Iron oxide hydroxide composite particles, pigment, paint and resin composition

Abstract

Iron oxide hydroxide composite particles having an average particle diameter of 0.005 to 1.0 μm, comprises:iron oxide hydroxide particles as core particles,a coating formed on surface of said iron oxide hydroxide particles, comprising at least one organosilicon compound selected from the group consisting of:(1) organosilane compounds obtainable from alkoxysilane compounds, and(2) polysiloxanes or modified polysiloxanes, andan organic pigment coat formed on said coating layer comprising said organosilicon compound, in an amount of from 1 to 30 parts by weight based on 100 parts by weight of said iron oxide hydroxide particles. The iron oxide hydroxide composite particles of the present invention contain no harmful elements and exhibit not only excellent chemical resistances such as acid resistance and alkali resistance, but also excellent heat resistance.

Description

BACKGROUND OF THE INVENTION

The present invention relates to iron oxide hydroxide composite particles, a pigment composed of the same, a paint containing the pigment, a resin composition containing the pigment and a process for producing the iron oxide hydroxide composite particles. More particularly, the present invention relates to iron oxide hydroxide composite particles containing no harmful elements and exhibiting not only excellent chemical resistances such as acid resistance and alkali resistance, but also excellent heat resistance, a pigment such as a green-based pigment or a orange-based pigment, composed of the iron oxide hydroxide composite particles, a paint containing the pigment, a resin composition containing the pigment and a process for producing the iron oxide hydroxide composite particles.

At present, as green-based pigments, there have been widely used inorganic pigments such as chrome green, chromium oxide and zinc green, and organic pigments such as phthalocyanine green. Also, as orange-based pigments, there have been used chrome vermilion, chrome orange, permanent orange, benzidine orange or the like. These pigments have been extensively applied to colorants of resins, paints, printing inks or the like.

However, it is known that the inorganic pigments such as chrome green, chromium oxide and zinc green tend to be deteriorated in chemical resistances such as acid resistance and alkali resistance though they are excellent in light resistance, and are expensive.

In addition, the inorganic pigments such as chrome green, chromium oxide and zinc green contain harmful elements such as lead and chromium. For this reason, it has been strongly required to develop alternate materials for these green-based pigments from viewpoints of hygiene, safety and environmental protection.

On the other hand, the organic green-based pigments such as phthalocyanine green exhibit a high tinting strength and a clear hue. However, it is known that these organic pigments are deteriorated in light resistance, i.e., suffer from bronze-bleeding (so-called bronzing) upon outdoor exposure.

Chrome vermilion and chrome orange exhibit a very clear hue. However, it is known that these orange-based pigments are deteriorated in chemical resistances such acid resistance and alkali resistance as well as light resistance and heat resistance, and are extensive.

In addition, the inorganic orange-based pigments such as chrome vermilion and chrome orange also contain harmful elements such as lead and chromium. Therefore, it has been strongly required to develop alternate materials for these orange-based pigments from viewpoints of hygiene, safety and environmental protection.

It is also known that the organic orange-based pigments such as permanent orange and benzidine orange exhibit a clear hue, but are deteriorated in light resistance.

Further, resin compositions using thermoplastic resins such as polyolefins, for example, polyethylenes, polypropylenes, styrene polymers or the like, polyamides and ABS resins are usually molded at a temperature as high as not less than 200° C. For this reason, pigments added as colorants to these resin compositions are required to exhibit a good heat resistance.

In consequence, green and orange-based pigments added to these resin compositions are strongly required to have not only excellent chemical resistances and tinting strength but also excellent heat resistance.

Hitherto, in order to improve properties of the pigments, it has been attempted to use inorganic and organic pigments in combination. For example, there have been proposed methods of co-precipitating chrome yellow and phthalocyanine blue together or adhering organic pigments onto the surfaces of inorganic pigments (Japanese Patent Application Laid-Open (KOKAI) Nos. 4-132770(1992), 10-88032(1998) and 11-181329(1999), etc.).

Thus, it has been strongly demanded to provide green and orange-based pigments exhibiting both excellent chemical resistances and excellent heat resistance without containing harmful elements. However, such pigments capable of satisfying these requirements have not been provided until now.

Namely, in the above method of co-precipitating chrome yellow and phthalocyanine blue together, the obtained pigments show a toxicity due to chrome yellow. Further, paints containing such pigments are insufficient in storage stability due to the use of co-precipitated pigments, so that coating films formed therefrom tend to suffer from bleeding.

In the method of precipitating organic pigments in the presence of inorganic pigments as described in Japanese Patent Application Laid-Open (KOKAI) No. 4-132770, the organic pigments are insufficient in adhesion to the inorganic pigments.

In the method of mechanically mixing and milling inorganic and organic pigments together as described in Japanese Patent Application Laid-Open (KOKAI) No. 10-88032(1998), the organic pigments are also insufficient in adhesion to the inorganic pigments.

Further, in Japanese Patent Application Laid-Open (KOKAI) No. 11-181329(1999), there is described the method of adding organic pigments to a solution prepared by dissolving organopolysiloxane in cyclic silicone to disperse therein the pigments as fine particles, impregnating the fine organic pigments with high oil-absorption inorganic pigments, and then evaporating cyclic silicone from the pigments. In this method, the organic pigments are also insufficient in adhesion to the inorganic pigments.

Meanwhile, in Japanese Patent Application Laid-Open (KOKAI) No. 11-323174(1999), there are described iron-based black composite particles obtained by forming an organosilane coating layer on black iron oxide particles or black iron oxide hydroxide particles, and then forming a carbon black coat on the organosilane coating layer. Since the iron-based black composite particles are black iron oxide hydroxide composite particles having the carbon black coat, the iron-based black composite particles are quite different from composite particles having green or orange-based pigments.

As a result of the present inventors' earnest studies, it has been found that by mixing as core particles iron oxide hydroxide particles with at least one compound selected from the group consisting of:

(1) alkoxysilane compounds, and

(2) polysiloxanes or modified polysiloxanes, by using an apparatus capable of applying a shear force to the core particles, thereby coating the surface of the black iron oxide hydroxide particle with the compounds;

mixing the obtained iron oxide hydroxide particles coated with the compounds and organic blue or red-based pigment in an amount of 1 to 30 parts by weight based on 100 parts by weight of the core particles by using an apparatus capable of applying a shear force to the core particles, thereby forming organic blue or red-based pigment coat on the surface of a coating layer comprising the organosilicon compounds, the thus obtained iron oxide hydroxide composite particles are harmless pigments which are excellent not only in chemical resistances such as acid resistance and alkali resistance, but also in heat resistance. The present invention has been attained on the basis of the above finding.

SUMMARY OF THE INVENTION

An object of the present invention is to provide a harmless pigment such as a harmless green or orange-based pigment exhibiting not only excellent chemical resistances such as acid resistance and alkali resistance, but also high hiding power, high tinting powder and excellent heat resistance.

Another object of the present invention is to provide a fine pigment such as a green or orange-based fine pigment which contains no harmful elements and is improved not only in chemical resistances such as acid resistance and alkali resistance but also in heat resistance, and further is capable of producing a paint and a resin composition exhibiting an excellent transparency.

To accomplish the aim of the present invention, in a first aspect of the present invention, there are provided iron oxide hydroxide composite particles having an average particle diameter (average major axial diameter) of 0.005 to 1.0 μm, comprising:

iron oxide hydroxide particles as core particles,

a coating formed on surface of the iron oxide hydroxide particles, comprising at least one organosilicon compound selected from the group consisting of:

(1) organosilane compounds obtainable from alkoxysilane compounds, and

(2) polysiloxanes or modified polysiloxanes, and

an organic pigment coat formed on the coating layer comprising the organosilicon compound, in an amount of from 1 to 30 parts by weight based on 100 parts by weight of the iron oxide hydroxide particles.

In a second aspect of the present invention, there are provided iron oxide hydroxide composite particles having an average particle diameter of 0.005 to 1.0 μm, comprising:

iron oxide hydroxide particles as core particles,

a coat formed on at least a part of the surface of the iron oxide hydroxide particles, comprising at least one compound selected from the group consisting of hydroxides of aluminum, oxides of aluminum, hydroxides of silicon and oxides of silicon;

a coating formed on surface of the said coat, comprising at least one organosilicon compound selected from the group consisting of:

(1) organosilane compounds obtainable from alkoxysilane compounds, and

(2) polysiloxanes or modified polysiloxanes, and

an organic pigment coat formed on the coating layer comprising the organosilicon compound, in an amount of from 1 to 30 parts by weight based on 100 parts by weight of the iron oxide hydroxide particles.

In a third aspect of the present invention, there are provided iron oxide hydroxide composite particles having an average particle diameter of from 0.005 to less than 0.1 μm, comprising:

iron oxide hydroxide particles as core particles,

a coating formed on surface of the iron oxide hydroxide particles, comprising at least one organosilicon compound selected from the group consisting of:

(1) organosilane compounds obtainable from alkoxysilane compounds, and

(2) polysiloxanes or modified polysiloxanes, and

an organic blue-based pigment coat formed on the coating layer comprising the organosilicon compound, in an amount of from 5 to 30 parts by weight based on 100 parts by weight of the iron oxide hydroxide particles.

In a fourth aspect of the present invention, there are provided iron oxide hydroxide composite particles having an average particle diameter of from 0.005 to less than 0.1 μm, comprising:

iron oxide hydroxide particles as core particles,

a coat formed on at least a part of the surface of the iron oxide hydroxide particles, comprising at least one compound selected from the group consisting of hydroxides of aluminum, oxides of aluminum, hydroxides of silicon and oxides of silicon;

a coating formed on surface of the said coat, comprising at least one organosilicon compound selected from the group consisting of:

(1) organosilane compounds obtainable from alkoxysilane compounds, and

(2) polysiloxanes or modified polysiloxanes, and

an organic blue-based pigment coat formed on the coating layer comprising the organosilicon compound, in an amount of from 5 to 30 parts by weight based on 100 parts by weight of the iron oxide hydroxide particles.

In a fifth aspect of the present invention, there are provided iron oxide hydroxide composite particles having an average particle diameter of from 0.005 to less than 0.1 μm, comprising:

iron oxide hydroxide particles as core particles,

a coating formed on surface of the iron oxide hydroxide particles, comprising at least one organosilicon compound selected from the group consisting of:

(1) organosilane compounds obtainable from alkoxysilane compounds, and

(2) polysiloxanes or modified polysiloxanes, and

an organic red-based pigment coat formed on the coating layer comprising the organosilicon compound, in an amount of from 1 to 30 parts by weight based on 100 parts by weight of the iron oxide hydroxide particles.

In a sixth aspect of the present invention, there are provided iron oxide hydroxide composite particles having an average particle diameter of from 0.005 to less than 0.1 μm, comprising:

iron oxide hydroxide particles as core particles,

a coat formed on at least a part of the surface of the iron oxide hydroxide particles, comprising at least one compound selected from the group consisting of hydroxides of aluminum, oxides of aluminum, hydroxides of silicon and oxides of silicon;

a coating formed on surface of the said coat, comprising at least one organosilicon compound selected from the group consisting of:

(1) organosilane compounds obtainable from alkoxysilane compounds, and

(2) polysiloxanes or modified polysiloxanes, and an organic red-based pigment coat formed on the coating layer comprising the organosilicon compound, in an amount of from 1 to 30 parts by weight based on 100 parts by weight of the iron oxide hydroxide particles.

In a seventh aspect of the present invention, there are provided iron oxide hydroxide composite particles having an average particle diameter of from 0.1 to 1.0 μm, comprising:

iron oxide hydroxide particles as core particles,

a coating formed on surface of the iron oxide hydroxide particles, comprising at least one organosilicon compound selected from the group consisting of:

(1) organosilane compounds obtainable from alkoxysilane compounds, and

(2) polysiloxanes or modified polysiloxanes, and an organic blue-based pigment coat formed on the coating layer comprising the organosilicon compound, in an amount of from 5 to 30 parts by weight based on 100 parts by weight of the iron oxide hydroxide particles.

In an eighth aspect of the present invention, there are provided iron oxide hydroxide composite particles having an average particle diameter of from 0.1 to 1.0 μm, comprising:

iron oxide hydroxide particles as core particles,

a coat formed on at least a part of the surface of the iron oxide hydroxide particles, comprising at least one compound selected from the group consisting of hydroxides of aluminum, oxides of aluminum, hydroxides of silicon and oxides of silicon;

a coating formed on surface of the said coat, comprising at least one organosilicon compound selected from the group consisting of:

(1) organosilane compounds obtainable from alkoxysilane compounds, and

(2) polysiloxanes or modified polysiloxanes, and

an organic blue-based pigment coat formed on the coating layer comprising the organosilicon compound, in an amount of from 5 to 30 parts by weight based on 100 parts by weight of the iron oxide hydroxide particles.

In a ninth aspect of the present invention, there are provided iron oxide hydroxide composite particles having an average particle diameter of from 0.1 to 1.0 μm, comprising:

iron oxide hydroxide particles as core particles,

a coating formed on surface of the iron oxide hydroxide particles, comprising at least one organosilicon compound selected from the group consisting of:

(1) organosilane compounds obtainable from alkoxysilane compounds, and

(2) polysiloxanes or modified polysiloxanes, and

an organic red-based pigment coat formed on the coating layer comprising the organosilicon compound, in an amount of from 1 to 30 parts by weight based on 100 parts by weight of the iron oxide hydroxide particles.

In a tenth aspect of the present invention, there are provided iron oxide hydroxide composite particles having an average particle diameter of from 0.1 to 1.0 μm, comprising:

iron oxide hydroxide particles as core particles,

a coat formed on at least a part of the surface of the iron oxide hydroxide particles, comprising at least one compound selected from the group consisting of hydroxides of aluminum, oxides of aluminum, hydroxides of silicon and oxides of silicon;

a coating formed on surface of the said coat, comprising at least one organosilicon compound selected from the group consisting of:

(1) organosilane compounds obtainable from alkoxysilane compounds, and

(2) polysiloxanes or modified polysiloxanes, and

an organic red-based pigment coat formed on the coating layer comprising the organosilicon compound, in an amount of from 1 to 30 parts by weight based on 100 parts by weight of the iron oxide hydroxide particles.

In an eleventh aspect of the present invention, there is provided a pigment comprising iron oxide hydroxide composite particles having an average particle diameter of 0.005 to 1.0 μm, comprising:

iron oxide hydroxide particles as core particles,

a coating formed on surface of the iron oxide hydroxide particles, comprising at least one organosilicon compound selected from the group consisting of:

(1) organosilane compounds obtainable from alkoxysilane compounds, and

(2) polysiloxanes or modified polysiloxanes, and

an organic pigment coat formed on the coating layer comprising the organosilicon compound, in an amount of from 1 to 30 parts by weight based on 100 parts by weight of the iron oxide hydroxide particles.

In a twelfth aspect of the present invention, there is provided a pigment comprising iron oxide hydroxide composite particles having an average particle diameter of 0.005 to 1.0 μm, comprising:

iron oxide hydroxide particles as core particles,

a coat formed on at least a part of the surface of the iron oxide hydroxide particles, comprising at least one compound selected from the group consisting of hydroxides of aluminum, oxides of aluminum, hydroxides of silicon and oxides of silicon;

a coating formed on surface of the said coat, comprising at least one organosilicon compound selected from the group consisting of:

(1) organosilane compounds obtainable from alkoxysilane compounds, and

(2) polysiloxanes or modified polysiloxanes, and

an organic pigment coat formed on the coating layer comprising the organosilicon compound, in an amount of from 1 to 30 parts by weight based on 100 parts by weight of the iron oxide hydroxide particles.

In a thirteenth aspect of the present invention, there is provided a green-based pigment comprising iron oxide hydroxide composite particles having an average particle diameter of 0.005 to 1.0 μm, comprising:

iron oxide hydroxide particles as core particles,

a coating formed on surface of the iron oxide hydroxide particles, comprising at least one organosilicon compound selected from the group consisting of:

(1) organosilane compounds obtainable from alkoxysilane compounds, and

(2) polysiloxanes or modified polysiloxanes, and

an organic blue-based pigment coat formed on the coating layer comprising the organosilicon compound, in an amount of from 5 to 30 parts by weight based on 100 parts by weight of the iron oxide hydroxide particles.

In fourteenth aspect of the present invention, there is provided an orange-based pigment comprising iron oxide hydroxide composite particles having an average particle diameter of 0.005 to 1.0 μm, comprising:

iron oxide hydroxide particles as core particles,

a coating formed on surface of the iron oxide hydroxide particles, comprising at least one organosilicon compound selected from the group consisting of:

(1) organosilane compounds obtainable from alkoxysilane compounds, and

(2) polysiloxanes or modified polysiloxanes, and

an organic red-based pigment coat formed on the coating layer comprising the organosilicon compound, in an amount of from 1 to 30 parts by weight based on 100 parts by weight of the iron oxide hydroxide particles.

In a fifteenth aspect of the present invention, there is provided a paint comprising:

a paint base material, and

a pigment comprising iron oxide hydroxide composite particles having an average particle diameter of 0.005 to 1.0 μm, comprising:

iron oxide hydroxide particles as core particles,

a coating formed on surface of the iron oxide hydroxide particles, comprising at least one organosilicon compound selected from the group consisting of:

(1) organosilane compounds obtainable from alkoxysilane compounds, and

(2) polysiloxanes or modified polysiloxanes, and an organic pigment coat formed on the coating layer comprising the organosilicon compound, in an amount of from 1 to 30 parts by weight based on 100 parts by weight of the iron oxide hydroxide particles.

In a sixteenth aspect of the present invention, there is provided a rubber or resin composition comprising:

a base material for rubber or resin composition, and

a pigment comprising iron oxide hydroxide composite particles having an average particle diameter of 0.005 to 1.0 μm, comprising:

iron oxide hydroxide particles as core particles,

a coating formed on surface of the iron oxide hydroxide particles, comprising at least one organosilicon compound selected from the group consisting of:

(1) organosilane compounds obtainable from alkoxysilane compounds, and

(2) polysiloxanes or modified polysiloxanes, and

an organic pigment coat formed on the coating layer comprising the organosilicon compound, in an amount of from 1 to 30 parts by weight based on 100 parts by weight of the iron oxide hydroxide particles.

DETAILED DESCRIPTION OF THE INVENTION

First, the pigment such as green or orange-based pigment according to the present invention will be explained below.

The pigment of the present invention is composed of iron oxide hydroxide composite particles which comprise iron oxide hydroxide particles as core particles, a coating layer of organosilicon compounds formed on the surface of the core particle, and an organic blue-based pigment or an organic red-based pigment adhered on the coating layer, and have an average major axial diameter of from 0.005 to 1.0 μm.

The above iron oxide hydroxide composite particles of the present invention are generally classified into:

(1) iron oxide hydroxide composite particles comprising iron oxide hydroxide particles as core particles, a coating layer of organosilicon compounds formed on the surface of the core particle, and an organic blue-based pigment or an organic red-based pigment adhered on the coating layer, and having an average major axial diameter of 0.1 to 1.0 μm; and

(2) fine iron oxide hydroxide composite particles comprising fine iron oxide hydroxide particles as core particles, a coating layer of organosilicon compounds formed on the surface of the core particle, and an organic blue-based pigment or an organic red-based pigment adhered on the coating layer, and having an average major axial diameter of from 0.005 to less than 0.1 μm.

The iron oxide hydroxide particles used as core particles in the present invention are of an acicular shape or a rectangular shape. The “acicular” shape used herein may include a spindle shape and a rice-ball shape in addition to literally acicular or needle-like shape.

The iron oxide hydroxide particles used in the present invention include goethite (α-FeOOH) particles and lepidocrocite (γ-FeOOH) particles. In the consideration of heat resistance of the obtained pigments, iron oxide hydroxide particles obtained by subjecting iron oxide hydroxide particles to heat resistance-imparting treatments is preferred. More specifically, the preferred iron oxide hydroxide particles used as core particles in the present invention may include iron oxide hydroxide particles whose surfaces are coated with at least one compound selected from the group consisting of hydroxides of aluminum and oxides of aluminum; iron oxide hydroxide particles containing aluminum inside thereof; iron oxide hydroxide particles having a coating layer composed of an iron and aluminum oxide hydroxide composite on the surface thereof; and iron oxide hydroxide particles subjected to any two or more of the above heat resistance-imparting treatments.

In the case of the iron oxide hydroxide particles whose surfaces are coated with at least one compound selected from the group consisting of hydroxides of aluminum and oxides of aluminum, the aluminum content thereof is 0.1 to 20.0% by weight (calculated as Al) based on the weight of the iron oxide hydroxide particles coated. In the case of the iron oxide hydroxide particles containing aluminum inside thereof, the aluminum content thereof is 0.05 to 50% by weight (calculated as Al) based on the weight of the iron oxide hydroxide particles containing aluminum inside thereof. In the case of the iron oxide hydroxide particles having a coasting layer composed of an iron and aluminum oxide hydroxide composite on the surfaces thereof, the aluminum content thereof is 0.1 to 10% by weight (calculated as Al) based on the weight of the iron oxide hydroxide particles, and the iron content thereof is 0.1 to 30% by weight (calculated as Fe) based on the weight of the iron oxide hydroxide particles.

The iron oxide hydroxide particles used in the present invention have an average major axial diameter of 0.005 to 1.0 μm; an average minor axial diameter of 0.0025 to 0.5 μm; an aspect ratio of 2:1 to 20:1; a BET specific surface area value of 5 to 300 m 2 /g; and a geometrical standard deviation of major axial diameters of 1.01 to 2.0. As to the hue of the iron oxide hydroxide particles, the L* value thereof is 40 to 80; the a* value thereof is −57.7 to +57.7 (a* value≢0); and the b* value thereof is from more than 0 to +100; and the h value thereof is from more than 60° to less than 120°.

More specifically, the following two kinds of iron oxide hydroxide particles as classified based on average major axial diameter thereof, are individually explained.

(1) In the case of iron oxide hydroxide particles having an average major axial diameter of 0.1 to 1.0 μm:

The average major axial diameter of the iron oxide hydroxide particles (1) is usually 0.1 to 1.0 μm, preferably 0.15 to 0.9 μm.

When the average major axial diameter is more than 1.0 μm, the obtained pigments become coarse particles, resulting in deteriorated tinting strength.

The average minor axial diameter of the iron oxide hydroxide particles (1) is usually 0.05 to 0.5 μm, preferably 0.075 to 0.45 μm.

The aspect ratio (ratio of average major axial diameter to average minor axial diameter; hereinafter referred to merely as “aspect ratio”) is usually not more than 20:1, preferably 2:1 to 15:1.

When the aspect ratio is more than 20:1, the particles may tend to be entangled or interlaced with each other, so that it may be difficult to uniformly form a coating layer of organosilicon compounds on the surface of each iron oxide hydroxide particle and uniformly adhere the organic pigment thereonto.

The geometrical standard deviation value of major axial diameters is usually not more than 2.0, preferably not more than 1.8, more preferably not more than 1.6.

When the geometrical standard deviation value is more than 2.0, a large amount of coarse particles may be present, so that the particles may be inhibited from being uniformly dispersed. As a result, it may be difficult to uniformly form a coating layer of organosilicon compounds on the surface of each iron oxide hydroxide particle and uniformly adhere the organic pigment thereonto. The lower limit of the geometrical standard deviation value is 1.01. It is difficult to industrially produce iron oxide hydroxide particles having a geometrical standard deviation value of less than 1.01.

The BET specific surface area value is usually 5 to 150 m 2 /g, preferably 10 to 120 m 2 /g, more preferably 15 to 100 m 2 /g.

When the BET specific surface area value is less than 5 m 2 /g, the iron oxide hydroxide particles may become coarse or tend to be sintered together. As a result, the obtained particles may become coarse, resulting in deteriorated tinting strength.

As to the hue of the iron oxide hydroxide particles (1), the L* value thereof is 40 to 80; the a* value thereof is −57.7 to +57.7 (a* value≢0); the b* value thereof is from more than 0 to +100; and the h value thereof is from more than 60° to less than 120°. When any of the L*, a*, b* and h values is out of the above specified range, the aimed pigments such as green or orange-based pigments according to the present invention may not be obtained.

(2) In the case of iron oxide hydroxide fine particles having an average major axial diameter of from 0.005 μm to less than 0.1 μm:

The average major axial diameter thereof is usually from 0.005 μm to less than 0.1 μm. When the average major axial diameter is less than 0.005 μm, the particles may tend to be agglomerated together due to increase in intermolecular force therebetween. As a result, it may be difficult to uniformly form a coating layer of organosilicon compounds on the surface of each iron oxide hydroxide fine particle and uniformly adhere the organic pigment thereonto.

In the consideration of uniform formation of the coating layer of organosilicon compounds on the surface of each iron oxide hydroxide fine particle, uniform adhesion of the organic pigment thereonto, and the average major axial diameter is preferably 0.008 to 0.096 μm, more preferably 0.01 to 0.092.

The average minor axial diameter thereof is usually from 0.0025 to less than 0.05 μm, preferably 0.004 to 0.048 μm, more preferably 0.005 to 0.046 μm; the aspect ratio thereof is usually not more than 20:1, preferably not more than 15:1, more preferably not more than 10:1 (lower limit of the aspect ratio: 2:1); the BET specific surface area value thereof is usually 50 to 300 m 2 /g, preferably 70 to 280 m 2 /g, more preferably 80 to 250 m 2 /g; and the geometrical standard deviation value of major axial diameters thereof is usually not more than 2.0, preferably not more than 1.8, more preferably not more than 1.6 (lower limit of the geometrical standard deviation value: 1.01).

When the average minor axial diameter is less than 0.0025 μm, the intermolecular force between the particles may become large due to fineness thereof, so that it may become difficult to uniformly form a coating layer of organosilicon compounds on the surface of each iron oxide hydroxide fine particle and uniformly adhere the organic pigment thereonto.

When the BET specific surface area value is more than 300 m 2 /g, the intermolecular force between the particles may become large due to fineness thereof, so that it may be difficult to uniformly form a coating layer of organosilicon compounds on the surface of each iron oxide hydroxide fine particle and uniformly adhere the organic pigment thereonto.

As to the hue of the iron oxide hydroxide fine particles (2) used in the present invention, the L* value thereof is 40 to 80; the a* value thereof is −57.7 to +57.7 (a* value≢0); the b* value thereof is from more than to +100; and the h value thereof is from more than 60° to less than 120°. When any of the L*, a* and b* values is out of the above specified range, the aimed fine pigments such as green or orange-based fine pigments according to the present invention may not be obtained.

The iron oxide hydroxide fine particles (2) used in the present invention have a hiding power of preferably less than 600 cm 2 /g, more preferably not more than 500 cm 2 /g. When the hiding power is not less than 600 cm 2 /g, the fine pigments obtained using the iron oxide hydroxide fine particles as core particles may show a too high hiding power.

As to the chemical resistances of the iron oxide hydroxide fine particles (2) used in the present invention, the acid resistance (ΔE*) thereof is preferably not more than 3.0, more preferably not more than 2.5; and the alkali resistance (ΔE*) thereof is preferably not more than 3.0, more preferably not more than 2.5, when measured by the evaluation methods described hereinafter. When any of the acid and alkali resistances (ΔE*) is more than 3.0, it may be difficult to obtain the aimed fine pigments such as green or orange-based fine pigments having excellent chemical resistances according to the present invention.

As to the heat resistance of the iron oxide hydroxide particles used in the present invention, the heat resistance temperature thereof is preferably not less than 180° C., more preferably not less than 185° C. In the consideration of the heat resistance of the obtained pigments such as green or orange-based pigments, the use of iron oxide hydroxide particles subjected to heat resistance-imparting treatments is preferred. In the case of the iron oxide hydroxide particles whose surfaces are coated with at least one compound selected from the group consisting of hydroxides of aluminum and oxides of aluminum, the heat resistance temperature thereof is about 240° C. In the case of the iron oxide hydroxide particles containing aluminum inside thereof, the heat resistance temperature thereof is about 245° C. Also, in the case of the iron oxide hydroxide particles having a coating layer composed of an aluminum and iron oxide hydroxide composite on the surfaces thereof, the heat resistance temperature thereof is about 250° C.

The coating formed on the surface of the core particle comprises at least one organosilicon compound selected from the group consisting of (1) organosilane compounds obtainable from alkoxysilane compounds; and (2) polysiloxanes and modified polysiloxanes selected from the group consisting of (2-A) polysiloxanes modified with at least one compound selected from the group consisting of polyethers, polyesters and epoxy compounds (hereinafter referred to merely as “modified polysiloxanes”), and (2-B) polysiloxanes whose molecular terminal is modified with at least one group selected from the group consisting of carboxylic acid groups, alcohol groups and a hydroxyl group (hereinafter referred to merely as “terminal-modified polysiloxanes”).

The organosilane compounds (1) may be produced by drying or heat-treating alkoxysilane compounds represented by the formula (I):

R 1 a SiX 4−a   (I)

wherein R 1 is C 6 H 5 —, (CH 3 ) 2 CHCH 2 — or n-C b H 2b+1 — (wherein b is an integer of 1 to 18); X is CH 3 O— or C 2 H 5 O—; and a is an integer of 0 to 3.

The drying or heat-treatment of the alkoxysilane compounds may be conducted, for example, at a temperature of usually 40 to 200° C., preferably 60 to 150° C. for usually 10 minutes to 12 hours, preferably 30 minutes to 3 hours.

Specific examples of the alkoxysilane compounds may include methyltriethoxysilane, dimethyldiethoxysilane, phenyltriethyoxysilane, diphenyldiethoxysilane, methyltrimethoxysilane, dimethyldimethoxysilane, phenyltrimethoxysilane, diphenyldimethoxysilane, isobutyltrimethoxysilane, decyltrimethoxysilane or the like. Among these alkoxysilane compounds, in view of the desorption percentage and the adhering effect of organic pigments, methyltriethoxysilane, phenyltriethyoxysilane, methyltrimethoxysilane, dimethyldimethoxysilane and isobutyltrimethoxysilane are preferred, and methyltriethoxysilane and methyltrimethoxysilane are more preferred.

As the polysiloxanes (2), there may be used those compounds represented by the formula (II):

wherein R 2 is H— or CH 3 —, and d is an integer of 15 to 450.

Among these polysiloxanes, in view of the desorption percentage and the adhering effect of the organic pigments, polysiloxanes having methyl hydrogen siloxane units are preferred.

As the modified polysiloxanes (2-A), there may be used:

(a) polysiloxanes modified with polyethers represented by the formula (III):

wherein R 3 is —(—CH 2 —) h —; R 4 is —(—CH 2 —) i —CH 3 ; R 5 is —OH, —COOH, —CH═CH 2 , —C(CH 3 )═CH 2 or —(—CH 2 —) j —CH 3 ; R 6 is —(—CH 2 —) k —CH 3 ; g and h are an integer of 1 to 15; i, j and k are an integer of 0 to 15; e is an integer of 1 to 50; and f is an integer of 1 to 300;

(b) polysiloxanes modified with polyesters represented by the formula (IV):

wherein R 7 , R 8 and R 9 are —(—CH 2 —) q — and may be the same or different; R 10 is —OH, —COOH, —CH═CH 2 , —C(CH 3 )═CH 2 or —(—CH 2 —) r —CH 3 ; R 11 is —(—CH 2 —) s —CH 3 ; n and q are an integer of 1 to 15; r and s are an integer of 0 to 15; e′ is an integer of 1 to 50; and f′ is an integer of 1 to 300;

(c) polysiloxanes modified with epoxy compounds represented by the formula (V):

wherein R 12 is —(—CH 2 —) v —; v is an integer of 1 to 15; t is an integer of 1 to 50; and u is an integer of 1 to 300; or a mixture thereof.

Among these modified polysiloxanes (2-A), in view of the desorption percentage and the adhering effect of the organic pigments, the polysiloxanes modified with the polyethers represented by the formula (III), are preferred.

As the terminal-modified polysiloxanes (2-B), there may be used those represented by the formula (VI):

wherein R 13 and R 14 are —OH, R 16 OH or R 17 COOH and may be the same or different; R 15 is —CH 3 or —C 6 H 5 ; R 16 and R 17 are —(—CH 2 —) y —; y is an integer of 1 to 15; w is an integer of 1 to 200; and x is an integer of 0 to 100.

Among these terminal-modified polysiloxanes, in view of the desorption percentage and the adhering effect of the organic pigments, the polysiloxanes whose terminals are modified with carboxylic acid groups are preferred.

The coating amount of the organosilicon compounds is usually 0.02 to 5.0% by weight, preferably 0.03 to 4.0% by weight, more preferably 0.05 to 3.0% by weight (calculated as Si) based on the weight of the iron oxide hydroxide particles coated with the organosilicon compounds.

When the coating amount of the organosilicon compounds is less than 0.02% by weight, it may be difficult to adhere the organic pigments in a predetermined.

When the coating amount of the organosilicon compounds is more than 5.0% by weight, the organic pigments can be adhered in a predetermined. Therefore, it is unnecessary and meaningless to coat the core particles with such a large amount of the organosilicon compounds.

As to the organic pigments used in the present invention, organic blue-based pigments and organic red-based pigments may be exemplified. The amount of the organic pigment such as organic blue-based pigments and organic red-based pigments adhered on the coating layer composed of organosilicon compounds is usually 1 to 30 parts based on 100 parts by weight of the iron oxide hydroxide particles.

As the organic blue-based pigments used in the present invention, there may be used phthalocyanine-based pigments such as metal-free phthalocyanine blue, phthalocyanine blue (copper phthalocyanine) and fast sky blue (sulfonated copper phthalocyanine), and alkali blue pigments, or the like. In the consideration of the hue of the obtained green-based fine pigments, among these pigments, the use of phthalocyanine blue is preferred.

In particular, in the consideration of light resistance, the use of low-chlorinated copper phthalocyanine, NC-type (non-crystallization-type) copper phthalocyanine or NC-type low-chlorinated copper phthalocyanine is preferred.

The amount of the organic blue-based pigment adhered is preferably 5 to 30 parts by weight based on 100 parts by weight of the iron oxide hydroxide particles.

When the amount of the organic blue-based pigment adhered is out of the above-mentioned range, it may be difficult to obtain the aimed green-based pigment of the present invention. The amount of the organic blue-based pigment adhered is more preferably 7.5 to 25 parts by weight based on 100 parts by weight of the iron oxide hydroxide particles.

As the organic red-based pigments used in the present invention, there may be used quinacridone-based pigments such as quinacridone red, azo-based pigments such as permanent red, condensed azo-based pigments such as condensed azo red, and perylene-based pigments such as perylene red. In the consideration of heat resistance and light resistance of the obtained orange-based pigments, the use of quinacridone-based pigments is preferred.

The amount of the organic red-based pigment adhered is usually 1 to 30 parts by weight based on 100 parts by weight of the iron oxide hydroxide particles. When the amount of the organic red-based pigment adhered is less than 1 part by weight or more than 30 parts by weight, it may be difficult to obtain the aimed orange-based pigment of the present invention. The amount of the organic red-based pigment adhered is preferably 3 to 25 parts by weight based on 100 parts by weight of the iron oxide hydroxide particles.

Phe shape and size of the green or orange-based pigments of the present invention considerably varies depending upon those of the iron oxide hydroxide particles as core particles, and usually have an analogous configuration to that of the iron oxide hydroxide particles.

For example, the green or orange-based pigment according to the present invention has an average major axial diameter of 0.005 to 1.0 μm; an average minor axial diameter of 0.0025 to 0.5 μm; an aspect ratio of 2.0:1 to 20:1; a BET specific surface area value of 6 to 300 m 2 /g; a geometrical standard deviation value of major axial diameters of 1.01 to 2.0; and a desorption percentage of the organic pigment of not more than 15%. As to the heat resistance of the green or orange-based pigment, the heat resistance temperature thereof is higher by +5 to +40° than that of the iron oxide hydroxide particles. As to the chemical resistances of the green or orange-based pigment, the acid resistance (ΔE* value) thereof is not more than 1.5, and the alkali resistance thereof is not more than 1.5, when evaluated by the method specified hereinafter.

Next, the properties of the green or orange-based pigments used on the present invention are more concretely explained as follows.

(1) In the case where iron oxide hydroxide particles having an average major axial diameter of 0.1 to 1.0 μm are used as core particles:

The green or orange-based pigment according to the present invention has an average major axial diameter of usually 0.1 to 1.0 μm, preferably 0.15 to 0.9 μm.

When the average major axial diameter of the green or orange-based pigment is more than 1.0 μm, the pigment particles may be larger, resulting in deteriorated tinting strength.

The green or orange-based pigment according to the present invention is of an acicular or rectangular shape.

The green or orange-based pigment according to the present invention has an aspect ratio of usually not more than 20:1, preferably 2:1 to 15:1, more preferably 2:1 to 10:1. When the aspect ratio of the green or orange-based pigment is more than 20:1, the pigment particles may tend to be entangled or interlaced with each other, resulting in poor dispersibility in vehicles or resin compositions as well as increased viscosity of the coating solution.

The green or orange-based pigment according to the present invention suitably has a geometrical standard deviation value of particle sizes of not more than 2.0. When the geometrical standard deviation value of particle sizes of the green or orange-based pigment is more than 2.0, a considerable amount of coarse particles are present, so that it may be difficult to uniformly disperse the pigment in vehicles or resin compositions. In the consideration of uniform dispersion in vehicles or resin compositions, the geometrical standard deviation value of particle sizes of the green or orange-based pigment is preferably not more than 1.8, more preferably not more than 1.6. In the consideration of industrial productivity, the lower limit of the geometrical standard deviation value of particle sizes of the green or orange-based pigment is 1.01, since it is difficult to industrially produce those pigments having a geometrical standard deviation value of less than 1.01.

The green or orange-based pigment according to the present invention has a BET specific surface area value of usually 6 to 160 M 2 /g, preferably 11 to 130 m 2 /g, more preferably 16 to 110 m 2 /g. When the BET specific surface area value of the green or orange-based pigment is less than 6 m 2 /g, the obtained green or orange-based pigment particles may be coarser, resulting in deteriorated tinting strength.

The green or orange-based pigment according to the present invention has a desorption percentage of the organic pigment of preferably not more than 15%, more preferably not more than 12%. When the desorption percentage of the organic pigment is more than 15%, the pigment particles may tend to be inhibited from being uniformly dispersed in vehicles or resin compositions due to desorbed organic pigment particles. Further, a portion of the surface of the iron oxide hydroxide core particle from which the organic pigment is desorbed, is exposed to outside, so that the obtained iron oxide hydroxide composite particles fail to exhibit a uniform hue.

Especially, as to the hue of the green-based pigment according to the present invention, the L* value thereof is 25 to 80; the a* value thereof is from −100 to less than 0; the b* value thereof is −100 to +100; and the h value thereof is 120° to 240°.

In addition, as to the hue of the orange-based pigment according to the present invention, the L* value thereof is 25 to 80; the a* value thereof is from more than 0 to +100; the b* value thereof is from more than 0 to +100; and the h value thereof is 30° to 60°.

As to the heat resistance of the green or orange-based pigment according to the present invention, the heat resistance temperature thereof is higher by +5 to +40° than that of the iron oxide hydroxide particles as core particles.

The green or orange-based pigment according to the present invention has a tinting strength of preferably not less than 115%, more preferably not less than 120%, when measured by the evaluation method specified hereinafter.

The green or orange-based pigment according to the present invention has a hiding power of preferably not less than 1,750 cm 2 /g, more preferably not less than 1,800 cm 2 /g, when measured by the evaluation method specified hereinafter.

As to the chemical resistances of the green or orange-based pigment according to the present invention, the acid resistance (ΔE* value) thereof is preferably not more than 1.5, more preferably not more than 1.2; and the alkali resistance (ΔE* value) thereof is preferably not more than 1.5, more preferably not more than 1.2, when measured by the evaluation method specified hereinafter.

(2) In the case where iron oxide hydroxide particles having an average major axial diameter of from 0.005 μm to less than 0.1 μm are used as core particles:

The green or orange-based fine pigment of the present invention has an average major axial diameter of from usually 0.005 μm to less than 0.1 μm, preferably 0.008 to 0.096 μm, more preferably 0.01 to 0.092 μm.

When the average major axial diameter of the green or orange-based fine pigment is less than 0.005 μm, the intermolecular force between the pigment particles may be increased due to fineness thereof, so that the particles may tend to be agglomerated together, resulting in poor dispersibility in vehicles or resin compositions.

The green or orange-based fine pigment of the present invention is also of an acicular or rectangular shape.

The green or orange-based fine pigment of the present invention has an aspect ratio of preferably not more than 20:1, more preferably 2:1 to 15:1, still more preferably 2:1 to 10:1. When the aspect ratio of the green or orange-based pigment is more than 20:1, the pigment particles may tend to be entangled or interlaced with each other, resulting in poor dispersibility in vehicles or resin compositions as well as increased viscosity of the obtained coating solution.

The green or orange-based fine pigment according to the present invention has an average minor axial diameter of usually from 0.0025 μm to less than 0.05 μm, preferably 0.004 to 0.048 μm, more preferably 0.005 to 0.046 μm. When the average minor axial diameter of the green or orange-based fine pigment is less than 0.0025 μm, the intermolecular force between the pigment particles may be increased due to fineness thereof, so that the particles may tend to be agglomerated together, resulting in poor dispersibility in vehicles or resin compositions.

The green or orange-based fine pigment according to the present invention suitably has a geometrical standard deviation value of particle sizes of usually not more than 2.0. When the geometrical standard deviation value of particle sizes of the green or orange-based fine pigment is more than 2.0, a considerable amount of coarse particles may be present, so that it may be difficult to uniformly disperse the fine pigment particles in vehicles or resin compositions. In the consideration of uniform dispersion in vehicles or resin compositions, the geometrical standard deviation value of particle sizes of the green or orange-based fine pigment is preferably not more than 1.8, more preferably not more than 1.6. In the consideration of industrial productivity, the lower limit of the geometrical standard deviation value of particle sizes of the green or orange-based fine pigment is 1.01, since it is difficult to industrially produce those pigments having a geometrical standard deviation value of less than 1.01.

The green or orange-based fine pigment according to the present invention has a BET specific surface area value of usually 50 to 300 m 2 /g, preferably 70 to 280 m 2 /g, more preferably 80 to 250 m 2 /g. When the BET specific surface area value of the green or orange-based fine pigment is less than 50 m 2 /g, the obtained green or orange-based fine pigment particles may be coarser, resulting in too high hiding power. As a result, coating films or resin compositions obtained using the green or orange-based fine pigment may fail to exhibit a sufficient transparency. On the other hand, when the BET specific surface area value of the green or orange-based fine pigment is more than 300 m 2 /g, the intermolecular force between the fine pigment particles may be increased due to fineness thereof, so that the particles may tend to be agglomerated together, resulting in poor dispersibility in vehicles or resin compositions.

The organic pigment constituting the green or orange-based fine pigment according to the present invention has a desorption percentage of the organic pigment of usually not more than 15%, preferably not more than 12%. When the desorption percentage of the organic pigment is more than 15%, the fine pigment particles tends to be inhibited from being uniformly dispersed in vehicles or resin compositions due to desorbed organic pigment particles. Further, a portion of the surface of the iron oxide hydroxide fine particles as core particle from which the organic pigment particles are desorbed, is exposed to outside, so that the obtained iron oxide hydroxide composite fine particles fail to exhibit a uniform hue.

Especially, as to the hue of the green-based fine pigment according to the present invention, the L* value thereof is usually 25 to 80; the a* value thereof is usually from −100 to less than 0; the b* value thereof is −100 to +100; and the h value thereof is usually 120 to 240°.

In addition, as to the hue of the orange-based fine pigment according to the present invention, the L* value thereof is usually 25 to 80; the a* value thereof is usually from more than 0 to +100; the b* value thereof is usually from more than 0 to +100; and the h value thereof is usually from 30° to 60°.

As to the heat resistance of the green or orange-based fine pigment according to the present invention, the heat resistance temperature thereof is usually higher by +5 to +40° than that of the iron oxide hydroxide fine particles as core particles, and is preferably not less than 210° C., more preferably not less than 215° C.

The green or orange-based fine pigment according to the present invention has a tinting strength of preferably not less than 115%, more preferably not less than 120%, when measured by the evaluation method specified hereinafter.

The green or orange-based fine pigment according to the present invention has a hiding power of preferably less than 600 cm 2 /g, more preferably not more than 500 cm 2 /g. When the hiding power of the green or orange-based fine pigment is not less than 600 cm 2 /g, coating films or resin compositions obtained using the green or orange-based fine pigment may fail to exhibit a sufficient transparency due to a too high hiding power thereof.

As to the chemical resistances of the green or orange-based fine pigment according to the present invention, the acid resistance (ΔE* value) thereof is preferably not more than 1.5, more preferably not more than 1.3; and the alkali resistance (ΔE* value) thereof is preferably not more than 1.5, more preferably not more than 1.3, when measured by the evaluation method specified hereinafter.

Before forming the coating layer comprising the organosilicon compound onto the iron oxide hydroxide particles, the surfaces of the core particles may be preliminarily coated with at least one compound selected from the group consisting of hydroxides of aluminum, oxides of aluminum, hydroxides of silicon and oxides of silicon (hereinafter referred to merely as “hydroxides and/or oxides of aluminum and/or silicon”). When the coating layer is formed on the surfaces of the core particles, the desorption percentage of the organic pigment from the surfaces of the iron oxide hydroxide particles can be reduced as compared to those having no coating layer, and the heat resistance of the obtained composite particles can be slightly increased.

The total coating amount of the hydroxides and/or oxides of aluminum and/or silicon is 0.01 to 20% by weight (calculated as Al, Si or a sum of Al and Si) based on the weight of the coated iron oxide hydroxide particles.

When the coating amount of the hydroxides and/or oxides of aluminum and/or silicon is less than 0.01% by weight, the effect of reducing the desorption percentage of the organic pigment may not be obtained. Since a sufficient effect of reducing the desorption percentage of the organic pigment can be obtained by adjusting the coating amount of the hydroxides and/or oxides of aluminum and/or silicon to 0.01 to 20% by weight, it is unnecessary and meaningless to coat the core particles with the hydroxides and/or oxides of aluminum and/or silicon in an amount of more than 20% by weight.

The green or orange-based pigment in which the iron oxide hydroxide particles coated with the hydroxides and/or oxides of aluminum and/or silicon are used as core particles, are substantially identical in particle size, geometrical standard deviation value, BET specific surface area value, hue, tinting strength, hiding power and chemical resistances to those used for the core particles having no coating layer composed of the hydroxides and/or oxides of aluminum and/or silicon. Also, by forming such a coating layer composed of the hydroxides and/or oxides of aluminum and/or silicon on the core particles, the desorption percentage of the organic pigment is improved, i.e., can be reduced to preferably not more than 12%, more preferably not more than 10%, and the heat resistance of the obtained composite particles becomes higher by +5 to +30° C. than those obtained by using the core particles having no coating layer composed of the hydroxides and/or oxides of aluminum and/or silicon.

Next, the paint containing the green or orange-based pigment according to the present invention, is described.

The paint containing the green or orange-based pigment according to the present invention has a storage stability (ΔE* value) of usually not more than 1.5, a gloss of 70 to 115% (in a coating film), a heat resistance temperature of usually not less than 220° C. (in a coating film), an acid resistance (ΔG value) as a chemical resistances of usually not more than 12% (in a coating film), an alkali resistance (ΔG value) as a chemical resistances of usually not more than 12% (in a coating film), and a L* value of usually 25 to 85 (in a coating film).

(A) Paint Containing the Green-Based Piment Having an Average Major Axial Diameter of 0.1 to 1.0 μm

The paint containing the green-based pigment according to the present invention has a storage stability (ΔE* value) of usually not more than 1.5, preferably not more than 1.2. When a coating film is produced by using the solvent-based paints, the gloss of the coating film is usually 75 to 110%, preferably 80 to 110%; and the heat resistance temperature of the coating film is usually not less than 240° C., preferably not less than 245° C. As to the chemical resistances of the coating film, the acid resistance (ΔG value) thereof is usually not more than 12%, preferably not more than 10%; and the alkali resistance (ΔG value) thereof is usually not more than 12%, preferably not more than 10%. As to the hue of the coating film produced from the paint, it is preferred that the L* value thereof is 25 to 85; the a* value thereof is from −100 to less than 0; the b* value thereof is −100 to +100; and the h value thereof is usually 120 to 240°.

The paint containing the green-based pigment obtained by using the core particles coated with the hydroxides and/or oxides of aluminum and/or silicon according to the present invention, has a storage stability (ΔE* value) of usually not more than 1.5, preferably not more than 1.2. When a coating film is produced by using the solvent-based paints, the gloss of the coating film is usually 80 to 115%, preferably 85 to 115%; and the heat resistance temperature of the coating film is usually not less than 245° C., preferably not less than 250° C. As to the chemical resistances of the coating film, the acid resistance (ΔG value) thereof is usually not more than 12%, preferably not more than 10%; and the alkali resistance (ΔG value) thereof is usually not more than 12%, preferably not more than 10%. As to the hue of the coating film produced from the paint, it is preferred that the L* value thereof is 25 to 85; the a* value thereof is from −100 to less than 0; the b* value thereof is −100 to +100; and the h value thereof is usually 120 to 240°.

The water-based paint containing the green-based pigment according to the present invention, has a storage stability (ΔE* value) of usually not more than 1.5, preferably not more than 1.2. When a coating film is produced by using the water-based paints, the gloss of the coating film is usually 70 to 110%, preferably 75 to 110%; and the heat resistance temperature of the coating film is usually not less than 235° C., preferably not less than 240° C. As to the chemical resistances of the coating film, the acid resistance (ΔG value) thereof is usually not more than 12%, preferably not more than 10%; and the alkali resistance (ΔG value) thereof is usually not more than 12%, preferably not more than 10%. As to the hue of the coating film produced from the water-based paint, it is preferred that the L* value thereof is 25 to 85; the a* value thereof is from −100 to less than 0; the b* value thereof is −100 to +100; and the h value thereof is usually 120 to 240°.

The water-based paint containing the green-based pigment obtained by using as the core particles iron oxide hydroxide particles coated with the hydroxides and/or oxides of aluminum and/or silicon according to the present invention, has a storage stability (ΔE* value) of usually not more than 1.5, preferably not more than 1.2. When a coating film is produced by using the water-based paints, the gloss of the coating film is usually 75 to 115%, preferably 80 to 115%; and the heat resistance temperature of the coating film is usually not less than 240° C., preferably not less than 245° C. As to the chemical resistances of the coating film, the acid resistance (ΔG value) thereof is usually not more than 12%, preferably not more than 10%; and the alkali resistance (ΔG value) thereof is usually not more than 12%, preferably not more than 10%. As to the hue of the coating film produced from the water-based paint, it is preferred that the L* value thereof is 25 to 85; the a* value thereof is from −100 to less than 0; the b* value thereof is −100 to +100; and the h value thereof is usually 120 to 240°.

(B) Paint Containing the Orange-Based Pigment Having an Average Major Axial Diameter of 0.1 to 1.0 μm

The paint containing the orange-based pigment according to the present invention has a storage stability (ΔE* value) of usually not more than 1.5, preferably not more than 1.2. When a coating film is produced by using the solvent-based paints, the gloss of the coating film is usually 75 to 110%, preferably 80 to 110%; and the heat resistance temperature of the coating film is usually not less than 240° C., preferably not less than 245° C. As to the chemical resistances of the coating film, the acid resistance (ΔG value) thereof is usually not more than 12%, preferably not more than 10%; and the alkali resistance (ΔG value) thereof is usually not more than 12%, preferably not more than 10%. As to the hue of the coating film produced from the paint, it is preferred that the L* value thereof is 25 to 85; the a* value thereof is from more than 0 to +100; the b* value thereof is from more than 0 to +100; and the h value thereof is 30 to 60°.

The paint containing the orange-based pigment obtained by using as the core particles iron oxide hydroxide particles coated with the hydroxides and/or oxides of aluminum and/or silicon according to the present invention, has a storage stability (ΔE* value) of usually not more than 1.5, preferably not more than 1.2. When a coating film is produced by using the solvent-based paints, the gloss of the coating film is usually 80 to 115%, preferably 85 to 115%; and the heat resistance temperature of the coating film is usually not less than 245° C., preferably not less than 250° C. As to the chemical resistances of the coating film, the acid resistance (ΔG value) thereof is usually not more than 12%, preferably not more than 10%; and the alkali resistance (ΔG value) thereof is usually not more than 12%, preferably not more than 10%. As to the hue of the coating film produced from the paint, it is preferred that the L* value thereof is 25 to 85; the a* value thereof is from more than 0 to +100; the b* value thereof is from more than 0 to +100; and the h value thereof is 30 to 60°.

The water-based paint containing the orange-based pigment according to the present invention, has a storage stability (ΔE* value) of usually not more than 1.5, preferably not more than 1.2. When a coating film is produced by using the water-based paints, the gloss of the coating film is usually 70 to 110%, preferably 75 to 110%; and the heat resistance temperature of the coating film is usually not less than 235° C., preferably not less than 240° C. As to the chemical resistances of the coating film, the acid resistance (ΔG value) thereof is usually not more than 12%, preferably not more than 10%; and the alkali resistance (ΔG value) thereof is usually not more than 12%, preferably not more than 10%. As to the hue of the coating film produced from the water-based paint, it is preferred that the L* value thereof is 25 to 85; the a* value thereof is from more than 0 to +100; the b* value thereof is from more than 0 to +100; and the h value thereof is 30 to 60°.

The water-based paint containing the orange-based pigment obtained by using as the core particles iron oxide hydroxide particles coated with the hydroxides and/or oxides of aluminum and/or silicon according to the present invention, has a storage stability (ΔE* value) of usually not more than 1.5, preferably not more than 1.2. When a coating film is produced by using the water-based paints, the gloss of the coating film is usually 75 to 115%, preferably 80 to 115%; and the heat resistance temperature of the coating film is usually not less than 240° C., preferably not less than 245° C. As to the chemical resistances of the coating film, the acid resistance (ΔG value) thereof is usually not more than 12%, preferably not more than 10%; and the alkali resistance (ΔG value) thereof is usually not more than 12%, preferably not more than 10%. As to the hue of the coating film produced from the water-based paint, it is preferred that the L* value thereof is 25 to 85; the a* value thereof is from more than 0 to +100; the b* value thereof is from more than 0 to +100; and the h value thereof is 30 to 60°.

(C) Paint Containing the Green-Based Fine Pigment Having an Average Major Axial Diameter of from 0.005 to Less Than 0.1 μm

The paint containing the green-based fine pigment according to the present invention has a storage stability (ΔE* value) of usually not more than 1.5, preferably not more than 1.3. When a coating film is produced by using the solvent-based paints, the gloss of the coating film is usually 75 to 110%, preferably 80 to 110%; and the heat resistance temperature of the coating film is usually not less than 220° C., preferably not less than 225° C. As to the chemical resistances of the coating film, the acid resistance (ΔG value) thereof is usually not more than 12%, more preferably not more than 10%; and the alkali resistance (ΔG value) thereof is usually not more than 12%, preferably not more than 10%. As to the hue of the coating film produced from the paint, it is preferred that the L* value thereof is 25 to 85; the a* value thereof is from −100 to less than 0; and the b* value thereof is −100 to +100; and the h value thereof is 120 to 240°. As to the transparency of the coating film, the linear absorption thereof is preferably not more than 0.05 μm −1 .

The paint containing the green-based fine pigment obtained by using as the core particles iron oxide hydroxide particles coated with the hydroxides and/or oxides of aluminum and/or silicon according to the present invention, has a storage stability (ΔE* value) of usually not more than 1.5, preferably not more than 1.3. When a coating film is produced by using the solvent-based paints, the gloss of the coating film is usually 80 to 115%, preferably 85 to 115%; and the heat resistance temperature of the coating film is usually not less than 230° C., preferably not less than 235° C. As to the chemical resistances of the coating film, the acid resistance (ΔG value) thereof is usually not more than 12%, preferably not more than 10%; and the alkali resistance (ΔG value) thereof is usually not more than 12%, preferably not more than 10%. As to the hue of the coating film produced from the paint, it is preferred that the L* value thereof is 25 to 85; the a* value thereof is from −100 to less than 0; the b* value thereof is −100 to +100; and the h value thereof is 120 to 240°. As to the transparency of the coating film, the linear absorption thereof is preferably not more than 0.05 μm −1 .

The water-based paint containing the green-based fine pigment according to the present invention, has a storage stability (ΔE* value) of usually not more than 1.5, preferably not more than 1.3. When a coating film is produced by using the water-based paints, the gloss of the coating film is usually 70 to 110%, preferably 75 to 110%; and the heat resistance temperature of the coating film is usually not less than 220° C., preferably not less than 225° C. As to the chemical resistances of the coating film, the acid resistance (ΔG value) thereof is usually not more than 12%, preferably not more than 10%; and the alkali resistance (ΔG value) thereof is usually not more than 12%, preferably not more than 10%. As to the hue of the coating film produced from the water-based paint, it is preferred that the L* value thereof is 25 to 85; the a* value thereof is from −100 to less than 0; and the b* value thereof is −100 to +100. As to the transparency of the coating film, the linear absorption thereof is preferably not more than 0.05 μm −1 .

The water-based paint containing the green-based fine pigment obtained by using as the core particles iron oxide hydroxide particles coated with the hydroxides and/or oxides of aluminum and/or silicon according to the present invention, has a storage stability (ΔE* value) of usually not more than 1.5, preferably not more than 1.3. When a coating film is produced by using the water-based paints, the gloss of the coating film is usually 75 to 115%, preferably 80 to 115%; and the heat resistance temperature of the coating film is usually not less than 230° C., preferably not less than 235° C. As to the chemical resistances of the coating film, the acid resistance (ΔG value) thereof is usually not more than 12%, preferably not more than 10%; and the alkali resistance (ΔG value) thereof is usually not more than 12%, preferably not more than 10%. As to the hue of the coating film produced from the water-based paint, it is preferred that the L* value thereof is 25 to 85; the a* value thereof is from −100 to less than 0; and the b* value thereof is −100 to +100; and the h value thereof is 120 to 240°. As to the transparency of the coating film, the linear absorption thereof is preferably not more than 0.05 μm −1 .

(D) Paint Containing the Orange-Based Fine Pigment Having an Average Major Axial Diameter of from 0.005 μm to Less Than 0.1 μm

The paint containing the orange-based fine pigment according to the present invention, has a storage stability (ΔE* value) of usually not more than 1.5, preferably not more than 1.3. When a coating film is produced by using the solvent-based paints, the gloss of the coating film is usually 75 to 110%, preferably 80 to 110%; and the heat resistance temperature of the coating film is usually not less than 220° C., preferably not less than 225° C. As to the chemical resistances of the coating film, the acid resistance (ΔG value) thereof is usually not more than 12%, preferably not more than 10%; and the alkali resistance (ΔG value) thereof is usually not more than 12%, preferably not more than 10%. As to the hue of the coating film produced from the paint, it is preferred that the L* value thereof is 25 to 85; the a* value thereof is from more than 0 to +100; the b* value thereof is from more than 0 to +100; and the h value thereof is 30 to 60°. As to the transparency of the coating film, the linear absorption thereof is preferably not more than 0.05 μm −1 .

The paint containing the orange-based fine pigment obtained by using as the core particles iron oxide hydroxide particles coated with the hydroxides and/or oxides of aluminum and/or silicon according to the present invention, has a storage stability (ΔE* value) of usually not more than 1.5, preferably not more than 1.3. When a coating film is produced by using the solvent-based paints, the gloss of the coating film is usually 80 to 115%, preferably 85 to 115%; and the heat resistance temperature of the coating film is usually not less than 230° C., preferably not less than 235° C. As to the chemical resistances of the coating film, the acid resistance (ΔG value) thereof is usually not more than 12%, preferably not more than 10%; and the alkali resistance (ΔG value) thereof is usually not more than 12%, preferably not more than 10%. As to the hue of the coating film produced from the paint, it is preferred that the L* value thereof is 25 to 85; the a* value thereof is from more than 0 to +100; the b* value thereof is from more than 0 to +100; and the h value thereof is 30 to 60°. As to the transparency of the coating film, the linear absorption thereof is preferably not more than 0.05 μm −1 .

The water-based paint containing the orange-based fine pigment according to the present invention, has a storage stability (ΔE* value) of usually not more than 1.5, preferably not more than 1.3. When a coating film is produced by using the water-based paints, the gloss of the coating film is usually 70 to 110%, preferably 75 to 110%; and the heat resistance temperature of the coating film is usually not less than 220° C., preferably not less than 225° C. As to the chemical resistances of the coating film, the acid resistance (ΔG value) thereof is usually not more than 12%, preferably not more than 10%; and the alkali resistance (ΔG value) thereof is usually not more than 12%, preferably not more than 10%. As to the hue of the coating film produced from the water-based paint, it is preferred that the L* value thereof is 25 to 85; the a* value thereof is from more than to +100; the b* value thereof is from more than to +100; and the h value thereof is 30 to 60°. As to the transparency of the coating film, the linear absorption thereof is preferably not more than 0.05 μm −1 .

The water-based paint containing the orange-based fine pigment obtained by using as the core particles iron oxide hydroxide particles coated with the hydroxides and/or oxides of aluminum and/or silicon according to the present invention, has a storage stability (ΔE* value) of usually not more than 1.5, preferably not more than 1.3. When a coating film is produced by using the water-based paints, the gloss of the coating film is usually 75 to 115%, preferably 80 to 115%; and the heat resistance temperature of the coating film is usually not less than 230° C., preferably not less than 235° C. As to the chemical resistances of the coating film, the acid resistance (ΔG value) thereof is usually not more than 12%, preferably not more than 10%; and the alkali resistance (ΔG value) thereof is usually not more than 12%, preferably not more than 10%. As to the hue of the coating film produced from the water-based paint, it is preferred that the L* value thereof is 25 to 85; the a* value thereof is from more than 0 to +100; the b* value thereof is from more than 0 to +100; and the h value thereof is 30 to 60°. As to the transparency of the coating film, the linear absorption thereof is preferably not more than 0.05 μm −1 .

In the paint of the present invention, the lower limit of the amount of the green or orange-based pigment blended therein usually 0.5 part by weight, preferably 1.0 part by weight, more preferably 2.0 parts by weight based on 100 parts by weight of a paint base material; and the upper limit of the amount of the green or orange-based pigment blended therein is usually 100 parts by weight, preferably 80 parts by weight, more preferably 50 parts by weight based on 100 parts by weight of the paint base material.

The paint based material contains green or orange-based pigments, resins and solvents, and may optionally contain defoamers, extender pigments, dryers, surfactants, hardeners, auxiliaries and the like, if required.

As the resins contained in the paint base material, there may be exemplified those ordinarily used for solvent-based paints such as acrylic resins, alkyd resins, polyester resins, polyurethane resins, epoxy resins, phenol resins, melamine resins, amino resins or the like. Also, as the resins for water-based paints, there may be exemplified ordinarily used ones such as water-soluble alkyd resins, water-soluble melamine resins, water-soluble acrylic resins, water-soluble urethane emulsion resins or the like.

As the solvents for solvent-based paints, there may be exemplified those ordinarily used for solvent-based paints such as toluene, xylene, thinner, butyl acetate, methyl acetate, methyl isobutyl ketone, butyl cellosolve, ethyl cellosolve, butyl alcohol, aliphatic hydrocarbons and mixtures thereof.

Also, as the solvents for water-based paints, there may be exemplified water, butyl cellosolve, butyl alcohol or the like which are ordinarily used for water-based paints, or mixtures thereof.

As the defoamer, there may be used commercially available products such as NOPCO 8034 (tradename), SN DEFOAMER 477 (tradename), SN DEFOAMER 5013 (tradename), SN DEFOAMER 247 (tradename) or SN DEFOAMER 382 (tradename) (all produced by SUN NOPCO LTD.); ANTIFOAM 08 (tradename) or EMULGEN 903 (tradename) (both produced by KAO CO., LTD.); or the like.

Next, the rubber or resin composition colored with the pigment according to the present invention will be described.

(A) Resin Composition Containing the Green-Based Pigment Having an Average Major Axial Diameter of 0.1 to 1.0 μm

The resin composition colored with the green-based pigment according to the present invention has a dispersing condition of usually rank 4 or 5, preferably rank 5 when visually observed and evaluated by the method described hereinafter; and a heat resistance temperature of usually not less than 215° C., preferably not less than 220° C. As to the hue of the resin composition, it is preferred that the L* value thereof is 25 to 85; the a* value thereof is from −100 to less than 0; and the b* value thereof is −100 to +100; and the h value thereof is 120 to 240°.

The resin composition colored with the green-based pigment obtained by using as the core particles iron oxide hydroxide particles coated with the hydroxides and/or oxides of aluminum and/or silicon according to the present invention, has a dispersing condition of usually rank 4 or 5, preferably rank 5 when visually observed and evaluated by the method described hereinafter; and a heat resistance temperature of usually not less than 220° C., preferably not less than 225° C. As to the hue of the resin composition, it is preferred that the L* value thereof is 25 to 85; the a* value thereof is from −100 to less than 0; the b* value thereof is −100 to +100; and the h value thereof is 120 to 240°.

(B) Resin Composition Containing the Orange-Based Pigment Having an Average Major Axial Diameter of 0.1 to 1.0 μm

The resin composition colored with the orange-based pigment according to the present invention has a dispersing condition of usually rank 4 or 5, preferably rank 5 when visually observed and evaluated by the method described hereinafter; and a heat resistance temperature of usually not less than 215° C., preferably not less than 220° C. As to the hue of the resin composition, it is preferred that the L* value thereof is 25 to 85; the a* value thereof is from more than 0 to +100; the b* value thereof is from more than 0 to +100; and the h value thereof is 30 to 60° C.

The resin composition colored with the orange-based pigment obtained by using as the core particles iron oxide hydroxide particles coated with the hydroxides and/or oxides of aluminum and/or silicon according to the present invention, has a dispersing condition of usually rank 4 or 5, preferably rank 5 when visually observed and evaluated by the method described hereinafter; and a heat resistance temperature of usually not less than 220° C., preferably not less than 225° C. As to the hue of the resin composition, it is preferred that the L* value thereof is 25 to 85; the a* value thereof is from more than 0 to +100; the b* value thereof is from more than 0 to +100; and the h value thereof is 30 to 60° C.

(C) Resin Composition Containing the Green-Based Fine Pigment Having an Average Major Axial Diameter of from 0.005 μm to Less Than 0.1 μm

The resin composition colored with the green-based fine pigment according to the present invention has a dispersing condition of usually rank 4 or 5, preferably rank 5 when visually observed and evaluated by the method described hereinafter; and a heat resistance temperature of usually not less than 210° C., preferably not less than 215° C. As to the hue of the resin composition, it is preferred that the L* value thereof is 25 to 85; the a* value thereof is from −100 to less than 0; the b* value thereof is −100 to +100; and the h value thereof is 120 to 240°. As to the transparency of the resin composition, the linear absorption thereof is preferably not more than 0.05 μm −1 .

The resin composition colored with the green-based fine pigment obtained by using as the core particles iron oxide hydroxide particles coated with the hydroxides and/or oxides of aluminum and/or silicon according to the present invention, has a dispersing condition of usually rank 4 or 5, preferably rank 5 when visually observed and evaluated by the method described hereinafter; and a heat resistance temperature of usually not less than 215° C., preferably not less than 220° C. As to the hue of the resin composition, it is preferred that the L* value thereof is 25 to 85; the a* value thereof is from −100 to less than 0; the b* value thereof is −100 to +100; and the h value thereof is 120 to 240°. As to the transparency of the resin composition, the linear absorption thereof is preferably not more than 0.05 μm −1 .

(D) Resin Composition Containing the Orange-Based Fine Pigment Having an Average Major Axial Diameter of from 0.005 to Less Than 0.1 μm

The resin composition colored with the orange-based fine pigment according to the present invention has a dispersing condition of usually rank 4 or 5, preferably rank 5 when visually observed and evaluated by the method described hereinafter; and a heat resistance temperature of usually not less than 210° C., preferably not less than 215° C. As to the hue of the resin composition, it is preferred that the L* value thereof is 25 to 85; the a* value thereof is from more than 0 to +100; the b* value thereof is from more than 0 to +100: and the h value thereof is 30 to 60°. As to the transparency of the resin composition, the linear absorption thereof is preferably not more than 0.05 μm −1 .

The resin composition colored with the orange-based fine pigment obtained by using as the core particles iron oxide hydroxide particles coated with the hydroxides and/or oxides of aluminum and/or silicon according to the present invention, has a dispersing condition of usually rank 4 or 5, preferably rank 5 when visually observed and evaluated by the method described hereinafter; and a heat resistance temperature of usually not less than 215° C., preferably not less than 220° C. As to the hue of the resin composition, it is preferred that the L* value thereof is 25 to 85; the a* value thereof is from more than 0 to +100; the b* value thereof is from more than 0 to +100; and the h value thereof is 30 to 60°. As to the transparency of the resin composition, the linear absorption thereof is preferably not more than 0.05 μm −1 .

In the resin composition according to the present invention, the amount of the green or orange-based pigment blended is usually 0.01 to 200 parts by weight based on 100 parts by weight of the rubber or resins composition.

In the case where the green or orange-based pigment having a particle size of 0.1 to 1.0 μm is used:

In the rubber or resin composition of the present invention, the amount of the green or orange-based pigment blended is usually 0.5 to 200 parts by weight based on 100 parts by weight of the rubber or resin composition. In the consideration of good handling property of the resin composition, the amount of the green or orange-based pigment blended is preferably 1.0 to 150 parts by weight, more preferably 2.5 to 100 parts by weight based on 100 parts by weight of the rubber or resin composition.

In the case where the green or orange-based fine pigment having a particle size of from 0.005 μm to less than 0.1 μm is used:

In the rubber or resin composition according to the present invention, the amount of the green or orange-based fine pigment blended is usually 0.01 to 50 parts by weight based on 100 parts by weight of the rubber or resin composition. In the consideration of good handling property of the resin composition, the amount of the green or orange-based fine pigment blended is preferably 0.05 to 45 parts by weight, more preferably 0.1 to 40 parts by weight based on 100 parts by weight of the rubber or resin composition.

The based material of the rubber or resin composition according to the present invention contains green or orange-based fine pigments and known thermoplastic resins, and may optionally contain various additives such as lubricants, plasticizers, antioxidants, ultraviolet light absorbers or the like, if required.

As the rubber or resins of the composition, there may be exemplified natural rubbers, synthetic rubbers, thermoplastic resins (e.g., polyolefins such as polyethylenes, polypropylenes, polybutenes and polyisobutylenes, polyvinyl chlorides, styrene polymers and polyamides) or the like.

The amount of the additives added is not more than 50% by weight based on the total weight of the green or orange-based fine pigments and resins. When the amount of the additives added is more than 50% by weight, the obtained rubber or resin composition is deteriorated in moldability.

The resin composition according to the present invention may be produced by preliminarily intimately mixing a raw resin material and the green or orange-based fine pigment together and applying a strong shear force to the mixture by a kneader or an extruder to deaggregate agglomerates of the green or orange-based fine pigment and uniformly disperse the individual green or orange-based fine pigment particles in the resin. The thus produced resin composition may be formed into an appropriate shape according to the application thereof upon use.

Next, the process for producing the green or orange-based pigment according to the present invention, is described.

The green or orange-based pigment of the present invention can be produced by mixing iron oxide hydroxide particles with alkoxysilane compounds or polysiloxanes to coat the surfaces of the iron oxide hydroxide particles with the alkoxysilane compounds or polysiloxanes; and then mixing the iron oxide hydroxide particles coated with the alkoxysilane compounds or polysiloxanes, with an organic pigment.

The coating of the iron oxide hydroxide particles with the alkoxysilane compounds, the polysiloxanes, the modified polysiloxanes, or the terminal-modified polysiloxanes, may be conducted (i) by mechanically mixing and stirring the iron oxide hydroxide particles together with the alkoxysilane compounds, the polysiloxanes, the modified polysiloxanes, or the terminal-modified polysiloxanes; or (ii) by mechanically mixing and stirring both the components together while spraying the alkoxysilane compounds, the polysiloxanes, the modified polysiloxanes, or the terminal-modified polysiloxanes onto the iron oxide hydroxide particles. In these cases, substantially whole amount of the alkoxysilane compounds, the polysiloxanes, the modified polysiloxanes, or the terminal-modified polysiloxanes added can be applied onto the surfaces of the iron oxide hydroxide particles.

In addition, by conducting the above-mentioned mixing or stirring treatment (i) of the iron oxide hydroxide particles as core particles together with the alkoxysilane compounds, at least a part of the alkoxysilane compounds coated on the iron oxide hydroxide particles as core particles may be changed to the organosilane compounds. In this case, there is also no affection against the formation of the organic pigment coat thereon.

In order to uniformly coat the surfaces of the iron oxide hydroxide particles with the alkoxysilane compounds, the polysiloxanes, the modified polysiloxanes, or the terminal-modified polysiloxanes, it is preferred that the iron oxide hydroxide particles s are preliminarily diaggregated by using a pulverizer.

As apparatus (a) for mixing and stirring treatment (i) of the core particles with the alkoxysilane compounds, the polysiloxanes, the modified polysiloxanes, or the terminal-modified polysiloxanes to form the coating layer thereof, and as apparatus (b) for mixing and stirring treatment (ii) of the organic pigment with the core particles whose surfaces are coated with the alkoxysilane compounds, the polysiloxanes, the modified polysiloxanes, or the terminal-modified polysiloxanes to form the organic pigment coat, there may be preferably used those apparatus capable of applying a shear force to the particles, more preferably those apparatuses capable of conducting the application of shear force, spaturate force and compressed force at the same time.

As such apparatuses, there may be exemplified wheel-type kneaders, ball-type kneaders, blade-type kneaders, roll-type kneaders or the like. Among them, wheel-type kneaders are preferred.

Specific examples of the wheel-type kneaders may include an edge runner (equal to a mix muller, a Simpson mill or a sand mill), a multi-mull, a Stotz mill, a wet pan mill, a Conner mill, a ring muller, or the like. Among them, an edge runner, a multi-mull, a Stotz mill, a wet pan mill and a ring muller are preferred, and an edge runner is more preferred.

Specific examples of the ball-type kneaders may include a vibrating mill or the like. Specific examples of the blade-type kneaders may include a Henschel mixer, a planetary mixer, a Nawter mixer or the like. Specific examples of the roll-type kneaders may include an extruder or the like.

In order to coat the surfaces of the core particles with the alkoxysilane compounds, the polysiloxanes, the modified polysiloxanes, or the terminal-modified polysiloxanes as uniformly as possible, the conditions of the above mixing or stirring treatment may be appropriately controlled such that the linear load is usually 2 to 200 Kg/cm (19.6 to 1960 N/cm), preferably 10 to 150 Kg/cm (98 to 1470 N/cm), more preferably 15 to 100 Kg/cm (147 to 980 N/cm); and the treating time is usually 5 to 120 minutes, preferably 10 to 90 minutes. It is preferred to appropriately adjust the stirring speed in the range of usually 2 to 2,000 rpm, preferably 5 to 1,000 rpm, more preferably 10 to 800 rpm.

The amount of the alkoxysilane compounds, the polysiloxanes, the modified polysiloxanes, or the terminal-modified polysiloxanes added, is preferably 0.15 to 45 parts by weight based on 100 parts by weight of the iron oxide hydroxide particles. When the amount of the alkoxysilane compounds, the polysiloxanes, the modified polysiloxanes or the terminal-modified polysiloxanes added is less than 0.15 part by weight, it may become difficult to adhere the organic pigment in such an amount enough to obtain the iron oxide hydroxide composite particles according to the present invention. On the other hand, when the amount of the alkoxysilane compounds, the polysiloxanes, the modified polysiloxanes or the terminal-modified polysiloxanes added is more than 45 parts by weight, since a sufficient amount of the organic pigment can be adhered on the surface of the coating layer, it is meaningless to add more than 45 parts by weight.

Next, the organic pigment are added to the iron oxide hydroxide particles coated with the alkoxysilane compounds, the polysiloxanes, the modified polysiloxanes, or the terminal-modified polysiloxanes, and the resultant mixture is mixed and stirred to form the organic pigment coat on the surfaces of the coating layer composed of the alkoxysilane compounds, the polysiloxanes, the modified polysiloxanes or the terminal-modified polysiloxanes. The drying or heat-treatment may be conducted.

It is preferred that the organic pigment are added little by little and slowly, especially about 5 to 60 minutes.

In order to form organic pigment coat onto the coating layer composed of the alkoxysilane compounds, the polysiloxanes, the modified polysiloxanes, or the terminal-modified polysiloxanes as uniformly as possible, the conditions of the above mixing or stirring treatment can be appropriately controlled such that the linear load is usually 2 to 200 Kg/cm (19.6 to 1960 N/cm), preferably 10 to 150 Kg/cm (98 to 1470 N/cm), more preferably 15 to 100 Kg/cm (147 to 980 N/cm); and the treating time is usually 5 to 120 minutes, preferably 10 to 90 minutes. It is preferred to appropriately adjust the stirring speed in the range of usually 2 to 2,000 rpm, preferably 5 to 1,000 rpm, more preferably 10 to 800 rpm.

The preferable amount of the organic blue-based pigment added is 5 to 30 parts by weight based on 100 parts by weight of the iron oxide hydroxide particles. When the amount of the organic blue-based pigment added is more than 30 parts by weight, the aimed green-based pigment of the present invention may not be obtained.

The preferable amount of the organic red-based pigment added is 1 to 30 parts by weight based on 100 parts by weight of the iron oxide hydroxide particles. When the amount of the organic red-based pigment added is out of the above specified range, the aimed orange-based pigment of the present invention may not be obtained.

The heating temperature used in the drying and heating steps is usually 40 to 200° C., preferably 60 to 150° C. The treating time of these steps is usually from 10 minutes to 12 hours, preferably from 30 minutes to 3 hours.

When the obtained green or orange-based pigment is subjected to the above drying and heating steps, the alkoxysilane compounds used as the coating thereof are finally converted into organosilane compounds.

If required, prior to mixing and stirring with the alkoxysilane compounds or polysiloxanes, the iron oxide hydroxide particles may be preliminarily coated with at least one compound selected from the group consisting of hydroxides of aluminum, oxides of aluminum, hydroxides of silicon and oxides of silicon to form an intermediate coating layer thereon.

At least a part of the surface of the iron oxide hydroxide particles may be coated with at least one compound selected from the group consisting of hydroxides of aluminum, oxides of aluminum, hydroxides of silicon and oxides of silicon (hereinafter referred to merely as “hydroxides and/or oxides of aluminum and/or silicon”), if required, in advance of mixing and stirring with the alkoxysilane compounds, the polysiloxanes, the modified polysiloxanes or the terminal-modified polysiloxanes.

The coating of the hydroxides and/or oxides of aluminum and/or silicon may be conducted by adding an aluminum compound, a silicon compound or both the compounds to a water suspension in which the iron oxide hydroxide particles are dispersed, followed by mixing and stirring, and further adjusting the pH value of the suspension, if required, thereby coating the surfaces of the iron oxide hydroxide particles with hydroxides and/or oxides of aluminum and/or silicon. The thus obtained iron oxide hydroxide particles coated with the hydroxides and/or oxides of aluminum and/or silicon are then filtered out, washed with water, dried and pulverized. Further, the iron oxide hydroxide particles coated with the hydroxides and/or oxides of aluminum and/or silicon may be subjected to post-treatments such as deaeration treatment and compaction treatment, if required.

As the aluminum compounds, there may be exemplified aluminum salts such as aluminum acetate, aluminum sulfate, aluminum chloride or aluminum nitrate, alkali aluminates such as sodium aluminate or the like.

The amount of the aluminum compound added is 0.01 to 20% by weight (calculated as Al) based on the weight of the iron oxide hydroxide particles. When the amount of the aluminum compound added is less than 0.01% by weight, it may be difficult to sufficiently coat the surfaces of the iron oxide hydroxide particles with hydroxides and/or oxides of aluminum, thereby failing to improve the effective reduction of the organic pigment desorption percentage. On the other hand, when the amount of the aluminum compound added is more than 20% by weight, the coating effect is saturated and, therefore, it is meaningless to add such an excess amount of the aluminum compound.

As the silicon compounds, there may be exemplified #3 water glass, sodium orthosilicate, sodium metasilicate or the like.

The amount of the silicon compound added is 0.01 to 20% by weight (calculated as SiO 2 ) based on the weight of the iron oxide hydroxide particles. When the amount of the silicon compound added is less than 0.01% by weight, it may be difficult to sufficiently coat the surfaces of the iron oxide hydroxide particles with hydroxides and/or oxides of silicon, thereby failing to improve the effective reduction of the organic pigment desorption percentage. On the other hand, when the amount of the silicon compound added is more than 20% by weight, the coating effect is saturated and, therefore, it is meaningless to add such an excess amount of the silicon compound.

In the case where both the aluminum and silicon compounds are used in combination for the coating, the total amount of the aluminum and silicon compounds added is preferably 0.01 to 20% by weight (calculated as a sum of Al and SiO 2 ) based on the weight of the iron oxide hydroxide particles.

The point of the present invention lies in the following. That is, the green or orange-based pigment obtained by coating the surfaces of iron oxide hydroxide particles having an average particle size of 0.1 to 1.0 μm with organosilicon compounds and then adhering an organic blue or red-based pigment onto the surface of coating composed of the organosilicon compounds, is a harmless green or orange-based pigment capable of exhibiting excellent chemical resistances, high hiding power and tinting strength, and improved heat resistance.

Another point of the present invention lies in the following. That is, the green or orange-based fine pigment obtained by coating the surfaces of iron oxide hydroxide particles having an average particle size of from 0.005 to less than 0.1 μm with organosilicon compounds and then adhering an organic blue or red-based pigment onto the surface of coating composed of the organosilicon compounds, is a harmless green or orange-based fine pigment capable of exhibiting excellent chemical resistances, excellent tinting strength and improved heat resistance.

The reason why the pigment exhibiting a green color can be obtained by the present invention, is considered as follows. That is, similarly to such a principle that a film exhibiting a green color is obtained by overlapping a blue film on a yellow film, when the iron oxide hydroxide particles having a yellow color is coated with the organic blue-based pigment having a low hiding power, the obtained composite particles can exhibit a green color.

Also, the reason why the pigment exhibiting an orange color can be obtained by the present invention, is considered as follows. That is, similarly to such a principle that a film exhibiting an orange color is obtained by overlapping a red film on a yellow film, when the iron oxide hydroxide particles having a yellow color is coated with the organic red-based pigment having a low hiding power, the obtained composite particles can exhibit an orange color.

The reason why the green or orange-based pigment of the present invention is excellent in chemical resistances, is considered as follows. That is, the iron oxide hydroxide particles as core particles themselves are excellent in chemical resistances. Further, by selecting the organic blue or red-based pigment to be adhered onto the particles from those pigments having excellent chemical resistances, the obtained green or orange-based pigment can also exhibit excellent chemical resistances as a whole.

The reason why the green or orange-based pigment of the present invention has excellent tinting strength, is considered as follows. That is, the organic blue or red-based pigment is strongly fixed onto the surfaces of the iron oxide hydroxide particles having excellent tinting strength through the coating layer composed of the organosilicon compounds to form composite particles. As a result, the obtained green or orange-based pigment can also exhibit an excellent tinting strength.

The reason why the green or orange-based pigment of the present invention has an excellent heat resistance, is considered as follows. That is, the iron oxide hydroxide particles which are inherently deteriorated in heat resistance, are coated with the organosilicon compounds having an excellent heat resistance. Further, the organic blue or red-based pigment having an excellent heat resistance is fixed onto the surface of the coating layer composed of the organosilicon compounds. As a result, the obtained green or orange-based pigment can be enhanced in heat resistance.

The organic green or orange-based pigment according to the present invention contains no harmful elements and compounds and, therefore, can show not only excellent hygiene and safety, but also is effective for environmental protection.

Also, the green or orange-based pigment having an average major axial diameter of 0.1 to 1.0 μm according to the present invention, has high tinting strength, and excellent heat resistance and chemical resistances, and are harmless.

In the paint and resin composition of the present invention, there is used the green or orange-based pigment which is not only excellent in heat resistance and chemical resistances but also harmless. Therefore, the paint and resin composition of the present invention is suitable as green or orange paints and resin compositions which are free from environmental pollution.

The green or orange-based fine pigment having an average major axial diameter of from 0.005 to less than 0.1 μm according to the present invention, is harmless and enhanced in chemical resistances and heat resistance. Further, by using such a green or orange-based fine pigment, it is possible to obtain paints and resin compositions having an excellent transparency. Therefore, the green or orange-based fine pigment of the present invention is suitable as coloring pigments for resins, paints and printing inks.

The paint and resin composition of the present invention are produced using the green or orange-based fine pigment which has excellent heat resistance and chemical resistances, and is harmless. Therefore, the paint and resin composition of the present invention are suitable as green or orange paints and resin compositions which are free from environmental pollution and have an excellent transparency.

EXAMPLES

The present invention is described in more detail by Examples and Comparative Examples, but the Examples are only illustrative and, therefore, not intended to limit the scope of the present invention.

Various properties were measured by the following methods.

(1) The average major axial diameter and average minor axial diameter of the particles were respectively expressed by average values (measured in a predetermined direction) of about 350 particles which were sampled from a micrograph obtained by magnifying an original electron micrograph by four times in each of the longitudinal and transverse directions.

(2) The aspect ratio of the particles was expressed by a ratio of average major axial diameter to average minor axial diameter thereof.

(3) The geometrical standard deviation of major axial diameters of the particles was expressed by values obtained by the following method. That is, the major axial diameters were measured from the above magnified electron micrograph. The actual major axial diameters and the number of the particles were obtained from the calculation on the basis of the measured values. On a logarithmic normal probability paper, the major axial diameters were plotted at regular intervals on the abscissa-axis and the accumulative number (under integration sieve) of particles belonging to each interval of the major axial diameters were plotted by percentage on the ordinate-axis by a statistical technique.

The major axial diameters corresponding to the number of particles of 50% and 84.13%, respectively, were read from the graph, and the geometrical standard deviation (under integration sieve) was measured from the following formula:

Geometrical standard deviation={major axial diameter corresponding to 84.13% under integration sieve)/{major axial diameter (geometrical average diameter) corresponding to 50% under integration sieve}

The closer to 1 the geometrical standard deviation value, the more excellent the particle size distribution of the major axial diameters of the particles.

(4) The specific surface area was expressed by values measured by a BET method.

(5) The amounts of Al and Si which were present within iron oxide hydroxide particles or on the surfaces thereof; the amount of Al contained in the aluminum and iron oxide hydroxide composite of adhered onto the surfaces of the iron oxide hydroxide particles; and the amount of Si contained in the coating layer composed of organosilicon compounds, were measured by a fluorescent X-ray spectroscopy device “3063 M-type” (manufactured by RIGAKU DENKI KOGYO CO., LTD.) according to JIS K0119 “General rule of fluorescent X-ray analysis”.

Meanwhile, the amount of Si contained in oxides of silicon, hydroxides of silicon and organosilicon compounds coated on the surfaces of the iron oxide hydroxide particles, is expressed by the value obtained by subtracting the amount of Si measured prior to the respective treatment steps from that measured after the respective treatment steps.

(6) The amount (wt. %) of Fe contained in aluminum and iron oxide hydroxide composite which was coated on the surfaces of the iron oxide hydroxide particles, is expressed by the value obtained by the following method.

That is, 0.25 g of the iron oxide hydroxide particles was weighed and charged into a 100 ml conical flask, and then mixed with 33.3 ml of ion exchange water. The flask was placed in a water bath heated to 60° C., and the contents of the flask were stirred for 20 minutes by a magnetic stirrer, thereby obtaining a suspension.

Next, the suspension was mixed with 16.7 ml of a 12N-hydrochloric acid solution and further stirred for 20 minutes. As a result, a portion of the coat of aluminum and iron oxide hydroxide composite adhered on the surface of each iron oxide hydroxide particle which portion extends from an outer surface of the coat up to approximately a mid point of the distance between the outer surface of the coat and an outer surface of each iron oxide hydroxide particle, and has a substantially uniform composition, was dissolved out with the acid from the outermost surface of the coated particle toward the inside thereof (This fact was already confirmed by many experiments). Thereafter, the suspension containing components dissolved-out by the acid was subjected to suction filtration using a 0.1 μm-membrane filter. The amounts (ppm) of Al and Fe in the obtained filtrate were measured by an inductively-coupled plasma atomic emission spectrometer (SPS-4000 manufactured by Seiko Denshi Kogyo Co., Ltd.).

Further, the amount of Fe contained in the aluminum and iron oxide hydroxide composite was calculated from the weight percentage of Al to Fe obtained from the measured amounts of Al and Fe in the filtrate and the amount (% by weight) of Al in the aluminum and iron oxide hydroxide composite obtained by the above-mentioned fluorescent X-ray analysis, according to the following formula (i):

Amount of Fe (% by weight)=Amount of Al (% by weight)/Weight ratio of Al to Fe

(7) The amount of the organic pigment adhered on the iron oxide hydroxide composite particles was obtained by measuring the carbon content thereof using “HORIBA METAL CARBON/SULFUR ANALYZER EMIA-2200 MODEL” (manufactured by Horiba Seisakusho Co., Ltd.).

(8) The desorption percentage of the organic pigment adhered on the iron oxide hydroxide composite particles, is expressed by the value measured by the following method. The closer to 0% the desorption percentage of the organic pigment, the less the amount of the organic pigment desorbed from the surface of the iron oxide hydroxide composite particles.

Three grams of the iron oxide hydroxide composite particles and 40 ml of ethanol were placed in a precipitation tube, and subjected to ultrasonic dispersion for 20 minutes. The obtained dispersion was allowed to stand for 120 minutes, thereby separating the dispersion into the iron oxide hydroxide composite particles and the organic pigment desorbed therefrom due to the difference in precipitating speed therebetween. Subsequently, the iron oxide hydroxide composite particles were mixed again with 40 ml of ethanol, and subjected to ultrasonic dispersion for 20 minutes. The obtained dispersion was allowed to stand for 120 minutes, thereby separating the dispersion into the iron oxide hydroxide composite particles and the organic pigment. The thus separated iron oxide hydroxide composite particles were dried at 80° C. for one hour to measure the amount of the organic pigment desorbed therefrom. The desorption percentage (%) of the organic pigment is calculated according to the following formula:

Desorption percentage (%) of organic pigment ={(Wa-We)/Wa}×100

wherein Wa represents an amount of the organic pigment adhered onto the iron oxide hydroxide composite particles; and We represents an amount of the organic pigment adhered onto the iron oxide hydroxide composite particles after desorption test.

(9) The hue of each of the iron oxide hydroxide particles, the organic pigment and the green or orange-based pigment, were measured by the following method.

That is, 0.5 g of each sample and 0.5 ml of castor oil were intimately kneaded together by a Hoover's muller to form a paste. 4.5 g of clear lacquer was added to the obtained paste and was intimately mixed to form a paint. The paint was applied on a cast-coated paper by using a 150 μm (6-mil) applicator to produce a coating film piece (having a film thickness of about 30 μm). The thus obtained coating film piece was measured by a Multi-spectro-colour-meter MSC-IS-2D (manufactured by SUGA TESTING MACHINES MANUFACTURING CO., LTD.) to determine L*, a* and b* values thereof.

Meanwhile, the h value is expressed by the value calculated from the above measured a* and b* values according to the following formulae:

h=tan −1 (b*/a*) (a*>0, b*≦0);

h=180+tan −1 (b*/a*) (a*<0); and

h=360+tan −1 (b*/a*) (a*>0, b*<0)

(10) The heat resistance of each of the iron oxide hydroxide particles, the organic pigment and the iron oxide hydroxide composite particles, was expressed by the temperature read out from a DSC chart obtained by subjecting a test sample to differential scanning calorimetry (DSC) using a thermal analyzing apparatus SSC-5000 (manufactured by SEIKO DENSHI KOGYO Co., Ltd.), which temperature was read at a crossing point of two tangential lines on two curves constituting the first one of two infection points which form a peak on the DSC chart.

(11-1) The tinting strengths of the green-based pigment were measured by the following method.

That is, a primary color enamel and a vehicle enamel prepared by the following methods were respectively applied on a cast-coated paper by using a 150 μm (6-mil) applicator to produce coating film pieces. The thus obtained coating film pieces were measured by a Multi-spectro-colour-meter MSC-IS-2D (manufactured by SUGA TESTING MACHINES MANUFACTURING CO., LTD.) to determine the L* values thereof. The difference between the measured L* values was expressed by ΔL*.

Based on the thus measured ΔL* value and the ΔLs* value obtained from chrome green (Comparative Example 6) as a reference sample, the tinting strength (%) was calculated according to the following formula:

Tinting strength (%)=100+{(ΔLs*−ΔL*)×10}

(11-2) The tinting strength of the orange-based pigment was measured by the following method.

That is, a primary color enamel and a vehicle enamel prepared by the following methods were respectively applied on a cast-coated paper by using a 150 μm (6-mil) applicator to produce coating film pieces. The thus obtained coating film pieces were measured by a Multi-spectro-colour-meter MSC-IS-2D (manufactured by SUGA TESTING MACHINES MANUFACTURING CO., LTD.) to determine the L* values thereof. The difference between the measured L* values was expressed by ΔL*.

Next, the organic red-based pigment and the iron oxide hydroxide particles were simply blended together at the same mixing ratio as used for the production of the orange-based pigment, thereby preparing a mixed pigment as a reference sample for the orange-based pigment. The thus prepared reference sample was used to produce coating film pieces of the primary color enamel and the vehicle enamel by the same method as used above, and then the obtained coating film pieces were measured by the same method as above to determine L* values of the respective coating film pieces. The difference between the measured L* values was expressed by ΔLs*.

Based on the thus obtained ΔL* and ΔLs* values for the orange-based pigment and the reference sample, respectively, the tinting strength (%) was calculated according to the following formula:

Tinting strength (%)=100+{(ΔLs* −ΔL*)×10}

Preparation of Primary Color Enamel

10 g of the above sample, 16 g of amino alkyd resin and 6 g of a thinner were blended together. The obtained mixture was charged together with 90 g of 3 mmφ glass beads into a 140-ml glass bottle, and then mixed and dispersed together for 45 minutes using a paint shaker. Thereafter, 50 g of amino alkyd resin was added to the obtained dispersion, and further dispersed together for 5 minutes using a paint shaker, thereby preparing a primary color enamel.

Preparation of Vehicle Enamel

12 g of the above-prepared primary color enamel and 40 g of AMIRAC WHITE (titanium dioxide-dispersed amino alkyd resin) were blended together, and then mixed and dispersed together for 15 minutes using a paint shaker, thereby preparing a vehicle enamel.

(12) The hiding power of the organic pigment and the green or orange-based pigment is expressed by the value measured by the criptometer method according to paragraph 8.2 of JIS K5101, using the above obtained primary color enamel.

(13) The acid resistance of the iron oxide hydroxide particles and the iron oxide hydroxide composite particles was measured by the following method.

That is, 10 g of sample particles were immersed in a 5% sulfuric acid solution for 10 minutes. Thereafter, the sample particles were taken out of the sulfuric acid solution, washed with water and then dried. The thus dried particles were used to form a coating film by the same method as described above. The L*, a* and b* values of the coating film were measured, and the acid resistance was expressed by the value of color difference ΔE* calculated according to the following formula:

ΔE* value=((ΔL*) 2 +(Δa*) 2 +(Δb*) 2 ) ½

wherein ΔL* represents the difference between the L* values before and after immersing the sample particles in acid or alkali; Δa* represents the difference between the a* values before and after immersing the sample particles in acid or alkali; and Δb* represents the difference between the a* values before and after immersing the sample particles in acid or alkali.

The smaller the ΔE* value, the more excellent the acid resistance.

(14) The alkali resistance of the iron oxide hydroxide particles and the iron oxide hydroxide composite particles was measured by the following method.

That is, 10 g of sample particles were immersed in a 1% sodium hydroxide solution for 15 minutes. Thereafter, the sample particles were taken out of the sodium hydroxide solution, washed with water and then dried. The thus dried particles were used to form a coating film by the same method as described above. The L*, a* and b* values of the coating film were measured, and the alkali resistance was expressed by the value of color difference ΔE* calculated according to the following formula:

ΔE* value=((ΔL*) 2 +(Δa*) 2 +(Δb*) 2 ) ½

wherein ΔL* represents the difference between the L* values before and after immersing the sample particles in acid or alkali; Δa* represents the difference between the a* values before and after immersing the sample particles in acid or alkali; and Δb* represents the difference between the a* values before and after immersing the sample particles in acid or alkali.

The smaller the ΔE* value, the more excellent the alkali resistance.

(15) The hue of the coating film obtained by using the solvent-based paint or water-based paint containing the green or orange-based pigment was determined by the following method.

That is, the paint produced by the method described hereinafter, was respectively coated on a cold-rolled steel plate (0.8 mm×70 mm×150 mm: JIS G-3141) and then dried to form a coating film having a thickness of 150 μm thereon, thereby preparing a coating film test piece. Also, the hue of the resin composition colored with the green or orange-based pigment was determined using a colored resin plate prepared by the method described hereinafter. The L*, a* and b* values of the thus prepared coating film test piece and colored resin plate were measured by using a Multi-spectro-colour-meter MSC-IS-2D (manufactured by SUGA TESTING MACHINES MANUFACTURING CO., LTD.).

Meanwhile, the h value of the paint or resin composition was calculated from the measured a* and b* values according to the above-specified formula:

h=tan −1 (b*/a*) (a*>0, b*≦0);

h=180+tan −1 (b*/a*) (a*<0); and

h=360+tan −1 (b*/a*) (a*>0, b*<0)

(16) The gloss of a coating film formed obtained by using the paint containing the green or orange-based pigment, was measured by irradiating light onto the above coating film test pieces at an incident angle of 60°, using a glossmeter UGV-5D (manufactured by SUGA TESTING MACHINES MANUFACTURING CO., LTD.).

The higher the gloss, the more excellent the dispersibility of the paint containing the green or orange-based pigment.

(17) The transparency of the solvent-based paint or water-based paint containing the green or orange-based fine pigment, was determined using a coating film having a thickness of 150 μm (6 mil) which was prepared by applying each paint prepared by the method described hereinafter onto a 100 μm-thick clear base film.

Also, the transparency of the rubber or resin composition was determined using a resin plate prepared by the method described hereinafter.

In order to determine the transparency of the paint or resin composition, the light transmittance of the coating film or the resin plate was measured by a self-recording photoelectric spectrophotometer “UV-2100” (manufactured by Shimadzu Seisakusho Co., Ltd.). Based on the measured light transmittance, the linear absorption thereof was calculated according to the following formula:

Linear absorption (μm −1 )=ln(1/t)/FT

wherein t represents a light transmittance at λ=900 nm; and FT is a thickness of the coating film or the resin plate used for the measurement.

The smaller the linear absorption, the higher the light transmittance of the paint or resin composition, i.e., the higher the transparency thereof.

(18-1) The heat resistance of a coating film formed from the solvent-based paint or water-based paint containing the green or orange-based pigment is determined as follows.

That is, the above prepared coating film test piece was placed in an electric furnace, and while varying the temperature of the electric furnace, heat-treated for 15 minutes at each temperature. The hues (L* value, a* value and b* value) of the coating film test piece before and after heat treatment at each temperature were respectively measured by a Multi-spectro-colour-meter MSC-IS-2D (manufactured by SUGA TESTING MACHINES MANUFACTURING CO., LTD.).

Based on the measured values before the heat treatment as standard values, the ΔE* value was calculated according to the below-mentioned formula. On the semi-logarithmic graph paper, the heating temperatures were plotted on the abscissa-axis, and the ΔE* values were plotted on the ordinate-axis. The temperature at which the ΔE* value was identical to just 1.5, was determined as the heat-resisting temperature of the coating film.

ΔE* value=((ΔL*) 2 +(Δa*) 2 +(Δb*) 2 ) ½

wherein ΔL* represents a difference between L* values of the coating film before and after the heat treatment; Δa* represents a difference between a* values of the coating film before and after the heat treatment; and Δb* represents a difference between b* values of the coating film before and after the heat treatment.

(18-2) The heat resistance of a coating film formed from the solvent-based paint or water-based paint containing the green or orange-based fine pigment is determined as follows.

That is, a paint prepared by the method described hereinafter was applied onto a transparent glass plate (0.8 mm (thickness)×70 mm (width)×150 mm (length)). The coated glass plate was placed in an electric furnace, and while varying the temperature of the electric furnace, heat-treated for 15 minutes at each temperature. The hues (L* value, a* value and b* value) of the coated glass plate on a standard white back plate before and after heat treatment at each temperature were respectively measured by a Multi-spectro-colour-meter MSC-IS-2D (manufactured by SUGA TESTING MACHINES MANUFACTURING CO., LTD.) according to JIS Z 8729.

Based on the measured values before the heat treatment as standard values, the ΔE* value was calculated according to the above-mentioned formula. On the semi-logarithmic graph paper, the heating temperatures were plotted on the abscissa-axis, and the ΔE* values were plotted on the ordinate-axis. The temperature at which the ΔE* value was identical to just 1.5, was determined as the heat-resisting temperature of the coating film.

ΔE* value=((ΔL*) 2 +(Δa*) 2 +(Δb*) 2 ) ½

wherein ΔL* represents a difference between L* values of the coating film before and after the heat treatment; Δa* represents a difference between a* values of the coating film before and after the heat treatment; and Δb* represents a difference between b* values of the coating film before and after the heat treatment.

(19) The heat resistance of a rubber or resin composition containing the green or orange-based pigment was determined as follow. That is, a resin plate prepared by the method described hereinafter was cut into 5 cm square, was placed in a hot press, and while varying the temperature of the hot press and applying a load of 98 MPa (1 ton/cm 2 ) thereto, heat-treated for 10 minutes at each temperature. The hues (L* value, a* value and b* value) of the resin plate before and after heat treatment at each temperature were respectively measured. Based on the measured values before the heat treatment as standard values, the ΔE* value was calculated according to the above-mentioned formula. On the semi-logarithmic graph paper, the heating temperatures were plotted on the abscissa-axis, and the ΔE* values were plotted on the ordinate-axis. The temperature at which the ΔE* value was identical to just 1.5, was determined as the heat-resisting temperature of the resin composition.

ΔE* value =((ΔL*) 2 +(Δa*) 2 +(Δb*) 2 ) ½

wherein ΔL* represents a difference between L* values of the coating film before and after the heat treatment; Δa* represents a difference between a* values of the coating film before and after the heat treatment; and Δb* represents a difference between b* values of the coating film before and after the heat treatment.

(20-1) The storage stability of a paint containing the green or orange-based pigment was determined by the following method.

That is, the paint produced by dispersing a mill base prepared by blending the below-mentioned components together at the predetermined mixing ratio, for 90 minutes, was coated on a cold-rolled steel plate (0.8 mm×70 mm×150 mm: JIS G-3141) and then dried to form a coating film having a thickness of 150 μm thereon. The hue (L*, a* and b* values) of the thus obtained coating film was measured. Further, after the paint was allowed to stand at 25° C. for one week, the paint was applied onto a cold-rolled steel plate and then dried to form a coating film by the same method as described above. Then, the hue (L*, a* and b* values) of the obtained coating film were also measured. Based on the thus measured L*, a* and b* values, the ΔE* value was calculated according to the below-mentioned formula:

ΔE* value ((ΔL*) 2 +(Δa*) 2 +(Δb*) 2 ) ½

wherein ΔL* represents a difference between L* values of the compared coating films prepared from the respective paints before and after the keeping test; Δa* represents a difference between a* values of the compared coating films prepared from the respective paints before and after the keeping test; and Δb* represents a difference between b* values of the compared coating films prepared from the respective paints before and after the keeping test.

(20-2) The storage stability of a paint containing the green or orange-based fine pigment was determined as follows.

That is, the paint prepared by the method described hereinafter, was applied onto a clear base film and then dried to form a coating film having a thickness of 150 μm (6 mil) thereon. The L*, a* and b* values of the obtained coating film were measured. Further, after the paint was allowed to stand at 25° C. for one week, the paint was applied onto a clear base film and then dried to form a coating film by the same method as described above. Then, the L*, a* and b* values of the obtained coating film were also measured. Based on the thus measured L*, a* and b* values, the ΔE* value was calculated according to the below-mentioned formula:

ΔE* value=((ΔL*) 2 +(Δa*) 2 +(Δb*) 2 ) ½

wherein ΔL* represents a difference between L* values of the compared coating films prepared from the respective paints before and after the keeping test; Δa* represents a difference between a* values of the compared coating films prepared from the respective paints before and after the keeping test; and Δb* represents a difference between b* values of the compared coating films prepared from the respective paints before and after the keeping test.

(21) The acid resistance of a coating film was measured by the following method.

That is, the coated plate was prepared by the same method as used above for the evaluation of heat resistance. The gloss of the coated plate was measured. Then, the coated plate suspended by a thread was immersed by about 120 mm in depth into a 5 wt. % aqueous sulfuric acid solution filled in a 1,000-ml beaker, and was allowed to stand in the suspended condition at 25° C. for 24 hours.

Next, the coated plate was removed from the aqueous sulfuric acid solution and gently washed with flowing water. After water attached to the coated plate was removed by shaking, the gloss of the coated plate was measured at a central portion thereof. Based on the measured gloss values before and after the immersion, the change in gloss (ΔG value) was calculated, thereby evaluating the acid resistance of the coating film. The smaller the ΔG value, the more excellent the acid resistance of the coating film.

(22) The alkali resistance of a coating film was measured by the following method. That is, the coated plate was prepared by the same method as used above for the evaluation of heat resistance. The gloss of the coated plate was measured. Then, the coated plate suspended by a thread was immersed by about 120 mm in depth into a 1 wt. % aqueous sodium hydroxide solution filled in a 1,000-ml beaker, and was allowed to stand in the suspended condition at 25° C. for 24 hours.

Next, the coated plate was removed from the aqueous sodium hydroxide solution and gently washed with flowing water. After water attached to the coated plate was removed by shaking, the gloss of the coated plate was measured at a central portion thereof. Based on the measured gloss values before and after the immersion, the change in gloss (ΔG value) was calculated, thereby evaluating the alkali resistance of the coating film. The smaller the ΔG value, the more excellent the alkali resistance of the coating film.

(23) The viscosity at 25° C. of the paint prepared by the method described hereinafter, was measured at a shear rate (D) of 1.92 sec −1 by E-type viscometer (cone plate-type viscometer) EMD-R (manufactured by TOKYO KEIKI CO., LTD.).

(24) The dispersibility of the green or orange-based pigment in resin composition was evaluated by visually counting the number of undispersed aggregate particles on a surface of the colored resin plate produced by the method described hereinafter, and by classifying the results into the following five ranks. The 5th rank represents the most excellent dispersing condition.

Rank 1: not less than 50 undispersed aggregate particles per 1 cm 2 were recognized;

Rank 2: 10 to 49 undispersed aggregate particles per 1 cm 2 were recognized;

Rank 3: 5 to 9 undispersed aggregate particles per 1 cm 2 were recognized;

Rank 4: 1 to 4 undispersed aggregate particles per 1 cm 2 were recognized;

Rank 5: No undispersed aggregate particles were recognized.

EXAMPLE 1

<Production of Green-Based Pigment>

11.0 kg of goethite particles (particle shape: acicular shape; average major axial diameter: 0.40 μm; aspect ratio: 5.3:1; geometrical standard deviation value: 1.44; BET specific surface area value: 18.8 m 2 /g; L* value: 59.3; a* value: 16.5; b* value: 53.9; h value: 73.0°; heat resistance temperature: 198° C.), were charged into an edge runner “MPUV-2 Model” (tradename, manufactured by MATSUMOTO CHUZO TEKKOSHO CO., LTD.). Then, a methyltriethoxysilane solution prepared by mixing and diluting 220 g of methyltriethoxysilane (tradename: TSL8123, produced by GE Toshiba Silicone Co., Ltd.) with 200 ml of ethanol was added to the goethite particles while operating the edge runner. The resultant mixture was mixed and stirred at a linear load of 392 N/cm (40 Kg/cm) and a stirring speed of 22 rpm for 20 minutes.

Next, 825 g of an organic blue pigment A (kind: copper phthalocyanine blue; particle shape: granular shape; average major axial diameter: 0.06 μm; hiding power: 240 cm 2 /g; L* value: 17.7; a* value: 9.7; b* value: −23.4; h value: 292.5°; heat resistance temperature: 256° C.), were added to the above mixture for 10 minutes while operating the edge runner. Further, the obtained mixture was mixed and stirred at a linear load of 392 N/cm (40 Kg/cm) and a stirring speed of 22 rpm for 20 minutes to form a coating layer composed of the organic blue pigment A on the methyltriethoxysilane coat, thereby obtaining a green-based pigment. The obtained green-based pigment was heat-treated at 105° C. for 60 minutes by using a drier.

The obtained green-based pigment was acicular particles having an average major axial diameter of 0.40 μm, an aspect ratio of 5.3:1, a geometrical standard deviation value of 1.44, a BET specific surface area value of 20.1 m 2 /g, a L* value of 39.9, an a* value of −13.2, a b* value of 19.8, a h value of 123.7°, a tinting strength of 141% and a hiding power of 1,950 cm 2 /g. As to the chemical resistances of the green-based pigment, the acid resistance (ΔE* value) thereof was 0.99, and the alkali resistance (ΔE* value) thereof was 0.86. As to the heat resistance of the green-based pigment, the heat resistance temperature thereof was 227° C. The desorption percentage of the organic blue pigment from the green-based pigment was 7.0% by weight. The amount of a coating layer composed of organosilane compounds produced from methyltriethoxysilane was 0.29% by weight (calculated as Si). The amount of the coating layer composed of the organic blue pigment A was 4.61% by weight (calculated as C) (corresponding to 7.5 parts by weight based on 100 parts by weight of the goethite core particles).

As a result of the observation of electron micrograph, almost no organic blue pigment A liberated was recognized, so that it was confirmed that a substantially whole amount of the organic blue pigment A added was adhered on the coating layer composed of the organosilane compounds produced from methyltriethoxysilane.

EXAMPLE 2

<Production of Solvent-Based Paint Containing Green-Based Pigment>

10 g of the green-based pigment produced in Example 1, was blended with an amino alkyd resin and a thinner at the following weight ratio, and charged into a 140-ml glass bottle together with 90 g of 3 mmφ glass beads. Next, the obtained mixture was mixed and dispersed for 90 minutes by a paint shaker, thereby preparing a mill base.

Composition of Mill Base:
Green-based pigment              12.2 parts by weight
Amino alkyd resin (AMILAC No. 1026, 19.5 parts by weight
produced by KANSAI PAINT CO., LTD.)
Thinner                          7.3 parts by weight

The above-prepared mill base was blended with an amino alkyd resin at the following weight ratio, and the obtained mixture was further mixed and dispersed for 15 minutes by a paint shaker, thereby obtaining a solvent-based paint containing the green-based pigment.

Composition of paint:
Mill base                        39.0 parts by weight
Amino Alkyd resin (AMILAC No. 1026, 61.0 parts by weight
KANSAI PAINT CO., LTD.)

The thus obtained solvent-based paint showed a viscosity of 1,452 cP. As to the storage stability of the solvent-based paint, the ΔE* value thereof was 0.92.

Then, the solvent-based paint was applied onto a cold-rolled steel plate (0.8 mm×70 mm×150 mm; JIS G-3141) and then dried to form a coating film having a thickness of 150 μm thereon. The thus obtained coating film showed a gloss of 87% and a heat resistance temperature of 249° C. As to the hue of the coating film, the L* value thereof was 40.2; the a* value thereof was −12.4; the b* value thereof was 20.5; and the h value thereof was 121.2°. As to the chemical resistances of the coating film, the acid resistance (ΔG value) thereof was 9.3%, and the alkali resistance (ΔG value) thereof was 7.9%.

EXAMPLE 3

<Production of Water-Based Paint Containing Green-Based Pigment>

7.62 g of the green-based pigment obtained in Example 1, was blended with a water-soluble alkyd resin at the following weight ratio, and charged into a 140-ml glass bottle together with 90 g of 3 mmφ glass beads. Next, the obtained mixture was mixed and dispersed for 90 minutes by a paint shaker, thereby preparing a mill base.

Composition of Mill Base:
Green-based pigment         12.4 parts by weight
Water-soluble alkyd resin   9.0 parts by weight
(tradename: “S-118”, produced by DAI-
NIPPON INK KAGAKU KOGYO CO., LTD.)
Defoamer (tradename: “NOPCO 8034”,
produced by SUN NOPCO LTD.) 0.1 parts by weight
Water                       4.8 parts by weight
Butyl cellosolve            4.1 parts by weight

The above-prepared mill base was blended with paint components at the following weight ratio, and the obtained mixture was further mixed and dispersed for 15 minutes by a paint shaker, thereby obtaining a water-soluble paint.

Composition of paint:
Mill base                        30.4 parts by weight
Water-soluble alkyd resin        46.2 parts by weight
(tradename: S-118, produced by DAI-
NIPPON INK KAGAKU KOGYO CO., LTD.)
Water-soluble melamine resin     12.6 parts by weight
(tradename: S-695, produced by DAI-
NIPPON INK KAGAKU KOGYO CO., LTD.)
Defoamer (tradename: “NOPCO 8034”, 0.1 parts by weight
produced by SUN NOPCO LTD.)
Water                            9.1 parts by weight
Butyl cellosolve                 1.6 parts by weight

The thus obtained water-based paint showed a viscosity of 2,118 cP. As to the storage stability of the water-based paint, the ΔE* value thereof was 1.00.

Then, the water-based paint was applied onto a cold-rolled steel plate (0.8 mm×70 mm×150 mm; JIS G-3141) and then dried to form a coating film having a thickness of 150 μm thereon. The thus obtained coating film showed a gloss of 82% and a heat resistance temperature of 247° C. As to the hue of the coating film, the L* value thereof was 40.7; the a* value thereof was −12.6; the b* value thereof was 20.9; and the h value thereof was 121.1°. As to the chemical resistances of the coating film, the acid resistance (ΔG value) thereof was 9.6%, and the alkali resistance (ΔG value) thereof was 8.8%.

EXAMPLE 4

<Production of Resin Composition>

2.5 g of the green-based pigment obtained in Example 1, and 47. 5 g of a polyvinyl chloride resin 103EP8D (produced by NIPPON ZEON CO., LTD.) were weighed and charged into a 100 ml beaker, and intimately mixed together by a spatula, thereby obtaining mixed particles.

0.5 g of calcium stearate was added to the mixed particles. The mixed particles were slowly supplied to hot rolls heated to 160° C. whose clearance was set to 0.2 mm, and continuously kneaded therebetween until a uniform resin composition was produced. The resin composition kneaded was separated from the hot rolls and used as a raw material for forming a colored resin plate.

Next, the thus-produced resin composition was interposed between a pair of surface-polished stainless steel plates, placed within a hot press heated to 180° C. and subjected to a pressure molding while applying a pressure of 1 ton/cm 2 thereto, thereby obtaining a colored resin plate having a thickness of 1 mm. The thus-produced colored resin plate had a dispersing condition of rank 5 and a heat resistance temperature of 223° C. As to the hue of the resin plate, the L* value thereof was 42.2; the a* value thereof was −10.8; the b* value thereof was 17.9; and the h value thereof was 121°.

EXAMPLE 5

<Production of Orange-Based Pigment>

11.0 kg of goethite particles (particle shape: acicular shape; average major axial diameter: 0.40 μm; aspect ratio: 5.3:1; geometrical standard deviation value: 1.44; BET specific surface area value: 18.8 m 2 /g; L* value: 59.3; a* value: 16.5; b* value: 53.9; h value: 73.0°; heat resistance temperature: 198° C.), were charged into an edge runner “MPUV-2 Model” (tradename, manufactured by MATSUMOTO CHUZO TEKKOSHO CO., LTD.). Then, a methyltriethoxysilane solution prepared by mixing and diluting 220 g of methyltriethoxysilane (tradename: TSL8123, produced by GE Toshiba Silicone Co., Ltd.) with 200 ml of ethanol was added to the goethite particles while operating the edge runner. The resultant mixture was mixed and stirred at a linear load of 392 N/cm (40 Kg/cm) and a stirring speed of 22 rpm for 20 minutes.

Next, 825 g of an organic red pigment D (kind: quinacridone red; particle shape: granular shape; average major axial diameter: 0.58 μm; hiding power: 480 cm 2 /g; heat resistance temperature: 488° C.; L* value: 37.0; a* value: 51.9; b* value: 20.6; h value: 21.6°), were added to the above mixture for 10 minutes while operating the edge runner. Further, the obtained mixture was mixed and stirred at a linear load of 392 N/cm (40 Kg/cm) and a stirring speed of 22 rpm for 20 minutes to form a coating layer composed of the organic red pigment D on the methyltriethoxysilane coat, thereby obtaining an orange-based pigment. The obtained orange-based pigment was heat-treated at 105° C. for 60 minutes by using a drier.

The obtained orange-based pigment was acicular particles having an average major axial diameter of 0.40 μm, an aspect ratio of 5.3:1, a geometrical standard deviation value of 1.44, a BET specific surface area value of 21.2 m 2 /g, a L* value of 46.3, an a* value of 37.1, a b* value of 42.6, a h value of 48.9°, a tinting strength of 137% and a hiding power of 1,970 cm 2 /g. As to the chemical resistances of the orange-based pigment, the acid resistance (ΔE* value) thereof was 0.97, and the alkali resistance (ΔE* value) thereof was 0.85. As to the heat resistance of the orange-based pigment, the heat resistance temperature thereof was 229° C. The desorption percentage of the organic red pigment from the orange-based pigment was 6.9%. The amount of a coating layer composed of organosilane compounds produced from methyltriethoxysilane was 0.30% by weight (calculated as Si). The amount of the coating layer composed of the organic red pigment D was 5.30% by weight (calculated as C) (corresponding to 7.5 parts by weight based on 100 parts by weight of the goethite core particles).

As a result of the observation of electron micrograph, almost no organic red pigment D liberated was recognized, so that it was confirmed that a substantially whole amount of the organic red pigment D added was adhered on the coating layer composed of the organosilane compounds produced from methyltriethoxysilane.

EXAMPLE 6

<Production of Solvent-Based Paint Containing Orange-Based Pigment>

10 g of the orange-based pigment produced in Example 5, was blended with an amino alkyd resin and a thinner at the following weight ratio, and charged into a 140-ml glass bottle together with 90 g of 3 mmφ glass beads. Next, the obtained mixture was mixed and dispersed for 90 minutes by a paint shaker, thereby preparing a mill base.

Composition of Mill Base:
Orange-based pigment             12.2 parts by weight
Amino alkyd resin (AMILAC No. 1026, 19.5 parts by weight
produced by KANSAI PAINT CO., LTD.)
Thinner                          7.3 parts by weight

The above-prepared mill base was blended with an amino alkyd resin at the following weight ratio, and the obtained mixture was further mixed and dispersed for 15 minutes by a paint shaker, thereby obtaining a solvent-based paint containing the orange-based pigment.

Composition of paint:
Mill base                        39.0 parts by weight
Amino alkyd resin (AMILAC No. 1026, 61.0 parts by weight
produced by KANSAI PAINT CO., LTD.)

The thus obtained solvent-based paint showed a viscosity of 1,315 cP. As to the storage stability of the solvent-based paint, the ΔE* value thereof was 0.86.

Then, the solvent-based paint was applied onto a cold-rolled steel plate (0.8 mm×70 mm×150 mm; JIS G-3141) and then dried to form a coating film having a thickness of 150 μm thereon. The thus obtained coating film showed a gloss of 87% and a heat resistance temperature of 250° C. As to the hue of the coating film, the L* value thereof was 48.0; the a* value thereof was 36.5; the b* value thereof was 42.1; and the h value thereof was 49.1°. As to the chemical resistances of the coating film, the acid resistance (ΔG value) thereof was 8.7%, and the alkali resistance (ΔG value) thereof was 7.7%.

EXAMPLE 7

<Production of Water-Based Paint Containing Orange-Based Pigment>

7.62 g of the orange-based pigment obtained in Example 5, was blended with a water-soluble alkyd resin and the like at the following weight ratio, and charged into a 140-ml glass bottle together with 90 g of 3 mmφ glass beads. Next, the obtained mixture was mixed and dispersed for 90 minutes by a paint shaker, thereby preparing a mill base.

Composition of Mill Base:
Orange-based pigment             12.4 parts by weight
Water-soluble alkyd resin        9.0 parts by weight
(tradename: “S-118”, produced by DAI-
NIPPON INK KAGAKU KOGYO CO., LTD.)
Defoamer (tradename: “NOPCO 8034”, 0.1 parts by weight
produced by SUN NOPCO LTD.)
Water                            4.8 parts by weight
Butyl cellosolve                 4.1 parts by weight

The above-prepared mill base was blended with paint components at the following weight ratio, and the obtained mixture was further mixed and dispersed for 15 minutes by a paint shaker, thereby obtaining a water-soluble paint.

Composition of paint:
Mill base                        30.4 parts by weight
Water-soluble alkyd resin        46.2 parts by weight
(tradename: S-118, produced by DAI-
NIPPON INK KAGAKU KOGYO CO., LTD.)
Water-soluble melamine resin     12.6 parts by weight
(tradename: S-695, produced by DAI-
NIPPON INK KAGAKU KOGYO CO., LTD.)
Defoamer (tradename: “NOPCO 8034”, 0.1 parts by weight
produced by SUN NOPCO LTD.)
Water                            9.1 parts by weight
Butyl cellosolve                 1.6 parts by weight

The thus obtained water-based paint showed a viscosity of 2,434 cP. As to the storage stability of the water-based paint, the ΔE* value thereof was 0.98.

Then, the water-based paint was applied onto a cold-rolled steel plate (0.8 mm×70 mm×150 mm; JIS G-3141) and then dried to form a coating film having a thickness of 150 μm thereon. The thus obtained coating film showed a gloss of 82% and a heat resistance temperature of 248° C. As to the hue of the coating film, the L* value thereof was 48.5; the a* value thereof was 36.7; the b* value thereof was 42.0; and the h value thereof was 48.9°. As to the chemical resistances of the coating film, the acid resistance (ΔG value) thereof was 9.4%, and the alkali resistance (ΔG value) thereof was 8.2%.

EXAMPLE 8

<Production of Resin Composition>

2.5 g of the orange-based pigment obtained in Example 5, and 47. 5 g of a polyvinyl chloride resin 103EP8D (produced by NIPPON ZEON CO., LTD.) were weighed and charged into a 100 ml beaker, and intimately mixed together by a spatula, thereby obtaining mixed particles.

0.5 g of calcium stearate was added to the mixed particles. The mixed particles were slowly supplied to hot rolls heated to 160° C. whose clearance was set to 0.2 mm, and continuously kneaded therebetween until a uniform resin composition was produced. The resin composition kneaded was separated from the hot rolls and used as a raw material for forming a colored resin plate.

Next, the thus-produced resin composition was interposed between a pair of surface-polished stainless steel plates, placed within a hot press heated to 180° C. and subjected to a pressure molding while applying a pressure of 98 MPa (1 ton/cm 2 ) thereto, thereby obtaining a colored resin plate having a thickness of 1 mm. The thus-produced colored resin plate had a dispersing condition of rank 5 and a heat resistance temperature of 224° C. As to the hue of the resin plate, the L* value thereof was 49.4; the a* value thereof was 36.2; the b* value thereof was 41.9; and the h value thereof was 49.20.

EXAMPLE 9

<Production of Green-Based Fine Pigment>

11.0 kg of goethite fine particles (particle shape: acicular shape; average major axial diameter: 0.0710 μm; average minor axial diameter: 0.0081 μm; aspect ratio: 8.8:1; geometrical standard deviation value: 1.38; BET specific surface area value: 159.8 m 2 /g; aluminum content: 0.83% by weight; L* value: 51.6; a* value: 31.4; b* value: 61.7; h value: 63.0°; acid resistance (ΔG value): 1.92; alkali resistance (ΔG value): 1.75; hiding power: 152 cm 2 /g; heat resistance temperature: 245° C.), were charged into an edge runner “MPUV-2 Model” (tradename, manufactured by MATSUMOTO CHUZO TEKKOSHO CO., LTD.). Then, a methyltriethoxysilane solution prepared by mixing and diluting 220 g of methyltriethoxysilane (tradename: TSL8123, produced by GE Toshiba Silicone Co., Ltd.) with 200 ml of ethanol was added to the goethite fine particles while operating the edge runner. The resultant mixture was mixed and stirred at a linear load of 392 N/cm (40 Kg/cm) and a stirring speed of 22 rpm for 20 minutes.

Next, 1,100 g of an organic blue pigment A (kind: copper phthalocyanine blue; particle shape: granular shape; average major axial diameter: 0.06 μm; hiding power: 240 cm 2 /g; L* value: 17.7; a* value: 9.7; b* value: −23.4; h value: 292.5°; heat resistance temperature: 256° C.), were added to the above mixture for 10 minutes while operating the edge runner. Further, the obtained mixture was mixed and stirred at a linear load of 392 N/cm (40 Kg/cm) and a stirring speed of 22 rpm for 20 minutes to form a coating layer composed of the organic blue pigment A on the methyltriethoxysilane coat. Then, the obtained particles were heat-treated at 105° C. for 60 minutes by using a dryer, thereby obtaining a green-based fine pigment.

The obtained green-based fine pigment was acicular particles having an average major axial diameter of 0.0722 μm, an average minor axial diameter of 0.0082 μm, an aspect ratio of 8.8:1, a geometrical standard deviation value of 1.33, a BET specific surface area value of 153.6 m 2 /g, a L* value of 31.6, an a* value of −8.7, a b* value of 0.3, a h value of 178.0°, a tinting strength of 123% and a hiding power of 159 cm 2 /g. As to the chemical resistances of the green-based fine pigment, the acid resistance (ΔE* value) thereof was 1.14, and the alkali resistance (ΔE* value) thereof was 1.06. As to the heat resistance of the green-based fine pigment, the heat resistance temperature thereof was 257° C. The desorption percentage of the organic blue pigment from the green-based fine pigment was 7.1%. The amount of a coating layer composed of organosilane compounds produced from methyltriethoxysilane was 0.30% by weight (calculated as Si). The amount of the coating layer composed of the organic blue pigment A was 5.99 % by weight (calculated as C) (corresponding to 10 parts by weight based on 100 parts by weight of the goethite core fine particles).

As a result of the observation of electron micrograph, almost no organic blue pigment A liberated was recognized. Therefore, it was confirmed that a substantially whole amount of the organic blue pigment A added was adhered on the coating layer composed of the organosilane compounds produced from methyltriethoxysilane.

EXAMPLE 10

<Production of Solvent-Based Paint Containing Green-Based Fine Pigment>

5 g of the green-based fine pigment produced in Example 9 was blended with the below-mentioned paint base materials at the following weight ratio in a 250-ml glass bottle. Next, the obtained mixture was mixed and dispersed together with 160 g of 3 mmφ glass beads for 120 minutes by a paint shaker, thereby preparing a solvent-based paint.

Composition of Solvent-based Paint:
Green-based fine pigment         9.9 parts by weight
Melamine resin (tradename: SUPER-PEKKAMINE 19.8 parts by weight
J-820-60, produced by DAI-NIPPON INK
KAGAKU KOGYO CO., LTD.)
Alkyd resin (tradename: BEKKOSOLE 1307-60EL, 39.6 parts by weight
produced by DAI-NIPPON INK KAGAKU
KOGYO CO., LTD.)
Xylene                           29.7 parts by weight
Butanol                          1.0 part by weight

The thus obtained solvent-based paint showed a viscosity of 1,676 cP. As to the storage stability of the solvent-based paint, the ΔE* value thereof was 0.87.

The solvent-based paint was applied onto a clear base film and then dried to form a coating film having a thickness of 150 μm (6 mil) thereon. The thus obtained coating film showed a gloss of 86.1%. As to the hue of the coating film, the L* value thereof was 32.3; the a* value thereof was −16.3; the b* value thereof was 2.0; and the h value thereof was 173.0°. The linear absorption of the coating film was 0.0184 μm −1 .

Then, the solvent-based paint was applied onto a transparent glass plate (0.8 mm in thickness×70 mm in width×150 mm in length) to form a coating film having a thickness of 150 μm (6 mil) thereon. As to the chemical resistances of the obtained coating film, the acid resistance (ΔG value) thereof was 8.2%, and the alkali resistance (ΔG value) thereof was 7.7%.

Then, the heat resistance of the coating film was determined as follows. That is, five coated plates were prepared using the solvent-based paint by the same method as described above. The respective coated plates were placed within Geer ovens heated to 210° C., 230° C., 250° C, 270° C. and 290° C., respectively, and heat-treated therein for 15 minutes. Thereafter, the coated plates were removed from the ovens to measure the hue values thereof. Based on the hue values before the heat treatment as standard values, the ΔE* value of each coated plate was measured. From the relationship between the heat-treating temperature and the ΔE* value, it was recognized that the temperature at which the ΔE* value was identical to just 1.5, was 269° C.

EXAMPLE 11

<Production of Water-Based Paint Containing Green-Based Fine Pigment>

5 g of the green-based fine pigment produced in Example 9 was blended with the below-mentioned paint base materials at the following weight ratio in a 250-ml glass bottle. Next, the obtained mixture was mixed and dispersed together with 160 g of 3 mmφ glass beads for 120 minutes by a paint shaker, thereby preparing a water-based paint.

Composition of Water-based Paint:
Green-based fine pigment         10.1 parts by weight
Water-soluble melamine resin (tradename: S-695, 9.3 parts by weight
produced by DAI-NIPPON INK KAGAKU
KOGYO CO., LTD.)
Water-soluble alkyd resin (tradename: S-118, 40.7 parts by weight
produced by DAI-NIPPON INK KAGAKU
KOGYO CO., LTD.)
Defoamer (tradename: “NOPCO 8034”, 0.2 part by weight
produced by SUN NOPCO LTD.)
Water                            28.2 parts by weight
Butyl cellosolve                 11.5 parts by weight

The thus obtained water-based paint showed a viscosity of 2,184 cP. As to the storage stability of the water-based paint, the ΔE* value thereof was 0.92.

The water-based paint was applied onto a clear base film and then dried to form a coating film having a thickness of 150 μm (6 mil) thereon. The thus obtained coating film showed a gloss of 82.3%. As to the hue of the coating film, the L* value thereof was 32.9; the a* value thereof was −16.2; the b* value thereof was 2.1; and the h value thereof was 172.6°. The linear absorption of the coating film was 0.0199 μm −1 .

Then, the water-based paint was applied onto a transparent glass plate (0.8 mm in thickness×70 mm in width×150 mm in length) to form a coating film having a thickness of 150 μm (6 mil) thereon. As to the chemical resistances of the obtained coating film, the acid resistance (ΔG value) thereof was 8.7%, and the alkali resistance (ΔG value) thereof was 8.0%.

Then, the heat resistance of the coating film was determined as follows. That is, five coated plates were prepared using the water-based paint by the same method as described above. The respective coated plates were placed within Geer ovens heated to 210° C., 230° C., 250° C., 270° C. and 290° C., respectively, and heat-treated therein for 15 minutes. Thereafter, the coated plates were removed from the ovens to measure the hue values thereof. Based on the hue values before the heat treatment as standard values, the ΔE* value of each coated plate was measured. From the relationship between the heat-treating temperature and the ΔE* value, it was recognized that the temperature at which the ΔE* value was identical to just 1.5, was 264° C.

EXAMPLE 12

<Production of Resin Composition>

0.5 g of the green-based fine pigment obtained in Example 9, and 49. 5 g of a polyvinyl chloride resin 103EP8D (produced by NIPPON ZEON CO., LTD.) were weighed and charged into a 100 ml beaker, and intimately mixed together by a spatula, thereby obtaining mixed particles.

1.0 g of calcium stearate was added to the mixed particles. The mixed particles were slowly supplied to hot rolls heated to 160° C. whose clearance was set to 0.2 mm, and continuously kneaded therebetween until a uniform resin composition was produced. The resin composition kneaded was separated from the hot rolls and used as a raw material for forming a colored resin plate.

Next, the thus-produced resin composition was interposed between a pair of surface-polished stainless steel plates, placed within a hot press heated to 180° C. and subjected to a pressure molding while applying a pressure of 98 MPa (1 ton/cm 2 ) thereto, thereby obtaining a colored resin plate having a thickness of 1 mm. As to the hue of the resin plate, the L* value thereof was 32.4; the a* value thereof was −12.6; the b* value thereof was 2.4; and the h value thereof was 169.2°. The thus-produced colored resin plate had a dispersing condition of rank 5 and a linear absorption of 0.0192 μm −1 .

Then, the heat resistance of the resin composition was determined as follows. That is, five colored resin plates were prepared using the resin composition and cut into 5 cm square to prepare 5 test specimens. The respective test specimens were placed within hot presses heated to 185° C., 200° C., 215° C., 230° C. and 245° C., respectively, and heat-treated therein for 10 minutes while applying a pressure of 98 MPa (1 ton/cm 2 ) thereto. Thereafter, the resin plates were removed from the presses to measure the hue values thereof. Based on the hue values before the heat treatment as standard values, the ΔE* value of each resin plate was measured. From the relationship between the heat-treating temperature and the ΔE* value, it was recognized that the temperature at which the ΔE* value was identical to just 1.5, was 231° C.

EXAMPLE 13

<Production of Orange-Based Fine Pigment>

11.0 kg of goethite fine particles (particle shape: acicular shape; average major axial diameter: 0.0710 μm; average minor axial diameter: 0.0081 μm; aspect ratio: 8.8:1; geometrical standard deviation value: 1.38; BET specific surface area value: 159.8 m 2 /g; aluminum content: 0.83% by weight; L* value: 51.6; a* value: 31.4; b* value: 61.7; h value: 63.0°; acid resistance: 1.92; alkali resistance: 1.75; hiding power: 152 cm 2 /g; heat resistance temperature: 245° C.), were charged into an edge runner “MPUV-2 Model” (tradename, manufactured by MATSUMOTO CHUZO TEKKOSHO CO., LTD.). Then, a methyltriethoxysilane solution prepared by mixing and diluting 220 g of methyltriethoxysilane (tradename: TSL8123, produced by GE Toshiba Silicone Co., Ltd.) with 200 ml of ethanol was added to the goethite fine particles while operating the edge runner. The resultant mixture was mixed and stirred at a linear load of 441 N/cm (45 Kg/cm) and a stirring speed of 22 rpm for 30 minutes.

Next, 1,100 g of an organic red pigment D (kind: quinacridone red; particle shape: granular shape; average major axial diameter: 0.58 μm; hiding power: 480 cm 2 /g; L* value: 37.0; a* value: 51.9; b* value: 20.6; h value: 21.6°; heat resistance temperature: 488° C.), was added to the above mixture for 10 minutes while operating the edge runner. Further, the obtained mixture was mixed and stirred at a linear load of 441 N/cm (45 Kg/cm) and a stirring speed of 22 rpm for 30 minutes to form a coating layer composed of the organic red pigment A on the methyltriethoxysilane coat. Then, the obtained particles were heat-treated at 105° C. for 60 minutes by using a dryer, thereby obtaining orange-based fine pigment.

The obtained orange-based fine pigment was acicular particles having an average major axial diameter of 0.0720 μm, an average minor axial diameter of 0.0084 μm, an aspect ratio of 8.6:1, a geometrical standard deviation value of 1.38, a BET specific surface area value of 162.1 m 2 /g, a L* value of 35.2, an a* value of 49.8, a b* value of 40.2, a h value of 38.9°, a tinting strength of 129% and a hiding power of 161 cm 2 /g. As to the chemical resistances of the orange-based fine pigment, the acid resistance (ΔE* value) thereof was 1.09, and the alkali resistance (ΔE* value) thereof was 1.04. As to the heat resistance of the orange-based fine pigment, the heat resistance temperature thereof was 254° C. The desorption percentage of the organic red pigment from the orange-based fine pigment was 7.0%. The amount of a coating layer composed of organosilane compounds produced from methyltriethoxysilane was 0.30% by weight (calculated as Si). The amount of the coating layer composed of the organic red pigment D was 6.89% by weight (calculated as C) (corresponding to 10 parts by weight based on 100 parts by weight of the goethite core fine particles).

As a result of the observation of electron micrograph, almost no organic red pigment D liberated was recognized. Therefore, it was confirmed that a substantially whole amount of the organic red pigment D added was adhered on the coating layer composed of the organosilane compounds produced from methyltriethoxysilane.

EXAMPLE 14

<Production of Solvent-Based Paint Containing Orange-Based Fine Pigment>

5 g of the orange-based fine pigment produced in Example 13 was blended with the below-mentioned paint base materials at the following weight ratio in a 250-ml glass bottle. Next, the obtained mixture was mixed and dispersed together with 160 g of 3 mmφ glass beads for 120 minutes by a paint shaker, thereby preparing a solvent-based paint.

Composition of Solvent-based Paint:
Orange-based fine pigment        9.9 parts by weight
Melamine resin (tradename: SUPER-PEKK- 19.8 parts by weight
AMINE J-820-60, produced by DAI-NIPPON
INK KAGAKU KOGYO CO., LTD.)
Alkyd resin (tradename: BEKKOSOLE 39.6 parts by weight
1307-60EL, produced by DAI-NIPPON
INK KAGAKU KOGYO CO., LTD.)
Xylene                           29.7 parts by weight
Butanol                          1.0 parts by weight

The thus obtained solvent-based paint showed a viscosity of 3,119 cP. As to the storage stability of the solvent-based paint, the ΔE* value thereof was 0.95.

The solvent-based paint was applied onto a clear base film and then dried to form a coating film having a thickness of 150 μm (6 mil) thereon. The thus obtained coating film showed a gloss of 82.2%. As to the hue of the coating film, the L* value thereof was 36.0; the a* value thereof was 49.5; the b* value thereof was 40.6; and the h value thereof 39.4°. The linear absorption of the coating film was 0.0202 μm −1 .

Then, the solvent-based paint was applied onto a transparent glass plate (0.8 mm in thickness×70 mm in width×150 mm in length) to form a coating film having a thickness of 150 μm (6 mil) thereon. As to the chemical resistances of the obtained coating film, the acid resistance (ΔG value) thereof was 8.5%, and the alkali resistance (ΔG value) thereof was 8.0%.

Then, the heat resistance of the coating film was determined as follows. That is, five coated plates were prepared using the solvent-based paint by the same method as described above. The respective coated plates were placed within Geer ovens heated to 210° C., 230° C., 250° C., 270° C. and 290° C., respectively, and heat-treated therein for 15 minutes. Thereafter, the coated plates were removed from the ovens to measure the hue values thereof. Based on the hue values before the heat treatment as standard values, the ΔE* value of each coated plate was measured. From the relationship between the heat-treating temperature and the ΔE* value, it was recognized that the temperature at which the ΔE* value was identical to just 1.5, was 259° C.

EXAMPLE 15

<Production of Water-Based Paint Containing Orange-Based Fine Pigment>

5 g of the orange-based fine pigment produced in Example 13 was blended with the below-mentioned paint base materials at the following weight ratio in a 250-ml glass bottle. Next, the obtained mixture was mixed and dispersed together with 160 g of 3 mmφ glass beads for 120 minutes by a paint shaker, thereby preparing a water-based paint.

Composition of Water-based Paint:
Orange-based fine pigment        10.1 parts by weight
Water-soluble melamine resin (tradename: 9.3 parts by weight
S-695, produced by DAI-NIPPON
INK KAGAKU KOGYO CO., LTD.)
Water-soluble alkyd resin (tradename: 40.7 parts by weight
S-118, produced by DAI-NIPPON
INK KAGAKU KOGYO CO., LTD.)
Defoamer (tradename:             0.2 parts by weight
“NOPCO 8034”, produced
by SUN NOPCO LTD.)
Water                            28.2 parts by weight
Butyl cellosolve                 11.5 parts by weight

The thus obtained water-based paint showed a viscosity of 3,209 cP. As to the storage stability of the water-based paint, the ΔE* value thereof was 0.92.

The water-based paint was applied onto a clear base film and then dried to form a coating film having a thickness of 150 μm (6 mil) thereon. The thus obtained coating film showed a gloss of 78.8%. As to the hue of the coating film, the L* value thereof was 36.1; the a* value thereof was 49.4; the b* value thereof was 40.2; and the h value thereof was 39.1°. The linear absorption of the coating film was 0.0215 μm −1 .

Then, the water-based paint was applied onto a transparent glass plate (0.8 mm in thickness×70 mm in width×150 mm in length) to form a coating film having a thickness of 150 μm (6 mil) thereon. As to the chemical resistances of the obtained coating film, the acid resistance (ΔG value) thereof was 8.7%, and the alkali resistance (ΔG value) thereof was 8.1%.

Then, the heat resistance of the coating film was determined as follows. That is, five coated plates were prepared using the water-based paint by the same method as described above. The respective coated plates were placed within Geer ovens heated to 210° C., 230° C., 250° C., 270° C. and 290° C., respectively, and heat-treated therein for 15 minutes. Thereafter, the coated plates were removed from the ovens to measure the hue values thereof. Based on the hue values before the heat treatment as standard values, the ΔE* value of each coated plate was measured. From the relationship between the heat-treating temperature and the ΔE* value, it was recognized that the temperature at which the ΔE* value was identical to just 1.5, was 256° C.

EXAMPLE 16

<Production of Resin Composition>

0.5 g of the orange-based fine pigment obtained in Example 13, and 49. 5 g of a polyvinyl chloride resin 103EP8D (produced by NIPPON ZEON CO., LTD.) were weighed and charged into a 100 ml beaker, and intimately mixed together by a spatula, thereby obtaining mixed particles.

1.0 g of calcium stearate was added to the mixed particles. The mixed particles were slowly supplied to hot rolls heated to 160° C. whose clearance was set to 0.2 mm, and continuously kneaded therebetween until a uniform resin composition was produced. The resin composition kneaded was separated from the hot rolls and used as a raw material for forming a colored resin plate.

Next, the thus-produced resin composition was interposed between a pair of surface-polished stainless steel plates, placed within a hot press heated to 180° C. and subjected to a pressure molding while applying a pressure of 98 MPa (1 ton/cm 2 ) thereto, thereby obtaining a colored resin plate having a thickness of 1 mm. As to the hue of the resin plate, the L* value thereof was 36.2; the a* value thereof was 49.9; the b* value thereof was 40.6; and the h value thereof was 39.1°. The thus-produced colored resin plate had a dispersing condition of rank 5 and a linear absorption of 0.0211 μm −1 .

Then, the heat resistance of the resin composition was determined as follows. That is, five colored resin plates were prepared from the resin composition and cut into 5 cm square to prepare 5 test specimens. The respective test specimens were placed within hot presses heated to 185° C., 200° C., 215° C., 230° C. and 245° C., respectively, and heat-treated therein for 10 minutes while applying a pressure of 98 MPa (1 ton/cm 2 ) thereto. Thereafter, the resin plates were removed from the presses to measure the hue values thereof. Based on the hue values before the heat treatment as standard values, the ΔE* value of each resin plate was measured. From the relationship between the heat-treating temperature and the ΔE* value, it was recognized that the temperature at which the ΔE* value was identical to just 1.5, was 229° C.

Core Particles 1 to 4

As core particles, iron oxide hydroxide particles having properties shown in Table 1 were prepared.

Core Particles 5

20 kg of acicular goethite particles (core particles 1) and 150 liters of water were mixed together, thereby obtaining a slurry containing the acicular goethite particles. The pH value of the obtained re-dispersed slurry containing the acicular goethite particles was adjusted to 10.5 using an aqueous sodium hydroxide solution, and then the concentration of the solid content in the slurry was adjusted to 98 g/liter by adding water thereto. After 150 liters of the slurry was heated to 60° C., 2,722 ml of a 1.0 mol/liter sodium aluminate solution (corresponding to 0.5% by weight (calculated as Al) based on the weight of the acicular goethite particles) was added to the slurry. After allowing the obtained slurry to stand for 30 minutes, the pH value of the obtained slurry was adjusted to 7.5 by adding acetic acid thereto. Further, after allowing the obtained slurry to stand for 30 minutes, the slurry was subjected to filtration, washing with water, drying and pulverization, thereby obtaining the acicular goethite particles whose surfaces were coated with hydroxides of aluminum.

The production condition are shown in Table 2, and various properties of the obtained surface-treated acicular goethite particles are shown in Table 3.

Core Particles 6 to 8

The same procedure as defined above for the production of the core particles 5, was conducted except that the respective iron oxide hydroxide particles (core particles 2 to 4) were used instead of the core particles 1, and kinds and amounts of coating materials to be adhered thereon were changed variously, thereby obtaining surface-coated iron oxide hydroxide particles.

The production condition are shown in Table 2, and various properties of the obtained surface-treated iron oxide hydroxide particles are shown in Table 3.

Core Particles 9 to 12

As core particles, iron oxide hydroxide fine particles having properties shown in Table 4 were prepared.

Core particles 13

20 kg of acicular goethite fine particles (core particles 9) and 150 liters of water were mixed together, thereby obtaining a slurry containing the acicular goethite fine particles. The pH value of the obtained re-dispersed slurry containing the acicular goethite fine particles was adjusted to 10.5 using an aqueous sodium hydroxide solution, and then the concentration of the solid content in the slurry was adjusted to 98 g/liter by adding water thereto. After 150 liters of the slurry was heated to 60° C., 5,444 ml of a 5.0 mol/liter sodium aluminate solution (corresponding to 5% by weight (calculated as Al) based on the weight of the acicular goethite fine particles) was added to the slurry. After allowing the obtained slurry to stand for 30 minutes, the pH value of the obtained slurry was adjusted to 7.5 by adding acetic acid thereto. Further, after allowing the obtained slurry to stand for 30 minutes, the slurry was subjected to filtration, washing with water, drying and pulverization, thereby obtaining the acicular goethite fine particles whose surfaces were coated with hydroxides of aluminum.

The production condition are shown in Table 5, and various properties of the obtained surface-treated acicular goethite fine particles are shown in Table 6.

Core Particles 14 to 16

The same procedure as defined above for the production of the core particles 13, was conducted except that the respective iron oxide hydroxide particles (core particles 10 to 12) were used instead to the core particles 9, and kinds and amounts of coating materials to be adhered were changed variously, thereby obtaining surface-coated iron oxide hydroxide fine particles.

The production condition are shown in Table 5, and various properties of the obtained surface-treated iron oxide hydroxide fine particles are shown in Table 6.

Meanwhile, in “Kind of coating material” of the “surface-treating step” as described in Tables, “A” represents hydroxides of aluminum, and “S” represents oxides of silicon.

Organic Blue Pigments A to C

The organic blue pigments having properties shown in Table 7 were prepared.

Organic Red Pigments D and E

The organic red pigments having properties shown in Table 7 were prepared.

EXAMPLES 17 to 24 and

Comparative Examples 1 to 5

The same procedure as defined in Example 1 was conducted except that kinds of the core particles, kinds and amounts of alkoxysilane compounds, polysiloxanes or silicon compounds added in the coating step, linear loads and times used for the edge runner treatment in the above coating step, kinds and amounts of organic blue pigments added in the organic blue pigment-adhering step, and linear loads and times used for the edge runner treatment in the above adhering step, were changed variously, thereby obtaining green-based pigments.

The production conditions are shown in Table 8, and various properties of the obtained green-based pigments are shown in Table 9.

Comparative Examples 6 to 8

In these Comparative Examples, chrome green (Comparative Example 6), chromium oxide (Comparative Example 7) and phthalocyanine green (Comparative Example 8) were used solely. The results are shown in Table 9.

EXAMPLES 25 to 32 and

Comparative Examples 9 to 16

The same procedure as defined in Example 2 was conducted except that kinds of green-based pigments were changed variously, thereby obtaining solvent-based paints.

Various properties of the obtained solvent-based paints and coating films are shown in Table 10.

EXAMPLES 33 to 40 and

Comparative Examples 17 to 24

The same procedure as defined in Example 3 was conducted except that kinds of green-based pigments were changed variously, thereby obtaining water-based paints.

Various properties of the obtained water-based paints and coating films are shown in Table 11.

EXAMPLES 41 to 48 and

Comparative Examples 25 to 32

The same procedure as defined in Example 4 was conducted except that kinds of green-based pigments were changed variously, thereby obtaining resin compositions.

The production conditions and various properties of the obtained resin compositions are shown in Table 12.

EXAMPLES 49 to 56 and

Comparative Examples 33 to 37

The same procedure as defined in Example 5 was conducted except that kinds of the core particles, kinds and amounts of alkoxysilane compounds, polysiloxanes or silicon compounds added in the coating step, linear loads and times used for the edge runner treatment in the above coating step, kinds and amounts of organic red pigments added in the organic red pigment-adhering step, and linear loads and times used for the edge runner treatment in the above adhering step, were changed variously, thereby obtaining orange-based pigments.

The production conditions are shown in Table 13, and various properties of the obtained orange-based pigments are shown in Table 14.

EXAMPLES 57 to 64 and

Comparative Examples 38 to 42

The same procedure as defined in Example 6 was conducted except that kinds of orange-based pigments were changed variously, thereby obtaining solvent-based paints.

Various properties of the obtained solvent-based paints and coating films are shown in Table 15.

EXAMPLES 65 to 72 and

Comparative Examples 43 to 47

The same procedure as defined in Example 7 was conducted except that kinds of orange-based pigments were changed variously, thereby obtaining water-based paints.

Various properties of the obtained water-based paints and coating films are shown in Table 16.

EXAMPLES 73 to 80 and

Comparative Examples 48 to 52

The same procedure as defined in Example 8 was conducted except that kinds of orange-based pigments were changed variously, thereby obtaining resin compositions.

The production conditions and various properties of the obtained resin compositions are shown in Table 17.

EXAMPLES 81 to 88 and

Comparative Examples 53 to 57

The same procedure as defined in Example 9 was conducted except that kinds of the core particles, kinds and amounts of alkoxysilane compounds, polysiloxanes or silicon compounds added in the coating step, linear loads and times used for the edge runner treatment in the above coating step, kinds and amounts of organic blue pigments added in the organic blue pigment-adhering step, and linear loads and times used for the edge runner treatment in the above adhering step, were changed variously, thereby obtaining green-based fine pigments.

The production conditions are shown in Table 18, and various properties of the obtained green-based fine pigments are shown in Table 19.

EXAMPLES 89 to 96 and

Comparative Examples 58 to 62

The same procedure as defined in Example 10 was conducted except that kinds of green-based fine pigments were changed variously, thereby obtaining solvent-based paints.

Various properties of the obtained solvent-based paints and coating films are shown in Table 20.

EXAMPLES 97 to 104 and

Comparative Examples 63 to 67

The same procedure as defined in Example 11 was conducted except that kinds of green-based fine pigments were changed variously, thereby obtaining water-based paints.

Various properties of the obtained water-based paints and coating films are shown in Table 21.

EXAMPLES 105 to 112 and

Comparative Examples 68 to 72

The same procedure as defined in Example 12 was conducted except that kinds of green-based fine pigments were changed variously, thereby obtaining resin compositions.

The production conditions and various properties of the obtained resin compositions are shown in Table 22.

EXAMPLES 113 to 120 and

Comparative Examples 73 to 77

The same procedure as defined in Example 13 was conducted except that kinds of the core particles, kinds and amounts of alkoxysilane compounds, polysiloxanes or silicon compounds added in the coating step, linear loads and times used for the edge runner treatment in the above coating step, kinds and amounts of organic red pigments added in the organic red pigment-adhering step, and linear loads and times used for the edge runner treatment in the above adhering step, were changed variously, thereby obtaining orange-based fine pigments.

The production conditions are shown in Table 23, and various properties of the obtained orange-based fine pigments are shown in Table 24.

EXAMPLES 121 to 128 and

Comparative Examples 78 to 82

The same procedure as defined in Example 14 was conducted except that kinds of orange-based fine pigments were changed variously, thereby obtaining solvent-based paints.

Various properties of the obtained solvent-based paints and coating films are shown in Table 25.

EXAMPLES 129 to 136 and

Comparative Examples 83 to 87

The same procedure as defined in Example 15 was conducted except that kinds of orange-based fine pigments were changed variously, thereby obtaining water-based paints.

Various properties of the obtained water-based paints and coating films are shown in Table 26.

EXAMPLES 137 to 144 and

Comparative Examples 88 to 92

The same procedure as defined in Example 16 was conducted except that kinds of orange-based fine pigments were changed variously, thereby obtaining resin compositions.

The production conditions and various properties of the obtained resin compositions are shown in Table 27.

	TABLE 1
	Properties of iron oxide
	hydroxide particles
		Kind of iron		Average
		oxide		major axial
	Core	hydroxide	Particle	diameter
	particles	particles	shape	(μm)
	Core	Goethite	Acicular	0.43
	particles 1
	Core	Goethite	Acicular	0.38
	particles 2
	Core	Goethite	Acicular	0.40
	particles 3
	Core	Lepidocrocite	Rectangular	0.20
	particles 4
	Properties of iron oxide hydroxide
	particles
			Geometrical	BET	Al
			standard	specific	content
		Aspect	deviation	surface	within
	Core	ratio	value	area value	particles
	particles	(−)	(−)	(m 2 /g)	(wt. %)
	Core	5.8:1	1.45	16.8	—
	particles 1
	Core	6.1:1	1.39	22.3	—
	particles 2
	Core	5.6:1	1.41	19.8	2.36
	particles 3
	Core	4.6:1	1.41	71.2	—
	particles 4
	Properties of iron oxide hydroxide
	particles
	Hue	Heat
		L*	a*	b*	h	resistance
	Core	value	value	value	value	temperature
	particles	(−)	(−)	(−)	(°)	(° C.)
	Core	61.2	15.3	54.8	74.4	202
	particles 1
	Core	58.6	17.1	52.1	71.8	195
	particles 2
	Core	60.6	14.9	55.0	74.8	250
	particles 3
	Core	54.8	20.4	37.6	61.5	193
	particles 4

	TABLE 2
		Surface-treating step
	Kind of	Additives
	Core	core		Calculated	Amount
	particles	particles	Kind	as	(wt. %)
	Core	Core	Sodium	A;	0.5
	particles 5	particles 1	aluminate
	Core	Core	Water	SiO 2	0.2
	particles 6	particles 2	glass #3
	Core	Core	Aluminum	Al	1.0
	particles 7	particles 3	sulfate
	Core	Core	Aluminum	Al	0.5
	particles 8	particles 4	sulfate
			Water	SiO 2	1.5
			glass #3
	Surface-treating step
	Coating material
	Core		Calculated	Amount
	particles	Kind	as	(wt. %)
	Core	A	Al	0.49
	particles 5
	Core	S	SiO 2	0.18
	particles 6
	Core	A	Al	0.97
	particles 7
	Core	A	Al	0.48
	particles 8	S	SiO 2	1.45

	TABLE 3
	Properties of surface-treated iron oxide
	hydroxide particles
			Average major
	Core	Particle	axial diameter	Aspect ratio
	particles	shape	(μm)	(−)
	Core	Acicular	0.43	5.8:1
	particles 5
	Core	Acicular	0.38	6.1:1
	particles 6
	Core	Acicular	0.40	5.6:1
	particles 7
	Core	Rectangular	0.21	4.6:1
	particles 8
	Properties of surface-treated iron oxide
	hydroxide particles
		Geometrical	BET specific	Al content
		standard	surface area	within
	Core	deviation value	value	particles
	particles	(−)	(m 2 /g)	(wt. %)
	Core	1.45	17.0	—
	particles 5
	Core	1.40	22.5	—
	particles 6
	Core	1.41	19.5	2.34
	particles 7
	Core	1.42	70.8	—
	particles 8
	Properties of surface-treated iron oxide
	hydroxide particles
	Hue	Heat
		L*	a*	b*	h	resistance
	Core	value	value	value	value	temperature
	particles	(−)	(−)	(−)	(°)	(° C.)
	Core	61.3	15.1	54.7	74.6	221
	particles 5
	Core	58.7	17.2	52.3	71.8	208
	particles 6
	Core	60.4	15.0	55.2	74.8	260
	particles 7
	Core	55.0	20.2	37.5	61.7	208
	particles 8

	TABLE 4
	Kind of iron	Properties of iron oxide
	oxide	hydroxide fine particles
		hydroxide		Average
	Core	fine	Particle	diameter
	particles	particles	shape	(μm)
	Core	Goethite	Acicular	0.0813
	particles 9
	Core	Goethite	Spindle-	0.0571
	particles 10		shaped
	Core	Goethite	Acicular	0.0763
	particles 11
	Core	Lepidocrocite	Rectangular	0.0900
	particles 12
	Properties of iron oxide hydroxide fine
	particles
		Average		Geometrical
		minor axial	Aspect	standard
	Core	diameter	ratio	deviation value
	particles	(μm)	(−)	(−)
	Core	0.0095	8.6:1	1.41
	particles 9
	Core	0.0093	6.1:1	1.35
	particles 10
	Core	0.0118	6.5:1	1.36
	particles 11
	Core	0.0179	5.0:1	1.40
	particles 12
	Properties of iron oxide hydroxide fine
	particles
			Al content within
		BET specific	particles
	Core	surface area	(calculated as Al)
	particles	value (m 2 /g)	(wt. %)
	Core	148.9	—
	particles 9
	Core	192.1	2.56
	particles 10
	Core	149.2	1.87
	particles 11
	Core	100.4	—
	particles 12
	Properties of iron oxide hydroxide fine
	particles
	Composite oxide hydroxide
		Coating amount	Coating amount
		of Al	of Fe
	Core	(calculated as Al)	(calculated as Fe)
	particles	(wt. %)	(wt. %)
	Core	—	—
	particles 9
	Core	—	—
	particles 10
	Core	1.31	11.0
	particles 11
	Core	—	—
	particles 12
	Properties of iron oxide hydroxide fine
	particles
	Hue
		L*	a*	b*	h	Hiding
	Core	value	value	value	value	power
	particles	(−)	(−)	(−)	(°)	(cm 2 /g)
	Core	50.1	29.4	54.2	61.5	171
	particles 9
	Core	52.6	29.6	57.0	65.6	144
	particles 10
	Core	54.3	27.3	58.9	65.1	158
	particles 11
	Core	48.4	33.6	59.4	60.5	209
	particles 12
	Properties of iron oxide hydroxide fine
	particles
	Chemical resistance
		Acid	Alkali	Heat
		resistance	resistance	resistance
	Core	ΔE* value	ΔE* value	temperature
	particles	(−)	(−)	(° C.)
	Core	2.05	1.83	192
	particles 9
	Core	1.96	1.72	246
	particles 10
	Core	1.77	1.67	270
	particles 11
	Core	2.24	2.11	189
	particles 12

	TABLE 5
		Surface-treating step
	Kind of	Additives
Core	core		Calculated	Amount
particles	particles	Kind	as	(wt. %)
Core	Core	Sodium	Al	5.0
particles 13	particles 9	aluminate
Core	Core	Water	SiO 2	2.0
particles 14	particles 10	glass #3
Core	Core	Sodium	Al	1.0
particles 15	particles 11	aluminate
		Water	SiO 2	0.5
		glass #3
Core	Core	Aluminum	Al	2.0
particles 16	particles 12	sulfate
	Surface-treating step
	Coating material
	Core		Calculated	Amount
	particles	Kind	as	(wt. %)
	Core	A	Al	4.75
	particles 13
	Core	S	SiO 2	1.96
	particles 14
	Core	A	Al	0.98
	particles 15	S	SiO 2	0.49
	Core	A	Al	1.96
	particles 16

	TABLE 6
	Properties of surface-treated iron
	oxide hydroxide fine particles
		Average	Average
		major axial	minor axial	Aspect
	Core	diameter	diameter	ratio
	particles	(μm)	(μm)	(−)
	Core	0.0816	0.0098	8.3:1
	particles 13
	Core	0.0572	0.0094	6.1:1
	particles 14
	Core	0.0765	0.0120	6.4:1
	particles 15
	Core	0.0901	0.0180	5.0:1
	particles 16
	Properties of surface-treated iron oxide
	hydroxide fine particles
				Al content* 1
		Geometrical		within
		standard		particles
		deviation	BET specific	(calculated
	Core	value	surface area	as Al)
	particles	(−)	value (m 2 /g)	(wt. %)
	Core	1.42	154.2	—
	particles 13
	Core	1.35	186.6	2.56
	particles 14
	Core	1.37	152.9	1.87
	particles 15
	Core	1.41	109.1	—
	particles 16
	Properties of surface-treated iron
	oxide hydroxide fine particles
	Composite oxide hydroxide
		Coating amount	Coating amount
		of Al* 1	of Fe* 1
	Core	(calculated as Al)	(calculated as Fe)
	particles	(wt. %)	(wt. %)
	Core	—	—
	particles 13
	Core	—	—
	particles 14
	Core	1.13	0.64
	particles 15
	Core	—	—
	particles 16
	Properties of surface-treated iron oxide
	hydroxide fine particles
	Hue
		L*	a*	b*	h	Hiding
	Core	value	value	value	value	power
	particles	(−)	(−)	(−)	(°)	(cm 2 /g)
	Core	51.1	29.1	54.3	61.8	166
	particles 13
	Core	53.8	29.3	57.6	63.0	140
	particles 14
	Core	55.2	26.1	58.1	65.8	152
	particles 15
	Core	49.3	34.0	60.2	60.5	207
	particles 16
	Properties of surface-treated iron oxide
	hydroxide fine particles
	Chemical resistances
		Acid	Alkali
		resistance	resistance	Heat
	Core	ΔE* value	ΔE* value	resistance
	particles	(−)	(−)	(° C.)
	Core	1.98	1.80	222
	particles 13
	Core	1.92	1.71	253
	particles 14
	Core	1.73	1.65	274
	particles 15
	Core	2.18	2.05	208
	particles 16
	* 1 : Coating amount on core particles

	TABLE 7
	Organic	Properties of organic pigment
	pigment	Kind
	Organic blue	Copper phthalocyanine blue
	pigment A	(C. I. Pigment Blue 15:1)
	Organic blue	Copper phthalocyanine blue
	pigment B	(C. I. Pigment Blue 15:4)
	Organic blue	Copper phthalocyanine blue
	pigment C	(C. I. Pigment Blue 15:2)
	Organic red	Quinacridone red
	pigment D
	Organic red	Quinacridone red
	pigment E
	Properties of organic pigment
			Average
			particle	Hiding
	Organic		size	power
	pigment	Particle shape	(μm)	(cm2/g)
	Organic blue	Granular	0.06	240
	pigment A
	Organic blue	Granular	0.08	272
	pigment B
	Organic blue	Granular	0.10	301
	pigment C
	Organic red	Granular	0.58	480
	pigment D
	Organic red	Granular	0.50	220
	pigment E
	Properties of organic pigment
	Hue	Heat
	L*	a*	b*	h	resistance
Organic	value	value	value	value	temperature
pigment	(−)	(−)	(−)	(°)	(° C.)
Organic blue	17.7	9.7	−23.4	292.5	256
pigment A
Organic blue	17.3	11.6	−26.5	293.6	273
pigment B
Organic blue	16.9	12.1	−28.8	292.8	266
pigment C
Organic red	37.0	51.9	20.6	21.6	488
pigment D
Organic red	28.3	58.0	20.6	19.5	319
pigment E

	TABLE 8
	Production of green-based
	pigment
	Coating step with
	alkoxysilane,
	polysiloxane or silicon
	compound
	Additives
			Amount
Examples			added
and			(part
Comparative	Kind of core		by
Examples	particles	Kind	weight)
Example 17	Core particles 1	Methyl	2.0
		triethoxysilane
Example 18	Core particles 2	Methyl	0.5
		trimethoxysilane
Example 19	Core particles 3	Phenyl	2.0
		triethoxysilane
Example 20	Core particles 4	Methyl hydrogen	1.0
		polysiloxane
Example 21	Core particles 5	Methyl	1.0
		triethoxysilane
Example 22	Core particles 6	BYK-080	1.0
Example 23	Core particles 7	Isobutyl	2.0
		trimethoxysilane
Example 24	Core particles 8	TSF4770	1.5
Comparative	Core particles 1	—	—
Example 1
Comparative	Core particles 1	Methyl	1.0
Example 2		triethoxysilane
Comparative	Core particles 1	Methyl	1.0
Example 3		triethoxysilane
Comparative	Core particles 1	Methyl	0.005
Example 4		triethoxysilane
Comparative	Core particles 1	γ-aminopropyl	1.0
Example 5		triethoxysilane
	Production of green-based pigment
	Coating step with alkoxysilane,
	polysiloxane or silicon compound
Examples		Coating amount
and	Edge runner treatment	(calculated as
Comparative	Linear load	Time	Si)
Examples	(N/cm)	(Kg/cm)	(min.)	(wt. %)
Example 17	392	40	15	0.30
Example 18	294	30	20	0.10
Example 19	392	40	20	0.26
Example 20	588	60	20	0.42
Example 21	490	50	15	0.15
Example 22	441	45	15	0.17
Example 23	392	40	20	0.30
Example 24	294	30	30	0.34
Comparative	—	—	—	—
Example 1
Comparative	392	40	20	0.15
Example 2
Comparative	392	40	20	0.15
Example 3
Comparative	392	40	20	7 × 10 −4
Example 4
Comparative	392	40	20	0.13
Example 5
		Production of green-based pigment
	Examples	Adhesion step with organic blue pigment
	and	Organic blue pigment
	Comparative		Amount adhered
	Examples	Kind	(part by weight)
	Example 17	A	10.0
	Example 18	A	7.5
	Example 19	A	20.0
	Example 20	A	5.0
	Example 21	A	7.5
	Example 22	B	15.0
	Example 23	B	10.0
	Example 24	B	25.0
	Comparative	A	10.0
	Example 1
	Comparative	A	1.0
	Example 2
	Comparative	A	35.0
	Example 3
	Comparative	A	10.0
	Example 4
	Comparative	A	10.0
	Example 5
	Production of green-based pigment
	Adhesion step with organic blue pigment
Examples		Amount adhered
and	Edge runner treatment	(calculated as
Comparative	Linear load	Time	C)
Examples	(N/cm)	(Kg/cm)	(min.)	(wt. %)
Example 17	392	40	20	6.03
Example 18	294	30	30	4.61
Example 19	294	30	20	11.07
Example 20	392	40	20	3.14
Example 21	490	50	15	4.62
Example 22	441	45	20	8.65
Example 23	294	30	20	6.04
Example 24	588	60	30	13.30
Comparative	392	40	20	6.02
Example 1
Comparative	392	40	20	0.63
Example 2
Comparative	392	40	20	17.26
Example 3
Comparative	392	40	20	6.02
Example 4
Comparative	392	40	20	6.03
Example 5

	TABLE 9
	Properties of green-based pigment
	Examples and	Average major axial
	Comparative	diameter	Aspect ratio
	Examples	(μm)	(−)
	Example 17	0.43	5.8:1
	Example 18	0.38	6.1:1
	Example 19	0.41	5.6:1
	Example 20	0.20	4.6:1
	Example 21	0.43	5.8:1
	Example 22	0.38	6.1:1
	Example 23	0.40	5.6:1
	Example 24	0.21	4.6:1
	Comparative	0.43	5.8:1
	Example 1
	Comparative	0.43	5.8:1
	Example 2
	Comparative	0.43	5.8:1
	Example 3
	Comparative	0.43	5.8:1
	Example 4
	Comparative	0.43	5.8:1
	Example 5
	Comparative	0.20	—
	Example 6
	Comparative	0.21	—
	Example 7
	Comparative	0.60	—
	Example 8
	Properties of green-based pigment
		Geometrical
		standard	BET specific	Al content
	Example and	deviation	surface area	within
	Comparative	value	value	particles
	Examples	(−)	(m 2 /g)	(wt. %)
	Example 17	1.45	18.3	—
	Example 18	1.39	24.6	—
	Example 19	1.41	22.1	1.94
	Example 20	1.41	73.6	—
	Example 21	1.45	19.1	—
	Example 22	1.39	25.9	—
	Example 23	1.41	20.2	2.09
	Example 24	1.41	76.5	—
	Comparative	—	26.8	—
	Example 1
	Comparative	1.45	17.9	—
	Example 2
	Comparative	—	29.3	—
	Example 3
	Comparative	—	26.3	—
	Example 4
	Comparative	—	25.8	—
	Example 5
	Comparative	1.89	10.5	—
	Example 6
	Comparative	2.32	68.2	—
	Example 7
	Comparative	1.76	2.1	—
	Example 8
	Properties of green-based pigment
Example and	Hue
Comparative	*L value	a* value	b* value	h value
Example	(−)	(−)	(−)	(°)
Example 17	35.5	−16.1	12.4	142.4
Example 18	38.8	−12.6	18.2	124.7
Example 19	28.5	−20.1	0.9	177.4
Example 20	36.1	−16.4	−1.2	184.2
Example 21	38.5	−12.3	18.0	124.3
Example 22	31.5	−19.6	4.7	166.5
Example 23	35.0	−16.6	12.8	142.4
Example 24	27.9	−14.8	−10.3	214.8
Comparative	30.5	−19.6	7.4	159.3
Example 1
Comparative	51.2	5.7	43.5	82.5
Example 2
Comparative	21.3	−18.6	−6.3	198.7
Example 3
Comparative	30.3	−19.1	7.6	158.3
Example 4
Comparative	31.0	−19.8	7.6	159.0
Example 5
Comparative	39.5	−20.0	22.1	132.1
Example 6
Comparative	11.3	−24.8	25.6	134.1
Example 7
Comparative	38.5	−19.1	20.8	132.6
Example 8
	Properties of green-based pigment
	Chemical resistance
			Acid	Alkali
Examples and	Tinting	Hiding	resistance	resistance
Comparative	strength	power	ΔE* value	ΔE* value
Examples	(%)	(cm 2 /g)	(−)	(−)
Example 17	134	1,920	0.93	0.78
Example 18	140	1,960	1.02	0.89
Example 19	125	1,830	0.83	0.71
Example 20	151	2,030	1.37	1.22
Example 21	143	1,950	0.74	0.61
Example 22	121	1,850	0.66	0.52
Example 23	138	1,970	0.79	0.67
Example 24	126	1,820	0.51	0.45
Comparative	4	1,730	2.16	2.01
Example 1
Comparative	186	1,950	1.88	1.75
Example 2
Comparative	7	1,680	0.76	0.68
Example 3
Comparative	5	1,730	2.05	1.93
Example 4
Comparative	5	1,740	2.04	1.92
Example 5
Comparative	100	1,180	2.58	2.13
Example 6
Comparative	98	420	1.89	2.15
Example 7
Comparative	78	680	1.16	1.88
Example 8
	Properties of green-based pigment
			Desorption
	Example and	Heat resistance	percentage of
	Comparative	temperature	organic pigment
	Examples	(° C.)	(%)
	Example 17	231	7.4
	Example 18	225	7.1
	Example 19	268	8.8
	Example 20	220	6.5
	Example 21	249	3.4
	Example 22	240	4.3
	Example 23	275	3.8
	Example 24	246	4.6
	Comparative	203	68.4
	Example 1
	Comparative	206	6.3
	Example 2
	Comparative	234	24.6
	Example 3
	Comparative	204	54.8
	Example 4
	Comparative	205	50.3
	Example 5
	Comparative	211	—
	Example 6	211	—
	Comparative	228	—
	Example 7
	Comparative	256	—
	Example 8

	TABLE 10
	Production
	of paint	Properties of paint
	Example and	Kind of		Storage
	Comparative	green-based	Viscosity	stability
	Examples	pigment	(cP)	(−)
	Example 25	Example 17	1,280	0.76
	Example 26	Example 18	1,357	0.91
	Example 27	Example 19	1,408	0.85
	Example 28	Example 20	1,408	0.98
	Example 29	Example 21	1,562	0.64
	Example 30	Example 22	1,178	0.58
	Example 31	Example 23	1,280	0.45
	Example 32	Example 24	1,433	0.51
	Comparative	Comparative	2,560	2.13
	Example 9	Example 1
	Comparative	Comparative	1,408	1.53
	Example 10	Example 2
	Comparative	Comparative	3,884	2.56
	Example 11	Example 3
	Comparative	Comparative	1,562	2.01
	Example 12	Example 4
	Comparative	Comparative	3,072	1.99
	Example 13	Example 5
	Comparative	Comparative	2,560	2.71
	Example 14	Example 6
	Comparative	Comparative	2,432	2.13
	Example 15	Example 7
	Comparative	Comparative	640	1.86
	Example 16	Example 8
	Properties of coating film
	Heat-	Chemical resistances
		resistance	Acid	Alkali
Examples and	60°	temperature	resistance	resistance
Comparative	gloss	of coating	ΔG value	ΔG value
Examples	(%)	film (° C.)	(%)	(%)
Example 25	86	253	8.1	7.0
Example 26	88	248	9.3	8.0
Example 27	90	270	7.8	6.6
Example 28	85	244	10.8	10.1
Example 29	91	263	6.5	5.6
Example 30	89	256	5.1	4.2
Example 31	93	276	5.4	4.5
Example 32	94	261	4.6	3.1
Comparative	68	213	16.8	14.8
Example 9
Comparative	83	220	14.8	13.9
Example 10
Comparative	56	255	7.7	6.7
Example 11
Comparative	68	215	15.9	14.3
Exmple 12
Comparative	71	216	15.5	14.1
Example 13
Comparative	73	236	31.6	28.3
Example 14
Comparative	69	253	21.8	16.9
Example 15
Comparative	51	266	11.6	10.2
Example 16
	Properties of coating film
Examples and	Hue
Comparative	L* value	a* value	b* value	h value
Examples	(−)	(−)	(−)	(°)
Example 25	37.1	−16.3	12.5	142.5
Example 26	39.9	−11.3	18.6	121.3
Example 27	29.6	−19.8	1.1	176.6
Example 28	37.4	−16.1	−0.6	182.1
Example 29	39.9	−12.0	17.6	124.3
Example 30	32.6	−19.3	4.9	165.8
Example 31	36.6	−15.6	12.6	141.1
Example 32	28.7	−14.3	−10.0	215.0
Comparative	31.4	−19.0	7.5	158.5
Example 9
Comparative	51.7	5.9	43.9	82.3
Example 10
Comparative	22.4	−18.1	−6.1	198.6
Example 11
Comparative	31.5	−18.9	7.7	157.8
Example 12
Comparative	32.0	−19.1	7.8	157.8
Example 13
Comparative	41.0	−19.3	21.6	131.8
Example 14
Comparative	12.6	−24.6	25.9	133.5
Example 15
Comparative	40.0	−18.3	21.6	130.3
Example 16

	TABLE 11
	Production
	of water-
	based paint	Properties of paint
Examples and	Kind of		Storage
Comparative	green-based	Viscosity	stability
Examples	pigment	(cP)	(−)
Example 33	Example 17	2,048	0.83
Example 34	Example 18	2,176	1.02
Example 35	Example 19	2,560	0.98
Example 36	Example 20	2,253	1.06
Example 37	Example 21	2,432	0.76
Example 38	Example 22	1,920	0.68
Example 39	Example 23	1,896	0.50
Example 40	Example 24	1,997	0.56
Comparative	Comparative	2,688	2.69
Example 17	Example 1
Comparative	Comparative	2,944	1.62
Example 18	Example 2
Comparative	Comparative	4,813	3.13
Example 19	Example 3
Comparative	Comparative	3,276	2.56
Example 20	Example 4
Comparative	Comparative	3,226	2.57
Example 21	Example 5
Comparative	Comparative	4,044	3.16
Example 22	Example 6
Comparative	Comparative	5,069	2.32
Example 23	Example 7
Comparative	Comparative	1,920	2.46
Example 24	Example 8
	Properties of coating film
	Heat-	Chemical resistance
		resistance	Acid	Alkali
Examples and	60°	temperature	resistance	resistance
Comparative	gloss	of coating	ΔG value	ΔG value
Examples	(%)	film (° C.)	(%)	(%)
Example 33	82	251	8.9	7.5
Example 34	83	246	9.7	8.9
Example 35	83	266	8.0	7.1
Example 26	81	238	11.5	10.6
Example 37	85	257	7.3	6.0
Example 38	86	246	6.0	4.9
Example 39	88	271	6.3	5.2
Example 40	87	252	5.2	4.4
Comparative	61	208	18.0	15.8
Example 17
Comparative	78	218	15.7	14.3
Example 18
Comparative	50	249	8.9	7.6
Example 19
Comparative	62	210	17.1	16.8
Example 20
Comparative	66	211	16.3	16.5
Example 21
Comparative	68	226	32.2	30.8
Example 22
Comparative	63	246	22.6	17.8
Example 23
Comparative	53	253	12.7	11.0
Example 24
	Properties of coating film
Example and	Hue
Comparative	L* value	a* value	b* value	h value
Examples	(−)	(−)	(−)	(°)
Example 33	37.6	−16.3	12.6	142.3
Example 34	39.8	−11.8	17.3	124.3
Example 35	29.7	−20.1	1.2	176.6
Example 36	37.1	−16.6	−1.1	183.8
Example 37	40.2	−11.8	17.9	123.4
Example 38	32.3	−19.5	4.4	167.3
Example 39	37.0	−15.2	12.2	141.2
Example 40	28.4	−15.0	−9.6	212.6
Comparative	31.1	−19.1	7.7	158.0
Example 17
Comparative	52.0	5.6	44.1	82.8
Example 18
Comparative	22.3	−18.0	−5.8	197.9
Example 19
Comparative	31.1	−19.0	7.8	157.7
Example 20
Comparative	31.7	−19.4	7.9	157.8
Example 21
Comparative	40.6	−19.0	22.8	129.8
Example 22
Comparative	12.5	−25.3	27.3	132.8
Example 23
Comparative	39.6	−19.6	23.6	129.7
Example 24

	TABLE 12
		Production of resin composition
	Examples and	Green-based pigment
	Comparative		Amount
	Examples	Kind	(part by weight)
	Example 41	Example 17	1.0
	Example 42	Example 18	1.0
	Example 43	Example 19	1.0
	Example 44	Example 20	1.0
	Example 45	Example 21	1.0
	Example 46	Example 22	1.0
	Example 47	Example 23	1.0
	Example 48	Example 24	1.0
	Comparative	Comparative	1.0
	Example 25	Example 1
	Comparative	Comparative	1.0
	Example 26	Example 2
	Comparative	Comparative	1.0
	Example 27	Example 3
	Comparative	Comparative	1.0
	Example 28	Example 4
	Comparative	Comparative	1.0
	Example 29	Example 5
	Comparative	Comparative	1.0
	Example 30	Example 6
	Comparative	Comparative	1.0
	Example 31	Example 7
	Comparative	Comparative	1.0
	Example 32	Example 8
	Production of resin composition
	Resin
	Example and		Amount
	Comparative		(part by
	Examples	Kind	weight)
	Example 41	Polyvinyl chloride resin	99.0
	Example 42	Polyvinyl chloride resin	99.0
	Example 43	Polyvinyl chloride resin	99.0
	Example 44	Polyvinyl chloride resin	99.0
	Example 45	Polyvinyl chloride resin	99.0
	Example 46	Polyvinyl chloride resin	99.0
	Example 47	Polyvinyl chloride resin	99.0
	Example 48	Polyvinyl chloride resin	99.0
	Comparative	Polyvinyl chloride resin	99.0
	Example 25
	Comparative	Polyvinyl chloride resin	99.0
	Example 26
	Comparative	Polyvinyl chloride resin	99.0
	Example 27
	Comparative	Polyvinyl chloride resin	99.0
	Example 28
	Comparative	Polyvinyl chloride resin	99.0
	Example 29
	Comparative	Polyvinyl chloride resin	99.0
	Example 30
	Comparative	Polyvinyl chloride resin	99.0
	Example 31
	Comparative	Polyvinyl chloride resin	99.0
	Example 32
	Production of resin composition
	Additives
	Examples and		Amount	Kneading
	Comparative		(part by	temperature
	Examples	Kind	weight)	(° C.)
	Example 41	Calcium Stearate	2.0	160
	Example 42	Calcium Stearate	2.0	160
	Example 43	Calcium Stearate	2.0	160
	Example 44	Calcium Stearate	2.0	160
	Example 45	Calcium Stearate	2.0	160
	Example 46	Calcium Stearate	2.0	160
	Example 47	Calcium Stearate	2.0	160
	Example 48	Calcium Stearate	2.0	160
	Comparative	Calcium Stearate	2.0	160
	Example 25
	Comparative	Calcium Stearate	2.0	160
	Example 26
	Comparative	Calcium Stearate	2.0	160
	Example 27
	Comparative	Calcium Stearate	2.0	160
	Example 28
	Comparative	Calcium Stearate	2.0	160
	Example 29
	Comparative	Calcium Stearate	2.0	160
	Example 30
	Comparative	Calcium Stearate	2.0	160
	Example 31
	Comparative	Calcium Stearate	2.0	160
	Example 32
	Properties of resin composition
			Heat-resistance
	Examples and	Dispersion	temperature of
	Comparative	condition	resin composition
	Examples	(−)	(° C.)
	Example 41	5	224
	Example 42	5	223
	Example 43	5	232
	Example 44	4	218
	Example 45	5	230
	Example 46	5	226
	Example 47	5	239
	Example 49	5	229
	Comparative	2	190
	Example 25
	Comparative	3	200
	Example 26
	Comparative	2	233
	Example 27
	Comparative	3	192
	Example 28
	Comparative	2	196
	Example 29
	Comparative	3	218
	Example 30
	Comparative	3	210
	Example 31
	Comparative	3	228
	Example 32
	Properties of coating film
Examples and	Hue
Comparative	L* value	a* value	b* value	h value
Examples	(−)	(−)	(−)	(°)
Example 41	39.8	−14.6	12.9	138.8
Example 42	41.3	−9.8	16.9	120.3
Example 43	31.5	−18.4	1.4	175.6
Example 44	38.5	−15.3	−0.8	183.0
Example 45	41.9	−10.8	18.1	120.8
Example 46	34.0	−17.6	4.7	165.0
Example 47	38.9	−14.4	12.5	139.0
Example 48	30.1	−13.6	−9.0	213.5
Comparative	32.0	−17.4	8.1	155.0
Example 25
Comparative	53.6	7.3	44.6	80.7
Example 26
Comparative	23.9	−16.2	−5.2	197.8
Example 27
Comparative	32.8	−17.3	8.1	154.9
Example 28
Comparative	33.6	−17.5	8.2	154.9
Example 29
Comparative	42.4	−17.8	23.0	127.7
Example 30
Comparative	13.8	−23.9	27.6	130.9
Example 31
Comparative	41.1	−18.6	24.0	127.8
Example 32

	TABLE 13
	Production of orange-
	based pigment
	Coating step with
	alkoxysilane,
	polysiloxane or silicon
	compound
	Additives
			Amount
Examples			added
and			(part
Comparative	Kind of core		by
Examples	particles	Kind	weight
Example 49	Core particles 1	Methyl	1.0
		triethoxysilane
Example 50	Core particles 2	Methyl	3.0
		triethoxysilane
Example 51	Core particles 3	Phenyl	2.0
		triethoxysilane
Example 52	Core particles 4	Methyl hydrogen	1.0
		polysiloxane
Example 53	Core particles 5	Methyl	1.0
		triethoxysilane
Example 54	Core particles 6	BYK-080	2.0
Example 55	Core particles 7	Isobutyl	1.0
		trimethoxysilane
Example 56	Core particles 8	TSF4770	1.0
Comparative	Core particles 1	—	—
Example 33
Comparative	Core particles 1	Methyl	1.0
Example 34		triethoxysilane
Comparative	Core particles 1	Methyl	1.0
Example 35		triethoxysilane
Comparative	Core particles 1	Methyl	0.005
Example 36		triethoxysilane
COmparative	Core particles 1	γ-aminopropyl	1.0
Example 37		triethoxysilane
	Production of orange-based pigment
	Coating step with alkoxysilane,
	polysiloxane or silicon compound
Example		Coating amount
and	Edge runner treatment	(calculated as
Comparative	Linear load	Time	Si)
Examples	(N/cm)	(Kg/cm)	(min.)	(wt. %)
Example 49	588	60	20	0.15
Example 50	294	30	30	0.59
Example 51	441	45	30	0.27
Example 52	588	60	20	0.44
Example 53	294	30	30	0.15
Example 54	392	40	30	0.36
Example 55	588	60	30	0.15
Example 56	392	40	20	0.34
Comparative	—	—	—	—
Example 33
Comparative	392	40	20	0.15
Example 34
Comparative	392	40	20	0.15
Example 35
Comparative	392	40	20	7 × 10 −4
Example 36
Comparative	392	40	20	0.13
Example 37
		Production of orange-based pigment
	Examples	Adhesion step with organic red pigment
	and	Organic red pigment
	Comparative		Amount adhered
	Examples	Kind	(part by weight)
	Example 49	D	10.0
	Example 50	E	20.0
	Example 51	D	15.0
	Example 52	E	20.0
	Example 53	D	10.0
	Example 54	E	7.5
	Example 55	D	10.0
	Example 56	E	20.0
	Comparative	D	10.0
	Example 33
	Comparative	D	100.0
	Example 34
	Comparative	D	0.5
	Example 35
	Comparative	D	10.0
	Example 36
	Comparative	D	10.0
	Example 37
	Production of orange-based pigment
	Adhesion step with organic red pigment
Examples		Amount adhered
and	Edge runner treatment	(calculated as
Comparative	Linear load	Time	C)
Examples	(N/cm)	(Kg/cm)	(min.)	(wt. %)
Example 49	392	40	20	6.95
Example 50	588	60	20	12.78
Example 51	294	30	30	9.99
Example 52	588	60	20	12.80
Example 53	441	45	30	6.96
Example 54	392	40	30	5.33
Example 55	588	60	20	6.93
Example 56	588	60	20	12.77
Comparative	392	40	20	6.92
Example 33
Comparative	392	40	20	38.26
Example 34
Comparative	392	40	20	0.35
Example 35
Comparative	392	40	20	6.95
Example 36
Comparative	392	40	20	6.94
Example 37

	TABLE 14
	Properties of orange-based pigment
Examples and	Average major axial
Comparative	diameter	Aspect ratio
Examples	(μm)	(−)
Example 49	0.43	5.8:1
Example 50	0.39	6.1:1
Example 51	0.40	5.6:1
Example 52	0.20	4.6:1
Example 53	0.43	5.8:1
Example 54	0.38	6.1:1
Example 55	0.40	5.6:1
Example 56	0.21	4.6:1
Comparative	0.43	5.8:1
Example 33
Comparative	0.43	5.8:1
Example 34
Comparative	0.43	5.8:1
Example 35
Comparative	0.43	5.8:1
Example 36
Comparative	0.43	5.8:1
Example 37
	Properties of oragne-based pigment
	Geometrical
	standard		Al content
Examples and	deviation	BET specific	within
Comparative	value	surface area	particles
Examples	(−)	value (m 2 /g)	(wt. %)
Example 49	1.45	21.3	—
Example 50	1.39	23.2	—
Example 51	1.41	21.6	2.00
Example 52	1.41	71.6	—
Example 53	1.45	21.8	—
Example 54	1.39	24.5	—
Example 55	1.41	23.8	2.09
Example 56	1.42	72.6	—
Comparative	—	28.6	—
Example 33
Comparative	—	34.0	—
Example 34
Comparative	1.45	16.3	—
Example 35
Comparative	—	26.8	—
Example 36
Comparative	—	24.6	—
Example 37
	Properties of orange-based pigment
Examples and	Hue
Comparative	L* value	a* value	b* value	h value
Examples	(−)	(−)	(−)	(°)
Example 49	45.7	38.3	38.6	45.2
Example 50	39.3	47.2	35.6	37.0
Example 51	40.3	46.2	38.3	39.7
Example 52	36.2	50.9	34.2	33.9
Example 53	46.1	39.6	36.6	42.7
Example 54	47.5	36.2	43.8	50.4
Example 55	42.8	38.4	41.1	46.9
Example 56	37.7	50.5	33.3	33.4
Comparative	46.3	37.6	40.4	47.1
Example 33
Comparative	31.2	51.2	27.0	27.8
Example 34
Comparative	52.8	20.1	45.5	66.2
Example 35
Comparative	46.9	38.2	39.2	45.7
Example 36
Comparative	47.3	37.9	40.1	46.6
Example 37
	Properties of orange-based pigment
	Chemical resistances
			Acid	Alkali
Examples and	Tinting	Hiding	resistance	resistance
Comparative	strength	power	ΔE* value	ΔE* value
Examples	(%)	(cm 2 /g)	(−)	(−)
Example 49	136	1,990	1.09	0.91
Example 50	138	1,950	0.94	0.85
Example 51	141	1,940	0.99	0.89
Example 52	145	1,920	1.20	1.19
Example 53	143	2,000	0.88	0.78
Example 54	138	2,070	0.90	0.80
Example 55	146	2,010	0.83	0.72
Example 56	146	1,960	0.97	0.90
Comparative	100	1,730	2.32	2.10
Example 33
Comparative	112	2,010	1.65	1.38
Example 34
Comparative	105	1,930	2.09	1.66
Example 35
Comparative	102	1,740	2.11	1.95
Example 36
Comparative	103	1,780	2.10	1.93
Example 37
	Properties of orange-based pigment
		Desorption
Examples and	Heat resistance	percentage of
Comparative	temperature	organic pigment
Examples	(° C.)	(%)
Example 49	233	7.2
Example 50	235	9.3
Example 51	270	8.6
Example 52	231	9.0
Example 53	250	4.3
Example 54	236	2.1
Example 55	279	3.8
Example 56	239	4.6
Comparative	205	69.2
Example 33
Comparative	241	59.4
Example 34
Comparative	203	—
Example 35
Comparative	205	58.1
Example 36
Comparative	206	56.6
Example 37

	TABLE 15
	Production	Properties of paint
		of paint		Storage
	Examples and	Kind of		stability
	Comparative	orange-based	Viscosity	ΔE* value
	Examples	pigment	(cP)	(−)
	Example 57	Example 49	1,280	0.81
	Example 59	Example 50	1,196	0.92
	Example 59	Example 51	982	0.88
	Example 60	Example 52	1,442	0.90
	Example 61	Example 53	1,386	0.60
	Example 62	Example 54	1,272	0.49
	Example 63	Example 55	1,071	0.55
	Example 64	Example 56	1,121	0.65
	Comparative	Comparative	2,560	2.16
	Example 38	Example 33
	Comparative	Comparative	2,883	2,93
	Example 39	Example 34
	Comparative	Comparative	982	1.62
	Example 40	Example 35
	Comparative	Comparative	3,160	2.09
	Example 41	Example 36
	Comparative	Comparative	2,830	2.06
	Example 42	Example 37
	Properties of coating film
	Heat-
	resistance	Chemical resistance
		temperature	Acid	Alkali
Examples and	60°	of coating	resistance	resistance
Comparative	gloss	film	ΔG value	ΔG value
Examples	(%)	(° C.)	(%)	(%)
Example 57	87	250	8.3	7.1
Example 58	86	252	7.8	6.9
Example 59	89	271	8.1	7.1
Example 60	85	248	10.4	10.0
Example 61	92	262	6.5	5.2
Example 62	93	253	6.6	5.4
Example 63	95	282	5.9	4.3
Example 64	90	257	7.7	7.0
Comparative	66	214	16.3	14.9
Example 38
Comparative	53	256	14.2	13.3
Example 39
Comparative	77	211	15.6	14.0
Example 40
Comparative	67	213	16.0	14.9
Example 41
Comparative	69	215	15.8	14.5
Example 42
	Properties of coating film
Examples and	Hue
Comparative	L* value	a* value	b* value	h value
Examples	(−)	(−)	(−)	(°)
Example 57	47.6	37.6	38.4	45.6
Example 58	41.7	46.6	35.1	37.0
Example 59	42.3	46.9	38.0	39.0
Example 60	37.4	49.1	34.6	35.2
Example 61	48.1	40.3	36.2	41.9
Example 62	49.2	35.5	44.6	51.5
Example 63	43.6	39.2	40.9	46.2
Example 64	49.3	49.8	33.0	33.5
Comparative	47.5	37.0	40.2	47.4
Example 38
Comparative	41.2	51.1	26.8	27.7
Example 39
Comparative	54.6	20.6	45.7	65.7
Example 40
Comparative	48.9	39.3	39.9	45.4
Example 41
Comparative	48.4	36.6	40.4	47.8
Example 42

	TABLE 16
	Production
	of water-	Properties of paint
		based paint		Storage
	Examples and	Kind of		stability
	Comparative	orange-based	Viscosity	ΔE* value
	Examples	pigment	(cP)	(−)
	Example 65	Example 49	2,560	0.92
	Example 66	Example 50	2,283	1.01
	Example 67	Example 51	2,762	0.96
	Example 68	Example 52	2,836	1.00
	Example 69	Example 53	2,401	0.71
	Example 70	Example 54	2,320	0.59
	Example 71	Example 55	2,532	0.64
	Example 72	Example 56	2,689	0.77
	Comparative	Comparative	3,882	2.62
	Example 43	Example 33
	Comparative	Comparative	4,156	3.36
	Example 44	Example 34
	Comparative	Comparative	2,160	1.74
	Example 45	Example 35
	Comparative	Comparative	4,442	2.47
	Example 46	Example 36
	Comparative	Comparative	3,716	2.43
	Example 47	Example 37
	Properties of coating film
	Heat-
	resistance	Chemical resistances
		temperature	Acid	Alklai
Examples and	60°	of coating	resistance	resistance
Comparative	gloss	film	ΔG value	ΔG value
Example	(%)	(° C.)	(%)	(%)
Example 65	84	246	8.9	8.2
Example 66	81	251	8.2	7.6
Example 67	85	268	8.6	7.8
Example 68	81	245	10.9	10.5
Example 69	87	259	6.8	5.7
Example 70	89	250	7.0	5.9
Example 71	90	280	6.3	5.0
Example 72	85	254	8.1	7.7
Comparative	60	211	17.5	15.6
Example 43
Comparative	47	252	15.5	15.0
Example 44
Comparative	71	207	16.4	14.8
Example 45
Comparative	62	210	16.8	15.6
Example 46
Comparative	63	212	17.2	15.3
Example 47
	Properties of coating film
Examples and	Hue
Comparative	L* value	a* value	b* value	h value
Examples	(−)	(−)	(−)	(°)
Example 65	47.7	37.5	38.0	45.4
Example 66	41.9	46.8	35.4	37.1
Example 67	42.0	46.6	38.3	39.4
Example 68	37.6	49.2	34.5	35.0
Example 69	47.8	40.6	36.0	41.6
Example 70	49.1	35.7	44.8	51.4
Example 71	43.3	39.5	41.1	46.1
Example 72	49.0	50.0	32.9	33.3
Comparative	47.2	37.3	40.3	47.2
Example 43
Comparative	41.6	51.4	26.5	27.3
Example 44
Comparative	55.0	20.9	45.8	65.5
Example 45
Comparative	48.3	39.1	39.7	45.4
Example 46
Comparative	48.1	36.8	40.2	47.5
Example 47

	TABLE 17
		Production of resin composition
	Examples and	Orange-based pigment
	Comparative		Amount
	Examples	Kind	(part by weight)
	Example 73	Example 49	1.0
	Example 74	Example 50	1.0
	Example 75	Example 51	1.0
	Example 76	Example 52	1.0
	Example 77	Example 53	1.0
	Example 78	Example 54	1.0
	Example 79	Example 55	1.0
	Example 80	Example 56	1.0
	Comparative	Comparative	1.0
	Example 48	Example 33
	Comparative	Comparative	1.0
	Example 49	Example 34
	Comparative	Comparative	1.0
	Example 50	Example 35
	Comparative	Comparative	1.0
	Example 51	Example 36
	Comparative	Comparative	1.0
	Example 52	Example 37
	Production of resin composition
	Resin
	Examples and		Amount
	Comparative		(part by
	Examples	Kind	weight)
	Example 73	Polyvinyl chloride resin	99.0
	Example 74	Polyvinyl chloride resin	99.0
	Example 75	Polyvinyl chloride resin	99.0
	Example 76	Polyvinyl chloride resin	99.0
	Example 77	Polyvinyl chloride resin	99.0
	Example 78	Polyvinyl chloride resin	99.0
	Example 79	Polyvinyl chloride resin	99.0
	Example 80	Polyvinyl chloride resin	99.0
	Comparative	Polyvinyl chloride resin	99.0
	Example 48
	Comparative	Polyvinyl chloride resin	99.0
	Example 49
	Comparative	Polyvinyl chloride resin	99.0
	Example 50
	Comparative	Polyvinyl chloride resin	99.0
	Example 51
	Comparative	Polyvinyl chloride resin	99.0
	Example 52
	Production of resin composition
	Additives
	Examples and		Amount	Kneading
	Comparative		(part by	temperature
	Examples	Kind	weight)	(° C.)
	Example 73	Calcium stearate	2.0	160
	Example 74	Calcium stearate	2.0	160
	Example 75	Calcium stearate	2.0	160
	Example 76	Calcium stearate	2.0	160
	Example 77	Calcium stearate	2.0	160
	Example 78	Calcium stearate	2.0	160
	Example 79	Calcium stearate	2.0	160
	Example 80	Calcium stearate	2.0	160
	Comparative	Calcium stearate	2.0	160
	Example 48
	Comparative	Calcium stearate	2.0	160
	Example 49
	Comparative	Calcium stearate	2.0	160
	Example 50
	Comparative	Calcium stearate	2.0	160
	Example 51
	Comparative	Calcium stearate	2.0	160
	Example 52
	Properties of resin composition
			Heat-resistance
	Examples and	Dispersion	temperatures of
	Comparative	condition	resin composition
	Examples	(−)	(° C.)
	Example 73	5	226
	Example 74	5	229
	Example 75	5	232
	Example 76	5	223
	Example 77	5	231
	Example 78	5	226
	Example 79	5	238
	Example 80	5	230
	Comparative	2	192
	Example 48
	Comparative	2	224
	Example 49
	Comparative	3	193
	Example 50
	Comparative	2	195
	Example 51
	Comparative	2	196
	Example 52
	Properties of resin composition
Examples and	Hue
Comparative	L* value	a* value	b* value	h value
Examples	(−)	(−)	(−)	(°)
Example 73	49.7	36.3	38.3	46.5
Example 74	43.8	45.3	35.0	37.7
Example 75	43.9	44.9	38.1	40.3
Example 76	39.5	47.8	34.7	36.0
Example 77	49.6	38.6	35.9	42.9
Example 78	51.0	34.1	44.5	52.5
Example 79	45.1	38.2	41.3	47.2
Example 80	50.7	48.2	32.8	34.2
Comparative	49.2	35.6	40.0	48.3
Example 48
Comparative	43.3	50.0	26.1	27.6
Example 49
Comparative	56.4	19.4	45.4	66.9
Example 50
Comparative	50.0	37.3	39.9	46.9
Example 51
Comparative	49.9	34.9	40.2	49.0
Example 52

	TABLE 18
	Production of green-based
	fine pigment
	Coating step with
	alkoxysilane,
	polysiloxane or silicon
	compound
	Additives
				Amount
	Examples			added
	and			(part
	Comparative	Kind of core		by
	Examples	particles	Kind	weight)
	Example 81	Core particles 9	Methyl	1.0
			triethoxysilane
	Example 82	Core particles 10	Methyl	0.5
			trimethoxysil-
			ane
	Example 83	Core particles 11	Phenyl	2.0
			triethoxysilane
	Example 84	Core particles 12	Methyl hydro-	1.0
			gen polysilox-
			ane
	Example 85	Core particles 13	Methyl	2.0
			triethoxysilane
	Example 86	Core particles 14	Methyl	1.0
			triethoxysilane
	Example 87	Core particles 15	Methyl	1.5
			triethoxysilane
	Example 88	Core particles 16	Methyl	3.0
			triethoxysilane
	Comparative	Core particles 9	—	—
	Example 53
	Comparative	Core particles 9	Methyl	1.0
	Example 54		triethoxysilane
	Comparative	Core particles 9	Methyl	0.005
	Example 55		triethoxysilane
	Comparative	Core particles 9	Methyl	1.0
	Example 56		triethoxysilane
	Comparative	Core particles 9	γ-aminopropyl	1.0
	Example 57		triethoxysilane
	Production of green-based fine pigment
	Coating step with alkoxysilane,
	polysiloxane or silicon compound
Examples		Coating amount
and	Edge runner treatment	(calculated as
Comparative	Linear load		Time	Si)
Examples	(N/cm)	(Kg/cm)	(min.)	(wt. %)
Example 81	392	40	30	0.15
Example 82	588	60	20	0.10
Example 83	490	50	20	0.26
Example 84	294	30	30	0.42
Example 85	588	60	20	0.30
Example 86	441	45	20	0.15
Example 87	735	75	20	0.23
Example 88	441	45	30	0.45
Comparative	—	—	—	—
Example 53
Comparative	588	60	20	0.15
Example 54
Comparative	588	60	20	6 × 10 −4
Example 55
Comparative	588	60	20	0.15
Example 56
Comparative	588	60	20	0.12
Example 57
		Production of green-based fine pigment
	Examples	Adhesion step with organic blue pigment
	and	Organic blue pigment
	Comparative		Amount adhered
	Examples	Kind	(part by weight)
	Example 81	A	10.0
	Example 82	B	7.5
	Example 83	C	15.0
	Example 84	A	20.0
	Example 85	A	15.0
	Example 86	A	12.0
	Example 87	A	7.5
	Example 88	A	10.0
	Comparative	A	10.0
	Example 53
	Comparative	—	—
	Example 54
	Comparative	A	10.0
	Example 55
	Comparative	A	1.0
	Example 56
	Comparative	A	10.0
	Example 57
	Production of green-based fine pigment
	Adhesion step with organic blue pigment
Examples		Amount adhered
and	Edge runner treatment	calculated
Comparative	Linear load	Time	as C)
Examples	(N/cm)	(Kg/cm)	(min.)	(wt. %)
Example 81	588	60	20	6.04
Example 82	441	45	30	4.60
Example 83	735	75	20	8.62
Example 84	588	60	20	11.09
Example 85	294	30	30	8.61
Example 86	441	45	20	7.09
Example 87	490	50	20	4.61
Example 88	588	60	20	6.05
Comparative	588	60	20	6.05
Example 53
Comparative	—	—	—	—
Example 54
Comparative	588	60	20	6.03
Example 55
Comparative	588	60	20	0.60
Example 56
Comparative	588	60	20	6.03
Example 57

	TABLE 19
	Properties of green-based fine pigment
		Average	Average
	Examples and	major axial	minor axial	Aspect
	Comparative	diameter	diameter	ratio
	Examples	(μm)	(μm)	(−)
	Example 81	0.0825	0.0100	8.3:1
	Example 82	0.0580	0.0097	6.0:1
	Example 83	0.0777	0.0125	6.2:1
	Example 84	0.0918	0.0188	4.9:1
	Example 85	0.0831	0.0102	8.1:1
	Example 86	0.0585	0.0101	5.8:1
	Example 87	0.0777	0.0125	6.2:1
	Example 88	0.0910	0.0185	4.9:1
	Comparative	0.0814	0.0096	8.5:1
	Example 53
	Comparative	0.0813	0.0096	8.5:1
	Example 54
	Comparative	0.0815	0.0097	8.4:1
	Example 55
	Comparative	0.0816	0.0097	8.4:1
	Example 56
	Comparative	0.0815	0.0097	8.4:1
	Example 57
	Properties of green-based fine pigment
		Geometrical
		standard		Al content* 1
	Examples and	deviation	BET specific	within
	Comparative	value	surface area	particles
	Examples	(−)	value (m 2 /g)	(wt. %)
	Example 81	1.41	142.2	—
	Example 82	1.36	189.6	2.56
	Example 83	1.37	143.8	1.87
	Example 84	1.41	96.0	—
	Example 85	1.42	148.1	—
	Example 86	1.36	180.5	2.56
	Example 87	1.37	149.6	1.87
	Example 88	1.41	106.2	—
	Comparative	—	164.7	—
	Example 53
	Comparative	1.41	149.2	—
	Example 54
	Comparative	—	160.1	—
	Example 55
	Comparative	1.41	147.6	—
	Example 56
	Comparative	—	161.3	—
	Example 57
	Properties of green-based fine pigment
	Composite oxide hydroxide
		Coating amount	Coating amount
	Examples and	of Al* 1	of Fe* 1
	Comparative	(calculated as Al)	(calculated as Fe)
	Examples	(wt. %)	(wt. %)
	Example 81	—	—
	Example 82	—	—
	Example 83	1.13	0.64
	Example 84	—	—
	Example 85	—	—
	Example 86	—	—
	Example 87	1.13	0.64
	Example 88	—	—
	Comparative	—	—
	Example 53
	Comparative	—	—
	Example 54
	Comparative	—	—
	Example 55
	Comparative	—	—
	Example 56
	Comparative	—	—
	Example 57
	Properties of green-based fine pigment
Examples and	Hue
Comparative	L* value	a* value	b* value	h value
Examples	(−)	(−)	(−)	(°)
Example 81	31.9	−14.2	3.8	165.0
Example 82	33.2	−11.2	5.2	155.1
Example 83	28.6	−16.8	0.6	178.0
Example 84	26.5	−16.9	−1.1	183.7
Example 85	30.1	−14.2	−1.9	187.6
Example 86	31.2	−18.2	0.4	178.7
Example 87	35.3	−10.8	6.6	148.6
Example 88	27.4	−12.0	9.1	142.8
Comparative	30.9	−9.3	4.6	153.7
Example 53
Comparative	50.2	29.8	54.0	61.1
Example 54
Comparative	31.2	−8.3	4.1	153.7
Example 55
Comparative	31.4	10.5	30.4	70.9
Example 56
Comparative	30.3	−8.0	4.4	151.2
Example 57
	Properties of green-based fine pigment
	Chemical resistances
				Acid	Alkali
	Examples and	Tinting	Hiding	resistance	resistance
	Comparative	strength	power	ΔE* value	ΔE* value
	Examples	(%)	(cm 2 /g)	(−)	(−)
	Example 81	133	177	1.26	1.12
	Example 82	126	152	1.05	1.00
	Example 83	142	176	0.98	0.91
	Example 84	148	215	1.23	1.02
	Example 85	146	175	1.14	1.03
	Example 86	140	150	1.01	0.95
	Example 87	131	158	0.95	0.87
	Example 88	134	211	1.23	0.97
	Comparative	110	208	2.04	1.83
	Example 53
	Comparative	104	172	2.00	1.81
	Example 54
	Comparative	112	203	2,04	1.81
	Example 55
	Comparative	108	172	1.97	1.78
	Example 56
	Comparative	111	202	1.99	1.80
	Example 57
	Properties of green-based fine pigment
			Desorption
	Examples and	Heat resistance	percentage of
	Comparative	temperature	organic pigment
	Examples	(° C.)	(%)
	Example 81	223	6.8
	Example 82	259	6.1
	Example 83	283	7.6
	Example 84	229	8.1
	Example 85	243	4.7
	Example 86	267	4.6
	Example 87	284	2.9
	Example 88	239	3.4
	Comparative	193	68.3
	Example 53
	Comparative	197	—
	Example 54
	Comparative	194	49.3
	Example 55
	Comparative	197	5.7
	Example 56
	Comparative	198	46.6
	Example 57
	* 1 : Coating amount on core particles

	TABLE 20
	Production	Properties of paint
	of paint	Storage
	Examples and	Kind of		stability
	Comparative	green-based	Viscosity	ΔE* value
	Examples	fine pigment	(cP)	(−)
	Example 89	Example 81	1,690	0.93
	Example 90	Example 82	1,741	0.88
	Example 91	Example 83	1,997	0.77
	Example 92	Example 84	1,796	0.93
	Example 93	Example 85	2,124	0.61
	Example 94	Example 86	1,920	0.52
	Example 95	Example 87	2,560	0.47
	Example 96	Example 88	2,051	0.64
	Comparative	Comparative	10,240	2.24
	Example 58	Example 53
	Comparative	Comparative	2,560	1.58
	Example 59	Example 54
	Comparative	Comparative	8,960	2.03
	Example 60	Example 55
	Comparative	Comparative	2,816	1.52
	Example 61	Example 56
	Comparative	Comparative	6,656	2.00
	Example 62	Example 57
	Properties of coating film
	Hue
	Examples and	60°	L*	a*	b*	h
	Comparative	gloss	value	value	value	value
	Examples	(%)	(−)	(−)	(−)	(°)
	Example 89	81.6	33.3	−20.2	4.8	166.6
	Example 90	85.3	35.4	−17.6	6.0	161.2
	Example 91	88.2	30.1	−22.4	1.6	175.9
	Example 92	81.3	27.5	−22.9	−0.8	182.0
	Example 93	86.7	32.2	−21.5	−1.1	182.9
	Example 94	88.1	33.8	−24.1	1.3	176.9
	Example 95	91.6	36.4	−16.9	2.5	171.6
	Example 96	85.4	29.6	−20.1	10.1	153.3
	Comparative	65.2	32.8	−10.1	6.6	146.8
	Example 58
	Comparative	79.8	54.3	28.6	62.3	65.3
	Example 59
	Comparative	68.9	33.9	−11.6	5.9	153.0
	Example 60
	Comparative	80.4	40.3	28.4	40.1	54.7
	Example 61
	Comparative	68.5	31.1	−12.4	6.1	153.8
	Example 62
	Properties of coating film
	Chemical resistances
	Examples and	Acid resistsnce	Alkali resistance
	Comparative	ΔG value	ΔG value
	Examples	(−)	(−)
	Example 89	8.4	7.6
	Example 90	8.0	7.1
	Example 91	7.6	6.8
	Example 92	9.1	8.7
	Example 93	6.7	5.5
	Example 94	6.4	5.2
	Example 95	4.3	3.9
	Example 96	6.0	5.6
	Comparative	14.9	13.2
	Example 58
	Comparative	13.1	12.6
	Example 59
	Comparative	14.4	12.4
	Example 60
	Comparative	12.8	12.1
	Example 61
	Comparative	14.5	12.4
	Example 62
	Properties of coating film
	Examples and	Heat resistance	Transparency
	Comparative	temperature	(linear absorption)
	Examples	(° C.)	(μm −1 )
	Example 89	241	0.0296
	Example 90	265	0.0182
	Example 91	285	0.0262
	Example 92	247	0.0360
	Example 93	258	0.0251
	Example 94	274	0.0177
	Example 95	286	0.0194
	Example 96	252	0.0312
	Comparative	213	0.0892
	Example 58
	Comparative	215	0.0532
	Example 59
	Comparative	214	0.0823
	Example 60
	Comparative	219	0.0666
	Example 61
	Comparative	215	0.0834
	Example 62

	TABLE 21
	Production
	of water-	Properties of paint
	based paint	Storage
	Examples and	Kind of		stability
	Comparative	green-based	Viscosity	ΔE* value
	Examples	fine pigment	(cP)	(−)
	Example 97	Example 81	2,867	1.00
	Example 98	Example 82	3,482	0.96
	Example 99	Example 83	3,200	0.87
	Example 100	Example 84	3,294	1.04
	Example 101	Example 85	3,123	0.71
	Example 102	Example 86	2,944	0.61
	Example 103	Example 87	2,816	0.55
	Example 104	Example 88	2,731	0.72
	Comparative	Comparative	11,385	2.38
	Example 63	Example 53
	Comparative	Comparative	3,482	1.69
	Example 64	Example 54
	Comparative	Comparative	12,800	2.26
	Example 65	Example 55
	Comparative	Comparative	3,123	1.65
	Example 66	Example 56
	Comparative	Comparative	6,400	2.21
	Example 67	Example 57
	Properties of coating film
	Hue
	Examples and	60°	L*	a*	b*	h
	Comparative	gloss	value	value	value	value
	Examples	(%)	(−)	(−)	(−)	(°)
	Example 97	77.8	33.5	−20.0	4.2	168.1
	Example 98	80.6	35.7	−17.5	5.6	162.3
	Example 99	83.2	30.6	−22.2	1.0	177.4
	Example 100	76.5	27.9	−22.7	−0.9	182.3
	Example 101	82.9	33.2	−21.4	−1.2	183.2
	Example 102	84.0	34.2	−24.0	1.4	176.7
	Example 103	87.4	36.9	−16.7	2.6	171.2
	Example 104	81.1	29.7	−20.4	10.0	153.9
	Comparative	60.1	33.1	−10.0	6.5	147.0
	Example 63
	Comparative	73.2	55.3	28.3	62.9	65.8
	Example 64
	Comparative	63.6	34.4	−11.5	6.1	152.1
	Example 65
	Comparative	74.2	40.8	27.9	41.4	56.0
	Example 66
	Comparative	62.3	31.7	−12.1	6.3	152.5
	Example 67
	Properties of coating film
	Chemical resistance
	Examples and	Acid resistance	Alkali resistance
	Comparative	ΔG value	ΔG value
	Examples	(−)	(−)
	Example 97	8.6	8.1
	Example 98	8.9	7.4
	Example 99	8.0	7.2
	Example 100	9.4	9.0
	Example 101	7.1	5.9
	Example 102	6.9	5.7
	Example 103	5.0	4.3
	Example 104	6.7	6.1
	Comparative	15.7	14.1
	Example 63
	Comparative	14.0	13.5
	Example 64
	Comparative	15.5	13.4
	Example 65
	Comparative	13.9	13.0
	Example 66
	Comparative	15.2	13.3
	Example 67
	Properties of coating film
	Examples and	Heat resistance	Transparency
	Comparative	temperature	(linear absorption)
	Examples	(° C.)	(μm −1 )
	Example 97	240	0.0314
	Example 98	262	0.0201
	Example 99	284	0.0285
	Example 100	245	0.0380
	Example 101	253	0.0262
	Example 102	271	0.0189
	Example 103	285	0.0211
	Example 104	251	0.0331
	Comparative	207	0.0951
	Example 63
	Comparative	210	0.0560
	Example 64
	Comparative	208	0.0853
	Example 65
	Comparative	214	0.0696
	Example 66
	Comparative	210	0.0854
	Example 67

	TABLE 22
		Production of
		resin composition	Properties of resin
	Examples and	Kind of green-	composition
	Comparative	based fine	Dispersion condition
	Examples	pigment	(−)
	Example 105	Example 81	4
	Example 106	Example 82	5
	Example 107	Example 83	5
	Example 108	Example 84	4
	Example 109	Example 85	5
	Example 110	Example 86	5
	Example 111	Example 87	5
	Example 112	Example 88	5
	Comparative	Comparative	2
	Example 68	Example 53
	Comparative	Comparative	3
	Example 69	Example 54
	Comparative	Comparative	2
	Example 70	Example 55
	Comparative	Comparative	2
	Example 71	Example 56
	Comparative	Comparative	2
	Example 72	Example 57
	Properties of resin composition
Examples and	Hue
Comparative	L* value	a* value	b* value	h value
Examples	(−)	(−)	(−)	(°)
Example 105	33.2	−17.2	6.6	159.0
Example 106	34.1	−15.6	7.1	155.5
Example 107	29.8	−18.6	3.2	170.2
Example 108	27.9	−19.5	0.7	177.9
Example 109	32.0	−19.8	−1.4	184.0
Example 110	32.3	−21.6	2.6	173.1
Example 111	36.3	−14.2	8.9	147.9
Example 112	29.7	−15.1	10.8	144.4
Comparative	32.8	−13.6	6.6	154.1
Example 68
Comparative	52.3	27.0	57.3	64.8
Example 69
Comparative	33.2	−12.2	6.3	152.7
Example 70
Comparative	34.3	6.6	34.2	79.1
Example 71
Comparative	32.1	−12.8	6.6	152.7
Example 72
	Properties of resin composition
	Examples and	Heat resistance	Transparency
	Comparative	temperature	(linear absorption)
	Examples	(° C.)	(μm −1 )
	Example 105	225	0.0312
	Example 106	234	0.0199
	Example 107	238	0.0274
	Example 108	227	0.0368
	Example 109	231	0.0261
	Example 110	235	0.0183
	Example 111	240	0.0200
	Example 112	231	0.0320
	Comparative	195	0.0919
	Example 68
	Comparative	200	0.0550
	Example 69
	Comparative	197	0.0851
	Example 70
	Comparative	202	0.0688
	Example 71
	Comparative	198	0.0857
	Example 72

	TABLE 23
	Production of orange-
	based fine pigment
	Coating step with
	alkoxysilane,
	polysiloxane or silicon
	compound
	Additives
				Amount
	Examples			added
	and			(part
	Comparative	Kind of core		by
	Examples	particles	Kind	weight)
	Example 113	Core particles 9	Methyl	2.0
			triethopxysilane
	Example 114	Core particles 10	Methyl	1.0
			trimethoxysilane
	Example 115	Core particles 11	Phenyl	1.5
			triethoxysilane
	Example 116	Core particles 12	Methyl hydrogen	1.0
			polysiloxane
	Example 117	Core particles 13	Methyl	2.0
			triethoxysilane
	Example 118	Core particles 14	Methyl	1.0
			triethoxysilane
	Example 119	Core particles 15	Methyl	1.5
			triethoxysilane
	Example 120	Core particles 16	Methyl	2.0
			triethoxysilane
	Comparative	Core particles 9	—	—
	Example 73
	Comparative	Core particles 9	Methyl	1.0
	Example 74		triethoxysilane
	Comparative	Core particles 9	Methyl	0.005
	Example 75		triethoxysilane
	Comparative	Core particles 9	Methyl	1.0
	Example 76		triethoxysilane
	Comparative	Core particles 9	γ-aminopropyl	1.0
	Example 77		triethoxysilane
	Production of orange-based fine pigment
	Coating step with alkoxysilane,
	polysiloxane or silicon compound
		Coating amount
Examples and	Edge runner treatment	(calculated as
Comparative	Linear load	Time	Si)
Examples	(N/cm)	(Kg/cm)	(min.)	(wt. %)
Example 113	588	60	20	0.30
Example 114	588	60	20	0.19
Example 115	441	45	30	0.20
Example 116	588	60	20	0.44
Example 117	294	30	30	0.30
Example 118	588	60	20	0.15
Example 119	441	45	30	0.23
Example 120	588	60	20	0.30
Comparative	—	—	—	—
Example 73
Comparative	588	60	20	0.15
Example 74
Comparative	588	60	20	6 × 10 −4
Example 75
Comparative	588	60	20	0.15
Example 76
Comparative	588	60	20	0.12
Example 77
		Production of orange-based fine pigment
		Adhesion step with organic red pigment
	Examples and	Organic red pigment
	Comparative		Amount adhered
	Examples	Kind	(part by weight)
	Example 113	D	10.0
	Example 114	E	15.0
	Example 115	D	20.0
	Example 116	E	15.0
	Example 117	D	10.0
	Example 118	E	5.0
	Example 119	D	10.0
	Example 120	E	25.0
	Comparative	D	10.0
	Example 73
	Comparative	D	100.0
	Example 74
	Comparative	D	10.0
	Example 75
	Comparative	D	0.5
	Example 76
	Comparative	D	10.0
	Example 77
	Production of orange-based fine pigment
	Adhesion step with organic red pigment
		Amount adhered
Examples and	Linear runner treatment	(calculated as
Comparative	Linear load	Time	C)
Examples	(N/cm)	(Kg/cm)	(min.)	(wt. %)
Example 113	588	60	20	6.93
Example 114	294	30	30	10.00
Example 115	441	45	30	12.77
Example 116	294	30	30	9.98
Example 117	588	60	20	6.91
Example 118	294	30	30	3.62
Example 119	441	45	20	6.94
Example 120	588	60	20	15.33
Comparative	588	60	20	6.92
Example 73
Comparative	588	60	20	38.31
Example 74
Comparative	588	60	20	6.90
Example 75
Comparative	588	60	20	0.34
Example 76
Comparative	588	60	20	6.91
Example 77

	TABLE 24
	Properties of orange-based fine pigment
		Average	Average
	Examples and	major axial	minor axial	Aspect
	Comparative	diameter	diameter	ratio
	Examples	(μm)	(μm)	(−)
	Example 113	0.0824	0.0098	8.4:1
	Example 114	0.0585	0.0100	5.9:1
	Example 115	0.0783	0.0127	6.2:1
	Example 116	0.0913	0.0186	4.9:1
	Example 117	0.0829	0.0102	8.1:1
	Example 118	0.0579	0.0097	6.0:1
	Example 119	0.0777	0.0125	6.2:1
	Example 120	0.0919	0.0193	4.8:1
	Comparative	0.0815	0.0096	8.5:1
	Example 73
	Comparative	0.0849	0.0107	7.9:1
	Example 74
	Comparative	0.0816	0.0097	8.4:1
	Example 75
	Comparative	0.0814	0.0096	8.5:1
	Example 76
	Comparative	0.0817	0.0097	8.4:1
	Example 77
	Properties of orange-based fine pigment
		Geometrical
		standard	BET specific	Al content* 1
	Examples and	deviation	surface area	within
	Comparative	value	value	particles
	Examples	(−)	(m 2 /g)	(wt. %)
	Example 113	1.41	151.2	—
	Example 114	1.35	190.6	2.56
	Example 115	1.36	150.6	1.87
	Example 116	1.41	100.6	—
	Example 117	1.41	152.6	—
	Example 118	1.35	184.3	2.56
	Example 119	1.37	152.1	1.87
	Example 120	1.42	111.1	—
	Comparative	—	135.8	—
	Example 73
	Comparative	—	146.8	—
	Example 74
	Comparative	—	140.4	—
	Example 75
	Comparative	1.41	141.2	—
	Example 76
	Comparative	—	146.6	—
	Example 77
	Properties of orange-based fine pigment
	Composite oxide hydroxide
		Coating amount	Coating amount
	Examples and	of Al* 1	of Fe* 1
	Comparative	(calculated as Al)	(calculated as Fe)
	Examples	(wt. %)	(wt. %)
	Example 113	—	—
	Example 114	—	—
	Example 115	1.13	0.64
	Example 116	—	—
	Example 117	—	—
	Example 118	—	—
	Example 119	1.13	0.64
	Example 120	—	—
	Comparative	—	—
	Example 73
	Comparative	—	—
	Example 74
	Comparative	—	—
	Example 75
	Comparative	—	—
	Example 76
	Comparative	—	—
	Example 77
	Properties of orange-based fine pigment
Example and	Hue
Comparative	L* value	a* value	b* value	h value
Examples	(−)	(−)	(−)	(°)
Example 113	34.6	49.1	38.0	37.7
Example 114	35.1	49.4	36.8	36.7
Example 115	34.4	49.3	33.7	34.4
Example 116	32.1	50.1	35.5	35.3
Example 117	35.6	49.2	37.6	37.4
Example 118	43.2	40.6	42.4	46.2
Example 119	38.9	48.4	38.9	38.8
Example 120	31.0	50.9	31.1	31.4
Comparative	35.1	46.7	40.6	41.0
Example 73
Comparative	28.3	51.2	23.4	24.6
Example 74
Comparative	34.9	47.2	39.9	40.2
Example 75
Comparative	46.2	32.9	51.4	57.4
Example 76
Comparative	34.8	47.3	39.7	40.0
Example 77
	Properties of orange-based fine pigment
	Chemical resistance
			Acid	Alkali
Examples and	Tinting	Hiding	resistance	resistance
Comparative	strength	power	ΔE* value	ΔE* value
Examples	(%)	(cm 2 /g)	(−)	(−)
Example 113	128	180	1.27	1.18
Example 114	132	152	1.08	1.00
Example 115	136	172	0.99	0.96
Example 116	126	223	1.29	1.21
Example 117	131	176	1.16	1.09
Example 118	130	145	1.06	0.98
Example 119	134	161	0.94	0.91
Example 120	133	224	1.21	1.13
Comparative	100	197	2.04	1.81
Example 73
Comparative	116	266	1.74	1.66
Example 74
Comparative	102	190	2.00	1.76
Example 75
Comparative	106	174	1.82	1.71
Example 76
Comparative	104	189	1.99	1.74
Example 77
	Properties of orange-based fine pigment
			Desorption
	Examples and	Heat resistance	percentage of
	Comparative	temperature	organic pigment
	Examples	(° C.)	(%)
	Example 113	224	7.1
	Example 114	253	8.3
	Example 115	276	9.2
	Example 116	226	8.7
	Example 117	238	3.9
	Example 118	267	2.2
	Example 119	281	2.6
	Example 120	230	4.8
	Comparative	194	69.4
	Example 73
	Comparative	231	60.1
	Example 74
	Comparative	197	57.2
	Example 75
	Comparative	200	6.8
	Example 76
	Comparative	199	56.6
	Example 77
	* 1 : Coating amount on core particles

	TABLE 25
	Production	Properties of paint
	of paint	Storage
	Examples and	Kind of		stability
	Comparative	orange-based	Viscosity	ΔE* value
	Examples	fine pigment	(cP)	(−)
	Example 121	Example 113	3,580	0.96
	Example 122	Example 114	3,180	0.92
	Example 123	Example 115	2,863	0.81
	Example 124	Example 116	3,265	0.99
	Example 125	Example 117	3,384	0.93
	Example 126	Example 118	3,062	0.90
	Example 127	Example 119	3,056	0.77
	Example 128	Example 120	2,786	0.97
	Comparative	Comparative	12,560	2.34
	Example 78	Example 73
	Comparative	Comparative	3,183	1.60
	Example 79	Example 74
	Comparative	Comparative	2,965	2.30
	Example 80	Example 75
	Comparative	Comparative	2,872	1.65
	Example 81	Example 76
	Comparative	Comparative	3,682	2.28
	Example 82	Example 77
	Properties of coating film
	Hue
	Examples and	60°	L*	a*	b*	h
	Comparative	gloss	value	value	value	value
	Examples	(%)	(−)	(−)	(−)	(°)
	Example 121	81.7	35.8	48.3	38.0	38.2
	Example 122	86.1	36.4	48.5	36.6	37.0
	Example 123	88.9	36.3	48.6	33.8	34.8
	Example 124	81.2	33.6	49.3	35.7	35.9
	Example 125	87.0	36.8	48.6	37.6	37.7
	Example 126	88.8	44.1	39.8	42.3	46.7
	Example 127	92.3	40.3	47.7	39.1	39.3
	Example 128	85.7	32.3	50.1	30.9	31.7
	Comparative	64.6	36.6	45.3	40.2	41.6
	Example 78
	Comparative	58.5	29.9	50.2	23.5	25.1
	Example 79
	Comparative	68.0	36.3	46.3	39.4	40.4
	Example 80
	Comparative	80.3	47.6	31.8	51.1	58.1
	Example 81
	Comparative	68.9	36.1	46.3	39.2	40.3
	Example 82
	Properties of coating film
	Chemical resistances
	Examples and	Acid resistance	Alkali resistance
	Comparative	ΔG value	ΔG value
	Examples	(−)	(−)
	Example 121	8.9	8.1
	Example 122	8.4	7.6
	Example 123	7.7	6.8
	Example 124	9.2	8.4
	Example 125	8.5	7.8
	Example 126	8.2	7.1
	Example 127	5.1	4.6
	Example 128	8.7	7.9
	Comparative	15.1	14.7
	Example 78
	Comparative	12.6	12.1
	Example 79
	Comparative	14.7	14.2
	Example 80
	Comparative	13.4	13.6
	Example 81
	Comparative	14.7	14.0
	Example 82
	Properties of coating film
	Examples and	Heat resistance	Transparency
	Comparative	temperature	(linear absorption)
	Examples	(° C.)	(μm −1 )
	Example 121	243	0.0300
	Example 122	261	0.0186
	Example 123	281	0.0260
	Example 124	246	0.0362
	Example 125	254	0.0261
	Example 126	273	0.0170
	Example 127	283	0.0199
	Example 128	248	0.0332
	Comparative	208	0.0872
	Example 78
	Comparative	246	0.1032
	Example 79
	Comparative	215	0.0828
	Example 80
	Comparative	216	0.0296
	Example 81
	Comparative	217	0.0816
	Example 82

	TABLE 26
	Production
	of water-	Properties of paint
	based paint	Storage
	Examples and	Kind of		Stability
	Comparative	orange-based	Viscosity	ΔE* value
	Examples	fine pigment	(cP)	(−)
	Example 129	Example 113	3,670	1.03
	Example 130	Example 114	3,281	0.98
	Example 131	Example 115	3,659	0.88
	Example 132	Example 116	3,263	1.05
	Example 133	Example 117	3,486	1.00
	Example 134	Example 118	3,365	0.96
	Example 135	Example 119	4,163	0.81
	Example 136	Example 120	3,887	1.04
	Comparative	Comparative	11,197	2.45
	Example 83	Example 73
	Comparative	Comparative	3,663	1.69
	Example 84	Example 74
	Comparative	Comparative	2,816	2.41
	Example 85	Example 75
	Comparative	Comparative	3,162	1.72
	Example 86	Example 76
	Comparative	Comparative	3,386	2.38
	Example 87	Example 77
	Properties of coating film
	Hue
	Examples and	60°	L*	a*	b*	h
	Comparative	gloss	value	value	value	value
	Examples	(%)	(−)	(−)	(−)	(°)
	Example 129	77.5	35.9	48.8	38.3	38.1
	Example 130	81.4	36.6	48.2	36.6	37.2
	Example 131	84.2	36.2	48.5	33.8	34.9
	Example 132	76.9	33.5	49.6	35.8	35.8
	Example 133	81.8	36.6	48.9	37.9	37.8
	Example 134	83.9	43.9	39.8	42.0	46.5
	Example 135	87.5	40.6	48.0	39.3	39.3
	Example 136	81.3	32.6	50.1	31.0	31.7
	Comparative	60.1	36.8	45.8	40.4	41.4
	Example 83
	Comparative	53.4	29.8	50.3	23.7	25.2
	Example 84
	Comparative	63.0	36.3	46.6	39.6	40.4
	Example 85
	Comparative	75.8	47.1	32.2	51.6	58.0
	Example 86
	Comparative	64.0	36.3	46.6	39.3	40.1
	Example 87
	Properties of coating film
	Chemical resistances
	Examples and	Acid resistance	Alkali resistance
	Comparative	ΔG value	ΔG value
	Examples	(−)	(−)
	Example 129	9.2	8.3
	Example 130	8.6	7.5
	Example 131	8.0	7.0
	Example 132	9.6	8.7
	Example 133	8.7	8.1
	Example 134	8.3	7.3
	Example 135	5.4	5.0
	Example 136	8.7	8.2
	Comparative	15.6	15.0
	Example 83
	COmparative	12.9	12.4
	Example 84
	Comparative	15.1	14.6
	Example 85
	Comparative	13.5	13.9
	Example 86
	Comparative	14.9	14.4
	Example 87
	Properties of coating film
	Examples and	Heat resistance	Transparency
	Comparative	temperature	(linear absorption)
	Examples	(° C.)	(μm −1 )
	Example 129	240	0.0319
	Example 130	259	0.0204
	Example 131	278	0.0280
	Example 132	243	0.0377
	Example 133	250	0.0282
	Example 134	271	0.0188
	Example 135	279	0.0216
	Example 136	244	0.0353
	Comparative	204	0.0893
	Example 83
	Comparative	240	0.1051
	Example 84
	Comparative	211	0.0849
	Example 85
	Comparative	214	0.0314
	Example 86
	Comparative	212	0.0833
	Example 87

	TABLE 27
		Production of
		resin composition	Properties of resin
	Examples and	Kind of orange-	composition
	Comparative	based fine	Dispersion condition
	Examples	pigment	(−)
	Example 137	Example 113	4
	Example 138	Example 114	5
	Example 139	Example 115	5
	Example 140	Example 116	5
	Example 141	Example 117	5
	Example 142	Example 118	5
	Example 143	Example 119	5
	Example 144	Example 120	5
	Comparative	Comparative	2
	Example 88	Example 73
	Comparative	Comparative	3
	Example 89	Example 74
	Comparative	Comparative	2
	Example 90	Example 75
	Comparative	Comparative	3
	Example 91	Example 76
	Comparative	Comparative	2
	Example 92	Example 77
	Properties of resin composition
Examples and	Hue
Comparative	L* value	a* value	b* value	h value
Examples	(−)	(−)	(−)	(°)
Example 137	35.8	49.5	38.7	38.0
Example 138	36.1	48.9	37.5	37.5
Example 139	36.6	49.6	35.0	35.2
Example 140	33.8	50.6	36.8	36.0
Example 141	36.9	49.9	39.2	38.2
Example 142	44.0	40.7	43.8	47.1
Example 143	40.5	49.1	40.3	39.4
Example 144	32.9	51.6	32.2	32.0
Comparative	36.9	46.5	41.6	41.8
Example 88
Comparative	29.9	51.5	24.6	25.5
Example 89
Comparative	36.1	47.9	41.0	40.6
Example 90
Comparative	47.2	32.6	52.6	58.2
Example 91
Comparative	36.5	48.0	40.2	39.9
Example 92
	Properties of resin composition
	Examples and	Heat resistance	Transparency
	Comparative	temperature	(linear absorption)
	Examples	(° C.)	(μm −1 )
	Example 137	223	0.0318
	Example 138	231	0.0203
	Example 139	236	0.0284
	Example 140	228	0.0356
	Example 141	235	0.0273
	Example 142	237	0.0180
	Example 143	239	0.0212
	Example 144	225	0.0352
	Comparative	195	0.0889
	Example 88
	Comparative	201	0.1045
	Example 89
	Comparative	197	0.0842
	Example 90
	Comparative	199	0.0310
	Example 91
	Comparative	198	0.0828
	Example 92

Claims

1. Iron oxide hydroxide composite particles having an average particle diameter of 0.005 to 1.0 μm, comprising:iron oxide hydroxide particles as core particles, a coating formed on surface of said iron oxide hydroxide particles, comprising at least one organosilicon compound selected from the group consisting of: (1) organosilane compounds obtainable from alkoxysilane compounds, and (2) polysiloxanes or modified polysiloxanes, and an organic pigment coat formed on said coating layer comprising said organosilicon compound, in an amount of from 1 to 30 parts by weight based on 100 parts by weight of said iron oxide hydroxide particles.

2. Iron oxide hydroxide composite particles according to claim 1, wherein said iron oxide hydroxide particles are particles having a coat which is formed on at least a part of the surface of said iron oxide hydroxide particles and which comprises at least one compound selected from the group consisting of hydroxides of aluminum, oxides of aluminum, hydroxides of silicon and oxides of silicon in an amount of 0.01 to 20% by weight, calculated as Al or SiO2, based on the total weight of the iron oxide hydroxide particles coated.

3. Iron oxide hydroxide composite particles according to claim 1, wherein said modified polysiloxanes are compounds selected from the group consisting of:(A) polysiloxanes modified with at least one compound selected from the group consisting of polyethers, polyesters and epoxy compounds, and (B) polysiloxanes whose molecular terminal is modified with at least one group selected from the group consisting of carboxylic acid groups, alcohol groups and a hydroxyl group.

4. Iron oxide hydroxide composite particles according to claim 1, wherein said alkoxysilane compound is represented by the general formula (I):R1aSiX4−a  (I) wherein R1 is C6H5—, (CH3)2CHCH2— or n-CbH2b+1— (wherein b is an integer of 1 to 18); X is CH3O— or C2H5O—; and a is an integer of 0 to 3.

5. Iron oxide hydroxide composite particles according to claim 4, wherein said alkoxysilane compound is methyltriethoxysilane, dimethyldiethoxysilane, phenyltriethoxysilane, diphenyldiethoxysilane, methyltrimethoxysilane, dimethyldimethoxysilane, phenyltrimethoxysilane, diphenyldimethoxysilane, isobutyltrimethoxysilane or decyltrimethoxysilane.

6. Iron oxide hydroxide composite particles according to claim 1, wherein said polysiloxanes are represented by the general formula (II): wherein R2 is H— or CH3—, and d is an integer of 15 to 450.

7. Iron oxide hydroxide composite particles according to claim 6, wherein said polysiloxanes are compounds having methyl hydrogen siloxane units.

8. Iron oxide hydroxide composite particles according to claim 3, wherein said polysiloxanes modified with at least one compound selected from the group consisting of polyethers, polyesters and epoxy compounds are represented by the general formula (III), (IV) or (V): wherein R3 is —(—CH2—)h—; R4 is —(—CH2—)i—CH3; R5 is —OH, —COOH, —CH═CH2, —C(CH3)═CH2 or —(—CH2—)j—CH3; R6 is —(—CH2—)k—CH3; g and h are an integer of 1 to 15; i, j and k are an integer of 0 to 15; e is an integer of 1 to 50; and f is an integer of 1 to 300; wherein R7, R8 and R9 are —(—CH2—)q— and may be the same or different; R10 is —OH, —COOH, —CH═CH2, —C(CH3)═CH2 or —(—CH2—)r—CH3; R11 is —(—CH2—)s—CH3; n and q are an integer of 1 to 15; r and s are an integer of 0 to 15; e′ is an integer of 1 to 50; and f′ is an integer of 1 to 300; or wherein R12 is —(—CH2—)v—; v is an integer of 1 to 15; t is an integer of 1 to 50; and u is an integer of 1 to 300.

9. Iron oxide hydroxide composite particles according to claim 3, wherein said polysiloxanes whose molecular terminal is modified with at least one group selected from the group consisting of carboxylic acid groups, alcohol groups and a hydroxyl group are represented by the general formula (VI): wherein R13 and R14 are —OH, R16OH or R17COOH and may be the same or different; R15 is —CH3 or —C6H5; R16 and R17 are —(—CH2—)y—; y is an integer of 1 to 15; w is an integer of 1 to 200; and x is an integer of 0 to 100.

10. Iron oxide hydroxide composite particles according to claim 1, wherein the amount of said coating organosilicon compounds is 0.02 to 5.0% by weight, calculated as Si, based on the total weight of the organosilicon compounds and said iron oxide hydroxide particles.

11. Iron oxide hydroxide composite particles according to claim 1, wherein said organic pigment is organic blue-based pigment or organic red-based pigment.

12. Iron oxide hydroxide composite particles according to claim 1, wherein said iron oxide hydroxide composite particles have an aspect ratio (average major axis diameter/average minor axis diameter) of 2.0:1 to 20.0:1.

13. Iron oxide hydroxide composite particles according to claim 1, wherein said iron oxide hydroxide composite particles have a BET specific surface area value of 6 to 300 m2/g.

14. Iron oxide hydroxide composite particles according to claim 1, wherein said iron oxide hydroxide composite particles have a geometrical standard deviation of major axis diameter of 1.01 to 2.0.

15. Iron oxide hydroxide composite particles according to claim 1, which have an average particle diameter of from 0.005 to less than 0.1 μm, comprise:iron oxide hydroxide particles as core particles, a coating formed on surface of said iron oxide hydroxide particles, comprising at least one organosilicon compound selected from the group consisting of: (1) organosilane compounds obtainable from alkoxysilane compounds, and (2) polysiloxanes or modified polysiloxanes, and an organic blue-based pigment coat formed on said coating layer comprising said organosilicon compound, in an amount of from 5 to 30 parts by weight based on 100 parts by weight of said iron oxide hydroxide particles.

16. Iron oxide hydroxide composite particles according to claim 15, wherein said iron oxide hydroxide particles are particles having a coat which is formed on at least a part of the surface of said iron oxide hydroxide particles and which comprises at least one compound selected from the group consisting of hydroxides of aluminum, oxides of aluminum, hydroxides of silicon and oxides of silicon in an amount of 0.01 to 20% by weight, calculated as Al or SiO2, based on the total weight of the iron oxide hydroxide particles coated.

17. Iron oxide hydroxide composite particles according to claim 15, wherein said organic blue-based pigment is a phthalocyanine-based pigment and an alkali blue pigment.

18. Iron oxide hydroxide composite particles according to claim 1, which have an average particle diameter of from 0.005 to less than 0.1 μm, comprise:iron oxide hydroxide particles as core particles, a coating formed on surface of said iron oxide hydroxide particles, comprising at least one organosilicon compound selected from the group consisting of: (1) organosilane compounds obtainable from alkoxysilane compounds, and (2) polysiloxanes or modified polysiloxanes, and an organic red-based pigment coat formed on said coating layer comprising said organosilicon compound, in an amount of from 1 to 30 parts by weight based on 100 parts by weight of said iron oxide hydroxide particles.

19. Iron oxide hydroxide composite particles according to claim 18, wherein said iron oxide hydroxide particles are particles having a coat which is formed on at least a part of the surface of said iron oxide hydroxide particles and which comprises at least one compound selected from the group consisting of hydroxides of aluminum, oxides of aluminum, hydroxides of silicon and oxides of silicon in an amount of 0.01 to 20% by weight, calculated as Al or SiO2, based on the total weight of the iron oxide hydroxide particles coated.

20. Iron oxide hydroxide composite particles according to claim 18, wherein said organic red-based pigment is quinacridone-based pigment, azo-based pigment, condensed azo-based pigment and perylene-based pigment.

21. Iron oxide hydroxide composite particles according to claim 1, which have an average particle diameter of from 0.1 to 1.0 μm, comprises:iron oxide hydroxide particles as core particles, a coating formed on surface of said iron oxide hydroxide particles, comprising at least one organosilicon compound selected from the group consisting of: (1) organosilane compounds obtainable from alkoxysilane compounds, and (2) polysiloxanes or modified polysiloxanes, and an organic blue-based pigment coat formed on said coating layer comprising said organosilicon compound, in an amount of from 5 to 30 parts by weight based on 100 parts by weight of said iron oxide hydroxide particles.

22. Iron oxide hydroxide composite particles according to claim 21, wherein said iron oxide hydroxide particles are particles having a coat which is formed on at least a part of the surface of said iron oxide hydroxide particles and which comprises at least one compound selected from the group consisting of hydroxides of aluminum, oxides of aluminum, hydroxides of silicon and oxides of silicon in an amount of 0.01 to 20% by weight, calculated as Al or SiO2, based on the total weight of the iron oxide hydroxide particles coated.

23. Iron oxide hydroxide composite particles according to claim 21, wherein organic blue-based pigment is a phthalocyanine-based pigment and an alkali blue pigment.

24. Iron oxide hydroxide composite particles according to claim 1, which have an average particle diameter of from 0.1 to 1.0 μm, and comprise:iron oxide hydroxide particles as core particles, a coating formed on surface of said iron oxide hydroxide particles, comprising at least one organosilicon compound selected from the group consisting of: (1) organosilane compounds obtainable from alkoxysilane compounds, and (2) polysiloxanes or modified polysiloxanes, and an organic red-based pigment coat formed on said coating layer comprising said organosilicon compound, in an amount of from 1 to 30 parts by weight based on 100 parts by weight of said iron oxide hydroxide particles.

25. Iron oxide hydroxide composite particles according to claim 24, wherein said iron oxide hydroxide particles are particles having a coat which is formed on at least a part of the surface of said iron oxide hydroxide particles and which comprises at least one compound selected from the group consisting of hydroxides of aluminum, oxides of aluminum, hydroxides of silicon and oxides of silicon in an amount of 0.01 to 20% by weight, calculated as Al or SiO2, based on the total weight of the iron oxide hydroxide particles coated.

26. Iron oxide hydroxide composite particles according to claim 24, wherein said organic red-based pigment is quinacridone-based pigment, azo-based pigment, condensed azo-based pigment and perylene-based pigment.

27. A pigment comprising the iron oxide hydroxide composite particles as defined in claim 1.

28. A green-based pigment comprising the iron oxide hydroxide composite particles as defined in claim 15 or 21.

29. A orange-based pigment comprising the iron oxide hydroxide composite particles as defined in claim 18 or 24.

30. A paint comprising:said pigment defined in claim 27; and a paint base material.

31. A paint according to claim 30, wherein the amount of said pigment is 0.5 to 100 parts by weight based on 100 parts by weight of said paint base material.

32. A rubber or resin composition comprising:said pigment defined in claim 27; and a base material for rubber or resin composition.

33. A rubber or resin composition according to claim 32, wherein the amount of said pigment is 0.01 to 200 parts by weight based on 100 parts by weight of said base material for rubber or resin composition.

34. A process for producing said iron oxide hydroxide composite particles defined in claim 1, which process comprises:mixing as core particles iron oxide hydroxide particles having an average particle diameter of 0.005 to 1.0 μm together with at least one compound selected from the group consisting of: (1) alkoxysilane compounds, and (2) polysiloxanes or modified polysiloxanes, by using an apparatus capable of applying a shear force to the core particles, thereby coating the surface of said iron oxide hydroxide particle with the said compounds; mixing the obtained iron oxide hydroxide particles coated with the said compounds and an organic pigment in an amount of 1 to 30 parts by weight based on 100 parts by weight of the core particles by using an apparatus capable of applying a shear force to the core particles, thereby forming an organic pigment coat on the surface of a coating layer comprising the organosilicon compounds.

35. A process for producing black iron oxide hydroxide composite particles according to claim 34, wherein said iron oxide hydroxide particles as core particles are coated with at least one compound selected from the group consisting of hydroxides of aluminum, oxides of aluminum, hydroxides of silicon and oxides of silicon.