Patent Application
20060063855
The present invention relates to a particularly advantageous process for preparing of fluorescent and non-fluorescent pigments derived from polymer soluble colorants and/or optical whiteners, to the products obtained by such process and to their use as valuable pigments.
Fluorescent pigments are basically the solutions of organic fluorescent dyes in clear and colourless polymeric resins. Typically, a polymer is colored with a fluorescent dye preferably during the condensation/polymerisation process. The resulting colored resin is usually clear, brittle and friable. It is pulverised into a fine powder, which is the final fluorescent pigment (Charles E. Moore in Pigment Handbook I-H Wiley N.Y. 1988). Postcuring and chemical modification can improve chemical and solvent resistance of such pigments (U.S. Pat. No. 3,412,036). Most fluorescent pigments are based on toluenesulfonamide-melamine-formaldehyde resin matrix (U.S. Pat. No. 2,9838,873). Also claimed are the polyamide-type (U.S. Pat. No. 3,915,884), the polyester-type (U.S. Pat. No. 3,922,232) and the urethane-type (U.S. Pat. No. 3,741,907) dye substrates.
In known processes for the manufacture of fluorescent pigments, these thermoset resins are formed by polycondensation of the above mixture in bulk, in non-continuous batches. Such processes are described e.g. in U.S. Pat. No. 3,939,093, in GB 1,341,602 or in U.S. Pat. No. 3,812,051. On the average the reaction takes 2 hours, per batch, in the reactor. After complete polymerisation a hard, tough solid is obtained. This solid must be taken out of the poly-merisation reactor as blocks. This can prove difficult and it is, therefore, often preferred to complete the reaction by casting the reacting mass, which is still pasty, into troughs and finishing the polymerisation in an oven. The blocks are then crushed and finally micronised. Such conventional processes for the manufacture are also described in Chem. Brit., 335 (1977).
The micronisation of this solid presents some difficulties: it requires a pregrinding before a fine microniser is fed, it being necessary for the two items of equipment to be cleaned after each batch. The U.S. Pat. No. 3,972,849 proposes the use of known grinding equipment, such as a ball mill.
The inconvenience of the conventional manufacturing processes and the disadvantages of the pigment particles obtained by these processes have led some manufacturers, on the other hand, to prefer the manufacture and the use of pigments based on thermoplastic resins whenever a high solvent and temperature resistance is not essential. U.S. Pat. No. 2,809,954, GB 869,801 and GB 980,583 describe the synthesis of pigments based on thermoplastic resins. These fusible, and hence heat-sensitive, resins do not lend themselves well to simple micronising by milling and hence to the manufacture of pigments of a fine and well-determined particle size. These resins generally require an additional stage of manufacture (dispersion, phase separation) to obtain pigment particles of well-determined particle size, which is described, for example, in U.S. Pat. Nos. 3,642,650 and 3,412,034.
The disadvantages of the two types of processes described above are avoided in the manufacture of amide (urea, melamine, and the like)/formaldehyde condensates of low molecular weight or of polyester alkyd resins, wherein to each type of said resins the colorant is fixed by adsorption. Such processes are described for example in GB 748,848, GB 786,678 or in GB 733,356. However, the applications of such pigments are in practice limited to inks and paints, because the colorant molecules are bound to the condensates only by adsorption.
U.S. Pat. No. 5,989,453 describes a process wherein the reactants for the formation of the polycondensation resin and the colorant are introduced continuously into an extruder; the mixture is caused to travel forward in the extruder, at the end of reaction the mixture is withdrawn continuously from the extruder, and is deposited continuously onto a conveyor belt, broken up into thermoset flakes, and cooled, the conveyor belt having means for cooling and means for detaching the flakes from the belt. The process still leads to hard thermoset flakes which are still difficult to grind. Besides that, the unreacted potentially toxic monomers, such as formaldehyde, and low molecular weight condensation products remain occluded into the product. Such toxic components are set free, particularly at elevated temperatures during the actual coloring of plastics therewith, causing environmental, health & safety problems.
The objective of the present invention is to manufacture fluorescent and non-fluorescent pigments comprising a white or a colored compound incorporated in a resin which encapsulates, confines and immobilizes the colored compound, which pigments withstand the action of heat or of solvents, while avoiding the disadvantages of the cumbersome processes of the prior art such as multistep processes, the handling, the crushing and the difficulties of micronisation, and especially the elimination of the residual monomers and/or low molecular weight condensation products.
This objective is attained by a process for the manufacture of pigments, comprising a colored compound and/or a fluorescent whitener incorporated in a polycondensation resin by bulk polycondensation of the reaction mixture, wherein the reactants for the formation of said polycondensation resin and the colored or whitening compound are introduced in an apparatus submitting the reaction mixture to enhanced driving power as expressed by a Froude number>1. The mixture is caused to react at a suitable elevated temperature, with or without vacuum, at the same time removing during and/or at the end the of the reaction any residual unreacted potentially toxic monomers and/or low molecular weight condensation products formed. The liquid resin composition thus formed is then cooled and allowed to solidify under stirring in the same reactor. Unlike any state-of-the art processes, pigments are thereby directly formed in a broken-up crushed state so that the subsequent micronisation is either not required and/or is facilitated. Furthermore, in situ crushing and micronisation also liberate any occluded monomers and low molecular weight condensation products enabling their easy elimination during the process of the present invention.
The Froude number Fr is defined by the formula
in which v is the velocity of the operative part, r is the radius of the operative part and g is the gravity of the treated materials. Such effect is obtained at overcritical speed>100 r/min and can be achieved independently of the appartus size. Examples of such apparatus are e.g. “All In One Reactor”® (Draiswerke GmbH, Germany), a kneader like the TurbuKneader® of the same company, a paddle dryer like the Turbudry® of the same company or a related system.
Also disclosed are compositions comprising non-fluorescent colorants and certain polyester or polyamide resins as well as a process for the preparation of the compositions. The products are useful for coloring polymeric material.
Particularly suitable polycondensation resins to be used according to the instant invention are products which are inelastic, non-fiber-forming and brittle and which consequently may easily be converted into particulate form. The resins should moreover have a relatively high softening point, preferably of more than about 100° C., because otherwise at the temperatures which arise during milling the particles of resin may agglomerate and stick together. The resins should also have little or no solubility in the solvents conventionally used in processing, such as e.g. painters' naphtha, toluene and xylenes and also should not swell in these solvents. Furthermore, the resins should exhibit good transparency and adequate fastness to light. Resins meeting these requirements are generally known, and some of them have already been used for the preparation of daylight fluorescent pigments.
Suitable polycondensation resins are for example those, wherein the reactants for the formation of said polycondensation resins are
(a) at least one component A chosen from aromatic sulfonamides containing 2 hydrogens bonded to the nitrogen of the sulfonamide group,
(b) at least one component B chosen from substances containing 2 or more NH2 groups, each of the said NH2 groups being bonded to a carbon, the said carbon being bonded by a double bond to an ═O, ═S or ═N, and
(c) at least one aldehyde component C.
Among the substances capable of forming the component A according to the present invention, there will be mentioned especially benzenesulfonamide and benzenesulfonamide derivatives of general formula:
wherein the groups R are hydrogen, alkyl or aryl groups. A particularly preferred substance A is para-toluenesulfonamide, ortho-toluenesulfonamide or mixtures of aromatic sulfonamides, such as mixtures of ortho- and para-toluene-sulfonamide (e.g. a 50:50 mixture of these components), can also be employed and are available on the market. C1-C4 alkyl-benzenesulfonamides, e.g. are also available commercially.
Among the substances which can be employed as component B according to the present invention there will be mentioned especially urea (NH2CONH2), thiourea (NH2CSNH2), guanidine (NH2)2C═NH, carbamylurea (C2H5N3O2), succinamide (C4H8N2O2), among the noncyclic compounds; among cyclic compounds and more particularly among nitrogenous heterocyclic rings there will be mentioned the molecules containing a plurality of NH2 groups, each of these groups being bonded to a carbon of a heterocyclic ring, the said carbon being linked by a double bond to a nitrogen of the heterocyclic ring; these heterocyclic rings include the triazole, diazine, triazine and pyrimidine nuclei; there will be mentioned in particular the guanamine derivatives of general formula:
where R′ is hydrogen, an aliphatic radical, an aromatic radical, a saturated or unsaturated cycloaliphatic or alkoxyaryloxy radical. Benzoguanamine may be mentioned among the preferred compounds B.
A compound B which is particularly preferred when it is intended to obtain a thermoset resin is melamine (where R′ is NH2). Diguanamines and triguanamines (whose synthesis from the corresponding nitriles and from dicyanodiamide is known, furthermore), or mixtures of the above substances can also be employed as component B according to the present invention, as well as the particular triazine compounds described in the U.S. Pat. No. 3,838,063. A certain amount of the component B according to the invention may be replaced by an isocyanuric ring containing compound, such as isocyanuric acid or its alkyl or aryl esters, or its N-alkyl or N-arylderivatives, respectively; pigment compositions comprising such resins are disclosed in U.S. Pat. No. 3,620,993.
The aldehyde or the mixture of aldehydes forming the component C according to the present invention are formaldehyde, acetaldehyde, propionaldehyde (higher aldehydes can be employed but do not offer any particular advantage within the meaning of the present invention). A particularly preferred compound is paraformaldehyde (CH2O)n, because of its ease of use.
In the process according to the present invention the concentration of component B, which is preferably between approximately 13% and 40% by weight, of the weight of sulfonamide component A in the reaction mixture, can be taken to values which are markedly higher than those employed in the processes for the manufacture of thermoplastic resins. The concentration of component C in the mixture is preferably between 27% and 40% by weight of the sulfonamide.
A harder and more brittle material is thus obtained, which lends itself better to micronisation and which withstands better the action of heat and of solvents. In the case where the amine chosen as component B is melamine, a decrease in the cost of manufacture is also obtained when the proportion of B is increased, given the low cost of this product.
The decrease in the cost of manufacture of the pigments according to the present invention particularly results from the incorporation of many unit operations such as condensation, pouring out of the reaction mass, solidification of the mass, post curing in a separate oven and pre-grinding, into a single operation. Moreover, the poly-condensation reaction is better controlled than in a continuous process.
Further examples of suitable polycondensation resins are i.a. polyamide resins, polyester resins, polycarbonates or polyurethanes. Other suitable resins are polyester/polyamide resins prepared by the reaction of aminoalcohols or aminophenols with polycarbocylic acids, such as the resins described in U.S. Pat. No. 4,975,220.
Particularly suitable polycondensation resins are polyester resins and especially polyamide resins.
Among the preferred resins are crosslinked polyester resins from aromatic polycarboxylic acids or their anhydrides, particularly aromatic dicarboxylic and tricarboxylic acids, such as phthalic acid, isophthalic acid or trimellitic acid, and bifunctional or polyfunctional alcohols, such as ethylene glycol, glycerol, pentaerythritol, trimethylolpropane and neopentyl glycol. Especially preferred are polyester resins from phthalic anhydride and pentaerythritol. Such preferred polyester resins are described for example in DE 961,575 or in the above mentioned U.S. Pat. No. 3,972,849.
Other preferred polyester resins are partially crystalline thermoplastic opaque polyester resins which have a substantial number of amorphous regions and which contain from 35 to 95 equivalent % of crystallinity-producing monomers and from 5 to 65 equivalent % of amorphous producing monomers. Such resins and their use for the preparation of fluorescent pigments are described in EP-A 489,482, especially on page 2, line 57 through page 4, line 40 which are hereby incorporated by reference.
Other preferred polycondensation resins to be prepared and used according to the invention are polyamide resins formed by the reaction of a polyfunctional amine with both a polycarboxylic acid and a monocarboxylic acid, said polyamide being in the molecular weight range from about 400 to about 2500. Such polyamide resins are substantially linear and have at least one carboxy group remaining on the majority of molecules, which permits a thermoplasitc resin to be formed which is extremely friable and grindable. The monocarboxylic acid may be added as such or may be formed in situ by reacting a monoamine and a dicarboxylic acid in sufficient quantity to form the desired corresponding monocarboxylic co-condensate to function as a terminator and control the molecular weight of the resin formed. Optionally, whether or not a monocarboxylic acid is added as such, or is formed in situ, a sufficient amount of stabilizing compound of an element from Groups IIA and IIB may be added to further stabilize the pigment. Such preferred polyamide resins are described in the U.S. Pat. No. 3,915,884, which document is incorporated herein by reference.
Preferred polyfunctional amines for the preparation of the instant polyamide resins are polyfunctional, preferably difunctional, primary amines. Particularly preferred are polyfunctional alicyclic primary amines, which form the most friable resins. Most preferred is isophorone diamine (1-amino-3-aminomethyl-3,5,5-trimethyl cyclohexane). Other suitable amines are aliphatic amines having an aromatic ring, such as the m- and p-xylylene diamines; aliphatic polyfunctional primary amines, such as ethylene diamine, diethylene triamine and the like.
Preferred monocarboxylic aromatic acids are benzoic acid and substituted benzoic acids, such as p-toluic, o-toluic, and 4-methoxy benzoic acid.
Preferred aromatic polycarboxylic acids are those which have carboxy groups on noncontiguous carbon atoms, such as isophthalic acid, terephthalic acid, trimesic acid and dicarboxy and tricarboxy naphthalene.
Other preferred polyamide resins are prepared by reaction of a diamine with an excess stoichiometric amount of a diacid. Such resins are described in U.S. Pat. No. 5,094,777, especially in column 2, line 13 through column 4, line 22, which are hereby incorporated by reference.
When a stabilizing compound of elements in Group IIA and Group IIB of the periodic table of elements is used, such compounds should preferably be compatible with the co-condensate and the coloring material. Suitable compounds are e.g. oxides, carbonates or organic acid salts of Group II elements, such as magnesium oxide, magnesium carbonate, zinc oxide, zinc stearate, calcium hydroxide and the like. Zinc oxide is preferred.
Other preferred polycondensation resins to be prepared and used according to the invention are epoxide resins based on bisphenol-A diglycidyl ethers and crosslinked with polyhydric phenols, such as bisphenol-A, with polycarboxylic acid anhydrides, with Lewis acids and particularly with dicyandiamides and related compounds; hybrid polyesters, such as solid saturated polyester resins having free carboxyl groups and being crosslinked with epoxide resins; polyesters, such as solid saturated polyesters having free carboxyl groups and being crosslinked with triglycidylisocyanurate (TGIC); polyurethanes, such as solid saturated polyesters with free hydroxyl groups being crosslinked with polyisocyanates.
The polycondensation resins to be used according to the instant invention may, if appropriate, also contain other additives, such as antioxidants, stabilizing compounds, such as UV-absorbers or light stabilizers as e.g. the hindered amine light stabilizers (HALS). Such stabilizers are well known in the art.
The U.S. Pat. No. 3,915,884 and U.S. Pat. No. 5,094,777 disclose, as mentioned above, the preferred polyamides and their use for the manufacture of fluorescent pigments. However, according to that reference the resins are synthesized by a state-of-the-art process. Such a process is characterized by all the disadvantages discussed above for similar prior art processes.
Surprisingly, with the process of the instant invention a much faster, simpler and more convenient synthesis of the above polycondensation resins and of the pigments, particularly fluorescent pigments, is provided.
The pigments according to the invention comprise preferably at least one colored or white compound which is soluble or partially soluble in the resin composition, the preferred concentration of said substance being between 1% and 5% by weight of the pigments. When non-fluorescent dyes, e.g. solvent dyes are used, the preferred concentration may be up to 10% by weight of the pigments.
Colorants and white materials capable of forming a solid solution in a resin are furthermore known and are, in general, listed in the Colour Index. Rhodamines, coumarines, xanthenes, perylenes and naphthalimides will be mentioned by way of example, no limitation being implied. Examples of appropriate colorants are also compounds described in GB 1,341,602, U.S. Pat. No. 3,939,093, U.S. Pat. No. 3,812,051, DE 3,703,495 and in EP-A 422,474.
Other suitable colorants are diketo-pyrrolo-pyrroles (DPP), especially those which are soluble or at least partially soluble in the resins used. Such DPP compounds are known and are described e.g. in U.S. Pat. No. 4,415,685; U.S. Pat. No. 4,810,802; U.S. Pat. No. 4,579,949 and especially in U.S. Pat. No. 4,585,878.
The present invention is particularly adapted to the manufacture of daylight fluorescent pigments, that is to say pigments whose colored composition comprises one or more substances which are fluorescent in daylight and/or optionally one or more common colored substances. However, it is not limited to pigments of this type: by including in a resin according to the invention a compound which does not absorb in the visible but which fluoresces when it is excited by UV radiation, “transparent” pigments are obtained, which can be employed for particular applications such as invisible inks.
The pigments of the invention are suitable for a wide variety of applications, such as paper coating, textile printing, preparation of paints, plastisols, pastes, inks, markers, toners for non-impact printing or cosmetics.
The instant pigments are characterized by high heat stability and high light stability. Therefore they are particularly suitable for the mass coloration of polymers, particularly of those thermoplastic polymers in which the instant pigments can easily be dispersed. Suitable such polymers are e.g. polyesters, polyamides, PVC-polymers, ABS-polymers, styrenics, acrylics or polyurethanes. Particularly suitable polymers are polyolefins, especially polyethylene or polypropylene. It is particularly convenient to use the instant pigments for the preparation of fluorescent polymer, especially polyolefin masterbatches. The instant pigments, particularly those prepared with basic dyes or with solvent dyes, can also advantageously be used in printing inks, e.g. for textile printing.
The present invention also makes it possible to manufacture nonfluorescent colored pigments.
The concentration of the fluorescent substances in the mixture which is to be polycondensed may be adjusted so that the intensity of colour and/or fluorescence are/is maximised. After polycondensation and micronisation the local microconcentration of colored substances dissolved in the polymeric matrix remains constant whatever the subsequent overall dilution of the pigment powder, according to its use.
In the process according to the present invention the polycondensation of the reaction mixture is preferably performed in a temperature range lying between 80° C. and 300° C.
When said polycondensation resin is a polyester resin, a hybrid polyester resin, a polyamide resin, an epoxide resin or a polyurethane resin, the temperature is more preferably between 160° C. and 300° C., especially preferred between 180° C. and 270° C.
When said polycondensation resin is a melamine formaldehyde resin obtained by the polycondensation of components A, B, and C described above, the reaction is preferably performed in a temperature range lying between 100° C. and 250° C.
The products are preferably micronised to a particle size of between 0.5 and 20 μm. The particularly preferred mean particle size is between 1 and 7 μm. An “All In One Reactor”® of Draiswerke Mannheim, Germany has been found particularly suited as a reactor for implementing the process according to the present invention.
The characteristics and the advantages of the present invention will be understood better with the aid of the examples below. A range of shades extending from yellow to green and black can be produced by mixing e.g. the following colorants, listed in the Colour Index:
Solvent Yellow 43
Solvent Yellow 44 (C.I. No. 56200)
Solvent Yellow 85
Solvent Yellow 98
Solvent Yellow 114
Solvent Yellow 163
Solvent Yellow 185
Solvent Yellow 172
Solvent Orange 63
Solvent Red 196
Solvent Red 197
Solvent Blue 104
Solvent Green 7
Basic Yellow 13
Basic Yellow 19
Basic Yellow 40
Basic Yellow 45
Basic Red 1 (Rhodamine 6G, C.I. No. 45160)
Basic Violet 10 (Rhodamine B, C.I. No. 45170)
Basic Blue 7 (C.I. No. 42595)
Disperse Yellow 232
Solvent Blue 104
Solvent Orange 60
A fluorescent whitening agent may also be used alone or be added to colorants.
Manufacture of Colored Melamine Formaldehyde Condensation Product:
A mixture comprising, by weight, 3420 g of p-toluenesulfonamide, 1500 g of paraformal-dehyde, 720 g of melamine and 180 g Solvent Yellow 43 colorant is introduced at 20-25° C. in a 10000 ml “All In One Reactor”® (Drais Mannheim Germany).
Under stirring and nitrogen flow the mixture is heated to 170° C. within 60 minutes. The temperature is maintained at 170° C. for fifteen minutes. The mixture is cooled under stirring to 70° C. and kept at 70° C. The material starts solidifying at 110 to 115° C. The brittle friable material thus formed largely disintegrates into an almost semi-powdery material. The reaction mixture is again heated to 100° C. in 30 minutes and kept at 100° C. for 30 minutes for post curing and the elnnination of any residual formaldehyde. The mixture is cooled to 50° C.
The material is emptied into a polyethylene sack, tightly fitted to the outlet of the reactor. The resin mass can be pulverised by impact milling to a still finer powder for example as described in example 2.
Micronisation
The material recovered from the reactor as described in example 1 is fed into a mill of the air jet microniser type (Alpine 200 AFG, Augsburg).
The operating conditions are: dry air at 7 bars, room temperature, 25 kg/hour flow rate.
More than 99% of the micronised material is between 0.9 and 14 μm in particle size.
According to the processes of example 1 and example 2, a fluorescent pink pigment is prepared from a mixture having 70% by weight of para-toluenesulfonamide, 18% by weight of paraformaldehyde, 9% by weight of melamine (dyed by 1.5% by weight of Basic Red 1 and 1.5% by weight of Basic Violet 10, the amount of colorant being relative to the total mixture).
A fluorescent pink pigment composition called masterbatch (cylindrical granulate forms with length: 5 mm-diameter: 2 mm) is obtained by including 35 g of pink fluorescent pigment of example 3 in 65 g of a polyvinyl chloride mixture composed of 55% of polyvinyl chloride, 31% of dioctyl phthalate and 2% of an organo-tin stabilizer, and passing said mixture through an extruder at 125° C. The strands of the colored masterbatch are cooled and cut by state-of-the art processes to provide the desired granulates.
Manufacture of Colored Polyester Resin:
A mixture comprising, by weight, 2740 g of phthalic anhydride, 1225 g of pentaerythritol and 40 g of Rhodamine B is introduced at 20-25° C. in a 10000 ml “All In One Reactor”® of (Drais Mannheim Germany). Under stirring and nitrogen flow the mixture is heated to 240° C. within 120 minutes. The temperature is maintained at 240° C. for fifteen minutes. The mixture is cooled to 50° C. and kept at 50° C. The brittle friable material thus formed largely disintegrates into an almost semi-powdery material. The material is emptied into a polyethylene sack, tightly fitted to the outlet of the reactor.
Micronisation
The material recovered from the reactor is fed into a mill of the air jet microniser type. The operating conditions are: dry air at 7 bars, room temperature, 20 kg/hour flow rate. The average particle size of the pigments obtained depends on the flow rate and ranges from 1 to 15 μm for more than 99% of the micronised material.
Manufacture of Colored Polyamide Pigment and its Micronisation:
According to the process of examples 5 and 6, a fluorescent yellow pigment is prepared from a mixture having 35.3% by weight of isophorone diamine, 34.5% by weight of isophthalic acid, 25.3% by weight of benzoic acid, 3.3% by weight of zinc oxide and 1.6% by weight of Solvent Yellow 98 (C.I. No. 56238).
Preparation of a Masterbatch:
A fluorescent pink pigment composition called masterbatch (cylindrical granulate forms with length: 5 mm-diameter: 2 mm) is obtained by including 30 parts of pink fluorescent polyester pigment of example 5 and micronised as described in example 6 in 70 parts of a polyethylene mixture composed of 64 parts of low density polyethylene, 5 parts of polyethylene wax AC 540.RTM. Allied Chemical Co.) and 1 part of zinc stearate, and passing said mixture through an extruder at 155° C. The filaments obtained are cooled to room temperature and granulated by state-of-the-art processes.
Preparation of a Masterbatch:
A fluorescent yellow pigment composition called masterbatch is obtained as described in example 8 above by using 30 parts of the yellow fluorescent polyamide pigment prepared in example 7 and micronised as described in example 6.
Manufacture of Polyamide based Pigment and its Micronisation:
According to the process of Examples 5 and 6 a fluorescent pink pigment is prepared from a mixture having 14.9% by weight of benzoic acid, 41.5% by weight of isophorone diamine, 40.5% by weight of isophthalic acid and 3.1% by weight of Rhodamine B (C.I. No. 45170).
According to the process of Examples 5 and 6 a fluorescent yellow pigment is prepared from a mixture having 10.5% by weight of benzoic acid, 43.7% by weight of isophorone diamine, 42.7% by weight of isophthalic acid and 3.1% by weight of C.I. Basic Yellow 40.
According to the process of examples 5 and 6 a fluorescent pink pigment is prepared from a mixture having 29.2% by weight of ethylene glycol, 69.8% by weight of phthalic anhydride and 1% by weight of Rhodamine B.
According to the process of examples 6 and 7 a blue pigment is prepared from a mixture having 14.9% by weight of benzoic acid, 41.5% by weight of isophorone diamine, 40.5% by weight of isophthalic acid and 3.1% by weight of Fliso Blue 630.RTM, (BASF AG).
Application in PVC Masstone
The preparation of a 0.1% colored PVC sheet is performed as follows: 100 parts of clear PVC are mixed with 0.1 part of pigment obtained according to Example 1 for 2 minutes. The mixture is passed between two rollers for 5 minutes, the front roller being heated at 130° C. and the rear roller being heated at 135° C. Then the sheet is pressed under a pressure of 25 tones between two chromium-plated steel plates heated at 165° C., for 5 minutes. The pressed sheet is colored with a red shade.
Application in PVC White Reduction
The preparation of a 0.1% colored PVC sheet with white is performed as follows: 100 parts of PVC-white (containing 5% TiO) are mixed with 0.1 part of pigment for 2 minutes. The mixture is passed between two rollers for 8 minutes, the front roller being heated at 160° C. and the rear roller being heated at 165° C. Then the sheet is pressed under a pressure of 25 tones between two chromium-plated steel plates heated at 160° C., for 5 minutes.
Application in Coatings Masstone
The preparation of the alkydmelamine resin coating is performed as follows: 3.6 g of pigment, 26.4 g of clear alkydmelamine paint (35%) and 85 g of glass beads are stirred in a Skandex stirrer for 30 minutes. 30 g of this preparation are mixed with 60 g of clear alkydmelamine paint (55.8%). The dispersion is sprayed on a cardboard sheet, air-dried for 15 minutes and baked at 140° C. in an oven for 30 minutes.
Application in Coatings White Reduction
The preparation of the alkydmelamine resin coating is performed as follows: 3.6 g of pigment, 26.4 g of clear alkydmelamine paint (35%) and 85 g of glass beads are stirred in a Skandex stirrer for 30 minutes. 7.5 g of this preparation are mixed with 20 g of alkydmelamine white paint (containing 30% TiO). The dispersion is sprayed on a cardboard sheet, air-dried for 15 minutes and baked at 140° C. in an oven for 30 minutes.
Application in Coatings for Paper
25 parts of blue pigment prepared in example 13, 25 parts of carbital 95, 25 parts of water, 25 parts of carbital 95, 25 parts of latex BASF SD 215.RTM are mixed together. The composition can be used for coating paper.
Application for Printing Inks
A fluorescent pink ink is prepared from a mixture having 100 parts of binder (Ecocryl.RTM. 0254, W. SIPPO Co., Millers Saint Paul, France), 20 parts of a fixer (fixer 99HD.RTM., W. SIPPO Co.), 10 parts of emulsifier (ATEPRINT E9183.RTM., Dr. Th. BÖHME, Germany), 820 parts of water and 20 parts of the pink pigment obtained in example 8. The fluorescent ink is used for application by the screen process (or any similar process) on cotton fabric, which is then heated (dry heat) for 3 minutes at 150° C.
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/IB03/01029 | 3/20/2003 | WO | 9/7/2005 |
