Toner for a two-component type developer

BACKGROUND OF THE INVENTION
1. Field of the Invention
The present invention relates to toner for a two-component type developer used for electrophotography. More particularly, the present invention relates to toner, which does not include a charge control agent, suitably used in an electrophotographic image forming apparatus such as an electrostatic copying machine and a laser beam printer.
2. Description of the Related Art
A two-component type developer is used as one of the developers used for developing an electrostatic latent image on a photosensitive body in an electrophotographic image forming apparatus. The two-component type developer includes toner comprising a binder resin and a coloring agent such as carbon black, and magnetic carrier such as iron powder and ferrite particles.
An electrostatic latent image is developed by the following steps: the developer forms a magnetic brush shape on a developing roller by a magnetic field thereof and is carried out to the photosensitive body. In this step, the toner is charged by friction with the carrier so as to have a desired charge and polarity of charge. Then, the developer is contacted with the photosensitive body by the developing roller, resulting in attaching the toner onto the electrostatic latent image formed thereon. Generally, the toner includes a charge control agent which controls and stabilizes the charge of the toner so as to attach a constant amount of the toner on the electrostatic latent image and provide a good developed image for a long period of time. Negatively charged toner includes a negative charge control agent such as a dye of a metal complex including a metal ion such as chrome(III) (for example, an azo compound-chrome(III) complex), and an oxycarboxylic acid-metal complex (for example, a salicylic acid-metal complex) (Japanese Laid-Open Patent Publication No. 3-67268). Positively charged toner includes a positive charge control agent such as an oil soluble dye including nigrosine and an amine type charge control agent (Japanese Laid-Open Patent Publication No. 56-106249).
Many metal complexes, including a heavy metal ion such as a chrome ion, are used as a conventional charge control agent. They are carefully selected, in terms of environmental safety, so that only those having passed various toxicity tests and safety tests alone are used. Therefore, although they would be safe in themselves or when included in toner, it is more preferable to refrain from using the metal complexes including a heavy metal as the charge control agent. In addition, the charge control agent is expensive as compared with the other materials for toner such as a binder resin and a coloring agent, for example, carbon black. Therefore, although the charge control agent has a content of merely several %, this results in increasing the price of the resultant toner. Accordingly, it is desired to develop toner having no charge control agent of a metal complex.
Furthermore, when conventional toner is used for a long period of time, the toner components tend to attach on a surface of the carrier particle. The attached components are called a spent. The spent makes the carrier charge with the same polarity as the toner, resulting in the disadvantages that the toner can be scattered and transfer efficiency of toner image is decreased.
SUMMARY OF THE INVENTION
The toner for a two-component type developer of this invention, which overcomes the above-discussed and numerous other disadvantages and deficiencies of the prior art, includes toner particles comprising a binder resin and magnetic powder dispersed in said binder resin, wherein said binder resin comprises a composition including at least one of the following:
(1) a polymer having an anionic group and a wax grafted portion; and
(2) a mixture of a polymer having an anionic group and a polymer having a wax grafted portion, and said magnetic powder is contained in said toner particles in an amount of 0.1 to 5 parts by weight per 100 parts by weight of said binder resin.
In a preferred embodiment, at least one of the polymers contained in the binder resin is a styrene-acrylic polymer, comprising portions having alkyl groups having 12 or more carbon atoms as side chains and having the following chemical properties:
(a) a peak of molecular weight distribution of said styrene-acrylic polymer being in the range between 4,000 and 30,000;
(b) a weight-average molecular weight of said styrene-acrylic polymer being in the range between 70,000 and 200,000; and
(c) an acid value of said styrene-acrylic polymer being in the range between 4 and 20.
In a preferred embodiment, an extract obtained by extracting the toner with methanol has substantially no absorption peak in the range of 280 to 350 nm, and has substantially zero absorbance in the range of 400 to 700 nm.
In a preferred embodiment, the magnetic powder is contained in an amount of 0.5 to 3 parts by weight per 100 parts by weight of the binder resin.
In a preferred embodiment, the toner particles have a volume-based average particle diameter of 5 through 15 .mu.m, and spacer particles with a volume-based average particle diameter of 0.05 through 1.0 .mu.m are attached onto surfaces of the toner particles.
In a preferred embodiment, the binder resin comprises a styrene-acrylic polymer having an anionic group, a portion having an alkyl group having 12 or more carbon atoms as side chains and a wax grafted portion.
Thus, the invention described herein makes possible the advantages of (1) providing toner with excellent chargeability including no charge control agent at all; (2) providing toner which realizes a copied image with a high quality due to little scattering in a development apparatus; and (3) providing toner in which a spent is not caused even when used for a long period of time, and hence, by which an excellent image quality can be maintained and transfer efficiency of toner image can be stabilized.
These and other advantages of the present invention will become apparent to those skilled in the art upon reading and understanding the following detailed description with reference to the accompanying figures.

BRIEF DESCRIPTION OF THE DRAWINGS
FIG. 1 is a graph showing absorbance of a methanol extracted solution of toner according to the present invention in the range of 200 to 700 nm;
FIG. 2 is a graph showing absorbance of a methanol extracted solution of toner having a dye of an azo compound-chrome complex as a charge control agent in the range of 200 to 700 nm;
FIG. 3 is a graph showing absorbance of a methanol extracted solution of toner having a salicylic acid-metal complex as the charge control agent in the range of 200 to 700 nm;
FIG. 4 is a graph showing absorbance of a methanol extracted solution of carrier in a two-component magnetic developer used for a long time in which toner has a dye of an azo compound-chrome complex as the charge control agent and chargeability of carrier is unstabilized by a spent in the range of 200 to 700 nm;
FIG. 5 is a graph showing a relationship between shaking time and a spent ratio obtained with regard to two kinds of two-component magnetic developer, one comprising toner having a charge control agent and magnetic carrier and another comprising toner having no charge control agent and magnetic carrier;
FIG. 6 is a graph showing a relationship between shaking time and quantity of charge of toner obtained with regard to two kinds of two-component magnetic developer, one comprising toner having a charge control agent and magnetic carrier and another comprising the toner having no charge control agent and magnetic carrier;
FIG. 7 is a graph showing a relationship between an amount of spent of carrier and content of a charge control agent in a toner particle;
FIG. 8 is a graph showing a relationship between shaking time and amount of spent obtained in the case where each component contained in a toner particle and magnetic carrier are individually mixed and shaken;
FIG. 9 illustrates a mechanism of charge failure caused by a spent in a conventional two-component magnetic developer; and
FIG. 10 is a schematic diagram of an original used in a copying performance test for observing a white dot in a black solid portion.

DESCRIPTION OF THE PREFERRED EMBODIMENTS
Toner for a two-component type developer according to the present invention has no charge control agent, such as a dye of an azo compound-metal complex and an oxycarboxylic acid-metal complex, at all. Therefore, a spent caused by a charge control agent, which will be described in detail below, scarcely occurs in the present toner, resulting in realizing a high quality copied image for a long period of time. Since the toner of the present invention has no charge control agent, it is impossible to detect any charge control agent, i.e., a dye type compound, from the toner by any chemical or physical method. For example, such a compound cannot be detected in the present toner by any chemical reaction. Alternatively, absorption peaks owing to such a compound cannot be detected in an organic solvent extracted solution of the present toner. For example, when the present toner is extracted with an organic solvent such as methanol, the extracted solution has substantially no absorption peak in the range of 280 to 350 nm, and has substantially zero absorbance in the range of 400 to 700 nm. Herein, "to have substantially no absorption peak" means, in an extracted solution obtained by extracting 0.1 g of the present toner with 50 ml of methanol, absorption peaks are not detected at all, or if detected, values of the absorbance peaks are 0.05 or less. Similarly, "to have substantially zero absorbance" means that values of the absorbance of the extracted solution obtained by extracting 0.1 g of the present toner with 50 ml of methanol are 0.05 or less.
In the present toner, instability of charge of toner due to a lack of a charge control agent is compensated for as follows: First, a polymer having an anionic group is used as a binder resin of a toner particle; and secondly, magnetic powder is contained in the toner particle at a predetermined proportion. In the present toner, in order to further enhance the function of the toner, a polymer having a portion where wax is grafted (hereinafter referred to as a wax grafted portion) is used as the binder resin. Therefore, the wax is well dispersed and prevented from attaching onto the surfaces of the carrier particles to cause the spent, thereby elongating the life time of the carrier. Furthermore, spacer particles having a desired particle diameter are attached on the surfaces of the toner particles, if necessary, thereby increasing the transfer efficiency of the toner.
The above-mentioned characteristics of the present toner will be described in detail.
FIG. 1 shows an UV-visible spectrum of a methanol extracted solution of the present toner in the range of 200 to 700 nm. As is shown in this spectrum, the extracted solution has no peak, which is otherwise formed because of a charge control agent. Specifically, the solution has substantially no absorption peak in the range of 280 to 350 nm, and the absorbance in the range of 400 to 700 nm is substantially zero. To the contrary, in an absorbance curve of a methanol extracted solution of toner having a dye of an azo compound-chrome complex as a charge control agent shown in FIG. 2, absorption peaks are found in the range of 400 to 700 nm, in particular, 550 to 570 nm. Furthermore, in the UV-visible spectrum of a methanol extracted solution of toner having a salicylic acid-metal complex as a charge control agent shown in FIG. 3, an absorption peak is found in the range of 280 to 350 nm.
It is because the charge control agent is present on the surfaces of the toner particles at a rather high concentration that the methanol extracted solution of the toner having the charge control agent has absorption peaks due to the charge control agent.
A carrier included in a developer which has insufficient chargeability owing to occurrence of a spent is extracted with methanol, and then the UV-visible spectrum of the extracted solution is measured to find absorption peaks in the range of 400 to 700 nm derived from a charge control agent. For example, the developer comprising the toner having a dye of an azo compound-chrome complex, whose UV-visible spectrum is shown in FIG. 2, was used for a long period of time to cause a spent therein. Then, UV-visible spectrum of a methanol extracted solution of the carrier in this developer was measured to give the spectrum shown in FIG. 4. As is shown in FIG. 4, absorption peaks are found at the same position as the spectrum in FIG. 2. It is conventionally understood that a spent is caused because a binder resin in the toner is attached to the surface of a carrier particle to form a resin film. The comparison between the absorbance curves in FIGS. 2 and 4, however, reveals that one of the major causes of a spent is the transfer of the charge control agent from the toner particles to the carrier particles.
The present inventors conducted the following experiments in order to find out more about the relationship between a charge control agent and a spent: First, toner comprising toner particles containing 1.5 wt % of the dye of the azo compound-chrome complex was mixed with a carrier to obtain a developer. The toner and the carrier was shaken for a predetermined period of time. FIG. 5 shows a relationship between the shaking time and amount of an attachment on the surfaces of the carrier particles. In FIG. 5, the amount of attachment is indicated as a spent ratio, that is, a percentage based on a total weight of the carrier particles bearing the attachment. Furthermore, FIG. 6 shows the relationship between the shaking time and the amount of charge of the toner. The same procedure was repeated with regard to a developer comprising toner having no charge control agent and carrier. The experimental results of this developer are also shown in FIGS. 5 and 6, wherein the results obtained by the developer including the toner having the charge control agent are plotted with black circles, and those by the developer including the toner having no charge control agent are plotted with white circles. It is apparent from FIGS. 5 and 6 that a larger amount of attachment is formed on the carrier particles as the spent and the charge amount of the toner has a greater decrease in the developer including the toner particle having the charge control agent than in the developer including the toner particle having no charge control agent.
Next, the weight of toner components attached on the surfaces of the carrier particles as the spent was measured with time. The results are shown in a graph of FIG. 7, wherein the abscissa indicates a measured amount of the spent and the ordinate indicates the content of the charge control agent in the toner particle. The broken line in FIG. 7 indicates the amount of the charge control agent calculated in assuming that the toner components attached as the spent are identical to the components in the toner particles. FIG. 7 reveals that a large amount of the charge control agent is deposited to be attached on the surfaces of the carrier particles at the initial stage. In FIG. 7, as amount of the spent increases, the measured values approximate the calculated values. This is because they are experimental results obtained in a close system having no supply of fresh toner. Therefore, when toner is exchanged as in a copying machine, the difference between the measured values and the calculated values would be much larger.
Furthermore, the present inventors measured the weight of the attachment on the surfaces of the carrier particles resulting from mixing the carrier with each of the toner components, that is, a charge control agent, a binder resin, carbon black as a coloring agent and wax, so as to find out the relationships between the respective toner components and the spent. The results are shown in FIG. 8 as a variation with time in the amount of the attachment (i.e., amount of the spent), wherein the results obtained from the mixture with the charge control agent is plotted with white circles, those from the carbon black with black circles, those from the binder resin with squares, and those from the wax with triangles. It is apparent from FIG. 8 that the charge control agent causes the largest amount of attachment due to the spent.
Based on the above-mentioned facts, the charge failure caused by the spent in a conventional two-component magnetic developer is explained as follows referring to FIG. 9. In the initial stage of the usage of a developer, a carrier particle 1 is positively charged and a toner particle 2 is negatively charged as is shown in an upper portion of FIG. 9. In this case, the toner particle works as a negative toner particle 21. When this developer is continued to be used, a component including the charge control agent as a main component in the toner particle is attached on the surface of the carrier particle 1. Attachment 201, which is the spent, is negatively charged. The negatively charged attachment 201 leads to the formation of a toner particle having positive charge, that is, a reversely charged toner particle 22. The reversely charged toner particle 22 is formed on the surface of the carrier particle 1 as is shown in a lower portion of FIG. 9, resulting in scattering of the toner and decreasing the transfer efficiency of the toner.
As described above, preferably, the toner does not have a charge control agent not only because the agent can include a heavy metal but also because the agent is the main cause of the spent, scatter of the toner and of a decrease in the transfer efficiency of the toner. Accordingly, the present toner has no charge control agent at all.
The instability of charge of the toner due to the lack of the charge control agent, in particular, the insufficiency in charge amount of the toner is compensated by using a binder resin having an anionic group as mentioned above. The insufficiency in charge amount of the toner particles can be supplemented because the binder resin has a negative charge in itself owing to the anionic group included therein. Since the anionic group is bonded to the main chain of the binder resin, it would never move onto the surface of the carrier particle as the charge control agent does, and hence it never causes the spent. On the contrary, charge around the surface of the toner particle caused by the anionic group of the binder resin is not so large that the electrostatic attraction between the toner particle and the carrier particle owing to the Coulomb force is insufficient when they are conveyed as a magnetic brush for development. Therefore, in a rapid copying operation, the toner cannot be sufficiently prevented from scattering because of insufficient coupling with the carrier particles. The scattered toner stains the inner wall of the copying machine, and can cause so-called a fog on a copied image.
In order to overcome such disadvantages, the present toner includes magnetic powder at a predetermined proportion, that is, 0.1 to 5 parts by weight on the basis of 100 parts by weight of the binder resin. The insufficiency in the charge amount of the toner particles can be thus compensated for. The magnetic powder contained in the toner particle causes magnetic attraction between the toner particle and the carrier particle. This magnetic attraction between the toner particle and the carrier particle together with electrostatic attraction prevents the toner from scattering. Moreover, since the number of the toner particles to be attached onto an electrostatic latent image is increased as the charge amount of one toner particle is smaller, apparent development sensitivity is increased.
The content of the magnetic powder in the toner particles is in the range of 0.1 to 5 parts by weight per 100 parts by weight of the binder resin as described above. When the content is less than 0.1 percent by weight, the charge amount of the toner particle is insufficient, resulting in insufficient coupling with the carrier particle and causing toner scattering. In this case, a fog can be disadvantageously formed on a copied image. Furthermore, the density of the copied image is low because of the insufficient charge amount. When the contents exceeds 5 percent by weight, the magnetic attraction between the carrier particle and the toner particle becomes so strong that the toner is not sufficiently attached onto an electrostatic latent image, resulting in decreasing the density of the copied image.
Several attempts have been made to improve the resolution of a copied image and the like by including (inclusively adding) magnetic powder as a toner component. For example, Japanese Laid-Open Patent Publication No. 56-106249 discloses a toner particle including 10 wt % of ferrite, and Japanese Laid-Open Patent Publication No. 59-162563 discloses a toner particle including 5 through 35 wt % of a magnetic fine particle. In either case, however, the content of the magnetic powder is excessive, and hence, the density of the copied image is low. Japanese Laid-Open Patent Publication No. 3-67268 discloses toner to which 0.05 to 2 wt % of magnetic powder is externally added. In this case, since the magnetic powder is not included in the toner particle, the powder is likely to be ununiformly attached onto the surface of the toner particle, resulting in insufficient magnetic attraction between the toner particle and the carrier particle. Furthermore, in either of the above-mentioned toners, the spent can be disadvantageously caused because a charge control agent is contained therein.
In the present toner, a polymer having a wax grafted portion is used as the binder resin for the toner particles. By grafting the wax in the polymer, compatibility of the wax with the binder resin is increased and thus the wax is well dispersed in the toner particle. As a result, when the developer comprising the present toner and carrier is used for a long period of time, the wax is scarcely attached onto the surface of the carrier particles to form the spent and the offset phenomenon scarcely occurs.
When a transferred toner image is fixed with heat rollers, a release agent is generally included in the toner particle to prevent offset onto the transfer paper. Various waxes are used as the release agent. Because such waxes have different SP values (the solubility parameters) from conventional binder resins, the wax has a poor compatibility with binder resins when heated and kneaded together with the binder resin and the magnetic powder in the production process of the toner. Therefore, the wax cannot be sufficiently dispersed in the binder resin in the heating and kneading process. As a result, the wax is ununiformly present in the resultant toner particles in the shape of a comparatively large grain, and the grain of the wax is present also on the surface of the toner particle. Therefore, when such a toner particle is mixed with a carrier, the wax, that is, the release agent, tends to be attached onto the surfaces of the carrier particles, thereby causing the spent.
The binder resin used in the present toner has the aforementioned excellent performance. The performance can be further improved in the following case: The binder resin comprises a styrene-acrylic polymer; and has a component including an alkyl group containing 12 or more carbon atoms as the side chain. In such a case, the wax added in the production process of the toner can attain a further high dispersibility, resulting in a longer life of the developer.
According to the present invention, the weight-average molecular weight, the peak of the molecular weight and the acid value of the styrene-acrylic polymer are specified so as to further reduce the spent and to improve the fixability of the toner, the crushability of a material of the toner in the production process of the toner, and the charge stability at a high humidity.
In the present invention, spacer particles having a particle diameter of 0.05 through 1.0 .mu.m are attached preferably onto the surfaces of the toner particles in order to increase the transfer efficiency of the toner image. The spacer particles can work to enhance fluidity of the toner, and in addition, form a gap between the photosensitive body and the toner particles when the toner is attached onto the electrostatic latent image formed on the photosensitive body. Therefore, the toner can be transferred from the photosensitive body onto the transfer paper with ease even when the toner attains a large quantity of charge through a long copying operation, resulting in a high transfer efficiency of the toner. When the spacer particle is similar to the particle of the magnetic powder included in the toner particle, the magnetic attraction between the toner particle and the carrier particle can be further enhanced, thereby further preventing toner scattering and a fog.
A fine particle having a particle diameter of approximately 0.015 .mu.m is used to enhance fluidity of a conventional toner. Such a small particle cannot form a sufficient gap between the photosensitive body and the toner particles, and cannot work as the spacer particle for the aforementioned purposes.
Now, preferable resins to be used as the binder resin in the present toner will be described. Herein, a "lower alkyl group" indicates alkyl having 1 to 5 carbon atoms; a "side chain" in a monomer indicates a site which is to be a side chain of a (co)polymer produced from the monomer; and a "wax portion" indicates a portion derived from a wax of a polymer having a wax grafted portion.
(Binder resin)
The binder resin contained in the toner particles of the present toner comprises a composition including at least one of the following: (1) a polymer having an anionic group and a wax grafted portion; and (2) a mixture of a polymer having an anionic group and a polymer having a wax grafted portion.
The polymer of item (1) is obtained by polymerizing a monomer having an anionic group or a mixture including the monomer having an anionic group together with a wax. The polymer having an anionic group used in the mixture of item (2) is obtained by polymerizing a monomer having an anionic group or a mixture including the monomer having an anionic group, and the resultant resin can be a homopolymer or a copolymer. The polymer having a wax grafted portion used in the mixture of item (2) is obtained by polymerizing a monomer having no anionic group together with a wax.
The polymer having a wax grafted portion can be prepared as follows: Part of a monomer to be polymerized is mixed with wax, then the mixture is polymerized, and the rest of the monomer is polymerized again with the resultant polymer. Alternatively, part of or an entire monomer to be polymerized is polymerized, then wax is added thereto, and the mixture is further polymerized.
The binder resin used in the present toner preferably comprises the composition including the polymer of item (1). This polymer has a wax grafted portion, which is obtained by polymerizing a monomer having an anionic group and another monomer together with the wax.
Examples of the monomer having an anionic group include monomers having a carboxylic acid group, a sulfonic acid group or a phosphoric acid group, and a monomer having a carboxylic acid group is generally used. Examples of the monomer having a carboxylic acid group include ethylenically unsaturated carboxylic acids such as acrylic acid, methacrylic acid, crotonic acid, maleic acid and fumaric acid; monomers that can form a carboxylic acid group such as maleic anhydride; and lower alkyl halfester of dicarboxylic acid such as maleic acid and fumaric acid. Examples of the monomer having a sulfonic acid group include styrene sulfonic acid and 2-acrylamido-2-methylpropane sulfonic acid. Examples of the monomer having a phosphoric acid group include 2-phosphonopropylmethacrylate, 2-phosphonooxypropylmethacrylate, 2-phosphonoethylmethacrylate, 2-phosphonooxy ethylmethacrylate, 3-chloro-2-phosphono propylmethacrylate 3-chloro-2-phosphonooxy propylmethacrylate.
Such a monomer having an anionic group can be a free acid, a salt of an alkaline metal such as sodium and potassium, a salt of an alkaline earth metal such as calcium and magnesium, and a salt such as zinc.
The monomer having no anionic group used to prepare the binder resin is selected so that the resultant binder resin has a sufficient fixability and chargeability required of toner, and is one or a combination of an ethylenically unsaturated monomer. Examples of such a monomer include ethylenically unsaturated carboxylic acid ester, monovinyl arene, vinyl ester, vinyl ether, diolefin and monoolefin.
The ethylenically unsaturated carboxylic acid esters are represented by the following Formula (I): ##STR1## wherein R.sup.1 is a hydrogen atom or a lower alkyl group; and R.sup.2 is a hydrocarbon group having 11 or less carbon atoms or a hydroxyalkyl group having 11 or less carbon atoms.
Examples of such ethylenically unsaturated carboxylic acid esters include methyl acrylate, ethyl acrylate, butyl acrylate, 2-ethylhexyl acrylate, cyclohexyl acrylate, phenyl acrylate, methyl methacrylate, hexyl methacrylate, 2-ethylhexyl methacrylate, .beta.-hydroxyethylacrylate, .tau.-hydroxypropylacrylate, .delta.-hydroxybutylacrylate and .beta.-hydroxyethylmethacrylate.
The monovinyl arenes are represented by the following Formula (II): ##STR2## wherein R.sup.3 is a hydrogen atom, a lower alkyl group or a halogen atom; R.sup.4 is a hydrogen atom, a lower alkyl group, a halogen atom, an alkoxy group, an amino group or a nitro group; and .phi. is a phenylene group.
Examples of such monovinyl arene include styrene, .alpha.-methylstyrene, vinyltoluene, .alpha.-chlorostyrene, o-chlorostyrene, m-chlorostyrene, p-chlorostyrene and p-ethylstyrene.
The vinyl esters are represented by the following Formula (III): ##STR3## wherein R.sup.5 is a hydrogen atom or a lower alkyl group.
Examples of such vinyl esters include vinyl formate, vinyl acetate and vinyl propionate.
The vinyl ethers are represented by the following Formula (IV):
CH.sub.2 .dbd.CH--O--R.sup.6 (IV)
wherein R.sup.6 is a monovalent hydrocarbon group having 11 or less carbon atoms.
Examples of such vinyl ethers include vinyl methyl ether, vinyl ethyl ether, vinyl n-butyl ether, vinyl phenyl ether and vinyl cyclohexyl ether.
The diolefins are represented by the following Formula (V): ##STR4## wherein R.sup.7, R.sup.8 and R.sup.9 are independently a hydrogen atom, a lower alkyl group or a halogen atom.
Examples of such diolefins include butadiene, isoprene and chloroprene.
The monoolefins are represented by the following Formula (VI): ##STR5## wherein R.sup.10 and R.sup.11 are independently a hydrogen atom or a lower alkyl group.
Examples of such monoolefins include ethylene, propylene, isobutylene, 1-butene, 1-pentene and 4-methyl-1-pentene.
The wax to be added at the time of the polymerization of the monomer having an anionic group and/or another monomer having no anionic group is selected from release agents usually used in toners. Specifically, the wax herein can be any of various kinds of natural wax and olefin resins. Examples of the olefin resins include polypropylene, polyethylene and propylene-ethylene copolymers, among which polypropylene is preferred.
The wax portion in the polymer having a wax grafted portion serves for preventing the offset of the toner in the thermal fixing process similarly to a release agent generally used in toner.
The content of the wax is determined so that the wax portion is in the range of 0.01 to 6 parts by weight, preferably 0.1 to 4 parts by weight per 100 parts by weight of the entire binder resin. When the content of the wax portion is less than 0.01 parts by weight, the offset of the resultant toner sometimes insufficiently prevented. When it exceeds 6 parts by weight, the charge failure can be caused, thereby decreasing the durability of the resultant toner.
The molecular weight of the wax is not herein specified, but the average molecular weight thereof is preferably in the range of 2,000 to 16,000, and more preferably 3,000 to 6,000.
Specific examples of the polymer having an anionic group, that is, a (co)polymer obtained through the polymerization of the aforementioned monomers, include styrene-acrylic acid copolymers, styrene-maleic acid copolymers and ionomer resins. Furthermore, a polyester resin having an anionic group can be also used. Also, the polymer having a wax grafted portion obtained by adding the wax at the time of the polymerization of the aforementioned monomers can contain, as a portion excluding the wax portion, a partial structure corresponding to a styrene-acrylic acid copolymer, a styrene-maleic acid copolymer or an ionomer resin.
The polymer having an anionic group and a wax grafted portion preferably includes the anionic group at a proportion for attaining an acid value of 4 through 20, and preferably 5 through 15, when the anionic group is present as a free acid. Also, the mixture including the polymer having an anionic group and the polymer having a wax grafted portion preferably has an acid value in the aforementioned range. When part or the entire anionic group is neutralized, the anionic group is preferably contained at such a proportion that the acid value would be in the aforementioned range in assuming that it is present as a free acid. When the acid value, i.e., the concentration of the anionic group, of the polymer or the composition is below the aforementioned range, the chargeability of the resultant toner is insufficient. When it exceeds the range, the resultant toner disadvantageously has a hygroscopic property. A preferable binder resin is a copolymer comprising the monomer having an anionic group, the wax, at least one of the ethylenically unsaturated carboxylic acid esters represented by Formula (I) as an indispensable components, and any of the monomers represented by Formulae (II) through (VI) as an optional component to be used if necessary. One or a combination of two or more of the aforementioned monomers is used for preparing the binder resin.
As described above, a composition comprising at least one of the following is used as the binder resin used in the present invention: (1) a polymer having an anionic group and a wax grafted portion; and (2) a mixture of a polymer having an anionic group and a polymer having a wax grafted portion. The composition can further comprise a polymer having neither an anionic group nor a wax grafted portion. In this case, the content of the anionic group in the entire composition is preferably within the aforementioned range.
Each of the polymers used in the binder resin is preferably a styrene-acrylic polymer that can include a component including an alkyl group containing 12 or more carbon atoms as the side chain thereof and can satisfy the following conditions:
(a) The peak in the molecular weight of the polymer is in the range between 4,000 and 30,000;
(b) the weight-average molecular weight of the polymer is in the range between 70,000 and 200,000; and
(c) the acid value of the polymer is in the range between 4 and 20.
Such a styrene-acrylic polymer can be obtained by copolymerizing a monovinyl arene and an acrylic monomer or a mixture with other monomers.
The component including an alkyl group containing 12 or more carbon atoms as the side chain is formed by polymerizing a monomer having an alkyl group containing 12 or more carbon atoms at the side chain or a mixture with other monomers. The resultant polymer can be a homopolymer or a copolymer. Such a styrene-acrylic polymer having an anionic group and/or a wax grafted portion and comprising a component including 12 or more carbon atoms as the side chain can be prepared as follows. For example, part of a monomer having an anionic group and/or a monomer including an alkyl group containing 12 or more carbon atoms at the side chain are polymerized together with wax. The resultant reactant is further polymerized with monomers such as a monomer having an anionic group and/or a monomer including an alkyl group containing 12 or more carbon atoms at the side chain. Alternatively, a reactant obtained by polymerizing part of a monomer or an entire monomer to be used is further polymerized together with wax. Alternatively, a styrene-acrylic polymer having an anionic group and/or a wax grafted portion is mixed with a polymer comprising a component including an alkyl group containing 12 or more carbon atoms as the side chain.
Any of the polymers obtained by the aforementioned methods can be a random copolymer, a block copolymer or a graft copolymer.
Examples of the monomer having an alkyl group containing 12 or more carbon atoms at the side chain include an ethylenically unsaturated carboxylic acid such as acrylate and methacrylate having an alkyl group containing 12 or more carbon atoms bonded through an ester bond; a vinyl ester having an alkyl group containing 12 or more carbon atoms bonded through an ester bond; a vinyl ether having an alkyl group containing 12 or more carbon atoms bonded through an ether bond; a 1-alkene having 14 or more carbon atoms; a monovinyl arene having at least one substituent including an alkyl group containing 12 or more carbon atoms; and a 1,3-alkadiene having at least one alkyl group containing 12 or more carbon atoms. One or a combination of two or more can be used. The alkyl group containing 12 or more carbon atoms herein comprises a linear hydrocarbon group, an acyclic branched hydrocarbon group and a cyclic hydrocarbon group.
The ethylenically unsaturated carboxylic acid ester having an alkyl group containing 12 or more carbon atoms as the side chain is represented by the following Formula (VII): ##STR6## wherein R.sup.12 is a hydrogen atom or a lower alkyl group; and R.sup.13 is an alkyl group containing 12 or more carbon atoms.
Examples of such an ester include lauryl acrylate, tridecyl acrylate, stearyl acrylate, docosyl acrylate, dicyclohexylmethyl acrylate, dicyclohexylpropyl acrylate, cyclododecyl acrylate, cycloundecanemethyl acrylate, lauryl methacrylate, tridecyl methacrylate, stearyl methacrylate, docosyl methacrylate, dicyclohexylmethyl methacrylate, dicyclohexylpropyl methacrylate, cyclododecyl methacrylate and cycloundecanemethyl methacrylate.
The vinyl ester having an alkyl group containing 12 or more carbon atoms as the side chain is represented by the following Formula (VIII): ##STR7## wherein R.sup.14 is an alkyl group containing 12 or more carbon atoms.
Examples of such a vinyl ester include vinyl laurate, vinyl tridecanoate, vinyl stearate, vinyl docosanoate, vinyl triacontanoate, vinyl pentylcyclohexanoate and vinyl dicyclohexylacetate.
The vinyl ether having an alkyl group containing 12 or more carbon atoms as the side chain is represented by the following Formula (IX):
CH.sub.2 .dbd.CH--O--R.sup.15 (IX)
wherein R.sup.15 is an alkyl group containing 12 or more carbon atoms.
Examples of such a vinyl ether include vinyl lauryl ether, vinyl stearyl ether, vinyl docosyl ether and vinyl cyclododecyl ether.
The 1-alkene having 14 or more carbon atoms is represented by the following Formula (X): ##STR8## wherein R.sup.16 and R.sup.17 are independently a hydrogen atom or an alkyl group containing 12 or more carbon atoms.
Examples of such an alkene include 1-tetradecene and 1-eicocene.
The monovinyl arene having at least one substituent having an alkyl group containing 12 or more carbon atoms is represented by the following Formula (XI): ##STR9## wherein R.sup.18 is a hydrogen atom, a lower alkyl group, an alkyl group containing 12 or more carbon atoms or a halogen atom; R.sup.19 is an alkoxy group, an amino group, a nitro group or an alkyl group containing 12 or more carbon atoms; and .phi. is a phenylene group. The phenylene group can include another substituent such as a lower alkyl group, a halogen atom, an alkoxy group, an amino group, a nitro group and an alkyl group containing 12 or more carbon atoms. The alkyl group containing 12 or more carbon atoms can be linked to the phenylene group through an ester bond, a (thio)ether bond or an amido bond.
Examples of such a monovinyl arene include m-laulylstyrene, p-laulylstyrene, m-stearylstyrene, p-stearylstyrene, .alpha.-methyl-3-stearylstyrene, m-stearoxystyrene, p-stearoxystyrene, stearyl 4-vinylbenzoate and 4-stearoylaminostyrene.
The 1,3-alkadiene having an alkyl group containing 12 or more carbon atoms is represented by the following Formula (XII): ##STR10## wherein R.sup.20, R.sup.21 and R.sup.22 are independently a hydrogen atom, a lower alkyl group, an alkyl group containing 12 or more carbon atoms or a halogen atom, respectively.
Examples of such a dialkene include 1,3-hexadecadiene, 1,3-docosadiene and 2-methyl-1,3-docosadiene.
The other monomers that are polymerized with the monomer having an alkyl group containing 12 or more carbon atoms as the side chain, if necessary, is selected so that the resultant polymer can attain a sufficient fixability and chargeability required of toner, and is prepared from one or a combination of two or more ethylenically unsaturated monomers. Examples of such a monomer include the ethylenically unsaturated carboxylic acid ester, the monovinyl arene, the vinyl ester, the vinyl ether, the 1-alkene and the 1,3-alkadiene represented by Formulae (I) through (VI), respectively.
The proportion of the monomer having an alkyl group containing 12 or more carbon atoms as the side chain to be copolymerized is in the range of 0.1 to 20 parts by weight, more preferably 0.5 to 10 parts by weight, and most preferably 1 to 5 parts by weight on the basis of the total weight of all the used monomers. When the content is below this range, the binder resin cannot have a sufficient compatibility with the wax, and when the content exceeds the range, the Tg of the binder resin is lowered and thus storage stability of the toner is lowered.
Examples of the polymer having an anionic group and an alkyl group containing 12 or more carbon atoms as the side chain, which is obtained through polymerization of any of the aforementioned monomers, include styrene-methacrylic acid (or acrylic acid)-stearyl methacrylate (or stearyl acrylate) copolymers, styrene-methacrylate (or acrylate)-stearyl methacrylate (or stearyl acrylate)-methacrylic acid (or acrylic acid) copolymers, and styrene-stearyl (meth)acrylate-maleic acid copolymers. Furthermore, a polyester resin having an anionic group can be also used. Similarly, the monomer having a wax grafted portion, which is obtained by polymerizing any of the aforementioned monomers together with wax, has a partial structure, as a portion except for the wax portion, corresponding to a styrene-methacrylic acid (or acrylic acid)-stearyl methacrylate (or stearyl acrylate) copolymer, a styrene-methacrylate (or acrylate)-stearyl methacrylate (or stearyl acrylate)-methacrylic acid (or acrylic acid) copolymer, and a styrene-stearyl methacrylate (or stearyl acrylate)-maleic acid copolymer.
The styrene-acrylic polymer used in the present invention includes the anionic group preferably at a proportion for attaining an acid value of 4 through 20, preferably 5 through 15, when the anionic group is present as a free acid. When part or the entire anionic group is neutralized, the anionic group is preferably contained at a proportion for attaining an acid value in the aforementioned range in assuming that it is present as a free acid. When the acid value of the polymer, i.e., the concentration of the anionic group, is below the aforementioned range, the chargeability of the resultant toner is insufficient. When it exceeds the range, the resultant toner disadvantageously has a hygroscopic property.
The peak in the molecular weight of the styrene-acrylic polymer is in the range between 4,000 and 30,000, and preferably 6,000 and 20,000. When the peak is below 4,000, the spent of the resultant toner cannot be sufficiently decreased, and when it exceeds 30,000, the crushability of the material of the toner is lowered in the producing process of the toner.
The weight-average molecular weight of the styrene-acrylic polymer is in the range between 70,000 and 200,000, and preferably 80,000 and 150,000. When it is smaller than 70,000, the resultant toner particles are likely to be broken with ease. When it exceeds 200,000, the crushability of the material of toner is lowered.
A preferable binder resin can be obtained by copolymerizing styrene, acrylic acid or methacrylic acid, and at least one of the ethylenically unsaturated carboxylic acid esters represented by Formula (VII), and simultaneously adding wax thereto, and any of the monomers represented by Formulae (I) through (VI) can be further copolymerized as an optional component, if necessary. Furthermore, another monomer can be copolymerized together, if necessary. The binder resin can be prepared from one or a combination of two or more of the aforementioned monomers. The resin can further include a polymer including a component having neither an anionic group nor an alkyl group containing 12 or more carbon atoms and having no wax grafted portion. In this case, the proportions of the anionic group, the component including an alkyl group containing 12 or more carbon atoms and the wax portion in the resultant resin are preferably in the aforementioned ranges, respectively.
(Production method for the preferred binder resin)
A preferable styrene-acrylic polymer having an anionic group and a wax grafted portion used for the present toner can be produced as follows.
Styrene, acrylic acid or methacrylic acid, at least one of the ethylenically unsaturated carboxylic acid esters represented by Formula (VII), a polymerization initiator and wax are mixed in a solvent such as toluene and xylene, and the mixture is stirred. The mixture is then charged in a reactor, and grafting of the wax and polymerization are effected at a temperature of 60.degree. through 250.degree. C. for 3 through 10 hours while stirring vigorously. The resultant solution is distilled and dried to give a polymer with low molecular weight. Next, the thus obtained polymer, styrene, acrylic acid or methacrylic acid, at least one of the ethylenically unsaturated carboxylic acid esters represented by Formula (VII) and a polymerization initiator are mixed in a solvent, and the mixture is stirred. The resultant mixture is then charged in a reactor and subjected to polymerization at a temperature of 60.degree. through 200.degree. C. for 5 through 24 hours while stirring vigorously. The resultant solution is distilled and dried to give the desired polymer.
(Magnetic powder)
The magnetic powder contained in (inclusively added to) the toner particles can be any magnetic powder used in a conventional one-component type developer. Examples of the material for the magnetic powder include triiron tetroxide (Fe.sub.3 O.sub.4), maghemite (.tau.-Fe.sub.2 O.sub.3), zinc iron oxide (ZnFe.sub.2 O.sub.4), yttrium iron oxide (Y.sub.3 Fe.sub.5 O.sub.12), cadmium iron oxide (CdFe.sub.2 O.sub.4), gadolinium iron oxide (Gd.sub.3 Fe.sub.5 O.sub.12), copper iron oxide (CuFe.sub.2 O.sub.4), lead iron oxide (PbFe.sub.12 O.sub.19), nickel iron oxide (NiFe.sub.2 O.sub.4), neodyum iron oxide (NdFeO.sub.3), barium iron oxide (BaFe.sub.12 O.sub.19), magnesium iron oxide (MgFe.sub.2 O.sub.4), manganese iron oxide (MnFe.sub.2 O.sub.4), lanthanum iron oxide (LaFeO.sub.3), iron (Fe), cobalt (Co) and Nickel (Ni). Particularly preferable magnetic powder is made from triiron tetroxide (magnetite) in the shape of fine particles. The particle of preferable magnetite is in the shape of a regular octahedron with a particle diameter of 0.05 through 1.0 .mu.m. Such a magnetite particle can be subjected to a surface treatment with a silane coupling agent or a titanium coupling agent. The particle diameter of the magnetic powder contained in the toner particle is generally 1.0 .mu.m or smaller, and preferably 0.05 through 1.0 .mu.m.
The content of the magnetic powder in the toner particle is in the range of 0.1 to 5 parts by weight, more preferably 0.5 to 4 parts by weight, and most preferably 0.5 to 3 parts by weight per 100 parts by weight of the binder resin. When the content is too small, the toner can be scattered during the development and the transfer efficiency of the toner can be decreased as described above.
(Inner additives in the toner particles)
The toner particle contains, as described above, the binder resin and the magnetic powder as indispensable components, and can optionally include some inner additive generally used for a toner, if necessary.
Examples of such additives include a coloring agent and a release agent.
As the coloring agent, the following pigments can be used:
Black pigment:
carbon black, acetylene black, lampblack, aniline black;
Extender:
barite powder, barium carbonate, clay, silica, white carbon, talc, alumina white.
Such a pigment is contained in the toner particle in the range of 2 to 20 parts by weight, and preferably 5 to 15 parts by weight per 100 parts by weight of the binder resin.
As the release agent, various wax and olefin resins can be used as in a conventional toner.
(Preparation of the toner)
The toner particles in the present toner can be produced by any ordinary method for toner particles such as crushing and classification, fusing granulation, spray granulation and polymerization, and are generally produced by the crushing and classification method.
For example, the components for the toner particles are previously mixed in a mixer such as a Henschel mixer, kneaded with a kneader such as a biaxial extruder, and then cooled. The resultant is crushed and classified to give toner particles. The particle diameter of the toner particle is generally in the range of 5 to 15 .mu.m and preferably 7 to 12 .mu.m in the volume-base averaged particle diameter (a medium size measured with a Coulter counter).
It is possible to improve the fluidity of the toner by attaching, as an outer additive, a fluidity enhancer such as hydrophobic vapor depositioned silica particles onto the surfaces of the toner particles, if necessary. The primary particle diameter of the fluidity enhancer such as the silica particles is generally approximately 0.015 .mu.m, and such a fluidity enhancer is added to the toner in the range of 0.1 to 2.0 percent by weight on the basis of the weight of the entire toner, i.e., the total weight of the toner particles and the fluidity enhancer.
Furthermore, spacer particles having a larger particle diameter than that of the fluidity enhancer are preferably added in the present invention. As the spacer particles, any of organic and inorganic inactive particles with a particle diameter of 0.05 through 1.0 .mu.m, more preferably 0.07 through 0.5 .mu.m can be used. Examples of the material for such inactive particles include silica, alumina, titanium oxide, magnesium carbonate, an acrylic resin, a styrene resin and magnetic materials. The spacer particle can not only work as a fluidity enhancer but also increase the transfer efficiency as described above. As the spacer particle, the same type of magnetic powder as included in the toner particle, in particular, triiron tetroxide (magnetite) in the shape of fine particle is preferably used. The magnetic powder, when used as the spacer particles, effectively suppresses the scattering of the toner as described above. The content of the spacer particles is 10 percent or less, more preferably in the range of 0.1 to 10 percent, and most preferably 0.1 to 5 percent by weight on the basis of the total weight of the toner. When the spacer particles are excessively included in toner, the density of a copied image is insufficient. When the magnetic powder is used as the spacer particles, the total amount of the magnetic powder together with that contained in the toner particles is preferably 10 parts by weight or less per 100 parts by weight of the binder resin. When it is excessively included, the density of a copied image can be decreased.
When the fluidity enhancer and the spacer particles are added to the toner particles, the following production method is preferred. The fluidity enhancer and the spacer particles are first sufficiently mixed with each other, and then the obtained mixture is added to the toner particles, and then is sufficiently unbound. Thus, the spacer particles can be attached onto the surfaces of the toner particles. To "be attached" herein means both to be held in contact with the surface of the toner particle and to be partly embedded in the toner particle. In this manner, the toner of the present invention is produced.
(Carrier particle)
In the present invention, generally used magnetite or ferrite can be used as a carrier for the two-component type developer. In such a compound, the electrical resistance is little varied with time or by the change of the environment, and hence, it can provide the resultant developer with a stable chargeability. Furthermore, such a compound is formed into a soft spicated shape in the developing apparatus when a magnetic field is applied. This prevents the turbulence of a toner image formed on the photosensitive body, thereby suppressing the formation of a white stripe in a copied image.
In the present invention, the carrier is charged preferably by allowing a resin having a cationic group to be contained in a coating layer of the carrier particle. Therefore, when this carrier is combined with toner including no charge control agent, the chargeability of the toner is remarkably improved, thereby stabilizing the chargeability of the toner. Furthermore, since the present toner does not include a charge control agent as the conventional developer does, the resultant developer can attain a longer life time by effectively preventing the spent from occurring on the carrier particles.
The carrier particle in the carrier used in the present invention is more preferably formed from a particle having a two-layered structure including a core particle and a coating layer over the core particle. The core particle comprises a magnetic material represented by the following Formula (A):
MOFe.sub.2 O.sub.3 (A)
wherein M is at least one metal selected from the group consisting of Cu, Zn, Fe, Ba, Ni, Mg, Mn, Al and Co.
The compound represented by Formula (A) is magnetite (wherein M is Fe) or ferrite (wherein M is one of the metals other than Fe), and ferrite, wherein M is Cu, Zn, Mn, Ni or Mg, is preferably used. Change of the electrical resistance of such magnetite and ferrite is little for a long time, and the magnetite and ferrite can be formed into a soft spicated shape in the developing apparatus when a magnetic field is applied. The core particle comprising such a magnetic material has a particle diameter between 30 and 200 .mu.m, and preferably between 50 and 150 .mu.m. The core particles are obtained by granulating the fine particles of the magnetic material by spray granulation and the like, and then heating the resultant particles. The core particle has a volume specific resistivity between 10.sup.5 and 10.sup.9 .OMEGA..cndot.cm, and preferably between 10.sup.6 and 10.sup.8 .OMEGA..cndot.cm. The saturation magnetization of the core particle is in the range of 30 to 70 emu/g, and preferably between 45 and 65 emu/g.
The resin having a cationic group included in the resin composition, which forms the coating layer of the carrier particle, can be a thermoplastic resin and a thermosetting resin, and is preferably a thermosetting resin or a mixture of a thermosetting resin and a thermoplastic resin in terms of the heat resistance and the durability. Examples of the cationic group include a basic nitrogen containing group such as primary, secondary and tertiary amino groups, a quaternary ammonium group, an amido group, an imino group, an imido group, a hydrazino group, a guanidino group and an amidino group, among which an amino group and a quaternary ammonium group are particularly preferred.
Examples of the thermoplastic resin having a cationic group include thermoplastic acrylic resins, thermoplastic styrene-acrylic resins, polyester resins, polyamide resins and olefin copolymer, each of which includes a cationic group. Examples of the thermosetting resin include modified and unmodified silicone resins, thermosetting acrylic resins, thermosetting styrene-acrylic resins, phenol resins, urethane resins, thermosetting polyester resins, epoxy resins and amino resins, each of which includes a cationic group. Such a resin including a cationic group is obtained by polymerizing a monomer having a cationic group or a mixture containing the monomer having a cationic group. Alternatively, such a resin is obtained by linking a compound having a cationic group with a resin having no cationic group. Furthermore, alternatively, a monomer having a cationic group and/or another monomer are (co)polymerized by using a polymerization initiator having a cationic group, thereby introducing the cationic group into the resultant resin.
When a resin prepared from alkoxysilane or alkoxytitanium is used, it is possible to produce the resin having a cationic group by allowing a silane coupling agent having a cationic polar group to react with the resin during or after the preparation of the resin. Examples of the silane coupling agent include N-(2-aminoethyl)-3-aminopropyltrimethoxysilane, N-(2-aminoethyl)-3-aminopropylmethyldimethoxysilane, .tau.-aminopropyltriethoxysilane and N-phenyl-3-aminopropyltrimethoxysilane. This type of silane coupling agent can be linked onto the surface of the core particle via a hydroxyl group generally present on the surface of the core particle. Therefore, such a silane coupling agent can form the coating layer by itself. Examples of the polymerization initiator having a cationic group include amidine type compound, e.g., azobis compounds.
The resin having a cationic group for forming the coating layer is used singly or together with any other of the aforementioned resins, or together with another resin having no cationic group.
The content of the cationic group in the resin having a cationic group is generally in the range of 0.1 to 2000 mmole, and preferably of 0.5 to 1,500 mmole per 100 g of the resin. When the resin having a cationic group is used with a resin having no cationic group, the cationic group is preferably contained in the entire resins forming the coating layer of the carrier particle at a proportion in the aforementioned range.
The resin composition forming the coating layer of the carrier particle includes at least one of the above-mentioned resins having a cationic group, together with another resin having no cationic group, if necessary. Examples of a mixture of the resin having a cationic group and the resin having no cationic polar group include a mixture of an alkylated melamine resin and a styrene-acrylic copolymer, and a mixture of an alkylated melamine resin and an acryl-modified silicone resin. The resin composition can further comprise an additive such as silica, alumina, carbon black, fatty acid metal salt, a silane coupling agent and silicone oil. These additives work for regulating physical properties of the coating layer.
(Preparation of the carrier)
The resin composition including a cationic group is applied to the surface of the core particle by a known method to form the coating layer. For example, the core particle is coated with a solution or a dispersion of the resin composition and dried, thereby forming the coating layer. Alternatively, when a thermosetting resin or a reactive resin oligomer is used, the core particle is coated with an uncured resin, or a solution or a dispersion of the oligomer, and then heated to cure the resin. The coating layer can be formed by any of the generally used methods such as immersion, spray, a fluidized bed method, a moving bed method and a tumbling layer method. As a solvent used to dissolve or disperse the resin composition, any of the ordinary organic solvents can be used. Examples of the solvent include aromatic hydrocarbons such as toluene and xylene; ketones such as acetone, methyl ethyl ketone, methyl isobutyl ketone and cyclohexanone; cyclic ethers such as tetrahydrofuran and dioxane; alcohols such as ethanol, propanol and butanol; cellosolves such as ethyl cellosolve and butyl cellosolve; esters such as ethyl acetate and butyl acetate; and amide type solvents such as dimethylformamide and dimethylacetoamide. The solvent is appropriately selected in accordance with the chemical properties of the resin such as the solubility.
The particle diameter of the thus obtained carrier particle is in the range of 30 to 200 .mu.m, and preferably of 50 to 150 .mu.m. The weight ratio of the coating layer on the carrier particle is in the range of 0.001 to 2.5 parts by weight, and preferably of 0.005 to 2.0 parts by weight per 100 parts by weight of the core particle. The obtained carrier particle has a volume specific resistivity in the range between 10.sup.5 and 10.sup.13 .OMEGA..cndot.cm, and preferably between 10.sup.7 and 10.sup.12 .OMEGA..cndot.cm, and a saturation magnetization in the range between 30 and 70 emu/g, and preferably between 45 and 65 emu/g.
(Preparation of a developer)
A two-component type developer is prepared by mixing the above-mentioned toner and carrier. The mixing ratio of the carrier and the toner is generally 98:2 through 90:10, and preferably 97:3 through 94:6, by weight.
A copying operation is conducted using the present toner by a general electrophotographic method. Specifically, for example, a photoconductive layer on a photosensitive body is uniformly charged, and an image is exposed to form an electrostatic latent image thereon. Then, a magnetic brush made of the two-component magnetic developer is allowed to come in contact with the photosensitive body, thereby developing the electrostatic latent image with ease into a toner image. The thus obtained toner image is transferred onto transfer paper to form a transfer image, which is then applied with heat and pressure by a heat roller to fix the image thereon.
EXAMPLES
The present invention will now be described by way of examples. It is noted that the invention is not limited to the following examples.
(Production Example 1)
A polymer having an anionic group and a wax grafted portion was prepared as follows.
A mixture (100 parts by weight) including styrene, butyl methacrylate and acrylic acid at a weight ratio of 80:15:5; polypropylene as wax (0.6 parts by weight; average molecular weight of 4,000); and a polymerization initiator were dissolved in a solvent while stirring. The resultant mixture was charged in a reactor, and polymerization was effected while stirring vigorously at 150.degree. C. for 5 hours to give a low molecular weight polymer. The polymerization for preparing the low molecular weight polymer is generally conducted at a temperature between 60.degree. and 250.degree. C. for 3 through 10 hours. Then, the solvent was removed from the reaction mixture, and the obtained residue was dried to give a low molecular weight polymer having a wax grafted portion.
The obtained polymer (100 parts by weight), polypropylene as wax (5.4 parts by weight; average molecular weight of 4,000), a mixture (100 parts by weight) of styrene, butyl methacrylate and acrylic acid at a weight ratio of 70:25:5, and a polymerization initiator were dissolved in a soluble solvent with stirring. The resultant mixture was charged in a reactor, and polymerization was effected with stirring vigorously at 80.degree. C. for 15 hours to give a high molecular-weight polymer. The polymerization reaction for preparing the high molecular weight polymer is generally conducted at a temperature between 50.degree. and 200.degree. C. for 5 through 24 hours. The solvent was removed from the obtained reaction mixture, and the residue was dried to give a binder resin comprising the polymer having a wax grafted portion with a low molecular weight part and a high molecular weight part.
(Production Example 2)
A styrene-acrylic polymer having an anionic group, an alkyl group containing 12 or more carbon atoms as the side chain and a wax grafted portion was prepared as follows.
A mixture (100 parts by weight) of styrene, butyl methacrylate and acrylic acid at a weight ratio of 80:17:3, polypropylene as wax (0.4 parts by weight; an average molecular weight of 4,000), and a polymerization initiator were dissolved in solvent with stirring. The resultant mixture was charged in a reactor, and polymerization was effected while stirring vigorously at 150.degree. C. for 5 hours to give a low molecular weight polymer. The polymerization for preparing the low molecular weight polymer is generally conducted at a temperature between 60.degree. and 250.degree. C. for 3 through 10 hours. The solvent was removed from the obtained reaction mixture, and the residue was dried to give a low molecular weight polymer having a wax grafted portion.
The thus obtained polymer (100 parts by weight), polypropylene as wax (3.6 parts by weight; an average molecular weight of 4,000), a mixture (100 parts by weight) of styrene, stearyl methacrylate, butyl methacrylate, and acrylic acid at a weight ratio of 66:4:20:10, and a polymerization initiator were dissolved in solvent with stirring. The resultant mixture was charged in a reactor, and polymerization was effected while stirring vigorously at 80.degree. C. for 15 hours to give a high molecular weight polymer. The polymerization for preparing the high molecular weight polymer is generally conducted at a temperature between 50.degree. and 200.degree. C. for 5 through 24 hours. The solvent was removed from the resultant reaction mixture, and the residue was dried to give a binder resin comprising the polymer having a wax grafted portion with a low molecular weight part and a high molecular weight part. The resin had a molecular weight peak of 10,000 in the low molecular weight part, and had a weight-average molecular weight of 100,000 and an acid value of 10.
(Example 1.1)
______________________________________Components of Partstoner by weight______________________________________Binder resin.sup.a) 103Coloring agent: Carbon black 10Magnetic powder: Magnetite 2______________________________________ .sup.a) The binder resin used in this example was that prepared in Production Example 1 (cornprising 3 parts by weight of the wax portion an 100 parts by weight of the other portion excluding the wax portion).
The components listed above were kneaded with a biaxial extruder, and the resultant was crushed with a jet mill and classified with a pneumatic classifier to give toner particles with an average particle diameter of 10.0 .mu.m.
To the obtained toner particles were added 0.3 parts by weight of hydrophobic silica fine particle with an average particle diameter of 0.015 .mu.m as a fluidity enhancer and 0.6 parts by weight of alumina particles with an average particle diameter of 0.3 .mu.m as spacer particles based on the 100 parts by weight of the toner particle, respectively. The resultant mixture was mixed with a Henschel mixer for 2 minutes to give toner.
<Preparation of a developer>
The thus obtained toner was homogeneously mixed with ferrite carrier having an average particle diameter of 100 .mu.m to give a two-component type developer with the toner concentration of 3.5 wt %.
(Comparative Example 1)
The same procedure was repeated as in Production Example 1 except that the polypropylene as the wax was not added in the polymerization process, thereby preparing a polymer having no wax grafted portion, as a binder resin. Then, in the same manner as in Example 1.1, toner was prepared except that wax (polypropylene; average molecular weight of 4,000) was added as a release agent to the polymer at a proportion of 3 parts by weight based on 100 parts by weight of the binder resin.
(Example 2.1)
The same procedure was repeated as in Example 1.1 to give the same type of toner.
<Preparation of a carrier>
Spherical ferrite particles with an average particle diameter of 100 .mu.m were used as magnetic core particles. To 1,000 parts by weight of the ferrite particles was added a coating agent having components as listed in Table 1, and the obtained mixture was stirred with a thermal stirrer. The solvent was removed from the resultant mixture and the resultant was subjected to a heat treatment at 200.degree. C. for 1 hour to give carrier particles having a coating layer.
<Preparation of a developer>
The thus obtained toner and carrier were uniformly mixed to give a two-component type developer having a toner concentration of 3.5 wt %.
(Example 2.2)
The same procedure was repeated as in Example 2.1 by using a coating agent having components as listed in Table 1 to give another type of developer.
(Example 2.3)
The same procedure was repeated as in Example 2.1 by using a coating agent having components as listed in Table 1 to give still another type of developer.
(Example 2.4)
The same procedure was repeated as in Example 2.1 except that a coating layer was not formed to give still another type of developer.
TABLE 1______________________________________Coating Agents of Examples 2.1-2.4.com- Exampleponent Example 2.1 Example 2.2 Example 2.3 2.4______________________________________Resin 1 Acryl-modified Metylphenyl Styrene-acrylic none silicone silicone polymerparts by 2.5 4.8 3.5weightResin 2 Metylated .gamma.-aminopropyl- Methylated none melamine triethoxysilane melamineparts by 2.5 0.2 1.5weightSolvent: 200 200 200 nonetoluene(parts byweight)______________________________________
(Example 3.1)
______________________________________Components of Partstoner by weight______________________________________Binder resin.sup.a) 102Polypropylene 1(average molecular weight of 4,000)Coloring agent: Carbon black 10Magnetic powder: Magnetite 2______________________________________ .sup.a) The binder resin used in this example was that prepared in Production Example 2 (comprising 2 parts by weight of the wax portion and 100 parts by weight of the other portion excluding the wax portion).
The components listed above were kneaded with a biaxial extruder, and the resultant was crushed with a jet mill and classified with a pneumatic classifier to give toner particles with an average particle diameter of 10.0 .mu.m.
To the obtained toner particles were added 0.3 parts by weight of hydrophobic silica fine particles with an average particle diameter of 0.015 .mu.m as a fluidity enhancer and 0.6 parts by weight of alumina particles with average particle diameter of 0.3 .mu.m as spacer particles based on 100 parts by weight of the toner particles, respectively. The resultant mixture was mixed with a Henschel mixer for 2 minutes to give toner.
<Preparation of a developer>
The thus obtained toner was uniformly mixed with a ferrite carrier having an average particle diameter of 100 .mu.m to give a two-component type developer having a toner concentration of 3.5 wt %.
(Comparative Example 3.1)
A binder resin used in this comparative example was a styrene-acrylic copolymer (a copolymer comprising styrene and acrylic acid at a weight ratio of 73:27) having an anionic group, but having neither a wax grafted portion nor an alkyl group containing 12 or more carbon atoms as the side chain. This binder resin had a molecular weight peak of 3,000 in the low molecular weight polymer, a weight-average molecular weight of 60,000 and an acid value of 2. By using this binder resin, toner was prepared in the same manner as in Example 3.1 except that wax (polypropylene; an average molecular weight of 4,000) was used as a release agent at a proportion of 3 parts by weight per 100 parts by weight of the binder resin.
<Preparation of a developer>
The thus obtained toner was uniformly mixed with a ferrite carrier with an average particle diameter of 100 .mu.m to give a two-component type developer having a toner concentration of 3.5 wt %.
(Comparative Example 3.2)
A binder resin used in this comparative example was a styrene-acrylic copolymer (a copolymer comprising styrene and acrylic acid at a weight ratio of 73:27) having an anionic group, but having neither a wax grafted portion nor an alkyl group containing 12 or more carbon atoms as the side chain. This binder resin had a molecular weight peak of 3,500 in the low molecular weight polymer, a weight-average molecular weight of 250,000 and an acid value of 25. By using this binder resin, toner was prepared in the same manner as in Example 3.1 except that wax (polypropylene; an average molecular weight of 4,000) was used as a release agent at a proportion of 3 parts by weight per 100 parts by weight of the binder resin.
<Preparation of a developer>
The thus obtained toner was homogeneously mixed with a ferrite carrier with an average particle diameter of 100 .mu.m to give a two-component type developer having a toner concentration of 3.5 wt %.
(Example 4.1)
The same procedure was repeated as in Example 3.1 to give the same type of toner.
<Preparation of a carrier>
Spherical ferrite particles with an average particle diameter of 100 .mu.m were used as magnetic core particles. To 1,000 parts by weight of the ferrite particles was added a coating agent having components as listed in Table 2, and the obtained mixture was stirred with a thermal stirrer. The solvent was removed from the resultant mixture by drying, and the resultant was subjected to a heat treatment at a temperature of 200.degree. C. for 1 hour to give carrier particles each having a coating layer.
<Preparation of a developer>
The thus obtained toner and carrier were homogeneously mixed to give a two-component type developer having a toner concentration of 3.5 wt %.
(Example 4.2)
The same procedure was repeated as in Example 4.1 by using a coating agent having components as listed in Table 2 to give another type of developer.
(Example 4.3)
The same procedure was repeated as in Example 4.1 by using a coating agent having components as listed in Table 2 to give still another type of developer.
(Example 4.4)
The same procedure was repeated as in Example 4.1 except that a coating layer was not formed to give still another type of developer.
TABLE 2______________________________________Coating Agents of Examples 4.1-4.4.com- Exampleponent Example 4.1 Example 4.2 Example 4.3 4.4______________________________________Resin 1 Acryl-modified Metylphenyl Styrene-acrylic none silicone silicone polymerparts by 2.5 4.8 3.5weightResin 2 Metylated .gamma.-aminopropyl- Methylated none melamine triethoxysilane melanineparts by 2.5 0.2 1.5weightSolvent: 200 200 200 nonetoluene(parts byweight)______________________________________
�Evaluation of the developers!
The developers obtained in the above described examples and comparative examples were evaluated with regard to the following items. An electric copying machine (manufactured by Mita Industrial Co., Ltd.; brand name: DC-4685) was modified so as to make evaluations easier, and the modified copying machine was used in the evaluation.
(a) Transfer efficiency:
The amount of toner in a toner hopper in the copying machine was measured at first, and a predetermined number of copies were made. Then, the amount of the toner left in the toner hopper was measured. From a difference between the amounts of the toner before and after the copying operation, a consumed amount of the toner was calculated. At the same time, the amount of the toner collected in a cleaning process during the copying operation was also measured as a collected amount. Based on these amounts, the transfer efficiency of the toner was calculated by using Equation (i) below. An original used in the copying operation bore characters with a black area ratio of 8%. This evaluation was conducted to perform various evaluation tests described in items (b) through (k). ##EQU1## (b) Image density (I.D.):
A copying operation was continued by using an original bearing characters with a black area ratio of 8% until the transfer efficiency became less than 70%. The density of a black portion in a copied image on every 5000 copies was measured by a reflection densitomer (manufactured by Tokyo Denshoku Co., Ltd.; TC-6D), and the average density of the black portion was taken as an image density (I.D.). An original used for sampling every 5000 copies had a black area ratio of 15% including a black solid portion. The results obtained from the developers of Example 1.1 and Comparative Example 1 are listed in Table 3, those of Examples 2.1 through 2.4 in Table 4, those of Example 3.1 and Comparative Examples 3.1 and 3.2 in Table 5 and those of Examples 4.1 through 4.4 in Table 6.
(c) Fog density (F.D.):
A copying operation was continued by using an original bearing characters with a black area ratio of 8% until the transfer efficiency became less than 70%. The density of a white portion in a copied image on every 5000 copies was measured by a reflection densitomer (manufactured by Tokyo Denshoku Co., Ltd.; TC-6D). A difference between the thus measured density and the density of the corresponding white portion in the original measured by the reflection densitomer was calculated, and the maximum difference was taken as a fog density (F.D.). An original used for sampling every 5000 copies had a black area ratio of 15% including a black solid portion. The results obtained from the developers of Example 1.1 and Comparative Example 1 are listed in Table 3, those of Examples 2.1 through 2.4 in Table 4, those of Example 3.1 and Comparative Examples 3.1 and 3.2 in Table 5 and those of Examples 4.1 through 4.4 in Table 6.
(d) Resolution:
A copying operation was conducted by using an original bearing characters with a black area ratio of 8%. When 50,000 copies were made (in the case where the transfer efficiency became less than 70% before making 50,000 copies, at that time), a normal chart original (an original bearing a plurality of patterns in each of which a predetermined number of parallel lines are drawn per 1 mm) was copied, and the obtained copied image was visually evaluated. The results obtained from the developers of Example 1.1 and Comparative Example 1 are listed in Table 3, those of Examples 2.1 through 2.4 in Table 4, those of Example 3.1 and Comparative Examples 3.1 and 3.2 in Table 5 and those of Examples 4.1 through 4.4 in Table 6.
(e) Charge amount:
A copying operation was continued by using an original bearing characters with a black area ratio of 8% until the transfer efficiency became less than 70%. During this copying operation, after making every 5,000 copies, the amount of charge of 200 mg of the developer was measured by a blowoff type powder charge amount measuring apparatus (manufactured by Toshiba Chemical Co., Ltd.), and the average of the amount of charge per 1 g of the toner was calculated based on the measured value. The results obtained from the developers of Example 1.1 and Comparative Example 1 are listed in Table 3, those of Examples 2.1 through 2.4 in Table 4, those of Example 3.1 and Comparative Examples 3.1 and 3.2 in Table 5 and those of Examples 4.1 through 4.4 in Table 6.
(f) Toner scattering:
A copying operation was continued by using an original bearing characters with a black area ratio of 8% until the transfer efficiency became less than 70%. Then, the toner scattering state in the copying machine was visually observed and evaluated. The results are listed in Table 5, wherein .smallcircle. indicates that the toner was not scattered; and X indicates that the toner was scattered.
(g) Durability:
After making every 10,000 copies, the transfer efficiency was calculated based on the consumed amount and the collected amount of the toner to find the number of copies that had been made before the transfer efficiency became less than 70%. The number was taken as an indicator for the durability of the developer. The results obtained from the developers of Example 1.1 and Comparative Example 1 are listed in Table 3, those of Examples 2.1 through 2.4 in Table 4, those of Example 3.1 and Comparative Examples 3.1 and 3.2 in Table 5 and those of Examples 4.1 through 4.4 in Table 6.
(h) Amount of attachment on the surface of the carrier particle as the spent:
A copying operation was conducted by using an original bearing characters with a black area ratio of 8%. After making 50,000 copies (in the case where the transfer efficiency became less than 70% before making 50,000 copies, at that time), the developer was tested as follows. The developer was placed on a screen of 400 mesh, and sucked from below with a blower, thereby separating the toner and the carrier. Five grams of the carrier remained on the screen and was charged in a beaker, to which toluene was added. Thus, the toner component attached onto the surfaces of the carrier particles as the spent was dissolved. Then, the toluene solution was discarded with the carrier attracted upon the bottom of the beaker with a magnet. This procedure was repeated several times until the resultant toluene solution became colorless. Then, the resultant carrier was heated with an oven to evaporate the toluene remaining thereto, and the weight of the obtained residue was measured. A difference between the weight of the carrier charged in the beaker at first (i.e., 5 g in this case) and the weight of the residue after evaporating the toluene was taken as the amount of the toner components attached onto the surfaces of the carrier particles as the spent (i.e., the spent amount). The spent amount is indicated as the weight in mg of the toner components attached to 1 g of the carrier. The results obtained from the developers of Example 1.1 and Comparative Example 1 are listed in Table 3, those of Examples 2.1 through 2.4 in Table 4, those of Example 3.1 and Comparative Examples 3.1 and 3.2 in Table 5 and those of Examples 4.1 through 4.4 in Table 6.
(i) Crushability:
A mixture obtained by kneading the respective components of the toner particles was supplied to a jet mill to be crushed at a predetermined pressure. At this point, a speed (g/min.) at which the mixture can be supplied to the jet mill was measured. The results are listed in Table 5, wherein .smallcircle. indicates the speed of 100 g/min. or more; and X indicates the speed of less than 100 g/min.
(j) Fixability:
Transfer paper bearing a toner image of an original bearing a black solid portion was allowed to pass through fixing rollers to fix the image, and an image density (A) of the thus obtained copied image was measured. A fixability measuring apparatus, which was produced by attaching a bleached cloth on the bottom of a counterbalance made of mild steel (with a diameter of 50 mm and a weight of 400 g) with an adhesive double coated tape, was allowed to slide upon the copied image between both the ends thereof five times by its own weight. Then, an image density (B) was measured. Based on the image densities (A) and (B), a fixing ratio was calculated by Equation (ii) below. The image density was measured with the reflection densitomer (manufactured by Tokyo Denshoku Co., Ltd.; TD-6D). ##EQU2##
The results are shown in Table 5, wherein .circleincircle. indicates a fixing ratio of 95% or more; .smallcircle. indicates a fixing ratio of 90% or more and less than 95%; .DELTA. indicates a fixing ratio of 80% or more and less than 90%; and X indicates a fixing ratio of less than 80%.
(k) High temperature offset property:
By using an original 3 with a size of 210 mm.times.297 mm bearing three black solid portions 31 each with a size of 50 mm.times.50 mm as is shown in FIG. 10, 500 copies were continuously made and the copied images were fixed with the heat rollers. The respective copied images were fed to the heat roller in the direction Pa as shown with a white arrow in FIG. 10. The offset phenomenon and the stain in a white portion on the 500th copied image were visually observed. The results are listed in Table 5, wherein .smallcircle. indicates that neither the offset phenomenon nor the stain was found; and X indicates that either the offset phenomenon or the stain was found.
TABLE 3______________________________________Toner component and Evaluation of Example 1.1 andComparative Example 1. Comparative Example 1.1 Example 1______________________________________Toner component (parts by weight)Binder resin*l 100 100;Wax grafred portion*.sup.2 present noneTotal wax 3 3Carbon black 10 10Magnetic powder 2 2Charge control agent none noneExternal additive 1 (silica; 0.015 .mu.m) 0.3 0.3External additive 2 (almina; 0.3 .mu.m) 0.6 0.6EvaluationI.D. 1.372 1.371F.D. 0.002 0.003Resolution 5 5Charge amount (.mu.C/g) -23.0 -22.2Spent amount (ag) 0.58 0.69Toner scattering .largecircle. .largecircle.Durability (copies) 100,000 60,000______________________________________ .sup.*.sup.1 When the binder resin has a wax grafted portion, the propotion in parts by weight of a portion excluding the wax grafted portion. .sup.*.sup.2 Whether or not a polymer having a wax grafted portion is present.
TABLE 4______________________________________Evaluation of Examples 2.1-2.4 Example 2.1 Example 2.2 Example 2.3 Example 2.4______________________________________I.D. 1.388 1.326 1.386 1.362F.D. 0.002 0.002 0.002 0.004Resolution 5 5 5 5Charge amount -23.1 -24.1 -24.2 -22.2(.mu.C/g)Toner .largecircle. .largecircle. .largecircle. .largecircle.scatteringDurability 140,000 140,000 140,000 70,000(copies)Spent amount 0.33 0.32 0.33 0.58(mg) at50,000 copies______________________________________
TABLE 5______________________________________Toner component and Evaluation of Example 3.1 and ComparativeExample 3.1 and 3.2. Comparative Comparative Example 3.1 Example 3.1 Example 3.2______________________________________Toner component (parts byweight)Binder resin*.sup.1 100 100 100;Peak molecular weight*.sup.2 10,000 3,000 35,000;Weight-average 100,000 60,000 250,000molecular weight (Mw);Acid value 10 2 25;Long-chain alkyl*.sup.3 present none none;Wax grafred portion*.sup.4 present none noneTotal wax 3 3 3Carbon black 10 10 10Magnetic powder 2 2 2Charge control agent none none noneExternal additive 1 0.3 0.3 0.3(silica; 0.015 .mu.m)External additive 2 0.6 0.6 0.6(almina: 0.3 .mu.m)EvaluationI.D. 1.378 1.362 1.359F.D. 0.002 0.004 0.003Resolution 5 5 5Charge amount (.mu.C/g) -23.7 -22 -23.1Spent amount (mg) 0.55 0.72*.sup.5 0.49Toner scattering .largecircle. .largecircle. .largecircle.Durability (copies) 120,000 30,000 110,000Crushablity .largecircle. .largecircle. .times.Fixability .largecircle. .largecircle. .times.High temperature offset .largecircle. .times. .largecircle.______________________________________ *.sup.1 When the binder resin has a wax grafted portion, the propotion in parts by weight of a portion excluding the wax grafted portion. *.sup.2 Peak of nolecular weight of a low molecular portion of the binder resin. *.sup.3 Alkyl group having 12 or more carbon atoms at the side chain. *.sup.4 Whether or not a polymer having a wax grafted portion is present. *.sup.5 Value at 30,000 copies.
TABLE 6______________________________________Evaluation of Examples 4.1-4.4 Example 4.1 Example 4.2 Example 4.3 Example 4.4______________________________________I.D. 1.380 1.313 1.377 1.361F.D. 0.002 0.002 0.002 0.004Resolution 5 5 5 5Charge amount -23.3 -25.2 -23.8 -22.3(.mu.C/g)Toner .largecircle. .largecircle. .largecircle. .largecircle.scatteringDurability 160,000 160,000 150,000 90,000(copies)Spent amount 0.28 0.27 0.30 0.50(mg) at50,000 copies______________________________________
�Review of the evaluation!
The developer produced in Example 1.1 comprising the toner having a wax grafted portion had a smaller spent amount and was superior in durability as compared with the developer produced in Comparative Example 1 comprising the toner having no wax grafted portion.
The developers produced in Examples 2.1 through 2.4 were excellently stable in fog density, resolution and charge amount. Furthermore, no toner scattering was observed when these developers were used. The developers produced in Examples 2.1 through 2.3 comprising the carrier particle having the coating layer had a lower fog density, a smaller spent amount and higher durability than the developer produced in Example 2.4 comprising the carrier particle having no coating layer.
The developer produced in Example 3.1 comprising the toner having a wax grafted portion and the component including an alkyl group containing 12 or more carbon atoms at the side chain was superior in durability, fixability, crushability and the high temperature offset property as compared with the developers produced in Comparative Examples 3.1 through 3.2 comprising the toner including none of such a portion and a component.
The developers produced in Examples 4.1 through 4.4 were excellently stable in resolution and the charge amount. Furthermore, no toner scattering was observed when they are used. The developers produced in Examples 4.1 through 4.3 comprising the carrier particle having the coating layer had a lower fog density, a smaller spent amount and a higher durability than the developer produced in Example 4.4 comprising the carrier particle having no coating layer.
Various other modifications will be apparent to and can be readily made by those skilled in the art without departing from the scope and spirit of this invention. Accordingly, it is not intended that the scope of the claims appended hereto be limited to the description as set forth herein, but rather that the claims be broadly construed.

Number	Date	Country	Kind
6-207412	Aug 1994	JPX
6-207444	Aug 1994	JPX

Number	Name	Date
5135833	Matsunaga et al.	Aug 1992
5364721	Asada et al.	Nov 1994
5384226	Kanakura et al.	Jan 1995
5500319	Funato et al.	Mar 1996

Number	Date	Country
0357042	Mar 1990	EPX
0407604	Jan 1991	EPX
56-106249	Aug 1981	JPX
59-162563	Sep 1984	JPX
60-4950	Jan 1985	JPX
60-222864	Nov 1985	JPX
367268	Mar 1991	JPX
91218582	Jun 1991	JPX

Toner for a two-component type developer

Information

Patent Number

Date Filed

Date Issued

Inventors

Original Assignees

Examiners

Agents

CPC

US Classifications

Field of Search

US

International Classifications

Abstract

Description

Claims

Priority Claims (2)

Parent Case Info

US Referenced Citations (4)

Foreign Referenced Citations (8)

Non-Patent Literature Citations (1)

Continuations (1)