Method of producing toner for developing electrostatic images

Patent metadata

Field	Value
Publication number	US-9971266-B2
Application number	US-201715440573-A
Country	US
Kind code	B2
Filing date	Feb 23, 2017
Priority date	Mar 2, 2016
Publication date	May 15, 2018
Grant date	May 15, 2018

Abstract

A method of producing a toner for developing electrostatic images includes Steps I to III is provided. The toner includes a toner matrix particle having a core-shell structure. The toner matrix particle includes a core particle including an amorphous resin A and a crystalline material, and a shell including an amorphous resin B. The shell includes a phase of the amorphous resin B that is not fused with the core particle at the interface. The amorphous resin A differs from the amorphous resin B.

First claim

What is claimed is:

1. A method of producing a toner for developing electrostatic images, the toner comprising a toner matrix particle having a core-shell structure, wherein
the toner matrix particle comprising a core particle comprising an amorphous resin A and a crystalline material, and a shell comprising an amorphous resin B,
the shell comprising a phase of the amorphous resin B that is not fused with the core particle at the interface, and
the amorphous resin A differing from the amorphous resin B, the method comprising the steps of:
Step I) dispersing at least the amorphous resin A and the crystalline material in an aqueous medium to prepare a dispersion, and adjusting a temperature of the dispersion to be equal to or higher than (a glass transition temperature (T g-a ) of the amorphous resin A+10)° C. and equal to or lower than (a melting point (T m-c ) of the crystalline material+10)° C., to prepare a core particle dispersion through coagulation and coalescence of at least the amorphous resin A and the crystalline material;
Step II) cooling the core particle dispersion prepared in Step I to a temperature equal to or lower than the glass transition temperature (T g-a ) of the amorphous resin A; and
Step III) adjusting a temperature of the core particle dispersion to be equal to or higher than (the glass transition temperature (T g-a ) of the amorphous resin A+5)° C. and equal to or lower than (a glass transition temperature (T g-b ) of the amorphous resin B+3)° C. after Step II, and then adding a dispersion of the amorphous resin B to the core particle dispersion,
wherein Expressions 1 and 2 are satisfied in Step III:
pH b ≤pH a , and  Expression 1:

2≤ pH b ≤5  Expression 2:

where pH a represents the pH of the core particle dispersion at 25° C., and pH b represents the pH of the dispersion of the amorphous resin B at 25° C.

2. The method according to claim 1 , wherein the core particle dispersion cooled in Step II contains a core particle having a shape factor SF-2 of 105 to 140.

3. The method according to claim 1 , wherein the amorphous resin B added in Step III is a particle having a volume median particle size of 30 to 300 rm.

4. The method according to claim 1 , wherein the amorphous resin A is a styrene-acrylic resin, and the amorphous resin B is a polyester resin.

5. The method according to claim 1 , wherein the amorphous resin A is a polyester resin, and the amorphous resin B is a styrene-acrylic resin.

6. The method according to claim 4 , wherein the polyester resin is an amorphous polyester resin chemically bonded to a styrene-acrylic resin.

7. The method according to claim 5 , wherein the polyester resin is an amorphous polyester resin chemically bonded to a styrene-acrylic resin.

8. The method according to claim 6 , wherein the amorphous polyester resin chemically bonded to the styrene-acrylic resin has a styrene-acrylic content of 5 to 30 mass %.

9. The method according to claim 7 , wherein the amorphous polyester resin chemically bonded to the styrene-acrylic resin has a styrene-acrylic content of 5 to 30 mass %.

10. The method according to claim 1 , wherein the amorphous resin A has a glass transition temperature T g-a of 35 to 50° C.

11. The method according to claim 1 , wherein the amorphous resin B has a glass transition temperature T g-b of 53 to 63° C.

12. The method according to claim 1 , wherein the crystalline material comprises a crystalline resin or a release agent, if the crystalline material is the releasing agent then the releasing agent is one selected from the group consisting of a hydrocarbon wax and an ester wax, and the crystalline material has a melting point (T m-c ) equal to or higher than (a glass transition temperature (T g-b ) of the amorphous resin B+3)° C.

13. The method according to claim 1 , wherein the ratio of the mass of the amorphous resin B added in Step III to the total mass of a binder resin is 5 to 35, and the binder resin comprises amorphous resin A and amorphous resin B.

Assignees

• Konica Minolta Inc

Inventors

• Tonegawa Naoya
• Kayamori Takanari
• Matsubara Masaharu
• Sekiguchi Kouji
• Iioka Atsushi

Classifications

• G03G9/09328

  obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds · CPC title

• G03G9/09364

  obtained by reactions only involving carbon-to-carbon unsaturated bonds · CPC title

• G03G9/09321

  obtained by reactions only involving carbon-to-carbon unsaturated bonds · CPC title

• G03G9/09392 Primary

  Preparation thereof · CPC title

• G03G9/09371

  obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds · CPC title