IP Library › Granted Patent US 7,820,350
Granted Patent B2
US 7,820,350 · App. 11/687,372 · Granted Oct 26, 2010

Toner, developer, toner container, process cartridge, image forming apparatus, and image forming method

Assignee: Ricoh Company, Ltd.
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Quick Facts
Patent No.
US 7,820,350
App. No.
11/687,372
Granted
Oct 26, 2010
Kind
B2
Abstract

A toner containing a colorant, and a binder resin, wherein the toner is prepared by dissolving or dispersing a colorant, a precursor of the binder resin having a site capable of reacting with an active hydrogen group-containing compound, the active hydrogen group-containing compound, in an organic solvent, to prepare a toner constituent mixture liquid, dispersing or emulsifying the toner constituent mixture liquid, in an aqueous medium while subjecting the precursor to a reaction with the active hydrogen group-containing compound, to prepare a toner dispersion, and removing the organic solvent from the toner dispersion; the binder resin contains a modified polyester having an isocyanate-derived binding site; the Sn content in the toner is 800 ppm or less; the content of a metal which is non Sn and derived from a polyesterified catalyst is 10 ppm to 200 ppm; and the content of a metal which is non Sn and derived from an isocyanated catalyst is 10 ppm to 200 ppm.

Claims (62)

1. A toner, comprising:

a colorant; and

a binder resin;

wherein:

the toner is prepared by:

dissolving or dispersing at least the colorant, a precursor of the binder resin having a site capable of reacting with an active hydrogen group-containing compound and the active hydrogen group-containing compound in an organic solvent to prepare a toner constituent mixture liquid;

dispersing or emulsifying the toner constituent mixture liquid in an aqueous medium while subjecting the precursor to a reaction with the active hydrogen group-containing compound to prepare a toner dispersion; and

removing the organic solvent from the toner dispersion to prepare the toner;

the binder resin comprises at least a modified polyester;

the modified polyester is derived from the precursor which has an isocyanate-derived functional group;

an Sn content of the toner is 800 ppm or less;

a content of Ti derived from a polyesterified catalyst in the toner is 10 ppm to 200 ppm; and

a content of Bi derived from an isocyanated catalyst in the toner is 10 ppm to 200 ppm.

2. The toner according to claim 1 , wherein:

the Sn content is 0 ppm to 500 ppm;

the content of Ti derived from the polyesterified catalyst is 10 ppm to 200 ppm; and

the content of Bi derived from the isocyanated catalyst is 10 ppm to 200 ppm.

3. The toner according to claim 1 , wherein the binding site derived from the isocyanate group is at least one of a urea bond and a urethane bond.

4. The toner according to claim 1 , wherein:

the modified polyester comprises an isocyanate terminal modified polyester; and

the isocyanate terminal modified polyester is prepared by reacting an unmodified polyester with a diisocyanate compound in the presence of the isocyanated catalyst.

5. The toner according to claim 4 , wherein the unmodified polyester consists of uncrosslinkable components.

6. The toner according to claim 4 , wherein the isocyanate terminal modified polyester has a ratio (NCO/OH) of a number of OH groups of the unmodified polyester relative to a number of NCO groups of the diisocyanate compound of from 2.0 to 2.5.

7. The toner according to claim 1 , wherein the unmodified polyester is polymerized using the polyesterified catalyst.

8. The toner according to claim 1 , wherein the toner comprises a crosslinkable polyester.

9. The toner according to claim 8 , wherein the crosslinkable polyester is formed by a reaction between the modified polyester and the active hydrogen group-containing compound.

10. The toner according to claim 1 , wherein:

the toner comprises a binder resin which differs from the polymer having a site capable of reacting with at least the active hydrogen group-containing compound; and

the glass transition temperature of the binder resin is 30° C. to 50° C.

11. The toner according to claim 10 , wherein the binder resin has an acid value of 1 mg KOH/g to 30 mg KOH/g.

12. The toner according to claim 1 , wherein the toner has a glass transition temperature of 40° C. to 70° C.

13. The toner according to claim 1 , wherein:

a weight average particle diameter of the toner is 3 μm to 8 μm; and

a ratio of the weight average particle diameter of the toner to a number average particle diameter of the toner is 1.25 or less.

14. A process cartridge comprising:

a latent electrostatic image bearing member; and

a developing unit configured to develop a latent electrostatic image formed on the latent electrostatic image bearing member using a toner to form a visible image;

wherein:

the toner is prepared by:

dissolving or dispersing at least a colorant, a precursor of a binder resin having a site capable of reacting with an active hydrogen group-containing, compound and the active hydrogen group-containing compound in an organic solvent to prepare a toner constituent mixture liquid;

dispersing or emulsifying the toner constituent mixture liquid in an aqueous medium while subjecting the precursor to a reaction with the active hydrogen group-containing compound to prepare a toner dispersion; and

removing the organic solvent from the toner dispersion to prepare the toner;

the binder resin comprises at least a modified polyester;

the modified polyester is derived from the precursor which has an isocyanate-derived functional group;

an Sn content of the toner is 800 ppm or less;

a content of Ti derived from a polyesterified catalyst in the toner is 10 ppm to 200 ppm; and

a content of Bi derived from an isocyanated catalyst in the toner is 10 ppm to 200 ppm.

15. An image forming method comprising:

forming a latent electrostatic image on a latent electrostatic image bearing member;

developing the latent electrostatic image using a toner to form a visible image;

transferring the visible image onto a recording medium; and

fixing the image transferred to the recording medium;

wherein:

the toner is prepared by:

dissolving or dispersing at least a colorant, a precursor of the binder resin having a site capable of reacting with an active hydrogen group-containing and the active hydrogen group-containing compound in an organic solvent to prepare a toner constituent mixture liquid;

dispersing or emulsifying the toner constituent mixture liquid in an aqueous medium while subjecting the precursor to a reaction with the active hydrogen group-containing compound to prepare a toner dispersion; and

removing the organic solvent from the toner dispersion to prepare the toner;

the binder resin comprises at least a modified polyester;

the modified polyester is derived from the precursor which has an isocyanate-derived functional group;

an Sn content of the toner is 800 ppm or less;

a content of Ti derived from a polyesterified catalyst in the toner is 10 ppm to 200 ppm; and

a content of Bi derived from an isocyanated catalyst in the toner is 10 ppm to 200 ppm.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 29, 2007
From: YAMADA, MASAHIDE; EMOTO, SHIGERU; WATANABE, NAOHIRO; OHKI, MASAHIRO; SAITOH, AKINORI; WAKAMATSU, SHINICHI
To: RICOH COMPANY, LTD.
Reel/Frame 019350/0866 →
Priority Claims (1)
JP 2006-074786 · Mar 17, 2006 · national
Continuity (1)
Related Publication 20070218392A1 · Sep 20, 2007