IP Library Granted Patent US 7,713,669
Granted Patent B2
US 7,713,669 · App. 11/187,929 · Granted May 11, 2010

Toner for developing electrostatic images, electrostatic image developer, and image-forming method

View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 7,713,669
App. No.
11/187,929
Granted
May 11, 2010
Kind
B2
Abstract

A toner for developing electrostatic images, comprising a binder resin and a colorant, the binder resin including a crystalline polyester resin and an amorphous resin. When, in differential scanning calorimetry of the toner according to ASTM D3418-8, the temperature of the endothermic peak derived from the crystalline polyester resin in a first heating process is defined as Tm1 (° C.), the endothermic quantity based on the endothermic peak in the first heating process is defined as ΔH1 (mW/g), and the endothermic quantity based on the endothermic peak in a second heating process is defined as ΔH2 (mW/g), Tm1 is 50 to 80° C., and ΔH1 and ΔH2 satisfy the relationship represented by the following Formula (1). When the softening temperature of the toner is defined as T f1/2 (° C.), Tf 1/2 is 85 to 135° C. Tm1 and T f1/2 satisfy the relationship represented by the following Formula (2): 0.35≦Δ H 2/Δ H 1≦0.95  Formula (1) T f1/2 ≦205−(1.4× Tm 1)  Formula (2).

Claims (26)

1. A toner for developing electrostatic images, comprising a binder resin and a colorant, the binder resin comprising a crystalline polyester resin and an amorphous resin, wherein:

when, in differential scanning calorimetry of the toner according to ASTM D3418-8, the temperature of an endothermic peak derived from the crystalline polyester resin in a first heating process is defined as Tm1 (° C.), an endothermic quantity based on the endothermic peak in the first heating process is defined as ΔH1 (mW/g), and an endothermic quantity based on an endothermic peak in a second heating process is defined as ΔH2 (mW/g), Tm1 is 50 to 80° C., and ΔH1 and ΔH2 satisfy the relationship represented by the following Formula (1);

when the softening temperature of the toner is defined as T f1/2 (° C.), T f1/2 is 85 to 135° C.;

Tm1 and T f1/2 satisfy the relationship represented by the following Formula (2):

0.35 ≦ΔH 2 /ΔH 1÷0.95  Formula (1)

T f1/2 ≦205−(1.4 ×Tm 1)  Formula (2);

when the crystalline polyester resin has an ester concentration M represented by the following Formula (3) of 0.01 to 0.12:

M=K/A   Formula (3);

where K represents the number of ester groups in the crystalline polyester resin and A represents the number of atoms constituting a polymer chain of the crystalline polyester resin;

the crystalline polyester resin includes an acid-derived constituent component derived from an aliphatic dicarboxylic acid and an alcohol-derived constituent component derived from an aliphatic diol; and

an amount of content of the acid-derived constituent derived from the aliphatic dicarboxylic acid, among all other acid-derived components, is 80-100 mole % by constitution.

2. The toner for developing electrostatic images according to claim 1 , wherein when the glass transition temperature in the first heating process is defined as Tg1 (° C.) and the glass transition temperature in the second heating process is defined as Tg2 (° C.), the difference (Tg1−Tg2) is 5 to 15° C.

3. The toner for developing electrostatic images according to claim 1 , wherein the glass transition temperature Tg1 (° C.) in the first heating process is in the range of 45 to 70° C.

4. The toner for developing electrostatic images according to claim 1 , wherein T f1/2 is 85 to 125° C.

5. The toner for developing electrostatic images according to claim 1 , wherein the melting point of the crystalline polyester resin is 60 to 120° C.

6. The toner for developing electrostatic images according to claim 1 , wherein the glass transition temperature of the amorphous resin is 45 to 65° C.

7. The toner for developing electrostatic images according to claim 1 , wherein the mass ratio (A/B) of the amount of the crystalline polyester resin (A) to the amount of amorphous resin (B) in the binder resin is 2/98 to 50/50.

8. The toner for developing electrostatic images according to claim 1 , further comprising two or more releasing agents.

9. The toner for developing electrostatic images according to claim 1 , wherein the volume-average particle size of the toner is 3 to 9 μm.

10. The toner for developing electrostatic images according to claim 1 , wherein the volume-average particle size distribution index GSDv is 1.35 or less.

11. The toner for developing electrostatic images according to claim 1 , wherein the ratio GSDv/GSDp of the volume-average particle distribution index GSDv to the number-average particle size distribution index GSDp is 0.90 or more.

12. The toner for developing electrostatic images according to claim 1 , prepared by a wet granulating method.

13. The toner for developing electrostatic images according to claim 12 , wherein the wet granulating method is an emulsion polymerization aggregation method.

14. The toner for developing electrostatic images according to claim 1 , wherein core particles containing the binder resin are coated with a coating resin on the surface thereof.

15. An electrostatic image developer, comprising the toner for developing electrostatic images according to claim 1 .

16. An image-forming method, comprising forming an electrostatic image on a latent image-holding member surface, developing the electrostatic image formed on the latent image-holding member surface with a developer containing a toner to form a toner image, transferring the toner image onto a transfer material surface, and heat-fixing the toner image transferred on the transfer material surface; wherein the toner used is the toner for developing electrostatic images according to claim 1 .

Assignments (2)
CHANGE OF NAME Recorded Aug 12, 2021
From: FUJI XEROX CO., LTD.
To: FUJIFILM BUSINESS INNOVATION CORP.
Reel/Frame 058287/0056 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 25, 2005
From: MIZUTANI, NORIYUKI; MAEHATA, HIDEO; HAMANO, HIROKAZU; TANAKA, HIROYUKI; IGUCHI, MOEGI; KITAGAWA, SOICHIRO; YOSHINO, SUSUMU; ISHIHARA, YUKA; TSURUMI, YOSUKE; MATSUMOTO, AKIRA; TAKAHASHI, MASARU
To: FUJI XEROX CO., LTD.
Reel/Frame 016812/0041 →