IP Library › Granted Patent US 12,748,358
Granted Patent B2
US 12,748,358 · App. 18/543,153 · Granted Sep 29, 2026

Toner and toner production method

Inventors: Megumi Shino (Chiba, JP); Takeshi Hashimoto (Ibaraki, JP); Gaku Sato (Chiba, JP); Hayato Ida (Ibaraki, JP)
Assignee: CANON KABUSHIKI KAISHA
G03G9/08728G03G9/081G03G9/0821G03G9/08782
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Quick Facts
Patent No.
US 12,748,358
App. No.
18/543,153
Granted
Sep 29, 2026
Kind
B2
Abstract

A toner comprises a toner particle that contains a binder resin having a crystalline resin and an amorphous resin, and a wax, wherein a matrix-domain structure made up of a matrix including the crystalline resin, and domains including the amorphous resin, is present in a cross-sectional observation of the toner, the crystalline resin has a specific monomer unit, in a differential curve, which is obtained through differentiation of a temperature-storage elastic modulus curve by temperature, with temperature being a horizontal axis and a common logarithm Log G′ of a storage elastic modulus G′ being a vertical axis as obtained in a viscoelasticity measurement of the toner, the differential curve has specific minimal values P1 and P2 within specific temperature ranges, and has storage elastic moduli G′ at the temperatures of the minimal values P1 and P2 lie in respective specific ranges.

Claims (67)

1 . A toner comprising a toner particle comprising

a binder resin comprising a crystalline resin and an amorphous resin, and

a wax, wherein

a matrix-domain structure made up of a matrix including the crystalline resin, and domains including the amorphous resin, is present in a cross-sectional observation of the toner under a transmission electron microscope,

the crystalline resin has a first monomer unit represented by Formula (1) below;

in a differential curve, which is obtained through differentiation of a temperature-storage elastic modulus curve by temperature, with temperature as a horizontal axis and a common logarithm Log G′ of a storage elastic modulus G′ as a vertical axis as obtained in a viscoelasticity measurement of the toner,

the differential curve has a minimal value P1 in a range of 50 to 70° C., the minimal value P1 being −0.50 to −0.20, and

the differential curve has a minimal value P2 in a range of 80 to 120° C., the minimal value P2 being −0.20 to −0.03;

the storage elastic modulus G′ of the toner at the temperature of the minimal value P1 is 5.0×10 5 to 2.0×10 7 Pa; and

the storage elastic modulus G′ of the toner at the temperature of the minimal value P2 is 1.0×10 2 to 1.0×10 4 Pa;

in Formula (1), R Z1 represents a hydrogen atom or a methyl group, and R 1 represents an alkyl group having 18 to 36 carbon atoms.

2 . The toner according to claim 1 , wherein

with ΔH(T) as a total endothermic quantity J/g per 1 g of wax, derived from the wax, in an endothermic quantity measurement of the toner using a differential scanning calorimeter,

and with ΔH(W) as a total endothermic quantity J/g per 1 g of wax, derived from the wax, in an endothermic quantity measurement of the wax,

ΔH(T) and ΔH(W) satisfy 0.70≤ΔH(T)/ΔH(W)≤0.90.

3 . The toner according to claim 1 , wherein a content ratio of the first monomer unit in the crystalline resin is at least 30.0 mass %, relative to mass of all monomer units in the crystalline resin.

4 . The toner according to claim 1 , wherein the amorphous resin is an amorphous polyester resin.

5 . The toner according to claim 1 ,

wherein in a cross-sectional observation of the toner under a transmission electron microscope,

a number-average diameter of the domains is 0.05 to 3.00 μm.

6 . The toner according to claim 1 , wherein

in a cross-sectional observation of the toner under a transmission electron microscope,

a ratio of the domains relative to a combined surface area of the matrix and the domains is 30 to 65 area %.

7 . The toner according to claim 1 , wherein the crystalline resin contains a second monomer unit represented by Formula (2) below, and a third monomer unit represented by Formula (3) below:

in Formula (2), R 2 represents a hydrogen atom or a methyl group, and

in Formula (3), X represents —O— or —NH—, R 4 represents a hydrogen atom or a methyl group, and R 3 represents an alkylene having 2 to 6 carbon atoms.

8 . The toner according to claim 1 , wherein

the wax is a hydrocarbon wax, and

a melting point of the wax is 90° C. or higher.

9 . The toner according to claim 1 , wherein

with SP1 being an SP value (J/cm 3 ) 0.5 of the crystalline resin, SP2 being an SP value (J/cm 3 ) 0.5 of the amorphous resin, and SP3 being an SP value (J/cm 3 ) 0.5 of the wax,

the SP1, SP2 and SP3 satisfy the following relationships:

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SP

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1

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.

10 . The toner according to claim 1 , wherein

the toner particle comprises an inorganic filler particle, and

a content ratio of the inorganic filler particle in the toner particle is 5 to 20 parts by mass, relative to 100 parts by mass of the binder resin.

11 . The toner according to claim 10 , wherein the inorganic filler particle is treated with a fatty acid.

12 . A method for producing the toner according to claim 1 ,

the method comprising:

a melt-kneading step of melt-kneading a mixture that contains the binder resin having the crystalline resin and the amorphous resin, and the wax; and

an annealing step of holding a melt-kneaded product obtained after the melt-kneading step at a temperature of 40 to 60° C., for 30 minutes or longer.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 28, 2024
From: SHINO, MEGUMI; HASHIMOTO, TAKESHI; SATO, GAKU; IDA, HAYATO
To: CANON KABUSHIKI KAISHA
Reel/Frame 066927/0797 →
Priority Claims (2)
JP 2022-207914 · Dec 26, 2022 · national
JP 2023-194259 · Nov 15, 2023 · national
Continuity (1)
Related Publication 20240219854A1 · Jul 4, 2024
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