Toner and method for producing toner

US12078960B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-12078960-B2
Application numberUS-202117493309-A
CountryUS
Kind codeB2
Filing dateOct 4, 2021
Priority dateOct 5, 2020
Publication dateSep 3, 2024
Grant dateSep 3, 2024

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  1. Title

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  2. Abstract

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  4. Key dates

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  5. First independent claim

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Abstract

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A toner including toner particles having a resin component containing a crystalline resin and an amorphous resin, in which the resin component contains a tetrahydrofuran-insoluble component, and the content of the tetrahydrofuran-insoluble component with respect to the content of the resin component is 5.0% to 80.0% by mass, wherein a maximum endothermic peak temperature of the tetrahydrofuran-insoluble component is 55.0 to 80.0° C., and the amount of heat absorption in the maximum endothermic peak of the tetrahydrofuran-insoluble component is 10.0 to 80.0 J/g, and toner particles have a structure which comprises a matrix containing the crystalline resin and domains containing the amorphous resin.

First claim

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What is claimed is: 1. A toner, comprising: toner particles containing: a resin component containing: a crystalline resin and an amorphous resin, wherein the resin component contains a tetrahydrofuran-insoluble component, and a content of the tetrahydrofuran-insoluble component with respect to a content of the resin component is 5.0% to 80.0% by mass, wherein when a maximum endothermic peak temperature in a differential scanning calorimetry measurement (DSC measurement) of the tetrahydrofuran-insoluble component is defined as Tm [° C.], and when an amount of heat absorption in the maximum endothermic peak determined from DSC measurement of the tetrahydrofuran-insoluble component is defined as H(I) [J/g], Tm [° C.] satisfies formula (1): 55.0≤ Tm≤ 80.0  (1), and H(I) [J/g] satisfies formula (2): 10.0≤ H ( I )≤80.0  (2), and wherein when cross sections of 100 particles of the toner particles are observed, each of the cross sections has a domain-matrix structure which comprises a matrix containing the crystalline resin, and domains each of which contains the amorphous resin, and among the 100 particles, the number of particle in which all the domains have a major diameter of 1.0 μm or less is 20 particles or more, and wherein the crystalline resin comprises a vinyl polymer A containing a monomer unit A1 represented by formula (A): where in formula (A), R 1 is H or CH 3 , and R 2 is an alkyl group having 18 to 36 carbon atoms. 2. The toner according to claim 1 , wherein when an amount of heat absorption in a maximum endothermic peak determined from DSC measurement of the toner is defined as H(T) [J/g], H(I) [J/g] and H(T) [J/g] satisfy formula (3): 3.0%≤ H ( I )/ H ( T )≤20.0%  (3). 3. The toner according to claim 1 , wherein a content of the monomer unit A1 with respect to a content of the vinyl polymer A is 30.0% to 99.9% by mass. 4. The toner according to claim 1 , wherein the vinyl polymer A further contains a monomer unit A2, and wherein when an SP value of the monomer unit A1 is defined as SP A1 (J/cm 3 ) 0.5 , and when an SP value of the monomer unit A2 is defined as SP A2 (J/cm 3 ) 0.5 SP A1 and SP A2 satisfy formula (4): 3.0≤SP A2 −SP A1 ≤25.0  (4). 5. The toner according to claim 1 , wherein the vinyl polymer A further contains a monomer unit A2, the monomer unit A2 is at least one monomer unit selected from the group consisting of a monomer unit represented by formula (A21) below and a monomer unit represented by formula (A22) below: where in formulae (A21) and (A22), X is a single bond or an alkylene group having 1 to 6 carbon atoms, R 4 is a cyano group (—C═N), —C(═O)NHR 7 (where R 7 is a hydrogen atom or an alkyl group having 1 to 4 carbon atoms), a hydroxy group, —COOR 8 (where R 8 is an alkyl group having 1 to 6 carbon atoms or a hydroxyalkyl group having 1 to 6 carbon atoms), —NHCOOR 9 (where R 9 is an alkyl group having 1 to 4 carbon atoms), —NH—C(═O)—NH(R 10 ) 2 (where each R 10 is independently a hydrogen atom or alkyl group having 1 to 6 carbon atoms), —COO(CH 2 ) 2 NHCOOR 11 (where R 11 is an alkyl group having 1 to 4 carbon atoms) or —COO(CH 2 ) 2 —NH—C(═O)—NH(R 12 ) 2 (where each R 12 is independently hydrogen atom or an alkyl group having 1 to 6 carbon atoms), R 6 is an alkyl group having 1 to 4 carbon atoms, and R 3 and R 5 are each independently a hydrogen atom or CH 3 . 6. The toner according to claim 4 , wherein a content of the monomer unit A2 with respect to a content of the vinyl polymer A is 1.0% to 70.0% by mass. 7. The toner according to claim 5 , wherein a content of the monomer unit A2 with respect to a content of the vinyl polymer A is 1.0% to 70.0% by mass. 8. The toner according to claim 5 , wherein the vinyl polymer A further contains a monomer unit A3, the monomer unit A3 is at least one monomer unit selected from the group consisting of a monomer unit represented by formula (A31) and a monomer unit represented by formula (A32): where in formula (A32), R 13 is H or CH 3 . 9. The toner according to claim 1 , wherein a content of the tetrahydrofuran-insoluble component with respect to a content of the resin component is 30.0% to 80.0% by mass.

Assignees

Inventors

Classifications

  • characterised by physical parameters (magnetic parameters G03G9/083) · CPC title

  • Polyesters · CPC title

  • Post-treatment · CPC title

  • by mixing the toner components in a liquefied state; melt kneading; reactive mixing · CPC title

  • Terephthalic acids · CPC title

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What does patent US12078960B2 cover?
A toner including toner particles having a resin component containing a crystalline resin and an amorphous resin, in which the resin component contains a tetrahydrofuran-insoluble component, and the content of the tetrahydrofuran-insoluble component with respect to the content of the resin component is 5.0% to 80.0% by mass, wherein a maximum endothermic peak temperature of the tetrahydrofuran-…
Who is the assignee on this patent?
Canon Kk
What technology area does this patent fall under?
Primary CPC classification G03G9/08731. Mapped technology areas include Physics.
When was this patent published?
Publication date Tue Sep 03 2024 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).