Crystalline polyester latex production by solvent reuse phase inversion emulsification
US-9267032-B1 · Feb 23, 2016 · US
US9829816B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9829816-B2 |
| Application number | US-201514736991-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jun 11, 2015 |
| Priority date | Jun 20, 2014 |
| Publication date | Nov 28, 2017 |
| Grant date | Nov 28, 2017 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
Provided is a toner for which the heat-resistant storability and the low-temperature fixability are able to co-exist at higher levels and for which the temporal stability of the low-temperature fixability is also excellent. The toner has a toner particle that contains a binder resin and a pigment, and this binder resin contains a polyester resin that has a specific structure and specific properties.
Opening claim text (preview).
What is claimed is: 1. A toner comprising a toner particle, said toner particle comprising: a pigment, the pigment being at least one member selected from the group consisting of an organic pigment and a carbon black; and a binder resin, the binder resin comprising styrene-acrylic resin, and a crystalline polyester resin, the crystalline polyester resin being obtained by condensation polymerization of a monomer (a) selected from monomer group A described below and a monomer (b) selected from monomer group B described below, wherein the crystalline polyester resin has a content X (mol %) of the unit derived from the monomer (b), as calculated by formula (1) of from 3.0 to 12.0 mol %: X={Mb /( Ma +Mb )}×100 (1) where Ma (mol/g) is the number of moles of the unit derived from the monomer (a) per unit mass, and Mb (mol/g) is the number of moles of the unit derived from the monomer (b) per unit mass, and a melting point of the crystalline polyester resin is from 50 to 85° C., monomer group A comprises a C 2-11 α,ω-straight-chain aliphatic diol, a C 2-13 α,ω-straight-chain aliphatic dicarboxylic acid, a C 2-12 α,ω-straight-chain aliphatic monohydroxymonocarboxylic acid, an intramolecular anhydride of a C 2-13 α,ω-straight-chain aliphatic dicarboxylic acid, an alkylester of a C 2-13 α,ω-straight-chain aliphatic dicarboxylic acid, an alkylester of a C 2-12 α,ω-straight-chain aliphatic monohydroxymonocarboxylic acid, or a lactonized compound of a C 2-12 α,ω-straight-chain aliphatic monohydroxymonocarboxylic acid, and monomer group B comprises a C 12-22 α,ω-straight-chain aliphatic diol, a C 14-24 α,ω-straight-chain aliphatic dicarboxylic acid, a C 13-23 α,ω-straight-chain aliphatic monohydroxymonocarboxylic acid, an intramolecular anhydride of a C 14-24 α,ω-straight-chain aliphatic dicarboxylic acid, an alkylester of a C 14-24 α,ω-straight-chain aliphatic dicarboxylic acid, an alkylester of a C 13-23 α,ω-straight-chain aliphatic monohydroxymonocarboxylic acid, or a lactonized compound of a C 13-23 α,ω-straight-chain aliphatic monohydroxymonocarboxylic acid. 2. The toner according to claim 1 , wherein the toner particle contains the crystalline polyester resin at from 3.0 to 30.0 mass% based on the total mass of the binder resin. 3. The toner according to claim 1 , wherein the crystalline polyester resin is a ternary copolymer. 4. The toner according to claim 1 , wherein the monomer group A comprises the C 2-10 α,ω-straight-chain aliphatic diol, the C 2-12 α,ω- straight-chain aliphatic dicarboxylic acid, or the C 2-11 α,ω-straight-chain aliphatic monohydroxymonocarboxylic acid. 5. The toner according to claim 1 , wherein the organic pigment is a cyan pigment, a magenta pigment, or a yellow pigment. 6. The toner according to claim 1 , wherein the monomer group A comprises the C 2-11 α,ω-straight-chain aliphatic diol, a C 5-13 α,ω-straight-chain aliphatic dicarboxylic acid, or the C 2-12 α,ω-straight-chain aliphatic monohydroxymonocarboxylic acid. 7. The toner according to claim 1 , wherein the monomer group A comprises the C 2-11 α,ω-straight-chain aliphatic diol, a C 10-13 α,ω-straight-chain aliphatic dicarboxylic acid, or the C 2-12 α,ω-straight-chain aliphatic monohydroxymonocarboxylic acid.
Organic dyes · CPC title
characterised by their chemical properties, e.g. acidity, molecular weight, sensitivity to reactants · CPC title
Polyesters · CPC title
characterised by their physical properties, e.g. viscosity, solubility, melting temperature, softening temperature, glass transition temperature · CPC title
with esters of acrylic or methacrylic acid · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.