Toner
US-8980517-B2 · Mar 17, 2015 · US
US9632441B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9632441-B2 |
| Application number | US-201414509257-A |
| Country | US |
| Kind code | B2 |
| Filing date | Oct 8, 2014 |
| Priority date | Oct 9, 2013 |
| Publication date | Apr 25, 2017 |
| Grant date | Apr 25, 2017 |
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The present invention is a toner that has toner particles that have a surface layer that contains an organosilicon polymer, wherein this organosilicon polymer has a specific substructure and the ratio [ST3], in a 29 Si-NMR measurement of a tetrahydrofuran-insoluble matter of the toner particles, of the peak area for this substructure to the total peak area for the organosilicon polymer satisfies the relationship ST3≧0.40.
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What is claimed is: 1. A toner comprising toner particles, each of which has a surface layer that contains an organosilicon polymer, the organosilicon polymer having a substructure represented by formula (T3) R—Si(O 1/2 ) 3 (T3) where R represents an alkyl group having 1 to 6 carbons or a phenyl group, wherein a ratio ST3 of the peak area for the substructure represented by formula (T3) to the total peak area for the organosilicon polymer in a 29 Si-NMR measurement of a tetrahydrofuran-insoluble matter in the toner particles satisfies the relationship ST3≧0.40, and a silicon atom concentration dSi with reference to a total concentration (dC+dO+dSi) of the silicon atom concentration dSi, an oxygen atom concentration dO, and a carbon atom concentration dC in electron spectroscopy for chemical analysis of a surface of the toner particles is 2.5 atom % or more. 2. The toner according to claim 1 , wherein ST3/SX2≧1.00 when SX2 is a ratio of the peak area for the structure in which the number of silicon-bonded O 1/2 is 2.0 to the total peak area for the organosilicon polymer in a 29 Si-NMR measurement of the tetrahydrofuran-insoluble matter in the toner particles. 3. The toner according to claim 1 , wherein the organosilicon polymer is obtained by polymerization of an organosilicon compound having a structure represented by formula (Z) where R 1 represents an alkyl group having 1 to 6 carbons or a phenyl group, and R 2 , R 3 , and R 4 each independently represent a halogen atom, hydroxy group, acetoxy group, or alkoxy group. 4. The toner according to claim 3 , wherein R 1 is a methyl group, ethyl group, propyl group, or phenyl group. 5. The toner according to claim 3 , wherein R 1 is an alkyl group having 1 to 3 carbons. 6. The toner according to claim 5 , wherein the alkyl group is a methyl group, ethyl group, or propyl group. 7. The toner according to claim 3 , wherein R 2 , R 3 , and R 4 are each independently an alkoxy group. 8. The toner according to claim 1 , wherein the silicon atom concentration dSi with reference to the total concentration (dC+dO+dSi) is 5.0 atomic % or more. 9. The toner according to claim 1 , wherein the silicon atom concentration dSi with reference to the total concentration (dC+dO+dSi) is 10.0 atomic % or more. 10. The toner according to claim 3 , wherein R 1 is a methyl group.
obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds · CPC title
Polymers having silicon in the main chain, with or without sulfur, oxygen, nitrogen or carbon only · CPC title
characterised by their structure; characterised by non-homogenuous distribution of components (microcapsular toners G03G9/093) · CPC title
treated with organic compounds · CPC title
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