Method for manufacturing core-shell structure fine particles and toner
US-9188894-B2 · Nov 17, 2015 · US
US9678450B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9678450-B2 |
| Application number | US-201414783945-A |
| Country | US |
| Kind code | B2 |
| Filing date | Apr 25, 2014 |
| Priority date | Apr 26, 2013 |
| Publication date | Jun 13, 2017 |
| Grant date | Jun 13, 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 [i] a toner including at least a colorant, a resin, and a releasing agent, wherein a spin-spin relaxation time (t 2 ) of the toner at 90° C. obtained by Hahn Echo method of pulse NMR analysis is from 1.80 msec to 7.00 msec. Also provided is [ii] a toner according to [i], wherein the spin-spin relaxation time (t 2 ) of the toner at 90° C. obtained by Hahn Echo method of pulse NMR analysis is from 3.80 msec to 5.90 msec.
Opening claim text (preview).
The invention claimed is: 1. A toner, comprising: a colorant; a crystalline resin; and a releasing agent, wherein a spin-spin relaxation time (t 2 ) of the toner at 90° C. obtained by Hahn Echo method of pulse NMR analysis is from 1.80 msec to 7.00 msec, wherein the crystalline resin comprises a crystalline polyester resin and the crystalline polyester resin comprises a urethane bond, a urea bond, or both thereof. 2. The toner according to claim 1 , wherein the spin-spin relaxation time (t 2 ) of the toner at 90° C. obtained by Hahn Echo method of pulse NMR analysis is from 3.80 msec to 5.90 msec. 3. The toner according to claim 1 , wherein of a soft component and a hard component of the toner at 90° C. obtained by Hahn Echo method of pulse NMR analysis, the hard component has a spin-spin relaxation time (t H ) that satisfies the following relational expression <1> or <2> where t S represents a spin-spin relaxation time attributed to the soft component: when t S ≧25.00 msec, t H ≦2.00 msec <1>, when t S <25.00 msec, t H ≧1.10 msec <2>. 4. The toner according to claim 1 , wherein in DSC of the toner in a range of from 0° C. to 100° C., a maximum endothermic peak temperature T1 of the toner at a first temperature raising and a maximum exothermic peak temperature T2 of the toner at a temperature lowering satisfy the following relational expression <3>: T 1− T 2≦30.0° C. and T 2≧30.0° C. <3>. 5. The toner according to claim 4 , wherein in the DSC of the toner in the range of from 0° C. to 100° C., a maximum endothermic peak temperature of the toner at a second temperature raising is in a range of from 50° C. to 70° C., and an amount of heat of melting of the toner at the second temperature raising is 30.0 J/g or greater. 6. The toner according to claim 1 , wherein when a tetrahydrofuran (THF) soluble content of the toner is measured with gel permeation chromatography (GPC), a ratio of a content of the THF soluble content that has a molecular weight of 100,000 or greater is 5% or greater, and a weight average molecular weight (Mw) of the THF soluble content is 20,000 or greater. 7. The toner according to claim 1 , wherein the toner has a core-shell structure, and a shell of the core-shell structure has a thickness of 40 nm or less. 8. A two-component developer, comprising: the toner according to claim 1 ; and a carrier having a magnetic property. 9. The toner according to claim 1 , which further comprises a non-crystalline polyester resin. 10. The toner according to claim 9 , wherein the non-crystalline polyester resin is a modified polyester resin. 11. The toner according to claim 9 , wherein the non-crystalline polyester resin is an unmodified polyester resin. 12. The toner according to claim 1 , which contains 10% by mass to 85% by mass of the crystalline resin. 13. The toner according to claim 1 , which has a glass transition temperature of 40° C. to 70° C. 14. The toner according to claim 1 , which contains 1% by mass to 15% by mass of the colorant. 15. The toner according to claim 1 , wherein the releasing agent is a wax. 16. The toner according to claim 1 , wherein the releasing agent is a wax having a melting point of 40° C. to 160° C. 17. The toner according to claim 1 , wherein the releasing agent is a wax and the toner comprises up to 40% by mass of the wax. 18. The toner according to claim 1 , wherein the releasing agent is a wax and the toner comprises 3% by mass to 30% by mass of the wax.
Polyesters · CPC title
characterised by their chemical properties, e.g. acidity, molecular weight, sensitivity to reactants · CPC title
Encapsulated toner particles · CPC title
characterised by their physical properties, e.g. viscosity, solubility, melting temperature, softening temperature, glass transition temperature · CPC title
with toner particles · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.