Toner formulations having improved toner usage efficiency and method to make the same
US-9217939-B2 · Dec 22, 2015 · US
US9671709B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9671709-B2 |
| Application number | US-201314145043-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 31, 2013 |
| Priority date | Dec 29, 2011 |
| Publication date | Jun 6, 2017 |
| Grant date | Jun 6, 2017 |
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A chemically prepared toner composition according to one example embodiment includes a core including a first polymer binder, a second polymer binder, a colorant and a release agent; a shell that is formed around the core and includes a third polymer binder; and a borax coupling agent between the core and the shell. The first and third polymer binders are different amorphous polyester resins. The second polymer binder is a crystalline polyester resin and acts as a plasticizing agent in the core. The borax coupling agent assists in adhering the shell to the outer surface of the core. Optionally, the toner of the present invention may be finished with a set of extra particulate additives.
Opening claim text (preview).
What is claimed is: 1. A chemically prepared toner composition, comprising: a core including a first polymer binder, a second polymer binder, a colorant and a release agent; a shell including a third polymer binder formed around the outer surface of the core; and a borax coupling agent between the core and the shell, wherein the borax coupling agent assists in adhering the shell to the outer surface of the core. 2. The chemically prepared toner composition of claim 1 , wherein the first polymer binder, the second polymer binder and the third polymer binder each include a polyester resin. 3. The chemically prepared toner composition of claim 2 , wherein the first polymer binder is an amorphous polyester resin. 4. The chemically prepared toner composition of claim 2 , wherein the second polymer binder is a crystalline polyester resin. 5. The chemically prepared toner composition of claim 2 , wherein the third polymer binder is an amorphous polyester resin. 6. The chemically prepared toner composition of claim 2 , wherein the first polymer binder and the third polymer binder are different amorphous polyester resins. 7. The chemically prepared toner of claim 1 further comprising extra particulate additives selected from the group consisting of medium sized silica particles a primary particle size in the range of 30 nm to 60 nm, large sized silica particles having a primary particle size in the range of 90 nm 120 nm, small sized silica particles having a primary particle size in the range of 2 nm to 20 nm, alumina particles and titania particles. 8. The toner composition of claim 7 , wherein said medium sized silica particles are treated with a surface treatment selected from the group consisting of hexamethyldisilazane and polydimethylsiloxane. 9. The toner composition of claim 7 , wherein said large sized silica particles are treated with a surface treatment selected from the group consisting of hexamethyldisilazane, polydimethylsiloxane, dimethyldichlorosilane, dimethyldiethoxysilane octyltrialkoxysilane and combinations thereof. 10. The toner composition of claim 7 , wherein said alumina particles are surface treated with octylsilane. 11. The chemically prepared toner composition of claim 1 , wherein the ratio of the first polymer binder and the second polymer binder to the third polymer binder is between about 20:80 and about 80:20 by weight. 12. The chemically prepared toner composition of claim 11 , wherein the ratio of the first polymer binder and the second polymer binder to the third polymer binder the ratio of the first polymer binder to the second polymer binder is between about 50:50 and about 70:30 by weight.
obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds · CPC title
Preparation thereof · CPC title
obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds · CPC title
Inorganic compounds · CPC title
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