Fluororubber composition
US-2015353720-A1 · Dec 10, 2015 · US
US9187587B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9187587-B2 |
| Application number | US-201313931983-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jun 30, 2013 |
| Priority date | Jun 30, 2013 |
| Publication date | Nov 17, 2015 |
| Grant date | Nov 17, 2015 |
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A marking system surface material includes a fluoroelastomer including grafted fluorinated polymers. The fluoroelastomer is a perfluoropolyether-grafted fluoroelastomer formed using an alkoxy-terminated fluorosilicone component, and exhibiting high contact angle and low sliding angle.
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What is claimed is: 1. A fluoropolymer composition, comprising: a fluoroelastomer component; and a perfluoropolyether component, the fluoroelastomer component being grafted to the perfluoropolyether component with an amino-functionalized alkoxy-terminated fluorosilicone component. 2. The composition of claim 1 , wherein in the fluoroelastomer is a terpolymer, the terpolymer being a peroxide curable terpolymer. 3. A method of forming a fluoroelastomer comprising grafted fluorinated polymers, the method comprising: combining a first solution comprising a fluoroelastomer component and a second solution comprising an amino-functionalized fluorosilicone crosslinker component including a perfluoropolyether component, the fluoroelastomer component being grafted to the perfluoropolyether component with an amino-functionalized alkoxy-terminated fluorosilicone component. 4. The method of claim 3 , the first solution being formed by preparing a surfactant mixture of fluorosurfactants and combining the mixture with the fluoroelastomer component. 5. The method of claim 4 , the first solution being a 17.5% solution of fluoroelastomer in MIBK. 6. The method of claim 3 , the second solution being formed by mixing the crosslinker and the perfluoropolyether component in a 1.5 to 1 mol ratio, respectively. 7. The method of claim 3 , the combining further comprising adding the second solution to the first solution dropwise. 8. The method of claim 3 , comprising: combining the mixture of the first solution and the second solution with MgO, CaO, or a mixture thereof. 9. The method of claim 8 , comprising mixing the combined first and second solution and MgO, CaO, or mixture thereof. 10. The method of claim 9 , the mixing being performed over 5 minutes at 23 degrees Celsius to form a mixed solution. 11. The method of claim 10 , comprising: pouring the solution. 12. The method of claim 11 , wherein the solution is poured onto a marking system surface. 13. The method of claim 10 , comprising: outgassing the mixed solution at 23 degrees Celsius overnight; and curing the mixed solution at 218 degrees Celsius thereafter. 14. An ink-based digital printing system, comprising: an imaging member having a reimageable surface layer, the surface layer comprising a fluoroelastomer component and a perfluoropolyether component, the fluoroelastomer component being grafted to the perfluoropolyether component with an amino-funetionalized alkoxy-terminated fluorosilicone component; a dampening fluid metering system, the dampening fluid metering system being configured to apply dampening fluid onto the reimageable surface; a dampening fluid patterning system, the dampening fluid patterning system being configured to form a pattern in the applied dampening fluid; and an inking system, the inking system being configured to apply ink to the imaging member surface, the surface having the patterned dampening fluid disposed thereon.
containing fluorine atoms · CPC title
Block or graft polymers not provided for in groups C09D101/00 - C09D185/04 · CPC title
Monomers containing fluorine · CPC title
Block or graft polymers containing only sequences of polymers of C08C or C08F · CPC title
containing three or more polymers in a blend · CPC title
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