Blanket materials for indirect printing methods
US-9200120-B2 · Dec 1, 2015 · US
US2016177133A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2016177133-A1 |
| Application number | US-201514842632-A |
| Country | US |
| Kind code | A1 |
| Filing date | Sep 1, 2015 |
| Priority date | Dec 19, 2014 |
| Publication date | Jun 23, 2016 |
| Grant date | — |
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A composition for forming a silica based layer includes a silicon-containing compound including polysilazane, polysiloxazane, or a combination thereof and one or more kinds of solvent, and having a turbidity increasing rate of less than or equal to about 0.13.
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What is claimed is: 1 . A composition for forming a silica based layer, comprising a silicon-containing compound comprising polysilazane, polysiloxazane, or a combination thereof and one or more kinds of solvent, and having a turbidity increasing rate of less than or equal to about 0.13, wherein the turbidity increasing rate is defined by Relationship Equation 1, and a gelation time in the Relationship Equation 1 is measured at temperature of about 23° C.±about 2° C. under a relative humidity of about 50%±about 10%: Turbidity increasing rate (NTU/hr)=(Turbidity at gelation−Initial turbidity)/Gelation time. Relationship Equation 1 2 . The composition of claim 1 , wherein the silicon-containing compound comprises polysilazane comprising a moiety represented by Chemical Formula 1: wherein, in Chemical Formula 1, R 1 to R 3 are each independently hydrogen, a substituted or unsubstituted C1 to C30 alkyl group, a substituted or unsubstituted C3 to C30 cycloalkyl group, a substituted or unsubstituted C6 to C30 aryl group, a substituted or unsubstituted C7 to C30 arylalkyl group, a substituted or unsubstituted C1 to C30 heteroalkyl group, a substituted or unsubstituted C2 to C30 heterocycloalkyl group, a substituted or unsubstituted C2 to C30 alkenyl group, a substituted or unsubstituted alkoxy group, a carboxyl group, an aldehyde group, a hydroxy group, or a combination thereof, and “*” indicates a linking point. 3 . The composition of claim 1 , wherein the silicon-containing compound comprises polysiloxazane comprising a moiety represented by Chemical Formula 2: wherein, in Chemical Formula 2, R 4 to R 7 are each independently hydrogen, a substituted or unsubstituted C1 to C30 alkyl group, a substituted or unsubstituted C3 to C30 cycloalkyl group, a substituted or unsubstituted C6 to C30 aryl group, a substituted or unsubstituted C7 to C30 arylalkyl group, a substituted or unsubstituted C1 to C30 heteroalkyl group, a substituted or unsubstituted C2 to C30 heterocycloalkyl group, a substituted or unsubstituted C2 to C30 alkenyl group, a substituted or unsubstituted alkoxy group, a carboxyl group, an aldehyde group, a hydroxy group, or a combination thereof, and “*” indicates a linking point. 4 . The composition of claim 1 , wherein the solvent comprises at least one selected from trimethylbenzene, triethylbenzene, decahydronaphthalene, tetrahydronaphthalene, indene, diethylbenzene, and methylnaphthalene. 5 . The composition of claim 1 , wherein the composition has the turbidity increasing rate of less than or equal to about 0.125. 6 . A method for manufacturing a silica based layer, the comprising coating the composition of claim 1 on a substrate, drying the substrate coated with the composition to produce a resultant, and curing the resultant under an inert atmosphere at a temperature of greater than or equal to about 150° C. to manufacture a silica based layer. 7 . The method of claim 6 , wherein the composition is coated utilizing a spin-on coating method. 8 . The method of claim 6 , wherein the silicon-containing compound comprises polysilazane comprising a moiety represented by Chemical Formula 1: wherein, in Chemical Formula 1, R 1 to R 3 are each independently hydrogen, a substituted or unsubstituted C1 to C30 alkyl group, a substituted or unsubstituted C3 to C30 cycloalkyl group, a substituted or unsubstituted C6 to C30 aryl group, a substituted or unsubstituted C7 to C30 arylalkyl group, a substituted or unsubstituted C1 to C30 heteroalkyl group, a substituted or unsubstituted C2 to C30 heterocycloalkyl group, a substituted or unsubstituted C2 to C30 alkenyl group, a substituted or unsubstituted alkoxy group, a carboxyl group, an aldehyde group, a hydroxy group, or a combination thereof, and “*” indicates a linking point. 9 . The method of claim 6 , wherein the silicon-containing compound comprises polysiloxazane comprising a moiety represented by Chemical Formula 2: wherein, in Chemical Formula 2, R 4 to R 7 are each independently hydrogen, a substituted or unsubstituted C1 to C30 alkyl group, a substituted or unsubstituted C3 to C30 cycloalkyl group, a substituted or unsubstituted C6 to C30 aryl group, a substituted or unsubstituted C7 to C30 arylalkyl group, a substituted or unsubstituted C1 to C30 heteroalkyl group, a substituted or unsubstituted C2 to C30 heterocycloalkyl group, a substituted or unsubstituted C2 to C30 alkenyl group, a substituted or unsubstituted alkoxy group, a carboxyl group, an aldehyde group, a hydroxy group, or a combination thereof, and “*” indicates a linking point. 10 . The method of claim 6 , wherein the solvent comprises at least one selected from trimethylbenzene, triethylbenzene, decahydronaphthalene, tetrahydronaphthalene, indene, diethylbenzene, and methylnaphthalene. 11 . The method of claim 6 , wherein the composition has the turbidity increasing rate of less than or equal to about 0.125. 12 . An electronic device comprising a silica based layer manufactured according to the method of claim 6 . 13 . The device of claim 12 , wherein the silicon-containing compound comprises polysilazane comprising a moiety represented by Chemical Formula 1: wherein, in Chemical Formula 1, R 1 to R 3 are each independently hydrogen, a substituted or unsubstituted C1 to C30 alkyl group, a substituted or unsubstituted C3 to C30 cycloalkyl group, a substituted or unsubstituted C6 to C30 aryl group, a substituted or unsubstituted C7 to C30 arylalkyl group, a substituted or unsubstituted C1 to C30 heteroalkyl group, a substituted or unsubstituted C2 to C30 heterocycloalkyl group, a substituted or unsubstituted C2 to C30 alkenyl group, a substituted or unsubstituted alkoxy group, a carboxyl group, an aldehyde group, a hydroxy group, or a combination thereof, and “*” indicates a linking point. 14 . The device of claim 12 , wherein the silicon-containing compound comprises polysiloxazane further comprising a moiety represented by Chemical Formula 2: wherein, in Chemical Formula 2, R 4 to R 7 are each independently hydrogen, a substituted or unsubstituted C1 to C30 alkyl group, a substituted or unsubstituted C3 to C30 cycloalkyl group, a substituted or unsubstituted C6 to C30 aryl group, a substituted or unsubstituted C7 to C30 arylalkyl group, a substituted or unsubstituted C1 to C30 heteroalkyl group, a substituted or unsubstituted C2 to C30 heterocycloalkyl group, a substituted or unsubstituted C2 to C30 alkenyl group, a substituted or unsubstituted alkoxy group, a carboxyl group, an aldehyde group, a hydroxy group, or a combination thereof, and “*” indicates a linking point. 15 . The device of claim 12 , wherein the solvent comprises at least one selected from trimethylbenzene, triethylbenzene, decahydronaphthalene, tetrahydronaphthalene, indene, diethylbenzene, and methylnaphthalene. 16 . The device of claim 12 ,
Hydrocarbons {(C08K5/0091 takes precedence)} · CPC title
Spin coating · CPC title
in which at least two but not all the silicon atoms are connected by linkages other than oxygen atoms (C09D183/10 takes precedence) · CPC title
in which all the silicon atoms are connected by linkages other than oxygen atoms · CPC title
Nitrogen atoms · CPC title
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