Moisture curable compositions
US-2024400829-A1 · Dec 5, 2024 · US
US9249338B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9249338-B2 |
| Application number | US-201213560714-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jul 27, 2012 |
| Priority date | Jul 27, 2011 |
| Publication date | Feb 2, 2016 |
| Grant date | Feb 2, 2016 |
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Disclosed herein is an anti-fingerprint coating composition, a coating composition for forming thin films that prevents fingerprints adhered to displays or touch panels from being remarkably visible and exhibits superior durability and slip properties, and a method for preparing the same. The anti-fingerprint coating composition is prepared by mixing a silane compound having an alkyl group with distilled water or acid.
Opening claim text (preview).
What is claimed is: 1. A coating composition comprising a silane oligomer having: an R 1 group represented by Formula 1 of [R a O—(CH 2 CH 2 O) p —R b —] wherein R a is selected from the group consisting of hydrogen and an alkyl group having 1 to 3 carbon atoms; R b is selected from the group consisting of an alkyl group having 5 to 20 carbon atoms, an alkenyl group having 5 to 20 carbon atoms, an alkynyl group having 5 to 20 carbon atoms, an aryl group having 5 to 20 carbon atoms, an arylalkyl group having 6 to 20 carbon atoms, a cycloalkyl group having 5 to 20 carbon atoms and a heteroalkyl group having 5 to 20 carbon atoms; and p is an integer of 1 to 12; and an R 2 group represented by Formula 2 of (R c ) q wherein R c is a cycloalkyl group having 3 to 20 carbon atoms; and q is an integer of 1 to 3, wherein at least one reactive group bonded to a silicon of the silane oligomer is substituted by a hydroxyl group (—OH). 2. The coating composition according to claim 1 , wherein the R 1 group is at least one selected from the group consisting of a methoxyethoxyundecyl group, a methoxytriglycoloxy-undecyl group, a 3-methoxyethoxy-4-acetoxycyclohexylethyl group, a 16-(2-methoxy-ethoxy)hexadecyl group and derivatives thereof. 3. The coating composition according to claim 1 , wherein the R 2 group is at least one selected from the group consisting of a 3-cyclopentadienylpropyl group, a dicyclopentyl group, a cyclopentyl group, a cyclohexyl group, a cyclooctyl group and derivatives thereof. 4. The coating composition according to claim 1 , wherein the silane oligomer has a molecular weight of about 100 to about 10000. 5. The coating composition according to claim 1 , wherein the silane oligomer has a structure of Formula 3 below, wherein m and n are each independently integers of 1 to 10. 6. An anti-fingerprint thin film formed by coating the coating composition according to claim 1 on a surface of a substrate. 7. The anti-fingerprint thin film according to claim 6 , wherein the thin film formed using the silane oligomer has a contact angle to water of about 60 to about 80 degrees and a contact angle to diiodomethane of about 0 to about 45 degrees. 8. A coating composition comprising: 45 to 49.5% by weight of a silane compound represented by Formula 1 of [R a O—(CH 2 CH 2 O) p —R b —] wherein R a is selected from the group consisting of hydrogen and an alkyl group having 1 to 3 carbon atoms; R b is selected from the group consisting of an alkyl group having 5 to 20 carbon atoms, an alkenyl group having 5 to 20 carbon atoms, an alkynyl group having 5 to 20 carbon atoms, an aryl group having 5 to 20 carbon atoms, an arylalkyl group having 6 to 20 carbon atoms, a cycloalkyl group having 5 to 20 carbon atoms and a heteroalkyl group having 5 to 20 carbon atoms; and p is an integer of 1 to 12; 45 to 49.5% by weight of the silane compound having an R 2 group represented by Formula 2 of (R c ) q wherein R c is a cycloalkyl group having 3 to 20 carbon atoms; and q is an integer of 1 to 3; and 1 to 10% by weight of H 2 O or acid, wherein at least one reactive group bonded to a silicon of the silane oligomer is substituted by a hydroxyl group (—OH). 9. The coating composition according to claim 8 , wherein Formula 1 is at least one selected from the group consisting of a methoxyethoxyundecyl group, a methoxytriglycoloxy-undecyl group, a 3-methoxyethoxy-4-acetoxycyclohexylethyl group, a 16-(2-methoxy-ethoxy)hexadecyl group and derivatives thereof. 10. The coating composition according to claim 8 , wherein the R 2 group is at least one selected from the group consisting of a 3-cyclopentadienylpropyl group, a dicyclopentyl group, a cyclopentyl group, a cyclohexyl group, a cyclooctyl group and derivatives thereof. 11. The coating composition according to claim 8 , wherein the coating composition has a molecular weight of about 100 to about 10000. 12. An anti-fingerprint thin film formed by coating the coating composition according to claim 8 on a surface of a substrate. 13. The anti-fingerprint thin film according to claim 12 , wherein the anti-fingerprint thin film has a contact angle to water of about 60 to about 80 degrees and a contact angle to diiodomethane of about 0 to about 45 degrees. 14. An electronic product having a display provided with an anti-fingerprint thin film, wherein the anti-fingerprint thin film has a contact angle to water of about 60 to about 80 degrees and a contact angle to diiodomethane of about 0 to about 45 degrees; wherein the anti-fingerprint thin film includes a silane oligomer having: an R 1 group represented by Formula 1 of [R a O—(CH 2 CH 2 O) p —R b —] wherein R a is selected from the group consisting of hydrogen and an alkyl group having 1 to 3 carbon atoms; R b is selected from the group consisting of an alkyl group having 5 to 20 carbon atoms, an alkenyl group having 5 to 20 carbon atoms, an alkynyl group having 5 to 20 carbon atoms, an aryl group having 5 to 20 carbon atoms, an arylalkyl group having 6 to 20 carbon atoms, a cycloalkyl group having 5 to 20 carbon atoms and a heteroalkyl group having 5 to 20 carbon atoms; and p is an integer of 1 to 12; and an R 2 group represented by Formula 2 of (R c ) q wherein R c is a cycloalkyl group having 3 to 20 carbon atoms; and q is an integer of 1 to 3, wherein at least one reactive group bonded to a silicon of the silane oligomer is substituted by a hydroxyl group (—OH). 15. The electronic product according to the claim 14 , wherein the R 1 group is at least one selected from the group consisting of a methoxyethoxyundecyl group, a ethoxytriglycoloxy-undecyl group, a 3-methoxyethoxy-4-acetoxycyclohexylethyl group, a 16-(2-methoxy-ethoxy)hexadecyl group and derivatives thereof. 16. The electronic product according to the claim 14 , wherein the R 2 group is at least one selected from the group consisting of a 3-cyclopentadienylpropyl group, a dicyclopentyl group, a cyclopentyl group, a cyclohexyl group, a cyclooctyl group and derivatives thereof. 17. The electronic product according to the claim 14 , wherein the silane oligomer has a structure of Formula 3 below, wherein m and n are each independently integers of 1 to 10.
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