Oligomer, composition and composite material employing the same
US-2018171068-A1 · Jun 21, 2018 · US
US11059938B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11059938-B2 |
| Application number | US-201916593320-A |
| Country | US |
| Kind code | B2 |
| Filing date | Oct 4, 2019 |
| Priority date | Oct 5, 2018 |
| Publication date | Jul 13, 2021 |
| Grant date | Jul 13, 2021 |
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.
The disclosure provides a film composition, wherein the film composition includes an oligomer and a crosslinking agent. The oligomer can have a structure represented by Formula (I) wherein R 1 and R 2 are independently hydrogen, C 1-20 alkyl group, C 2-20 alkenyl group, C 6-12 aryl group, C 6-12 alkylaryl group, C 5-12 cycloalkyl group, C 6-20 cycloalkylalkyl group, alkoxycarbonyl group, or alkylcarbonyloxy group; R 1 is not hydrogen when R 2 is hydrogen; a is 0 or 1; 100≥n≥1; 100≥m≥1; and when n is not 0, the ratio of n to m is from 3:1 to 1:4. The weight ratio of the oligomer and the crosslinking agent can be from 9:1 to 3:7. The oligomer has a number average molecular weight (Mn) from 1,000 to 8,000.
Opening claim text (preview).
What is claimed is: 1. A film composition, comprising: a crosslinking agent; and an oligomer, wherein the weight ratio of the oligomer to the crosslinking agent is from 9:1 to 3:7, wherein the crosslinking agent is a compound having at least two crosslinkable functional groups or a bismaleimide, wherein the crosslinkable functional group is alkenyl group, methacrylate group, acrylate group, acryloyl group, epoxy group, carboxyl group, or a combination thereof, wherein the oligomer has a number average molecular weight (Mn) from 1,000 to 8,000, wherein the oligomer has a structure represented by Formula (I) wherein R 1 and R 2 are independently hydrogen, C 1-20 alkyl group, C 2-20 alkenyl group, C 6-12 aryl group, C 6-12 alkylaryl group, C 5-12 cycloalkyl group, C 6-20 cycloalkylalkyl group, alkoxycarbonyl group, or alkylcarbonyloxy group; R 1 is not hydrogen when R 2 is hydrogen; a is 0 or 1; n≥0; m≥1, and when n is not 0, the ratio of n to m is from 3:1 to 1:4; and the repeat unit and the repeat unit are arranged in a random or block fashion. 2. The film composition as claimed in claim 1 , wherein R 1 and R 2 are independently hydrogen, or wherein b is 0, or an integer from 1 to 19; and, R 1 is not hydrogen when R 2 is hydrogen. 3. The film composition as claimed in claim 1 , wherein R 1 and R 2 are independently hydrogen, or wherein c is 0, or an integer from 1 to 6; and, R 1 is not hydrogen when R 2 is hydrogen. 4. The film composition as claimed in claim 1 , wherein R 1 and R 2 are independently hydrogen, or and wherein d is 0, or an integer from 1 to 6; and, R 1 is not hydrogen when R 2 is hydrogen. 5. The film composition as claimed in claim 1 , wherein R 1 and R 2 are independently hydrogen, or wherein e is 0, or an integer from 1 to 6; and, R 1 is not hydrogen when R 2 is hydrogen. 6. The film composition as claimed in claim 1 , wherein R 1 and R 2 are independently hydrogen, or and wherein f is 0, or an integer from 1 to 6; R 3 is C 1-6 alkyl group; and, R 1 is not hydrogen when R 2 is hydrogen. 7. The film composition as claimed in claim 1 , wherein R 1 and R 2 are independently hydrogen, or and wherein g is 0, or an integer from 1 to 6; R 4 is C 1-6 alkyl group; and, R 1 is not hydrogen when R 2 is hydrogen. 8. The film composition as claimed in claim 1 , wherein R 1 and R 2 are independently hydrogen, or wherein h is an integer from 1 to 6; and, R 1 is not hydrogen when R 2 is hydrogen. 9. The film composition as claimed in claim 1 , wherein R 1 and R 2 are independently hydrogen, or wherein i is 0 or an integer from 1 to 6; and, R 1 is not hydrogen when R 2 is hydrogen. 10. The film composition as claimed in claim 1 , wherein R 1 and R 2 are independently hydrogen, or wherein j is 0 or an integer from 1 to 6; and, R 1 is not hydrogen when R 2 is hydrogen. 11. The film composition as claimed in claim 1 , further comprising a solvent, wherein the ratio of the weight of the solvent to the total weight of the oligomer and the crosslinking agent is from 0.01 to 60. 12. The film composition as claimed in claim 1 , wherein the crosslinking agent is a bismaleimide having a structure represented by Formula (II) or Formula (III) wherein R 5 is —CR 2 —, —NR—, —C(O)CH 2 —, —CH 2 OCH 2 —, —C(O)—, —O—, —O—O—, —S—, —S—S—, —S(O)—, —CH 2 S(O)CH 2 —, —(O)S(O)—, —C 6 R 4 —, —CH 2 (C 6 R 4 )CH 2 —, —CH 2 (C 6 R 4 )(O)—, or substituted phenylene or substituted diphenylene; R 6 is —CR 2 —, —C(O)—, —O—, —O—O—, —S—, —S—S—, —(O)S(O)— or —S(O)—; and R is independently hydrogen or C 1-4 alkyl group. 13. The film composition as claimed in claim 1 , wherein the crosslinking agent is N′-bismaleimide-4,4′-diphenylmethane, 1,1′-(methylenedi-4,1-phenylene)bismaleimide, N,N′-(1,1′-biphenyl-4,4′-diyl) bismaleimide, N,N′-(4-methyl-1,3-phenylene)bismaleimide, 1,1′-(3,3′ dimethyl-1,1′-biphenyl-4,4′-diyl)bismaleimide, N,N′-ethylenedimaleimide, N,N′-(1,2-phenylene)dimaleimide, N,N′-(1,3-phenylene)dimaleimide, N,N′-thiodimaleimide, N,N′-dithiodimaleimide, N,N′-ketonedimaleimide, N,N′-methylene-bis-maleinimide, bis-maleinimidomethyl-ether, 1,2-bis-(maleimido)-1,2-ethandiol, N,N′-4,4′-diphenylether-bis-maleimid, or 4,4′-bis(maleimido)-diphenylsulfone. 14. A film, which is a cured product of the film composition as claimed in claim 1 .
of carbocyclic compounds containing one or more carbon-to-carbon double bonds in the ring · CPC title
Compositions of macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain (C08L7/00 - C08L57/00, C08L61/00 take precedence); Compositions of derivatives of such polymers · CPC title
used for films · CPC title
containing carboxy groups (COOH) and/or -C(=O)O-moieties · CPC title
Saturated aliphatic units · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.