Poly aryl ether ketone polymer blends
US-8945694-B2 · Feb 3, 2015 · US
US9102792B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9102792-B2 |
| Application number | US-201414183834-A |
| Country | US |
| Kind code | B2 |
| Filing date | Feb 19, 2014 |
| Priority date | Feb 22, 2013 |
| Publication date | Aug 11, 2015 |
| Grant date | Aug 11, 2015 |
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A polymer composition that contains at least one high performance polymer and at least one aromatic amide oligomer is provided. The oligomer can serve as a flow aid that lowers the overall viscosity of the polymer matrix under shear.
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What is claimed is: 1. A polymer composition comprising a high performance polymer having a glass transition temperature of about 100° C. or more and an aromatic amide oligomer having the following general formula (I): wherein, ring B is a 6-membered aromatic ring wherein 1 to 3 ring carbon atoms are optionally replaced by nitrogen or oxygen, wherein each nitrogen is optionally oxidized, and wherein ring B may be optionally fused or linked to a 5- or 6-membered aryl, heteroaryl, cycloalkyl, or heterocyclyl; R 5 is halo, haloalkyl, alkyl, alkenyl, aryl, heteroaryl, cycloalkyl, or heterocyclyl; m is from 0 to 4; X 1 and X 2 are independently C(O)HN or NHC(O); and R 1 and R 2 are independently selected from aryl, heteroaryl, cycloalkyl, and heterocyclyl, wherein the high performance polymer is a polyetherimide. 2. The polymer composition of claim 1 , wherein the aromatic amide oligomer has a molecular weight of about 2,000 grams per mole or less. 3. The polymer composition of claim 1 , wherein ring B is phenyl. 4. The polymer composition of claim 1 , wherein the aromatic amide oligomer has the following general formula (II): wherein, X 1 and X 2 are independently C(O)HN or NHC(O); R 5 , R 8 , and R 9 are independently selected from halo, haloalkyl, alkyl, alkenyl, alkynyl, aryl, heteroaryl, cycloalkyl, and heterocyclyl; m is from 0 to 4; and q and r are independently from 0 to 5. 5. The polymer composition of claim 4 , wherein m, q, and r are 0. 6. The polymer composition of claim 4 , wherein R 8 and R 9 are phenyl substituted with —C(O)HN— or —NHC(O)—. 7. The polymer composition of claim 1 , wherein the oligomer is selected from the group consisting of the following compounds and combinations thereof: Structure Name N1,N4- diphenylterephthalamide N1,N4- diphenylisophthalamide N1,N4-bis(2,3,4,5,6- pentafluorophenyl)- terephthalamide N1,N4-bis(4- benzamidophenyl) terephthalamide N4-phenyl-N1-[4-[[4- (phenylcarbamoyl) benzoyl]amino]phenyl] terephthalamide N4-phenyl-N1-[3-[[4- (phenylcarbamoyl) benzoyl]amino]phenyl] terephthalamide N1,N3-bis(4- benzamidophenyl) benzene-1,3- dicarboxamide N3-phenyl-N1-[3-[[3- (phenylcarbamoyl) benzoyl]amino]phenyl] benzene-1,3- dicarboxamide N1,N3-bis(3- benzamidophenyl) benzene-1,3- dicarboxamide N1,N4-bis(4-pyridyl) terephthalamide N1,N3-bis(4- phenylphenyl)benzene- 1,3-dicarboxamide N1,N3,N5- triphenylbenzene- 1,3,5-tricarboxamide N-(4,6-dibenzamido- 1,3,5-triazin-2- yl)benzamide N2,N7- dicyclohexylnaphthalene- 2,7-dicarboxamide N2,N6- dicyclohexylnaphthalene- 2,6-dicarboxamide N1,N3-dicyclohexyl-1,3- Benzenedicarboxamide
linked by a chain containing carbon and nitrogen atoms as chain links, e.g. Schiff bases · CPC title
Polyimides; Polyester-imides; Polyamide-imides; Polyamide acids or similar polyimide precursors · CPC title
in which at least two rings are linked by a chain containing nitrogen atoms · CPC title
Polymers modified by chemical after-treatment · CPC title
Additives having no specific mesophase {characterised by their chemical composition} · CPC title
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