CS101191A2 - Mixtures containing polyketone polymer - Google Patents

Mixtures containing polyketone polymer Download PDF

Info

Publication number: CS101191A2
Authority: CS; Czechoslovakia
Prior art keywords: polymer; weight; copolymer; optionally; composition
Prior art date: 1990-04-12

Application number

CS911011A

Other languages

Czech (cs)

English (en)

Inventor

Joseph Michael Machado

Original Assignee

Shell Int Research

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1990-04-12

Filing date

1991-04-10

Publication date

1991-11-12

Family has litigation

First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=24020676&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=CS101191(A2) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.

1991-04-10 Application filed by Shell Int Research filed Critical Shell Int Research

1991-11-12 Publication of CS101191A2 publication Critical patent/CS101191A2/cs

Links

229920000642 polymer Polymers 0.000 title claims abstract description 82
239000000203 mixture Substances 0.000 title claims abstract description 69
229920001470 polyketone Polymers 0.000 title claims description 37
229920001971 elastomer Polymers 0.000 claims abstract description 38
239000005060 rubber Substances 0.000 claims abstract description 38
UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 claims abstract description 15
230000002378 acidificating effect Effects 0.000 claims abstract description 15
229910002091 carbon monoxide Inorganic materials 0.000 claims abstract description 15
229930195735 unsaturated hydrocarbon Natural products 0.000 claims abstract description 14
150000001732 carboxylic acid derivatives Chemical class 0.000 claims abstract description 11
229920000578 graft copolymer Polymers 0.000 claims abstract description 9
229920002959 polymer blend Polymers 0.000 claims abstract description 8
239000000178 monomer Substances 0.000 claims description 43
229920001577 copolymer Polymers 0.000 claims description 17
239000000758 substrate Substances 0.000 claims description 16
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 14
229920002554 vinyl polymer Polymers 0.000 claims description 13
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 10
239000005977 Ethylene Substances 0.000 claims description 10
125000004432 carbon atom Chemical group C* 0.000 claims description 10
-1 vinyl nitrile Chemical class 0.000 claims description 10
NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 7
NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 claims description 6
238000006116 polymerization reaction Methods 0.000 claims description 5
LLVWLCAZSOLOTF-UHFFFAOYSA-N 1-methyl-4-[1,4,4-tris(4-methylphenyl)buta-1,3-dienyl]benzene Chemical compound C1=CC(C)=CC=C1C(C=1C=CC(C)=CC=1)=CC=C(C=1C=CC(C)=CC=1)C1=CC=C(C)C=C1 LLVWLCAZSOLOTF-UHFFFAOYSA-N 0.000 claims description 4
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 4
CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 4
VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 claims description 4
239000005062 Polybutadiene Substances 0.000 claims description 4
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 4
229920002857 polybutadiene Polymers 0.000 claims description 4
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 4
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 3
229910052783 alkali metal Inorganic materials 0.000 claims description 3
150000001340 alkali metals Chemical class 0.000 claims description 3
229910052782 aluminium Inorganic materials 0.000 claims description 3
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 3
229910052725 zinc Inorganic materials 0.000 claims description 3
239000011701 zinc Substances 0.000 claims description 3
FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 2
229910052749 magnesium Inorganic materials 0.000 claims description 2
239000011777 magnesium Substances 0.000 claims description 2
229920001195 polyisoprene Polymers 0.000 claims description 2
125000005396 acrylic acid ester group Chemical group 0.000 claims 1
239000004711 α-olefin Substances 0.000 abstract 1
239000003607 modifier Substances 0.000 description 18
238000012360 testing method Methods 0.000 description 18
239000002253 acid Substances 0.000 description 10
239000000463 material Substances 0.000 description 10
238000000034 method Methods 0.000 description 9
229920001897 terpolymer Polymers 0.000 description 9
229910052751 metal Inorganic materials 0.000 description 8
239000002184 metal Substances 0.000 description 8
238000002156 mixing Methods 0.000 description 7
150000002430 hydrocarbons Chemical group 0.000 description 6
RLSSMJSEOOYNOY-UHFFFAOYSA-N m-cresol Chemical compound CC1=CC=CC(O)=C1 RLSSMJSEOOYNOY-UHFFFAOYSA-N 0.000 description 6
238000004519 manufacturing process Methods 0.000 description 6
239000004215 Carbon black (E152) Substances 0.000 description 5
229930195733 hydrocarbon Natural products 0.000 description 5
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 5
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 5
KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 description 4
VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical compound CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 4
KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 4
239000003054 catalyst Substances 0.000 description 4
229910021645 metal ion Inorganic materials 0.000 description 4
238000006386 neutralization reaction Methods 0.000 description 4
229910052698 phosphorus Inorganic materials 0.000 description 4
230000008569 process Effects 0.000 description 4
150000003839 salts Chemical class 0.000 description 4
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 3
150000001450 anions Chemical class 0.000 description 3
239000002585 base Substances 0.000 description 3
239000002274 desiccant Substances 0.000 description 3
239000003446 ligand Substances 0.000 description 3
238000002844 melting Methods 0.000 description 3
230000008018 melting Effects 0.000 description 3
230000004048 modification Effects 0.000 description 3
238000012986 modification Methods 0.000 description 3
125000004437 phosphorous atom Chemical group 0.000 description 3
AFFLGGQVNFXPEV-UHFFFAOYSA-N 1-decene Chemical compound CCCCCCCCC=C AFFLGGQVNFXPEV-UHFFFAOYSA-N 0.000 description 2
CRSBERNSMYQZNG-UHFFFAOYSA-N 1-dodecene Chemical compound CCCCCCCCCCC=C CRSBERNSMYQZNG-UHFFFAOYSA-N 0.000 description 2
LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 2
BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 2
239000000654 additive Substances 0.000 description 2
125000001931 aliphatic group Chemical group 0.000 description 2
125000003118 aryl group Chemical group 0.000 description 2
230000015556 catabolic process Effects 0.000 description 2
150000001875 compounds Chemical class 0.000 description 2
230000007423 decrease Effects 0.000 description 2
238000006731 degradation reaction Methods 0.000 description 2
238000013461 design Methods 0.000 description 2
230000009477 glass transition Effects 0.000 description 2
150000002736 metal compounds Chemical class 0.000 description 2
BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
TVMXDCGIABBOFY-UHFFFAOYSA-N n-Octanol Natural products CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 2
229910052763 palladium Inorganic materials 0.000 description 2
230000000704 physical effect Effects 0.000 description 2
229920005989 resin Polymers 0.000 description 2
239000011347 resin Substances 0.000 description 2
229920003048 styrene butadiene rubber Polymers 0.000 description 2
JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 2
NIONDZDPPYHYKY-SNAWJCMRSA-N (2E)-hexenoic acid Chemical compound CCC\C=C\C(O)=O NIONDZDPPYHYKY-SNAWJCMRSA-N 0.000 description 1
WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 1
BYYLJVQCWRRFMP-UHFFFAOYSA-N 1-ethenyl-3-propan-2-ylbenzene Chemical compound CC(C)C1=CC=CC(C=C)=C1 BYYLJVQCWRRFMP-UHFFFAOYSA-N 0.000 description 1
WHFHDVDXYKOSKI-UHFFFAOYSA-N 1-ethenyl-4-ethylbenzene Chemical compound CCC1=CC=C(C=C)C=C1 WHFHDVDXYKOSKI-UHFFFAOYSA-N 0.000 description 1
ILPBINAXDRFYPL-UHFFFAOYSA-N 2-octene Chemical compound CCCCCC=CC ILPBINAXDRFYPL-UHFFFAOYSA-N 0.000 description 1
LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
SXXPTCXIFIOPQF-UHFFFAOYSA-N 3-bis(2-methoxyphenyl)phosphanylpropyl-bis(2-methoxyphenyl)phosphane Chemical compound COC1=CC=CC=C1P(C=1C(=CC=CC=1)OC)CCCP(C=1C(=CC=CC=1)OC)C1=CC=CC=C1OC SXXPTCXIFIOPQF-UHFFFAOYSA-N 0.000 description 1
OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
JLBJTVDPSNHSKJ-UHFFFAOYSA-N 4-Methylstyrene Chemical compound CC1=CC=C(C=C)C=C1 JLBJTVDPSNHSKJ-UHFFFAOYSA-N 0.000 description 1
QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
229920000089 Cyclic olefin copolymer Polymers 0.000 description 1
JLVVSXFLKOJNIY-UHFFFAOYSA-N Magnesium ion Chemical compound [Mg+2] JLVVSXFLKOJNIY-UHFFFAOYSA-N 0.000 description 1
239000005642 Oleic acid Substances 0.000 description 1
ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
235000021355 Stearic acid Nutrition 0.000 description 1
XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
NIONDZDPPYHYKY-UHFFFAOYSA-N Z-hexenoic acid Natural products CCCC=CC(O)=O NIONDZDPPYHYKY-UHFFFAOYSA-N 0.000 description 1
ZOIORXHNWRGPMV-UHFFFAOYSA-N acetic acid;zinc Chemical compound [Zn].CC(O)=O.CC(O)=O ZOIORXHNWRGPMV-UHFFFAOYSA-N 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 1
239000004676 acrylonitrile butadiene styrene Substances 0.000 description 1
230000009471 action Effects 0.000 description 1
150000001336 alkenes Chemical class 0.000 description 1
229910052787 antimony Inorganic materials 0.000 description 1
WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical group [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 description 1
239000003963 antioxidant agent Substances 0.000 description 1
229910052785 arsenic Inorganic materials 0.000 description 1
RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical group [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 description 1
238000003556 assay Methods 0.000 description 1
235000013361 beverage Nutrition 0.000 description 1
238000012662 bulk polymerization Methods 0.000 description 1
IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 description 1
CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
125000002843 carboxylic acid group Chemical group 0.000 description 1
150000001735 carboxylic acids Chemical class 0.000 description 1
150000001768 cations Chemical class 0.000 description 1
230000008859 change Effects 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
230000015271 coagulation Effects 0.000 description 1
238000005345 coagulation Methods 0.000 description 1
229910017052 cobalt Inorganic materials 0.000 description 1
239000010941 cobalt Substances 0.000 description 1
GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
239000003086 colorant Substances 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
238000004132 cross linking Methods 0.000 description 1
LDHQCZJRKDOVOX-NSCUHMNNSA-N crotonic acid Chemical compound C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 description 1
150000001993 dienes Chemical class 0.000 description 1
229940069096 dodecene Drugs 0.000 description 1
230000000694 effects Effects 0.000 description 1
239000000839 emulsion Substances 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
125000002573 ethenylidene group Chemical group [*]=C=C([H])[H] 0.000 description 1
SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 1
229920006242 ethylene acrylic acid copolymer Polymers 0.000 description 1
229920001038 ethylene copolymer Polymers 0.000 description 1
229920005648 ethylene methacrylic acid copolymer Polymers 0.000 description 1
238000001125 extrusion Methods 0.000 description 1
239000000945 filler Substances 0.000 description 1
239000010408 film Substances 0.000 description 1
239000003063 flame retardant Substances 0.000 description 1
XUCNUKMRBVNAPB-UHFFFAOYSA-N fluoroethene Chemical compound FC=C XUCNUKMRBVNAPB-UHFFFAOYSA-N 0.000 description 1
235000013305 food Nutrition 0.000 description 1
235000019253 formic acid Nutrition 0.000 description 1
238000010528 free radical solution polymerization reaction Methods 0.000 description 1
238000005227 gel permeation chromatography Methods 0.000 description 1
150000008282 halocarbons Chemical class 0.000 description 1
229920001519 homopolymer Polymers 0.000 description 1
239000012433 hydrogen halide Substances 0.000 description 1
229910000039 hydrogen halide Inorganic materials 0.000 description 1
238000002347 injection Methods 0.000 description 1
239000007924 injection Substances 0.000 description 1
238000001746 injection moulding Methods 0.000 description 1
230000003993 interaction Effects 0.000 description 1
229920000554 ionomer Polymers 0.000 description 1
QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
125000000468 ketone group Chemical group 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
238000002372 labelling Methods 0.000 description 1
229910001425 magnesium ion Inorganic materials 0.000 description 1
239000011159 matrix material Substances 0.000 description 1
DEAKWVKQKRNPHF-UHFFFAOYSA-N methyl 2-methylprop-2-enoate;prop-2-enenitrile;styrene Chemical compound C=CC#N.COC(=O)C(C)=C.C=CC1=CC=CC=C1 DEAKWVKQKRNPHF-UHFFFAOYSA-N 0.000 description 1
229910052759 nickel Inorganic materials 0.000 description 1
125000002560 nitrile group Chemical group 0.000 description 1
150000002825 nitriles Chemical class 0.000 description 1
QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
150000002941 palladium compounds Chemical class 0.000 description 1
YJVFFLUZDVXJQI-UHFFFAOYSA-L palladium(ii) acetate Chemical compound [Pd+2].CC([O-])=O.CC([O-])=O YJVFFLUZDVXJQI-UHFFFAOYSA-L 0.000 description 1
230000000737 periodic effect Effects 0.000 description 1
230000010399 physical interaction Effects 0.000 description 1
229920003023 plastic Polymers 0.000 description 1
239000004033 plastic Substances 0.000 description 1
SCUZVMOVTVSBLE-UHFFFAOYSA-N prop-2-enenitrile;styrene Chemical compound C=CC#N.C=CC1=CC=CC=C1 SCUZVMOVTVSBLE-UHFFFAOYSA-N 0.000 description 1
230000035939 shock Effects 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
239000007858 starting material Substances 0.000 description 1
239000008117 stearic acid Substances 0.000 description 1
229920000638 styrene acrylonitrile Polymers 0.000 description 1
239000000725 suspension Substances 0.000 description 1
229920001169 thermoplastic Polymers 0.000 description 1
229920002725 thermoplastic elastomer Polymers 0.000 description 1
239000004416 thermosoftening plastic Substances 0.000 description 1
LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
238000009827 uniform distribution Methods 0.000 description 1
238000011144 upstream manufacturing Methods 0.000 description 1
238000004073 vulcanization Methods 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
150000003751 zinc Chemical class 0.000 description 1
239000004246 zinc acetate Substances 0.000 description 1
239000011592 zinc chloride Substances 0.000 description 1
235000005074 zinc chloride Nutrition 0.000 description 1
150000003752 zinc compounds Chemical class 0.000 description 1
SRWMQSFFRFWREA-UHFFFAOYSA-M zinc formate Chemical compound [Zn+2].[O-]C=O SRWMQSFFRFWREA-UHFFFAOYSA-M 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F210/00—Copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
- C08F210/02—Ethene
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L73/00—Compositions of macromolecular compounds obtained by reactions forming a linkage containing oxygen or oxygen and carbon in the main chain, not provided for in groups C08L59/00 - C08L71/00; Compositions of derivatives of such polymers
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G67/00—Macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing oxygen or oxygen and carbon, not provided for in groups C08G2/00 - C08G65/00
- C08G67/02—Copolymers of carbon monoxide and aliphatic unsaturated compounds
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L55/00—Compositions of homopolymers or copolymers, obtained by polymerisation reactions only involving carbon-to-carbon unsaturated bonds, not provided for in groups C08L23/00 - C08L53/00
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S525/00—Synthetic resins or natural rubbers -- part of the class 520 series
- Y10S525/942—Polymer derived from nitrile, conjugated diene and aromatic co-monomers

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Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
Compositions Of Macromolecular Compounds (AREA)
Polyethers (AREA)
External Artificial Organs (AREA)
Professional, Industrial, Or Sporting Protective Garments (AREA)
Orthopedics, Nursing, And Contraception (AREA)
Materials For Medical Uses (AREA)
Gloves (AREA)
Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

CS911011A 1990-04-12 1991-04-10 Mixtures containing polyketone polymer CS101191A2 (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US07/507,925 US5162432A (en)	1990-04-12	1990-04-12	Polyketone polymer blends

Publications (1)

Publication Number	Publication Date
CS101191A2 true CS101191A2 (en)	1991-11-12

Family

ID=24020676

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CS911011A CS101191A2 (en)	1990-04-12	1991-04-10	Mixtures containing polyketone polymer

Country Status (16)

Country	Link
US (1)	US5162432A (de)
EP (1)	EP0451918B1 (de)
JP (1)	JP3059532B2 (de)
KR (1)	KR910018424A (de)
CN (1)	CN1055750A (de)
AT (1)	ATE140254T1 (de)
AU (1)	AU644640B2 (de)
BR (1)	BR9101442A (de)
CA (1)	CA2040203A1 (de)
CS (1)	CS101191A2 (de)
DE (1)	DE69120713T2 (de)
FI (1)	FI911717L (de)
HU (1)	HUT58356A (de)
NO (1)	NO911392L (de)
PL (1)	PL289813A1 (de)
PT (1)	PT97307B (de)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
AU7543698A (en) *	1997-05-29	1998-12-30	Bp Chemicals Limited	Toughened polyketone composition
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- 1991-04-09 KR KR1019910005683A patent/KR910018424A/ko not_active Withdrawn
- 1991-04-09 AT AT91200824T patent/ATE140254T1/de not_active IP Right Cessation
- 1991-04-09 DE DE69120713T patent/DE69120713T2/de not_active Expired - Fee Related
- 1991-04-10 BR BR919101442A patent/BR9101442A/pt unknown
- 1991-04-10 PT PT97307A patent/PT97307B/pt not_active IP Right Cessation
- 1991-04-10 JP JP3166928A patent/JP3059532B2/ja not_active Expired - Lifetime
- 1991-04-10 FI FI911717A patent/FI911717L/fi unknown
- 1991-04-10 NO NO91911392A patent/NO911392L/no unknown
- 1991-04-10 CN CN91102286A patent/CN1055750A/zh active Pending
- 1991-04-10 PL PL28981391A patent/PL289813A1/xx unknown
- 1991-04-10 AU AU74336/91A patent/AU644640B2/en not_active Ceased
- 1991-04-10 HU HU911159A patent/HUT58356A/hu unknown
- 1991-04-10 CS CS911011A patent/CS101191A2/cs unknown
- 1991-04-10 CA CA002040203A patent/CA2040203A1/en not_active Abandoned

Also Published As

Publication number	Publication date
NO911392D0 (no)	1991-04-10
AU7433691A (en)	1991-10-17
EP0451918A3 (en)	1992-11-25
PL289813A1 (en)	1991-10-21
EP0451918A2 (de)	1991-10-16
FI911717A7 (fi)	1991-10-13
PT97307A (pt)	1992-01-31
PT97307B (pt)	1999-12-31
FI911717A0 (fi)	1991-04-10
BR9101442A (pt)	1991-11-26
KR910018424A (ko)	1991-11-30
US5162432A (en)	1992-11-10
NO911392L (no)	1991-10-14
JP3059532B2 (ja)	2000-07-04
DE69120713T2 (de)	1997-02-13
DE69120713D1 (de)	1996-08-14
JPH06228430A (ja)	1994-08-16
FI911717L (fi)	1991-10-13
HUT58356A (en)	1992-02-28
AU644640B2 (en)	1993-12-16
CA2040203A1 (en)	1991-10-13
ATE140254T1 (de)	1996-07-15
EP0451918B1 (de)	1996-07-10
CN1055750A (zh)	1991-10-30
HU911159D0 (en)	1991-10-28

Publication	Publication Date	Title
KR101098242B1 (ko)	2011-12-23	폴리케톤 블렌드 및 그 제조방법
CS101191A2 (en)	1991-11-12	Mixtures containing polyketone polymer
JPH06505521A (ja)	1994-06-23	ナイロンを含んで成る可撓性の熱可塑性組成物
CA1283233C (en)	1991-04-16	Polymer blends containing a polymer having pendant oxazoline groups
US5160475A (en)	1992-11-03	Method of producing shaped articles having excellent impact resistance
JP3015108B2 (ja)	2000-03-06	ポリケトンポリマー組成物
JPH05500980A (ja)	1993-02-25	ポリオレフィン／サーモプラスチック配合物
EP0457374A2 (de)	1991-11-21	Polyketon/Polymermischungen, die ein lineares alternierendes Polymer aus Kohlenmonoxid und einer ethylenisch ungesättigten Verbindung enthalten
JPH07216178A (ja)	1995-08-15	熱可塑性樹脂組成物
JPH0543798A (ja)	1993-02-23	ポリアミド・ポリオレフイン樹脂組成物
JPH04249579A (ja)	1992-09-04	ポリケトンポリマー組成物
KR20170041988A (ko)	2017-04-18	젤화 억제 열가소성 폴리케톤 수지 조성물
JPH11315184A (ja)	1999-11-16	ビニル芳香族／ケトンポリマ―組成物
JPS5820980B2 (ja)	1983-04-26	ポリアミド樹脂組成物
JPS59164359A (ja)	1984-09-17	耐衝撃性ポリアミドの製法
CA2035571A1 (en)	1991-08-02	Method of production shaped articles having excellent impact resistance
JPS58198501A (ja)	1983-11-18	変性ポリオレフイン架橋物の製造方法
JPH0543796A (ja)	1993-02-23	ポリアミド・ポリオレフイン樹脂組成物
USH1403H (en)	1995-01-03	Polyketone polymer blends
JP3135408B2 (ja)	2001-02-13	ポリアセタール樹脂組成物
JP2872779B2 (ja)	1999-03-24	熱可塑性樹脂組成物
CA2019459A1 (en)	1990-12-29	Agent for making abs resin and polyolefin compatible, and abs resin-polyolefin thermoplastic resin composition
JPS6156249B2 (de)	1986-12-01
JPH0333158A (ja)	1991-02-13	Ａｂｓ樹脂―ポリアミド用相溶化剤および該相溶化剤を含有してなる熱可塑樹脂組成物
JPS629618B2 (de)	1987-03-02