NL1020366C2 - Polymeersamenstelling met verbeterde temperatuurbestendigheid. - Google Patents
Polymeersamenstelling met verbeterde temperatuurbestendigheid. Download PDFInfo
- Publication number
- NL1020366C2 NL1020366C2 NL1020366A NL1020366A NL1020366C2 NL 1020366 C2 NL1020366 C2 NL 1020366C2 NL 1020366 A NL1020366 A NL 1020366A NL 1020366 A NL1020366 A NL 1020366A NL 1020366 C2 NL1020366 C2 NL 1020366C2
- Authority
- NL
- Netherlands
- Prior art keywords
- polymer
- grafted
- ethylenically unsaturated
- polyolefin
- reactive
- Prior art date
Links
- 229920000642 polymer Polymers 0.000 title claims abstract description 67
- 239000000203 mixture Substances 0.000 title claims abstract description 54
- 150000001875 compounds Chemical class 0.000 claims abstract description 39
- 229920005601 base polymer Polymers 0.000 claims abstract description 35
- 229920000098 polyolefin Polymers 0.000 claims abstract description 30
- 229920001169 thermoplastic Polymers 0.000 claims abstract description 30
- 125000000524 functional group Chemical group 0.000 claims abstract description 24
- 238000000034 method Methods 0.000 claims abstract description 15
- 229920001112 grafted polyolefin Polymers 0.000 claims abstract description 14
- 229920013730 reactive polymer Polymers 0.000 claims description 21
- -1 polyethylene Polymers 0.000 claims description 11
- 229920000573 polyethylene Polymers 0.000 claims description 7
- 229920000034 Plastomer Polymers 0.000 claims description 6
- 239000004952 Polyamide Substances 0.000 claims description 3
- 229920002647 polyamide Polymers 0.000 claims description 3
- 239000004698 Polyethylene Substances 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 claims description 2
- 229920002397 thermoplastic olefin Polymers 0.000 claims 1
- 239000003054 catalyst Substances 0.000 abstract description 6
- 238000002360 preparation method Methods 0.000 abstract description 2
- 238000002844 melting Methods 0.000 description 17
- 230000008018 melting Effects 0.000 description 17
- 238000002156 mixing Methods 0.000 description 10
- 239000000155 melt Substances 0.000 description 8
- 238000012360 testing method Methods 0.000 description 8
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 7
- 239000005977 Ethylene Substances 0.000 description 7
- 239000007795 chemical reaction product Substances 0.000 description 7
- 229920001577 copolymer Polymers 0.000 description 7
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
- 239000000654 additive Substances 0.000 description 6
- 235000019441 ethanol Nutrition 0.000 description 6
- 239000004593 Epoxy Substances 0.000 description 5
- 150000001735 carboxylic acids Chemical class 0.000 description 5
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 4
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 4
- KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 description 4
- 150000008064 anhydrides Chemical class 0.000 description 4
- 239000000178 monomer Substances 0.000 description 4
- 229920001155 polypropylene Polymers 0.000 description 4
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 3
- QQONPFPTGQHPMA-UHFFFAOYSA-N Propene Chemical compound CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 3
- 125000003158 alcohol group Chemical group 0.000 description 3
- 150000001298 alcohols Chemical class 0.000 description 3
- 150000001412 amines Chemical group 0.000 description 3
- 230000008859 change Effects 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 229910052736 halogen Inorganic materials 0.000 description 3
- 150000002367 halogens Chemical class 0.000 description 3
- 229920001519 homopolymer Polymers 0.000 description 3
- 230000008569 process Effects 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 2
- 125000003504 2-oxazolinyl group Chemical class O1C(=NCC1)* 0.000 description 2
- WSSSPWUEQFSQQG-UHFFFAOYSA-N 4-methyl-1-pentene Chemical compound CC(C)CC=C WSSSPWUEQFSQQG-UHFFFAOYSA-N 0.000 description 2
- 229920013339 Akulon® K122 Polymers 0.000 description 2
- VVJKKWFAADXIJK-UHFFFAOYSA-N Allylamine Chemical compound NCC=C VVJKKWFAADXIJK-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical compound CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 2
- 239000006057 Non-nutritive feed additive Substances 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- 125000003277 amino group Chemical group 0.000 description 2
- 229920006125 amorphous polymer Polymers 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 239000000975 dye Substances 0.000 description 2
- 238000001125 extrusion Methods 0.000 description 2
- 230000002349 favourable effect Effects 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 239000003063 flame retardant Substances 0.000 description 2
- 230000009477 glass transition Effects 0.000 description 2
- 229920000578 graft copolymer Polymers 0.000 description 2
- 229920001903 high density polyethylene Polymers 0.000 description 2
- 239000004700 high-density polyethylene Substances 0.000 description 2
- 229920001684 low density polyethylene Polymers 0.000 description 2
- 239000004702 low-density polyethylene Substances 0.000 description 2
- RLSSMJSEOOYNOY-UHFFFAOYSA-N m-cresol Chemical compound CC1=CC=CC(O)=C1 RLSSMJSEOOYNOY-UHFFFAOYSA-N 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
- 229920001707 polybutylene terephthalate Polymers 0.000 description 2
- 239000004417 polycarbonate Substances 0.000 description 2
- 229920000515 polycarbonate Polymers 0.000 description 2
- 229920000139 polyethylene terephthalate Polymers 0.000 description 2
- 239000005020 polyethylene terephthalate Substances 0.000 description 2
- 239000012783 reinforcing fiber Substances 0.000 description 2
- 229920006126 semicrystalline polymer Polymers 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- 125000000101 thioether group Chemical group 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- WBYWAXJHAXSJNI-VOTSOKGWSA-M .beta-Phenylacrylic acid Natural products [O-]C(=O)\C=C\C1=CC=CC=C1 WBYWAXJHAXSJNI-VOTSOKGWSA-M 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- YYPNJNDODFVZLE-UHFFFAOYSA-N 3-methylbut-2-enoic acid Chemical compound CC(C)=CC(O)=O YYPNJNDODFVZLE-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
- JRXNBYBCTNEZQY-UHFFFAOYSA-N 4-amino-2-methylidene-4-oxobutanoic acid Chemical compound NC(=O)CC(=C)C(O)=O JRXNBYBCTNEZQY-UHFFFAOYSA-N 0.000 description 1
- QISOBCMNUJQOJU-UHFFFAOYSA-N 4-bromo-1h-pyrazole-5-carboxylic acid Chemical compound OC(=O)C=1NN=CC=1Br QISOBCMNUJQOJU-UHFFFAOYSA-N 0.000 description 1
- 229920006045 Akulon® Polymers 0.000 description 1
- WBYWAXJHAXSJNI-SREVYHEPSA-N Cinnamic acid Chemical compound OC(=O)\C=C/C1=CC=CC=C1 WBYWAXJHAXSJNI-SREVYHEPSA-N 0.000 description 1
- 241001448862 Croton Species 0.000 description 1
- 229920000219 Ethylene vinyl alcohol Polymers 0.000 description 1
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Natural products OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 1
- 229920010126 Linear Low Density Polyethylene (LLDPE) Polymers 0.000 description 1
- 229920002292 Nylon 6 Polymers 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 239000004708 Very-low-density polyethylene Substances 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical class C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 125000005233 alkylalcohol group Chemical group 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 150000005840 aryl radicals Chemical class 0.000 description 1
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 1
- 125000004369 butenyl group Chemical group C(=CCC)* 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 229930016911 cinnamic acid Natural products 0.000 description 1
- 235000013985 cinnamic acid Nutrition 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000007796 conventional method 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
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical class C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000003623 enhancer Substances 0.000 description 1
- 125000003700 epoxy group Chemical group 0.000 description 1
- JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 description 1
- 239000004715 ethylene vinyl alcohol Substances 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 1
- VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical compound CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-UHFFFAOYSA-N 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- RUDVQBCFUZDOTA-UHFFFAOYSA-N hex-1-en-1-amine Chemical compound CCCCC=CN RUDVQBCFUZDOTA-UHFFFAOYSA-N 0.000 description 1
- RZXDTJIXPSCHCI-UHFFFAOYSA-N hexa-1,5-diene-2,5-diol Chemical compound OC(=C)CCC(O)=C RZXDTJIXPSCHCI-UHFFFAOYSA-N 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 125000004356 hydroxy functional group Chemical group O* 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 239000011261 inert gas Substances 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
- 230000002427 irreversible effect Effects 0.000 description 1
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 1
- 238000005304 joining Methods 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000012968 metallocene catalyst Substances 0.000 description 1
- WBYWAXJHAXSJNI-UHFFFAOYSA-N methyl p-hydroxycinnamate Natural products OC(=O)C=CC1=CC=CC=C1 WBYWAXJHAXSJNI-UHFFFAOYSA-N 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- RZAMBPVOOSUBJW-UHFFFAOYSA-N n-ethyl-n-prop-1-en-2-ylaniline Chemical compound CCN(C(C)=C)C1=CC=CC=C1 RZAMBPVOOSUBJW-UHFFFAOYSA-N 0.000 description 1
- 238000010899 nucleation Methods 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 125000002255 pentenyl group Chemical group C(=CCCC)* 0.000 description 1
- 238000005191 phase separation Methods 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 229920005606 polypropylene copolymer Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 238000012545 processing Methods 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
- 125000004368 propenyl group Chemical group C(=CC)* 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 229920006114 semi-crystalline semi-aromatic polyamide Polymers 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000008247 solid mixture Substances 0.000 description 1
- 229920000638 styrene acrylonitrile Polymers 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 229920000468 styrene butadiene styrene block copolymer Polymers 0.000 description 1
- 229920001935 styrene-ethylene-butadiene-styrene 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
- 238000011144 upstream manufacturing Methods 0.000 description 1
- 229920001866 very low density polyethylene Polymers 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
Classifications
-
- 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
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/04—Homopolymers or copolymers of ethene
- C08L23/08—Copolymers of ethene
- C08L23/0807—Copolymers of ethene with unsaturated hydrocarbons only containing four or more carbon atoms
- C08L23/0815—Copolymers of ethene with unsaturated hydrocarbons only containing four or more carbon atoms with aliphatic 1-olefins containing one carbon-to-carbon double bond
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2314/00—Polymer mixtures characterised by way of preparation
- C08L2314/06—Metallocene or single site catalysts
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L51/00—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
- C08L51/06—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers grafted on to homopolymers or copolymers of aliphatic hydrocarbons containing only one carbon-to-carbon double bond
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L77/00—Compositions of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Compositions of derivatives of such polymers
Landscapes
- 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)
- Other Resins Obtained By Reactions Not Involving Carbon-To-Carbon Unsaturated Bonds (AREA)
Priority Applications (11)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| NL1020366A NL1020366C2 (nl) | 2002-04-11 | 2002-04-11 | Polymeersamenstelling met verbeterde temperatuurbestendigheid. |
| JP2003584167A JP2005522550A (ja) | 2002-04-11 | 2003-04-07 | 改善された温度耐性を有するポリマー組成物 |
| ES03723501T ES2263969T3 (es) | 2002-04-11 | 2003-04-07 | Composicion de polimero con resistencia mejorada a la temperatura. |
| AT03723501T ATE330994T1 (de) | 2002-04-11 | 2003-04-07 | Polymerzusammensetzung mit verbesserter temperaturbeständigkeit |
| AU2003230446A AU2003230446A1 (en) | 2002-04-11 | 2003-04-07 | Polymer composition with improved temperature resistance |
| DE60306351T DE60306351T2 (de) | 2002-04-11 | 2003-04-07 | Polymerzusammensetzung mit verbesserter temperaturbeständigkeit |
| CNB038080524A CN1297603C (zh) | 2002-04-11 | 2003-04-07 | 有改善耐温性的聚合物组合物 |
| EP03723501A EP1492843B1 (en) | 2002-04-11 | 2003-04-07 | Polymer composition with improved temperature resistance |
| PCT/NL2003/000259 WO2003087216A1 (en) | 2002-04-11 | 2003-04-07 | Polymer composition with improved temperature resistance |
| US10/510,598 US20050222328A1 (en) | 2002-04-11 | 2003-04-07 | Polymer composition with improved temperature resistance |
| TW092108457A TWI288156B (en) | 2002-04-11 | 2003-04-11 | Polymer composition with improved temperature resistance |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| NL1020366 | 2002-04-11 | ||
| NL1020366A NL1020366C2 (nl) | 2002-04-11 | 2002-04-11 | Polymeersamenstelling met verbeterde temperatuurbestendigheid. |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NL1020366C2 true NL1020366C2 (nl) | 2003-10-14 |
Family
ID=29244978
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NL1020366A NL1020366C2 (nl) | 2002-04-11 | 2002-04-11 | Polymeersamenstelling met verbeterde temperatuurbestendigheid. |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US20050222328A1 (https=) |
| EP (1) | EP1492843B1 (https=) |
| JP (1) | JP2005522550A (https=) |
| CN (1) | CN1297603C (https=) |
| AT (1) | ATE330994T1 (https=) |
| AU (1) | AU2003230446A1 (https=) |
| DE (1) | DE60306351T2 (https=) |
| ES (1) | ES2263969T3 (https=) |
| NL (1) | NL1020366C2 (https=) |
| TW (1) | TWI288156B (https=) |
| WO (1) | WO2003087216A1 (https=) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103013108A (zh) * | 2012-11-25 | 2013-04-03 | 安徽六方重联机械股份有限公司 | 一种含有尼龙pa66的包装用塑料薄膜 |
| CN103044909A (zh) * | 2012-11-25 | 2013-04-17 | 安徽六方重联机械股份有限公司 | 一种含有尼龙pa6的包装用塑料基材薄膜 |
| FR3016167B1 (fr) * | 2014-01-03 | 2017-05-19 | Arkema France | Composition thermoplastique a base de polypropylene et de polyolefine greffee polyamide |
| EP4055216B1 (en) | 2019-11-04 | 2024-08-14 | Avient Protective Materials B.V. | Polymer filled polyolefin fiber |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1993025617A2 (en) * | 1992-06-05 | 1993-12-23 | The Dow Chemical Company | Paintable polyethylenes |
| WO1997012919A1 (en) * | 1995-10-06 | 1997-04-10 | The Dow Chemical Company | Branched block ethylene polymers, their preparation and compositions comprising the same |
| EP0866081A1 (en) * | 1995-12-08 | 1998-09-23 | Kaneka Corporation | Grafted polyolefin resin and thermoplastic resin composition containing the same |
| US5849844A (en) * | 1993-12-22 | 1998-12-15 | Borealis A/S | Polyolefin-condensation polymer blend |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DD20232A (https=) * | 1957-01-09 | 1900-01-01 | ||
| US4950541A (en) * | 1984-08-15 | 1990-08-21 | The Dow Chemical Company | Maleic anhydride grafts of olefin polymers |
| US5225483A (en) * | 1991-07-22 | 1993-07-06 | Exxon Chemical Patents Inc. | Thermoplastic composition of polypropylene and styrene copolymer resins |
| AU7309096A (en) * | 1995-10-27 | 1997-05-15 | Elf Atochem S.A. | Mixture of polyolefin and polyamide alloy, and fabrication process |
| EP1057870A1 (fr) * | 1999-06-02 | 2000-12-06 | Atofina | Compositions à base de polyoléfine et de polyamide à bas point de fusion |
| NL1012324C2 (nl) * | 1999-06-14 | 2000-12-15 | Dsm Nv | Werkwijze voor de bereiding van een slagvaste polymeer samenstellling. |
-
2002
- 2002-04-11 NL NL1020366A patent/NL1020366C2/nl not_active IP Right Cessation
-
2003
- 2003-04-07 JP JP2003584167A patent/JP2005522550A/ja not_active Withdrawn
- 2003-04-07 DE DE60306351T patent/DE60306351T2/de not_active Expired - Fee Related
- 2003-04-07 AT AT03723501T patent/ATE330994T1/de not_active IP Right Cessation
- 2003-04-07 AU AU2003230446A patent/AU2003230446A1/en not_active Abandoned
- 2003-04-07 ES ES03723501T patent/ES2263969T3/es not_active Expired - Lifetime
- 2003-04-07 WO PCT/NL2003/000259 patent/WO2003087216A1/en not_active Ceased
- 2003-04-07 US US10/510,598 patent/US20050222328A1/en not_active Abandoned
- 2003-04-07 EP EP03723501A patent/EP1492843B1/en not_active Expired - Lifetime
- 2003-04-07 CN CNB038080524A patent/CN1297603C/zh not_active Expired - Fee Related
- 2003-04-11 TW TW092108457A patent/TWI288156B/zh active
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1993025617A2 (en) * | 1992-06-05 | 1993-12-23 | The Dow Chemical Company | Paintable polyethylenes |
| US5849844A (en) * | 1993-12-22 | 1998-12-15 | Borealis A/S | Polyolefin-condensation polymer blend |
| WO1997012919A1 (en) * | 1995-10-06 | 1997-04-10 | The Dow Chemical Company | Branched block ethylene polymers, their preparation and compositions comprising the same |
| EP0866081A1 (en) * | 1995-12-08 | 1998-09-23 | Kaneka Corporation | Grafted polyolefin resin and thermoplastic resin composition containing the same |
Also Published As
| Publication number | Publication date |
|---|---|
| JP2005522550A (ja) | 2005-07-28 |
| ES2263969T3 (es) | 2006-12-16 |
| US20050222328A1 (en) | 2005-10-06 |
| DE60306351T2 (de) | 2007-09-06 |
| CN1646620A (zh) | 2005-07-27 |
| EP1492843A1 (en) | 2005-01-05 |
| ATE330994T1 (de) | 2006-07-15 |
| TWI288156B (en) | 2007-10-11 |
| DE60306351D1 (de) | 2006-08-03 |
| TW200404852A (en) | 2004-04-01 |
| AU2003230446A1 (en) | 2003-10-27 |
| CN1297603C (zh) | 2007-01-31 |
| WO2003087216A1 (en) | 2003-10-23 |
| EP1492843B1 (en) | 2006-06-21 |
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