NO309985B1 - Blandinger av polyolefinpodekopolymerer og polykarbonater - Google Patents

Blandinger av polyolefinpodekopolymerer og polykarbonater Download PDF

Info

Publication number: NO309985B1
Authority: NO; Norway
Prior art keywords: weight; propylene; composition according; ethylene; polycarbonate
Prior art date: 1995-05-31

Application number

NO962180A

Other languages

English (en)

Norwegian (no)

Other versions

NO962180D0 (no

NO962180L (no

Inventor

Jr Anthony J Denicola

Kyle D Eastenson

Tam T M Phan

Original Assignee

Montell North America Inc

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.)

1995-05-31

Filing date

1996-05-29

Publication date

2001-04-30

1996-05-29 Application filed by Montell North America Inc filed Critical Montell North America Inc

1996-05-29 Publication of NO962180D0 publication Critical patent/NO962180D0/no

1996-12-02 Publication of NO962180L publication Critical patent/NO962180L/no

2001-04-30 Publication of NO309985B1 publication Critical patent/NO309985B1/no

Links

239000000203 mixture Substances 0.000 title claims abstract description 93
229920000515 polycarbonate Polymers 0.000 title claims abstract description 74
239000004417 polycarbonate Substances 0.000 title claims abstract description 74
229920000578 graft copolymer Polymers 0.000 title claims abstract description 62
229920000098 polyolefin Polymers 0.000 title description 8
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims abstract description 77
239000000178 monomer Substances 0.000 claims abstract description 60
229920001971 elastomer Polymers 0.000 claims abstract description 59
239000005060 rubber Substances 0.000 claims abstract description 57
229920001155 polypropylene Polymers 0.000 claims abstract description 44
239000002861 polymer material Substances 0.000 claims abstract description 41
NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 claims abstract description 17
FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims abstract description 16
XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 claims abstract description 14
229920001897 terpolymer Polymers 0.000 claims abstract description 13
229920003232 aliphatic polyester Polymers 0.000 claims abstract description 11
125000003118 aryl group Chemical group 0.000 claims abstract description 11
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 26
239000005977 Ethylene Substances 0.000 claims description 26
-1 polybutylene adipate Polymers 0.000 claims description 25
150000001336 alkenes Chemical class 0.000 claims description 23
229920001400 block copolymer Polymers 0.000 claims description 23
JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims description 22
229920001610 polycaprolactone Polymers 0.000 claims description 17
239000004632 polycaprolactone Substances 0.000 claims description 17
229920001384 propylene homopolymer Polymers 0.000 claims description 17
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims description 15
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 15
229920000642 polymer Polymers 0.000 claims description 14
HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 claims description 13
229920002635 polyurethane Polymers 0.000 claims description 9
239000004814 polyurethane Substances 0.000 claims description 9
150000004945 aromatic hydrocarbons Chemical class 0.000 claims description 8
150000001993 dienes Chemical class 0.000 claims description 7
229920001519 homopolymer Polymers 0.000 claims description 7
VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 claims description 6
RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 claims description 6
229920000402 bisphenol A polycarbonate polymer Polymers 0.000 claims description 6
238000002156 mixing Methods 0.000 claims description 6
229920005604 random copolymer Polymers 0.000 claims description 6
150000003440 styrenes Chemical group 0.000 claims description 6
125000000217 alkyl group Chemical group 0.000 claims description 5
IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 claims description 5
IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 claims description 4
239000011258 core-shell material Substances 0.000 claims description 4
150000002148 esters Chemical class 0.000 claims description 4
229920006132 styrene block copolymer Polymers 0.000 claims description 4
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 3
229920000089 Cyclic olefin copolymer Polymers 0.000 claims description 2
229920000921 polyethylene adipate Polymers 0.000 claims description 2
229920001577 copolymer Polymers 0.000 abstract description 14
229920000728 polyester Polymers 0.000 description 45
230000000052 comparative effect Effects 0.000 description 15
230000000694 effects Effects 0.000 description 14
238000000034 method Methods 0.000 description 14
230000000704 physical effect Effects 0.000 description 13
239000000463 material Substances 0.000 description 12
239000003999 initiator Substances 0.000 description 11
150000002978 peroxides Chemical class 0.000 description 10
101150004822 PSAN gene Proteins 0.000 description 8
150000003254 radicals Chemical class 0.000 description 8
229920001169 thermoplastic Polymers 0.000 description 8
239000004416 thermosoftening plastic Substances 0.000 description 8
102100041003 Glutamate carboxypeptidase 2 Human genes 0.000 description 7
101000892862 Homo sapiens Glutamate carboxypeptidase 2 Proteins 0.000 description 7
229920001481 poly(stearyl methacrylate) Polymers 0.000 description 7
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
239000000126 substance Substances 0.000 description 6
229920000428 triblock copolymer Polymers 0.000 description 6
KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 5
239000004743 Polypropylene Substances 0.000 description 4
230000001590 oxidative effect Effects 0.000 description 4
229920006124 polyolefin elastomer Polymers 0.000 description 4
229920006395 saturated elastomer Polymers 0.000 description 4
RYECOJGRJDOGPP-UHFFFAOYSA-N Ethylurea Chemical compound CCNC(N)=O RYECOJGRJDOGPP-UHFFFAOYSA-N 0.000 description 3
239000002253 acid Substances 0.000 description 3
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
238000006243 chemical reaction Methods 0.000 description 3
150000001875 compounds Chemical class 0.000 description 3
230000009849 deactivation Effects 0.000 description 3
238000010559 graft polymerization reaction Methods 0.000 description 3
238000001746 injection moulding Methods 0.000 description 3
239000011159 matrix material Substances 0.000 description 3
229910052757 nitrogen Inorganic materials 0.000 description 3
239000001301 oxygen Substances 0.000 description 3
229910052760 oxygen Inorganic materials 0.000 description 3
ZGEGCLOFRBLKSE-UHFFFAOYSA-N 1-Heptene Chemical compound CCCCCC=C ZGEGCLOFRBLKSE-UHFFFAOYSA-N 0.000 description 2
LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 2
WSSSPWUEQFSQQG-UHFFFAOYSA-N 4-methyl-1-pentene Chemical compound CC(C)CC=C WSSSPWUEQFSQQG-UHFFFAOYSA-N 0.000 description 2
NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 2
XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 2
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 description 2
150000008064 anhydrides Chemical group 0.000 description 2
235000019400 benzoyl peroxide Nutrition 0.000 description 2
238000005266 casting Methods 0.000 description 2
229920003244 diene elastomer Polymers 0.000 description 2
125000005442 diisocyanate group Chemical group 0.000 description 2
239000000806 elastomer Substances 0.000 description 2
238000001125 extrusion Methods 0.000 description 2
239000000945 filler Substances 0.000 description 2
WOLATMHLPFJRGC-UHFFFAOYSA-N furan-2,5-dione;styrene Chemical compound O=C1OC(=O)C=C1.C=CC1=CC=CC=C1 WOLATMHLPFJRGC-UHFFFAOYSA-N 0.000 description 2
239000007789 gas Substances 0.000 description 2
238000010438 heat treatment Methods 0.000 description 2
239000004615 ingredient Substances 0.000 description 2
238000002347 injection Methods 0.000 description 2
239000007924 injection Substances 0.000 description 2
229910052500 inorganic mineral Inorganic materials 0.000 description 2
230000005865 ionizing radiation Effects 0.000 description 2
229920003049 isoprene rubber Polymers 0.000 description 2
239000000155 melt Substances 0.000 description 2
239000011707 mineral Substances 0.000 description 2
YWAKXRMUMFPDSH-UHFFFAOYSA-N pentene Chemical compound CCCC=C YWAKXRMUMFPDSH-UHFFFAOYSA-N 0.000 description 2
229920002857 polybutadiene Polymers 0.000 description 2
238000006116 polymerization reaction Methods 0.000 description 2
238000010926 purge Methods 0.000 description 2
235000015096 spirit Nutrition 0.000 description 2
239000008096 xylene Substances 0.000 description 2
HGXJDMCMYLEZMJ-UHFFFAOYSA-N (2-methylpropan-2-yl)oxy 2,2-dimethylpropaneperoxoate Chemical compound CC(C)(C)OOOC(=O)C(C)(C)C HGXJDMCMYLEZMJ-UHFFFAOYSA-N 0.000 description 1
NOBYOEQUFMGXBP-UHFFFAOYSA-N (4-tert-butylcyclohexyl) (4-tert-butylcyclohexyl)oxycarbonyloxy carbonate Chemical compound C1CC(C(C)(C)C)CCC1OC(=O)OOC(=O)OC1CCC(C(C)(C)C)CC1 NOBYOEQUFMGXBP-UHFFFAOYSA-N 0.000 description 1
BEQKKZICTDFVMG-UHFFFAOYSA-N 1,2,3,4,6-pentaoxepane-5,7-dione Chemical compound O=C1OOOOC(=O)O1 BEQKKZICTDFVMG-UHFFFAOYSA-N 0.000 description 1
PAOHAQSLJSMLAT-UHFFFAOYSA-N 1-butylperoxybutane Chemical compound CCCCOOCCCC PAOHAQSLJSMLAT-UHFFFAOYSA-N 0.000 description 1
XMNIXWIUMCBBBL-UHFFFAOYSA-N 2-(2-phenylpropan-2-ylperoxy)propan-2-ylbenzene Chemical compound C=1C=CC=CC=1C(C)(C)OOC(C)(C)C1=CC=CC=C1 XMNIXWIUMCBBBL-UHFFFAOYSA-N 0.000 description 1
FALRKNHUBBKYCC-UHFFFAOYSA-N 2-(chloromethyl)pyridine-3-carbonitrile Chemical compound ClCC1=NC=CC=C1C#N FALRKNHUBBKYCC-UHFFFAOYSA-N 0.000 description 1
GLVYLTSKTCWWJR-UHFFFAOYSA-N 2-carbonoperoxoylbenzoic acid Chemical compound OOC(=O)C1=CC=CC=C1C(O)=O GLVYLTSKTCWWJR-UHFFFAOYSA-N 0.000 description 1
ZACVGCNKGYYQHA-UHFFFAOYSA-N 2-ethylhexoxycarbonyloxy 2-ethylhexyl carbonate Chemical compound CCCCC(CC)COC(=O)OOC(=O)OCC(CC)CCCC ZACVGCNKGYYQHA-UHFFFAOYSA-N 0.000 description 1
BIISIZOQPWZPPS-UHFFFAOYSA-N 2-tert-butylperoxypropan-2-ylbenzene Chemical compound CC(C)(C)OOC(C)(C)C1=CC=CC=C1 BIISIZOQPWZPPS-UHFFFAOYSA-N 0.000 description 1
YHQXBTXEYZIYOV-UHFFFAOYSA-N 3-methylbut-1-ene Chemical compound CC(C)C=C YHQXBTXEYZIYOV-UHFFFAOYSA-N 0.000 description 1
RITONZMLZWYPHW-UHFFFAOYSA-N 3-methylhex-1-ene Chemical compound CCCC(C)C=C RITONZMLZWYPHW-UHFFFAOYSA-N 0.000 description 1
LDTAOIUHUHHCMU-UHFFFAOYSA-N 3-methylpent-1-ene Chemical compound CCC(C)C=C LDTAOIUHUHHCMU-UHFFFAOYSA-N 0.000 description 1
OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical class C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
239000004215 Carbon black (E152) Substances 0.000 description 1
238000012695 Interfacial polymerization Methods 0.000 description 1
OWYWGLHRNBIFJP-UHFFFAOYSA-N Ipazine Chemical compound CCN(CC)C1=NC(Cl)=NC(NC(C)C)=N1 OWYWGLHRNBIFJP-UHFFFAOYSA-N 0.000 description 1
VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
JKIJEFPNVSHHEI-UHFFFAOYSA-N Phenol, 2,4-bis(1,1-dimethylethyl)-, phosphite (3:1) Chemical compound CC(C)(C)C1=CC(C(C)(C)C)=CC=C1OP(OC=1C(=CC(=CC=1)C(C)(C)C)C(C)(C)C)OC1=CC=C(C(C)(C)C)C=C1C(C)(C)C JKIJEFPNVSHHEI-UHFFFAOYSA-N 0.000 description 1
229920000616 Poly(1,4-butylene adipate) Polymers 0.000 description 1
229920000562 Poly(ethylene adipate) Polymers 0.000 description 1
239000004698 Polyethylene Substances 0.000 description 1
239000004721 Polyphenylene oxide Substances 0.000 description 1
239000004433 Thermoplastic polyurethane Substances 0.000 description 1
BGYHLZZASRKEJE-UHFFFAOYSA-N [3-[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxy]-2,2-bis[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxymethyl]propyl] 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CCC(=O)OCC(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 BGYHLZZASRKEJE-UHFFFAOYSA-N 0.000 description 1
239000000654 additive Substances 0.000 description 1
125000003342 alkenyl group Chemical group 0.000 description 1
229910052786 argon Inorganic materials 0.000 description 1
230000004888 barrier function Effects 0.000 description 1
238000010923 batch production Methods 0.000 description 1
125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
229940106691 bisphenol a Drugs 0.000 description 1
229910000019 calcium carbonate Inorganic materials 0.000 description 1
CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 1
239000008116 calcium stearate Substances 0.000 description 1
235000013539 calcium stearate Nutrition 0.000 description 1
239000006229 carbon black Substances 0.000 description 1
239000001569 carbon dioxide Substances 0.000 description 1
229910002092 carbon dioxide Inorganic materials 0.000 description 1
239000004568 cement Substances 0.000 description 1
238000013329 compounding Methods 0.000 description 1
238000001816 cooling Methods 0.000 description 1
230000006378 damage Effects 0.000 description 1
238000000354 decomposition reaction Methods 0.000 description 1
229940057404 di-(4-tert-butylcyclohexyl)peroxydicarbonate Drugs 0.000 description 1
LSXWFXONGKSEMY-UHFFFAOYSA-N di-tert-butyl peroxide Chemical compound CC(C)(C)OOC(C)(C)C LSXWFXONGKSEMY-UHFFFAOYSA-N 0.000 description 1
238000009826 distribution Methods 0.000 description 1
125000000524 functional group Chemical group 0.000 description 1
238000007306 functionalization reaction Methods 0.000 description 1
238000001641 gel filtration chromatography Methods 0.000 description 1
239000011521 glass Substances 0.000 description 1
239000003365 glass fiber Substances 0.000 description 1
239000001307 helium Substances 0.000 description 1
229910052734 helium Inorganic materials 0.000 description 1
SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
150000002430 hydrocarbons Chemical class 0.000 description 1
125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
239000011261 inert gas Substances 0.000 description 1
239000012948 isocyanate Substances 0.000 description 1
150000002513 isocyanates Chemical class 0.000 description 1
239000010445 mica Substances 0.000 description 1
229910052618 mica group Inorganic materials 0.000 description 1
150000002825 nitriles Chemical class 0.000 description 1
150000001451 organic peroxides Chemical class 0.000 description 1
239000002245 particle Substances 0.000 description 1
150000004978 peroxycarbonates Chemical class 0.000 description 1
229920000570 polyether Polymers 0.000 description 1
229920000573 polyethylene Polymers 0.000 description 1
229920001228 polyisocyanate Polymers 0.000 description 1
239000005056 polyisocyanate Substances 0.000 description 1
229920002959 polymer blend Polymers 0.000 description 1
229920005862 polyol Polymers 0.000 description 1
150000003077 polyols Chemical class 0.000 description 1
229920000379 polypropylene carbonate Polymers 0.000 description 1
229920005629 polypropylene homopolymer Polymers 0.000 description 1
229920001296 polysiloxane Polymers 0.000 description 1
239000000843 powder Substances 0.000 description 1
239000002243 precursor Substances 0.000 description 1
HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
239000007870 radical polymerization initiator Substances 0.000 description 1
239000012744 reinforcing agent Substances 0.000 description 1
239000011347 resin Substances 0.000 description 1
229920005989 resin Polymers 0.000 description 1
238000007127 saponification reaction Methods 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
125000003011 styrenyl group Chemical group [H]\C(*)=C(/[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
RINCXYDBBGOEEQ-UHFFFAOYSA-N succinic anhydride Chemical group O=C1CCC(=O)O1 RINCXYDBBGOEEQ-UHFFFAOYSA-N 0.000 description 1
229940014800 succinic anhydride Drugs 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
WYKYCHHWIJXDAO-UHFFFAOYSA-N tert-butyl 2-ethylhexaneperoxoate Chemical compound CCCCC(CC)C(=O)OOC(C)(C)C WYKYCHHWIJXDAO-UHFFFAOYSA-N 0.000 description 1
GJBRNHKUVLOCEB-UHFFFAOYSA-N tert-butyl benzenecarboperoxoate Chemical compound CC(C)(C)OOC(=O)C1=CC=CC=C1 GJBRNHKUVLOCEB-UHFFFAOYSA-N 0.000 description 1
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
238000010998 test method Methods 0.000 description 1
229920002397 thermoplastic olefin Polymers 0.000 description 1
229920002803 thermoplastic polyurethane Polymers 0.000 description 1
238000005809 transesterification reaction Methods 0.000 description 1
229920006032 ungrafted co-polymer Polymers 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
- 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
- C08L69/00—Compositions of polycarbonates; Compositions of derivatives of polycarbonates

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)
Confectionery (AREA)

NO962180A 1995-05-31 1996-05-29 Blandinger av polyolefinpodekopolymerer og polykarbonater NO309985B1 (no)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US08/455,607 US5585434A (en)	1995-05-31	1995-05-31	Blends of polyolefin graft copolymers and polycarbonate

Publications (3)

Publication Number	Publication Date
NO962180D0 NO962180D0 (no)	1996-05-29
NO962180L NO962180L (no)	1996-12-02
NO309985B1 true NO309985B1 (no)	2001-04-30

Family

ID=23809528

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO962180A NO309985B1 (no)	1995-05-31	1996-05-29	Blandinger av polyolefinpodekopolymerer og polykarbonater

Country Status (16)

Country	Link
US (1)	US5585434A (fr)
EP (1)	EP0745647B1 (fr)
JP (1)	JP3611924B2 (fr)
KR (1)	KR960041273A (fr)
CN (1)	CN1061066C (fr)
AT (1)	ATE183535T1 (fr)
AU (1)	AU698214B2 (fr)
BR (1)	BR9602568A (fr)
CA (1)	CA2177238C (fr)
DE (1)	DE69603786T2 (fr)
DK (1)	DK0745647T3 (fr)
ES (1)	ES2138776T3 (fr)
MX (1)	MX9601935A (fr)
NO (1)	NO309985B1 (fr)
RU (1)	RU2171821C2 (fr)
TW (1)	TW372999B (fr)

Families Citing this family (35)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US5952423A (en) *	1997-07-18	1999-09-14	Baxter International Inc.	Plastic compositions for medical containers and methods for providing such containers and for storing red blood cells
US6468258B1 (en)	1997-07-18	2002-10-22	Baxter International Inc.	Plastic compositions including vitamin E for medical containers and methods for providing such compositions and containers
US6248827B1 (en)	1997-12-22	2001-06-19	Bridgestone Corporation	Centipede polymers and preparation and application in rubber compositions
US6248825B1 (en)	1998-05-06	2001-06-19	Bridgestone Corporation	Gels derived from extending grafted centipede polymers and polypropylene
US6204354B1 (en)	1998-05-06	2001-03-20	Bridgestone Corporation	Soft compounds derived from polypropylene grafted disubstituted ethylene- maleimide copolymers
US6207763B1 (en)	1998-06-12	2001-03-27	Bridgestone Corporation	Application of disubstituted ethylene-maleimide copolymers in rubber compounds
US6184292B1 (en)	1998-10-05	2001-02-06	Bridgestone Corporation	Soft gel polymers for high temperature use
US6133354A (en) *	1998-11-17	2000-10-17	Bridgestone Corporation	Copolymers as additives in thermoplastic elastomer gels
US6191217B1 (en)	1998-11-17	2001-02-20	Bridgestone Corporation	Gels derived from polypropylene grafted alkyl vinylether-maleimide copolymers
WO2000036011A1 (fr) *	1998-12-17	2000-06-22	Montell Technology Company B.V.	Melange de copolymere greffe de polyolefine et de polyamide
US6476117B1 (en)	2000-06-05	2002-11-05	Bridgestone Corporation	Grafted near-gelation polymers having high damping properties
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1995
- 1995-05-31 US US08/455,607 patent/US5585434A/en not_active Expired - Fee Related
1996
- 1996-05-22 MX MX9601935A patent/MX9601935A/es unknown
- 1996-05-23 CA CA002177238A patent/CA2177238C/fr not_active Expired - Fee Related
- 1996-05-24 AT AT96108298T patent/ATE183535T1/de not_active IP Right Cessation
- 1996-05-24 ES ES96108298T patent/ES2138776T3/es not_active Expired - Lifetime
- 1996-05-24 EP EP96108298A patent/EP0745647B1/fr not_active Expired - Lifetime
- 1996-05-24 DK DK96108298T patent/DK0745647T3/da active
- 1996-05-24 DE DE69603786T patent/DE69603786T2/de not_active Expired - Fee Related
- 1996-05-25 TW TW085106228A patent/TW372999B/zh active
- 1996-05-29 AU AU54586/96A patent/AU698214B2/en not_active Ceased
- 1996-05-29 JP JP13514496A patent/JP3611924B2/ja not_active Expired - Fee Related
- 1996-05-29 NO NO962180A patent/NO309985B1/no not_active IP Right Cessation
- 1996-05-30 RU RU96110404/04A patent/RU2171821C2/ru not_active IP Right Cessation
- 1996-05-31 BR BR9602568A patent/BR9602568A/pt not_active IP Right Cessation
- 1996-05-31 CN CN96106810A patent/CN1061066C/zh not_active Expired - Fee Related
- 1996-05-31 KR KR1019960018985A patent/KR960041273A/ko not_active Abandoned

Also Published As

Publication number	Publication date
KR960041273A (ko)	1996-12-19
ES2138776T3 (es)	2000-01-16
NO962180D0 (no)	1996-05-29
EP0745647A1 (fr)	1996-12-04
JP3611924B2 (ja)	2005-01-19
AU698214B2 (en)	1998-10-29
CN1061066C (zh)	2001-01-24
JPH0912830A (ja)	1997-01-14
ATE183535T1 (de)	1999-09-15
MX9601935A (es)	1997-01-31
DK0745647T3 (da)	1999-12-06
NO962180L (no)	1996-12-02
RU2171821C2 (ru)	2001-08-10
TW372999B (en)	1999-11-01
CA2177238C (fr)	2002-11-26
EP0745647B1 (fr)	1999-08-18
AU5458696A (en)	1996-12-12
US5585434A (en)	1996-12-17
CN1148063A (zh)	1997-04-23
BR9602568A (pt)	1998-10-06
DE69603786T2 (de)	2000-03-09
CA2177238A1 (fr)	1996-12-01
DE69603786D1 (de)	1999-09-23

Legal Events

Date	Code	Title	Description
2005-01-03	MM1K	Lapsed by not paying the annual fees

Publication	Publication Date	Title
US5585434A (en)	1996-12-17	Blends of polyolefin graft copolymers and polycarbonate
KR100257498B1 (ko)	2000-06-01	엔지니어링 수지-프로필렌 중합체 그래프트 조성물
US5370813A (en)	1994-12-06	Heat resistant composition of polyphenylene ether and/or polystyrene block copolymer(s) and styrenic grafted propylene polymer
US4990558A (en)	1991-02-05	Graft copolymer compositions
CA2087486C (fr)	2000-05-09	Melanges pour ameliorer les proprietes de copolymeres bloques de composes aromatiques vinyliques-dienes conjugues
US6140425A (en)	2000-10-31	Process for making polypropylene graft copolymers containing anhydride groups
CA2091533C (fr)	2000-10-31	Melanges thermoplastiques contenant des copolymeres greffes de polyacrylates qui modifient la resistance a l'impact
US4490508A (en)	1984-12-25	Graft-modified copolymer and compounding agent for styrene-type polymer containing the same
KR0179386B1 (ko)	1999-05-15	폴리올레핀 및 비닐 방향족 중합체 기재 열가소성 조성물
AU751574B2 (en)	2002-08-22	Thermal stability of alpha-substituted acrylate graft copolymers
JP3534479B2 (ja)	2004-06-07	ポリプロピレン系樹脂組成物
MXPA99001883A (en)	2000-04-24	Improvement of thermal stability of sterile acrylate copolymers replaced in position a