NO850205L - Vannherdbare azid-sulfonyl-silan-modifiserte etylen-polymerer - Google Patents

Vannherdbare azid-sulfonyl-silan-modifiserte etylen-polymerer

Info

Publication number: NO850205L
Authority: NO; Norway
Prior art keywords: polymer; ethylene; silane; approx; water
Prior art date: 1984-01-18

Application number

NO850205A

Other languages

English (en)

Norwegian (no)

Inventor

Austin Emidio Barnabeo

Original Assignee

Union Carbide Corp

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.)

1984-01-18

Filing date

1985-01-17

Publication date

1985-07-19

1985-01-17 Application filed by Union Carbide Corp filed Critical Union Carbide Corp

1985-07-19 Publication of NO850205L publication Critical patent/NO850205L/no

Links

229920000573 polyethylene Polymers 0.000 title claims abstract description 23
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical class C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 title claims description 5
229920000642 polymer Polymers 0.000 claims abstract description 17
KTVHISUWGUWQPT-UHFFFAOYSA-N sulfonylsilane azide Chemical compound S(=O)(=O)=[SiH2].[N-]=[N+]=[N-] KTVHISUWGUWQPT-UHFFFAOYSA-N 0.000 claims abstract description 10
229920001577 copolymer Polymers 0.000 claims description 12
150000002430 hydrocarbons Chemical group 0.000 claims description 9
YNQLUTRBYVCPMQ-UHFFFAOYSA-N Ethylbenzene Chemical group CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 claims description 6
239000002253 acid Substances 0.000 claims description 6
239000000203 mixture Substances 0.000 claims description 6
239000005977 Ethylene Substances 0.000 claims description 4
239000001257 hydrogen Substances 0.000 claims description 4
229910052739 hydrogen Inorganic materials 0.000 claims description 4
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 4
BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 claims description 3
125000003545 alkoxy group Chemical group 0.000 claims description 3
JEHQYUIXQHYENR-UHFFFAOYSA-N n-diazo-2-(2-trimethoxysilylethyl)benzenesulfonamide Chemical group CO[Si](OC)(OC)CCC1=CC=CC=C1S(=O)(=O)N=[N+]=[N-] JEHQYUIXQHYENR-UHFFFAOYSA-N 0.000 claims description 3
229910000077 silane Inorganic materials 0.000 claims description 3
239000004711 α-olefin Substances 0.000 claims description 3
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 2
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 7
238000009413 insulation Methods 0.000 abstract description 3
240000005572 Syzygium cordatum Species 0.000 description 11
235000006650 Syzygium cordatum Nutrition 0.000 description 11
230000015572 biosynthetic process Effects 0.000 description 11
125000004432 carbon atom Chemical group C* 0.000 description 10
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 9
-1 methylene, ethylene, propylene, butylene, hexylene Chemical group 0.000 description 8
238000006243 chemical reaction Methods 0.000 description 7
229920000098 polyolefin Polymers 0.000 description 7
VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 6
239000000126 substance Substances 0.000 description 6
125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 description 5
VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 4
239000000654 additive Substances 0.000 description 4
239000002023 wood Substances 0.000 description 4
229940123457 Free radical scavenger Drugs 0.000 description 3
239000003963 antioxidant agent Substances 0.000 description 3
238000004132 cross linking Methods 0.000 description 3
239000000155 melt Substances 0.000 description 3
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 3
239000002516 radical scavenger Substances 0.000 description 3
YXIWHUQXZSMYRE-UHFFFAOYSA-N 1,3-benzothiazole-2-thiol Chemical compound C1=CC=C2SC(S)=NC2=C1 YXIWHUQXZSMYRE-UHFFFAOYSA-N 0.000 description 2
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
KFHLAQZSZAJKKJ-UHFFFAOYSA-N 2,3,4-trimethyl-1,2-dihydroquinoline Chemical compound C1=CC=C2C(C)=C(C)C(C)NC2=C1 KFHLAQZSZAJKKJ-UHFFFAOYSA-N 0.000 description 2
QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 2
CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 2
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
150000007513 acids Chemical class 0.000 description 2
125000003118 aryl group Chemical group 0.000 description 2
239000012298 atmosphere Substances 0.000 description 2
229910000019 calcium carbonate Inorganic materials 0.000 description 2
OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 2
239000003054 catalyst Substances 0.000 description 2
239000007795 chemical reaction product Substances 0.000 description 2
238000009833 condensation Methods 0.000 description 2
230000005494 condensation Effects 0.000 description 2
JQVDAXLFBXTEQA-UHFFFAOYSA-N dibutylamine Chemical compound CCCCNCCCC JQVDAXLFBXTEQA-UHFFFAOYSA-N 0.000 description 2
239000003063 flame retardant Substances 0.000 description 2
239000007789 gas Substances 0.000 description 2
229910052736 halogen Inorganic materials 0.000 description 2
150000002367 halogens Chemical class 0.000 description 2
239000012774 insulation material Substances 0.000 description 2
238000004519 manufacturing process Methods 0.000 description 2
229910052751 metal Inorganic materials 0.000 description 2
239000002184 metal Substances 0.000 description 2
238000000034 method Methods 0.000 description 2
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
SCPYDCQAZCOKTP-UHFFFAOYSA-N silanol Chemical compound [SiH3]O SCPYDCQAZCOKTP-UHFFFAOYSA-N 0.000 description 2
BMVXCPBXGZKUPN-UHFFFAOYSA-N 1-hexanamine Chemical compound CCCCCCN BMVXCPBXGZKUPN-UHFFFAOYSA-N 0.000 description 1
LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 1
BIGOJJYDFLNSGB-UHFFFAOYSA-N 3-isocyanopropyl(trimethoxy)silane Chemical group CO[Si](OC)(OC)CCC[N+]#[C-] BIGOJJYDFLNSGB-UHFFFAOYSA-N 0.000 description 1
WSSSPWUEQFSQQG-UHFFFAOYSA-N 4-methyl-1-pentene Chemical compound CC(C)CC=C WSSSPWUEQFSQQG-UHFFFAOYSA-N 0.000 description 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
239000004801 Chlorinated PVC Substances 0.000 description 1
239000004709 Chlorinated polyethylene Substances 0.000 description 1
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
239000004698 Polyethylene Substances 0.000 description 1
XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 1
239000005864 Sulphur Substances 0.000 description 1
UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 1
230000032683 aging Effects 0.000 description 1
150000001341 alkaline earth metal compounds Chemical class 0.000 description 1
229910000287 alkaline earth metal oxide Inorganic materials 0.000 description 1
125000000217 alkyl group Chemical group 0.000 description 1
125000002947 alkylene group Chemical group 0.000 description 1
WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
229940058905 antimony compound for treatment of leishmaniasis and trypanosomiasis Drugs 0.000 description 1
150000001463 antimony compounds Chemical class 0.000 description 1
229910000410 antimony oxide Inorganic materials 0.000 description 1
230000003078 antioxidant effect Effects 0.000 description 1
239000012300 argon atmosphere Substances 0.000 description 1
150000001540 azides Chemical class 0.000 description 1
AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
239000000920 calcium hydroxide Substances 0.000 description 1
229910001861 calcium hydroxide Inorganic materials 0.000 description 1
BRPQOXSCLDDYGP-UHFFFAOYSA-N calcium oxide Chemical compound [O-2].[Ca+2] BRPQOXSCLDDYGP-UHFFFAOYSA-N 0.000 description 1
239000000292 calcium oxide Substances 0.000 description 1
ODINCKMPIJJUCX-UHFFFAOYSA-N calcium oxide Inorganic materials [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 1
239000001175 calcium sulphate Substances 0.000 description 1
235000011132 calcium sulphate Nutrition 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
239000006229 carbon black Substances 0.000 description 1
150000004649 carbonic acid derivatives Chemical class 0.000 description 1
150000007942 carboxylates Chemical class 0.000 description 1
150000001732 carboxylic acid derivatives Chemical group 0.000 description 1
230000015556 catabolic process Effects 0.000 description 1
239000000460 chlorine Substances 0.000 description 1
229910052801 chlorine Inorganic materials 0.000 description 1
239000004927 clay Substances 0.000 description 1
238000005260 corrosion Methods 0.000 description 1
230000007797 corrosion Effects 0.000 description 1
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
125000004956 cyclohexylene group Chemical group 0.000 description 1
125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
WHHGLZMJPXIBIX-UHFFFAOYSA-N decabromodiphenyl ether Chemical compound BrC1=C(Br)C(Br)=C(Br)C(Br)=C1OC1=C(Br)C(Br)=C(Br)C(Br)=C1Br WHHGLZMJPXIBIX-UHFFFAOYSA-N 0.000 description 1
238000006731 degradation reaction Methods 0.000 description 1
230000018109 developmental process Effects 0.000 description 1
239000012975 dibutyltin dilaurate Substances 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
PWWSSIYVTQUJQQ-UHFFFAOYSA-N distearyl thiodipropionate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)CCSCCC(=O)OCCCCCCCCCCCCCCCCCC PWWSSIYVTQUJQQ-UHFFFAOYSA-N 0.000 description 1
230000005684 electric field Effects 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
239000000194 fatty acid Substances 0.000 description 1
229930195729 fatty acid Natural products 0.000 description 1
150000004665 fatty acids Chemical class 0.000 description 1
239000000945 filler Substances 0.000 description 1
229920001519 homopolymer Polymers 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
150000004679 hydroxides Chemical class 0.000 description 1
238000007654 immersion Methods 0.000 description 1
229910052500 inorganic mineral Inorganic materials 0.000 description 1
ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
239000001095 magnesium carbonate Substances 0.000 description 1
229910000021 magnesium carbonate Inorganic materials 0.000 description 1
VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 description 1
239000000347 magnesium hydroxide Substances 0.000 description 1
229910001862 magnesium hydroxide Inorganic materials 0.000 description 1
HCWCAKKEBCNQJP-UHFFFAOYSA-N magnesium orthosilicate Chemical compound [Mg+2].[Mg+2].[O-][Si]([O-])([O-])[O-] HCWCAKKEBCNQJP-UHFFFAOYSA-N 0.000 description 1
239000000395 magnesium oxide Substances 0.000 description 1
CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
239000000391 magnesium silicate Substances 0.000 description 1
229910052919 magnesium silicate Inorganic materials 0.000 description 1
235000019792 magnesium silicate Nutrition 0.000 description 1
229910052943 magnesium sulfate Inorganic materials 0.000 description 1
235000019341 magnesium sulphate Nutrition 0.000 description 1
AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
239000011707 mineral Substances 0.000 description 1
235000010755 mineral Nutrition 0.000 description 1
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
KHIXUMMSSFAASU-UHFFFAOYSA-N n-diazo-1-trimethoxysilylpentane-1-sulfonamide Chemical class CCCCC([Si](OC)(OC)OC)S(=O)(=O)N=[N+]=[N-] KHIXUMMSSFAASU-UHFFFAOYSA-N 0.000 description 1
GQBCSFCTJPGYMA-UHFFFAOYSA-N n-diazo-2-methyl-4-trichlorosilylbutane-1-sulfonamide Chemical class Cl[Si](Cl)(Cl)CCC(C)CS(=O)(=O)N=[N+]=[N-] GQBCSFCTJPGYMA-UHFFFAOYSA-N 0.000 description 1
SIJNXHOWVIALDH-UHFFFAOYSA-N n-diazo-2-trichlorosilylethanesulfonamide Chemical class Cl[Si](Cl)(Cl)CCS(=O)(=O)N=[N+]=[N-] SIJNXHOWVIALDH-UHFFFAOYSA-N 0.000 description 1
IXYPUNHEMAGTLK-UHFFFAOYSA-N n-diazo-3-[dimethoxy(methyl)silyl]propane-1-sulfonamide Chemical class CO[Si](C)(OC)CCCS(=O)(=O)N=[N+]=[N-] IXYPUNHEMAGTLK-UHFFFAOYSA-N 0.000 description 1
URUASLMRRXKWEX-UHFFFAOYSA-N n-diazo-4-triethoxysilylcyclohexane-1-sulfonamide Chemical class CCO[Si](OCC)(OCC)C1CCC(S(=O)(=O)N=[N+]=[N-])CC1 URUASLMRRXKWEX-UHFFFAOYSA-N 0.000 description 1
PRLJJVPZYYCGBL-UHFFFAOYSA-N n-diazo-4-trimethoxysilylbenzenesulfonamide Chemical class CO[Si](OC)(OC)C1=CC=C(S(=O)(=O)N=[N+]=[N-])C=C1 PRLJJVPZYYCGBL-UHFFFAOYSA-N 0.000 description 1
HVQHIIITRIMPTG-UHFFFAOYSA-N n-diazo-6-trimethoxysilylhexane-1-sulfonamide Chemical class CO[Si](OC)(OC)CCCCCCS(=O)(=O)N=[N+]=[N-] HVQHIIITRIMPTG-UHFFFAOYSA-N 0.000 description 1
125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 1
125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
150000007530 organic bases Chemical class 0.000 description 1
VTRUBDSFZJNXHI-UHFFFAOYSA-N oxoantimony Chemical compound [Sb]=O VTRUBDSFZJNXHI-UHFFFAOYSA-N 0.000 description 1
239000012188 paraffin wax Substances 0.000 description 1
235000019809 paraffin wax Nutrition 0.000 description 1
YWAKXRMUMFPDSH-UHFFFAOYSA-N pentene Chemical compound CCCC=C YWAKXRMUMFPDSH-UHFFFAOYSA-N 0.000 description 1
235000019271 petrolatum Nutrition 0.000 description 1
239000002861 polymer material Substances 0.000 description 1
229920000915 polyvinyl chloride Polymers 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
239000000047 product Substances 0.000 description 1
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
238000011084 recovery Methods 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
235000012239 silicon dioxide Nutrition 0.000 description 1
239000003707 silyl modified polymer Substances 0.000 description 1
238000003860 storage Methods 0.000 description 1
150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 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
- C08F8/00—Chemical modification by after-treatment
- C08F8/42—Introducing metal atoms or metal-containing groups

Landscapes

Chemical & Material Sciences (AREA)
General Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Organic Insulating Materials (AREA)
Insulated Conductors (AREA)
Compositions Of Macromolecular Compounds (AREA)

NO850205A 1984-01-18 1985-01-17 Vannherdbare azid-sulfonyl-silan-modifiserte etylen-polymerer NO850205L (no)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US06/570,784 US4551504A (en)	1984-01-18	1984-01-18	Water curable, azide sulfonyl silane modified ethylene polymers

Publications (1)

Publication Number	Publication Date
NO850205L true NO850205L (no)	1985-07-19

Family

ID=24281041

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO850205A NO850205L (no)	1984-01-18	1985-01-17	Vannherdbare azid-sulfonyl-silan-modifiserte etylen-polymerer

Country Status (7)

Country	Link
US (1)	US4551504A (de)
EP (1)	EP0150773B1 (de)
JP (1)	JPS60228502A (de)
AT (1)	ATE42752T1 (de)
CA (1)	CA1229447A (de)
DE (1)	DE3569933D1 (de)
NO (1)	NO850205L (de)

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CN112678774A (zh) *	2020-12-23	2021-04-20	四川天采科技有限责任公司	乙烯与硅烷反应的SiC-CVD无氯外延制程尾气FTrPSA回收与循环再利用方法

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US3697551A (en) *	1968-12-31	1972-10-10	Hercules Inc	Silane sulfonyl azides
US3813351A (en) *	1968-12-31	1974-05-28	Hercules Inc	Priming composition
GB1264432A (de) *	1969-04-28	1972-02-23
GB1377737A (en) *	1971-07-15	1974-12-18	Dow Corning Ltd	Crosslinking of olefin polymers
US3706592A (en) *	1971-07-30	1972-12-19	Hercules Inc	Adhesion promoting agents
US3705911A (en) *	1971-11-16	1972-12-12	Hercules Inc	Silyl-azidoformates
US3715371A (en) *	1971-11-16	1973-02-06	Hercules Inc	Adhesion promoting agents
NL7207689A (de) *	1972-06-07	1973-12-11
JPS5369245A (en) *	1976-12-02	1978-06-20	Dainichi Nippon Cables Ltd	Extrusion and crosslinking of polyolefin
JPS5493049A (en) *	1977-12-30	1979-07-23	Showa Electric Wire & Cable Co Ltd	Manufacture of crosslinked molded article
JPS6017353B2 (ja) *	1978-03-03	1985-05-02	古河電気工業株式会社	ポリオレフイン系樹脂の架橋方法
US4291136A (en) *	1978-03-31	1981-09-22	Union Carbide Corporation	Water-curable silane modified alkylene alkylacrylate copolymer and a process for its production
US4328323A (en) *	1979-08-29	1982-05-04	Union Carbide Corporation	Production of silane modified copolymers of alkylene-alkyl acrylates
JPS575913A (en) *	1980-05-27	1982-01-12	Showa Electric Wire & Cable Co Ltd	Crosslinked polyolefin fiber
JPS57153004A (en) *	1981-03-19	1982-09-21	Nippon Oil Co Ltd	Production of silane-crosslinked polyolefin
GB2101138A (en) *	1981-05-28	1983-01-12	Bicc Plc	Polymer compositions

1984
- 1984-01-18 US US06/570,784 patent/US4551504A/en not_active Expired - Fee Related
1985
- 1985-01-11 CA CA000471989A patent/CA1229447A/en not_active Expired
- 1985-01-17 JP JP60005119A patent/JPS60228502A/ja active Pending
- 1985-01-17 EP EP85100449A patent/EP0150773B1/de not_active Expired
- 1985-01-17 AT AT85100449T patent/ATE42752T1/de not_active IP Right Cessation
- 1985-01-17 NO NO850205A patent/NO850205L/no unknown
- 1985-01-17 DE DE8585100449T patent/DE3569933D1/de not_active Expired

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CN112678774A (zh) *	2020-12-23	2021-04-20	四川天采科技有限责任公司	乙烯与硅烷反应的SiC-CVD无氯外延制程尾气FTrPSA回收与循环再利用方法
CN112678774B (zh) *	2020-12-23	2023-05-30	四川天采科技有限责任公司	乙烯与硅烷反应的SiC-CVD无氯外延制程尾气FTrPSA回收与循环再利用方法

Also Published As

Publication number	Publication date
DE3569933D1 (en)	1989-06-08
CA1229447A (en)	1987-11-17
EP0150773A3 (en)	1986-08-13
JPS60228502A (ja)	1985-11-13
EP0150773A2 (de)	1985-08-07
US4551504A (en)	1985-11-05
ATE42752T1 (de)	1989-05-15
EP0150773B1 (de)	1989-05-03

Publication	Publication Date	Title
NO850205L (no)	1985-07-19	Vannherdbare azid-sulfonyl-silan-modifiserte etylen-polymerer
US4369289A (en)	1983-01-18	Masterbatch composition comprising a matrix having a polysiloxane dispersed therein and a method for the preparation thereof
US4446279A (en)	1984-05-01	Compositions based on a polysiloxane and an organo titanate and the use thereof in the preparation of water curable, silane modified alkylene-alkyl acrylate copolymers
US4526930A (en)	1985-07-02	Production of water-curable, silane modified thermoplastic polymers
US4343917A (en)	1982-08-10	Water curable, amino silane modified alkylene-alkyl acrylate copolymers
EP0049155B1 (de)	1986-02-12	Verfahren zur Herstellung silanmodifizierter Copolymere aus Olefinen und Alkylacrylaten, zu deren Herstellung verwendbare Polysiloxane, die Organotitanate gebunden enthalten, Verfahren zur Herstellung dieser Polysiloxane und elektrische Leiter, die mit vernetzten, silanmodifizierten Copolymeren isoliert sind
US4328323A (en)	1982-05-04	Production of silane modified copolymers of alkylene-alkyl acrylates
US4291136A (en)	1981-09-22	Water-curable silane modified alkylene alkylacrylate copolymer and a process for its production
US4575535A (en)	1986-03-11	Water-curable, silane modified alkylene-alkyl acrylate copolymers and a process for the production thereof
US4440907A (en)	1984-04-03	Process of producing a water-curable, silane modified alkylene-alkyl acrylate copolymer by reacting an alkylene-alkyl acrylate copolymer with a polysiloxane predispersed in a thermoplastic resin matrix
US4408011A (en)	1983-10-04	Polysiloxanes and the use thereof in the production of silane modified alkylene-alkyl acrylate copolymers
NZ233370A (en)	1991-06-25	Flame retardent compositions comprising an ethylene containing copolymer, a silicone and an inorganic filler which is an alkaline-earth compound
US4493924A (en)	1985-01-15	Water-curable, silane modified chlorosulfonated olefinic polymers and a process for the preparation thereof
US4767820A (en)	1988-08-30	Compositions of a relatively water-stable thermoplastic polymer and tetramethyl titanate dispersed in an alkylene-alkyl acrylate copolymer matrix
CA2952592A1 (en)	2015-12-23	Moisture-curable polymeric compositions having halogenated polymers and metal mercaptides
CA1205936A (en)	1986-06-10	Ethylene polymers stabilized against water-treeing by n-phenyl substituted amino silanes; and the use of these compositions as insulation about electrical conductors
EP3589681B1 (de)	2021-12-01	Flammhemmende, feuchtigkeitshärtende draht- und kabelkonstruktionen mit verbesserter glanzschlagleistung
EP0150774B1 (de)	1989-05-03	Wasservernetzbare azid-sulfonyl-silanmodifizierte Alkylen-Alkylacrylat-Copolymere
US4404349A (en)	1983-09-13	Polysiloxanes having combined therein organo titanates
JPH01186707A (ja)	1989-07-26	難燃性電気絶縁組成物
JPS6218577B2 (de)	1987-04-23
JPH01186709A (ja)	1989-07-26	難燃性電気絶縁組成物