NO791064L - Varmherdbar silanmodifisert alkylenalkylakrylatkopolymer samt fremgangsmaate for fremstilling derav - Google Patents

Varmherdbar silanmodifisert alkylenalkylakrylatkopolymer samt fremgangsmaate for fremstilling derav

Info

Publication number: NO791064L
Authority: NO; Norway
Prior art keywords: silane; acrylate copolymer; alkyl; alkyl acrylate; radical
Prior art date: 1978-03-31

Application number

NO791064A

Other languages

English (en)

Norwegian (no)

Inventor

Michael John Keogh

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.)

1978-03-31

Filing date

1979-03-30

Publication date

1979-10-02

1979-03-30 Application filed by Union Carbide Corp filed Critical Union Carbide Corp

1979-10-02 Publication of NO791064L publication Critical patent/NO791064L/no

Links

238000000034 method Methods 0.000 title claims description 50
238000002360 preparation method Methods 0.000 title description 6
125000002947 alkylene group Chemical group 0.000 claims description 37
229920000800 acrylic rubber Polymers 0.000 claims description 32
239000003054 catalyst Substances 0.000 claims description 30
229920001577 copolymer Polymers 0.000 claims description 30
238000006243 chemical reaction Methods 0.000 claims description 25
BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 claims description 23
VXUYXOFXAQZZMF-UHFFFAOYSA-N titanium(IV) isopropoxide Chemical group CC(C)O[Ti](OC(C)C)(OC(C)C)OC(C)C VXUYXOFXAQZZMF-UHFFFAOYSA-N 0.000 claims description 22
229910000077 silane Inorganic materials 0.000 claims description 20
125000004432 carbon atom Chemical group C* 0.000 claims description 18
229920006244 ethylene-ethyl acrylate Polymers 0.000 claims description 13
239000001257 hydrogen Substances 0.000 claims description 12
229910052739 hydrogen Inorganic materials 0.000 claims description 12
125000000217 alkyl group Chemical group 0.000 claims description 10
238000009833 condensation Methods 0.000 claims description 7
230000005494 condensation Effects 0.000 claims description 7
SCPYDCQAZCOKTP-UHFFFAOYSA-N silanol Chemical compound [SiH3]O SCPYDCQAZCOKTP-UHFFFAOYSA-N 0.000 claims description 7
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 6
238000004519 manufacturing process Methods 0.000 claims description 6
239000004215 Carbon black (E152) Substances 0.000 claims description 5
229930195733 hydrocarbon Natural products 0.000 claims description 5
229920000642 polymer Polymers 0.000 claims description 5
229910052799 carbon Inorganic materials 0.000 claims description 4
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 4
239000004711 α-olefin Substances 0.000 claims description 4
125000003545 alkoxy group Chemical group 0.000 claims description 2
230000003197 catalytic effect Effects 0.000 claims description 2
229910052710 silicon Inorganic materials 0.000 claims description 2
239000010703 silicon Substances 0.000 claims description 2
150000002431 hydrogen Chemical class 0.000 claims 2
BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 claims 1
238000004132 cross linking Methods 0.000 description 14
-1 polyethylene Polymers 0.000 description 14
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 11
NNBZCPXTIHJBJL-UHFFFAOYSA-N decalin Chemical compound C1CCCC2CCCCC21 NNBZCPXTIHJBJL-UHFFFAOYSA-N 0.000 description 10
JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 9
PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 9
238000000576 coating method Methods 0.000 description 8
150000002978 peroxides Chemical class 0.000 description 8
239000012632 extractable Substances 0.000 description 7
NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 6
239000011248 coating agent Substances 0.000 description 6
238000010438 heat treatment Methods 0.000 description 6
239000000155 melt Substances 0.000 description 6
239000000203 mixture Substances 0.000 description 6
229920000098 polyolefin Polymers 0.000 description 6
150000003254 radicals Chemical class 0.000 description 6
229920005989 resin Polymers 0.000 description 6
239000011347 resin Substances 0.000 description 6
125000005907 alkyl ester group Chemical group 0.000 description 5
239000000463 material Substances 0.000 description 5
PXXNTAGJWPJAGM-UHFFFAOYSA-N vertaline Natural products C1C2C=3C=C(OC)C(OC)=CC=3OC(C=C3)=CC=C3CCC(=O)OC1CC1N2CCCC1 PXXNTAGJWPJAGM-UHFFFAOYSA-N 0.000 description 5
238000004073 vulcanization Methods 0.000 description 5
XDLMVUHYZWKMMD-UHFFFAOYSA-N 3-trimethoxysilylpropyl 2-methylprop-2-enoate Chemical compound CO[Si](OC)(OC)CCCOC(=O)C(C)=C XDLMVUHYZWKMMD-UHFFFAOYSA-N 0.000 description 4
XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 4
239000004698 Polyethylene Substances 0.000 description 4
UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 4
125000005250 alkyl acrylate group Chemical group 0.000 description 4
239000012975 dibutyltin dilaurate Substances 0.000 description 4
CGPRUXZTHGTMKW-UHFFFAOYSA-N ethene;ethyl prop-2-enoate Chemical class C=C.CCOC(=O)C=C CGPRUXZTHGTMKW-UHFFFAOYSA-N 0.000 description 4
150000001282 organosilanes Chemical class 0.000 description 4
229920000573 polyethylene Polymers 0.000 description 4
150000004756 silanes Chemical class 0.000 description 4
239000000126 substance Substances 0.000 description 4
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
230000000694 effects Effects 0.000 description 3
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-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
QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 2
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 2
RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 2
239000002253 acid Substances 0.000 description 2
150000007513 acids Chemical class 0.000 description 2
150000001253 acrylic acids Chemical class 0.000 description 2
239000000654 additive Substances 0.000 description 2
239000000853 adhesive Substances 0.000 description 2
230000001070 adhesive effect Effects 0.000 description 2
230000032683 aging Effects 0.000 description 2
229910052786 argon Inorganic materials 0.000 description 2
238000005266 casting Methods 0.000 description 2
JQVDAXLFBXTEQA-UHFFFAOYSA-N dibutylamine Chemical compound CCCCNCCCC JQVDAXLFBXTEQA-UHFFFAOYSA-N 0.000 description 2
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
238000001125 extrusion Methods 0.000 description 2
238000009413 insulation Methods 0.000 description 2
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
239000000047 product Substances 0.000 description 2
230000005855 radiation Effects 0.000 description 2
239000002904 solvent Substances 0.000 description 2
RYSXWUYLAWPLES-MTOQALJVSA-N (Z)-4-hydroxypent-3-en-2-one titanium Chemical compound [Ti].C\C(O)=C\C(C)=O.C\C(O)=C\C(C)=O.C\C(O)=C\C(C)=O.C\C(O)=C\C(C)=O RYSXWUYLAWPLES-MTOQALJVSA-N 0.000 description 1
BMVXCPBXGZKUPN-UHFFFAOYSA-N 1-hexanamine Chemical compound CCCCCCN BMVXCPBXGZKUPN-UHFFFAOYSA-N 0.000 description 1
IHEDBVUTTQXGSJ-UHFFFAOYSA-M 2-[bis(2-oxidoethyl)amino]ethanolate;titanium(4+);hydroxide Chemical compound [OH-].[Ti+4].[O-]CCN(CC[O-])CC[O-] IHEDBVUTTQXGSJ-UHFFFAOYSA-M 0.000 description 1
AIFLGMNWQFPTAJ-UHFFFAOYSA-J 2-hydroxypropanoate;titanium(4+) Chemical compound [Ti+4].CC(O)C([O-])=O.CC(O)C([O-])=O.CC(O)C([O-])=O.CC(O)C([O-])=O AIFLGMNWQFPTAJ-UHFFFAOYSA-J 0.000 description 1
239000004925 Acrylic resin Substances 0.000 description 1
229920000178 Acrylic resin Polymers 0.000 description 1
RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
239000005977 Ethylene Substances 0.000 description 1
CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
125000002252 acyl group Chemical group 0.000 description 1
125000002877 alkyl aryl 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
125000003710 aryl alkyl group Chemical group 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
YHWCPXVTRSHPNY-UHFFFAOYSA-N butan-1-olate;titanium(4+) Chemical compound [Ti+4].CCCC[O-].CCCC[O-].CCCC[O-].CCCC[O-] YHWCPXVTRSHPNY-UHFFFAOYSA-N 0.000 description 1
CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical class CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
229910000019 calcium carbonate Inorganic materials 0.000 description 1
239000000378 calcium silicate Substances 0.000 description 1
229910052918 calcium silicate Inorganic materials 0.000 description 1
OYACROKNLOSFPA-UHFFFAOYSA-N calcium;dioxido(oxo)silane Chemical compound [Ca+2].[O-][Si]([O-])=O OYACROKNLOSFPA-UHFFFAOYSA-N 0.000 description 1
150000007942 carboxylates Chemical class 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
239000004927 clay Substances 0.000 description 1
238000010960 commercial process Methods 0.000 description 1
150000001875 compounds Chemical class 0.000 description 1
230000003750 conditioning effect Effects 0.000 description 1
125000000753 cycloalkyl group Chemical group 0.000 description 1
238000000354 decomposition reaction Methods 0.000 description 1
125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
230000001934 delay Effects 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
238000010894 electron beam technology Methods 0.000 description 1
238000005265 energy consumption Methods 0.000 description 1
238000005886 esterification reaction Methods 0.000 description 1
150000002148 esters Chemical group 0.000 description 1
239000005038 ethylene vinyl acetate Substances 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
239000007789 gas Substances 0.000 description 1
125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
150000002430 hydrocarbons Chemical class 0.000 description 1
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
238000007654 immersion Methods 0.000 description 1
239000003999 initiator Substances 0.000 description 1
229910052500 inorganic mineral Inorganic materials 0.000 description 1
229910052742 iron Inorganic materials 0.000 description 1
125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
GIWKOZXJDKMGQC-UHFFFAOYSA-L lead(2+);naphthalene-2-carboxylate Chemical compound [Pb+2].C1=CC=CC2=CC(C(=O)[O-])=CC=C21.C1=CC=CC2=CC(C(=O)[O-])=CC=C21 GIWKOZXJDKMGQC-UHFFFAOYSA-L 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
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
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
150000002734 metacrylic acid derivatives Chemical class 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
125000005395 methacrylic acid group Chemical class 0.000 description 1
239000011707 mineral Substances 0.000 description 1
239000000178 monomer Substances 0.000 description 1
GEMHFKXPOCTAIP-UHFFFAOYSA-N n,n-dimethyl-n'-phenylcarbamimidoyl chloride Chemical compound CN(C)C(Cl)=NC1=CC=CC=C1 GEMHFKXPOCTAIP-UHFFFAOYSA-N 0.000 description 1
150000007530 organic bases Chemical class 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
230000002035 prolonged effect Effects 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 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
239000000376 reactant Substances 0.000 description 1
238000007493 shaping process Methods 0.000 description 1
238000007086 side reaction Methods 0.000 description 1
LIVNPJMFVYWSIS-UHFFFAOYSA-N silicon monoxide Chemical class [Si-]#[O+] LIVNPJMFVYWSIS-UHFFFAOYSA-N 0.000 description 1
229910052814 silicon oxide Inorganic materials 0.000 description 1
239000004071 soot Substances 0.000 description 1
125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 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
125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
239000012815 thermoplastic material Substances 0.000 description 1
KSBAEPSJVUENNK-UHFFFAOYSA-L tin(ii) 2-ethylhexanoate Chemical compound [Sn+2].CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O KSBAEPSJVUENNK-UHFFFAOYSA-L 0.000 description 1
239000010936 titanium Substances 0.000 description 1
229910052719 titanium Inorganic materials 0.000 description 1
229910052723 transition metal Inorganic materials 0.000 description 1
YJGJRYWNNHUESM-UHFFFAOYSA-J triacetyloxystannyl acetate Chemical compound [Sn+4].CC([O-])=O.CC([O-])=O.CC([O-])=O.CC([O-])=O YJGJRYWNNHUESM-UHFFFAOYSA-J 0.000 description 1
CHJMFFKHPHCQIJ-UHFFFAOYSA-L zinc;octanoate Chemical compound [Zn+2].CCCCCCCC([O-])=O.CCCCCCCC([O-])=O CHJMFFKHPHCQIJ-UHFFFAOYSA-L 0.000 description 1

Classifications

- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B3/00—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties
- H01B3/18—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances
- H01B3/30—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes
- H01B3/46—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes silicones
- 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
- 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
- C08G81/00—Macromolecular compounds obtained by interreacting polymers in the absence of monomers, e.g. block polymers
- C08G81/02—Macromolecular compounds obtained by interreacting polymers in the absence of monomers, e.g. block polymers at least one of the polymers being obtained by reactions involving only carbon-to-carbon unsaturated bonds
- C08G81/024—Block or graft polymers containing sequences of polymers of C08C or C08F and of polymers of C08G
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K13/00—Use of mixtures of ingredients not covered by one single of the preceding main groups, each of these compounds being essential
- C08K13/02—Organic and inorganic ingredients
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/34—Heterocyclic compounds having nitrogen in the ring
- C08K5/3412—Heterocyclic compounds having nitrogen in the ring having one nitrogen atom in the ring
- C08K5/3415—Five-membered rings
- C08K5/3417—Five-membered rings condensed with carbocyclic rings
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L83/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers
- C08L83/16—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers in which all the silicon atoms are connected by linkages other than oxygen atoms
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B3/00—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties
- H01B3/18—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances
- H01B3/30—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes
- H01B3/44—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes vinyl resins; acrylic resins
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B3/00—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties
- H01B3/18—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances
- H01B3/30—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes
- H01B3/44—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes vinyl resins; acrylic resins
- H01B3/441—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes vinyl resins; acrylic resins from alkenes

Landscapes

Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
Physics & Mathematics (AREA)
Spectroscopy & Molecular Physics (AREA)
General Chemical & Material Sciences (AREA)
Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Compositions Of Macromolecular Compounds (AREA)
Organic Insulating Materials (AREA)
Heat Sensitive Colour Forming Recording (AREA)

NO791064A 1978-03-31 1979-03-30 Varmherdbar silanmodifisert alkylenalkylakrylatkopolymer samt fremgangsmaate for fremstilling derav NO791064L (no)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US89215378A	1978-03-31	1978-03-31

Publications (1)

Publication Number	Publication Date
NO791064L true NO791064L (no)	1979-10-02

Family

ID=25399465

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO791064A NO791064L (no)	1978-03-31	1979-03-30	Varmherdbar silanmodifisert alkylenalkylakrylatkopolymer samt fremgangsmaate for fremstilling derav

Country Status (13)

Country	Link
EP (2)	EP0004752B1 (de)
JP (1)	JPS6030325B2 (de)
AR (1)	AR222995A1 (de)
AT (1)	AT366704B (de)
AU (1)	AU525628B2 (de)
BR (1)	BR7901936A (de)
CA (1)	CA1124438A (de)
DE (1)	DE2966569D1 (de)
DK (1)	DK131579A (de)
ES (1)	ES479103A1 (de)
NO (1)	NO791064L (de)
NZ (1)	NZ190052A (de)
ZA (1)	ZA791416B (de)

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ZA787062B (en) *	1977-12-27	1980-04-30	Union Carbide Corp	Wire or cable insulated with a dielectric composition stabilized against water treeing with organo silane compounds
US4351926A (en) *	1979-12-26	1982-09-28	Union Carbide Corporation	Heat curable polymer
US4321263A (en) *	1980-09-30	1982-03-23	Rowell Laboratories, Inc.	Psyllium compositions
US4369289A (en) *	1980-09-30	1983-01-18	Union Carbide Corporation	Masterbatch composition comprising a matrix having a polysiloxane dispersed therein and a method for the preparation thereof
US4452937A (en) *	1980-12-22	1984-06-05	Union Carbide Corporation	Ethylene polymer compositions stabilized against water treeing and electrical treeing by an organo titanium chelate; and the use thereof as insulation about electrical conductors
US4446279A (en) *	1982-02-22	1984-05-01	Union Carbide Corporation	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
CH660744A5 (de) *	1982-11-05	1987-06-15	Inventa Ag	Verfahren zur herstellung hochviskoser bzw. thermisch formstabiler, mindestens teilvernetzter polyamide.
US4526930A (en) *	1983-09-23	1985-07-02	Union Carbide Corporation	Production of water-curable, silane modified thermoplastic polymers
DE3682088D1 (de) *	1985-03-18	1991-11-28	Mitsubishi Petrochemical Co	Verfahren zur herstellung von wasserabsorbierenden polymeren.
DE3544085A1 (de) *	1985-12-13	1987-06-19	Kabelmetal Electro Gmbh	Elektrisches luftkabel mit lichtwellenleitern
JPS63112244U (de) *	1987-01-13	1988-07-19
FR2618152B1 (fr) *	1987-07-16	1992-02-28	Filergie Sa	Procede de reticulation de polyolefines halogenees
GB8811615D0 (en) *	1988-05-17	1988-06-22	Swift Adhesives Ltd	Adhesive compositions
AU654361B2 (en)	1991-05-31	1994-11-03	Bp Chemicals Limited	Cross linkable polymeric composition
ES2049580B1 (es) *	1991-07-09	1995-01-16	Union Carbide Corp	Procedimiento para preparar una composicion ignifuga reticulada a base de un copolimero de alquileno-acrilato de alquilo.
DE4132683A1 (de) *	1991-10-01	1993-04-08	Basf Ag	Extrusionsverfahren zur herstellung von ionisch vernetzten ethylencopolymerisaten (ionomeren)
DE102010003108A1 (de)	2010-03-22	2011-09-22	Wacker Chemie Ag	Silaoxacyclen
DE102010003110A1 (de)	2010-03-22	2011-09-22	Wacker Chemie Ag	Herstellung von Silaoxacyclen
CN105163715A (zh) *	2013-05-10	2015-12-16	宝洁公司	包含硅烷改性的油的消费产品
US11319425B2 (en) *	2017-09-26	2022-05-03	Dow Global Technologies Llc	Compositions comprising a tin-based catalyst and titanium dioxide for moisture cure of silane-functionalized ethylenic polymers

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US3408420A (en) *	1964-04-30	1968-10-29	Du Pont	Silane-modified olefinic copolymers
BE707365A (de) *	1965-12-27	1968-05-30
US4247446A (en) *	1979-06-01	1981-01-27	General Electric Company	Flame-resistant composition, and electrical product thereof
JPS5695940A (en) *	1979-12-28	1981-08-03	Mitsubishi Petrochem Co Ltd	Ethylene polymer composition
CA1161182A (en) *	1980-03-05	1984-01-24	Michael J. Keogh	Compositions of alkylene-alkyl acrylate copolymers having improved flame retardant properties
US4321263A (en) *	1980-09-30	1982-03-23	Rowell Laboratories, Inc.	Psyllium compositions

1979
- 1979-03-20 NZ NZ190052A patent/NZ190052A/xx unknown
- 1979-03-26 ZA ZA791416A patent/ZA791416B/xx unknown
- 1979-03-30 JP JP54037153A patent/JPS6030325B2/ja not_active Expired
- 1979-03-30 AR AR275999A patent/AR222995A1/es active
- 1979-03-30 AT AT0238579A patent/AT366704B/de not_active IP Right Cessation
- 1979-03-30 BR BR7901936A patent/BR7901936A/pt unknown
- 1979-03-30 ES ES479103A patent/ES479103A1/es not_active Expired
- 1979-03-30 NO NO791064A patent/NO791064L/no unknown
- 1979-03-30 AU AU45653/79A patent/AU525628B2/en not_active Ceased
- 1979-03-30 EP EP79300521A patent/EP0004752B1/de not_active Expired
- 1979-03-30 DK DK131579A patent/DK131579A/da not_active IP Right Cessation
- 1979-03-30 DE DE7979300521T patent/DE2966569D1/de not_active Expired
- 1979-03-30 CA CA324,723A patent/CA1124438A/en not_active Expired
1982
- 1982-04-16 EP EP82301976A patent/EP0093806A1/de not_active Ceased

Also Published As

Publication number	Publication date
AR222995A1 (es)	1981-07-15
ES479103A1 (es)	1979-08-01
ATA238579A (de)	1981-09-15
EP0004752A2 (de)	1979-10-17
BR7901936A (pt)	1979-11-27
EP0004752A3 (en)	1979-10-31
AT366704B (de)	1982-05-10
AU4565379A (en)	1979-10-18
NZ190052A (en)	1980-11-14
DE2966569D1 (en)	1984-03-01
ZA791416B (en)	1980-04-30
CA1124438A (en)	1982-05-25
EP0093806A1 (de)	1983-11-16
JPS54154491A (en)	1979-12-05
JPS6030325B2 (ja)	1985-07-16
AU525628B2 (en)	1982-11-18
EP0004752B1 (de)	1984-01-25
DK131579A (da)	1979-10-01

Publication	Publication Date	Title
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
US4369289A (en)	1983-01-18	Masterbatch composition comprising a matrix having a polysiloxane dispersed therein and a method for the preparation thereof
KR860001033B1 (ko)	1986-07-28	알킬렌-알킬 아크릴레이트의 실란 개질된 혼성중합체를 제조하는 방법
EP0004752B1 (de)	1984-01-25	Durch Wasser vernetzbare mit Silan modifizierte Alkylen-Alkylacrylat-Kopolymere, ihre Herstellung und daraus verfertigte Produkte
US4328323A (en)	1982-05-04	Production of silane modified copolymers of alkylene-alkyl acrylates
US4575535A (en)	1986-03-11	Water-curable, silane modified alkylene-alkyl acrylate copolymers and a process for the production thereof
US4434272A (en)	1984-02-28	Water-curable, silane modified alkyl acrylate copolymers and a process for the preparation thereof
NO169395B (no)	1992-03-09	Tverrbindbart polymermateriale paa basis av en silylmodifisert etylenpolymer samt anvendelse av polymermaterialet for isolering av traad eller kabel
JPH0144254B2 (de)	1989-09-26
EP0106062B1 (de)	1988-01-27	Polysiloxane und ihre Anwendung in der Herstellung von mit Silanen modifizierten Alkylenacrylatcopolymeren
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
DE69406572T2 (de)	1998-03-05	Härtbare Harzmasse, die ein Silicionharz mit Epoxy- und Phenylgruppen im Molekül und ein Vinylpolymer enthält, das eine mit der Epoxygruppe reaktive Gruppe hat
JPS61155462A (ja)	1986-07-15	加水分解可能なペンダントシラン部分を有する水硬化性熱可塑性重合体及び有機チタネ−トを基材とする耐スコ−チ性組成物
US4404349A (en)	1983-09-13	Polysiloxanes having combined therein organo titanates
CA1242835A (en)	1988-10-04	Water curable, azide sulfonyl silane modified, alkylene-alkyl acrylate copolymers
KR830000409B1 (ko)	1983-03-07	수경성 실란변형 알킬렌알킬아크릴레이트 공중합체의 제조방법
JPS6218577B2 (de)	1987-04-23
CA1186437A (en)	1985-04-30	Production of silane modified copolymers of alkylene- alkyl acrylates, polysiloxanes having combined therein organo titanates and the use thereof in the production of silane modified copolymers of alkylene- alkyl acrylates
NO821247L (no)	1983-10-17	Preparat basert paa vannbare silanmodifiserte kopolymere av alkylen-alkylakrylater
JPS6352642B2 (de)	1988-10-19
JPS61223012A (ja)	1986-10-03	シラン架橋エチレン共重合体の製造方法