NO301019B1 - Fornettbare blandinger som inneholder siloxankopolymerer som oppviser alkenylgrupper, slike siloxankopolymerer, og anvendelse av blandingene - Google Patents
Fornettbare blandinger som inneholder siloxankopolymerer som oppviser alkenylgrupper, slike siloxankopolymerer, og anvendelse av blandingene Download PDFInfo
- Publication number
- NO301019B1 NO301019B1 NO922772A NO922772A NO301019B1 NO 301019 B1 NO301019 B1 NO 301019B1 NO 922772 A NO922772 A NO 922772A NO 922772 A NO922772 A NO 922772A NO 301019 B1 NO301019 B1 NO 301019B1
- Authority
- NO
- Norway
- Prior art keywords
- radical
- formula
- alkenyl groups
- siloxane
- groups
- Prior art date
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- 229920001577 copolymer Polymers 0.000 title claims abstract description 75
- 125000003342 alkenyl group Chemical group 0.000 title claims abstract description 48
- 239000000203 mixture Substances 0.000 title claims description 57
- 230000001747 exhibiting effect Effects 0.000 title claims description 22
- -1 siloxane units Chemical group 0.000 claims abstract description 82
- 229920001296 polysiloxane Polymers 0.000 claims description 72
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 33
- 239000001257 hydrogen Substances 0.000 claims description 30
- 229910052739 hydrogen Inorganic materials 0.000 claims description 30
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 26
- 239000003054 catalyst Substances 0.000 claims description 25
- 125000004432 carbon atom Chemical group C* 0.000 claims description 21
- 238000004519 manufacturing process Methods 0.000 claims description 19
- 239000004215 Carbon black (E152) Substances 0.000 claims description 17
- 229930195733 hydrocarbon Natural products 0.000 claims description 17
- 239000000126 substance Substances 0.000 claims description 11
- 239000003112 inhibitor Substances 0.000 claims description 10
- 125000000217 alkyl group Chemical group 0.000 claims description 9
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 9
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 3
- 125000001931 aliphatic group Chemical group 0.000 claims description 2
- 125000003118 aryl group Chemical group 0.000 claims description 2
- 239000000123 paper Substances 0.000 description 44
- 229920000642 polymer Polymers 0.000 description 31
- 238000000034 method Methods 0.000 description 30
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical group [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 26
- 150000003254 radicals Chemical class 0.000 description 23
- 150000002894 organic compounds Chemical class 0.000 description 21
- 239000000853 adhesive Substances 0.000 description 16
- 150000002430 hydrocarbons Chemical group 0.000 description 13
- 230000001070 adhesive effect Effects 0.000 description 12
- 229910052697 platinum Inorganic materials 0.000 description 12
- 229920001843 polymethylhydrosiloxane Chemical group 0.000 description 11
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 10
- 239000011630 iodine Substances 0.000 description 10
- 229910052740 iodine Inorganic materials 0.000 description 10
- NWVVVBRKAWDGAB-UHFFFAOYSA-N p-methoxyphenol Chemical compound COC1=CC=C(O)C=C1 NWVVVBRKAWDGAB-UHFFFAOYSA-N 0.000 description 10
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 9
- FBEIPJNQGITEBL-UHFFFAOYSA-J tetrachloroplatinum Chemical compound Cl[Pt](Cl)(Cl)Cl FBEIPJNQGITEBL-UHFFFAOYSA-J 0.000 description 9
- KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 description 8
- 238000000576 coating method Methods 0.000 description 7
- 239000011888 foil Substances 0.000 description 7
- 239000012299 nitrogen atmosphere Substances 0.000 description 7
- KTRQRAQRHBLCSQ-UHFFFAOYSA-N 1,2,4-tris(ethenyl)cyclohexane Chemical compound C=CC1CCC(C=C)C(C=C)C1 KTRQRAQRHBLCSQ-UHFFFAOYSA-N 0.000 description 6
- 230000008021 deposition Effects 0.000 description 6
- PRBHEGAFLDMLAL-UHFFFAOYSA-N 1,5-Hexadiene Natural products CC=CCC=C PRBHEGAFLDMLAL-UHFFFAOYSA-N 0.000 description 5
- 239000011111 cardboard Substances 0.000 description 5
- 238000004132 cross linking Methods 0.000 description 5
- 125000000753 cycloalkyl group Chemical group 0.000 description 5
- PYGSKMBEVAICCR-UHFFFAOYSA-N hexa-1,5-diene Chemical compound C=CCCC=C PYGSKMBEVAICCR-UHFFFAOYSA-N 0.000 description 5
- 239000010410 layer Substances 0.000 description 5
- TVMXDCGIABBOFY-UHFFFAOYSA-N n-Octanol Natural products CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 5
- 239000003960 organic solvent Substances 0.000 description 5
- 238000000926 separation method Methods 0.000 description 5
- 125000006043 5-hexenyl group Chemical group 0.000 description 4
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 4
- 239000004698 Polyethylene Substances 0.000 description 4
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 4
- 239000004205 dimethyl polysiloxane Substances 0.000 description 4
- 235000013870 dimethyl polysiloxane Nutrition 0.000 description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
- 239000003921 oil Substances 0.000 description 4
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 4
- 229920000573 polyethylene Polymers 0.000 description 4
- 239000004447 silicone coating Substances 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 238000005160 1H NMR spectroscopy Methods 0.000 description 3
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical group O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000003522 acrylic cement Substances 0.000 description 3
- 229910001854 alkali hydroxide Inorganic materials 0.000 description 3
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 3
- 125000004429 atom Chemical group 0.000 description 3
- 238000003490 calendering Methods 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- BITPLIXHRASDQB-UHFFFAOYSA-N ethenyl-[ethenyl(dimethyl)silyl]oxy-dimethylsilane Chemical compound C=C[Si](C)(C)O[Si](C)(C)C=C BITPLIXHRASDQB-UHFFFAOYSA-N 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 125000006038 hexenyl group Chemical group 0.000 description 3
- 150000002431 hydrogen Chemical class 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 150000004756 silanes Chemical class 0.000 description 3
- 238000001228 spectrum Methods 0.000 description 3
- 239000002023 wood Substances 0.000 description 3
- KWEKXPWNFQBJAY-UHFFFAOYSA-N (dimethyl-$l^{3}-silanyl)oxy-dimethylsilicon Chemical compound C[Si](C)O[Si](C)C KWEKXPWNFQBJAY-UHFFFAOYSA-N 0.000 description 2
- XWJBRBSPAODJER-UHFFFAOYSA-N 1,7-octadiene Chemical compound C=CCCCCC=C XWJBRBSPAODJER-UHFFFAOYSA-N 0.000 description 2
- CEBKHWWANWSNTI-UHFFFAOYSA-N 2-methylbut-3-yn-2-ol Chemical compound CC(C)(O)C#C CEBKHWWANWSNTI-UHFFFAOYSA-N 0.000 description 2
- FKNQCJSGGFJEIZ-UHFFFAOYSA-N 4-methylpyridine Chemical compound CC1=CC=NC=C1 FKNQCJSGGFJEIZ-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 2
- 229910002621 H2PtCl6 Inorganic materials 0.000 description 2
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 239000002250 absorbent Substances 0.000 description 2
- 230000002745 absorbent Effects 0.000 description 2
- 239000002390 adhesive tape Substances 0.000 description 2
- 150000001335 aliphatic alkanes Chemical class 0.000 description 2
- 239000010426 asphalt Substances 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 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 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 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 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 2
- 239000002655 kraft paper Substances 0.000 description 2
- 229920005684 linear copolymer Polymers 0.000 description 2
- 125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 2
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- 239000010893 paper waste Substances 0.000 description 2
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- CLSUSRZJUQMOHH-UHFFFAOYSA-L platinum dichloride Chemical compound Cl[Pt]Cl CLSUSRZJUQMOHH-UHFFFAOYSA-L 0.000 description 2
- 150000003141 primary amines Chemical class 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 230000002940 repellent Effects 0.000 description 2
- 239000005871 repellent Substances 0.000 description 2
- 150000003335 secondary amines Chemical class 0.000 description 2
- 229910052710 silicon Inorganic materials 0.000 description 2
- 229920002050 silicone resin Polymers 0.000 description 2
- XMRSTLBCBDIKFI-UHFFFAOYSA-N tetradeca-1,13-diene Chemical compound C=CCCCCCCCCCCC=C XMRSTLBCBDIKFI-UHFFFAOYSA-N 0.000 description 2
- WGTYBPLFGIVFAS-UHFFFAOYSA-M tetramethylammonium hydroxide Chemical compound [OH-].C[N+](C)(C)C WGTYBPLFGIVFAS-UHFFFAOYSA-M 0.000 description 2
- 239000008096 xylene Substances 0.000 description 2
- PFTAWBLQPZVEMU-DZGCQCFKSA-N (+)-catechin Chemical compound C1([C@H]2OC3=CC(O)=CC(O)=C3C[C@@H]2O)=CC=C(O)C(O)=C1 PFTAWBLQPZVEMU-DZGCQCFKSA-N 0.000 description 1
- XXHDHKZTASMVSX-UHFFFAOYSA-N 1,2,3,4-tetrakis(ethenyl)cyclobutane Chemical compound C=CC1C(C=C)C(C=C)C1C=C XXHDHKZTASMVSX-UHFFFAOYSA-N 0.000 description 1
- WEERVPDNCOGWJF-UHFFFAOYSA-N 1,4-bis(ethenyl)benzene Chemical compound C=CC1=CC=C(C=C)C=C1 WEERVPDNCOGWJF-UHFFFAOYSA-N 0.000 description 1
- DURPTKYDGMDSBL-UHFFFAOYSA-N 1-butoxybutane Chemical compound CCCCOCCCC DURPTKYDGMDSBL-UHFFFAOYSA-N 0.000 description 1
- QYLFHLNFIHBCPR-UHFFFAOYSA-N 1-ethynylcyclohexan-1-ol Chemical compound C#CC1(O)CCCCC1 QYLFHLNFIHBCPR-UHFFFAOYSA-N 0.000 description 1
- WJFKNYWRSNBZNX-UHFFFAOYSA-N 10H-phenothiazine Chemical compound C1=CC=C2NC3=CC=CC=C3SC2=C1 WJFKNYWRSNBZNX-UHFFFAOYSA-N 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- IILUPZLCNCGGHZ-UHFFFAOYSA-N 3,5-dimethylhepta-1,6-diene Chemical compound C=CC(C)CC(C)C=C IILUPZLCNCGGHZ-UHFFFAOYSA-N 0.000 description 1
- RJBKAMWYBWMHRY-UHFFFAOYSA-N 4-ethenyl-3,5-dimethylhepta-1,6-diene Chemical compound C=CC(C)C(C=C)C(C)C=C RJBKAMWYBWMHRY-UHFFFAOYSA-N 0.000 description 1
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- CYTYCFOTNPOANT-UHFFFAOYSA-N Perchloroethylene Chemical group ClC(Cl)=C(Cl)Cl CYTYCFOTNPOANT-UHFFFAOYSA-N 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 229910019029 PtCl4 Inorganic materials 0.000 description 1
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical group ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000002313 adhesive film Substances 0.000 description 1
- 239000012790 adhesive layer Substances 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- 125000005428 anthryl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C3C(*)=C([H])C([H])=C([H])C3=C([H])C2=C1[H] 0.000 description 1
- 125000003710 aryl alkyl group Chemical group 0.000 description 1
- 239000010425 asbestos Substances 0.000 description 1
- QSKKXNSTGHZSQB-UHFFFAOYSA-N azane;platinum(2+) Chemical class N.[Pt+2] QSKKXNSTGHZSQB-UHFFFAOYSA-N 0.000 description 1
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- NDKBVBUGCNGSJJ-UHFFFAOYSA-M benzyltrimethylammonium hydroxide Chemical compound [OH-].C[N+](C)(C)CC1=CC=CC=C1 NDKBVBUGCNGSJJ-UHFFFAOYSA-M 0.000 description 1
- ZPOLOEWJWXZUSP-WAYWQWQTSA-N bis(prop-2-enyl) (z)-but-2-enedioate Chemical compound C=CCOC(=O)\C=C/C(=O)OCC=C ZPOLOEWJWXZUSP-WAYWQWQTSA-N 0.000 description 1
- 125000004369 butenyl group Chemical group C(=CCC)* 0.000 description 1
- 235000012970 cakes Nutrition 0.000 description 1
- 235000013736 caramel Nutrition 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
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- 230000003197 catalytic effect Effects 0.000 description 1
- ADRVNXBAWSRFAJ-UHFFFAOYSA-N catechin Natural products OC1Cc2cc(O)cc(O)c2OC1c3ccc(O)c(O)c3 ADRVNXBAWSRFAJ-UHFFFAOYSA-N 0.000 description 1
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- 125000004122 cyclic group Chemical group 0.000 description 1
- 125000000582 cycloheptyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 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
- YAJIVAPCZRKADM-UHFFFAOYSA-L cycloocta-1,3-diene;platinum(2+);dichloride Chemical compound Cl[Pt]Cl.C1CCC=CC=CC1 YAJIVAPCZRKADM-UHFFFAOYSA-L 0.000 description 1
- UBDOHRFXPUJBOY-UHFFFAOYSA-L cyclopenta-1,3-diene;dichloroplatinum Chemical compound Cl[Pt]Cl.C1C=CC=C1 UBDOHRFXPUJBOY-UHFFFAOYSA-L 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
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- 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
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- 125000005448 ethoxyethyl group Chemical group [H]C([H])([H])C([H])([H])OC([H])([H])C([H])([H])* 0.000 description 1
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- PQPVPZTVJLXQAS-UHFFFAOYSA-N hydroxy-methyl-phenylsilicon Chemical class C[Si](O)C1=CC=CC=C1 PQPVPZTVJLXQAS-UHFFFAOYSA-N 0.000 description 1
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- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
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- 150000002576 ketones Chemical class 0.000 description 1
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- QXLPXWSKPNOQLE-UHFFFAOYSA-N methylpentynol Chemical compound CCC(C)(O)C#C QXLPXWSKPNOQLE-UHFFFAOYSA-N 0.000 description 1
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- 125000003136 n-heptyl 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])* 0.000 description 1
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- 125000001624 naphthyl group Chemical group 0.000 description 1
- 239000005445 natural material Substances 0.000 description 1
- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- 125000001400 nonyl 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])[H] 0.000 description 1
- SJYNFBVQFBRSIB-UHFFFAOYSA-N norbornadiene Chemical compound C1=CC2C=CC1C2 SJYNFBVQFBRSIB-UHFFFAOYSA-N 0.000 description 1
- 125000003261 o-tolyl group Chemical group [H]C1=C([H])C(*)=C(C([H])=C1[H])C([H])([H])[H] 0.000 description 1
- 125000002347 octyl 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])[H] 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 229920000620 organic polymer Polymers 0.000 description 1
- 150000003961 organosilicon compounds Chemical class 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 description 1
- 125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 description 1
- 239000005022 packaging material Substances 0.000 description 1
- 125000002255 pentenyl group Chemical group C(=CCCC)* 0.000 description 1
- 125000005561 phenanthryl group Chemical group 0.000 description 1
- 229950000688 phenothiazine Drugs 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 238000007639 printing Methods 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 229910052895 riebeckite Inorganic materials 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- DCKVNWZUADLDEH-UHFFFAOYSA-N sec-butyl acetate Chemical compound CCC(C)OC(C)=O DCKVNWZUADLDEH-UHFFFAOYSA-N 0.000 description 1
- BHRZNVHARXXAHW-UHFFFAOYSA-N sec-butylamine Chemical compound CCC(C)N BHRZNVHARXXAHW-UHFFFAOYSA-N 0.000 description 1
- 229910000077 silane Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000005507 spraying Methods 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
- 238000003860 storage Methods 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 229950011008 tetrachloroethylene Drugs 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 125000003396 thiol group Chemical group [H]S* 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- UHUUYVZLXJHWDV-UHFFFAOYSA-N trimethyl(methylsilyloxy)silane Chemical group C[SiH2]O[Si](C)(C)C UHUUYVZLXJHWDV-UHFFFAOYSA-N 0.000 description 1
- 239000002759 woven fabric Substances 0.000 description 1
- 150000003738 xylenes Chemical class 0.000 description 1
- 125000005023 xylyl group Chemical group 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
- 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
- C08L83/14—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 at least two but not all the silicon atoms are connected by linkages other than oxygen atoms
-
- 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
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/48—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule in which at least two but not all the silicon atoms are connected by linkages other than oxygen atoms
- C08G77/50—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule in which at least two but not all the silicon atoms are connected by linkages other than oxygen atoms by carbon linkages
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D183/00—Coating compositions based on 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; Coating compositions based on derivatives of such polymers
- C09D183/14—Coating compositions based on 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; Coating compositions based on derivatives of such polymers in which at least two but not all the silicon atoms are connected by linkages other than oxygen atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Materials Engineering (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Silicon Polymers (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Paints Or Removers (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Seasonings (AREA)
- Crystals, And After-Treatments Of Crystals (AREA)
- Separation, Sorting, Adjustment, Or Bending Of Sheets To Be Conveyed (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE4123423A DE4123423A1 (de) | 1991-07-15 | 1991-07-15 | Alkenylgruppen aufweisende siloxancopolymere, deren herstellung und verwendung |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| NO922772D0 NO922772D0 (no) | 1992-07-14 |
| NO922772L NO922772L (no) | 1993-01-18 |
| NO301019B1 true NO301019B1 (no) | 1997-09-01 |
Family
ID=6436197
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO922772A NO301019B1 (no) | 1991-07-15 | 1992-07-14 | Fornettbare blandinger som inneholder siloxankopolymerer som oppviser alkenylgrupper, slike siloxankopolymerer, og anvendelse av blandingene |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US5241034A (ja) |
| EP (1) | EP0523660B1 (ja) |
| JP (1) | JPH0794557B2 (ja) |
| AT (1) | ATE149541T1 (ja) |
| CA (1) | CA2073813C (ja) |
| DE (2) | DE4123423A1 (ja) |
| ES (1) | ES2097836T3 (ja) |
| FI (1) | FI923223A (ja) |
| NO (1) | NO301019B1 (ja) |
Families Citing this family (44)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE4215030A1 (de) * | 1992-05-07 | 1993-11-11 | Wacker Chemie Gmbh | Vinyloxygruppen aufweisende Siloxancopolymere, deren Herstellung und Verwendung |
| DE4300809A1 (de) * | 1993-01-14 | 1994-07-21 | Wacker Chemie Gmbh | Alkenylgruppen aufweisende Siloxancopolymere, deren Herstellung und Verwendung |
| JPH0770324A (ja) * | 1993-09-03 | 1995-03-14 | Toray Dow Corning Silicone Co Ltd | 有機ケイ素重合体の製造方法 |
| US5545831A (en) * | 1993-10-22 | 1996-08-13 | Dow Corning Toray Silicone Co., Ltd. | Silicone compositions for the formation of cured release coatings |
| DE4336703A1 (de) * | 1993-10-27 | 1995-05-04 | Wacker Chemie Gmbh | Vernetzbare Zusammensetzungen und deren Verwendung zur Herstellung von klebrige Stoffe abweisenden Überzügen |
| GB9322793D0 (en) * | 1993-11-05 | 1993-12-22 | Dow Corning | Silicone release compositions |
| GB9322794D0 (en) * | 1993-11-05 | 1993-12-22 | Dow Corning | Silicone release compositions |
| FR2720752B1 (fr) | 1994-06-07 | 1996-10-31 | Rhone Poulenc Chimie | Composition silicone réticulable ou réticulée, antiadhérente et imprimable. |
| DE19535005A1 (de) * | 1995-09-21 | 1997-03-27 | Wacker Chemie Gmbh | Wäßrige Organopolysiloxanemulsionen sowie Emulgatoren zu deren Herstellung |
| DE19541451A1 (de) * | 1995-11-07 | 1997-05-15 | Wacker Chemie Gmbh | Vernetzbare Zusammensetzungen |
| DE19548474A1 (de) * | 1995-12-22 | 1997-06-26 | Wacker Chemie Gmbh | Aliphatisch ungesättigte Reste aufweisende Organopolysiloxane, deren Herstellung und deren Verwendung in vernetzbaren Massen |
| GB9526498D0 (en) | 1995-12-23 | 1996-02-28 | Dow Corning | Silicone release coating compositions |
| US5691435A (en) | 1996-01-25 | 1997-11-25 | Wacker-Chemie Gmbh | Crosslinkable compositions |
| DE19629053A1 (de) * | 1996-07-17 | 1998-01-22 | Wacker Chemie Gmbh | Aliphatisch ungesättigte Kohlenwasserstoffgruppen aufweisende Organosiliciumverbindungen |
| DE19637158A1 (de) * | 1996-09-12 | 1998-03-19 | Wacker Chemie Gmbh | Si-gebundene Wasserstoffatome aufweisende Organosiliciumverbindungen in vernetzbaren Zusammensetzungen |
| DE19638125A1 (de) * | 1996-09-18 | 1998-03-19 | Wacker Chemie Gmbh | Aminogruppen aufweisende Organosiliciumverbindungen, deren Herstellung und Verwendung |
| US5708075A (en) * | 1996-12-30 | 1998-01-13 | Dow Corning Corporation | Silicone release coating compositions |
| DE19701393A1 (de) * | 1997-01-16 | 1998-07-23 | Wacker Chemie Gmbh | Polymere Organosiliciumverbindungen, deren Herstellung und Verwendung |
| DE19718470A1 (de) * | 1997-04-30 | 1998-11-05 | Wacker Chemie Gmbh | Verfahren zur Herstellung von Si-gebundene Wasserstoffatome aufweisenden Organosiliciumverbindungen |
| DE19718634A1 (de) * | 1997-05-02 | 1998-11-05 | Wacker Chemie Gmbh | Strahlungs- oder thermischhärtende Organosiloxanmassen mit (Methyl)styrolgruppen |
| DE19723669A1 (de) * | 1997-06-05 | 1998-12-10 | Wacker Chemie Gmbh | Vernetzbare Zusammensetzungen |
| DE19755151A1 (de) * | 1997-12-11 | 1999-06-24 | Wacker Chemie Gmbh | Vernetzbare Zusammensetzungen |
| US6080829A (en) * | 1998-06-24 | 2000-06-27 | Medtronic, Inc. | Silalkylenesiloxane copolymer materials and methods for their preparation |
| DE19856115A1 (de) * | 1998-12-04 | 2000-06-21 | Wacker Chemie Gmbh | Alkenylgruppen aufweisende Siloxancopolymere |
| US6265515B1 (en) | 1999-06-14 | 2001-07-24 | The United States Of America As Represented By The Secretary Of The Navy | Fluorinated silicone resin fouling release composition |
| DE19960291A1 (de) * | 1999-12-14 | 2001-07-12 | Wacker Chemie Gmbh | Mehrphasige Zubereitungen von Organosiliciumverbindungen |
| DE50201143D1 (de) * | 2001-07-19 | 2004-11-04 | Wacker Chemie Gmbh | Verzweigte Organosiloxan(co)polymere und deren Verwendung als Antimisting Additive für Siliconbeschichtungszusammensetzungen |
| US20050165194A1 (en) * | 2001-11-20 | 2005-07-28 | Rhodia Chimie | Crosslinking agent for a silicone composition which can be crosslinked at low temperature based on a hydrogenated silicone oil comprising Si-H units at the chain end and in the chain |
| FR2832414B1 (fr) * | 2001-11-20 | 2004-01-30 | Rhodia Chimie Sa | Reticulant pour composition silicone reticulable a basse temperature a base d'une huile silicone hydrogenee comprenant des motifs si-h en bout de chaine et dans la chaine |
| DE10161334A1 (de) * | 2001-12-13 | 2003-07-17 | Wacker Chemie Gmbh | Alkenylgruppen aufweisende Siloxancopolymere als Antimisting Additive für Siliconbeschichtungszusammensetzungen |
| FR2833963B1 (fr) * | 2001-12-21 | 2004-03-12 | Rhodia Chimie Sa | RETICULANT POUR UNE COMPOSITION SILICONE RETICULABLE AVEC DE BAS TAUX DE PLATINE, A BASE D'UNE HUILE SILICONE HYDROGENEE COMPORTANT DES MOTIFS Si-H EN BOUT DE CHAINE ET DANS LA CHAINE |
| DE50302603D1 (de) * | 2002-02-04 | 2006-05-04 | Basf Ag | Verwendung von anti-adhäsiven verpackungsmaterialien für die verpackung von chemikalien und lebensmitteln |
| DE10210014A1 (de) * | 2002-03-07 | 2003-09-25 | Wacker Chemie Gmbh | Si-gebundene Wasserstoffatome aufweisende Siloxancopolymere als Antimisting Additive für Siliconbeschichtungszusammensetzungen |
| DE10210015A1 (de) | 2002-03-07 | 2003-09-25 | Wacker Chemie Gmbh | Verwendung von Alkenylgruppen aufweisenden Siloxancopolymeren als Antimisting Additive in vernetzbaren Siliconbeschichtungszusammensetzungen |
| DE10210026A1 (de) * | 2002-03-07 | 2003-09-25 | Wacker Chemie Gmbh | Verzweigte Organosiliciumverbindungen als Antimisting Additive für Siliconbeschichtungszusammensetzungen |
| EP1573086A4 (en) * | 2002-09-18 | 2012-10-03 | Air Prod & Chem | ADDITIVES FOR PREVENTING DETERIORATION OF ALKYL-HYDROGEN SILOXANES |
| DE10358060A1 (de) * | 2003-12-11 | 2005-07-14 | Wacker-Chemie Gmbh | Verfahren zur Herstellung hochviskoser Organopolysiloxane |
| DE102004038148A1 (de) * | 2004-08-05 | 2006-03-16 | Wacker Chemie Ag | Verfahren zur Herstellung von Emulsionen von hochviskosen Organopolysiloxanen |
| JP4743757B2 (ja) * | 2004-10-22 | 2011-08-10 | 信越化学工業株式会社 | シリコーン紙処理剤 |
| DE102006052730A1 (de) * | 2006-11-08 | 2008-05-15 | Wacker Chemie Ag | Verfahren zur Behandlung von Füllfasern mit wässrigen Dispersionen von Organopolysiloxanen |
| DE102007055844A1 (de) | 2007-12-17 | 2009-06-25 | Wacker Chemie Ag | Vernetzbare Siliconbeschichtungszusammensetzungen |
| DE102008027502A1 (de) | 2008-06-10 | 2009-12-17 | Tesa Se | Verfahren zur Herstellung von Releaselinern |
| BRPI0916596B1 (pt) | 2008-07-30 | 2019-09-17 | Bluestar Silicones France Sas | Composição de silicone para o revestimento de um suporte flexível destinado a formar um revestimento reticulado que tem fixação aumentada, resistência mecânica e reatividade |
| KR101902167B1 (ko) | 2014-04-28 | 2018-10-01 | 다우 실리콘즈 코포레이션 | 가교결합된 조성물 및 이를 포함하는 화장 조성물 |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2575085B1 (fr) * | 1984-12-20 | 1987-02-20 | Rhone Poulenc Spec Chim | Complexe platine-triene comme catalyseur de reaction d'hydrosilylation et son procede de preparation |
| JPS63235367A (ja) * | 1987-03-24 | 1988-09-30 | Shin Etsu Chem Co Ltd | オルガノポリシロキサン組成物 |
| EP0414938A1 (en) * | 1989-08-30 | 1991-03-06 | Nippon Unicar Company Limited | A crosslinkable composition |
| DE4002922A1 (de) * | 1990-02-01 | 1991-08-08 | Wacker Chemie Gmbh | Alkenyloxygruppen aufweisende siloxancopolymere, deren herstellung und verwendung |
| DE4002879A1 (de) * | 1990-02-01 | 1991-08-08 | Wacker Chemie Gmbh | Alkenylgruppen aufweisende siloxancopolymere, deren herstellung und verwendung |
| JP2866181B2 (ja) * | 1990-10-04 | 1999-03-08 | 鐘淵化学工業株式会社 | 粘着剤組成物 |
-
1991
- 1991-07-15 DE DE4123423A patent/DE4123423A1/de not_active Withdrawn
-
1992
- 1992-07-14 US US07/913,089 patent/US5241034A/en not_active Expired - Lifetime
- 1992-07-14 JP JP4186659A patent/JPH0794557B2/ja not_active Expired - Fee Related
- 1992-07-14 CA CA002073813A patent/CA2073813C/en not_active Expired - Fee Related
- 1992-07-14 FI FI923223A patent/FI923223A/fi not_active Application Discontinuation
- 1992-07-14 NO NO922772A patent/NO301019B1/no unknown
- 1992-07-15 ES ES92112080T patent/ES2097836T3/es not_active Expired - Lifetime
- 1992-07-15 DE DE59208091T patent/DE59208091D1/de not_active Expired - Fee Related
- 1992-07-15 AT AT92112080T patent/ATE149541T1/de not_active IP Right Cessation
- 1992-07-15 EP EP92112080A patent/EP0523660B1/de not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| ATE149541T1 (de) | 1997-03-15 |
| EP0523660A1 (de) | 1993-01-20 |
| DE4123423A1 (de) | 1993-01-21 |
| EP0523660B1 (de) | 1997-03-05 |
| DE59208091D1 (de) | 1997-04-10 |
| JPH0794557B2 (ja) | 1995-10-11 |
| US5241034A (en) | 1993-08-31 |
| NO922772L (no) | 1993-01-18 |
| JPH05194743A (ja) | 1993-08-03 |
| CA2073813C (en) | 1997-03-04 |
| FI923223A (fi) | 1993-01-16 |
| CA2073813A1 (en) | 1993-01-16 |
| ES2097836T3 (es) | 1997-04-16 |
| FI923223A0 (fi) | 1992-07-14 |
| NO922772D0 (no) | 1992-07-14 |
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