NL7908083A - Werkwijze voor het bekleden van verknoopt organopoly- siloxan. - Google Patents

Werkwijze voor het bekleden van verknoopt organopoly- siloxan. Download PDF

Info

Publication number: NL7908083A
Authority: NL; Netherlands
Prior art keywords: cross; group; linked; optionally substituted; organopolysiloxane
Prior art date: 1978-12-01

Application number

NL7908083A

Other languages

English (en)

Dutch (nl)

Original Assignee

Wacker Chemie Gmbh

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.)

1978-12-01

Filing date

1979-11-05

Publication date

1980-06-03

1979-11-05 Application filed by Wacker Chemie Gmbh filed Critical Wacker Chemie Gmbh

1980-06-03 Publication of NL7908083A publication Critical patent/NL7908083A/nl

Links

229920001296 polysiloxane Polymers 0.000 title claims description 45
238000000576 coating method Methods 0.000 title claims description 20
239000011248 coating agent Substances 0.000 title claims description 19
238000000034 method Methods 0.000 title claims description 16
239000000975 dye Substances 0.000 claims description 27
239000004215 Carbon black (E152) Substances 0.000 claims description 16
229930195733 hydrocarbon Natural products 0.000 claims description 16
125000003277 amino group Chemical group 0.000 claims description 14
229910000077 silane Inorganic materials 0.000 claims description 13
BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 claims description 12
125000003545 alkoxy group Chemical group 0.000 claims description 9
125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 9
150000004756 silanes Chemical class 0.000 claims description 9
239000003054 catalyst Substances 0.000 claims description 8
239000003795 chemical substances by application Substances 0.000 claims description 7
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 7
229910052710 silicon Inorganic materials 0.000 claims description 7
239000010703 silicon Substances 0.000 claims description 7
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 5
238000009833 condensation Methods 0.000 claims description 5
230000005494 condensation Effects 0.000 claims description 5
229910052799 carbon Inorganic materials 0.000 claims description 4
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 3
238000004043 dyeing Methods 0.000 claims description 3
230000007062 hydrolysis Effects 0.000 claims description 3
238000006460 hydrolysis reaction Methods 0.000 claims description 3
239000001301 oxygen Substances 0.000 claims description 3
229910052760 oxygen Inorganic materials 0.000 claims description 3
125000004430 oxygen atom Chemical group O* 0.000 claims description 2
KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 claims 1
-1 hydrocarbon radical Chemical class 0.000 description 34
229920001971 elastomer Polymers 0.000 description 22
239000000806 elastomer Substances 0.000 description 22
150000003961 organosilicon compounds Chemical class 0.000 description 13
239000000203 mixture Substances 0.000 description 10
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 6
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
238000004132 cross linking Methods 0.000 description 6
VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 4
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 4
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 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
239000012975 dibutyltin dilaurate Substances 0.000 description 4
239000004205 dimethyl polysiloxane Substances 0.000 description 4
235000013870 dimethyl polysiloxane Nutrition 0.000 description 4
229920005645 diorganopolysiloxane polymer Polymers 0.000 description 4
239000006185 dispersion Substances 0.000 description 4
150000002430 hydrocarbons Chemical group 0.000 description 4
230000014759 maintenance of location Effects 0.000 description 4
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
238000002156 mixing Methods 0.000 description 4
229920000435 poly(dimethylsiloxane) Polymers 0.000 description 4
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
229920000180 alkyd Polymers 0.000 description 3
230000000052 comparative effect Effects 0.000 description 3
229920001577 copolymer Polymers 0.000 description 3
125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
238000010409 ironing Methods 0.000 description 3
239000004922 lacquer Substances 0.000 description 3
229920002635 polyurethane Polymers 0.000 description 3
239000004814 polyurethane Substances 0.000 description 3
238000002360 preparation method Methods 0.000 description 3
239000012262 resinous product Substances 0.000 description 3
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
125000004442 acylamino group Chemical group 0.000 description 2
125000000217 alkyl group Chemical group 0.000 description 2
125000002344 aminooxy group Chemical group [H]N([H])O[*] 0.000 description 2
125000003710 aryl alkyl group Chemical group 0.000 description 2
125000003118 aryl group Chemical group 0.000 description 2
SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 2
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 2
229910000019 calcium carbonate Inorganic materials 0.000 description 2
125000004432 carbon atom Chemical group C* 0.000 description 2
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 2
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
239000000945 filler Substances 0.000 description 2
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 2
229910052742 iron Inorganic materials 0.000 description 2
229910052751 metal Inorganic materials 0.000 description 2
239000002184 metal Substances 0.000 description 2
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
125000003544 oxime group Chemical group 0.000 description 2
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
125000002467 phosphate group Chemical group [H]OP(=O)(O[H])O[*] 0.000 description 2
239000011118 polyvinyl acetate Substances 0.000 description 2
229920002689 polyvinyl acetate Polymers 0.000 description 2
229920000915 polyvinyl chloride Polymers 0.000 description 2
239000004800 polyvinyl chloride Substances 0.000 description 2
239000002510 pyrogen Substances 0.000 description 2
150000003254 radicals Chemical class 0.000 description 2
150000003377 silicon compounds Chemical class 0.000 description 2
239000000377 silicon dioxide Substances 0.000 description 2
239000000243 solution Substances 0.000 description 2
239000000126 substance Substances 0.000 description 2
239000000758 substrate Substances 0.000 description 2
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
239000002023 wood Substances 0.000 description 2
WYTZZXDRDKSJID-UHFFFAOYSA-N (3-aminopropyl)triethoxysilane Chemical compound CCO[Si](OCC)(OCC)CCCN WYTZZXDRDKSJID-UHFFFAOYSA-N 0.000 description 1
ODIGIKRIUKFKHP-UHFFFAOYSA-N (n-propan-2-yloxycarbonylanilino) acetate Chemical group CC(C)OC(=O)N(OC(C)=O)C1=CC=CC=C1 ODIGIKRIUKFKHP-UHFFFAOYSA-N 0.000 description 1
BMVXCPBXGZKUPN-UHFFFAOYSA-N 1-hexanamine Chemical compound CCCCCCN BMVXCPBXGZKUPN-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
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
BHWUCEATHBXPOV-UHFFFAOYSA-N 2-triethoxysilylethanamine Chemical compound CCO[Si](CCN)(OCC)OCC BHWUCEATHBXPOV-UHFFFAOYSA-N 0.000 description 1
SWDDLRSGGCWDPH-UHFFFAOYSA-N 4-triethoxysilylbutan-1-amine Chemical compound CCO[Si](OCC)(OCC)CCCCN SWDDLRSGGCWDPH-UHFFFAOYSA-N 0.000 description 1
239000004925 Acrylic resin Substances 0.000 description 1
229920000178 Acrylic resin Polymers 0.000 description 1
AOAHANATESKGQL-UHFFFAOYSA-N ClC(Cl)OOC(Cl)Cl Chemical compound ClC(Cl)OOC(Cl)Cl AOAHANATESKGQL-UHFFFAOYSA-N 0.000 description 1
JYFHYPJRHGVZDY-UHFFFAOYSA-N Dibutyl phosphate Chemical group CCCCOP(O)(=O)OCCCC JYFHYPJRHGVZDY-UHFFFAOYSA-N 0.000 description 1
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 1
239000000020 Nitrocellulose Substances 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
239000004820 Pressure-sensitive adhesive Substances 0.000 description 1
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
235000021355 Stearic acid Nutrition 0.000 description 1
ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-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
ISKQADXMHQSTHK-UHFFFAOYSA-N [4-(aminomethyl)phenyl]methanamine Chemical compound NCC1=CC=C(CN)C=C1 ISKQADXMHQSTHK-UHFFFAOYSA-N 0.000 description 1
NBJODVYWAQLZOC-UHFFFAOYSA-L [dibutyl(octanoyloxy)stannyl] octanoate Chemical group CCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCC NBJODVYWAQLZOC-UHFFFAOYSA-L 0.000 description 1
DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 1
PXAJQJMDEXJWFB-UHFFFAOYSA-N acetone oxime Chemical compound CC(C)=NO PXAJQJMDEXJWFB-UHFFFAOYSA-N 0.000 description 1
125000003668 acetyloxy group Chemical group [H]C([H])([H])C(=O)O[*] 0.000 description 1
239000002253 acid Substances 0.000 description 1
150000007513 acids Chemical group 0.000 description 1
125000004423 acyloxy group Chemical group 0.000 description 1
239000000654 additive Substances 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
150000001335 aliphatic alkanes Chemical class 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
125000003342 alkenyl group Chemical group 0.000 description 1
125000004183 alkoxy alkyl group Chemical group 0.000 description 1
125000002877 alkyl aryl group Chemical group 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
125000004103 aminoalkyl group Chemical group 0.000 description 1
150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
125000000043 benzamido group Chemical group [H]N([*])C(=O)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
238000009835 boiling Methods 0.000 description 1
125000004799 bromophenyl group Chemical group 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
LXTKCTMGEWVPTB-UHFFFAOYSA-N butylazanium;acetate Chemical compound CC(O)=O.CCCCN LXTKCTMGEWVPTB-UHFFFAOYSA-N 0.000 description 1
150000001721 carbon Chemical group 0.000 description 1
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
150000001734 carboxylic acid salts Chemical class 0.000 description 1
150000001735 carboxylic acids Chemical class 0.000 description 1
150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
125000000068 chlorophenyl group Chemical group 0.000 description 1
150000001875 compounds Chemical class 0.000 description 1
125000004966 cyanoalkyl group Chemical group 0.000 description 1
125000000753 cycloalkyl group Chemical group 0.000 description 1
125000000596 cyclohexenyl group Chemical group C1(=CCCCC1)* 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
AYOHIQLKSOJJQH-UHFFFAOYSA-N dibutyltin Chemical compound CCCC[Sn]CCCC AYOHIQLKSOJJQH-UHFFFAOYSA-N 0.000 description 1
239000012895 dilution Substances 0.000 description 1
238000010790 dilution Methods 0.000 description 1
125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
238000007598 dipping method Methods 0.000 description 1
POULHZVOKOAJMA-UHFFFAOYSA-M dodecanoate Chemical compound CCCCCCCCCCCC([O-])=O POULHZVOKOAJMA-UHFFFAOYSA-M 0.000 description 1
239000007789 gas Substances 0.000 description 1
125000003106 haloaryl group Chemical group 0.000 description 1
XKDUZXVNQOZCFC-UHFFFAOYSA-N hexan-1-amine;hydron;chloride Chemical compound Cl.CCCCCCN XKDUZXVNQOZCFC-UHFFFAOYSA-N 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
229940070765 laurate Drugs 0.000 description 1
VQPKAMAVKYTPLB-UHFFFAOYSA-N lead;octanoic acid Chemical compound [Pb].CCCCCCCC(O)=O VQPKAMAVKYTPLB-UHFFFAOYSA-N 0.000 description 1
239000007788 liquid Substances 0.000 description 1
229910052748 manganese Inorganic materials 0.000 description 1
239000011572 manganese Substances 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
239000000463 material Substances 0.000 description 1
238000005259 measurement Methods 0.000 description 1
150000002739 metals Chemical class 0.000 description 1
WHIVNJATOVLWBW-SNAWJCMRSA-N methylethyl ketone oxime Chemical group CC\C(C)=N\O WHIVNJATOVLWBW-SNAWJCMRSA-N 0.000 description 1
238000005065 mining Methods 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
HDNXAGOHLKHJOA-UHFFFAOYSA-N n-[bis(cyclohexylamino)-methylsilyl]cyclohexanamine Chemical compound C1CCCCC1N[Si](NC1CCCCC1)(C)NC1CCCCC1 HDNXAGOHLKHJOA-UHFFFAOYSA-N 0.000 description 1
WHIVNJATOVLWBW-UHFFFAOYSA-N n-butan-2-ylidenehydroxylamine Chemical compound CCC(C)=NO WHIVNJATOVLWBW-UHFFFAOYSA-N 0.000 description 1
125000002004 n-butylamino group Chemical group [H]N(*)C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
229920001220 nitrocellulos Polymers 0.000 description 1
QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
125000005375 organosiloxane group Chemical group 0.000 description 1
150000002924 oxiranes Chemical class 0.000 description 1
239000002245 particle Substances 0.000 description 1
239000012466 permeate Substances 0.000 description 1
239000004014 plasticizer Substances 0.000 description 1
150000003058 platinum compounds Chemical class 0.000 description 1
229920000728 polyester Polymers 0.000 description 1
229920005553 polystyrene-acrylate Polymers 0.000 description 1
238000002203 pretreatment Methods 0.000 description 1
230000001698 pyrogenic effect Effects 0.000 description 1
238000005096 rolling process Methods 0.000 description 1
125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
239000002904 solvent Substances 0.000 description 1
238000005507 spraying Methods 0.000 description 1
238000003892 spreading Methods 0.000 description 1
239000007858 starting material Substances 0.000 description 1
239000008117 stearic acid 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
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
150000003608 titanium Chemical class 0.000 description 1
125000005425 toluyl group Chemical group 0.000 description 1
ARKBFSWVHXKMSD-UHFFFAOYSA-N trimethoxysilylmethanamine Chemical compound CO[Si](CN)(OC)OC ARKBFSWVHXKMSD-UHFFFAOYSA-N 0.000 description 1
RZOPLESFSUHKPZ-UHFFFAOYSA-N trimethyl(methylstannyloxy)stannane Chemical compound C[SnH2]O[Sn](C)(C)C RZOPLESFSUHKPZ-UHFFFAOYSA-N 0.000 description 1
229920002554 vinyl polymer Polymers 0.000 description 1
239000008096 xylene Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J7/00—Chemical treatment or coating of shaped articles made of macromolecular substances
- C08J7/04—Coating
- C08J7/043—Improving the adhesiveness of the coatings per se, e.g. forming primers
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J7/00—Chemical treatment or coating of shaped articles made of macromolecular substances
- C08J7/04—Coating
- C08J7/042—Coating with two or more layers, where at least one layer of a composition contains a polymer binder
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2383/00—Characterised by the use 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; Derivatives of such polymers
- C08J2383/04—Polysiloxanes
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2477/00—Characterised by the use of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Derivatives of such polymers
- C08J2477/10—Polyamides derived from aromatically bound amino and carboxyl groups of amino carboxylic acids or of polyamines and polycarboxylic acids

Landscapes

Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
Paints Or Removers (AREA)
Compositions Of Macromolecular Compounds (AREA)
Coating Of Shaped Articles Made Of Macromolecular Substances (AREA)
Application Of Or Painting With Fluid Materials (AREA)
Supply Devices, Intensifiers, Converters, And Telemotors (AREA)
Insulating Bodies (AREA)
Silicon Polymers (AREA)
Laminated Bodies (AREA)

NL7908083A 1978-12-01 1979-11-05 Werkwijze voor het bekleden van verknoopt organopoly- siloxan. NL7908083A (nl)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
DE2852090A DE2852090C2 (de)	1978-12-01	1978-12-01	Verfahren zum Überziehen von vernetztem Organopolysiloxan
DE2852090		1978-12-01

Publications (1)

Publication Number	Publication Date
NL7908083A true NL7908083A (nl)	1980-06-03

Family

ID=6056100

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NL7908083A NL7908083A (nl)	1978-12-01	1979-11-05	Werkwijze voor het bekleden van verknoopt organopoly- siloxan.

Country Status (13)

Country	Link
JP (1)	JPS5575430A (fr)
AU (1)	AU5339679A (fr)
BE (1)	BE880329A (fr)
CA (1)	CA1142818A (fr)
CH (1)	CH641191A5 (fr)
DE (1)	DE2852090C2 (fr)
ES (1)	ES486473A1 (fr)
FR (1)	FR2442668A1 (fr)
GB (1)	GB2039231A (fr)
IT (1)	IT7950946A0 (fr)
NL (1)	NL7908083A (fr)
NO (1)	NO793902L (fr)
SE (1)	SE438610B (fr)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS57180674A (en) *	1981-04-30	1982-11-06	Toray Silicone Co Ltd	Primer composition for heat-curable silicone elastomer
JPH066680B2 (ja) *	1985-10-30	1994-01-26	東レ・ダウコーニング・シリコーン株式会社	プライマ−組成物
US5248334A (en) *	1988-12-12	1993-09-28	Dow Corning Corporation	Primer composition, coating method and coated silicone substrates
US4923946A (en) *	1988-12-12	1990-05-08	Dow Corning Corporation	Composition and method for priming and coating silicone substrates
US4992312A (en) *	1989-03-13	1991-02-12	Dow Corning Wright Corporation	Methods of forming permeation-resistant, silicone elastomer-containing composite laminates and devices produced thereby
US5213617A (en) *	1991-06-13	1993-05-25	Dow Corning Corporation	Primer for silicone substrates
JP6054060B2 (ja) *	2012-05-17	2016-12-27	株式会社フコク	ゴム部材、ゴム用コーティング剤、およびゴム部材製造方法
DE102018100214A1 (de) *	2018-01-08	2019-07-11	Jörg Nass	Verfahren zum Grundieren von Silikonoberflächen

1978
- 1978-12-01 DE DE2852090A patent/DE2852090C2/de not_active Expired
1979
- 1979-11-05 NL NL7908083A patent/NL7908083A/nl not_active Application Discontinuation
- 1979-11-29 BE BE0/198344A patent/BE880329A/fr not_active IP Right Cessation
- 1979-11-29 IT IT7950946A patent/IT7950946A0/it unknown
- 1979-11-30 NO NO793902A patent/NO793902L/no unknown
- 1979-11-30 CH CH1067079A patent/CH641191A5/de not_active IP Right Cessation
- 1979-11-30 SE SE7909907A patent/SE438610B/sv unknown
- 1979-11-30 GB GB7941492A patent/GB2039231A/en not_active Withdrawn
- 1979-11-30 ES ES486473A patent/ES486473A1/es not_active Expired
- 1979-11-30 JP JP15451979A patent/JPS5575430A/ja active Pending
- 1979-12-03 AU AU53396/79A patent/AU5339679A/en not_active Abandoned
- 1979-12-03 CA CA000341042A patent/CA1142818A/fr not_active Expired
- 1979-12-03 FR FR7929649A patent/FR2442668A1/fr active Granted

Also Published As

Publication number	Publication date
NO793902L (no)	1980-06-03
CA1142818A (fr)	1983-03-15
SE7909907L (sv)	1980-06-02
FR2442668A1 (fr)	1980-06-27
GB2039231A (en)	1980-08-06
ES486473A1 (es)	1980-05-16
IT7950946A0 (it)	1979-11-29
FR2442668B1 (fr)	1984-12-14
DE2852090C2 (de)	1984-01-12
AU5339679A (en)	1980-06-05
JPS5575430A (en)	1980-06-06
SE438610B (sv)	1985-04-29
DE2852090A1 (de)	1980-06-12
CH641191A5 (de)	1984-02-15
BE880329A (fr)	1980-05-29

Legal Events

Date	Code	Title	Description
1985-01-01	A85	Still pending on 85-01-01
1986-07-01	BV	The patent application has lapsed

Publication	Publication Date	Title
US7005475B2 (en)	2006-02-28	Curable silicone compositions having improved adhesion to polymeric films
EP0467406B1 (fr)	1994-08-17	Composition filmogène d'organopolysiloxane
US6716533B2 (en)	2004-04-06	Paper release compositions having improved adhesion to paper and polymeric films
US4252933A (en)	1981-02-24	Self-bonding silicone coating composition
US4033924A (en)	1977-07-05	Heat curable organopolysiloxane compositions containing adhesion additives
US4157357A (en)	1979-06-05	Curable two-part silicone rubber compositions with improved adhesion properties
EP3119847B1 (fr)	2017-06-28	Silicones comprenant des groupes alkoxy et des groupes fonctionels ayant une réactivité spécifique
JPH05140459A (ja)	1993-06-08	シリコーンゴム組成物およびシリコーンゴム加工布
DE4414653A1 (de)	1994-11-17	Schneller klebende Silicon-Klebstoffzusammensetzungen
EP0171442A1 (fr)	1986-02-19	Revêtements anti-adhérents à base de siloxanes et d'agents inhibiteurs
EP0446030A2 (fr)	1991-09-11	Organopolysiloxanes sans solvant pour revêtements anti-adhésifs
JPH10501272A (ja)	1998-02-03	抗付着汚損および付着物除去性コーティング
US3576905A (en)	1971-04-27	Arc resistant siloxane vulcanizable at room temperature
JP4194683B2 (ja)	2008-12-10	噴霧可能な付加硬化性シリコーン汚損除去コーティング並びに該コーティングで被覆された物品
JPH05179159A (ja)	1993-07-20	プライマー組成物及びシリコーン支持体の上塗方法
KR940703896A (ko)	1994-12-12	코팅조성물
US5561184A (en)	1996-10-01	Room temperature curable silicone composition
US4704419A (en)	1987-11-03	Organosiloxane primer composition
NL7908083A (nl)	1980-06-03	Werkwijze voor het bekleden van verknoopt organopoly- siloxan.
US6387451B1 (en)	2002-05-14	Curable coating compositions
EP0044672B1 (fr)	1984-04-11	Promoteurs d'adhérence à base d'une résine phénylsiloxane et d'un polysiloxane ayant des groupes vinyliques
JPS5811900B2 (ja)	1983-03-05	オルガノポリシロキサンソセイブツ
JPH0341108B2 (fr)	1991-06-21
US5270110A (en)	1993-12-14	Film-forming organopolysiloxane composition
US2934519A (en)	1960-04-26	Room temperature curing silicone