CA1142818A - Elastomeres au silicone peinturables - Google Patents

Elastomeres au silicone peinturables

Info

Publication number: CA1142818A
Authority: CA; Canada
Prior art keywords: group; radicals; monovalent hydrocarbon; paint; hydrocarbon radicals
Prior art date: 1978-12-01
Legal status (The legal status 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 status listed.): Expired

Application number

CA000341042A

Other languages

English (en)

Inventor

August Schiller

Alois Strasser

Oswin Sommer

Eckhart Louis

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Wacker Chemie AG

Original Assignee

Wacker Chemie AG

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

1979-12-03

Publication date

1983-03-15

1979-12-03 Application filed by Wacker Chemie AG filed Critical Wacker Chemie AG

1983-03-15 Application granted granted Critical

1983-03-15 Publication of CA1142818A publication Critical patent/CA1142818A/fr

Status Expired legal-status Critical Current

Links

229920002379 silicone rubber Polymers 0.000 title description 8
239000004215 Carbon black (E152) Substances 0.000 claims abstract description 36
229930195733 hydrocarbon Natural products 0.000 claims abstract description 36
229920001296 polysiloxane Polymers 0.000 claims abstract description 35
239000003973 paint Substances 0.000 claims abstract description 33
239000000203 mixture Substances 0.000 claims abstract description 28
238000000034 method Methods 0.000 claims abstract description 27
229910000077 silane Inorganic materials 0.000 claims abstract description 23
BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 claims abstract description 21
229910052710 silicon Inorganic materials 0.000 claims abstract description 21
239000010703 silicon Substances 0.000 claims abstract description 20
125000003277 amino group Chemical group 0.000 claims abstract description 16
150000003961 organosilicon compounds Chemical class 0.000 claims abstract description 16
229910052799 carbon Inorganic materials 0.000 claims abstract description 12
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 11
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims abstract description 10
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 10
239000001301 oxygen Substances 0.000 claims abstract description 10
229910052760 oxygen Inorganic materials 0.000 claims abstract description 10
229920001577 copolymer Polymers 0.000 claims abstract description 9
239000011118 polyvinyl acetate Substances 0.000 claims abstract description 7
239000006185 dispersion Substances 0.000 claims abstract description 6
239000002966 varnish Substances 0.000 claims abstract description 6
239000004922 lacquer Substances 0.000 claims abstract description 5
229920002689 polyvinyl acetate Polymers 0.000 claims abstract description 5
239000004800 polyvinyl chloride Substances 0.000 claims abstract description 5
239000000020 Nitrocellulose Substances 0.000 claims abstract description 4
229920001220 nitrocellulos Polymers 0.000 claims abstract description 4
229920000915 polyvinyl chloride Polymers 0.000 claims abstract description 4
-1 hydrocarbon radicals Chemical class 0.000 claims description 86
239000003054 catalyst Substances 0.000 claims description 18
125000003545 alkoxy group Chemical group 0.000 claims description 10
238000009833 condensation Methods 0.000 claims description 8
230000005494 condensation Effects 0.000 claims description 8
230000007062 hydrolysis Effects 0.000 claims description 6
238000006460 hydrolysis reaction Methods 0.000 claims description 6
239000001257 hydrogen Substances 0.000 claims description 5
229910052739 hydrogen Inorganic materials 0.000 claims description 5
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 5
125000000217 alkyl group Chemical group 0.000 claims description 3
150000002430 hydrocarbons Chemical class 0.000 claims description 3
229940075065 polyvinyl acetate Drugs 0.000 abstract description 5
239000002023 wood Substances 0.000 abstract description 4
239000000758 substrate Substances 0.000 abstract description 3
239000000806 elastomer Substances 0.000 description 30
229920001971 elastomer Polymers 0.000 description 29
XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 19
150000003254 radicals Chemical group 0.000 description 13
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 7
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 6
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
150000004756 silanes Chemical class 0.000 description 6
235000013870 dimethyl polysiloxane Nutrition 0.000 description 5
VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 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
239000004205 dimethyl polysiloxane Substances 0.000 description 4
125000002887 hydroxy group Chemical group [H]O* 0.000 description 4
229920000435 poly(dimethylsiloxane) Polymers 0.000 description 4
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
229920000180 alkyd Polymers 0.000 description 3
239000011248 coating agent Substances 0.000 description 3
238000000576 coating method Methods 0.000 description 3
239000012975 dibutyltin dilaurate Substances 0.000 description 3
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 3
239000000463 material Substances 0.000 description 3
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
239000004814 polyurethane Substances 0.000 description 3
239000000047 product Substances 0.000 description 3
235000012239 silicon dioxide Nutrition 0.000 description 3
239000000377 silicon dioxide Substances 0.000 description 3
239000002904 solvent Substances 0.000 description 3
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 2
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
102220644355 Laminin subunit alpha-5_R22N_mutation Human genes 0.000 description 2
229910019142 PO4 Inorganic materials 0.000 description 2
CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 description 2
239000002253 acid Substances 0.000 description 2
125000001931 aliphatic group Chemical group 0.000 description 2
150000005840 aryl radicals Chemical class 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
229910000019 calcium carbonate Inorganic materials 0.000 description 2
125000004432 carbon atom Chemical group C* 0.000 description 2
239000000470 constituent Substances 0.000 description 2
229920005645 diorganopolysiloxane polymer Polymers 0.000 description 2
239000000945 filler Substances 0.000 description 2
239000000413 hydrolysate Substances 0.000 description 2
230000014759 maintenance of location Effects 0.000 description 2
229910052751 metal Inorganic materials 0.000 description 2
239000002184 metal Substances 0.000 description 2
239000010452 phosphate Substances 0.000 description 2
229920002635 polyurethane Polymers 0.000 description 2
239000011369 resultant mixture Substances 0.000 description 2
230000000717 retained effect Effects 0.000 description 2
150000003839 salts Chemical class 0.000 description 2
150000003377 silicon compounds Chemical class 0.000 description 2
WYTZZXDRDKSJID-UHFFFAOYSA-N (3-aminopropyl)triethoxysilane Chemical compound CCO[Si](OCC)(OCC)CCCN WYTZZXDRDKSJID-UHFFFAOYSA-N 0.000 description 1
FZENGILVLUJGJX-NSCUHMNNSA-N (E)-acetaldehyde oxime Chemical compound C\C=N\O FZENGILVLUJGJX-NSCUHMNNSA-N 0.000 description 1
BMVXCPBXGZKUPN-UHFFFAOYSA-N 1-hexanamine Chemical compound CCCCCCN BMVXCPBXGZKUPN-UHFFFAOYSA-N 0.000 description 1
BHWUCEATHBXPOV-UHFFFAOYSA-N 2-triethoxysilylethanamine Chemical compound CCO[Si](CCN)(OCC)OCC BHWUCEATHBXPOV-UHFFFAOYSA-N 0.000 description 1
SLRMQYXOBQWXCR-UHFFFAOYSA-N 2154-56-5 Chemical compound [CH2]C1=CC=CC=C1 SLRMQYXOBQWXCR-UHFFFAOYSA-N 0.000 description 1
QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
239000004925 Acrylic resin Substances 0.000 description 1
229920000178 Acrylic resin Polymers 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
PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 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
229910018540 Si C Inorganic materials 0.000 description 1
235000021355 Stearic acid Nutrition 0.000 description 1
BOTDANWDWHJENH-UHFFFAOYSA-N Tetraethyl orthosilicate Chemical compound CCO[Si](OCC)(OCC)OCC BOTDANWDWHJENH-UHFFFAOYSA-N 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
YUDRVAHLXDBKSR-UHFFFAOYSA-N [CH]1CCCCC1 Chemical compound [CH]1CCCCC1 YUDRVAHLXDBKSR-UHFFFAOYSA-N 0.000 description 1
OBNDGIHQAIXEAO-UHFFFAOYSA-N [O].[Si] Chemical compound [O].[Si] OBNDGIHQAIXEAO-UHFFFAOYSA-N 0.000 description 1
JLHADLTXDDGZFX-UHFFFAOYSA-L [[acetyloxy(dibutyl)stannyl]oxy-dibutylstannyl] acetate Chemical compound CCCC[Sn](CCCC)(OC(C)=O)O[Sn](CCCC)(CCCC)OC(C)=O JLHADLTXDDGZFX-UHFFFAOYSA-L 0.000 description 1
NBJODVYWAQLZOC-UHFFFAOYSA-L [dibutyl(octanoyloxy)stannyl] octanoate Chemical compound CCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCC NBJODVYWAQLZOC-UHFFFAOYSA-L 0.000 description 1
PXAJQJMDEXJWFB-UHFFFAOYSA-N acetone oxime Chemical compound CC(C)=NO PXAJQJMDEXJWFB-UHFFFAOYSA-N 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
239000000654 additive Substances 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
150000001408 amides Chemical class 0.000 description 1
150000001412 amines Chemical class 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
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
238000009835 boiling Methods 0.000 description 1
230000001680 brushing effect 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
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 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
150000001723 carbon free-radicals Chemical class 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
238000004132 cross linking Methods 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
POULHZVOKOAJMA-UHFFFAOYSA-M dodecanoate Chemical compound CCCCCCCCCCCC([O-])=O POULHZVOKOAJMA-UHFFFAOYSA-M 0.000 description 1
239000000975 dye Substances 0.000 description 1
239000003974 emollient agent Substances 0.000 description 1
LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 1
ZVBWPVOCTORPLM-UHFFFAOYSA-N formylsilicon Chemical compound [Si]C=O ZVBWPVOCTORPLM-UHFFFAOYSA-N 0.000 description 1
ZZUFCTLCJUWOSV-UHFFFAOYSA-N furosemide Chemical compound C1=C(Cl)C(S(=O)(=O)N)=CC(C(O)=O)=C1NCC1=CC=CO1 ZZUFCTLCJUWOSV-UHFFFAOYSA-N 0.000 description 1
239000007792 gaseous phase Substances 0.000 description 1
150000002334 glycols Chemical class 0.000 description 1
XKDUZXVNQOZCFC-UHFFFAOYSA-N hexan-1-amine;hydron;chloride Chemical compound Cl.CCCCCCN XKDUZXVNQOZCFC-UHFFFAOYSA-N 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
XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 1
229910052742 iron Inorganic materials 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
238000005259 measurement Methods 0.000 description 1
150000002739 metals Chemical class 0.000 description 1
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical compound [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 description 1
238000002156 mixing Methods 0.000 description 1
MYBHTTGTUGMYGS-UHFFFAOYSA-N n'-(4-triethoxysilylbutyl)ethane-1,2-diamine Chemical compound CCO[Si](OCC)(OCC)CCCCNCCN MYBHTTGTUGMYGS-UHFFFAOYSA-N 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
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([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
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
238000010422 painting Methods 0.000 description 1
239000002245 particle 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
238000002360 preparation method Methods 0.000 description 1
239000002994 raw material Substances 0.000 description 1
238000005096 rolling process Methods 0.000 description 1
238000007789 sealing Methods 0.000 description 1
229910010271 silicon carbide Inorganic materials 0.000 description 1
238000005507 spraying Methods 0.000 description 1
239000008117 stearic acid Substances 0.000 description 1
150000003608 titanium Chemical class 0.000 description 1
UBOXGVDOUJQMTN-UHFFFAOYSA-N trichloroethylene Natural products ClCC(Cl)Cl UBOXGVDOUJQMTN-UHFFFAOYSA-N 0.000 description 1
ARKBFSWVHXKMSD-UHFFFAOYSA-N trimethoxysilylmethanamine Chemical compound CO[Si](CN)(OC)OC ARKBFSWVHXKMSD-UHFFFAOYSA-N 0.000 description 1
229940117958 vinyl acetate Drugs 0.000 description 1
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 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)
Application Of Or Painting With Fluid Materials (AREA)
Laminated Bodies (AREA)
Coating Of Shaped Articles Made Of Macromolecular Substances (AREA)
Silicon Polymers (AREA)
Supply Devices, Intensifiers, Converters, And Telemotors (AREA)
Insulating Bodies (AREA)

CA000341042A 1978-12-01 1979-12-03 Elastomeres au silicone peinturables Expired CA1142818A (fr)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
DEP2852090.3		1978-12-01
DE2852090A DE2852090C2 (de)	1978-12-01	1978-12-01	Verfahren zum Überziehen von vernetztem Organopolysiloxan

Publications (1)

Publication Number	Publication Date
CA1142818A true CA1142818A (fr)	1983-03-15

Family

ID=6056100

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA000341042A Expired CA1142818A (fr)	1978-12-01	1979-12-03	Elastomeres au silicone peinturables

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

Also Published As

Publication number	Publication date
JPS5575430A (en)	1980-06-06
SE438610B (sv)	1985-04-29
GB2039231A (en)	1980-08-06
BE880329A (fr)	1980-05-29
NL7908083A (nl)	1980-06-03
IT7950946A0 (it)	1979-11-29
DE2852090A1 (de)	1980-06-12
AU5339679A (en)	1980-06-05
CH641191A5 (de)	1984-02-15
FR2442668A1 (fr)	1980-06-27
FR2442668B1 (fr)	1984-12-14
ES486473A1 (es)	1980-05-16
DE2852090C2 (de)	1984-01-12
SE7909907L (sv)	1980-06-02
NO793902L (no)	1980-06-03

Legal Events

Date	Code	Title	Description
2000-03-15	MKEX	Expiry

Publication	Publication Date	Title
US5338574A (en)	1994-08-16	Method for producing a painted silicone elastomer
US3701753A (en)	1972-10-31	Solutions of room temperature vulcanizable silicone rubber compositions
US4267297A (en)	1981-05-12	Room temperature curable silicone resins
US5904988A (en)	1999-05-18	Sprayable, condensation curable silicone foul release coatings and articles coated therewith
US5525660A (en)	1996-06-11	Organopolysiloxane compositions and rubber articles
JP2994699B2 (ja)	1999-12-27	皮膜形成性オルガノポリシロキサン組成物
EP0390154B1 (fr)	1995-01-11	Composition de revêtement de silicone sans solvant
EP3119847B1 (fr)	2017-06-28	Silicones comprenant des groupes alkoxy et des groupes fonctionels ayant une réactivité spécifique
JPS60115660A (ja)	1985-06-22	微生物耐性の単一成分有機ポリシロキサン組成物
JPH1143647A (ja)	1999-02-16	表面処理剤および表面処理されたｅｐｄｍ物品
EP0334190A2 (fr)	1989-09-27	Composition de revêtement antiadhésif pour ustensiles de cuisine
EP0482480B1 (fr)	1995-01-11	Agent de traitement de surfaces et article en EPDM dont la surface est traitée
US4704419A (en)	1987-11-03	Organosiloxane primer composition
US5561184A (en)	1996-10-01	Room temperature curable silicone composition
JPH04214764A (ja)	1992-08-05	室温硬化性オルガノポリシロキサン組成物
GB2039231A (en)	1980-08-06	Coating crosslinked organopolysiloxanes
JPH0343310B2 (fr)	1991-07-02
US5486567A (en)	1996-01-23	Primer compositions
JP3154206B2 (ja)	2001-04-09	オルガノポリシロキサン組成物及びゴム部品
JPH04283248A (ja)	1992-10-08	塗膜形成剤組成物およびシリコーン弾性体表面の汚損防止方法
JPS5939306B2 (ja)	1984-09-21	皮膜形成方法
JPH0776680A (ja)	1995-03-20	プライマー組成物
JP3967717B2 (ja)	2007-08-29	有機珪素化合物を基礎とする架橋可能な材料
JPH107988A (ja)	1998-01-13	海洋構築物用室温硬化性オルガノシロキサンコーティング材
KR100208416B1 (ko)	1999-07-15	유기폴리실록산 조성물 및 그 도막을 갖는 고무부품