CA1162692A - Caoutchoucs au silicone auto-collants vulcanisables a la temperature ambiante interieure - Google Patents

Caoutchoucs au silicone auto-collants vulcanisables a la temperature ambiante interieure

Info

Publication number: CA1162692A
Authority: CA; Canada
Prior art keywords: parts; weight; radicals; varies; monovalent hydrocarbon
Prior art date: 1980-08-29
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

CA000359263A

Other languages

English (en)

Inventor

Alfred H. Smith, Jr.

George P. Dezuba

Tyrone D. Mitchell

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.)

General Electric Co

Original Assignee

General Electric Co

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.)

1980-08-29

Filing date

1980-08-29

Publication date

1984-02-21

1980-08-29 Application filed by General Electric Co filed Critical General Electric Co

1980-08-29 Priority to CA000359263A priority Critical patent/CA1162692A/fr

1984-02-21 Application granted granted Critical

1984-02-21 Publication of CA1162692A publication Critical patent/CA1162692A/fr

Status Expired legal-status Critical Current

Links

239000000203 mixture Substances 0.000 title claims abstract description 134
229920002379 silicone rubber Polymers 0.000 title claims abstract description 31
239000004945 silicone rubber Substances 0.000 title claims abstract description 26
-1 polysiloxane Polymers 0.000 claims abstract description 123
239000000654 additive Substances 0.000 claims abstract description 51
229920001296 polysiloxane Polymers 0.000 claims abstract description 51
230000000996 additive effect Effects 0.000 claims abstract description 33
239000003054 catalyst Substances 0.000 claims abstract description 32
239000003431 cross linking reagent Substances 0.000 claims abstract description 31
239000000758 substrate Substances 0.000 claims abstract description 23
239000000945 filler Substances 0.000 claims abstract description 20
150000004756 silanes Chemical class 0.000 claims abstract description 20
229920005645 diorganopolysiloxane polymer Polymers 0.000 claims abstract description 16
229910052751 metal Inorganic materials 0.000 claims abstract description 13
239000002184 metal Substances 0.000 claims abstract description 13
239000004033 plastic Substances 0.000 claims abstract description 6
229920003023 plastic Polymers 0.000 claims abstract description 6
239000004215 Carbon black (E152) Substances 0.000 claims description 44
229930195733 hydrocarbon Natural products 0.000 claims description 44
125000004432 carbon atom Chemical group C* 0.000 claims description 30
SCPYDCQAZCOKTP-UHFFFAOYSA-N silanol Chemical compound [SiH3]O SCPYDCQAZCOKTP-UHFFFAOYSA-N 0.000 claims description 30
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 29
UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 claims description 24
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 24
229910052739 hydrogen Inorganic materials 0.000 claims description 21
239000001257 hydrogen Substances 0.000 claims description 21
125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 17
150000007524 organic acids Chemical class 0.000 claims description 15
239000012530 fluid Substances 0.000 claims description 14
ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical class [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims description 13
150000003254 radicals Chemical class 0.000 claims description 13
229910021626 Tin(II) chloride Inorganic materials 0.000 claims description 12
238000000034 method Methods 0.000 claims description 10
239000000377 silicon dioxide Substances 0.000 claims description 8
150000001734 carboxylic acid salts Chemical class 0.000 claims description 7
125000000962 organic group Chemical group 0.000 claims description 7
125000004469 siloxy group Chemical group [SiH3]O* 0.000 claims description 7
XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 5
125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 claims description 5
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 5
125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 claims description 5
229910052710 silicon Inorganic materials 0.000 claims description 5
125000005389 trialkylsiloxy group Chemical group 0.000 claims description 5
150000005840 aryl radicals Chemical class 0.000 claims description 4
150000002430 hydrocarbons Chemical class 0.000 claims description 4
239000010703 silicon Substances 0.000 claims description 4
239000002253 acid Substances 0.000 claims description 3
125000001183 hydrocarbyl group Chemical group 0.000 claims description 3
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims description 3
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 3
ISKQADXMHQSTHK-UHFFFAOYSA-N [4-(aminomethyl)phenyl]methanamine Chemical group NCC1=CC=C(CN)C=C1 ISKQADXMHQSTHK-UHFFFAOYSA-N 0.000 claims description 2
125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 claims description 2
PNOXNTGLSKTMQO-UHFFFAOYSA-L diacetyloxytin Chemical compound CC(=O)O[Sn]OC(C)=O PNOXNTGLSKTMQO-UHFFFAOYSA-L 0.000 claims description 2
239000003017 thermal stabilizer Substances 0.000 claims 2
BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 abstract description 36
229910000077 silane Inorganic materials 0.000 abstract description 36
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract description 26
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 abstract description 17
SXUXGFHXUDLTFO-UHFFFAOYSA-N (Z)-4-oxo-4-silyloxybut-2-enoic acid Chemical compound OC(=O)C=C/C(=O)O[SiH3] SXUXGFHXUDLTFO-UHFFFAOYSA-N 0.000 abstract description 13
229920005601 base polymer Polymers 0.000 abstract description 13
VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 abstract description 10
QPEZXRRQLZVKSU-UHFFFAOYSA-N 4-oxo-4-silyloxybutanoic acid Chemical compound OC(=O)CCC(=O)O[SiH3] QPEZXRRQLZVKSU-UHFFFAOYSA-N 0.000 abstract description 9
VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 abstract description 7
KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 abstract description 5
229920000642 polymer Polymers 0.000 description 31
239000000306 component Substances 0.000 description 28
239000003795 chemical substances by application Substances 0.000 description 13
VZCYOOQTPOCHFL-OWOJBTEDSA-L fumarate(2-) Chemical class [O-]C(=O)\C=C\C([O-])=O VZCYOOQTPOCHFL-OWOJBTEDSA-L 0.000 description 12
229910021485 fumed silica Inorganic materials 0.000 description 11
150000003900 succinic acid esters Chemical class 0.000 description 10
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
150000002688 maleic acid derivatives Chemical class 0.000 description 8
150000001732 carboxylic acid derivatives Chemical class 0.000 description 7
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 6
229910052799 carbon Inorganic materials 0.000 description 6
239000004615 ingredient Substances 0.000 description 6
BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 6
239000007983 Tris buffer Substances 0.000 description 5
125000003545 alkoxy group Chemical group 0.000 description 5
229910052782 aluminium Inorganic materials 0.000 description 5
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 5
235000010210 aluminium Nutrition 0.000 description 5
239000003921 oil Substances 0.000 description 5
150000003839 salts Chemical class 0.000 description 5
239000000565 sealant Substances 0.000 description 5
229940086735 succinate Drugs 0.000 description 5
229910000989 Alclad Inorganic materials 0.000 description 4
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-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
238000006243 chemical reaction Methods 0.000 description 4
150000001875 compounds Chemical class 0.000 description 4
239000012975 dibutyltin dilaurate Substances 0.000 description 4
229920001971 elastomer Polymers 0.000 description 4
239000000463 material Substances 0.000 description 4
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 4
239000000047 product Substances 0.000 description 4
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 3
JOPQOJFZJSAFHO-UHFFFAOYSA-N [bis(2-ethylhexanoyloxy)-methylsilyl] 2-ethylhexanoate Chemical compound CCCCC(CC)C(=O)O[Si](C)(OC(=O)C(CC)CCCC)OC(=O)C(CC)CCCC JOPQOJFZJSAFHO-UHFFFAOYSA-N 0.000 description 3
TVJPBVNWVPUZBM-UHFFFAOYSA-N [diacetyloxy(methyl)silyl] acetate Chemical compound CC(=O)O[Si](C)(OC(C)=O)OC(C)=O TVJPBVNWVPUZBM-UHFFFAOYSA-N 0.000 description 3
238000004132 cross linking Methods 0.000 description 3
238000011067 equilibration Methods 0.000 description 3
238000006460 hydrolysis reaction Methods 0.000 description 3
125000001181 organosilyl group Chemical group [SiH3]* 0.000 description 3
229910052697 platinum Inorganic materials 0.000 description 3
238000002360 preparation method Methods 0.000 description 3
239000005060 rubber Substances 0.000 description 3
239000003381 stabilizer Substances 0.000 description 3
239000005046 Chlorosilane Substances 0.000 description 2
PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 2
VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 2
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
125000004423 acyloxy group Chemical group 0.000 description 2
125000000217 alkyl group Chemical group 0.000 description 2
230000015572 biosynthetic process Effects 0.000 description 2
239000013522 chelant Substances 0.000 description 2
238000010276 construction Methods 0.000 description 2
229920001577 copolymer Polymers 0.000 description 2
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 2
DDJSWKLBKSLAAZ-UHFFFAOYSA-N cyclotetrasiloxane Chemical class O1[SiH2]O[SiH2]O[SiH2]O[SiH2]1 DDJSWKLBKSLAAZ-UHFFFAOYSA-N 0.000 description 2
238000011161 development Methods 0.000 description 2
230000018109 developmental process Effects 0.000 description 2
239000004205 dimethyl polysiloxane Substances 0.000 description 2
235000013870 dimethyl polysiloxane Nutrition 0.000 description 2
239000000806 elastomer Substances 0.000 description 2
238000013023 gasketing Methods 0.000 description 2
238000010438 heat treatment Methods 0.000 description 2
FFUAGWLWBBFQJT-UHFFFAOYSA-N hexamethyldisilazane Chemical compound C[Si](C)(C)N[Si](C)(C)C FFUAGWLWBBFQJT-UHFFFAOYSA-N 0.000 description 2
230000007062 hydrolysis Effects 0.000 description 2
150000002500 ions Chemical class 0.000 description 2
229910052748 manganese Inorganic materials 0.000 description 2
239000011572 manganese Substances 0.000 description 2
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 2
GEIHDEVWPDTQIM-UHFFFAOYSA-N methyl-tris(phenylmethoxy)silane Chemical compound C=1C=CC=CC=1CO[Si](OCC=1C=CC=CC=1)(C)OCC1=CC=CC=C1 GEIHDEVWPDTQIM-UHFFFAOYSA-N 0.000 description 2
BFXIKLCIZHOAAZ-UHFFFAOYSA-N methyltrimethoxysilane Chemical compound CO[Si](C)(OC)OC BFXIKLCIZHOAAZ-UHFFFAOYSA-N 0.000 description 2
229910052757 nitrogen Inorganic materials 0.000 description 2
HMMGMWAXVFQUOA-UHFFFAOYSA-N octamethylcyclotetrasiloxane Chemical compound C[Si]1(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O1 HMMGMWAXVFQUOA-UHFFFAOYSA-N 0.000 description 2
230000000737 periodic effect Effects 0.000 description 2
150000002978 peroxides Chemical class 0.000 description 2
239000004014 plasticizer Substances 0.000 description 2
229920000435 poly(dimethylsiloxane) Polymers 0.000 description 2
125000005372 silanol group Chemical group 0.000 description 2
229910001220 stainless steel Inorganic materials 0.000 description 2
239000010935 stainless steel Substances 0.000 description 2
239000010936 titanium Substances 0.000 description 2
229910052719 titanium Inorganic materials 0.000 description 2
125000003944 tolyl group Chemical group 0.000 description 2
NGZXDRGWBULKFA-NSOVKSMOSA-N (+)-Bebeerine Chemical compound C([C@@H]1N(C)CCC=2C=C(C(=C(OC3=CC=C(C=C3)C[C@H]3C=4C=C(C(=CC=4CCN3C)OC)O3)C=21)O)OC)C1=CC=C(O)C3=C1 NGZXDRGWBULKFA-NSOVKSMOSA-N 0.000 description 1
OATXJMYZMZLOTG-UHFFFAOYSA-N 4-[3,3-bis(trimethoxysilyl)propoxy]-4-oxobutanoic acid Chemical compound CO[Si](C(CCOC(=O)CCC(=O)O)[Si](OC)(OC)OC)(OC)OC OATXJMYZMZLOTG-UHFFFAOYSA-N 0.000 description 1
229920002972 Acrylic fiber Polymers 0.000 description 1
BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 1
BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
241000725101 Clea Species 0.000 description 1
229920000742 Cotton Polymers 0.000 description 1
239000004971 Cross linker Substances 0.000 description 1
102100025027 E3 ubiquitin-protein ligase TRIM69 Human genes 0.000 description 1
OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 1
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-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
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
101000830203 Homo sapiens E3 ubiquitin-protein ligase TRIM69 Proteins 0.000 description 1
125000000520 N-substituted aminocarbonyl group Chemical group [*]NC(=O)* 0.000 description 1
241000282320 Panthera leo Species 0.000 description 1
229920005372 Plexiglas® Polymers 0.000 description 1
239000004721 Polyphenylene oxide Substances 0.000 description 1
239000004614 Process Aid Substances 0.000 description 1
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical group CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
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244000166490 Tetrameles nudiflora Species 0.000 description 1
241000030538 Thecla Species 0.000 description 1
VGRYURJKXZNDAS-UHFFFAOYSA-N [SiH4].C(C=C/C(=O)O)(=O)O Chemical class [SiH4].C(C=C/C(=O)O)(=O)O VGRYURJKXZNDAS-UHFFFAOYSA-N 0.000 description 1
RTSDIJDRLOTGRD-UHFFFAOYSA-L [dibutyl(hexanoyloxy)stannyl] hexanoate Chemical compound CCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCC RTSDIJDRLOTGRD-UHFFFAOYSA-L 0.000 description 1
125000003668 acetyloxy group Chemical group [H]C([H])([H])C(=O)O[*] 0.000 description 1
229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 1
150000001408 amides Chemical class 0.000 description 1
239000007864 aqueous solution Substances 0.000 description 1
239000010425 asbestos Substances 0.000 description 1
238000010533 azeotropic distillation Methods 0.000 description 1
235000013405 beer Nutrition 0.000 description 1
GPWPWELMLCKXRP-MDZDMXLPSA-N bis(3-trimethoxysilylpropyl) (e)-but-2-enedioate Chemical compound CO[Si](OC)(OC)CCCOC(=O)\C=C\C(=O)OCCC[Si](OC)(OC)OC GPWPWELMLCKXRP-MDZDMXLPSA-N 0.000 description 1
GPWPWELMLCKXRP-KTKRTIGZSA-N bis(3-trimethoxysilylpropyl) (z)-but-2-enedioate Chemical compound CO[Si](OC)(OC)CCCOC(=O)\C=C/C(=O)OCCC[Si](OC)(OC)OC GPWPWELMLCKXRP-KTKRTIGZSA-N 0.000 description 1
INPMCZQFKXISAE-UHFFFAOYSA-L butanoate;tin(2+) Chemical compound [Sn+2].CCCC([O-])=O.CCCC([O-])=O INPMCZQFKXISAE-UHFFFAOYSA-L 0.000 description 1
FAOSYNUKPVJLNZ-UHFFFAOYSA-N butylstannane Chemical compound CCCC[SnH3] FAOSYNUKPVJLNZ-UHFFFAOYSA-N 0.000 description 1
239000006227 byproduct Substances 0.000 description 1
150000001721 carbon Chemical group 0.000 description 1
239000004927 clay Substances 0.000 description 1
229910052570 clay Inorganic materials 0.000 description 1
238000009833 condensation Methods 0.000 description 1
230000005494 condensation Effects 0.000 description 1
239000007799 cork Substances 0.000 description 1
238000005336 cracking Methods 0.000 description 1
125000000753 cycloalkyl group Chemical group 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
PYRZPBDTPRQYKG-UHFFFAOYSA-N cyclopentene-1-carboxylic acid Chemical compound OC(=O)C1=CCCC1 PYRZPBDTPRQYKG-UHFFFAOYSA-N 0.000 description 1
DIVTWACHZOQOBF-UHFFFAOYSA-K diacetyloxy(butyl)stannanylium;acetate Chemical compound CCCC[Sn](OC(C)=O)(OC(C)=O)OC(C)=O DIVTWACHZOQOBF-UHFFFAOYSA-K 0.000 description 1
AYOHIQLKSOJJQH-UHFFFAOYSA-N dibutyltin Chemical compound CCCC[Sn]CCCC AYOHIQLKSOJJQH-UHFFFAOYSA-N 0.000 description 1
SGIBEPSSERDAHS-UHFFFAOYSA-L dibutyltin(2+);hexanedioate Chemical compound CCCC[Sn+2]CCCC.[O-]C(=O)CCCCC([O-])=O SGIBEPSSERDAHS-UHFFFAOYSA-L 0.000 description 1
DSTWFRCNXMNXTR-WAYWQWQTSA-N dipropyl (z)-but-2-enedioate Chemical compound CCCOC(=O)\C=C/C(=O)OCCC DSTWFRCNXMNXTR-WAYWQWQTSA-N 0.000 description 1
KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical compound [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 1
238000004821 distillation Methods 0.000 description 1
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125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
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125000001188 haloalkyl group Chemical group 0.000 description 1
229910052736 halogen Inorganic materials 0.000 description 1
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150000002367 halogens Chemical class 0.000 description 1
230000003301 hydrolyzing effect Effects 0.000 description 1
ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 1
239000004816 latex Substances 0.000 description 1
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CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
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238000006386 neutralization reaction Methods 0.000 description 1
XULSCZPZVQIMFM-IPZQJPLYSA-N odevixibat Chemical compound C12=CC(SC)=C(OCC(=O)N[C@@H](C(=O)N[C@@H](CC)C(O)=O)C=3C=CC(O)=CC=3)C=C2S(=O)(=O)NC(CCCC)(CCCC)CN1C1=CC=CC=C1 XULSCZPZVQIMFM-IPZQJPLYSA-N 0.000 description 1
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125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000000376 reactant Substances 0.000 description 1
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229910052895 riebeckite Inorganic materials 0.000 description 1
UIIMBOGNXHQVGW-UHFFFAOYSA-M sodium bicarbonate Substances [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 1
229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
235000017557 sodium bicarbonate Nutrition 0.000 description 1
229910000029 sodium carbonate Inorganic materials 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
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150000003609 titanium compounds Chemical class 0.000 description 1
239000004408 titanium dioxide Substances 0.000 description 1
JZBMWXZOUSTRDA-UHFFFAOYSA-J tri(hexanoyloxy)stannyl hexanoate Chemical compound [Sn+4].CCCCCC([O-])=O.CCCCCC([O-])=O.CCCCCC([O-])=O.CCCCCC([O-])=O JZBMWXZOUSTRDA-UHFFFAOYSA-J 0.000 description 1
125000005270 trialkylamine group Chemical group 0.000 description 1
PZJJKWKADRNWSW-UHFFFAOYSA-N trimethoxysilicon Chemical group CO[Si](OC)OC PZJJKWKADRNWSW-UHFFFAOYSA-N 0.000 description 1
DVYQCRRVXOXJSA-UHFFFAOYSA-N tris(2-ethylhexoxy)-methylsilane Chemical compound CCCCC(CC)CO[Si](C)(OCC(CC)CCCC)OCC(CC)CCCC DVYQCRRVXOXJSA-UHFFFAOYSA-N 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
238000005406 washing Methods 0.000 description 1
239000002023 wood Substances 0.000 description 1
GFQYVLUOOAAOGM-UHFFFAOYSA-N zirconium(iv) silicate Chemical compound [Zr+4].[O-][Si]([O-])([O-])[O-] GFQYVLUOOAAOGM-UHFFFAOYSA-N 0.000 description 1
229910021489 α-quartz Inorganic materials 0.000 description 1

Landscapes

Adhesives Or Adhesive Processes (AREA)
Compositions Of Macromolecular Compounds (AREA)

CA000359263A 1980-08-29 1980-08-29 Caoutchoucs au silicone auto-collants vulcanisables a la temperature ambiante interieure Expired CA1162692A (fr)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
CA000359263A CA1162692A (fr)	1980-08-29	1980-08-29	Caoutchoucs au silicone auto-collants vulcanisables a la temperature ambiante interieure

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CA000359263A CA1162692A (fr)	1980-08-29	1980-08-29	Caoutchoucs au silicone auto-collants vulcanisables a la temperature ambiante interieure

Publications (1)

Publication Number	Publication Date
CA1162692A true CA1162692A (fr)	1984-02-21

Family

ID=4117770

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA000359263A Expired CA1162692A (fr)	1980-08-29	1980-08-29	Caoutchoucs au silicone auto-collants vulcanisables a la temperature ambiante interieure

Country Status (1)

Country	Link
CA (1)	CA1162692A (fr)

1980
- 1980-08-29 CA CA000359263A patent/CA1162692A/fr not_active Expired

Legal Events

Date	Code	Title	Description
2001-02-21	MKEX	Expiry

Publication	Publication Date	Title
US4273698A (en)	1981-06-16	Self-bonding room temperature vulcanizable silicone rubber compositions
US4672003A (en)	1987-06-09	RTV organopolysiloxane compositions and self-adhesive elastomers therefrom
JP6215312B2 (ja)	2017-10-18	有機ケイ素化合物をベースとした架橋性組成物
JP2698268B2 (ja)	1998-01-19	改良された室温硬化性シリコ―ン組成物
US4483972A (en)	1984-11-20	Integrated cross-linkers and amine functional siloxane scavengers for RTV silicone rubber compositions
US4599394A (en)	1986-07-08	Process for producing alkoxy-terminated polysiloxanes
EP0104179A1 (fr)	1984-04-04	Coprecipitateurs pour des compositions rtv alkoxy-fonctionnelles a un composant et procedes.
JPS60202152A (ja)	1985-10-12	室温加硫性オルガノポリシロキサン組成物及びその製造法
JPS625943B2 (fr)	1987-02-07
GB2144442A (en)	1985-03-06	Room temperature vulcanizable organopolysiloxane compositions
KR20040054499A (ko)	2004-06-25	오르가노폴리실록산조성물 및 그 제조방법
JPH07107135B2 (ja)	1995-11-15	オルガノポリシロキサン材料の安定化方法
KR840001492B1 (ko)	1984-09-28	저장-안정성 촉매 조성물
US6001948A (en)	1999-12-14	Alkoxy-crosslinking RTV1 silicone rubber mixtures
US4731411A (en)	1988-03-15	Process for producing alkoxy-terminated polysiloxanes
JPH0543803A (ja)	1993-02-23	低モジユラス１成分型ｒｔｖ組成物およびその製造方法
JP2000169587A (ja)	2000-06-20	Ｒｔｖ―１―アルコキシ材料、その製造方法およびその使用
CA1293736C (fr)	1991-12-31	Methode de preparation d'un catalyseur de traitement a base d'un complexe d'etain
AU735954B2 (en)	2001-07-19	Organopolysiloxane compositions crosslinkable with elimination of alcohols to give elastomers
JPH0323106B2 (fr)	1991-03-28
JPH038657B2 (fr)	1991-02-06
FR2569414A1 (fr)	1986-02-28	Compositions de polyorganosiloxane vulcanisables a temperature ambiante a stabilite de conservation amelioree
JPS6352673B2 (fr)	1988-10-19
CA1162692A (fr)	1984-02-21	Caoutchoucs au silicone auto-collants vulcanisables a la temperature ambiante interieure
JP7516563B2 (ja)	2024-07-16	有機ケイ素化合物をベースとする架橋性部分