JPS61108682A - シリコーン感圧接着組成物 - Google Patents

シリコーン感圧接着組成物

Info

Publication number: JPS61108682A
Authority: JP; Japan
Prior art keywords: units; group; groups; polydiorganosiloxane; condensation
Prior art date: 1984-10-29
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.): Granted

Application number

JP60241233A

Other languages

English (en)

Japanese (ja)

Other versions

JPH0236633B2 (2

Inventor

ゲイリイ　レツクス　ホウマン

ハロルド　ルイズ　ビンセント

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.)

Dow Silicones Corp

Original Assignee

Dow Corning Corp

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1984-10-29

Filing date

1985-10-28

Publication date

1986-05-27

1985-10-28 Application filed by Dow Corning Corp filed Critical Dow Corning Corp

1986-05-27 Publication of JPS61108682A publication Critical patent/JPS61108682A/ja

1990-08-20 Publication of JPH0236633B2 publication Critical patent/JPH0236633B2/ja

Status Granted legal-status Critical Current

Links

239000000203 mixture Substances 0.000 title claims description 114
239000004820 Pressure-sensitive adhesive Substances 0.000 title claims description 85
229920001296 polysiloxane Polymers 0.000 title claims description 52
238000000034 method Methods 0.000 claims description 63
229920005989 resin Polymers 0.000 claims description 54
239000011347 resin Substances 0.000 claims description 54
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 45
150000001875 compounds Chemical class 0.000 claims description 36
238000009833 condensation Methods 0.000 claims description 34
230000005494 condensation Effects 0.000 claims description 34
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 29
229910001868 water Inorganic materials 0.000 claims description 29
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 28
239000003795 chemical substances by application Substances 0.000 claims description 26
239000002904 solvent Substances 0.000 claims description 25
239000000047 product Substances 0.000 claims description 19
229940121848 Ammonia scavenger Drugs 0.000 claims description 18
239000006227 byproduct Substances 0.000 claims description 16
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 16
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 15
238000004519 manufacturing process Methods 0.000 claims description 14
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 13
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 12
125000004432 carbon atom Chemical group C* 0.000 claims description 12
238000010992 reflux Methods 0.000 claims description 11
238000002156 mixing Methods 0.000 claims description 10
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims description 9
239000008096 xylene Substances 0.000 claims description 9
239000007859 condensation product Substances 0.000 claims description 8
238000006482 condensation reaction Methods 0.000 claims description 8
230000015572 biosynthetic process Effects 0.000 claims description 7
229920001577 copolymer Polymers 0.000 claims description 7
125000000524 functional group Chemical group 0.000 claims description 7
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 6
239000007787 solid Substances 0.000 claims description 6
229920002554 vinyl polymer Polymers 0.000 claims description 6
150000002430 hydrocarbons Chemical group 0.000 claims description 5
239000004215 Carbon black (E152) Substances 0.000 claims description 4
125000000217 alkyl group Chemical group 0.000 claims description 4
229930195733 hydrocarbon Natural products 0.000 claims description 4
125000000962 organic group Chemical group 0.000 claims description 4
125000002947 alkylene group Chemical group 0.000 claims description 2
150000005826 halohydrocarbons Chemical group 0.000 claims description 2
239000003607 modifier Substances 0.000 claims description 2
229920002050 silicone resin Polymers 0.000 claims description 2
239000011541 reaction mixture Substances 0.000 claims 3
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 55
230000001070 adhesive effect Effects 0.000 description 29
229910021529 ammonia Inorganic materials 0.000 description 27
239000000853 adhesive Substances 0.000 description 25
230000008569 process Effects 0.000 description 22
FFUAGWLWBBFQJT-UHFFFAOYSA-N hexamethyldisilazane Chemical compound C[Si](C)(C)N[Si](C)(C)C FFUAGWLWBBFQJT-UHFFFAOYSA-N 0.000 description 20
230000014759 maintenance of location Effects 0.000 description 18
229910052799 carbon Inorganic materials 0.000 description 16
239000003960 organic solvent Substances 0.000 description 16
-1 trimethylmethoxy Chemical group 0.000 description 14
238000010438 heat treatment Methods 0.000 description 13
230000000704 physical effect Effects 0.000 description 13
239000003054 catalyst Substances 0.000 description 12
229920006026 co-polymeric resin Polymers 0.000 description 9
ZPUCINDJVBIVPJ-LJISPDSOSA-N cocaine Chemical compound O([C@H]1C[C@@H]2CC[C@@H](N2C)[C@H]1C(=O)OC)C(=O)C1=CC=CC=C1 ZPUCINDJVBIVPJ-LJISPDSOSA-N 0.000 description 9
239000004615 ingredient Substances 0.000 description 9
239000000463 material Substances 0.000 description 9
SCPYDCQAZCOKTP-UHFFFAOYSA-N silanol Chemical compound [SiH3]O SCPYDCQAZCOKTP-UHFFFAOYSA-N 0.000 description 9
238000012360 testing method Methods 0.000 description 8
238000012545 processing Methods 0.000 description 6
125000001931 aliphatic group Chemical group 0.000 description 5
239000000523 sample Substances 0.000 description 5
125000005372 silanol group Chemical group 0.000 description 5
229910052710 silicon Inorganic materials 0.000 description 5
239000010703 silicon Substances 0.000 description 5
238000003786 synthesis reaction Methods 0.000 description 5
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical group CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
239000004205 dimethyl polysiloxane Substances 0.000 description 4
150000002978 peroxides Chemical class 0.000 description 4
229920000435 poly(dimethylsiloxane) Polymers 0.000 description 4
239000004342 Benzoyl peroxide Substances 0.000 description 3
OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 3
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-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
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 3
230000032683 aging Effects 0.000 description 3
229910052782 aluminium Inorganic materials 0.000 description 3
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
150000001412 amines Chemical class 0.000 description 3
238000010533 azeotropic distillation Methods 0.000 description 3
235000019400 benzoyl peroxide Nutrition 0.000 description 3
238000006243 chemical reaction Methods 0.000 description 3
238000004132 cross linking Methods 0.000 description 3
239000012530 fluid Substances 0.000 description 3
238000005259 measurement Methods 0.000 description 3
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 3
229910001220 stainless steel Inorganic materials 0.000 description 3
239000010935 stainless steel Substances 0.000 description 3
SVTBMSDMJJWYQN-UHFFFAOYSA-N 2-methylpentane-2,4-diol Chemical compound CC(O)CC(C)(C)O SVTBMSDMJJWYQN-UHFFFAOYSA-N 0.000 description 2
229920002799 BoPET Polymers 0.000 description 2
QMMFVYPAHWMCMS-UHFFFAOYSA-N Dimethyl sulfide Chemical compound CSC QMMFVYPAHWMCMS-UHFFFAOYSA-N 0.000 description 2
239000005041 Mylar™ Substances 0.000 description 2
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 2
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
239000002253 acid Substances 0.000 description 2
239000002313 adhesive film Substances 0.000 description 2
150000001298 alcohols Chemical class 0.000 description 2
238000004458 analytical method Methods 0.000 description 2
230000008901 benefit Effects 0.000 description 2
239000002981 blocking agent Substances 0.000 description 2
230000008859 change Effects 0.000 description 2
238000003776 cleavage reaction Methods 0.000 description 2
125000004093 cyano group Chemical group *C#N 0.000 description 2
XLYOFNOQVPJJNP-DYCDLGHISA-N deuterium hydrogen oxide Chemical compound [2H]O XLYOFNOQVPJJNP-DYCDLGHISA-N 0.000 description 2
KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 2
239000003814 drug Substances 0.000 description 2
229940079593 drug Drugs 0.000 description 2
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
FKRCODPIKNYEAC-UHFFFAOYSA-N ethyl propionate Chemical compound CCOC(=O)CC FKRCODPIKNYEAC-UHFFFAOYSA-N 0.000 description 2
239000011888 foil Substances 0.000 description 2
AOGQPLXWSUTHQB-UHFFFAOYSA-N hexyl acetate Chemical compound CCCCCCOC(C)=O AOGQPLXWSUTHQB-UHFFFAOYSA-N 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
125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
238000010348 incorporation Methods 0.000 description 2
229910052500 inorganic mineral Inorganic materials 0.000 description 2
ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 2
125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 2
150000002576 ketones Chemical class 0.000 description 2
229910052751 metal Inorganic materials 0.000 description 2
239000002184 metal Substances 0.000 description 2
239000011707 mineral Substances 0.000 description 2
229920000642 polymer Polymers 0.000 description 2
229910052700 potassium Inorganic materials 0.000 description 2
239000011591 potassium Substances 0.000 description 2
238000002360 preparation method Methods 0.000 description 2
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
150000003333 secondary alcohols Chemical class 0.000 description 2
150000004756 silanes Chemical class 0.000 description 2
238000003756 stirring Methods 0.000 description 2
238000003860 storage Methods 0.000 description 2
239000000126 substance Substances 0.000 description 2
238000013271 transdermal drug delivery Methods 0.000 description 2
BOOBDAVNHSOIDB-UHFFFAOYSA-N (2,3-dichlorobenzoyl) 2,3-dichlorobenzenecarboperoxoate Chemical compound ClC1=CC=CC(C(=O)OOC(=O)C=2C(=C(Cl)C=CC=2)Cl)=C1Cl BOOBDAVNHSOIDB-UHFFFAOYSA-N 0.000 description 1
UUFQTNFCRMXOAE-UHFFFAOYSA-N 1-methylmethylene Chemical compound C[CH] UUFQTNFCRMXOAE-UHFFFAOYSA-N 0.000 description 1
IXEHTHNYIWZCSI-UHFFFAOYSA-N 2,2,3-trichlorocyclopropan-1-one Chemical compound ClC1C(=O)C1(Cl)Cl IXEHTHNYIWZCSI-UHFFFAOYSA-N 0.000 description 1
GVNVAWHJIKLAGL-UHFFFAOYSA-N 2-(cyclohexen-1-yl)cyclohexan-1-one Chemical compound O=C1CCCCC1C1=CCCCC1 GVNVAWHJIKLAGL-UHFFFAOYSA-N 0.000 description 1
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
ATRRKUHOCOJYRX-UHFFFAOYSA-N Ammonium bicarbonate Chemical compound [NH4+].OC([O-])=O ATRRKUHOCOJYRX-UHFFFAOYSA-N 0.000 description 1
DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 1
101150065749 Churc1 gene Proteins 0.000 description 1
239000004338 Dichlorodifluoromethane Substances 0.000 description 1
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
CYTYCFOTNPOANT-UHFFFAOYSA-N Perchloroethylene Chemical group ClC(Cl)=C(Cl)Cl CYTYCFOTNPOANT-UHFFFAOYSA-N 0.000 description 1
102100038239 Protein Churchill Human genes 0.000 description 1
229910020485 SiO4/2 Inorganic materials 0.000 description 1
239000004115 Sodium Silicate Substances 0.000 description 1
XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical group ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 1
KXKVLQRXCPHEJC-UHFFFAOYSA-N acetic acid trimethyl ester Natural products COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 description 1
239000003377 acid catalyst Substances 0.000 description 1
230000009471 action Effects 0.000 description 1
230000002411 adverse Effects 0.000 description 1
230000001476 alcoholic effect Effects 0.000 description 1
150000001408 amides Chemical group 0.000 description 1
239000001099 ammonium carbonate Substances 0.000 description 1
235000012501 ammonium carbonate Nutrition 0.000 description 1
229940072049 amyl acetate Drugs 0.000 description 1
PGMYKACGEOXYJE-UHFFFAOYSA-N anhydrous amyl acetate Natural products CCCCCOC(C)=O PGMYKACGEOXYJE-UHFFFAOYSA-N 0.000 description 1
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
239000011230 binding agent Substances 0.000 description 1
230000000903 blocking effect Effects 0.000 description 1
238000009835 boiling Methods 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
230000003197 catalytic effect Effects 0.000 description 1
150000001768 cations Chemical class 0.000 description 1
125000004218 chloromethyl group Chemical group [H]C([H])(Cl)* 0.000 description 1
238000001816 cooling Methods 0.000 description 1
125000004122 cyclic 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
239000008367 deionised water Substances 0.000 description 1
229910021641 deionized water Inorganic materials 0.000 description 1
230000002939 deleterious effect Effects 0.000 description 1
230000001627 detrimental effect Effects 0.000 description 1
PXBRQCKWGAHEHS-UHFFFAOYSA-N dichlorodifluoromethane Chemical compound FC(F)(Cl)Cl PXBRQCKWGAHEHS-UHFFFAOYSA-N 0.000 description 1
235000019404 dichlorodifluoromethane Nutrition 0.000 description 1
HALQELOKLVRWRI-VDBOFHIQSA-N doxycycline hyclate Chemical group O.[Cl-].[Cl-].CCO.O=C1C2=C(O)C=CC=C2[C@H](C)[C@@H]2C1=C(O)[C@]1(O)C(=O)C(C(N)=O)=C(O)[C@@H]([NH+](C)C)[C@@H]1[C@H]2O.O=C1C2=C(O)C=CC=C2[C@H](C)[C@@H]2C1=C(O)[C@]1(O)C(=O)C(C(N)=O)=C(O)[C@@H]([NH+](C)C)[C@@H]1[C@H]2O HALQELOKLVRWRI-VDBOFHIQSA-N 0.000 description 1
238000010894 electron beam technology Methods 0.000 description 1
150000002148 esters Chemical group 0.000 description 1
XJRPTMORGOIMMI-UHFFFAOYSA-N ethyl 2-amino-4-(trifluoromethyl)-1,3-thiazole-5-carboxylate Chemical compound CCOC(=O)C=1SC(N)=NC=1C(F)(F)F XJRPTMORGOIMMI-UHFFFAOYSA-N 0.000 description 1
239000004744 fabric Substances 0.000 description 1
239000000945 filler Substances 0.000 description 1
239000012467 final product Substances 0.000 description 1
WBJINCZRORDGAQ-UHFFFAOYSA-N formic acid ethyl ester Natural products CCOC=O WBJINCZRORDGAQ-UHFFFAOYSA-N 0.000 description 1
230000005484 gravity Effects 0.000 description 1
150000008282 halocarbons Chemical class 0.000 description 1
MNWFXJYAOYHMED-UHFFFAOYSA-M heptanoate Chemical compound CCCCCCC([O-])=O MNWFXJYAOYHMED-UHFFFAOYSA-M 0.000 description 1
125000004836 hexamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 description 1
FUZZWVXGSFPDMH-UHFFFAOYSA-M hexanoate Chemical compound CCCCCC([O-])=O FUZZWVXGSFPDMH-UHFFFAOYSA-M 0.000 description 1
229940051250 hexylene glycol Drugs 0.000 description 1
230000003301 hydrolyzing effect Effects 0.000 description 1
230000000774 hypoallergenic effect Effects 0.000 description 1
230000006872 improvement Effects 0.000 description 1
230000010354 integration Effects 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
229910052744 lithium Inorganic materials 0.000 description 1
239000012280 lithium aluminium hydride Substances 0.000 description 1
238000000691 measurement method Methods 0.000 description 1
WKWOFMSUGVVZIV-UHFFFAOYSA-N n-bis(ethenyl)silyl-n-trimethylsilylmethanamine Chemical compound C[Si](C)(C)N(C)[SiH](C=C)C=C WKWOFMSUGVVZIV-UHFFFAOYSA-N 0.000 description 1
229910000510 noble metal Inorganic materials 0.000 description 1
231100000344 non-irritating Toxicity 0.000 description 1
150000002894 organic compounds Chemical class 0.000 description 1
125000001181 organosilyl group Chemical group [SiH3]* 0.000 description 1
125000001820 oxy group Chemical group [*:1]O[*:2] 0.000 description 1
239000001301 oxygen Substances 0.000 description 1
229910052760 oxygen Inorganic materials 0.000 description 1
239000000049 pigment Substances 0.000 description 1
BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 1
229920006267 polyester film Polymers 0.000 description 1
150000003138 primary alcohols Chemical class 0.000 description 1
230000005855 radiation Effects 0.000 description 1
150000003254 radicals Chemical class 0.000 description 1
239000000376 reactant Substances 0.000 description 1
230000009467 reduction Effects 0.000 description 1
239000012260 resinous material Substances 0.000 description 1
229910052703 rhodium Inorganic materials 0.000 description 1
239000010948 rhodium Substances 0.000 description 1
MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 description 1
230000007017 scission Effects 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
239000013464 silicone adhesive Substances 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
239000011734 sodium Substances 0.000 description 1
NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 1
229910052911 sodium silicate Inorganic materials 0.000 description 1
235000015096 spirit Nutrition 0.000 description 1
239000012258 stirred mixture Substances 0.000 description 1
230000035882 stress Effects 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
239000000758 substrate Substances 0.000 description 1
150000003509 tertiary alcohols Chemical class 0.000 description 1
229950011008 tetrachloroethylene Drugs 0.000 description 1
238000004448 titration Methods 0.000 description 1
238000012546 transfer Methods 0.000 description 1
239000013638 trimer Substances 0.000 description 1
125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
238000005303 weighing Methods 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J183/00—Adhesives 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; Adhesives based on derivatives of such polymers
- C09J183/10—Block or graft copolymers containing polysiloxane sequences
- 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
- C08G77/42—Block-or graft-polymers containing polysiloxane sequences
- C08G77/44—Block-or graft-polymers containing polysiloxane sequences containing only polysiloxane sequences

Landscapes

Chemical & Material Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Adhesives Or Adhesive Processes (AREA)
Silicon Polymers (AREA)
Compositions Of Macromolecular Compounds (AREA)

JP60241233A 1984-10-29 1985-10-28 シリコーン感圧接着組成物 Granted JPS61108682A (ja)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US06/665,796 US4585836A (en)	1984-10-29	1984-10-29	Silicone pressure-sensitive adhesive process and product with improved lap-shear stability-II
US665796		1984-10-29

Publications (2)

Publication Number	Publication Date
JPS61108682A true JPS61108682A (ja)	1986-05-27
JPH0236633B2 JPH0236633B2 (2)	1990-08-20

Family

ID=24671610

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP60241233A Granted JPS61108682A (ja)	1984-10-29	1985-10-28	シリコーン感圧接着組成物

Country Status (5)

Country	Link
US (1)	US4585836A (2)
EP (1)	EP0183378B1 (2)
JP (1)	JPS61108682A (2)
CA (1)	CA1271580A (2)
DE (1)	DE3574267D1 (2)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
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JPS5027837A (2) *	1973-05-29	1975-03-22
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- 1985-10-22 EP EP85307608A patent/EP0183378B1/en not_active Expired
- 1985-10-22 DE DE8585307608T patent/DE3574267D1/de not_active Expired
- 1985-10-28 JP JP60241233A patent/JPS61108682A/ja active Granted

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JPS5027837A (2) *	1973-05-29	1975-03-22
JPS56110730A (en) *	1980-01-29	1981-09-02	Wacker Chemie Gmbh	Manufacture of organosiloxane block copolymer
JPS5790045A (en) *	1980-10-29	1982-06-04	Toshiba Silicone Co Ltd	Adherent polyorganosiloxane composition
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JPH05209163A (ja) *	1991-08-22	1993-08-20	Dow Corning Corp	湿分硬化性シリコーン感圧接着剤

Also Published As

Publication number	Publication date
CA1271580A (en)	1990-07-10
DE3574267D1 (en)	1989-12-21
US4585836A (en)	1986-04-29
JPH0236633B2 (2)	1990-08-20
EP0183378B1 (en)	1989-11-15
EP0183378A3 (en)	1987-03-25
EP0183378A2 (en)	1986-06-04

Publication	Publication Date	Title
JPS61108682A (ja)	1986-05-27	シリコーン感圧接着組成物
EP0183377B1 (en)	1989-11-15	Silicone pressure-sensitive adhesive process and product with improved lapshear stability-i
JPS61158920A (ja)	1986-07-18	アミン抵抗性シリコ−ン接着剤を使用した経皮薬物送達デバイス
US4591622A (en)	1986-05-27	Silicone pressure-sensitive adhesive process and product thereof
JP4220001B2 (ja)	2009-02-04	シリコーン感圧接着剤を製造する方法
KR100466907B1 (ko)	2006-01-12	실리콘감압성접착제조성물의제조방법
EP0253601A2 (en)	1988-01-20	Silicone pressure-sensitive adhesive composition
JPH07197008A (ja)	1995-08-01	シリコーン感圧接着剤
JP2000265150A (ja)	2000-09-26	シリコーン組成物およびシリコーン感圧接着剤
JP2002285129A (ja)	2002-10-03	シリコーン感圧接着剤組成物
JP2519571B2 (ja)	1996-07-31	剥離性に優れたシリコ―ン組成物
US5288830A (en)	1994-02-22	Curable organopolysiloxane composition
JPH10110156A (ja)	1998-04-28	シリコーン系感圧接着剤
JPH0711228A (ja)	1995-01-13	シリコーン粘着剤組成物、粘着テープ及び粘着方法
JPH05140458A (ja)	1993-06-08	湿気硬化型シリコーン粘着剤組成物
JPH09118871A (ja)	1997-05-06	シリコーン系感圧接着剤用オルガノポリシロキサンおよびシリコーン系感圧接着剤
JPH05209163A (ja)	1993-08-20	湿分硬化性シリコーン感圧接着剤
US5470923A (en)	1995-11-28	Moisture-curable silicone pressure-sensitive adhesives
JP2002161208A (ja)	2002-06-04	シリコーン剥離剤組成物及び剥離紙
JPH10195414A (ja)	1998-07-28	付加反応型シリコーン粘着剤組成物
JPS6027703B2 (ja)	1985-07-01	接着剤被覆物品と用法
JP3934866B2 (ja)	2007-06-20	付加反応型シリコーン粘着剤組成物
JP2000080345A (ja)	2000-03-21	シリコーン系感圧接着剤、および粘着材
JP2002097440A (ja)	2002-04-02	シリコーン接着剤組成物
JPH0273878A (ja)	1990-03-13	硬化シリコーンゴム用接着剤組成物

JPS61108682A - シリコーン感圧接着組成物 - Google Patents

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Cited By (1)

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Citations (6)

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Patent Citations (6)

Cited By (1)

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