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 JPS61108682A JP60241233A JP24123385A JPS61108682A JP S61108682 A JPS61108682 A JP S61108682A JP 60241233 A JP60241233 A JP 60241233A JP 24123385 A JP24123385 A JP 24123385A JP S61108682 A JPS61108682 A JP S61108682A
- Authority
- JP
- Japan
- Prior art keywords
- units
- group
- groups
- polydiorganosiloxane
- condensation
- Prior art date
- 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
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)
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 (enExample) | 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 (enExample) |
| EP (1) | EP0183378B1 (enExample) |
| JP (1) | JPS61108682A (enExample) |
| CA (1) | CA1271580A (enExample) |
| DE (1) | DE3574267D1 (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| 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 |
Families Citing this family (192)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4831070A (en) * | 1987-11-02 | 1989-05-16 | Dow Corning Corporation | Moldable elastomeric pressure sensitive adhesives |
| US4865920A (en) * | 1988-09-20 | 1989-09-12 | Dow Corning Corporation | Hot-melt pressure sensitive adhesive article and method of making |
| US4882377A (en) * | 1988-09-21 | 1989-11-21 | Dow Corning Corporation | Low-viscosity pressure-adherent silicone elastomer compositions |
| WO1992016590A1 (en) * | 1991-03-20 | 1992-10-01 | Minnesota Mining And Manufacturing Company | Radiation curable vinyl/silicone release coating |
| WO1992016593A2 (en) * | 1991-03-20 | 1992-10-01 | Minnesota Mining And Manufacturing Company | Radiation-curable acrylate/silicone pressure-sensitive adhesive compositions |
| US5308887A (en) * | 1991-05-23 | 1994-05-03 | Minnesota Mining & Manufacturing Company | Pressure-sensitive adhesives |
| US5464659A (en) * | 1991-05-23 | 1995-11-07 | Minnesota Mining And Manufacturing Company | Silicone/acrylate vibration dampers |
| US5387465A (en) * | 1992-07-30 | 1995-02-07 | General Electric Company | Paper adhesive release system |
| JPH06100694A (ja) * | 1992-09-22 | 1994-04-12 | Nippon Dow Corning Kk | 分岐状ポリオルガノシロキサンの製造方法 |
| JP3324166B2 (ja) * | 1992-12-10 | 2002-09-17 | 信越化学工業株式会社 | 接着性シリコーンゴム組成物 |
| US5319040A (en) * | 1993-03-12 | 1994-06-07 | General Electric Company | Method for making substantially silanol-free silicone resin powder, product and use |
| DE4414653A1 (de) * | 1993-05-13 | 1994-11-17 | Gen Electric | Schneller klebende Silicon-Klebstoffzusammensetzungen |
| US5545700A (en) * | 1994-01-10 | 1996-08-13 | Dow Corning Corporation | Moisture-curable silicone pressure sensitive adhesives |
| US5371128A (en) * | 1994-01-14 | 1994-12-06 | Dow Corning Corporation | Hot-melt silicone pressure sensitive adhesive with siloxylated allyloxypropane diol copolymers as additives |
| US5482988A (en) * | 1994-01-14 | 1996-01-09 | Dow Corning Corporation | Hot-melt silicone pressure sensitive adhesive with siloxylated polyether waxes as additives |
| US5561203A (en) | 1994-06-20 | 1996-10-01 | Dow Corning Corporation | Silicone pressure sensitive adhesive composition |
| US5473026A (en) * | 1994-06-20 | 1995-12-05 | Dow Corning Corporation | Moisture-curable hot melt silicone pressure-sensitive adhesives |
| US5562917A (en) * | 1994-12-23 | 1996-10-08 | Pentech Pharmaceuticals, Inc. | Transdermal administration of apomorphine |
| US5510430A (en) * | 1995-03-31 | 1996-04-23 | General Electric Company | Method of functionalizing organosiloxane condensation products |
| US6316022B1 (en) | 1995-06-07 | 2001-11-13 | Noven Pharmaceuticals, Inc. | Transdermal compositions containing low molecular weight drugs which are liquid at room temperatures |
| US5726256A (en) * | 1996-10-22 | 1998-03-10 | Dow Corning Corporation | Method of making silicone pressure sensitive adhesives |
| US5939477A (en) * | 1998-02-02 | 1999-08-17 | Dow Corning Corporation | Silicone pressure sensitive adhesive composition containing functionalized polyisobutylene |
| AU3470600A (en) * | 1999-01-14 | 2000-08-01 | David Houze | Compositions and methods for drug delivery |
| US20030170195A1 (en) * | 2000-01-10 | 2003-09-11 | Noven Pharmaceuticals, Inc. | Compositions and methods for drug delivery |
| US6337086B1 (en) | 1999-02-06 | 2002-01-08 | Dow Corning Corporation | Pressure sensitive adhesive compositions for transdermal drug delivery devices |
| US6201055B1 (en) | 1999-03-11 | 2001-03-13 | Dow Corning Corporation | Silicone composition and silicone pressure sensitive adhesive |
| US20020004065A1 (en) | 2000-01-20 | 2002-01-10 | David Kanios | Compositions and methods to effect the release profile in the transdermal administration of active agents |
| US6433057B1 (en) | 2000-03-28 | 2002-08-13 | Dow Corning Corporation | Silicone composition and electrically conductive silicone adhesive formed therefrom |
| EP1406633B1 (en) * | 2001-06-18 | 2011-10-05 | Noven Pharmaceuticals, Inc. | Enhanced drug delivery in transdermal systems |
| US20060205887A1 (en) * | 2003-01-22 | 2006-09-14 | Yoshiki Nakagawa | Polymer and curable compositions improved in storage stability |
| US20040243042A1 (en) * | 2003-05-20 | 2004-12-02 | Lipman Roger D. A. | Facial masks for managing skin wounds |
| EP1663179A1 (en) * | 2003-07-21 | 2006-06-07 | Noven Pharmaceuticals, Inc. | Composition and method for controlling drug delivery from silicone adhesive blends |
| US7517808B2 (en) * | 2003-07-28 | 2009-04-14 | Dow Corning Corporation | Method for forming and removing a patterned silicone film |
| US7045586B2 (en) * | 2003-08-14 | 2006-05-16 | Dow Corning Corporation | Adhesives having improved chemical resistance and curable silicone compositions for preparing the adhesives |
| US20050038188A1 (en) * | 2003-08-14 | 2005-02-17 | Dongchan Ahn | Silicones having improved chemical resistance and curable silicone compositions having improved migration resistance |
| US20050038183A1 (en) * | 2003-08-14 | 2005-02-17 | Dongchan Ahn | Silicones having improved surface properties and curable silicone compositions for preparing the silicones |
| US8815215B2 (en) | 2003-08-15 | 2014-08-26 | Colgate-Palmolive Company | Hydrophobic tooth whitening system and methods of use |
| US20050036957A1 (en) * | 2003-08-15 | 2005-02-17 | Michael Prencipe | Tooth whitening dental tray and method of use |
| WO2005025549A2 (en) * | 2003-09-10 | 2005-03-24 | Noven Pharmaceuticals, Inc. | Multi-layer transdermal drug delivery device |
| KR101246638B1 (ko) * | 2003-10-28 | 2013-03-25 | 다우 코닝 코포레이션 | 플랫-탑 패드의 제조방법 |
| ES2626784T3 (es) * | 2003-10-28 | 2017-07-26 | Noven Pharmaceuticals, Inc. | Dispositivo de administración transdérmica de fármacos |
| ATE425210T1 (de) * | 2004-01-22 | 2009-03-15 | Dow Corning | Zusammensetzung mit verbesserter haftung gegenüber einem additionshärtbaren material und verbundgegenstand mit der zusammensetzung |
| US20050182443A1 (en) | 2004-02-18 | 2005-08-18 | Closure Medical Corporation | Adhesive-containing wound closure device and method |
| EP1574227A1 (en) * | 2004-03-09 | 2005-09-14 | The Procter & Gamble Company | Disposable absorbent articles with improved fastening performance to hydrophobic materials, particularly microfibre materials |
| EP1574226B1 (en) * | 2004-03-09 | 2017-06-28 | The Procter & Gamble Company | Disposable absorbent articles with improved peel force on hydrophobic garment materials, particularly microfibre materials |
| US20070172518A1 (en) | 2004-03-12 | 2007-07-26 | Dow Corning Corporation | Method of making silicone pressure sensitive adhesives for delivering hydrophilic drugs |
| US20060009099A1 (en) | 2004-07-12 | 2006-01-12 | Closure Medical Corporation | Adhesive-containing wound closure device and method |
| JP4880603B2 (ja) * | 2004-08-11 | 2012-02-22 | ダウ・コーニング・コーポレイション | センサ応用のための半透膜を形成する光重合性シリコーン物質 |
| ES2596809T3 (es) * | 2004-10-08 | 2017-01-12 | Noven Pharmaceuticals, Inc. | Dispositivo de administración transdérmica de fármacos que incluye un refuerzo oclusivo |
| WO2006041908A2 (en) | 2004-10-08 | 2006-04-20 | Noven Pharmaceuticals, Inc. | Transdermal delivery of estradiol |
| WO2006041907A2 (en) | 2004-10-08 | 2006-04-20 | Noven Pharmaceuticals, Inc. | Transdermal delivery of estradiol |
| US20060078602A1 (en) | 2004-10-08 | 2006-04-13 | Noven Pharmaceuticals, Inc. | Device for transdermal administration of drugs including acrylic polymers |
| US7850870B2 (en) * | 2004-10-28 | 2010-12-14 | Dow Corning Corporation | Conductive curable compositions |
| WO2006071772A2 (en) | 2004-12-23 | 2006-07-06 | Dow Corning Corporation | Crosslinkable saccharide-siloxane compositions, and networks, coatings and articles formed therefrom |
| JP5090182B2 (ja) * | 2005-01-04 | 2012-12-05 | ダウ・コーニング・コーポレイション | オルガノボランアミン錯体によって硬化されたシロキサンおよびシラン |
| DE602005015766D1 (de) * | 2005-01-04 | 2009-09-10 | Dow Corning | Organosiliciumfunktionelle bor-amin-katalysatorkomplexe und daraus hergestellte härtbare zusammensetzungen |
| EP1913040B1 (en) | 2005-02-16 | 2021-03-31 | Dow Silicones Corporation | Polymer particles and encapsulated compositions using organoborane amine complexes |
| EP1854136A1 (en) * | 2005-03-01 | 2007-11-14 | Dow Corning Corporation | Temporary wafer bonding method for semiconductor processing |
| US8877216B2 (en) * | 2005-05-23 | 2014-11-04 | Dow Corning Corporation | Cosmetic and skin-care compositions comprising saccharide-siloxane copolymers |
| DE602006017829D1 (de) * | 2005-05-23 | 2010-12-09 | Dow Corning | Oberflächenbehandlungszusammensetzungen mit saccharid-siloxan-polymeren |
| CN101267949A (zh) * | 2005-09-21 | 2008-09-17 | 陶氏康宁公司 | 使用有机基硼烷胺络合物的环境平版印刷方法 |
| US20080300358A1 (en) * | 2005-12-08 | 2008-12-04 | Leon Neal Cook | Continuous Process For Production Of Silicone Pressure Sensitive Adhesives |
| US20070166244A1 (en) * | 2006-01-19 | 2007-07-19 | The Procter & Gamble Company | Compositions comprising silicone pressure sensitive adhesives for delivering oral care substances |
| WO2007084266A2 (en) * | 2006-01-19 | 2007-07-26 | Dow Corning Corporation | Silicone adhesive for adhesion to wet surfaces |
| US7410704B2 (en) * | 2006-04-14 | 2008-08-12 | 3M Innovative Properties Company | Composition containing fluoroalkyl hydrosilicone |
| US7407710B2 (en) * | 2006-04-14 | 2008-08-05 | 3M Innovative Properties Company | Composition containing fluoroalkyl silicone and hydrosilicone |
| US7413807B2 (en) * | 2006-04-14 | 2008-08-19 | 3M Innovative Properties Company | Fluoroalkyl silicone composition |
| KR101409252B1 (ko) | 2006-05-23 | 2014-07-03 | 다우 코닝 코포레이션 | 아마이드 작용성 중합체와의 보레인 촉매 착물 및 이로부터제조된 경화성 조성물 |
| WO2007139812A2 (en) * | 2006-05-23 | 2007-12-06 | Dow Corning Corporation | Novel silicone film former for delivery of actives |
| MY153136A (en) * | 2006-08-14 | 2014-12-31 | Dow Corning | Method of preparing a patterned film with a developing solvent |
| MX2009004358A (es) * | 2006-10-27 | 2009-06-17 | Noven Pharma | Suministro transdermico de derivados polares de cetoprofeno. |
| US7709092B2 (en) * | 2007-01-19 | 2010-05-04 | 3M Innovative Properties Company | Solar control multilayer film |
| WO2008103219A1 (en) * | 2007-02-20 | 2008-08-28 | Dow Corning Coration | Filler treating agents based on hydrogen bonding polyorganosiloxanes |
| US20080302487A1 (en) | 2007-06-07 | 2008-12-11 | Closure Medical Corporation | Mesh dispenser |
| US8377852B2 (en) * | 2007-10-26 | 2013-02-19 | Dow Corning Corporation | Method of preparing a substrate with a composition including an organoborane initiator |
| WO2009021249A2 (en) | 2007-10-29 | 2009-02-12 | Dow Corning Corporation | Polar polydimethylsiloxane molds, methods of making the molds, and methods of using the molds for pattern transfer |
| US20090270884A1 (en) * | 2008-04-25 | 2009-10-29 | Closure Medical Corporation | Mesh Dispensing Device Having a Closed Loop of Backing Film |
| US8231906B2 (en) * | 2008-07-10 | 2012-07-31 | Noven Pharmaceuticals, Inc. | Transdermal estrogen device and delivery |
| WO2010104534A1 (en) | 2009-03-12 | 2010-09-16 | Dow Corning Corporation | Thermal interface materials and mehtods for their preparation and use |
| US9320742B2 (en) | 2009-12-01 | 2016-04-26 | Noven Pharmaceuticals, Inc. | Transdermal testosterone device and delivery |
| US8647964B2 (en) | 2010-02-12 | 2014-02-11 | Dow Corning Corporation | Temporary wafer bonding method for semiconductor processing |
| EP3064199B1 (en) | 2010-04-02 | 2023-12-20 | Buzzz Pharmaceuticals Limited | Abuse-deterrent transdermal formulations of opiate agonists and agonist-antagonists |
| ES2555258T3 (es) | 2010-04-02 | 2015-12-30 | Zynerba Pharmaceuticals, Inc. | Profármacos de opioides administrables por vía transdérmica, composiciones que no inducen al abuso y procedimientos de uso de los profármacos opioides |
| CA2807336A1 (en) | 2010-08-05 | 2012-02-09 | Biofilm Ip, Llc | Cyclosiloxane-substituted polysiloxane compounds, compositions containing the compounds and methods of use thereof |
| US8853372B2 (en) | 2010-08-23 | 2014-10-07 | Dow Corning Corporation | Saccharide siloxanes stable in aqueous environments and methods for the preparation and use of such saccharide siloxanes |
| WO2012071330A1 (en) | 2010-11-24 | 2012-05-31 | Dow Corning Corporation | Controlling morphology of block copolymers |
| WO2012092165A1 (en) | 2010-12-29 | 2012-07-05 | Noven Pharmaceuticals, Inc. | Transdermal drug delivery system comprising levonorgestrel acetate |
| WO2012128875A1 (en) | 2011-03-22 | 2012-09-27 | Dow Corning Corporation | Thermal management within an led assembly |
| CN103619861A (zh) | 2011-06-29 | 2014-03-05 | 道康宁公司 | 硅氢加成反应可固化组合物及其制备和使用方法 |
| JP6117210B2 (ja) | 2011-09-20 | 2017-04-19 | ダウ コーニング コーポレーションＤｏｗ Ｃｏｒｎｉｎｇ Ｃｏｒｐｏｒａｔｉｏｎ | イリジウムを含有するヒドロシリル化触媒及びその触媒を含有する組成物 |
| US20140182483A1 (en) | 2011-09-20 | 2014-07-03 | Dow Corning Corporation | Titanium Containing Hydrosilylation Catalysts And Compositions Containing The Catalysts |
| JP2015501287A (ja) | 2011-09-20 | 2015-01-15 | ダウ コーニング コーポレーションＤｏｗ Ｃｏｒｎｉｎｇ Ｃｏｒｐｏｒａｔｉｏｎ | バナジウム含有ヒドロシリル化触媒及びこの触媒を含有する組成物 |
| CN104024267A (zh) | 2011-09-20 | 2014-09-03 | 道康宁公司 | 含铁硅氢加成催化剂及含有该催化剂的组合物 |
| WO2013043767A2 (en) | 2011-09-20 | 2013-03-28 | Dow Corning Corporation | Rhenium containing hydrosilylation catalysts and compositions containing the catalysts |
| JP6117211B2 (ja) | 2011-09-20 | 2017-04-19 | ダウ コーニング コーポレーションＤｏｗ Ｃｏｒｎｉｎｇ Ｃｏｒｐｏｒａｔｉｏｎ | ルテニウム含有ヒドロシリル化触媒及びこの触媒を含有する組成物 |
| WO2013043765A2 (en) | 2011-09-20 | 2013-03-28 | Dow Corning Corporation | Hafnium containing hydrosilylation catalysts and compositions containing the catalysts |
| WO2013043785A2 (en) | 2011-09-20 | 2013-03-28 | Dow Corning Corporation | Nickel containing hydrosilylation catalysts and compositions containing the catalysts |
| CN103814037A (zh) | 2011-09-20 | 2014-05-21 | 道康宁公司 | 含锰硅氢加成催化剂及含有该催化剂的组合物 |
| US20140225027A1 (en) | 2011-09-20 | 2014-08-14 | Dow Corning Corporation | Silver Containing Hydrosilylation Catalysts And Compositions Containing The Catalysts |
| WO2013043766A1 (en) | 2011-09-20 | 2013-03-28 | Dow Corning Corporation | Molybdenum containing hydrosilylation reaction catalysts and compositions containing the catalysts |
| WO2013043792A2 (en) | 2011-09-20 | 2013-03-28 | Dow Corning Corporation | Copper containing hydrosilylation catalysts and compositions containing the catalysts |
| WO2013043799A1 (en) | 2011-09-20 | 2013-03-28 | Dow Corning Corporation | Zirconium containing hydrosilylation catalysts and compositions containing the catalysts |
| US20140228570A1 (en) | 2011-09-20 | 2014-08-14 | Dow Corning Corporation | Hydrosilylation Catalysts Made With Terdentate Nitrogen Ligands And Compositions Containing The Catalysts |
| WO2013043798A2 (en) | 2011-09-20 | 2013-03-28 | Dow Corning Corporation | Zinc containing hydrosilylation catalysts and compositions containing the catalysts |
| EP2758417A2 (en) | 2011-09-20 | 2014-07-30 | Dow Corning Corporation | Cobalt containing hydrosilylation catalysts and compositions containing the catalysts |
| US9139699B2 (en) | 2012-10-04 | 2015-09-22 | Dow Corning Corporation | Metal containing condensation reaction catalysts, methods for preparing the catalysts, and compositions containing the catalysts |
| EP2773304B1 (en) | 2011-10-31 | 2016-03-30 | Avery Dennison Corporation | Disruptable adhesive layer for fluid activated debonding |
| WO2013081794A1 (en) | 2011-12-01 | 2013-06-06 | Dow Corning Corporation | Hydrosilylation reaction catalysts and curable compositions and methods for their preparation and use |
| EP2790684B1 (en) | 2011-12-16 | 2016-10-12 | 3M Innovative Properties Company | Foldable adhesive composite dressing |
| BR112014014828A2 (pt) | 2011-12-21 | 2017-06-13 | 3M Innovative Properties Co | conjunto de emplastros adesivos com revestimento de sobreposição e sistema e método para a produção do mesmo |
| US9144671B2 (en) | 2011-12-21 | 2015-09-29 | 3M Innovative Properties Company | Transdermal adhesive patch assembly with removable microneedle array and method of using same |
| JP2015506978A (ja) | 2012-02-08 | 2015-03-05 | ダウ コーニング コーポレーションＤｏｗ Ｃｏｒｎｉｎｇ Ｃｏｒｐｏｒａｔｉｏｎ | ヘルスケア有効成分の送達用シリコーンエマルション |
| JP2015508116A (ja) | 2012-02-08 | 2015-03-16 | ダウ コーニング コーポレーションＤｏｗ Ｃｏｒｎｉｎｇ Ｃｏｒｐｏｒａｔｉｏｎ | シリコーン樹脂エマルション |
| WO2014059104A1 (en) | 2012-10-10 | 2014-04-17 | 3M Innovative Properties Company | Applicator and method for applying a microneedle device to skin |
| EP2909270A1 (en) | 2012-10-22 | 2015-08-26 | Avery Dennison Corporation | Hybrid material of crosslinked microgel particles dispersed in an adhesive |
| WO2014078545A1 (en) | 2012-11-16 | 2014-05-22 | 3M Innovative Properties Company | Force-controlled applicator for applying a microneedle device to skin |
| TW201439264A (zh) | 2012-12-20 | 2014-10-16 | 道康寧公司 | 製造電子裝置的方法 |
| US20150342899A1 (en) | 2012-12-28 | 2015-12-03 | Noven Pharmaceuticals, Inc. | Compositions and methods for transdermal delivery of amphetamine and clonidine |
| WO2014130846A1 (en) | 2013-02-22 | 2014-08-28 | Seungpyo Hong | Transdermal drug delivery using amphiphilic dendron-coil micelles |
| AR095259A1 (es) | 2013-03-15 | 2015-09-30 | Noven Pharma | Composiciones y métodos para la administración transdérmica de fármacos de amina terciaria |
| WO2014143757A1 (en) | 2013-03-15 | 2014-09-18 | Dow Corning Corporation | Cosmetic compositions containing silicone resin emulsions |
| JP6494602B2 (ja) | 2013-05-31 | 2019-04-03 | スリーエム イノベイティブ プロパティズ カンパニー | 二重カバーを備えるマイクロニードル注射装置 |
| ES2686362T3 (es) | 2013-05-31 | 2018-10-17 | 3M Innovative Properties Company | Aparato de inyección de microagujas que comprende una accionador inverso |
| KR102274902B1 (ko) | 2013-05-31 | 2021-07-07 | 쓰리엠 이노베이티브 프로퍼티즈 컴파니 | 마이크로니들 주사 및 주입 장치 및 그의 사용 방법 |
| US20160230047A1 (en) | 2013-09-23 | 2016-08-11 | Lubrizol Advanced Materials, Inc. | A combined hot-melt adhesive and pressure sensitive adhesive system and composite materials made from the same |
| AR098878A1 (es) | 2013-12-23 | 2016-06-22 | Noven Pharma | Composiciones y métodos para administración transdérmica de anfetamina |
| US20170112126A1 (en) | 2014-06-10 | 2017-04-27 | Sabic Global Technologies B.V. | Insecticide-containing coating composition and method for protecting palm trees from pests |
| EP3155060A1 (en) | 2014-06-13 | 2017-04-19 | Avery Dennison Corporation | Improved pressure-sensitive adhesives used for medical applications |
| US10071090B2 (en) | 2014-07-18 | 2018-09-11 | Buzzz Pharmaceuticals Limited | Oxymorphone transdermal patch |
| EP3172262B1 (en) | 2014-07-23 | 2023-07-05 | Dow Silicones Corporation | Silicone emulsions |
| USD824525S1 (en) | 2014-09-25 | 2018-07-31 | Ethicon Llc | Release paper for wound treament devices |
| EP3233800A4 (en) | 2014-12-19 | 2018-08-01 | Dow Silicones Corporation | Ligand components, associated reaction products, activated reaction products, hydrosilylation catalysts and hydrosilylation curable compositions including the ligand components, and associated methods for preparing same |
| WO2016126438A1 (en) | 2015-02-03 | 2016-08-11 | Dow Corning Corporation | Curable silicone formulations and related cured products, methods, articles, and devices |
| EP3288505B1 (en) | 2015-04-30 | 2020-02-26 | Coloplast A/S | Ostomy device |
| US20170000745A1 (en) | 2015-07-02 | 2017-01-05 | Noven Pharmaceuticals, Inc. | Transdermal drug delivery systems for levonorgestrel and ethinyl estradiol |
| TWI678551B (zh) | 2015-07-28 | 2019-12-01 | 美商道康寧公司 | 智慧型光學材料、配方、方法、用途、物品、及裝置 |
| ES3013888T3 (en) | 2015-09-24 | 2025-04-15 | Ethicon Llc | Devices for wound closure |
| JP7531821B2 (ja) | 2015-11-16 | 2024-08-13 | ノーヴェン ファーマシューティカルズ インコーポレイテッド | 経皮薬物送達システムのための伸縮可能なバッキング層 |
| US20210100754A1 (en) | 2016-02-05 | 2021-04-08 | 3M Innovative Properties Company | Transdermal drug delivery systems with fluorosilicone release liners |
| US10792024B2 (en) | 2016-09-28 | 2020-10-06 | Ethicon, Inc. | Scaffolds with channels for joining layers of tissue at discrete points |
| US10687986B2 (en) | 2016-09-29 | 2020-06-23 | Ethicon, Inc. | Methods and devices for skin closure |
| US10470934B2 (en) | 2016-09-29 | 2019-11-12 | Ethicon, Inc. | Methods and devices for skin closure |
| USD848624S1 (en) | 2016-09-29 | 2019-05-14 | Ethicon, Inc. | Release paper for wound treatment devices |
| CN110382083B (zh) | 2017-03-14 | 2022-03-29 | 美国陶氏有机硅公司 | 使用吸附剂共聚物耗减混合物中的有机硅组分的方法和用于实施该方法的装置 |
| US10470935B2 (en) | 2017-03-23 | 2019-11-12 | Ethicon, Inc. | Skin closure systems and devices of improved flexibility and stretchability for bendable joints |
| US20180271505A1 (en) | 2017-03-23 | 2018-09-27 | Ethicon, Inc. | Scaffolds for Joining Layers of Tissue at Discrete Points |
| US11504446B2 (en) | 2017-04-25 | 2022-11-22 | Ethicon, Inc. | Skin closure devices with self-forming exudate drainage channels |
| EP3665210B1 (en) | 2017-07-25 | 2022-02-23 | Dow Silicones Corporation | Method for preparing a graft copolymer with a polyolefin backbone and polyorganosiloxane pendant groups |
| CN111051461B (zh) | 2017-08-22 | 2022-04-26 | 美国陶氏有机硅公司 | 双重固化粘合剂组合物及其制备和使用方法 |
| CN111032814B (zh) | 2017-10-19 | 2022-06-28 | 美国陶氏有机硅公司 | 压敏粘着剂组合物及其制备方法以及在柔性有机发光二极管应用中的用途 |
| TW201917148A (zh) | 2017-10-27 | 2019-05-01 | 美商陶氏有機矽公司 | 可固化矽氧烷黏著劑 |
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Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5027837A (enExample) * | 1973-05-29 | 1975-03-22 | ||
| SU413836A1 (ru) * | 1971-03-03 | 1978-01-30 | Karlin A V | Способ получени полиорганосилоксанов |
| 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 |
| JPS57168974A (en) * | 1981-01-05 | 1982-10-18 | Dow Corning | Silicone pressure-sensitive adhesive composition |
| US4460371A (en) * | 1981-11-24 | 1984-07-17 | Dennison Manufacturing Company | Silicone pressure sensitive adhesive and uses |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA575664A (en) * | 1959-05-12 | Bartell Charles | Process for curing compositions containing organopolysiloxane and organo-amines | |
| CA711756A (en) * | 1965-06-15 | R. Pail Daniel | Organosiloxane pressure-sensitive adhesive composition | |
| US2736721A (en) * | 1952-10-08 | 1956-02-28 | Optionally | |
| US2814601A (en) * | 1954-04-29 | 1957-11-26 | Dow Corning | Organopolysiloxane adhesive and pressure-sensitive adhesive tape containing same |
| DE1017883B (de) * | 1954-07-08 | 1957-10-17 | Fellows Gear Shaper Co | Schalt- und Vorschubeinrichtung fuer Zahnradherstellungsmaschinen |
| US3528940A (en) * | 1966-12-15 | 1970-09-15 | Gen Electric | Silicone pressure-sensitive adhesive of improved strength |
| US3929704A (en) * | 1973-06-07 | 1975-12-30 | Gen Electric | Silicone pressure sensitive adhesives and tapes |
| US3983298A (en) * | 1975-04-18 | 1976-09-28 | Dow Corning Corporation | Polyorganosiloxane pressure sensitive adhesives and articles therefrom |
| US4255316A (en) * | 1979-04-26 | 1981-03-10 | Dow Corning Corporation | Ceramifiable silicone adhesives |
| US4417042A (en) * | 1982-02-17 | 1983-11-22 | General Electric Company | Scavengers for one-component alkoxy-functional RTV compositions and processes |
-
1984
- 1984-10-29 US US06/665,796 patent/US4585836A/en not_active Expired - Lifetime
-
1985
- 1985-10-04 CA CA000492257A patent/CA1271580A/en not_active Expired
- 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
Patent Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SU413836A1 (ru) * | 1971-03-03 | 1978-01-30 | Karlin A V | Способ получени полиорганосилоксанов |
| JPS5027837A (enExample) * | 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 |
| JPS57168974A (en) * | 1981-01-05 | 1982-10-18 | Dow Corning | Silicone pressure-sensitive adhesive composition |
| US4460371A (en) * | 1981-11-24 | 1984-07-17 | Dennison Manufacturing Company | Silicone pressure sensitive adhesive and uses |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| 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 |
|---|---|
| EP0183378A2 (en) | 1986-06-04 |
| JPH0236633B2 (enExample) | 1990-08-20 |
| EP0183378A3 (en) | 1987-03-25 |
| US4585836A (en) | 1986-04-29 |
| DE3574267D1 (en) | 1989-12-21 |
| CA1271580A (en) | 1990-07-10 |
| EP0183378B1 (en) | 1989-11-15 |
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