JPH03425B2 - - Google Patents
Info
- Publication number
- JPH03425B2 JPH03425B2 JP61002364A JP236486A JPH03425B2 JP H03425 B2 JPH03425 B2 JP H03425B2 JP 61002364 A JP61002364 A JP 61002364A JP 236486 A JP236486 A JP 236486A JP H03425 B2 JPH03425 B2 JP H03425B2
- Authority
- JP
- Japan
- Prior art keywords
- parts
- organopolysiloxane
- group
- sio
- component
- 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.)
- Expired
Links
- 229920001296 polysiloxane Polymers 0.000 claims description 76
- 125000005358 mercaptoalkyl group Chemical group 0.000 claims description 42
- 239000000203 mixture Substances 0.000 claims description 42
- 125000003342 alkenyl group Chemical group 0.000 claims description 14
- 229910004298 SiO 2 Inorganic materials 0.000 claims description 13
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 5
- 125000001183 hydrocarbyl group Chemical group 0.000 claims description 5
- 239000003504 photosensitizing agent Substances 0.000 claims description 5
- 229920005645 diorganopolysiloxane polymer Polymers 0.000 claims description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
- 229910052799 carbon Inorganic materials 0.000 claims 1
- 230000000704 physical effect Effects 0.000 description 14
- -1 Polysiloxane Polymers 0.000 description 11
- IJOOHPMOJXWVHK-UHFFFAOYSA-N chlorotrimethylsilane Chemical compound C[Si](C)(C)Cl IJOOHPMOJXWVHK-UHFFFAOYSA-N 0.000 description 10
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
- 229920002379 silicone rubber Polymers 0.000 description 9
- 239000004945 silicone rubber Substances 0.000 description 9
- DKEGCUDAFWNSSO-UHFFFAOYSA-N 1,8-dibromooctane Chemical compound BrCCCCCCCCBr DKEGCUDAFWNSSO-UHFFFAOYSA-N 0.000 description 8
- 239000000463 material Substances 0.000 description 8
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 6
- 239000007788 liquid Substances 0.000 description 6
- 238000004519 manufacturing process Methods 0.000 description 6
- UUEWCQRISZBELL-UHFFFAOYSA-N 3-trimethoxysilylpropane-1-thiol Chemical compound CO[Si](OC)(OC)CCCS UUEWCQRISZBELL-UHFFFAOYSA-N 0.000 description 5
- 230000015572 biosynthetic process Effects 0.000 description 5
- YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 description 5
- 238000005259 measurement Methods 0.000 description 5
- 238000003786 synthesis reaction Methods 0.000 description 5
- 239000005051 trimethylchlorosilane Substances 0.000 description 5
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 5
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
- 238000004132 cross linking Methods 0.000 description 3
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 229910052710 silicon Inorganic materials 0.000 description 3
- 239000000377 silicon dioxide Substances 0.000 description 3
- 125000003396 thiol group Chemical group [H]S* 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 2
- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- ISAOCJYIOMOJEB-UHFFFAOYSA-N benzoin Chemical compound C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1 ISAOCJYIOMOJEB-UHFFFAOYSA-N 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 229910052681 coesite Inorganic materials 0.000 description 2
- 229910052906 cristobalite Inorganic materials 0.000 description 2
- 125000004122 cyclic group Chemical group 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 238000012676 equilibrium polymerization Methods 0.000 description 2
- 125000005843 halogen group Chemical group 0.000 description 2
- 230000001678 irradiating effect Effects 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 150000001451 organic peroxides Chemical class 0.000 description 2
- 235000012239 silicon dioxide Nutrition 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 229910052682 stishovite Inorganic materials 0.000 description 2
- 229910052905 tridymite Inorganic materials 0.000 description 2
- 150000005206 1,2-dihydroxybenzenes Chemical class 0.000 description 1
- MSAHTMIQULFMRG-UHFFFAOYSA-N 1,2-diphenyl-2-propan-2-yloxyethanone Chemical compound C=1C=CC=CC=1C(OC(C)C)C(=O)C1=CC=CC=C1 MSAHTMIQULFMRG-UHFFFAOYSA-N 0.000 description 1
- DURPTKYDGMDSBL-UHFFFAOYSA-N 1-butoxybutane Chemical compound CCCCOCCCC DURPTKYDGMDSBL-UHFFFAOYSA-N 0.000 description 1
- VZSRBBMJRBPUNF-UHFFFAOYSA-N 2-(2,3-dihydro-1H-inden-2-ylamino)-N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]pyrimidine-5-carboxamide Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C(=O)NCCC(N1CC2=C(CC1)NN=N2)=O VZSRBBMJRBPUNF-UHFFFAOYSA-N 0.000 description 1
- XMNIXWIUMCBBBL-UHFFFAOYSA-N 2-(2-phenylpropan-2-ylperoxy)propan-2-ylbenzene Chemical compound C=1C=CC=CC=1C(C)(C)OOC(C)(C)C1=CC=CC=C1 XMNIXWIUMCBBBL-UHFFFAOYSA-N 0.000 description 1
- SXAMGRAIZSSWIH-UHFFFAOYSA-N 2-[3-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]-1,2,4-oxadiazol-5-yl]-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethanone Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C1=NOC(=N1)CC(=O)N1CC2=C(CC1)NN=N2 SXAMGRAIZSSWIH-UHFFFAOYSA-N 0.000 description 1
- WZFUQSJFWNHZHM-UHFFFAOYSA-N 2-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperazin-1-yl]-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethanone Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)N1CCN(CC1)CC(=O)N1CC2=C(CC1)NN=N2 WZFUQSJFWNHZHM-UHFFFAOYSA-N 0.000 description 1
- KMNCBSZOIQAUFX-UHFFFAOYSA-N 2-ethoxy-1,2-diphenylethanone Chemical compound C=1C=CC=CC=1C(OCC)C(=O)C1=CC=CC=C1 KMNCBSZOIQAUFX-UHFFFAOYSA-N 0.000 description 1
- LOOUJXUUGIUEBC-UHFFFAOYSA-N 3-(dimethoxymethylsilyl)propane-1-thiol Chemical compound COC(OC)[SiH2]CCCS LOOUJXUUGIUEBC-UHFFFAOYSA-N 0.000 description 1
- DQMRXALBJIVORP-UHFFFAOYSA-N 3-[methoxy(dimethyl)silyl]propane-1-thiol Chemical compound CO[Si](C)(C)CCCS DQMRXALBJIVORP-UHFFFAOYSA-N 0.000 description 1
- CONKBQPVFMXDOV-QHCPKHFHSA-N 6-[(5S)-5-[[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperazin-1-yl]methyl]-2-oxo-1,3-oxazolidin-3-yl]-3H-1,3-benzoxazol-2-one Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)N1CCN(CC1)C[C@H]1CN(C(O1)=O)C1=CC2=C(NC(O2)=O)C=C1 CONKBQPVFMXDOV-QHCPKHFHSA-N 0.000 description 1
- 239000004342 Benzoyl peroxide Substances 0.000 description 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- AFCARXCZXQIEQB-UHFFFAOYSA-N N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(CCNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 AFCARXCZXQIEQB-UHFFFAOYSA-N 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- 244000028419 Styrax benzoin Species 0.000 description 1
- 235000000126 Styrax benzoin Nutrition 0.000 description 1
- 235000008411 Sumatra benzointree Nutrition 0.000 description 1
- BOTDANWDWHJENH-UHFFFAOYSA-N Tetraethyl orthosilicate Chemical compound CCO[Si](OCC)(OCC)OCC BOTDANWDWHJENH-UHFFFAOYSA-N 0.000 description 1
- 239000003377 acid catalyst Substances 0.000 description 1
- 239000002318 adhesion promoter Substances 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 150000008365 aromatic ketones Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 229960002130 benzoin Drugs 0.000 description 1
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 1
- 239000012965 benzophenone Substances 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 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
- 239000000919 ceramic Substances 0.000 description 1
- 125000004218 chloromethyl group Chemical group [H]C([H])(Cl)* 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 125000004093 cyano group Chemical group *C#N 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
- 238000006481 deamination reaction Methods 0.000 description 1
- 230000002542 deteriorative effect Effects 0.000 description 1
- LSXWFXONGKSEMY-UHFFFAOYSA-N di-tert-butyl peroxide Chemical compound CC(C)(C)OOC(C)(C)C LSXWFXONGKSEMY-UHFFFAOYSA-N 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000000806 elastomer Substances 0.000 description 1
- 238000010292 electrical insulation Methods 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000003517 fume Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 235000019382 gum benzoic Nutrition 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical group 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000011810 insulating material Substances 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000011259 mixed solution Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000006082 mold release agent Substances 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 125000000962 organic group Chemical group 0.000 description 1
- 239000012044 organic layer Substances 0.000 description 1
- 150000001282 organosilanes Chemical class 0.000 description 1
- 125000005375 organosiloxane group Chemical class 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 238000004382 potting Methods 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 239000012763 reinforcing filler Substances 0.000 description 1
- 239000000565 sealant Substances 0.000 description 1
- 238000007493 shaping process Methods 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- GJBRNHKUVLOCEB-UHFFFAOYSA-N tert-butyl benzenecarboperoxoate Chemical compound CC(C)(C)OOC(=O)C1=CC=CC=C1 GJBRNHKUVLOCEB-UHFFFAOYSA-N 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- 125000000725 trifluoropropyl group Chemical group [H]C([H])(*)C([H])([H])C(F)(F)F 0.000 description 1
- 238000009281 ultraviolet germicidal irradiation Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L83/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers
- C08L83/04—Polysiloxanes
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L83/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers
- C08L83/04—Polysiloxanes
- C08L83/08—Polysiloxanes containing silicon bound to organic groups containing atoms other than carbon, hydrogen and oxygen
-
- 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
- C08G77/04—Polysiloxanes
- C08G77/20—Polysiloxanes containing silicon bound to unsaturated aliphatic groups
-
- 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
- C08G77/04—Polysiloxanes
- C08G77/22—Polysiloxanes containing silicon bound to organic groups containing atoms other than carbon, hydrogen and oxygen
- C08G77/28—Polysiloxanes containing silicon bound to organic groups containing atoms other than carbon, hydrogen and oxygen sulfur-containing groups
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Silicon Polymers (AREA)
Description
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Claims (1)
- ãç¹èš±è«æ±ã®ç¯å²ã ïŒ ïŒ ïŒååäžã«ããçŽ ååã«çµåããã¢ã«ã±
ãã«åºãå°ãªããšãïŒåæããã25âã«ããã
ç²åºŠã100000cps以äžã§ãããªã«ã¬ãããªã·ã
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ã®é眮æïŒäŸ¡çåæ°ŽçŽ åºãR2ã¯ççŽ æ°ïŒãïŒ
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ãåŒãåäœãšã®åã®ã¢ã«æ¯ã 0.5ã2.5ã§HSåºå«æéã0.4ã6.0ééïŒ ã§ãã
ã¡ã«ã«ããã¢ã«ãã«åºå«æãªã«ã¬ãããªã·ãã
ãµã³ ïŒã300éééšã ïŒ ïŒååäžã«ããçŽ ååã«çµåããã¡ã«ã«ãã
ã¢ã«ãã«åºãå°ãªããšãïŒåæãããç²åºŠã
100000cps以äžã®ã¡ã«ã«ããã¢ã«ãã«åºå«æãž
ãªã«ã¬ãããªã·ãããµã³ ïŒã300éééšã ïŒ æå å€ äžèšïŒïŒãïŒïŒæåã®åèšé100é
ééšã«å¯Ÿã0.01ã10éééš ãšãããªãã第ïŒæåã第ïŒæåäžã®ã¡ã«ã«ãã
ã¢ã«ãã«åºãšç¬¬ïŒæåäžã®ã¢ã«ã±ãã«åºãšã®ã¢ã«
æ¯ã0.2ïŒ1.0ã5.0ïŒ1.0ãšãªãããã«ããŠãªãã
ãšãç¹åŸŽãšãã玫å€ç·ç¡¬åæ§ãªã«ã¬ãããªã·ãã
ãµã³çµæç©ã
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP61002364A JPS62161856A (ja) | 1986-01-09 | 1986-01-09 | 玫å€ç·ç¡¬åæ§ãªã«ã¬ãããªã·ãããµã³çµæç© |
| US07/179,832 US4810731A (en) | 1986-01-09 | 1988-04-08 | Ultraviolet-curable organopolysiloxane composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP61002364A JPS62161856A (ja) | 1986-01-09 | 1986-01-09 | 玫å€ç·ç¡¬åæ§ãªã«ã¬ãããªã·ãããµã³çµæç© |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS62161856A JPS62161856A (ja) | 1987-07-17 |
| JPH03425B2 true JPH03425B2 (ja) | 1991-01-08 |
Family
ID=11527202
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP61002364A Granted JPS62161856A (ja) | 1986-01-09 | 1986-01-09 | 玫å€ç·ç¡¬åæ§ãªã«ã¬ãããªã·ãããµã³çµæç© |
Country Status (2)
| Country | Link |
|---|---|
| US (1) | US4810731A (ja) |
| JP (1) | JPS62161856A (ja) |
Families Citing this family (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH02245060A (ja) * | 1989-03-17 | 1990-09-28 | Toshiba Silicone Co Ltd | 玫å€ç·ç¡¬åæ§ã·ãªã³ãŒã³ã²ã«çµæç© |
| US5091440A (en) * | 1989-12-08 | 1992-02-25 | Wacker Silicones Corporation | Acrylate- or methacrylate-functional organopolysiloxanes |
| DE4120418A1 (de) * | 1991-06-20 | 1992-12-24 | Wacker Chemie Gmbh | Haertbare organo(poly)siloxanmassen |
| US5340620A (en) * | 1993-09-13 | 1994-08-23 | International Paper Company | Process for producing an improved oxygen barrier structure on paper |
| JPH09183908A (ja) * | 1995-12-28 | 1997-07-15 | Toray Dow Corning Silicone Co Ltd | 硬åæ§ãªã«ã¬ãããªã·ãããµã³çµæç©ããã³è©²çµæç©ã䜿çšããŠåºæãšè¢«çäœãæ¥çãããæ¹æ³ |
| EP0795584A3 (en) * | 1996-03-14 | 1998-02-11 | Dow Corning Corporation | Radiation-curable fluorinated organosiloxane compositions |
| US8293810B2 (en) * | 2005-08-29 | 2012-10-23 | Cmet Inc. | Rapid prototyping resin compositions |
| KR101762990B1 (ko) | 2010-04-26 | 2017-07-28 | ì°ëŠ¬ë³žë íìž ìŒë¯žì¹Œ ê°ë¶ìí€ê°ìŽì€ | êŽê²œíì± ì€ëŠ¬ìœê² ì¡°ì±ë¬Œ ë° ê·žì ì©ë |
| US8716362B2 (en) * | 2010-12-22 | 2014-05-06 | Momentive Performance Materials Japan Llc | Ultraviolet-curable silicone resin composition, and image display device using the same |
| JP6173764B2 (ja) * | 2013-05-08 | 2017-08-02 | ã¢ã¡ã³ãã£ãã»ããã©ãŒãã³ã¹ã»ãããªã¢ã«ãºã»ãžã£ãã³ååäŒç€Ÿ | ç»åè¡šç€ºè£ çœ®çšã®ãã æçµæç©ãåã³ãããçšããç»åè¡šç€ºè£ çœ® |
| JP6426023B2 (ja) * | 2015-02-16 | 2018-11-21 | ã¢ã¡ã³ãã£ãã»ããã©ãŒãã³ã¹ã»ãããªã¢ã«ãºã»ãžã£ãã³ååäŒç€Ÿ | 玫å€ç·ç¡¬ååã·ãªã³ãŒã³æš¹èçµæç©ãåã³ãããçšããç»åè¡šç€ºè£ çœ® |
| WO2017082180A1 (en) * | 2015-11-13 | 2017-05-18 | Dow Corning Toray Co., Ltd. | Curable organopolysiloxane composition and cured product thereof |
| CN110494498A (zh) * | 2017-04-13 | 2019-11-22 | ä¿¡è¶ååŠå·¥äžæ ªåŒäŒç€Ÿ | å¥çŠ»æ§æŸå°çº¿åºåæ§ææºç¡ ç»åç©åå¥çŠ»ç |
| WO2021168075A1 (en) * | 2020-02-23 | 2021-08-26 | Dow Silicones Corporation | Photocurable silicone composition and cured product thereof |
| JP7694933B2 (ja) * | 2020-02-28 | 2025-06-18 | ãã¥ãã³ã»æ±ã¬ã»ã¹ãã·ã£ã«ãã£ã»ãããªã¢ã«æ ªåŒäŒç€Ÿ | 玫å€ç·ç¡¬åæ§ã·ãªã³ãŒã³çµæç©åã³ãããå©çšããŠãªãå°æ¢æãŸãã¯ã·ãŒããã£ã«ã |
| JP2022191716A (ja) * | 2021-06-16 | 2022-12-28 | ããŒã ã»ã¢ã³ãã»ããŒã¹ã»ãšã¬ã¯ããããã¯ã»ãããªã¢ã«ãºã»ã³ãªã¢ã»ãªãããã | ïœç¡¬åæ§ã·ãªã³ãŒã³çµæç©åã³ãã®ç¡¬åç© |
| CN113861426B (zh) * | 2021-11-05 | 2022-06-21 | å京çå·¥å€§åŠ | äžç§å æå液äœç¡ æ©¡è¶åå ¶å¶å€æ¹æ³ |
| JP7474007B2 (ja) * | 2022-03-31 | 2024-04-24 | æ ªåŒäŒç€Ÿã¿ã€ã« | å 硬åæ§ã·ãªã³ãŒã³æš¹èçµæç© |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3337497A (en) * | 1966-04-11 | 1967-08-22 | Gen Electric | Ordered organopolysiloxanes |
| JPS5239701B2 (ja) * | 1974-12-28 | 1977-10-06 | ||
| US4163082A (en) * | 1978-10-23 | 1979-07-31 | Dow Corning Corporation | U.V.-radiation method for decreasing surface tack of disposed organopolysiloxane greases and gels |
-
1986
- 1986-01-09 JP JP61002364A patent/JPS62161856A/ja active Granted
-
1988
- 1988-04-08 US US07/179,832 patent/US4810731A/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| US4810731A (en) | 1989-03-07 |
| JPS62161856A (ja) | 1987-07-17 |
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