JP2016527344A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2016527344A5 JP2016527344A5 JP2016524341A JP2016524341A JP2016527344A5 JP 2016527344 A5 JP2016527344 A5 JP 2016527344A5 JP 2016524341 A JP2016524341 A JP 2016524341A JP 2016524341 A JP2016524341 A JP 2016524341A JP 2016527344 A5 JP2016527344 A5 JP 2016527344A5
- Authority
- JP
- Japan
- Prior art keywords
- silane
- alkyl
- group
- substituted
- composition
- 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.)
- Pending
Links
- 239000000203 mixture Substances 0.000 claims 29
- -1 amide compound Chemical class 0.000 claims 19
- 125000000217 alkyl group Chemical group 0.000 claims 18
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 claims 15
- 229910000077 silane Inorganic materials 0.000 claims 15
- 229920000642 polymer Polymers 0.000 claims 11
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims 10
- 125000003118 aryl group Chemical group 0.000 claims 10
- 125000003545 alkoxy group Chemical group 0.000 claims 8
- 125000003710 aryl alkyl group Chemical group 0.000 claims 8
- 125000003342 alkenyl group Chemical group 0.000 claims 7
- 125000002877 alkyl aryl group Chemical group 0.000 claims 7
- 125000001072 heteroaryl group Chemical group 0.000 claims 6
- 239000002318 adhesion promoter Substances 0.000 claims 5
- 150000003377 silicon compounds Chemical class 0.000 claims 5
- 125000004104 aryloxy group Chemical group 0.000 claims 4
- 238000009835 boiling Methods 0.000 claims 4
- 229910052799 carbon Inorganic materials 0.000 claims 4
- 239000003431 cross linking reagent Substances 0.000 claims 4
- 239000000945 filler Substances 0.000 claims 4
- 125000004475 heteroaralkyl group Chemical group 0.000 claims 4
- 229910052739 hydrogen Inorganic materials 0.000 claims 4
- 239000001257 hydrogen Substances 0.000 claims 4
- 229920000728 polyester Polymers 0.000 claims 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 3
- 239000004721 Polyphenylene oxide Substances 0.000 claims 3
- 229910004298 SiO 2 Inorganic materials 0.000 claims 3
- 239000007983 Tris buffer Substances 0.000 claims 3
- 150000007513 acids Chemical class 0.000 claims 3
- 125000003302 alkenyloxy group Chemical group 0.000 claims 3
- 125000005248 alkyl aryloxy group Chemical group 0.000 claims 3
- 125000000304 alkynyl group Chemical group 0.000 claims 3
- 150000001412 amines Chemical class 0.000 claims 3
- 125000004103 aminoalkyl group Chemical group 0.000 claims 3
- 125000000000 cycloalkoxy group Chemical group 0.000 claims 3
- 125000000753 cycloalkyl group Chemical group 0.000 claims 3
- 125000000524 functional group Chemical group 0.000 claims 3
- 125000004404 heteroalkyl group Chemical group 0.000 claims 3
- 229910052757 nitrogen Inorganic materials 0.000 claims 3
- 229920000620 organic polymer Polymers 0.000 claims 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 3
- 229910052698 phosphorus Inorganic materials 0.000 claims 3
- 229920000570 polyether Polymers 0.000 claims 3
- 229910052710 silicon Inorganic materials 0.000 claims 3
- 239000002904 solvent Substances 0.000 claims 3
- 229910052717 sulfur Chemical group 0.000 claims 3
- 241000723420 Celtis Species 0.000 claims 2
- 235000018962 Celtis occidentalis Nutrition 0.000 claims 2
- 239000004971 Cross linker Substances 0.000 claims 2
- ZRALSGWEFCBTJO-UHFFFAOYSA-N Guanidine Chemical compound NC(N)=N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 claims 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 2
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 claims 2
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical group [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims 2
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 2
- BOTDANWDWHJENH-UHFFFAOYSA-N Tetraethyl orthosilicate Chemical compound CCO[Si](OCC)(OCC)OCC BOTDANWDWHJENH-UHFFFAOYSA-N 0.000 claims 2
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims 2
- 125000004181 carboxyalkyl group Chemical group 0.000 claims 2
- 229910052801 chlorine Inorganic materials 0.000 claims 2
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 claims 2
- 125000001033 ether group Chemical group 0.000 claims 2
- 229910052731 fluorine Inorganic materials 0.000 claims 2
- 125000000623 heterocyclic group Chemical group 0.000 claims 2
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims 2
- 150000002431 hydrogen Chemical class 0.000 claims 2
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 claims 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 2
- ZWXYOPPJTRVTST-UHFFFAOYSA-N methyl-tris(prop-1-en-2-yloxy)silane Chemical compound CC(=C)O[Si](C)(OC(C)=C)OC(C)=C ZWXYOPPJTRVTST-UHFFFAOYSA-N 0.000 claims 2
- BFXIKLCIZHOAAZ-UHFFFAOYSA-N methyltrimethoxysilane Chemical compound CO[Si](C)(OC)OC BFXIKLCIZHOAAZ-UHFFFAOYSA-N 0.000 claims 2
- 229910052760 oxygen Inorganic materials 0.000 claims 2
- 239000011574 phosphorus Chemical group 0.000 claims 2
- 229920001281 polyalkylene Polymers 0.000 claims 2
- 229920000515 polycarbonate Polymers 0.000 claims 2
- 239000004417 polycarbonate Substances 0.000 claims 2
- 229920000098 polyolefin Polymers 0.000 claims 2
- 229920002635 polyurethane Polymers 0.000 claims 2
- 239000004814 polyurethane Substances 0.000 claims 2
- 229920006395 saturated elastomer Polymers 0.000 claims 2
- 239000010703 silicon Substances 0.000 claims 2
- 239000011593 sulfur Chemical group 0.000 claims 2
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 1
- OGZPYBBKQGPQNU-DABLZPOSSA-N (e)-n-[bis[[(e)-butan-2-ylideneamino]oxy]-methylsilyl]oxybutan-2-imine Chemical compound CC\C(C)=N\O[Si](C)(O\N=C(/C)CC)O\N=C(/C)CC OGZPYBBKQGPQNU-DABLZPOSSA-N 0.000 claims 1
- SOIOCWRKKDYODY-UHFFFAOYSA-N 1-[dimethoxy(methyl)silyl]-1,3,3-trimethylurea Chemical compound CO[Si](C)(OC)N(C)C(=O)N(C)C SOIOCWRKKDYODY-UHFFFAOYSA-N 0.000 claims 1
- HYJFCKNSOVNEDU-UHFFFAOYSA-N 1-[dimethoxy(methyl)silyl]-3,3-dimethyl-1-phenylurea Chemical compound CO[Si](C)(OC)N(C(=O)N(C)C)C1=CC=CC=C1 HYJFCKNSOVNEDU-UHFFFAOYSA-N 0.000 claims 1
- YNOOJRKYZUJKMX-UHFFFAOYSA-N C(C)[Si](N(C(C)=O)C)(OC)OC.C[Si](N(C(C)=O)C)(N(C(C)=O)C)N(C(C)=O)C Chemical compound C(C)[Si](N(C(C)=O)C)(OC)OC.C[Si](N(C(C)=O)C)(N(C(C)=O)C)N(C(C)=O)C YNOOJRKYZUJKMX-UHFFFAOYSA-N 0.000 claims 1
- 125000005915 C6-C14 aryl group Chemical group 0.000 claims 1
- 239000004215 Carbon black (E152) Substances 0.000 claims 1
- 239000004970 Chain extender Substances 0.000 claims 1
- 239000004593 Epoxy Substances 0.000 claims 1
- CHJJGSNFBQVOTG-UHFFFAOYSA-N N-methyl-guanidine Natural products CNC(N)=N CHJJGSNFBQVOTG-UHFFFAOYSA-N 0.000 claims 1
- 229910019142 PO4 Inorganic materials 0.000 claims 1
- 239000004743 Polypropylene Substances 0.000 claims 1
- 240000007653 Pometia tomentosa Species 0.000 claims 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 claims 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims 1
- 235000018936 Vitellaria paradoxa Nutrition 0.000 claims 1
- OYZAFCBNUHKGAM-UHFFFAOYSA-N [SiH4].C(C)NC(CC)=O Chemical compound [SiH4].C(C)NC(CC)=O OYZAFCBNUHKGAM-UHFFFAOYSA-N 0.000 claims 1
- ZAEXPVSOLSDZRQ-UHFFFAOYSA-N [acetyloxy(dibutoxy)silyl] acetate Chemical compound CCCCO[Si](OC(C)=O)(OC(C)=O)OCCCC ZAEXPVSOLSDZRQ-UHFFFAOYSA-N 0.000 claims 1
- NOZAQBYNLKNDRT-UHFFFAOYSA-N [diacetyloxy(ethenyl)silyl] acetate Chemical compound CC(=O)O[Si](OC(C)=O)(OC(C)=O)C=C NOZAQBYNLKNDRT-UHFFFAOYSA-N 0.000 claims 1
- KXJLGCBCRCSXQF-UHFFFAOYSA-N [diacetyloxy(ethyl)silyl] acetate Chemical compound CC(=O)O[Si](CC)(OC(C)=O)OC(C)=O KXJLGCBCRCSXQF-UHFFFAOYSA-N 0.000 claims 1
- TVJPBVNWVPUZBM-UHFFFAOYSA-N [diacetyloxy(methyl)silyl] acetate Chemical compound CC(=O)O[Si](C)(OC(C)=O)OC(C)=O TVJPBVNWVPUZBM-UHFFFAOYSA-N 0.000 claims 1
- MCZCJVXEOMJCBE-UHFFFAOYSA-N [dimethyl(triacetyloxysilyloxy)silyl] acetate Chemical compound CC(=O)O[Si](C)(C)O[Si](OC(C)=O)(OC(C)=O)OC(C)=O MCZCJVXEOMJCBE-UHFFFAOYSA-N 0.000 claims 1
- BEIRWWZHJZKPCX-UHFFFAOYSA-N [phenyl-di(propanoyloxy)silyl] propanoate Chemical compound CCC(=O)O[Si](OC(=O)CC)(OC(=O)CC)C1=CC=CC=C1 BEIRWWZHJZKPCX-UHFFFAOYSA-N 0.000 claims 1
- 239000000853 adhesive Substances 0.000 claims 1
- 230000001070 adhesive effect Effects 0.000 claims 1
- 125000005055 alkyl alkoxy group Chemical group 0.000 claims 1
- 125000002947 alkylene group Chemical group 0.000 claims 1
- 150000001409 amidines Chemical class 0.000 claims 1
- 125000005001 aminoaryl group Chemical group 0.000 claims 1
- 125000004429 atom Chemical group 0.000 claims 1
- 125000002837 carbocyclic group Chemical group 0.000 claims 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims 1
- YENOLDYITNSPMQ-UHFFFAOYSA-N carboxysilicon Chemical compound OC([Si])=O YENOLDYITNSPMQ-UHFFFAOYSA-N 0.000 claims 1
- 239000011248 coating agent Substances 0.000 claims 1
- 238000000576 coating method Methods 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 claims 1
- 238000009833 condensation Methods 0.000 claims 1
- 230000005494 condensation Effects 0.000 claims 1
- IJKVHSBPTUYDLN-UHFFFAOYSA-N dihydroxy(oxo)silane Chemical compound O[Si](O)=O IJKVHSBPTUYDLN-UHFFFAOYSA-N 0.000 claims 1
- QIXFYORLWOFUQF-UHFFFAOYSA-N diisocyanato(dimethoxy)silane Chemical compound O=C=N[Si](OC)(OC)N=C=O QIXFYORLWOFUQF-UHFFFAOYSA-N 0.000 claims 1
- MRGUOKJJTKDIIC-UHFFFAOYSA-N diisothiocyanato-methoxy-methylsilane Chemical compound S=C=N[Si](C)(OC)N=C=S MRGUOKJJTKDIIC-UHFFFAOYSA-N 0.000 claims 1
- OQRBGEUZNWMSQN-UHFFFAOYSA-N dimethoxy-methyl-(1-phenylethenoxy)silane Chemical compound CO[Si](C)(OC)OC(=C)C1=CC=CC=C1 OQRBGEUZNWMSQN-UHFFFAOYSA-N 0.000 claims 1
- CVQVSVBUMVSJES-UHFFFAOYSA-N dimethoxy-methyl-phenylsilane Chemical compound CO[Si](C)(OC)C1=CC=CC=C1 CVQVSVBUMVSJES-UHFFFAOYSA-N 0.000 claims 1
- YTPNLBCMTSWLKJ-UHFFFAOYSA-N dimethoxy-methyl-prop-1-en-2-yloxysilane Chemical compound CO[Si](C)(OC)OC(C)=C YTPNLBCMTSWLKJ-UHFFFAOYSA-N 0.000 claims 1
- SWSQBOPZIKWTGO-UHFFFAOYSA-N dimethylaminoamidine Natural products CN(C)C(N)=N SWSQBOPZIKWTGO-UHFFFAOYSA-N 0.000 claims 1
- 229920001971 elastomer Polymers 0.000 claims 1
- 239000000806 elastomer Substances 0.000 claims 1
- FWDBOZPQNFPOLF-UHFFFAOYSA-N ethenyl(triethoxy)silane Chemical compound CCO[Si](OCC)(OCC)C=C FWDBOZPQNFPOLF-UHFFFAOYSA-N 0.000 claims 1
- NKSJNEHGWDZZQF-UHFFFAOYSA-N ethenyl(trimethoxy)silane Chemical compound CO[Si](OC)(OC)C=C NKSJNEHGWDZZQF-UHFFFAOYSA-N 0.000 claims 1
- GBFVZTUQONJGSL-UHFFFAOYSA-N ethenyl-tris(prop-1-en-2-yloxy)silane Chemical compound CC(=C)O[Si](OC(C)=C)(OC(C)=C)C=C GBFVZTUQONJGSL-UHFFFAOYSA-N 0.000 claims 1
- 150000004678 hydrides Chemical class 0.000 claims 1
- 229930195733 hydrocarbon Natural products 0.000 claims 1
- 150000002430 hydrocarbons Chemical class 0.000 claims 1
- 125000004356 hydroxy functional group Chemical group O* 0.000 claims 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 1
- 150000007529 inorganic bases Chemical class 0.000 claims 1
- MAMPQFAGGHUOQJ-UHFFFAOYSA-N isocyanato-dimethoxy-methylsilane Chemical compound CO[Si](C)(OC)N=C=O MAMPQFAGGHUOQJ-UHFFFAOYSA-N 0.000 claims 1
- 239000000463 material Substances 0.000 claims 1
- 238000000034 method Methods 0.000 claims 1
- 150000007522 mineralic acids Chemical class 0.000 claims 1
- 239000003607 modifier Substances 0.000 claims 1
- SBSPZXNNGHZVCR-UHFFFAOYSA-N n-[[acetyl(methyl)amino]-methoxy-methylsilyl]-n-methylacetamide Chemical compound CC(=O)N(C)[Si](C)(OC)N(C)C(C)=O SBSPZXNNGHZVCR-UHFFFAOYSA-N 0.000 claims 1
- HDNXAGOHLKHJOA-UHFFFAOYSA-N n-[bis(cyclohexylamino)-methylsilyl]cyclohexanamine Chemical compound C1CCCCC1N[Si](NC1CCCCC1)(C)NC1CCCCC1 HDNXAGOHLKHJOA-UHFFFAOYSA-N 0.000 claims 1
- NCWLQWGQNUJBNB-UHFFFAOYSA-N n-[bis[benzoyl(methyl)amino]-methylsilyl]-n-methylbenzamide Chemical compound C=1C=CC=CC=1C(=O)N(C)[Si](C)(N(C)C(=O)C=1C=CC=CC=1)N(C)C(=O)C1=CC=CC=C1 NCWLQWGQNUJBNB-UHFFFAOYSA-N 0.000 claims 1
- XIFOKLGEKUNZTI-UHFFFAOYSA-N n-[diethylamino(dimethyl)silyl]-n-ethylethanamine Chemical compound CCN(CC)[Si](C)(C)N(CC)CC XIFOKLGEKUNZTI-UHFFFAOYSA-N 0.000 claims 1
- QREFMLYPZMSWJC-UHFFFAOYSA-N n-[dimethoxy(methyl)silyl]-n-methylacetamide Chemical compound CO[Si](C)(OC)N(C)C(C)=O QREFMLYPZMSWJC-UHFFFAOYSA-N 0.000 claims 1
- HIAYOADWINTDQT-UHFFFAOYSA-N n-[dimethoxy(methyl)silyl]ethanamine Chemical compound CCN[Si](C)(OC)OC HIAYOADWINTDQT-UHFFFAOYSA-N 0.000 claims 1
- CHQGKZGNKCXMIG-UHFFFAOYSA-N n-[dimethoxy(methyl)silyl]methanamine Chemical compound CN[Si](C)(OC)OC CHQGKZGNKCXMIG-UHFFFAOYSA-N 0.000 claims 1
- ZWRBXRIQPXAXNU-UHFFFAOYSA-N n-[dimethoxy(methyl)silyl]propan-2-amine Chemical compound CO[Si](C)(OC)NC(C)C ZWRBXRIQPXAXNU-UHFFFAOYSA-N 0.000 claims 1
- WZXSAXDNMYMUBG-UHFFFAOYSA-N n-methyl-n-trimethoxysilylacetamide Chemical compound CO[Si](OC)(OC)N(C)C(C)=O WZXSAXDNMYMUBG-UHFFFAOYSA-N 0.000 claims 1
- 125000000962 organic group Chemical group 0.000 claims 1
- 150000001282 organosilanes Chemical class 0.000 claims 1
- 125000005375 organosiloxane group Chemical group 0.000 claims 1
- 239000010452 phosphate Substances 0.000 claims 1
- 229920000233 poly(alkylene oxides) Polymers 0.000 claims 1
- 229920005862 polyol Polymers 0.000 claims 1
- 150000003077 polyols Chemical class 0.000 claims 1
- 229920001155 polypropylene Polymers 0.000 claims 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 1
- 239000011347 resin Substances 0.000 claims 1
- 229920005989 resin Polymers 0.000 claims 1
- 239000000565 sealant Substances 0.000 claims 1
- FZHAPNGMFPVSLP-UHFFFAOYSA-N silanamine Chemical compound [SiH3]N FZHAPNGMFPVSLP-UHFFFAOYSA-N 0.000 claims 1
- 125000003808 silyl group Chemical group [H][Si]([H])([H])[*] 0.000 claims 1
- 125000005017 substituted alkenyl group Chemical group 0.000 claims 1
- 125000000547 substituted alkyl group Chemical group 0.000 claims 1
- 125000004426 substituted alkynyl group Chemical group 0.000 claims 1
- ISIJQEHRDSCQIU-UHFFFAOYSA-N tert-butyl 2,7-diazaspiro[4.5]decane-7-carboxylate Chemical compound C1N(C(=O)OC(C)(C)C)CCCC11CNCC1 ISIJQEHRDSCQIU-UHFFFAOYSA-N 0.000 claims 1
- ZQZCOBSUOFHDEE-UHFFFAOYSA-N tetrapropyl silicate Chemical compound CCCO[Si](OCCC)(OCCC)OCCC ZQZCOBSUOFHDEE-UHFFFAOYSA-N 0.000 claims 1
- 229920001187 thermosetting polymer Polymers 0.000 claims 1
- CPUDPFPXCZDNGI-UHFFFAOYSA-N triethoxy(methyl)silane Chemical compound CCO[Si](C)(OCC)OCC CPUDPFPXCZDNGI-UHFFFAOYSA-N 0.000 claims 1
- JLGNHOJUQFHYEZ-UHFFFAOYSA-N trimethoxy(3,3,3-trifluoropropyl)silane Chemical compound CO[Si](OC)(OC)CCC(F)(F)F JLGNHOJUQFHYEZ-UHFFFAOYSA-N 0.000 claims 1
- SDDVFEDYRCTTKO-UHFFFAOYSA-N trimethyl prop-1-en-2-yl silicate Chemical compound CO[Si](OC)(OC)OC(C)=C SDDVFEDYRCTTKO-UHFFFAOYSA-N 0.000 claims 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims 1
- 229920002554 vinyl polymer Polymers 0.000 claims 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201361842205P | 2013-07-02 | 2013-07-02 | |
| US61/842,205 | 2013-07-02 | ||
| PCT/US2014/045222 WO2015003045A1 (en) | 2013-07-02 | 2014-07-02 | Moisture curable compositions |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2016527344A JP2016527344A (ja) | 2016-09-08 |
| JP2016527344A5 true JP2016527344A5 (enExample) | 2017-08-17 |
Family
ID=52144189
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2016524341A Pending JP2016527344A (ja) | 2013-07-02 | 2014-07-02 | 湿気硬化性組成物 |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US20160369061A1 (enExample) |
| EP (1) | EP3017002A4 (enExample) |
| JP (1) | JP2016527344A (enExample) |
| KR (1) | KR20160027014A (enExample) |
| CN (1) | CN105392831A (enExample) |
| WO (1) | WO2015003045A1 (enExample) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2017184416A1 (en) * | 2016-04-19 | 2017-10-26 | Dow Global Technologies Llc | Long open-time water based primer composition for isocyanate and silane functional adhesives |
| KR20190086685A (ko) * | 2016-11-30 | 2019-07-23 | 닛토덴코 가부시키가이샤 | 점착제 조성물, 점착제층 및 점착 시트 |
| WO2019027955A1 (en) * | 2017-07-31 | 2019-02-07 | Dow Global Technologies Llc | HUMIDITY-CURABLE COMPOSITION FOR ISOLATION AND SHEATH LAYERS OF WIRES AND CABLE |
| KR102230635B1 (ko) * | 2018-01-16 | 2021-03-22 | 주식회사 신광화학산업 | 유기주석 비함유 1액 습기 경화형 실릴화 폴리에테르 실란트 접착 조성물 및 이의 제조방법 |
| KR102457648B1 (ko) * | 2018-02-13 | 2022-10-24 | 샌트랄 글래스 컴퍼니 리미티드 | 발수성 보호막 형성용 약액, 그 조제 방법, 및 표면 처리체의 제조 방법 |
| US11441034B2 (en) | 2018-04-19 | 2022-09-13 | Wacker Chemie Ag | Polysiloxane composition |
| CN113748177B (zh) * | 2019-01-28 | 2023-10-03 | 科慕埃弗西有限公司 | 用于制造钝化层的组合物和使用所述组合物的钝化层 |
| DE102021131400A1 (de) * | 2021-11-30 | 2023-06-01 | Nitrochemie Aschau Gmbh | Zusammensetzung für Silikonkautschukmassen |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| LU35994A1 (fr) * | 1957-07-12 | 1958-06-17 | Rhone Poulenc Sa | Procédé de fabrication d'elastomères à base de diorgano-polysiloxanes et produits ainsi obtenus. |
| JPS62295958A (ja) * | 1986-06-13 | 1987-12-23 | Shin Etsu Chem Co Ltd | 室温硬化性オルガノシロキサン組成物 |
| JP2811140B2 (ja) * | 1993-01-19 | 1998-10-15 | 信越化学工業株式会社 | 室温硬化性組成物 |
| US5502144A (en) * | 1994-07-15 | 1996-03-26 | University Of Cincinnati | Composition and method for preparing silicone elastomers |
| ATE243212T1 (de) * | 1996-10-14 | 2003-07-15 | Asahi Chemical Ind | Verfahren zur herstellung acylierter hexaazaisowurtzitan-derivate |
| DE19855619A1 (de) * | 1998-12-02 | 2000-06-08 | Wacker Chemie Gmbh | Unter Abspaltung von Alkoholen zu Elastomeren vernetzbare Organopolysiloxanmassen |
| US6627721B1 (en) * | 2002-09-19 | 2003-09-30 | The Goodyear Tire & Rubber Company | Functionalized elastomers |
| JP4146695B2 (ja) * | 2002-09-13 | 2008-09-10 | 積水化学工業株式会社 | 硬化性組成物 |
| WO2007085622A1 (de) * | 2006-01-26 | 2007-08-02 | Sika Technology Ag | Feuchtigkeitshärtende zusammensetzungen enthaltend silanfunktionelle polymere und aminosilan-addukte mit guter haftung |
| EP1849845A1 (de) * | 2006-04-26 | 2007-10-31 | Sika Technology AG | Feuchtigkeitshärtende Zusammensetzungen enthaltend silanfunktionelle Polymere und Aminosilan-Addukte |
| JP5945881B2 (ja) * | 2011-05-20 | 2016-07-05 | ナガセケムテックス株式会社 | 帯電防止離型剤組成物及び離型フィルム |
| CN104114598B (zh) * | 2011-12-15 | 2017-03-01 | 莫门蒂夫性能材料股份有限公司 | 湿固化的有机聚硅氧烷组合物 |
-
2014
- 2014-07-02 CN CN201480038096.9A patent/CN105392831A/zh active Pending
- 2014-07-02 KR KR1020167001791A patent/KR20160027014A/ko not_active Withdrawn
- 2014-07-02 WO PCT/US2014/045222 patent/WO2015003045A1/en not_active Ceased
- 2014-07-02 JP JP2016524341A patent/JP2016527344A/ja active Pending
- 2014-07-02 US US14/902,219 patent/US20160369061A1/en not_active Abandoned
- 2014-07-02 EP EP14819562.1A patent/EP3017002A4/en not_active Withdrawn
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2016527344A5 (enExample) | ||
| JP2016514191A5 (enExample) | ||
| EP3102325A1 (en) | Moisture curable silicone composition | |
| KR20170088891A (ko) | 수분 경화성 조성물 | |
| JP6748256B2 (ja) | チオ尿素を有する湿気硬化性化合物 | |
| JP2016522308A5 (enExample) | ||
| JP2015524003A (ja) | 湿気硬化性オルガノポリシロキサン組成物 | |
| CN105392831A (zh) | 可湿固化组合物 | |
| JP2016521309A5 (enExample) | ||
| JP2015504946A (ja) | 湿気硬化性オルガノポリシロキサン組成物 | |
| KR20160052611A (ko) | 아미노산을 갖는 수분 경화성 화합물 | |
| CN105658695A (zh) | 可湿固化的组合物 | |
| WO2015081146A1 (en) | Moisture curable compound with metal-arene complexes | |
| WO2014210492A1 (en) | Moisture curable composition with strontium | |
| JP6319168B2 (ja) | 縮合反応生成物の製造方法、該縮合反応生成物を含有する室温硬化性オルガノポリシロキサン組成物の製造方法 | |
| JP2016524637A5 (enExample) | ||
| KR101856788B1 (ko) | 경화성 오르가노폴리실록산 조성물 | |
| WO2016106390A2 (en) | Moisture curable compositions | |
| CN105246947A (zh) | 用于硅氧烷合成的催化剂 | |
| WO2015081148A1 (en) | Moisture curable compositions |