BRPI1007886B1 - Polímero sililado curável por umidade e composição de revestimento ou selante, adesiva curável por umidade - Google Patents
Polímero sililado curável por umidade e composição de revestimento ou selante, adesiva curável por umidade Download PDFInfo
- Publication number
- BRPI1007886B1 BRPI1007886B1 BRPI1007886-0A BRPI1007886A BRPI1007886B1 BR PI1007886 B1 BRPI1007886 B1 BR PI1007886B1 BR PI1007886 A BRPI1007886 A BR PI1007886A BR PI1007886 B1 BRPI1007886 B1 BR PI1007886B1
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- BR
- Brazil
- Prior art keywords
- moisture
- amino
- silane
- group
- fact
- Prior art date
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- 229920000642 polymer Polymers 0.000 title claims abstract description 125
- 239000000203 mixture Substances 0.000 title claims abstract description 116
- 239000000853 adhesive Substances 0.000 title claims abstract description 26
- 230000001070 adhesive effect Effects 0.000 title claims abstract description 26
- 238000000576 coating method Methods 0.000 title claims abstract description 10
- 239000011248 coating agent Substances 0.000 title claims abstract description 7
- 238000007789 sealing Methods 0.000 title description 3
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 claims abstract description 113
- 229910000077 silane Inorganic materials 0.000 claims abstract description 72
- 239000003153 chemical reaction reagent Substances 0.000 claims abstract description 30
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 25
- 239000000565 sealant Substances 0.000 claims abstract description 23
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims abstract description 22
- 125000003545 alkoxy group Chemical group 0.000 claims abstract description 13
- -1 3-trimethoxysilyl-2-methylpropyl Chemical group 0.000 claims description 104
- 229920001730 Moisture cure polyurethane Polymers 0.000 claims description 38
- 239000003054 catalyst Substances 0.000 claims description 37
- 238000006884 silylation reaction Methods 0.000 claims description 34
- 239000012948 isocyanate Substances 0.000 claims description 28
- 150000002513 isocyanates Chemical class 0.000 claims description 26
- 239000000945 filler Substances 0.000 claims description 24
- 239000002516 radical scavenger Substances 0.000 claims description 22
- 239000002253 acid Substances 0.000 claims description 21
- 150000001412 amines Chemical group 0.000 claims description 21
- 229920000570 polyether Polymers 0.000 claims description 18
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 15
- 239000004014 plasticizer Substances 0.000 claims description 15
- 239000004721 Polyphenylene oxide Substances 0.000 claims description 14
- 239000002318 adhesion promoter Substances 0.000 claims description 14
- 239000011236 particulate material Substances 0.000 claims description 14
- 239000000126 substance Substances 0.000 claims description 14
- 150000002009 diols Chemical class 0.000 claims description 13
- FMGBDYLOANULLW-UHFFFAOYSA-N 3-isocyanatopropyl(trimethoxy)silane Chemical compound CO[Si](OC)(OC)CCCN=C=O FMGBDYLOANULLW-UHFFFAOYSA-N 0.000 claims description 12
- SJECZPVISLOESU-UHFFFAOYSA-N 3-trimethoxysilylpropan-1-amine Chemical compound CO[Si](OC)(OC)CCCN SJECZPVISLOESU-UHFFFAOYSA-N 0.000 claims description 12
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical group N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 12
- 230000001464 adherent effect Effects 0.000 claims description 12
- 125000005442 diisocyanate group Chemical group 0.000 claims description 12
- 239000004971 Cross linker Substances 0.000 claims description 11
- 239000003963 antioxidant agent Substances 0.000 claims description 11
- OJURWUUOVGOHJZ-UHFFFAOYSA-N methyl 2-[(2-acetyloxyphenyl)methyl-[2-[(2-acetyloxyphenyl)methyl-(2-methoxy-2-oxoethyl)amino]ethyl]amino]acetate Chemical compound C=1C=CC=C(OC(C)=O)C=1CN(CC(=O)OC)CCN(CC(=O)OC)CC1=CC=CC=C1OC(C)=O OJURWUUOVGOHJZ-UHFFFAOYSA-N 0.000 claims description 11
- 239000003960 organic solvent Substances 0.000 claims description 11
- 239000004094 surface-active agent Substances 0.000 claims description 11
- 239000013008 thixotropic agent Substances 0.000 claims description 11
- FRGPKMWIYVTFIQ-UHFFFAOYSA-N triethoxy(3-isocyanatopropyl)silane Chemical compound CCO[Si](OCC)(OCC)CCCN=C=O FRGPKMWIYVTFIQ-UHFFFAOYSA-N 0.000 claims description 11
- 150000002148 esters Chemical class 0.000 claims description 9
- 239000012963 UV stabilizer Substances 0.000 claims description 8
- 239000001257 hydrogen Substances 0.000 claims description 8
- 229910052739 hydrogen Inorganic materials 0.000 claims description 8
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 claims description 8
- WYTZZXDRDKSJID-UHFFFAOYSA-N (3-aminopropyl)triethoxysilane Chemical compound CCO[Si](OCC)(OCC)CCCN WYTZZXDRDKSJID-UHFFFAOYSA-N 0.000 claims description 7
- 229910052751 metal Inorganic materials 0.000 claims description 7
- 239000002184 metal Substances 0.000 claims description 7
- BUZRAOJSFRKWPD-UHFFFAOYSA-N isocyanatosilane Chemical class [SiH3]N=C=O BUZRAOJSFRKWPD-UHFFFAOYSA-N 0.000 claims description 6
- 229910052757 nitrogen Inorganic materials 0.000 claims description 6
- FZHAPNGMFPVSLP-UHFFFAOYSA-N silanamine Chemical class [SiH3]N FZHAPNGMFPVSLP-UHFFFAOYSA-N 0.000 claims description 6
- XYWBBDSPFGNYOJ-UHFFFAOYSA-N 3-[diethoxy(methoxy)silyl]propan-1-amine Chemical compound CCO[Si](OCC)(OC)CCCN XYWBBDSPFGNYOJ-UHFFFAOYSA-N 0.000 claims description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 5
- 239000005058 Isophorone diisocyanate Substances 0.000 claims description 5
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical group CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 claims description 5
- NZVVXILCYZGAEE-UHFFFAOYSA-N 2-(trimethoxysilylmethylamino)butanedioic acid Chemical compound CO[Si](OC)(OC)CNC(C(O)=O)CC(O)=O NZVVXILCYZGAEE-UHFFFAOYSA-N 0.000 claims description 4
- AVRBSCLVFWGLFA-UHFFFAOYSA-N 3-(2,2-dimethoxyethoxysilyl)propan-1-amine Chemical compound NCCC[SiH2]OCC(OC)OC AVRBSCLVFWGLFA-UHFFFAOYSA-N 0.000 claims description 4
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 4
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 4
- 125000000524 functional group Chemical group 0.000 claims description 4
- 229910052760 oxygen Inorganic materials 0.000 claims description 4
- 239000001301 oxygen Substances 0.000 claims description 4
- 229910052717 sulfur Chemical group 0.000 claims description 4
- 239000011593 sulfur Chemical group 0.000 claims description 4
- JQKBYCKXGRPGAV-UHFFFAOYSA-N 3-isocyanatopropyl-tri(propan-2-yloxy)silane Chemical compound CC(C)O[Si](OC(C)C)(OC(C)C)CCCN=C=O JQKBYCKXGRPGAV-UHFFFAOYSA-N 0.000 claims description 3
- IVJJAJZLEWCWMI-UHFFFAOYSA-N diethoxy-(3-isocyanatopropyl)-methoxysilane Chemical compound CCO[Si](OCC)(OC)CCCN=C=O IVJJAJZLEWCWMI-UHFFFAOYSA-N 0.000 claims description 3
- 125000005842 heteroatom Chemical group 0.000 claims description 3
- 150000002431 hydrogen Chemical class 0.000 claims description 3
- DQKJNMYIIVPNPU-UHFFFAOYSA-N 2,2-dimethoxyethoxy(isocyanatomethyl)silane Chemical compound N(=C=O)C[SiH2]OCC(OC)OC DQKJNMYIIVPNPU-UHFFFAOYSA-N 0.000 claims description 2
- YOTMZTYBCNXBNS-UHFFFAOYSA-N 2,2-dimethoxyethoxysilylmethylurea Chemical compound N(C(=O)N)C[SiH2]OCC(OC)OC YOTMZTYBCNXBNS-UHFFFAOYSA-N 0.000 claims description 2
- TXMKKXXLZRAQMQ-UHFFFAOYSA-N 2-(2,2-dimethoxyethoxysilyl)ethylurea Chemical compound N(C(=O)N)CC[SiH2]OCC(OC)OC TXMKKXXLZRAQMQ-UHFFFAOYSA-N 0.000 claims description 2
- HGCUSTFCEUEVNF-UHFFFAOYSA-N 2-[2,2-dimethoxyethoxy(phenyl)silyl]ethanethiol Chemical compound COC(CO[SiH](CCS)c1ccccc1)OC HGCUSTFCEUEVNF-UHFFFAOYSA-N 0.000 claims description 2
- KDNAICGMNAVDKR-UHFFFAOYSA-N 2-[3-(2,2-dimethoxyethoxysilyl)propoxy]-N-methylpropan-1-amine Chemical compound CNCC(OCCC[SiH2]OCC(OC)OC)C KDNAICGMNAVDKR-UHFFFAOYSA-N 0.000 claims description 2
- HZKTYPHGKLZRSS-UHFFFAOYSA-N 2-[diethoxy(methoxy)silyl]ethylurea Chemical compound CCO[Si](OCC)(OC)CCNC(N)=O HZKTYPHGKLZRSS-UHFFFAOYSA-N 0.000 claims description 2
- XTSYFXWVAUUYEF-UHFFFAOYSA-N 2-[diethoxy(phenylmethoxy)silyl]ethanethiol Chemical compound CCO[Si](CCS)(OCC)OCC1=CC=CC=C1 XTSYFXWVAUUYEF-UHFFFAOYSA-N 0.000 claims description 2
- IHZHYITXFSSZIZ-UHFFFAOYSA-N 2-isocyanatoethyl(trimethoxy)silane Chemical compound CO[Si](OC)(OC)CCN=C=O IHZHYITXFSSZIZ-UHFFFAOYSA-N 0.000 claims description 2
- PABWYMSXHPGZFP-UHFFFAOYSA-N 2-methyl-3-trimethoxysilyl-n-(3-trimethoxysilylpropyl)propan-1-amine Chemical compound CO[Si](OC)(OC)CCCNCC(C)C[Si](OC)(OC)OC PABWYMSXHPGZFP-UHFFFAOYSA-N 0.000 claims description 2
- LOSLJXKHQKRRFN-UHFFFAOYSA-N 2-trimethoxysilylethanethiol Chemical compound CO[Si](OC)(OC)CCS LOSLJXKHQKRRFN-UHFFFAOYSA-N 0.000 claims description 2
- CZBAFHYBQOCXFP-UHFFFAOYSA-N 2-trimethoxysilylethylurea Chemical compound CO[Si](OC)(OC)CCNC(N)=O CZBAFHYBQOCXFP-UHFFFAOYSA-N 0.000 claims description 2
- CTNYQLTXYKSXFH-UHFFFAOYSA-N 3-[2,2-dimethoxyethoxy(phenyl)silyl]propane-1-thiol Chemical compound COC(CO[SiH](CCCS)c1ccccc1)OC CTNYQLTXYKSXFH-UHFFFAOYSA-N 0.000 claims description 2
- ZYBGOKPABPWCAK-UHFFFAOYSA-N 3-[diethoxy(methoxy)silyl]propylurea Chemical compound CCO[Si](OCC)(OC)CCCNC(N)=O ZYBGOKPABPWCAK-UHFFFAOYSA-N 0.000 claims description 2
- YUERZCNJGJYZPO-UHFFFAOYSA-N 3-[diethoxy(phenylmethoxy)silyl]propane-1-thiol Chemical compound SCCC[Si](OCC)(OCC)OCC1=CC=CC=C1 YUERZCNJGJYZPO-UHFFFAOYSA-N 0.000 claims description 2
- DCQBZYNUSLHVJC-UHFFFAOYSA-N 3-triethoxysilylpropane-1-thiol Chemical compound CCO[Si](OCC)(OCC)CCCS DCQBZYNUSLHVJC-UHFFFAOYSA-N 0.000 claims description 2
- UUEWCQRISZBELL-UHFFFAOYSA-N 3-trimethoxysilylpropane-1-thiol Chemical compound CO[Si](OC)(OC)CCCS UUEWCQRISZBELL-UHFFFAOYSA-N 0.000 claims description 2
- LVACOMKKELLCHJ-UHFFFAOYSA-N 3-trimethoxysilylpropylurea Chemical compound CO[Si](OC)(OC)CCCNC(N)=O LVACOMKKELLCHJ-UHFFFAOYSA-N 0.000 claims description 2
- ZKUHSYZUFLIKBN-UHFFFAOYSA-N 4-(2,2-dimethoxyethoxysilyl)-N-ethyl-2,2-dimethylbutan-1-amine Chemical compound C(C)NCC(CC[SiH2]OCC(OC)OC)(C)C ZKUHSYZUFLIKBN-UHFFFAOYSA-N 0.000 claims description 2
- DXKAYKQALOWPOL-UHFFFAOYSA-N 4-[diethoxy(methoxy)silyl]-n-ethyl-2,2-dimethylbutan-1-amine Chemical compound CCNCC(C)(C)CC[Si](OC)(OCC)OCC DXKAYKQALOWPOL-UHFFFAOYSA-N 0.000 claims description 2
- FLYKYQZCCVFXBO-UHFFFAOYSA-N 4-[diethoxy(phenyl)silyl]oxybutane-1-thiol Chemical compound SCCCCO[Si](OCC)(OCC)C1=CC=CC=C1 FLYKYQZCCVFXBO-UHFFFAOYSA-N 0.000 claims description 2
- AIGMOEXVBDSLEO-UHFFFAOYSA-N 4-methyl-4-[phenyl-di(propan-2-yloxy)silyl]oxypentane-1-thiol Chemical compound SCCCC(C)(C)O[Si](OC(C)C)(OC(C)C)C1=CC=CC=C1 AIGMOEXVBDSLEO-UHFFFAOYSA-N 0.000 claims description 2
- LMAFAQBMCIYHQS-UHFFFAOYSA-N 4-trimethoxysilylbutane-1-thiol Chemical compound CO[Si](OC)(OC)CCCCS LMAFAQBMCIYHQS-UHFFFAOYSA-N 0.000 claims description 2
- XFXPMWWXUTWYJX-UHFFFAOYSA-N Cyanide Chemical compound N#[C-] XFXPMWWXUTWYJX-UHFFFAOYSA-N 0.000 claims description 2
- WFZTZIQBPHRIKH-UHFFFAOYSA-N [diethoxy(methoxy)silyl]methylurea Chemical compound CCO[Si](OCC)(OC)CNC(N)=O WFZTZIQBPHRIKH-UHFFFAOYSA-N 0.000 claims description 2
- PBPWOJWEWAPHRO-UHFFFAOYSA-N diethoxy-(isocyanatomethyl)-methoxysilane Chemical compound CCO[Si](OCC)(OC)CN=C=O PBPWOJWEWAPHRO-UHFFFAOYSA-N 0.000 claims description 2
- QRFPECUQGPJPMV-UHFFFAOYSA-N isocyanatomethyl(trimethoxy)silane Chemical compound CO[Si](OC)(OC)CN=C=O QRFPECUQGPJPMV-UHFFFAOYSA-N 0.000 claims description 2
- SMIDUPHNWFRONB-UHFFFAOYSA-N n,2-dimethyl-3-trimethoxysilylpropan-1-amine Chemical compound CNCC(C)C[Si](OC)(OC)OC SMIDUPHNWFRONB-UHFFFAOYSA-N 0.000 claims description 2
- YFBFAHMPVMWKIM-UHFFFAOYSA-N n-(3-triethoxysilylpropyl)cyclohexanamine Chemical compound CCO[Si](OCC)(OCC)CCCNC1CCCCC1 YFBFAHMPVMWKIM-UHFFFAOYSA-N 0.000 claims description 2
- XCOASYLMDUQBHW-UHFFFAOYSA-N n-(3-trimethoxysilylpropyl)butan-1-amine Chemical compound CCCCNCCC[Si](OC)(OC)OC XCOASYLMDUQBHW-UHFFFAOYSA-N 0.000 claims description 2
- KGNDVXPHQJMHLX-UHFFFAOYSA-N n-(3-trimethoxysilylpropyl)cyclohexanamine Chemical compound CO[Si](OC)(OC)CCCNC1CCCCC1 KGNDVXPHQJMHLX-UHFFFAOYSA-N 0.000 claims description 2
- AAWMXDDKBSXJOE-UHFFFAOYSA-N n-ethyl-2,2-dimethyl-4-triethoxysilylbutan-1-amine Chemical compound CCNCC(C)(C)CC[Si](OCC)(OCC)OCC AAWMXDDKBSXJOE-UHFFFAOYSA-N 0.000 claims description 2
- YJOGKUUQSLYPQJ-UHFFFAOYSA-N n-ethyl-2,2-dimethyl-4-trimethoxysilylbutan-1-amine Chemical compound CCNCC(C)(C)CC[Si](OC)(OC)OC YJOGKUUQSLYPQJ-UHFFFAOYSA-N 0.000 claims description 2
- FRDNYWXDODPUJV-UHFFFAOYSA-N n-ethyl-2-methyl-3-trimethoxysilylpropan-1-amine Chemical compound CCNCC(C)C[Si](OC)(OC)OC FRDNYWXDODPUJV-UHFFFAOYSA-N 0.000 claims description 2
- OKIKLSJWTXOVSF-UHFFFAOYSA-N n-methyl-2-(3-trimethoxysilylpropoxy)propan-1-amine Chemical compound CNCC(C)OCCC[Si](OC)(OC)OC OKIKLSJWTXOVSF-UHFFFAOYSA-N 0.000 claims description 2
- 230000003078 antioxidant effect Effects 0.000 claims 9
- 125000001183 hydrocarbyl group Chemical group 0.000 claims 4
- 239000003381 stabilizer Substances 0.000 claims 2
- VREPHMROZZKOOL-UHFFFAOYSA-N 12-trimethoxysilyldodecane-1-thiol Chemical compound CO[Si](OC)(OC)CCCCCCCCCCCCS VREPHMROZZKOOL-UHFFFAOYSA-N 0.000 claims 1
- IKOPJOGLZWEOFM-UHFFFAOYSA-N 18-(2,2-dimethoxyethoxysilyl)octadecane-1-thiol Chemical compound SCCCCCCCCCCCCCCCCCC[SiH2]OCC(OC)OC IKOPJOGLZWEOFM-UHFFFAOYSA-N 0.000 claims 1
- UAXHQOHEACNJSR-UHFFFAOYSA-N 18-trimethoxysilyloctadecane-1-thiol Chemical compound CO[Si](OC)(OC)CCCCCCCCCCCCCCCCCCS UAXHQOHEACNJSR-UHFFFAOYSA-N 0.000 claims 1
- TVZFBIOTLWINEV-UHFFFAOYSA-N 2,2-dimethoxyethoxy(2-isocyanatoethyl)silane Chemical compound N(=C=O)CC[SiH2]OCC(OC)OC TVZFBIOTLWINEV-UHFFFAOYSA-N 0.000 claims 1
- RGCOBWOVZMXWDG-UHFFFAOYSA-N 2-(2,2-dimethoxyethoxysilyl)benzenethiol Chemical compound SC1=C(C=CC=C1)[SiH2]OCC(OC)OC RGCOBWOVZMXWDG-UHFFFAOYSA-N 0.000 claims 1
- KFEVWIIWNXMTGM-UHFFFAOYSA-N 2-(2,2-dimethoxyethoxysilyl)ethanethiol Chemical compound SCC[SiH2]OCC(OC)OC KFEVWIIWNXMTGM-UHFFFAOYSA-N 0.000 claims 1
- FJUSHUZNBSJTMD-UHFFFAOYSA-N 2-[diethoxy(methoxy)silyl]ethanethiol Chemical compound CCO[Si](CCS)(OC)OCC FJUSHUZNBSJTMD-UHFFFAOYSA-N 0.000 claims 1
- IPJLELCCCCILNT-UHFFFAOYSA-N 2-methyl-3-triethoxysilylpropane-1-thiol Chemical compound CCO[Si](OCC)(OCC)CC(C)CS IPJLELCCCCILNT-UHFFFAOYSA-N 0.000 claims 1
- NYLOHBUGPHJQSL-UHFFFAOYSA-N 2-methyl-3-trimethoxysilylpropane-1-thiol Chemical compound CO[Si](OC)(OC)CC(C)CS NYLOHBUGPHJQSL-UHFFFAOYSA-N 0.000 claims 1
- JEELSXJQQHJRII-UHFFFAOYSA-N 2-methyl-6-trimethoxysilylbenzenethiol Chemical compound CO[Si](OC)(OC)C1=CC=CC(C)=C1S JEELSXJQQHJRII-UHFFFAOYSA-N 0.000 claims 1
- DVNPFNZTPMWRAX-UHFFFAOYSA-N 2-triethoxysilylethanethiol Chemical compound CCO[Si](CCS)(OCC)OCC DVNPFNZTPMWRAX-UHFFFAOYSA-N 0.000 claims 1
- ZCEAVTLUHHSQTE-UHFFFAOYSA-N 2-triethoxysilylethylurea Chemical compound CCO[Si](OCC)(OCC)CCNC(N)=O ZCEAVTLUHHSQTE-UHFFFAOYSA-N 0.000 claims 1
- UANAJLMWAZQBKE-UHFFFAOYSA-N 2-trimethoxysilylbenzenethiol Chemical compound CO[Si](OC)(OC)C1=CC=CC=C1S UANAJLMWAZQBKE-UHFFFAOYSA-N 0.000 claims 1
- QFQSTSHUTJIPRQ-UHFFFAOYSA-N 3-(2,2-dimethoxyethoxysilyl)-2-methylpropane-1-thiol Chemical compound COC(CO[SiH2]CC(C)CS)OC QFQSTSHUTJIPRQ-UHFFFAOYSA-N 0.000 claims 1
- TZZRMTWZNLVNJP-UHFFFAOYSA-N 3-(2,2-dimethoxyethoxysilyl)-N-[3-(2,2-dimethoxyethoxysilyl)propyl]-2-methylpropan-1-amine Chemical compound COC(CO[SiH2]CCCNCC(C[SiH2]OCC(OC)OC)C)OC TZZRMTWZNLVNJP-UHFFFAOYSA-N 0.000 claims 1
- JEHYFNDDEVMHAX-UHFFFAOYSA-N 3-(2,2-dimethoxyethoxysilyl)propane-1-thiol Chemical compound COC(CO[SiH2]CCCS)OC JEHYFNDDEVMHAX-UHFFFAOYSA-N 0.000 claims 1
- YVPIIPDBSLVJGP-UHFFFAOYSA-N 3-[diethoxy(methoxy)silyl]-2-methylpropane-1-thiol Chemical compound CCO[Si](OCC)(OC)CC(C)CS YVPIIPDBSLVJGP-UHFFFAOYSA-N 0.000 claims 1
- RDXXFOAUYDPYHA-UHFFFAOYSA-N 3-[diethoxy(methoxy)silyl]-N-(3-diethoxysilyl-3-methoxypropyl)-2-methylpropan-1-amine Chemical compound COC(CCNCC(C[Si](OCC)(OCC)OC)C)[SiH](OCC)OCC RDXXFOAUYDPYHA-UHFFFAOYSA-N 0.000 claims 1
- VXXWKJGMMZLDEQ-UHFFFAOYSA-N 3-[diethoxy(methoxy)silyl]-n,2-dimethylpropan-1-amine Chemical compound CCO[Si](OCC)(OC)CC(C)CNC VXXWKJGMMZLDEQ-UHFFFAOYSA-N 0.000 claims 1
- FDRUIFJGFGHVQL-UHFFFAOYSA-N 3-[diethoxy(methoxy)silyl]-n-ethyl-2-methylpropan-1-amine Chemical compound CCNCC(C)C[Si](OC)(OCC)OCC FDRUIFJGFGHVQL-UHFFFAOYSA-N 0.000 claims 1
- VXHQTKWHGVQQAE-UHFFFAOYSA-N 3-[diethoxy(methoxy)silyl]propane-1-thiol Chemical compound CCO[Si](OCC)(OC)CCCS VXHQTKWHGVQQAE-UHFFFAOYSA-N 0.000 claims 1
- CLHDHUPZLNNYCB-UHFFFAOYSA-N 3-[dimethoxy(phenyl)silyl]oxypropane-1-thiol Chemical compound SCCCO[Si](OC)(OC)C1=CC=CC=C1 CLHDHUPZLNNYCB-UHFFFAOYSA-N 0.000 claims 1
- AQSKFYRGZPZSEX-UHFFFAOYSA-N 3-isocyanatopropyl(tripropoxy)silane Chemical compound CCCO[Si](OCCC)(OCCC)CCCN=C=O AQSKFYRGZPZSEX-UHFFFAOYSA-N 0.000 claims 1
- RAGWTBZZWJGPGR-UHFFFAOYSA-N 3-isocyanatopropyl-methoxy-dipropoxysilane Chemical compound CCCO[Si](OCCC)(OC)CCCN=C=O RAGWTBZZWJGPGR-UHFFFAOYSA-N 0.000 claims 1
- IMTQZALMIBBSKC-UHFFFAOYSA-N 3-triethoxysilylcyclohexane-1-thiol Chemical compound CCO[Si](OCC)(OCC)C1CCCC(S)C1 IMTQZALMIBBSKC-UHFFFAOYSA-N 0.000 claims 1
- LVNLBBGBASVLLI-UHFFFAOYSA-N 3-triethoxysilylpropylurea Chemical compound CCO[Si](OCC)(OCC)CCCNC(N)=O LVNLBBGBASVLLI-UHFFFAOYSA-N 0.000 claims 1
- QSUKAUDXXCSABB-UHFFFAOYSA-N 3-trimethoxysilylcyclohexane-1-thiol Chemical compound CO[Si](OC)(OC)C1CCCC(S)C1 QSUKAUDXXCSABB-UHFFFAOYSA-N 0.000 claims 1
- XHAQMECHRHFMLO-UHFFFAOYSA-N 4-(2,2-dimethoxyethoxysilyl)butane-1-thiol Chemical compound SCCCC[SiH2]OCC(OC)OC XHAQMECHRHFMLO-UHFFFAOYSA-N 0.000 claims 1
- MQLVSALTTHLHPB-UHFFFAOYSA-N 4-(2,2-dimethoxyethoxysilyl)butane-2-thiol Chemical compound SC(CC[SiH2]OCC(OC)OC)C MQLVSALTTHLHPB-UHFFFAOYSA-N 0.000 claims 1
- WNJBXSGUYBRPDX-UHFFFAOYSA-N 4-[diethoxy(methoxy)silyl]butane-2-thiol Chemical compound CCO[Si](OCC)(OC)CCC(C)S WNJBXSGUYBRPDX-UHFFFAOYSA-N 0.000 claims 1
- MPGJPVZZFPGZQG-UHFFFAOYSA-N 4-[dimethoxy(phenyl)silyl]oxybutane-1-thiol Chemical compound SCCCCO[Si](OC)(OC)C1=CC=CC=C1 MPGJPVZZFPGZQG-UHFFFAOYSA-N 0.000 claims 1
- RVAVYOJYNISEQK-UHFFFAOYSA-N 4-triethoxysilylbutane-1-thiol Chemical compound CCO[Si](OCC)(OCC)CCCCS RVAVYOJYNISEQK-UHFFFAOYSA-N 0.000 claims 1
- XUGBJJNOIWRRPH-UHFFFAOYSA-N 4-triethoxysilylbutane-2-thiol Chemical compound CCO[Si](OCC)(OCC)CCC(C)S XUGBJJNOIWRRPH-UHFFFAOYSA-N 0.000 claims 1
- ZWLDNGJSJBLBFK-UHFFFAOYSA-N 4-trimethoxysilylbutane-2-thiol Chemical compound CO[Si](OC)(OC)CCC(C)S ZWLDNGJSJBLBFK-UHFFFAOYSA-N 0.000 claims 1
- 150000001413 amino acids Chemical class 0.000 claims 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 claims 1
- BMUGBDVZQVLOIT-UHFFFAOYSA-N dibutoxy-(3-isocyanatopropyl)-methoxysilane Chemical compound CCCCO[Si](OCCCC)(OC)CCCN=C=O BMUGBDVZQVLOIT-UHFFFAOYSA-N 0.000 claims 1
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- FIYGHLYYOVFEJL-BUTJMFNXSA-N bombinin-like peptide-3 Chemical compound C([C@H](NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](C)NC(=O)[C@H](CC(C)C)NC(=O)CNC(=O)[C@H](CCCCN)NC(=O)[C@H](C)NC(=O)[C@H](CC(C)C)NC(=O)CNC(=O)[C@H](CCCCN)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](C)NC(=O)[C@H](CO)NC(=O)[C@H](CCCCN)NC(=O)CNC(=O)[C@H](C)NC(=O)[C@H](CO)NC(=O)[C@H](CC(C)C)NC(=O)[C@H]([C@@H](C)CC)NC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)CNC(=O)[C@@H](NC(=O)CN)[C@@H](C)CC)C(=O)N[C@@H](CC=1C=CC=CC=1)C(N)=O)C1C=NC=N1 FIYGHLYYOVFEJL-BUTJMFNXSA-N 0.000 description 1
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 238000013005 condensation curing Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- WXGNPLOJWLOIIC-UHFFFAOYSA-N di(butan-2-yloxy)-(3-isocyanatopropyl)-methoxysilane Chemical compound CCC(C)O[Si](OC(C)CC)(OC)CCCN=C=O WXGNPLOJWLOIIC-UHFFFAOYSA-N 0.000 description 1
- PNOXNTGLSKTMQO-UHFFFAOYSA-L diacetyloxytin Chemical compound CC(=O)O[Sn]OC(C)=O PNOXNTGLSKTMQO-UHFFFAOYSA-L 0.000 description 1
- AYOHIQLKSOJJQH-UHFFFAOYSA-N dibutyltin Chemical group CCCC[Sn]CCCC AYOHIQLKSOJJQH-UHFFFAOYSA-N 0.000 description 1
- ZXDVQYBUEVYUCG-UHFFFAOYSA-N dibutyltin(2+);methanolate Chemical compound CCCC[Sn](OC)(OC)CCCC ZXDVQYBUEVYUCG-UHFFFAOYSA-N 0.000 description 1
- KORSJDCBLAPZEQ-UHFFFAOYSA-N dicyclohexylmethane-4,4'-diisocyanate Chemical compound C1CC(N=C=O)CCC1CC1CCC(N=C=O)CC1 KORSJDCBLAPZEQ-UHFFFAOYSA-N 0.000 description 1
- PJKZHPDNDUQMNP-UHFFFAOYSA-N diethoxy-methoxy-propylsilane Chemical compound CCC[Si](OC)(OCC)OCC PJKZHPDNDUQMNP-UHFFFAOYSA-N 0.000 description 1
- MOXVGLPDBJFDLM-UHFFFAOYSA-N dimethyl 2-[propyl(trimethoxysilyl)amino]butanedioate Chemical compound CCCN([Si](OC)(OC)OC)C(C(=O)OC)CC(=O)OC MOXVGLPDBJFDLM-UHFFFAOYSA-N 0.000 description 1
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical group OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 1
- YCZJVRCZIPDYHH-UHFFFAOYSA-N ditridecyl benzene-1,2-dicarboxylate Chemical compound CCCCCCCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCCCCCCC YCZJVRCZIPDYHH-UHFFFAOYSA-N 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- NKSJNEHGWDZZQF-UHFFFAOYSA-N ethenyl(trimethoxy)silane Chemical compound CO[Si](OC)(OC)C=C NKSJNEHGWDZZQF-UHFFFAOYSA-N 0.000 description 1
- XYIBRDXRRQCHLP-UHFFFAOYSA-N ethyl acetoacetate Chemical compound CCOC(=O)CC(C)=O XYIBRDXRRQCHLP-UHFFFAOYSA-N 0.000 description 1
- 229940093858 ethyl acetoacetate Drugs 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 230000007717 exclusion Effects 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 238000005755 formation reaction Methods 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 230000035876 healing Effects 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 238000002513 implantation Methods 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000011133 lead Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- ARYZCSRUUPFYMY-UHFFFAOYSA-N methoxysilane Chemical class CO[SiH3] ARYZCSRUUPFYMY-UHFFFAOYSA-N 0.000 description 1
- BFXIKLCIZHOAAZ-UHFFFAOYSA-N methyltrimethoxysilane Chemical compound CO[Si](C)(OC)OC BFXIKLCIZHOAAZ-UHFFFAOYSA-N 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- MBAUOPQYSQVYJV-UHFFFAOYSA-N octyl 3-[4-hydroxy-3,5-di(propan-2-yl)phenyl]propanoate Chemical compound OC1=C(C=C(C=C1C(C)C)CCC(=O)OCCCCCCCC)C(C)C MBAUOPQYSQVYJV-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 235000019198 oils Nutrition 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 125000002524 organometallic group Chemical group 0.000 description 1
- 125000001181 organosilyl group Chemical group [SiH3]* 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 125000005498 phthalate group Chemical class 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 229920001748 polybutylene Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920006149 polyester-amide block copolymer Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920006324 polyoxymethylene Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- YUVZWFKROIQRKD-UHFFFAOYSA-N silane triethoxysilane Chemical compound [SiH4].CCO[SiH](OCC)OCC YUVZWFKROIQRKD-UHFFFAOYSA-N 0.000 description 1
- 150000004819 silanols Chemical class 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- APSBXTVYXVQYAB-UHFFFAOYSA-M sodium docusate Chemical group [Na+].CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC APSBXTVYXVQYAB-UHFFFAOYSA-M 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000007655 standard test method Methods 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 150000003505 terpenes Chemical class 0.000 description 1
- 235000007586 terpenes Nutrition 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 239000012974 tin catalyst Substances 0.000 description 1
- KSBAEPSJVUENNK-UHFFFAOYSA-L tin(ii) 2-ethylhexanoate Chemical compound [Sn+2].CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O KSBAEPSJVUENNK-UHFFFAOYSA-L 0.000 description 1
- 150000003609 titanium compounds Chemical class 0.000 description 1
- YXFVVABEGXRONW-UHFFFAOYSA-N toluene Substances CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 1
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 1
- WCLDITPGPXSPGV-UHFFFAOYSA-N tricamba Chemical compound COC1=C(Cl)C=C(Cl)C(Cl)=C1C(O)=O WCLDITPGPXSPGV-UHFFFAOYSA-N 0.000 description 1
- BPSIOYPQMFLKFR-UHFFFAOYSA-N trimethoxy-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CO[Si](OC)(OC)CCCOCC1CO1 BPSIOYPQMFLKFR-UHFFFAOYSA-N 0.000 description 1
- 150000004072 triols Chemical class 0.000 description 1
- AVWRKZWQTYIKIY-UHFFFAOYSA-N urea-1-carboxylic acid Chemical compound NC(=O)NC(O)=O AVWRKZWQTYIKIY-UHFFFAOYSA-N 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N urethane group Chemical group NC(=O)OCC JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- 239000003039 volatile agent Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- PAPBSGBWRJIAAV-UHFFFAOYSA-N ε-Caprolactone Chemical compound O=C1CCCCCO1 PAPBSGBWRJIAAV-UHFFFAOYSA-N 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
- C09J175/00—Adhesives based on polyureas or polyurethanes; Adhesives based on derivatives of such polymers
- C09J175/04—Polyurethanes
-
- 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
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/08—Processes
- C08G18/10—Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step
-
- 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
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/08—Processes
- C08G18/10—Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step
- C08G18/12—Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step using two or more compounds having active hydrogen in the first polymerisation step
-
- 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
- C08G2190/00—Compositions for sealing or packing joints
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Sealing Material Composition (AREA)
- Paints Or Removers (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Polyurethanes Or Polyureas (AREA)
- Silicon Polymers (AREA)
- Polyethers (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US12/322,882 US8138297B2 (en) | 2009-02-09 | 2009-02-09 | Moisture-curable silylated polymer possessing improved storage stability |
| US12/322.882 | 2009-02-09 | ||
| PCT/US2010/023456 WO2010091338A1 (en) | 2009-02-09 | 2010-02-08 | Moisture-curable silylated polymer possessing improved storage stability |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| BRPI1007886A2 BRPI1007886A2 (pt) | 2017-01-17 |
| BRPI1007886B1 true BRPI1007886B1 (pt) | 2020-02-11 |
Family
ID=42272554
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BRPI1007886-0A BRPI1007886B1 (pt) | 2009-02-09 | 2010-02-08 | Polímero sililado curável por umidade e composição de revestimento ou selante, adesiva curável por umidade |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US8138297B2 (enExample) |
| EP (1) | EP2393861B1 (enExample) |
| JP (1) | JP5653368B2 (enExample) |
| CN (1) | CN102361901B (enExample) |
| BR (1) | BRPI1007886B1 (enExample) |
| WO (1) | WO2010091338A1 (enExample) |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2969621B1 (fr) * | 2010-12-22 | 2013-01-18 | Bostik Sa | Polyurethane a blocs polyether et polyester et groupe terminal alkoxysilane |
| CN102432793B (zh) * | 2011-11-25 | 2014-02-05 | 广州杰锐体育设施有限公司 | 一种环保型聚氨酯预聚体及其合成方法 |
| CN104583222A (zh) * | 2012-09-04 | 2015-04-29 | 拜耳材料科技股份有限公司 | 具有硫代氨基甲酸酯结构的异氰酸根合硅烷 |
| CN105579484B (zh) * | 2013-02-26 | 2019-06-04 | 霍尼韦尔国际公司 | 含有卤代烯烃发泡剂的聚氨酯泡沫预混物和由其制造的泡沫 |
| CN103436216B (zh) * | 2013-09-05 | 2014-12-31 | 江苏天辰新材料有限公司 | 一种脱醇型低模量高伸长率的有机硅密封胶及其制备方法 |
| CN103509517B (zh) * | 2013-09-05 | 2015-10-28 | 江苏天辰硅材料有限公司 | 一种瓷化阻燃防火硅酮密封胶及其制备方法 |
| CN103436217A (zh) * | 2013-09-06 | 2013-12-11 | 江苏天辰硅材料有限公司 | 一种单组份脱醇型耐油硅酮密封胶及其制备方法 |
| CN103602306B (zh) * | 2013-09-06 | 2016-01-20 | 江苏天辰新材料股份有限公司 | 一种单组份室温硫化透明脱醇型防霉硅酮密封胶及其制备方法 |
| US9321878B2 (en) * | 2013-12-16 | 2016-04-26 | Momentive Performance Materials Inc. | Process for the preparation of silylated polyurethane polymers using titanium-containing and zirconium-containing catalysts |
| US20150203624A1 (en) * | 2014-01-21 | 2015-07-23 | Vladimyr Wolan | Second generation hybrid silane modified polymers of low viscosity for low toxicity rtv sealants and adhesives |
| PL3067375T3 (pl) * | 2015-03-11 | 2018-01-31 | Henkel Ag & Co Kgaa | Sililowane poliuretany, ich wytwarzanie i zastosowanie |
| WO2018043238A1 (ja) * | 2016-08-31 | 2018-03-08 | 富士フイルム株式会社 | 半導体ナノ粒子複合体の製造方法、半導体ナノ粒子複合体およびフィルム |
| DE102017205444A1 (de) * | 2017-03-30 | 2018-10-04 | Evonik Degussa Gmbh | Zusammensetzung umfassend ein Gemisch von Bis(triethoxysilylpropyl)amin und Bis(trimethoxysilylpropyl)amin sowie dessen Verwendung in einer 2K-Beschichtungszusammensetzung |
| FR3068633B1 (fr) * | 2017-07-04 | 2019-08-23 | Bostik Sa | Preparation d'une composition adhesive dans une extrudeuse |
| EP3565857B1 (de) * | 2017-12-15 | 2020-03-25 | Wacker Chemie AG | Vernetzbare massen auf der basis von organyloxygruppen aufweisenden organopolysiloxanen |
| CA3113952C (en) | 2018-09-24 | 2023-09-19 | Building Materials Investment Corporation | Roofing membranes with improved adhesive bonding strength |
| EP3992252A4 (en) * | 2019-06-26 | 2023-07-19 | Sekisui Polymatech Co., Ltd. | PACKAGING FOR THERMAL CONDUCTIVE COMPOSITION AND TWO COMPONENT CURING THERMAL COMPOSITION |
| CN112142945B (zh) * | 2019-06-27 | 2022-07-12 | 万华化学集团股份有限公司 | 一种高稳定性的端硅烷基聚合物树脂及其制备方法 |
| EP4110842B1 (en) | 2020-02-26 | 2024-02-07 | Akzo Nobel Coatings International B.V. | Alkoxysilane functional polyurethane-urea for adhesive or coating |
| JP2023519822A (ja) * | 2020-04-08 | 2023-05-15 | シーカ テクノロジー アクチェンゲゼルシャフト | 向上された上塗り性を有するシラン官能性ポリマーをベースとする組成物 |
| KR102820691B1 (ko) * | 2020-06-24 | 2025-06-12 | 와커 헤미 아게 | 수분-경화 컨포멀 코팅 조성물 |
| US11760900B2 (en) | 2021-10-27 | 2023-09-19 | Momentive Performance Materials Inc. | Condensation curable composition |
| CN114574155A (zh) * | 2021-12-17 | 2022-06-03 | 浙江新安化工集团股份有限公司 | 一种安全环保型单组份橡皮泥状硅酮密封胶及其制备方法 |
| CN114479741B (zh) * | 2022-02-23 | 2023-03-31 | 广州市白云化工实业有限公司 | 一种低温可快速深层固化的单组分有机硅改性密封胶及其制备方法 |
| CN119053644A (zh) | 2022-05-04 | 2024-11-29 | 美国陶氏有机硅公司 | 硅酮-聚醚共聚物、包含硅酮-聚醚共聚物的密封剂和相关方法 |
| CN116606415A (zh) * | 2023-05-31 | 2023-08-18 | 湖北回天新材料股份有限公司 | 梳型硅烷封端聚氨酯聚合物树脂及其制备方法和应用 |
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| EP0976766B1 (en) | 1997-04-18 | 2006-03-08 | Kaneka Corporation | Polymers, processes for producing the same, and curable compositions produced therefrom |
| US6274688B1 (en) | 1997-07-28 | 2001-08-14 | Kaneka Corporation | Functional groups-terminated vinyl polymers |
| WO1999005215A1 (en) | 1997-07-28 | 1999-02-04 | Kaneka Corporation | Curable adhesive composition |
| US5990257A (en) * | 1998-01-22 | 1999-11-23 | Witco Corporation | Process for producing prepolymers which cure to improved sealants, and products formed thereby |
| DE69933945T2 (de) | 1998-09-02 | 2007-09-13 | Kaneka Corp. | Polymer, verfahren zu seiner herstellung und zusammensetzung |
| US6197912B1 (en) * | 1999-08-20 | 2001-03-06 | Ck Witco Corporation | Silane endcapped moisture curable compositions |
| DE60216966T2 (de) | 2001-11-29 | 2007-10-04 | Kaneka Corp. | Härtbare zusammensetzung |
| US7307134B2 (en) * | 2002-02-22 | 2007-12-11 | Henkel Corporation | Mixed alkoxysilyl functional polymers |
| JP4951889B2 (ja) * | 2004-07-29 | 2012-06-13 | 旭硝子株式会社 | 室温硬化性組成物 |
| US7253238B2 (en) | 2005-04-12 | 2007-08-07 | Momentine Performance Materials Inc. | Fluoroalkylsilylated MQ resin and solvent-resistant pressure sensitive adhesive composition containing same |
| US7405259B2 (en) | 2005-04-29 | 2008-07-29 | Momentive Performance Materials Inc. | Silylated polymer derived from butadiene and solvent-resistant pressure sensitive adhesive composition containing same |
| US8232362B2 (en) * | 2005-09-15 | 2012-07-31 | Momentive Performance Materials Inc. | Preparation of amino-silane terminated polymer by using organic bismuth catalyst and cured polymer therefrom by using non-tin catalyst |
| US20070129528A1 (en) * | 2005-12-01 | 2007-06-07 | Misty Huang | Two-part curable composition and polyurethane-polysiloxane resin mixture obtained therefrom |
| US7732554B2 (en) | 2006-09-21 | 2010-06-08 | Momentive Performance Materials Inc. | Process for preparing a curable silylated polyurethane resin |
| US8207252B2 (en) | 2007-03-07 | 2012-06-26 | Momentive Performance Materials Inc. | Moisture-curable silylated polymer resin composition |
-
2009
- 2009-02-09 US US12/322,882 patent/US8138297B2/en not_active Expired - Fee Related
-
2010
- 2010-02-08 WO PCT/US2010/023456 patent/WO2010091338A1/en not_active Ceased
- 2010-02-08 JP JP2011549306A patent/JP5653368B2/ja not_active Expired - Fee Related
- 2010-02-08 CN CN201080013146.XA patent/CN102361901B/zh not_active Expired - Fee Related
- 2010-02-08 EP EP10703778.0A patent/EP2393861B1/en not_active Not-in-force
- 2010-02-08 BR BRPI1007886-0A patent/BRPI1007886B1/pt active IP Right Grant
Also Published As
| Publication number | Publication date |
|---|---|
| EP2393861A1 (en) | 2011-12-14 |
| BRPI1007886A2 (pt) | 2017-01-17 |
| JP5653368B2 (ja) | 2015-01-14 |
| CN102361901A (zh) | 2012-02-22 |
| US20100204384A1 (en) | 2010-08-12 |
| WO2010091338A1 (en) | 2010-08-12 |
| EP2393861B1 (en) | 2013-10-23 |
| CN102361901B (zh) | 2014-06-11 |
| JP2012517505A (ja) | 2012-08-02 |
| US8138297B2 (en) | 2012-03-20 |
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