JP2013509476A5 - - Google Patents
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- JP2013509476A5 JP2013509476A5 JP2012535866A JP2012535866A JP2013509476A5 JP 2013509476 A5 JP2013509476 A5 JP 2013509476A5 JP 2012535866 A JP2012535866 A JP 2012535866A JP 2012535866 A JP2012535866 A JP 2012535866A JP 2013509476 A5 JP2013509476 A5 JP 2013509476A5
- Authority
- JP
- Japan
- Prior art keywords
- diisocyanate
- carbon atoms
- group
- urea
- equal
- 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
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- -1 polyoxytetramethylene Polymers 0.000 claims description 9
- 238000006243 chemical reaction Methods 0.000 claims description 4
- 150000001875 compounds Chemical class 0.000 claims description 4
- 239000000203 mixture Substances 0.000 claims description 3
- 229910000077 silane Inorganic materials 0.000 claims description 3
- 125000004432 carbon atom Chemical group C* 0.000 claims 10
- 239000004721 Polyphenylene oxide Substances 0.000 claims 6
- 238000000034 method Methods 0.000 claims 6
- 229920000570 polyether Polymers 0.000 claims 6
- 125000005442 diisocyanate group Chemical group 0.000 claims 5
- 125000000217 alkyl group Chemical group 0.000 claims 4
- 125000000962 organic group Chemical group 0.000 claims 4
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 3
- NNOZGCICXAYKLW-UHFFFAOYSA-N 1,2-bis(2-isocyanatopropan-2-yl)benzene Chemical compound O=C=NC(C)(C)C1=CC=CC=C1C(C)(C)N=C=O NNOZGCICXAYKLW-UHFFFAOYSA-N 0.000 claims 2
- 239000005058 Isophorone diisocyanate Substances 0.000 claims 2
- 229920003171 Poly (ethylene oxide) Polymers 0.000 claims 2
- 239000004952 Polyamide Substances 0.000 claims 2
- 239000005062 Polybutadiene Substances 0.000 claims 2
- 125000002947 alkylene group Chemical group 0.000 claims 2
- 229920001400 block copolymer Polymers 0.000 claims 2
- 229910052739 hydrogen Inorganic materials 0.000 claims 2
- 239000001257 hydrogen Substances 0.000 claims 2
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 claims 2
- 229920000058 polyacrylate Polymers 0.000 claims 2
- 229920002647 polyamide Polymers 0.000 claims 2
- 229920002857 polybutadiene Polymers 0.000 claims 2
- 229920000728 polyester Polymers 0.000 claims 2
- 229920001195 polyisoprene Polymers 0.000 claims 2
- 229920000193 polymethacrylate Polymers 0.000 claims 2
- 229920002635 polyurethane Polymers 0.000 claims 2
- 239000004814 polyurethane Substances 0.000 claims 2
- LFSYUSUFCBOHGU-UHFFFAOYSA-N 1-isocyanato-2-[(4-isocyanatophenyl)methyl]benzene Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=CC=C1N=C=O LFSYUSUFCBOHGU-UHFFFAOYSA-N 0.000 claims 1
- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 claims 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 claims 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims 1
- 239000000853 adhesive Substances 0.000 claims 1
- 230000001070 adhesive effect Effects 0.000 claims 1
- 239000004202 carbamide Substances 0.000 claims 1
- 239000011248 coating agent Substances 0.000 claims 1
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- 238000002360 preparation method Methods 0.000 claims 1
- 239000011541 reaction mixture Substances 0.000 claims 1
- 239000000565 sealant Substances 0.000 claims 1
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical group CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 claims 1
- RUELTTOHQODFPA-UHFFFAOYSA-N toluene 2,6-diisocyanate Chemical compound CC1=C(N=C=O)C=CC=C1N=C=O RUELTTOHQODFPA-UHFFFAOYSA-N 0.000 claims 1
- SJRJJKPEHAURKC-UHFFFAOYSA-N N-Methylmorpholine Chemical compound CN1CCOCC1 SJRJJKPEHAURKC-UHFFFAOYSA-N 0.000 description 3
- GQHTUMJGOHRCHB-UHFFFAOYSA-N 2,3,4,6,7,8,9,10-octahydropyrimido[1,2-a]azepine Chemical compound C1CCCCN2CCCN=C21 GQHTUMJGOHRCHB-UHFFFAOYSA-N 0.000 description 2
- ZRALSGWEFCBTJO-UHFFFAOYSA-N Guanidine Chemical compound NC(N)=N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 description 2
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 2
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical group [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 2
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 2
- ISKQADXMHQSTHK-UHFFFAOYSA-N [4-(aminomethyl)phenyl]methanamine Chemical compound NCC1=CC=C(CN)C=C1 ISKQADXMHQSTHK-UHFFFAOYSA-N 0.000 description 2
- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 2
- WGQKYBSKWIADBV-UHFFFAOYSA-N benzylamine Chemical compound NCC1=CC=CC=C1 WGQKYBSKWIADBV-UHFFFAOYSA-N 0.000 description 2
- HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- PAFZNILMFXTMIY-UHFFFAOYSA-N cyclohexylamine Chemical compound NC1CCCCC1 PAFZNILMFXTMIY-UHFFFAOYSA-N 0.000 description 2
- JGFBRKRYDCGYKD-UHFFFAOYSA-N dibutyl(oxo)tin Chemical compound CCCC[Sn](=O)CCCC JGFBRKRYDCGYKD-UHFFFAOYSA-N 0.000 description 2
- JQVDAXLFBXTEQA-UHFFFAOYSA-N dibutylamine Chemical compound CCCCNCCCC JQVDAXLFBXTEQA-UHFFFAOYSA-N 0.000 description 2
- 239000012975 dibutyltin dilaurate Substances 0.000 description 2
- 229920000768 polyamine Polymers 0.000 description 2
- IMNIMPAHZVJRPE-UHFFFAOYSA-N triethylenediamine Chemical compound C1CN2CCN1CC2 IMNIMPAHZVJRPE-UHFFFAOYSA-N 0.000 description 2
- YOBOXHGSEJBUPB-MTOQALJVSA-N (z)-4-hydroxypent-3-en-2-one;zirconium Chemical compound [Zr].C\C(O)=C\C(C)=O.C\C(O)=C\C(C)=O.C\C(O)=C\C(C)=O.C\C(O)=C\C(C)=O YOBOXHGSEJBUPB-MTOQALJVSA-N 0.000 description 1
- TYKCBTYOMAUNLH-MTOQALJVSA-J (z)-4-oxopent-2-en-2-olate;titanium(4+) Chemical compound [Ti+4].C\C([O-])=C\C(C)=O.C\C([O-])=C\C(C)=O.C\C([O-])=C\C(C)=O.C\C([O-])=C\C(C)=O TYKCBTYOMAUNLH-MTOQALJVSA-J 0.000 description 1
- ZBBLRPRYYSJUCZ-GRHBHMESSA-L (z)-but-2-enedioate;dibutyltin(2+) Chemical compound [O-]C(=O)\C=C/C([O-])=O.CCCC[Sn+2]CCCC ZBBLRPRYYSJUCZ-GRHBHMESSA-L 0.000 description 1
- QGLWBTPVKHMVHM-KTKRTIGZSA-N (z)-octadec-9-en-1-amine Chemical compound CCCCCCCC\C=C/CCCCCCCCN QGLWBTPVKHMVHM-KTKRTIGZSA-N 0.000 description 1
- OWRCNXZUPFZXOS-UHFFFAOYSA-N 1,3-diphenylguanidine Chemical compound C=1C=CC=CC=1NC(=N)NC1=CC=CC=C1 OWRCNXZUPFZXOS-UHFFFAOYSA-N 0.000 description 1
- VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 description 1
- AHDSRXYHVZECER-UHFFFAOYSA-N 2,4,6-tris[(dimethylamino)methyl]phenol Chemical compound CN(C)CC1=CC(CN(C)C)=C(O)C(CN(C)C)=C1 AHDSRXYHVZECER-UHFFFAOYSA-N 0.000 description 1
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 1
- SJECZPVISLOESU-UHFFFAOYSA-N 3-trimethoxysilylpropan-1-amine Chemical compound CO[Si](OC)(OC)CCCN SJECZPVISLOESU-UHFFFAOYSA-N 0.000 description 1
- ULKLGIFJWFIQFF-UHFFFAOYSA-N 5K8XI641G3 Chemical compound CCC1=NC=C(C)N1 ULKLGIFJWFIQFF-UHFFFAOYSA-N 0.000 description 1
- RSIOIDACLNBIHM-UHFFFAOYSA-N C(C=C/C(=O)OCC)(=O)OCC.C(CCCCCCC)[Sn]CCCCCCCC Chemical compound C(C=C/C(=O)OCC)(=O)OCC.C(CCCCCCC)[Sn]CCCCCCCC RSIOIDACLNBIHM-UHFFFAOYSA-N 0.000 description 1
- KWADETUNAHTOCO-UHFFFAOYSA-N C(C=C/C(=O)OCC1=CC=CC=C1)(=O)OCC1=CC=CC=C1.C(CCC)[Sn]CCCC Chemical compound C(C=C/C(=O)OCC1=CC=CC=C1)(=O)OCC1=CC=CC=C1.C(CCC)[Sn]CCCC KWADETUNAHTOCO-UHFFFAOYSA-N 0.000 description 1
- 0 C**(*N(C)CCC1*C1)N Chemical compound C**(*N(C)CCC1*C1)N 0.000 description 1
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 1
- CHJJGSNFBQVOTG-UHFFFAOYSA-N N-methyl-guanidine Natural products CNC(N)=N CHJJGSNFBQVOTG-UHFFFAOYSA-N 0.000 description 1
- 229910008051 Si-OH Inorganic materials 0.000 description 1
- 229910006358 Si—OH Inorganic materials 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- GKXVJHDEWHKBFH-UHFFFAOYSA-N [2-(aminomethyl)phenyl]methanamine Chemical compound NCC1=CC=CC=C1CN GKXVJHDEWHKBFH-UHFFFAOYSA-N 0.000 description 1
- CQQXCSFSYHAZOO-UHFFFAOYSA-L [acetyloxy(dioctyl)stannyl] acetate Chemical compound CCCCCCCC[Sn](OC(C)=O)(OC(C)=O)CCCCCCCC CQQXCSFSYHAZOO-UHFFFAOYSA-L 0.000 description 1
- NBJODVYWAQLZOC-UHFFFAOYSA-L [dibutyl(octanoyloxy)stannyl] octanoate Chemical compound CCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCC NBJODVYWAQLZOC-UHFFFAOYSA-L 0.000 description 1
- XQBCVRSTVUHIGH-UHFFFAOYSA-L [dodecanoyloxy(dioctyl)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCCCCCC)(CCCCCCCC)OC(=O)CCCCCCCCCCC XQBCVRSTVUHIGH-UHFFFAOYSA-L 0.000 description 1
- UZFVQGTYOXJWTF-UHFFFAOYSA-L [octadecanoyloxy(dioctyl)stannyl] octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)O[Sn](CCCCCCCC)(CCCCCCCC)OC(=O)CCCCCCCCCCCCCCCCC UZFVQGTYOXJWTF-UHFFFAOYSA-L 0.000 description 1
- 239000002318 adhesion promoter Substances 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- IKHOZNOYZQPPCK-UHFFFAOYSA-K aluminum;4,4-diethyl-3-oxohexanoate Chemical compound [Al+3].CCC(CC)(CC)C(=O)CC([O-])=O.CCC(CC)(CC)C(=O)CC([O-])=O.CCC(CC)(CC)C(=O)CC([O-])=O IKHOZNOYZQPPCK-UHFFFAOYSA-K 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- HZXXNQUMSGYIKQ-JRYLAINFSA-N bis(6-methylheptyl) (Z)-but-2-enedioate dibutyltin Chemical compound CCCC[Sn]CCCC.CC(C)CCCCCOC(=O)\C=C/C(=O)OCCCCCC(C)C HZXXNQUMSGYIKQ-JRYLAINFSA-N 0.000 description 1
- BCPQQVJRGVNJMJ-JRYLAINFSA-N bis(6-methylheptyl) (Z)-but-2-enedioate dioctyltin Chemical compound CCCCCCCC[Sn]CCCCCCCC.CC(C)CCCCCOC(=O)\C=C/C(=O)OCCCCCC(C)C BCPQQVJRGVNJMJ-JRYLAINFSA-N 0.000 description 1
- YHWCPXVTRSHPNY-UHFFFAOYSA-N butan-1-olate;titanium(4+) Chemical compound [Ti+4].CCCC[O-].CCCC[O-].CCCC[O-].CCCC[O-] YHWCPXVTRSHPNY-UHFFFAOYSA-N 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000002738 chelating agent Substances 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 238000003776 cleavage reaction Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- XAUKEHTUWXPUBM-IRYVOTIRSA-N dibutyl (z)-but-2-enedioate;dibutyltin Chemical compound CCCC[Sn]CCCC.CCCCOC(=O)\C=C/C(=O)OCCCC XAUKEHTUWXPUBM-IRYVOTIRSA-N 0.000 description 1
- UROKUKHYYXBCQE-UHFFFAOYSA-L dibutyl(diphenoxy)stannane Chemical compound C=1C=CC=CC=1O[Sn](CCCC)(CCCC)OC1=CC=CC=C1 UROKUKHYYXBCQE-UHFFFAOYSA-L 0.000 description 1
- CBFGPUOFLQMQAZ-UHFFFAOYSA-N dibutyl-di(propan-2-yloxy)stannane Chemical compound CC(C)[O-].CC(C)[O-].CCCC[Sn+2]CCCC CBFGPUOFLQMQAZ-UHFFFAOYSA-N 0.000 description 1
- AYOHIQLKSOJJQH-UHFFFAOYSA-N dibutyltin Chemical compound CCCC[Sn]CCCC AYOHIQLKSOJJQH-UHFFFAOYSA-N 0.000 description 1
- JFHKCZFPXJVELF-UHFFFAOYSA-L dibutyltin(2+);2,2-diethylhexanoate Chemical compound CCCC[Sn+2]CCCC.CCCCC(CC)(CC)C([O-])=O.CCCCC(CC)(CC)C([O-])=O JFHKCZFPXJVELF-UHFFFAOYSA-L 0.000 description 1
- ZXDVQYBUEVYUCG-UHFFFAOYSA-N dibutyltin(2+);methanolate Chemical compound CCCC[Sn](OC)(OC)CCCC ZXDVQYBUEVYUCG-UHFFFAOYSA-N 0.000 description 1
- NVOGEOJJWIEKGO-WTUPQPTJSA-N dibutyltin;diethyl (z)-but-2-enedioate Chemical compound CCCC[Sn]CCCC.CCOC(=O)\C=C/C(=O)OCC NVOGEOJJWIEKGO-WTUPQPTJSA-N 0.000 description 1
- IIFKGJGNMKYHLT-FGSKAQBVSA-N dibutyltin;dimethyl (z)-but-2-enedioate Chemical compound CCCC[Sn]CCCC.COC(=O)\C=C/C(=O)OC IIFKGJGNMKYHLT-FGSKAQBVSA-N 0.000 description 1
- MMFHQUJCZSYDEK-SWLCOABPSA-N dibutyltin;ditridecyl (z)-but-2-enedioate Chemical compound CCCC[Sn]CCCC.CCCCCCCCCCCCCOC(=O)\C=C/C(=O)OCCCCCCCCCCCCC MMFHQUJCZSYDEK-SWLCOABPSA-N 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- SWSQBOPZIKWTGO-UHFFFAOYSA-N dimethylaminoamidine Natural products CN(C)C(N)=N SWSQBOPZIKWTGO-UHFFFAOYSA-N 0.000 description 1
- LQRUPWUPINJLMU-UHFFFAOYSA-N dioctyl(oxo)tin Chemical compound CCCCCCCC[Sn](=O)CCCCCCCC LQRUPWUPINJLMU-UHFFFAOYSA-N 0.000 description 1
- JRBPAEWTRLWTQC-UHFFFAOYSA-N dodecylamine Chemical compound CCCCCCCCCCCCN JRBPAEWTRLWTQC-UHFFFAOYSA-N 0.000 description 1
- 150000002118 epoxides Chemical class 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- YMQPOZUUTMLSEK-UHFFFAOYSA-L lead(2+);octanoate Chemical compound [Pb+2].CCCCCCCC([O-])=O.CCCCCCCC([O-])=O YMQPOZUUTMLSEK-UHFFFAOYSA-L 0.000 description 1
- QOHMWDJIBGVPIF-UHFFFAOYSA-N n',n'-diethylpropane-1,3-diamine Chemical compound CCN(CC)CCCN QOHMWDJIBGVPIF-UHFFFAOYSA-N 0.000 description 1
- IOQPZZOEVPZRBK-UHFFFAOYSA-N octan-1-amine Chemical compound CCCCCCCCN IOQPZZOEVPZRBK-UHFFFAOYSA-N 0.000 description 1
- 125000005498 phthalate group Chemical class 0.000 description 1
- 229920006122 polyamide resin Polymers 0.000 description 1
- 150000007519 polyprotic acids Polymers 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- HKJYVRJHDIPMQB-UHFFFAOYSA-N propan-1-olate;titanium(4+) Chemical compound CCCO[Ti](OCCC)(OCCC)OCCC HKJYVRJHDIPMQB-UHFFFAOYSA-N 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 230000007017 scission Effects 0.000 description 1
- 125000005373 siloxane group Chemical group [SiH2](O*)* 0.000 description 1
- 229910001887 tin oxide Inorganic materials 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
- QHGNHLZPVBIIPX-UHFFFAOYSA-N tin(ii) oxide Chemical class [Sn]=O QHGNHLZPVBIIPX-UHFFFAOYSA-N 0.000 description 1
- 229960001124 trientine Drugs 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102009046269A DE102009046269A1 (de) | 2009-10-30 | 2009-10-30 | Harnstoffgebundende Alkoxysilane zum Einsatz in Dicht- und Klebstoffen |
| DE102009046269.4 | 2009-10-30 | ||
| PCT/EP2010/066592 WO2011051491A1 (de) | 2009-10-30 | 2010-11-02 | Harnstoffgebundende alkoxysilane zum einsatz in dicht- und klebstoffen |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2013509476A JP2013509476A (ja) | 2013-03-14 |
| JP2013509476A5 true JP2013509476A5 (enExample) | 2013-12-19 |
| JP5688091B2 JP5688091B2 (ja) | 2015-03-25 |
Family
ID=43661898
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2012535866A Expired - Fee Related JP5688091B2 (ja) | 2009-10-30 | 2010-11-02 | シーラントおよび接着剤において使用するための尿素結合型アルコキシシラン |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US8501903B2 (enExample) |
| EP (1) | EP2493957B1 (enExample) |
| JP (1) | JP5688091B2 (enExample) |
| CN (1) | CN102666648B (enExample) |
| DE (1) | DE102009046269A1 (enExample) |
| ES (1) | ES2435633T3 (enExample) |
| PL (1) | PL2493957T3 (enExample) |
| WO (1) | WO2011051491A1 (enExample) |
Families Citing this family (26)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102010001470A1 (de) * | 2010-02-02 | 2011-08-04 | Henkel AG & Co. KGaA, 40589 | Polyetherblockcopolymere und daraus erhältliche Zusammensetzungen |
| JP5584575B2 (ja) * | 2010-09-30 | 2014-09-03 | 株式会社カネカ | プライマー組成物 |
| TWI575049B (zh) * | 2011-12-22 | 2017-03-21 | 漢高股份有限公司 | 紫外線硬化型和濕氣硬化型黏膠組成物 |
| CN102604071B (zh) * | 2012-03-01 | 2013-12-04 | 西北工业大学 | 端羟基聚丁二烯-聚四氢呋喃三嵌段共聚物及其制备方法 |
| CN103045056A (zh) * | 2012-12-12 | 2013-04-17 | 优利康达（天津）科技有限公司 | 一种高耐候性的不饱和树脂涂层封闭剂及使用方法 |
| US9765247B2 (en) | 2013-09-11 | 2017-09-19 | Dow Global Technologies Llc | Silyl terminated prepolymers, method for making them and adhesive compositions made therefrom |
| CA2933163A1 (en) * | 2013-09-30 | 2015-04-02 | Virginia Commonwealth University | Ice release coatings |
| CN103694709B (zh) * | 2013-12-09 | 2016-04-13 | 华南理工大学 | 加成型液体硅橡胶用耐漏电起痕剂及其制备方法和应用 |
| US9920199B2 (en) | 2014-09-02 | 2018-03-20 | Dow Global Technologies Llc | Silyl terminated prepolymers, method for making them and adhesive compositions made therefrom |
| CN104559916B (zh) * | 2015-01-16 | 2016-09-21 | 北京天山新材料技术有限公司 | 一种食品安全的加成型硅橡胶密封剂及其制备方法 |
| CN105348507A (zh) * | 2015-12-04 | 2016-02-24 | 西北工业大学 | 窄分布的高1，4结构端羟基聚丁二烯-聚四氢呋喃三嵌段共聚物及制备方法 |
| ES2896477T3 (es) | 2016-10-14 | 2022-02-24 | Basf Se | Composición estabilizante |
| CN110062796B (zh) | 2016-10-14 | 2021-09-03 | 巴斯夫欧洲公司 | 可硬化的聚合物组合物 |
| JP2021522382A (ja) * | 2018-04-25 | 2021-08-30 | ヘンケル・アクチェンゲゼルシャフト・ウント・コムパニー・コマンディットゲゼルシャフト・アウフ・アクチェンＨｅｎｋｅｌ ＡＧ ＆ Ｃｏ． ＫＧａＡ | ヒドロキシル官能化ポリエーテルポリシロキサンブロックコポリマーの調製用プロセス |
| EP3613785A1 (de) * | 2018-08-21 | 2020-02-26 | Covestro Deutschland AG | Trocknungsmittel für feuchtigkeitshärtende zusammensetzungen |
| CN111117489B (zh) * | 2018-10-31 | 2022-01-07 | 娄从江 | 一种快速成膜和高阻隔性硅烷改性类建筑密封胶的底涂剂 |
| US20220073821A1 (en) | 2019-01-16 | 2022-03-10 | Basf Se | Stabilizer composition for sealants and adhesives |
| EP3715396A1 (de) | 2019-03-26 | 2020-09-30 | PolyU GmbH | Zusammensetzung und verfahren zur herstellung silylierter polymere und deren verwendung |
| SE1950486A1 (en) * | 2019-04-17 | 2020-10-18 | Essve Produkter Ab | Adhesive sealant composition |
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| CN111154445B (zh) * | 2020-01-17 | 2021-03-19 | 杭州之江新材料有限公司 | 一种双组份防水密封胶 |
| US20230183425A1 (en) * | 2021-12-10 | 2023-06-15 | Thanikaivelan Tindivanam Veeraraghavan | Two-component moisture curable thermal interface material for thermal management systems |
| 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 |
| CN114686082B (zh) * | 2022-05-09 | 2022-10-11 | 上海予通管道工程技术有限公司 | 一种用于管道修复的耐腐蚀聚脲涂料及其制备方法 |
| CN116144013B (zh) * | 2023-02-15 | 2025-02-11 | 西安近代化学研究所 | 一种端四烯基聚醚粘合剂及其合成方法 |
| CN119751894B (zh) * | 2024-12-17 | 2025-11-04 | 广州白云科技股份有限公司 | 硅烷改性聚醚-聚丁二烯、透明耐水解的硅烷改性聚醚密封胶及其制备方法 |
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-
2009
- 2009-10-30 DE DE102009046269A patent/DE102009046269A1/de not_active Ceased
-
2010
- 2010-11-02 WO PCT/EP2010/066592 patent/WO2011051491A1/de not_active Ceased
- 2010-11-02 PL PL10771480T patent/PL2493957T3/pl unknown
- 2010-11-02 JP JP2012535866A patent/JP5688091B2/ja not_active Expired - Fee Related
- 2010-11-02 ES ES10771480T patent/ES2435633T3/es active Active
- 2010-11-02 EP EP10771480.0A patent/EP2493957B1/de active Active
- 2010-11-02 CN CN201080048663.0A patent/CN102666648B/zh not_active Expired - Fee Related
-
2012
- 2012-04-26 US US13/456,314 patent/US8501903B2/en not_active Expired - Fee Related
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