DK2089490T4 - Præpolymerblandinger indeholdende silylgrupper og anvendelse heraf - Google Patents
Præpolymerblandinger indeholdende silylgrupper og anvendelse heraf Download PDFInfo
- Publication number
- DK2089490T4 DK2089490T4 DK07787732.2T DK07787732T DK2089490T4 DK 2089490 T4 DK2089490 T4 DK 2089490T4 DK 07787732 T DK07787732 T DK 07787732T DK 2089490 T4 DK2089490 T4 DK 2089490T4
- Authority
- DK
- Denmark
- Prior art keywords
- silane
- seal
- groups
- adhesion
- functional
- Prior art date
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- 125000003808 silyl group Chemical group [H][Si]([H])([H])[*] 0.000 title description 3
- 229920002959 polymer blend Polymers 0.000 title 1
- 239000000203 mixture Substances 0.000 claims abstract description 46
- 239000000758 substrate Substances 0.000 claims abstract description 16
- 229920000098 polyolefin Polymers 0.000 claims abstract description 13
- 239000000945 filler Substances 0.000 claims abstract description 11
- 239000003054 catalyst Substances 0.000 claims abstract description 8
- 239000004033 plastic Substances 0.000 claims abstract description 5
- 229920003023 plastic Polymers 0.000 claims abstract description 5
- 239000004014 plasticizer Substances 0.000 claims abstract description 5
- 150000004756 silanes Chemical class 0.000 claims description 16
- 239000002318 adhesion promoter Substances 0.000 claims description 12
- 229920001451 polypropylene glycol Polymers 0.000 claims description 9
- 239000001993 wax Substances 0.000 claims description 7
- 239000011248 coating agent Substances 0.000 claims description 6
- 239000003208 petroleum Substances 0.000 claims description 6
- 229920002367 Polyisobutene Polymers 0.000 claims description 5
- 125000003118 aryl group Chemical group 0.000 claims description 5
- 238000000576 coating method Methods 0.000 claims description 4
- 125000005369 trialkoxysilyl group Chemical group 0.000 claims description 4
- 238000007789 sealing Methods 0.000 claims description 3
- RWLDCNACDPTRMY-UHFFFAOYSA-N 3-triethoxysilyl-n-(3-triethoxysilylpropyl)propan-1-amine Chemical compound CCO[Si](OCC)(OCC)CCCNCCC[Si](OCC)(OCC)OCC RWLDCNACDPTRMY-UHFFFAOYSA-N 0.000 claims description 2
- TZZGHGKTHXIOMN-UHFFFAOYSA-N 3-trimethoxysilyl-n-(3-trimethoxysilylpropyl)propan-1-amine Chemical compound CO[Si](OC)(OC)CCCNCCC[Si](OC)(OC)OC TZZGHGKTHXIOMN-UHFFFAOYSA-N 0.000 claims description 2
- 125000001931 aliphatic group Chemical group 0.000 claims description 2
- 239000004839 Moisture curing adhesive Substances 0.000 claims 6
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 5
- ZPZDIFSPRVHGIF-UHFFFAOYSA-N 3-aminopropylsilicon Chemical compound NCCC[Si] ZPZDIFSPRVHGIF-UHFFFAOYSA-N 0.000 claims 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 claims 2
- 238000013008 moisture curing Methods 0.000 claims 2
- 125000000022 2-aminoethyl group Chemical group [H]C([*])([H])C([H])([H])N([H])[H] 0.000 claims 1
- 239000004698 Polyethylene Substances 0.000 claims 1
- 238000004026 adhesive bonding Methods 0.000 claims 1
- 150000001336 alkenes Chemical class 0.000 claims 1
- 229920013640 amorphous poly alpha olefin Polymers 0.000 claims 1
- 239000003112 inhibitor Substances 0.000 claims 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims 1
- 239000012188 paraffin wax Substances 0.000 claims 1
- 229920000573 polyethylene Polymers 0.000 claims 1
- 239000000853 adhesive Substances 0.000 abstract description 18
- 230000001070 adhesive effect Effects 0.000 abstract description 18
- 239000000565 sealant Substances 0.000 abstract description 14
- 238000003860 storage Methods 0.000 abstract description 10
- 150000001875 compounds Chemical class 0.000 description 12
- 238000012360 testing method Methods 0.000 description 11
- -1 allyl chloride Chemical class 0.000 description 10
- 229920000570 polyether Polymers 0.000 description 10
- 229920000642 polymer Polymers 0.000 description 9
- 239000013466 adhesive and sealant Substances 0.000 description 7
- 229920001897 terpolymer Polymers 0.000 description 7
- 229920001577 copolymer Polymers 0.000 description 6
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 5
- SJECZPVISLOESU-UHFFFAOYSA-N 3-trimethoxysilylpropan-1-amine Chemical compound CO[Si](OC)(OC)CCCN SJECZPVISLOESU-UHFFFAOYSA-N 0.000 description 4
- VTYYLEPIZMXCLO-UHFFFAOYSA-L calcium carbonate Substances [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 239000012948 isocyanate Substances 0.000 description 4
- 150000002513 isocyanates Chemical class 0.000 description 4
- 239000003921 oil Substances 0.000 description 4
- 239000005011 phenolic resin Substances 0.000 description 4
- 229920000768 polyamine Polymers 0.000 description 4
- 229910000077 silane Inorganic materials 0.000 description 4
- SJRJJKPEHAURKC-UHFFFAOYSA-N N-Methylmorpholine Chemical compound CN1CCOCC1 SJRJJKPEHAURKC-UHFFFAOYSA-N 0.000 description 3
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 125000003277 amino group Chemical group 0.000 description 3
- 230000003712 anti-aging effect Effects 0.000 description 3
- 239000011324 bead Substances 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 238000009833 condensation Methods 0.000 description 3
- 230000005494 condensation Effects 0.000 description 3
- AYOHIQLKSOJJQH-UHFFFAOYSA-N dibutyltin Chemical compound CCCC[Sn]CCCC AYOHIQLKSOJJQH-UHFFFAOYSA-N 0.000 description 3
- NKSJNEHGWDZZQF-UHFFFAOYSA-N ethenyl(trimethoxy)silane Chemical compound CO[Si](OC)(OC)C=C NKSJNEHGWDZZQF-UHFFFAOYSA-N 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 239000000049 pigment Substances 0.000 description 3
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- 238000000518 rheometry Methods 0.000 description 3
- 229910052710 silicon Inorganic materials 0.000 description 3
- 238000003786 synthesis reaction Methods 0.000 description 3
- WYTZZXDRDKSJID-UHFFFAOYSA-N (3-aminopropyl)triethoxysilane Chemical compound CCO[Si](OCC)(OCC)CCCN WYTZZXDRDKSJID-UHFFFAOYSA-N 0.000 description 2
- ZYAASQNKCWTPKI-UHFFFAOYSA-N 3-[dimethoxy(methyl)silyl]propan-1-amine Chemical compound CO[Si](C)(OC)CCCN ZYAASQNKCWTPKI-UHFFFAOYSA-N 0.000 description 2
- UUEWCQRISZBELL-UHFFFAOYSA-N 3-trimethoxysilylpropane-1-thiol Chemical compound CO[Si](OC)(OC)CCCS UUEWCQRISZBELL-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 239000004606 Fillers/Extenders Substances 0.000 description 2
- ZRALSGWEFCBTJO-UHFFFAOYSA-N Guanidine Chemical compound NC(N)=N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 description 2
- 238000004566 IR spectroscopy Methods 0.000 description 2
- 229920001730 Moisture cure polyurethane Polymers 0.000 description 2
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 2
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-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
- 239000002253 acid Substances 0.000 description 2
- 125000003545 alkoxy group Chemical group 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 150000008064 anhydrides Chemical class 0.000 description 2
- WGQKYBSKWIADBV-UHFFFAOYSA-N benzylamine Chemical compound NCC1=CC=CC=C1 WGQKYBSKWIADBV-UHFFFAOYSA-N 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 description 2
- 235000010216 calcium carbonate Nutrition 0.000 description 2
- 239000006229 carbon black Substances 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 239000013256 coordination polymer 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
- 125000005442 diisocyanate group Chemical group 0.000 description 2
- 150000002118 epoxides Chemical group 0.000 description 2
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- PHQOGHDTIVQXHL-UHFFFAOYSA-N n'-(3-trimethoxysilylpropyl)ethane-1,2-diamine Chemical compound CO[Si](OC)(OC)CCCNCCN PHQOGHDTIVQXHL-UHFFFAOYSA-N 0.000 description 2
- 229920001568 phenolic resin Polymers 0.000 description 2
- 229920002635 polyurethane Polymers 0.000 description 2
- 239000004814 polyurethane Substances 0.000 description 2
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 2
- 239000010703 silicon Substances 0.000 description 2
- 238000001228 spectrum Methods 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- GSUGNQKJVLXBHC-UHFFFAOYSA-N triethoxy-[4-(oxiran-2-ylmethoxy)butyl]silane Chemical compound CCO[Si](OCC)(OCC)CCCCOCC1CO1 GSUGNQKJVLXBHC-UHFFFAOYSA-N 0.000 description 2
- IMNIMPAHZVJRPE-UHFFFAOYSA-N triethylenediamine Chemical compound C1CN2CCN1CC2 IMNIMPAHZVJRPE-UHFFFAOYSA-N 0.000 description 2
- ZNXDCSVNCSSUNB-UHFFFAOYSA-N trimethoxy-[2-(oxiran-2-ylmethoxy)ethyl]silane Chemical compound CO[Si](OC)(OC)CCOCC1CO1 ZNXDCSVNCSSUNB-UHFFFAOYSA-N 0.000 description 2
- GUKYSRVOOIKHHB-UHFFFAOYSA-N trimethoxy-[4-(oxiran-2-ylmethoxy)butyl]silane Chemical compound CO[Si](OC)(OC)CCCCOCC1CO1 GUKYSRVOOIKHHB-UHFFFAOYSA-N 0.000 description 2
- BYBCYIPRGOCREE-UHFFFAOYSA-N (1-dimethoxysilyl-3-isocyanatopropoxy)-trimethylsilane Chemical compound C[Si](OC(CCN=C=O)[SiH](OC)OC)(C)C BYBCYIPRGOCREE-UHFFFAOYSA-N 0.000 description 1
- POZSTGZKLIJTEG-UHFFFAOYSA-N (1-dimethylsilyl-3-isocyanatopropyl) trimethyl silicate Chemical compound CO[Si](OC(CCN=C=O)[SiH](C)C)(OC)OC POZSTGZKLIJTEG-UHFFFAOYSA-N 0.000 description 1
- VDOXMPDWSJMMPK-UHFFFAOYSA-N (2-isocyanato-1,1-dimethoxybutyl)silane Chemical compound C(C)C(C([SiH3])(OC)OC)N=C=O VDOXMPDWSJMMPK-UHFFFAOYSA-N 0.000 description 1
- SHIIKOYLGKOEBS-UHFFFAOYSA-N (3-ethyl-6-isocyanatohexan-3-yl)-methoxysilane Chemical compound C(C)C(CCCN=C=O)([SiH2]OC)CC SHIIKOYLGKOEBS-UHFFFAOYSA-N 0.000 description 1
- 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
- 150000005207 1,3-dihydroxybenzenes Chemical class 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
- QLUOTIPAKQNTGM-UHFFFAOYSA-N 1-(oxiran-2-ylmethoxy)butyl-tripropoxysilane Chemical compound CCCO[Si](OCCC)(OCCC)C(CCC)OCC1CO1 QLUOTIPAKQNTGM-UHFFFAOYSA-N 0.000 description 1
- YDLRHJCZKKFTCD-UHFFFAOYSA-N 1-(oxiran-2-ylmethoxy)ethyl-tripropoxysilane Chemical compound CCCO[Si](OCCC)(OCCC)C(C)OCC1CO1 YDLRHJCZKKFTCD-UHFFFAOYSA-N 0.000 description 1
- RSZSZOBFBLDTDV-UHFFFAOYSA-N 1-(oxiran-2-ylmethoxy)propyl-tripropoxysilane Chemical compound CCCO[Si](OCCC)(OCCC)C(CC)OCC1CO1 RSZSZOBFBLDTDV-UHFFFAOYSA-N 0.000 description 1
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 1
- QKBCXIWITQACLO-UHFFFAOYSA-N 1-isocyanatoethyl(dimethoxy)silane Chemical compound CC([SiH](OC)OC)N=C=O QKBCXIWITQACLO-UHFFFAOYSA-N 0.000 description 1
- JVVDURMXZZATIC-UHFFFAOYSA-N 1-isocyanatopentan-3-yl(dimethoxy)silane Chemical compound C(C)C(CCN=C=O)[SiH](OC)OC JVVDURMXZZATIC-UHFFFAOYSA-N 0.000 description 1
- LKSVDBOSJYQVTG-UHFFFAOYSA-N 1-isocyanatopropan-2-yl(dimethoxy)silane Chemical compound CC(CN=C=O)[SiH](OC)OC LKSVDBOSJYQVTG-UHFFFAOYSA-N 0.000 description 1
- KJSMLNSOCULBBO-UHFFFAOYSA-N 1-isocyanatopropyl(dimethoxy)silane Chemical compound C(C)C([SiH](OC)OC)N=C=O KJSMLNSOCULBBO-UHFFFAOYSA-N 0.000 description 1
- DJBYTWGZUGZIKL-UHFFFAOYSA-N 1-n-(3-triethoxysilylpropyl)butane-1,2-diamine Chemical compound CCO[Si](OCC)(OCC)CCCNCC(N)CC DJBYTWGZUGZIKL-UHFFFAOYSA-N 0.000 description 1
- VYIVCWZGVYMHJG-UHFFFAOYSA-N 1-n-(3-trimethoxysilylpropyl)butane-1,2-diamine Chemical compound CCC(N)CNCCC[Si](OC)(OC)OC VYIVCWZGVYMHJG-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
- ROYZOPPLNMOKCU-UHFFFAOYSA-N 2-(7-oxabicyclo[4.1.0]heptan-4-yl)ethyl-tripropoxysilane Chemical compound C1C(CC[Si](OCCC)(OCCC)OCCC)CCC2OC21 ROYZOPPLNMOKCU-UHFFFAOYSA-N 0.000 description 1
- KRSNNVWORUWKSH-UHFFFAOYSA-N 2-(oxiran-2-ylmethoxy)ethyl-tripropoxysilane Chemical compound CCCO[Si](OCCC)(OCCC)CCOCC1CO1 KRSNNVWORUWKSH-UHFFFAOYSA-N 0.000 description 1
- ALRJENJPEPZEBR-UHFFFAOYSA-N 2-(oxiran-2-ylmethoxy)propyl-tripropoxysilane Chemical compound CCCO[Si](OCCC)(OCCC)CC(C)OCC1CO1 ALRJENJPEPZEBR-UHFFFAOYSA-N 0.000 description 1
- IHZHYITXFSSZIZ-UHFFFAOYSA-N 2-isocyanatoethyl(trimethoxy)silane Chemical compound CO[Si](OC)(OC)CCN=C=O IHZHYITXFSSZIZ-UHFFFAOYSA-N 0.000 description 1
- ANIJZNSAIQYDCF-UHFFFAOYSA-N 2-methoxysilylethanamine Chemical compound CO[SiH2]CCN ANIJZNSAIQYDCF-UHFFFAOYSA-N 0.000 description 1
- GFJUOMJGSXRJJY-UHFFFAOYSA-N 2-methylprop-1-ene Chemical compound CC(C)=C.CC(C)=C GFJUOMJGSXRJJY-UHFFFAOYSA-N 0.000 description 1
- YXYCGBBZGQNOFX-UHFFFAOYSA-N 3-(7-oxabicyclo[4.1.0]heptan-4-yl)propyl-tripropoxysilane Chemical compound C1C(CCC[Si](OCCC)(OCCC)OCCC)CCC2OC21 YXYCGBBZGQNOFX-UHFFFAOYSA-N 0.000 description 1
- WVMAJYXLIWGTHZ-UHFFFAOYSA-N 3-(oxiran-2-ylmethoxy)butyl-tripropoxysilane Chemical compound CCCO[Si](OCCC)(OCCC)CCC(C)OCC1CO1 WVMAJYXLIWGTHZ-UHFFFAOYSA-N 0.000 description 1
- DAJFVZRDKCROQC-UHFFFAOYSA-N 3-(oxiran-2-ylmethoxy)propyl-tripropoxysilane Chemical compound CCCO[Si](OCCC)(OCCC)CCCOCC1CO1 DAJFVZRDKCROQC-UHFFFAOYSA-N 0.000 description 1
- HXLAEGYMDGUSBD-UHFFFAOYSA-N 3-[diethoxy(methyl)silyl]propan-1-amine Chemical compound CCO[Si](C)(OCC)CCCN HXLAEGYMDGUSBD-UHFFFAOYSA-N 0.000 description 1
- NVWDNGGULHAGRO-UHFFFAOYSA-N 3-isocyanatopentan-3-yl(methoxy)silane Chemical compound C(C)C([SiH2]OC)(CC)N=C=O NVWDNGGULHAGRO-UHFFFAOYSA-N 0.000 description 1
- FMGBDYLOANULLW-UHFFFAOYSA-N 3-isocyanatopropyl(trimethoxy)silane Chemical compound CO[Si](OC)(OC)CCCN=C=O FMGBDYLOANULLW-UHFFFAOYSA-N 0.000 description 1
- BYIMSFXYUSZVLI-UHFFFAOYSA-N 3-methoxysilylpropan-1-amine Chemical compound CO[SiH2]CCCN BYIMSFXYUSZVLI-UHFFFAOYSA-N 0.000 description 1
- URDOJQUSEUXVRP-UHFFFAOYSA-N 3-triethoxysilylpropyl 2-methylprop-2-enoate Chemical compound CCO[Si](OCC)(OCC)CCCOC(=O)C(C)=C URDOJQUSEUXVRP-UHFFFAOYSA-N 0.000 description 1
- XDLMVUHYZWKMMD-UHFFFAOYSA-N 3-trimethoxysilylpropyl 2-methylprop-2-enoate Chemical compound CO[Si](OC)(OC)CCCOC(=O)C(C)=C XDLMVUHYZWKMMD-UHFFFAOYSA-N 0.000 description 1
- BTXXTMOWISPQSJ-UHFFFAOYSA-N 4,4,4-trifluorobutan-2-one Chemical class CC(=O)CC(F)(F)F BTXXTMOWISPQSJ-UHFFFAOYSA-N 0.000 description 1
- JMPSRHHNRPTGKD-UHFFFAOYSA-N 4-(7-oxabicyclo[4.1.0]heptan-4-yl)butyl-tripropoxysilane Chemical compound C1C(CCCC[Si](OCCC)(OCCC)OCCC)CCC2OC21 JMPSRHHNRPTGKD-UHFFFAOYSA-N 0.000 description 1
- QVQROLPFTKFLBU-UHFFFAOYSA-N 4-(oxiran-2-ylmethoxy)butyl-tripropoxysilane Chemical compound CCCO[Si](OCCC)(OCCC)CCCCOCC1CO1 QVQROLPFTKFLBU-UHFFFAOYSA-N 0.000 description 1
- AQXPJYFPHOGPBW-UHFFFAOYSA-N 4-isocyanatobutan-2-yl(dimethoxy)silane Chemical compound CC(CCN=C=O)[SiH](OC)OC AQXPJYFPHOGPBW-UHFFFAOYSA-N 0.000 description 1
- AONXMESMHBIONB-UHFFFAOYSA-N 4-isocyanatobutyl(trimethoxy)silane Chemical compound CO[Si](OC)(OC)CCCCN=C=O AONXMESMHBIONB-UHFFFAOYSA-N 0.000 description 1
- DSBLXLMAHMQMPF-UHFFFAOYSA-N 5-isocyanatopentan-2-yl(dimethoxy)silane Chemical compound CC(CCCN=C=O)[SiH](OC)OC DSBLXLMAHMQMPF-UHFFFAOYSA-N 0.000 description 1
- ZQNXOVPHAFNYIZ-UHFFFAOYSA-N 5-isocyanatopentyl(trimethoxy)silane Chemical compound CO[Si](OC)(OC)CCCCCN=C=O ZQNXOVPHAFNYIZ-UHFFFAOYSA-N 0.000 description 1
- ULKLGIFJWFIQFF-UHFFFAOYSA-N 5K8XI641G3 Chemical compound CCC1=NC=C(C)N1 ULKLGIFJWFIQFF-UHFFFAOYSA-N 0.000 description 1
- OWBNPAWCKWLFGD-UHFFFAOYSA-N 6-isocyanatohexan-2-yl(dimethoxy)silane Chemical compound CC(CCCCN=C=O)[SiH](OC)OC OWBNPAWCKWLFGD-UHFFFAOYSA-N 0.000 description 1
- VZLHAKDPXIPRFW-UHFFFAOYSA-N 6-isocyanatohexan-3-yl(dimethoxy)silane Chemical compound C(C)C(CCCN=C=O)[SiH](OC)OC VZLHAKDPXIPRFW-UHFFFAOYSA-N 0.000 description 1
- HUHGKBBIOFENOY-UHFFFAOYSA-N 6-isocyanatohexyl(trimethoxy)silane Chemical compound CO[Si](OC)(OC)CCCCCCN=C=O HUHGKBBIOFENOY-UHFFFAOYSA-N 0.000 description 1
- DYLRLWGHBDMWAM-UHFFFAOYSA-N 7-isocyanatoheptan-2-yl(dimethoxy)silane Chemical compound CC(CCCCCN=C=O)[SiH](OC)OC DYLRLWGHBDMWAM-UHFFFAOYSA-N 0.000 description 1
- XWRPTSGHSYJZTA-UHFFFAOYSA-N 7-isocyanatoheptan-3-yl(dimethoxy)silane Chemical compound C(C)C(CCCCN=C=O)[SiH](OC)OC XWRPTSGHSYJZTA-UHFFFAOYSA-N 0.000 description 1
- PTOCVXOZAZOZTJ-UHFFFAOYSA-N 7-oxabicyclo[4.1.0]heptan-4-ylmethyl(tripropoxy)silane Chemical compound C1C(C[Si](OCCC)(OCCC)OCCC)CCC2OC21 PTOCVXOZAZOZTJ-UHFFFAOYSA-N 0.000 description 1
- TWXOYZZHTUAXGV-UHFFFAOYSA-N 8-isocyanatooctan-3-yl(dimethoxy)silane Chemical compound C(C)C(CCCCCN=C=O)[SiH](OC)OC TWXOYZZHTUAXGV-UHFFFAOYSA-N 0.000 description 1
- BQACOLQNOUYJCE-FYZZASKESA-N Abietic acid Natural products CC(C)C1=CC2=CC[C@]3(C)[C@](C)(CCC[C@@]3(C)C(=O)O)[C@H]2CC1 BQACOLQNOUYJCE-FYZZASKESA-N 0.000 description 1
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- 150000003623 transition metal compounds Chemical class 0.000 description 1
- ZWLBKGYXAYDBPG-UHFFFAOYSA-N tributoxy(3-propoxybutyl)silane Chemical compound CCCCO[Si](OCCCC)(OCCCC)CCC(C)OCCC ZWLBKGYXAYDBPG-UHFFFAOYSA-N 0.000 description 1
- OZFSVMFLPOAUOR-UHFFFAOYSA-N tributoxy(7-oxabicyclo[4.1.0]heptan-4-ylmethyl)silane Chemical compound C1C(C[Si](OCCCC)(OCCCC)OCCCC)CCC2OC21 OZFSVMFLPOAUOR-UHFFFAOYSA-N 0.000 description 1
- VBZKZUHVIFHDDD-UHFFFAOYSA-N tributoxy-[1-(oxiran-2-ylmethoxy)butyl]silane Chemical compound CCCCO[Si](OCCCC)(OCCCC)C(CCC)OCC1CO1 VBZKZUHVIFHDDD-UHFFFAOYSA-N 0.000 description 1
- HBXRMPFDHZIUFJ-UHFFFAOYSA-N tributoxy-[1-(oxiran-2-ylmethoxy)ethyl]silane Chemical compound CCCCO[Si](OCCCC)(OCCCC)C(C)OCC1CO1 HBXRMPFDHZIUFJ-UHFFFAOYSA-N 0.000 description 1
- XQDYAOWPTAJENA-UHFFFAOYSA-N tributoxy-[1-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CCCCO[Si](OCCCC)(OCCCC)C(CC)OCC1CO1 XQDYAOWPTAJENA-UHFFFAOYSA-N 0.000 description 1
- OAVPBWLGJVKEGZ-UHFFFAOYSA-N tributoxy-[2-(7-oxabicyclo[4.1.0]heptan-4-yl)ethyl]silane Chemical compound C1C(CC[Si](OCCCC)(OCCCC)OCCCC)CCC2OC21 OAVPBWLGJVKEGZ-UHFFFAOYSA-N 0.000 description 1
- AAIBUMCPBXSZDU-UHFFFAOYSA-N tributoxy-[2-(oxiran-2-ylmethoxy)ethyl]silane Chemical compound CCCCO[Si](OCCCC)(OCCCC)CCOCC1CO1 AAIBUMCPBXSZDU-UHFFFAOYSA-N 0.000 description 1
- RXTGGEGRYABTMQ-UHFFFAOYSA-N tributoxy-[2-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CCCCO[Si](OCCCC)(OCCCC)CC(C)OCC1CO1 RXTGGEGRYABTMQ-UHFFFAOYSA-N 0.000 description 1
- NKLKGGCLDYNMKP-UHFFFAOYSA-N tributoxy-[3-(7-oxabicyclo[4.1.0]heptan-4-yl)propyl]silane Chemical compound C1C(CCC[Si](OCCCC)(OCCCC)OCCCC)CCC2OC21 NKLKGGCLDYNMKP-UHFFFAOYSA-N 0.000 description 1
- GTOPGQCTLBXYNX-UHFFFAOYSA-N tributoxy-[4-(7-oxabicyclo[4.1.0]heptan-4-yl)butyl]silane Chemical compound C1C(CCCC[Si](OCCCC)(OCCCC)OCCCC)CCC2OC21 GTOPGQCTLBXYNX-UHFFFAOYSA-N 0.000 description 1
- CBUYJESDGBAFOZ-UHFFFAOYSA-N tributoxy-[4-(oxiran-2-ylmethoxy)butyl]silane Chemical compound CCCCO[Si](OCCCC)(OCCCC)CCCCOCC1CO1 CBUYJESDGBAFOZ-UHFFFAOYSA-N 0.000 description 1
- KEIBTGABMNALIT-UHFFFAOYSA-N triethoxy(2-isocyanatoethyl)silane Chemical compound CCO[Si](OCC)(OCC)CCN=C=O KEIBTGABMNALIT-UHFFFAOYSA-N 0.000 description 1
- FRGPKMWIYVTFIQ-UHFFFAOYSA-N triethoxy(3-isocyanatopropyl)silane Chemical compound CCO[Si](OCC)(OCC)CCCN=C=O FRGPKMWIYVTFIQ-UHFFFAOYSA-N 0.000 description 1
- ASUUSZXVXTVKDD-UHFFFAOYSA-N triethoxy(4-isocyanatobutyl)silane Chemical compound CCO[Si](OCC)(OCC)CCCCN=C=O ASUUSZXVXTVKDD-UHFFFAOYSA-N 0.000 description 1
- IWQBIRQQKBICKW-UHFFFAOYSA-N triethoxy(5-isocyanatopentyl)silane Chemical compound CCO[Si](OCC)(OCC)CCCCCN=C=O IWQBIRQQKBICKW-UHFFFAOYSA-N 0.000 description 1
- QKJDKLUGDDTSNP-UHFFFAOYSA-N triethoxy(6-isocyanatohexyl)silane Chemical compound CCO[Si](OCC)(OCC)CCCCCCN=C=O QKJDKLUGDDTSNP-UHFFFAOYSA-N 0.000 description 1
- VQFQVYFUZUTIMU-UHFFFAOYSA-N triethoxy(7-oxabicyclo[4.1.0]heptan-4-ylmethyl)silane Chemical compound C1C(C[Si](OCC)(OCC)OCC)CCC2OC21 VQFQVYFUZUTIMU-UHFFFAOYSA-N 0.000 description 1
- BOTMPGMIDPRZGP-UHFFFAOYSA-N triethoxy(isocyanatomethyl)silane Chemical compound CCO[Si](OCC)(OCC)CN=C=O BOTMPGMIDPRZGP-UHFFFAOYSA-N 0.000 description 1
- OHKFEBYBHZXHMM-UHFFFAOYSA-N triethoxy-[1-(oxiran-2-ylmethoxy)butyl]silane Chemical compound CCO[Si](OCC)(OCC)C(CCC)OCC1CO1 OHKFEBYBHZXHMM-UHFFFAOYSA-N 0.000 description 1
- SJQPASOTJGFOMU-UHFFFAOYSA-N triethoxy-[1-(oxiran-2-ylmethoxy)ethyl]silane Chemical compound CCO[Si](OCC)(OCC)C(C)OCC1CO1 SJQPASOTJGFOMU-UHFFFAOYSA-N 0.000 description 1
- NFRRMEMOPXUROM-UHFFFAOYSA-N triethoxy-[1-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CCO[Si](OCC)(OCC)C(CC)OCC1CO1 NFRRMEMOPXUROM-UHFFFAOYSA-N 0.000 description 1
- UDUKMRHNZZLJRB-UHFFFAOYSA-N triethoxy-[2-(7-oxabicyclo[4.1.0]heptan-4-yl)ethyl]silane Chemical compound C1C(CC[Si](OCC)(OCC)OCC)CCC2OC21 UDUKMRHNZZLJRB-UHFFFAOYSA-N 0.000 description 1
- RWJUTPORTOUFDY-UHFFFAOYSA-N triethoxy-[2-(oxiran-2-ylmethoxy)ethyl]silane Chemical compound CCO[Si](OCC)(OCC)CCOCC1CO1 RWJUTPORTOUFDY-UHFFFAOYSA-N 0.000 description 1
- CFUDQABJYSJIQY-UHFFFAOYSA-N triethoxy-[2-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CCO[Si](OCC)(OCC)CC(C)OCC1CO1 CFUDQABJYSJIQY-UHFFFAOYSA-N 0.000 description 1
- NLKPPXKQMJDBFO-UHFFFAOYSA-N triethoxy-[3-(7-oxabicyclo[4.1.0]heptan-4-yl)propyl]silane Chemical compound C1C(CCC[Si](OCC)(OCC)OCC)CCC2OC21 NLKPPXKQMJDBFO-UHFFFAOYSA-N 0.000 description 1
- KPNCYSTUWLXFOE-UHFFFAOYSA-N triethoxy-[3-(oxiran-2-ylmethoxy)butyl]silane Chemical compound CCO[Si](OCC)(OCC)CCC(C)OCC1CO1 KPNCYSTUWLXFOE-UHFFFAOYSA-N 0.000 description 1
- JXUKBNICSRJFAP-UHFFFAOYSA-N triethoxy-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CCO[Si](OCC)(OCC)CCCOCC1CO1 JXUKBNICSRJFAP-UHFFFAOYSA-N 0.000 description 1
- PSUKBUSXHYKMLU-UHFFFAOYSA-N triethoxy-[4-(7-oxabicyclo[4.1.0]heptan-4-yl)butyl]silane Chemical compound C1C(CCCC[Si](OCC)(OCC)OCC)CCC2OC21 PSUKBUSXHYKMLU-UHFFFAOYSA-N 0.000 description 1
- QQQSFSZALRVCSZ-UHFFFAOYSA-N triethoxysilane Chemical compound CCO[SiH](OCC)OCC QQQSFSZALRVCSZ-UHFFFAOYSA-N 0.000 description 1
- CVLRAFKSANUAQP-UHFFFAOYSA-N triethyl (3-ethyl-3-isocyanatopentyl) silicate Chemical compound CCO[Si](OCC)(OCC)OCCC(CC)(CC)N=C=O CVLRAFKSANUAQP-UHFFFAOYSA-N 0.000 description 1
- KLUOEGRKDKATMH-UHFFFAOYSA-N triethyl(4-isocyanatobutyl)silane Chemical compound CC[Si](CC)(CC)CCCCN=C=O KLUOEGRKDKATMH-UHFFFAOYSA-N 0.000 description 1
- QQXCLWWJKOROLE-UHFFFAOYSA-N triethyl(5-isocyanatopentyl)silane Chemical compound CC[Si](CC)(CC)CCCCCN=C=O QQXCLWWJKOROLE-UHFFFAOYSA-N 0.000 description 1
- HGCVEHIYVPDFMS-UHFFFAOYSA-N trimethoxy(7-oxabicyclo[4.1.0]heptan-4-ylmethyl)silane Chemical compound C1C(C[Si](OC)(OC)OC)CCC2OC21 HGCVEHIYVPDFMS-UHFFFAOYSA-N 0.000 description 1
- FNBIAJGPJUOAPB-UHFFFAOYSA-N trimethoxy-[1-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CO[Si](OC)(OC)C(CC)OCC1CO1 FNBIAJGPJUOAPB-UHFFFAOYSA-N 0.000 description 1
- DQZNLOXENNXVAD-UHFFFAOYSA-N trimethoxy-[2-(7-oxabicyclo[4.1.0]heptan-4-yl)ethyl]silane Chemical compound C1C(CC[Si](OC)(OC)OC)CCC2OC21 DQZNLOXENNXVAD-UHFFFAOYSA-N 0.000 description 1
- HTVULPNMIHOVRU-UHFFFAOYSA-N trimethoxy-[2-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CO[Si](OC)(OC)CC(C)OCC1CO1 HTVULPNMIHOVRU-UHFFFAOYSA-N 0.000 description 1
- DBUFXGVMAMMWSD-UHFFFAOYSA-N trimethoxy-[3-(7-oxabicyclo[4.1.0]heptan-4-yl)propyl]silane Chemical compound C1C(CCC[Si](OC)(OC)OC)CCC2OC21 DBUFXGVMAMMWSD-UHFFFAOYSA-N 0.000 description 1
- ZQPNGHDNBNMPON-UHFFFAOYSA-N trimethoxy-[3-(oxiran-2-ylmethoxy)butyl]silane Chemical compound CO[Si](OC)(OC)CCC(C)OCC1CO1 ZQPNGHDNBNMPON-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
- ZOWVSEMGATXETK-UHFFFAOYSA-N trimethoxy-[4-(7-oxabicyclo[4.1.0]heptan-4-yl)butyl]silane Chemical compound C1C(CCCC[Si](OC)(OC)OC)CCC2OC21 ZOWVSEMGATXETK-UHFFFAOYSA-N 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N urea group Chemical group NC(=O)N XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- 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
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/32—Polymers modified by chemical after-treatment
- C08G65/329—Polymers modified by chemical after-treatment with organic compounds
- C08G65/336—Polymers modified by chemical after-treatment with organic compounds containing silicon
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D171/00—Coating compositions based on polyethers obtained by reactions forming an ether link in the main chain; Coating compositions based on derivatives of such polymers
- C09D171/02—Polyalkylene oxides
-
- 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
- C09J171/00—Adhesives based on polyethers obtained by reactions forming an ether link in the main chain; Adhesives based on derivatives of such polymers
- C09J171/02—Polyalkylene oxides
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/26—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers modified by chemical after-treatment
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2666/00—Composition of polymers characterized by a further compound in the blend, being organic macromolecular compounds, natural resins, waxes or and bituminous materials, non-macromolecular organic substances, inorganic substances or characterized by their function in the composition
- C08L2666/02—Organic macromolecular compounds, natural resins, waxes or and bituminous materials
- C08L2666/04—Macromolecular compounds according to groups C08L7/00 - C08L49/00, or C08L55/00 - C08L57/00; Derivatives thereof
- C08L2666/06—Homopolymers or copolymers of unsaturated hydrocarbons; Derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L51/00—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
- C08L51/06—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers grafted on to homopolymers or copolymers of aliphatic hydrocarbons containing only one carbon-to-carbon double bond
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Sealing Material Composition (AREA)
- Ceramic Products (AREA)
Claims (9)
1. Fugthærdende adhæsions/forseglingsmonokomponentsammensætning indeholdende (a) mindst én silanfunktionel polyoxyalkylenpræpolymer, og (b) mindst én silanfunktionel polyolefin, og (c) mindst én apolær blødgører, hvorved den mindst ene silanfunktionelle polyoxyalkylenpræpolymer er på basis af polyethere.
2. Fugthærdende adhæsions/forseglingsmonokomponentsammensætning ifølge krav 1 indeholdende som apolær blødgører mindst énallifatisk, naphtha-len- eller aromatisk petroleumsolie.
3. Fugthærdende adhæsions/forseglingsmonokomponentsammensætning ifølge krav 1 eller 2, som yderligere indeholder mindste én katalysator.
4. Fugthærdende adhæsions/forseglingsmonokomponentsammensætning ifølge kravene 1 til 3, som yderligere indeholder mindst ét fyldstof og/eller mindst én adhæsionsfremmer.
5. Fugthærdende adhæsions/forseglingsmonokomponentsammensætning ifølge kravene 1 til 4, kendetegnet ved, at den silanfunktionelle polyoxyalkylenpræpolymer er valgt blandt lineære eller forgrenede polypropylenglycoler med methyldialkoxysilylgrupper og/eller trialkoxysilylgrupper eller blandinger heraf.
6. Fugthærdende adhæsions/forseglingsmonokomponentsammensætning ifølge kravene 1 til 5, kendetegnet ved, at den silanfunktionelle polyolefin er en amorf poly-a-olefin, en polyisobutylen eller en modificeret polyolefinvoks med methyldialkoxysilylgrupper og/eller trialkoxysilylgrupper.
7. Fugthærdende adhæsions/forseglingsmonokomponentsammensætning ifølge kravene 1 til 6, kendetegnet ved, at afhæsionspromotoren er valgt blandt 3-glycidoxypropylalkoxysilan, 3-mercaptopropylalkoxysilan, 3-methacryloxypro-pylalkoxysilan, 3-aminopropylalkoxysilan, N-(2-aminoethyl)-3-aminopropylalko-xysilan, N-(2-aminoethyl)-N'-(2-aminoethyl)-3-aminopropylmethyldiethoxysilan, bis-(triethoxysilylpropyl)amin, bis-(trimethoxysilylpropyl)-amin, vinylalkoxysilan, co-kondensater af amino-funktionelle silaner eller blandinger af de førnævnte silaner.
8. Fugthærdende adhæsions/forseglingsmonokomponentsammensætning ifølge kravene 1 til 7 indeholdende (a) 5 til 30 vægt% forgrenet polypropylenglycol med methyldialkoxysilylgrupper, (b) 5 til 30 vægt% lineær polypropylenglycol med methyldialkoxysilylgrupper, (c) 1 til 10 vægt% amorf poly-a-olefin med methyldialkoxysilylgrupper og/eller trialkoxysilylgrupper, (d) 1 til 15 vægt% paraffin-, naphthen- og/eller aromatisk jordolie, (e) 0,1 til 5 vægt% af én eller flere adhæsionsf remmere, (f) 0 til 60 vægt%, fortrinsvis 30 til 60 vægt% af ét eller flere fyldstoffer, (g) 0 til 2 vægt%, fortrinsvis 0,05 til 1,5 vægt% katalysator, hvor summen af de indgåede dele er 100%.
9. Anvendelse af adhæsions/forseglingssammensætningen ifølge kravene 1 til 8 til adhæsiv binding og/eller overtræk og/eller forsegling af plastdele eller malede substrater uden forbehandling af substratet.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102006059473A DE102006059473A1 (de) | 2006-12-14 | 2006-12-14 | Silylgruppen enthaltende Mischung von Prepolymeren und deren Verwendung |
| PCT/EP2007/057474 WO2008071461A1 (de) | 2006-12-14 | 2007-07-19 | Silylgruppen enthaltende mischung von prepolymeren und deren verwendung |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DK2089490T3 DK2089490T3 (da) | 2010-12-20 |
| DK2089490T4 true DK2089490T4 (da) | 2017-04-10 |
Family
ID=38544153
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DK07787732.2T DK2089490T4 (da) | 2006-12-14 | 2007-07-19 | Præpolymerblandinger indeholdende silylgrupper og anvendelse heraf |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US8101681B2 (da) |
| EP (1) | EP2089490B2 (da) |
| AT (1) | ATE481462T1 (da) |
| CA (1) | CA2672379C (da) |
| DE (2) | DE102006059473A1 (da) |
| DK (1) | DK2089490T4 (da) |
| WO (1) | WO2008071461A1 (da) |
Families Citing this family (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9579869B2 (en) * | 2009-02-17 | 2017-02-28 | Henkel IP & Holding GmbH | Liquid moisture curable polyurethane adhesives for lamination and assembly |
| DE102009001771A1 (de) | 2009-03-24 | 2010-09-30 | Henkel Ag & Co. Kgaa | Erstarrende Klebstoffe mit Silanvernetzung |
| DE102009046190A1 (de) | 2009-10-30 | 2011-05-05 | Henkel Ag & Co. Kgaa | Kaschierklebstoff mit Silanvernetzung |
| WO2013164413A1 (de) | 2012-05-03 | 2013-11-07 | Henkel Ag & Co. Kgaa | Zwei - komponenten schmelzklebstoff |
| US9040622B2 (en) | 2012-05-03 | 2015-05-26 | Ppg Industries Ohio, Inc. | Solvent-based primer solution based on silylated polyurethane (SPUR) chemistry for polycarbonate substrates |
| US9365751B2 (en) | 2012-07-24 | 2016-06-14 | Henkel IP & Holding GmbH | Reactive hot melt adhesive |
| JP2015530998A (ja) | 2012-08-24 | 2015-10-29 | ダウ グローバル テクノロジーズ エルエルシー | テトラメチルスタンノキシ化合物 |
| ES2691483T3 (es) | 2014-01-14 | 2018-11-27 | Henkel IP & Holding GmbH | Adhesivos reactivos de fusión en caliente con adherencia mejorada |
| US20150344698A1 (en) * | 2014-06-03 | 2015-12-03 | Corning Incorporated | Adhesion primer for glass and ceramics |
| US20160326408A1 (en) * | 2015-05-08 | 2016-11-10 | Henkel lP & Holding GmbH | Moisture curable hot melt adhesive with high adhesion strength and fast set time |
| WO2019159972A1 (ja) * | 2018-02-13 | 2019-08-22 | 株式会社カネカ | ワーキングジョイント用1成分型硬化性組成物 |
| JP7491149B2 (ja) * | 2020-09-03 | 2024-05-28 | 株式会社オートネットワーク技術研究所 | 難燃性樹脂組成物、絶縁電線、ワイヤーハーネス |
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| JP2001311056A (ja) † | 2000-04-28 | 2001-11-09 | Kanegafuchi Chem Ind Co Ltd | 被着体の接着方法 |
| JP2001329126A (ja) | 2000-05-22 | 2001-11-27 | Bridgestone Corp | 硬化性組成物 |
| DE10053545A1 (de) | 2000-10-27 | 2002-05-08 | Henkel Kgaa | Polymere mit Harnstoffgruppen und Silylgruppen, deren Herstellung und Verwendung |
| DE10139132A1 (de) * | 2001-08-09 | 2003-02-27 | Consortium Elektrochem Ind | Alkoxyvernetzende einkomponentige feuchtigkeitshärtende Massen |
| DE50303577D1 (de) | 2002-03-04 | 2006-07-06 | Basf Ag | Verfahren zur herstellung von isobutenpolymeren |
| DE10212523A1 (de) | 2002-03-21 | 2003-10-02 | Degussa | Lufttrocknende, silanhaltige Beschichtungsmittel |
| KR20050021521A (ko) | 2002-07-19 | 2005-03-07 | 쉘 인터내셔날 리써취 마트샤피지 비.브이. | 신전유를 포함하는 규소 고무 및 상기 신전유의 제조방법 |
| DE10237271A1 (de) | 2002-08-14 | 2004-03-04 | Consortium für elektrochemische Industrie GmbH | Polymermassen auf Basis alkoxysilanterminierter Polymere mit regulierbarer Härtungsgeschwindigkeit |
| US7449629B2 (en) † | 2002-08-21 | 2008-11-11 | Truseal Technologies, Inc. | Solar panel including a low moisture vapor transmission rate adhesive composition |
| TW200407390A (en) * | 2002-09-03 | 2004-05-16 | Rohm & Haas | Reactive hot-melt adhesive compositions with improved adhesion to difficult substrates |
| EP1462500A1 (en) † | 2003-03-28 | 2004-09-29 | Le Joint Francais | Single component, chemically curing warm applied sealant for durable insulating glazing units |
| DE10328844A1 (de) * | 2003-06-26 | 2005-02-03 | Consortium für elektrochemische Industrie GmbH | Alkoxysilanterminierte Prepolymere |
| DE10338344A1 (de) | 2003-08-21 | 2005-03-24 | Clariant Gmbh | Modifizierte Polyolefinwachse |
| DE10351804A1 (de) * | 2003-11-06 | 2005-06-09 | Wacker-Chemie Gmbh | Verfahren zur Erhöhung der Elastizität von feuchtigkeitsgehärteten Elastomeren |
| DE102005023319A1 (de) * | 2005-05-17 | 2006-11-23 | Den Braven Sealants Bv | Lösungsmittelfreier Kleb- und Dichtstoff |
-
2006
- 2006-12-14 DE DE102006059473A patent/DE102006059473A1/de not_active Ceased
-
2007
- 2007-07-19 EP EP07787732.2A patent/EP2089490B2/de not_active Not-in-force
- 2007-07-19 AT AT07787732T patent/ATE481462T1/de active
- 2007-07-19 CA CA2672379A patent/CA2672379C/en not_active Expired - Fee Related
- 2007-07-19 WO PCT/EP2007/057474 patent/WO2008071461A1/de not_active Ceased
- 2007-07-19 DE DE502007005094T patent/DE502007005094D1/de active Active
- 2007-07-19 DK DK07787732.2T patent/DK2089490T4/da active
-
2009
- 2009-06-12 US US12/483,521 patent/US8101681B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| US8101681B2 (en) | 2012-01-24 |
| ATE481462T1 (de) | 2010-10-15 |
| DE102006059473A1 (de) | 2008-06-19 |
| CA2672379A1 (en) | 2008-06-19 |
| DK2089490T3 (da) | 2010-12-20 |
| EP2089490A1 (de) | 2009-08-19 |
| EP2089490B2 (de) | 2017-01-04 |
| US20090306283A1 (en) | 2009-12-10 |
| CA2672379C (en) | 2014-12-02 |
| EP2089490B1 (de) | 2010-09-15 |
| WO2008071461A1 (de) | 2008-06-19 |
| DE502007005094D1 (de) | 2010-10-28 |
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