EP1771496A1 - Cross-linkable siloxane urea copolymers - Google Patents
Cross-linkable siloxane urea copolymersInfo
- Publication number
- EP1771496A1 EP1771496A1 EP05771820A EP05771820A EP1771496A1 EP 1771496 A1 EP1771496 A1 EP 1771496A1 EP 05771820 A EP05771820 A EP 05771820A EP 05771820 A EP05771820 A EP 05771820A EP 1771496 A1 EP1771496 A1 EP 1771496A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- radical
- formula
- different
- optionally
- radicals
- 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.)
- Withdrawn
Links
- 229920001577 copolymer Polymers 0.000 title claims abstract description 50
- 239000004202 carbamide Substances 0.000 title description 3
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 title 1
- 239000000203 mixture Substances 0.000 claims abstract description 60
- 238000000034 method Methods 0.000 claims abstract description 23
- 229910003849 O-Si Inorganic materials 0.000 claims abstract description 12
- 229910003872 O—Si Inorganic materials 0.000 claims abstract description 12
- 229910009257 Y—Si Inorganic materials 0.000 claims abstract description 11
- 125000004432 carbon atom Chemical group C* 0.000 claims description 28
- 229920000642 polymer Polymers 0.000 claims description 25
- 229930195733 hydrocarbon Natural products 0.000 claims description 17
- 230000008569 process Effects 0.000 claims description 16
- 239000003054 catalyst Substances 0.000 claims description 14
- 239000004215 Carbon black (E152) Substances 0.000 claims description 13
- 239000002904 solvent Substances 0.000 claims description 13
- 150000001875 compounds Chemical class 0.000 claims description 12
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 12
- 239000000945 filler Substances 0.000 claims description 11
- 238000002360 preparation method Methods 0.000 claims description 11
- 238000004132 cross linking Methods 0.000 claims description 10
- 239000001257 hydrogen Substances 0.000 claims description 10
- 229910052739 hydrogen Inorganic materials 0.000 claims description 10
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 8
- 239000004971 Cross linker Substances 0.000 claims description 8
- 239000002318 adhesion promoter Substances 0.000 claims description 8
- 239000000460 chlorine Chemical group 0.000 claims description 8
- 229910052801 chlorine Inorganic materials 0.000 claims description 8
- 125000005442 diisocyanate group Chemical group 0.000 claims description 8
- 229910052731 fluorine Inorganic materials 0.000 claims description 8
- 239000011737 fluorine Substances 0.000 claims description 8
- 125000001153 fluoro group Chemical group F* 0.000 claims description 8
- 239000000126 substance Substances 0.000 claims description 8
- 239000000470 constituent Substances 0.000 claims description 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 5
- 238000006243 chemical reaction Methods 0.000 claims description 5
- 239000003063 flame retardant Substances 0.000 claims description 5
- 239000000049 pigment Substances 0.000 claims description 5
- 239000004014 plasticizer Substances 0.000 claims description 5
- 239000003381 stabilizer Substances 0.000 claims description 5
- 239000003963 antioxidant agent Substances 0.000 claims description 3
- 150000002148 esters Chemical class 0.000 claims description 3
- 239000012948 isocyanate Substances 0.000 claims description 3
- 150000002513 isocyanates Chemical class 0.000 claims description 3
- 239000004611 light stabiliser Substances 0.000 claims description 3
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 3
- 125000003277 amino group Chemical group 0.000 claims description 2
- 150000002431 hydrogen Chemical class 0.000 claims description 2
- 150000002989 phenols Chemical class 0.000 claims description 2
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 claims 2
- YZCKVEUIGOORGS-IGMARMGPSA-N Protium Chemical compound [1H] YZCKVEUIGOORGS-IGMARMGPSA-N 0.000 claims 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 1
- 239000012084 conversion product Substances 0.000 claims 1
- 239000001301 oxygen Substances 0.000 claims 1
- 229910052760 oxygen Inorganic materials 0.000 claims 1
- 229920002396 Polyurea Polymers 0.000 abstract description 7
- 238000004519 manufacturing process Methods 0.000 abstract description 4
- 229920001296 polysiloxane Polymers 0.000 abstract description 4
- 238000004073 vulcanization Methods 0.000 abstract description 2
- -1 siloxanes Chemical class 0.000 description 94
- 150000003254 radicals Chemical class 0.000 description 43
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 26
- 239000000463 material Substances 0.000 description 15
- 235000013870 dimethyl polysiloxane Nutrition 0.000 description 13
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 13
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 13
- 230000008901 benefit Effects 0.000 description 12
- 238000000576 coating method Methods 0.000 description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- PHQOGHDTIVQXHL-UHFFFAOYSA-N n'-(3-trimethoxysilylpropyl)ethane-1,2-diamine Chemical compound CO[Si](OC)(OC)CCCNCCN PHQOGHDTIVQXHL-UHFFFAOYSA-N 0.000 description 8
- 239000000243 solution Substances 0.000 description 8
- 239000000654 additive Substances 0.000 description 7
- 239000011248 coating agent Substances 0.000 description 7
- 238000012360 testing method Methods 0.000 description 7
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 6
- 239000000853 adhesive Substances 0.000 description 6
- 230000001070 adhesive effect Effects 0.000 description 6
- 238000009833 condensation Methods 0.000 description 6
- 230000005494 condensation Effects 0.000 description 6
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 6
- 229920002725 thermoplastic elastomer Polymers 0.000 description 6
- 125000002947 alkylene group Chemical group 0.000 description 5
- 229910052799 carbon Inorganic materials 0.000 description 5
- 238000001816 cooling Methods 0.000 description 5
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 5
- 238000012545 processing Methods 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- 239000000565 sealant Substances 0.000 description 5
- 239000004753 textile Substances 0.000 description 5
- 229920001169 thermoplastic Polymers 0.000 description 5
- 239000004416 thermosoftening plastic Substances 0.000 description 5
- 239000004831 Hot glue Substances 0.000 description 4
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 4
- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 4
- 230000000996 additive effect Effects 0.000 description 4
- 239000012298 atmosphere Substances 0.000 description 4
- 229920001400 block copolymer Polymers 0.000 description 4
- 239000004205 dimethyl polysiloxane Substances 0.000 description 4
- 230000007717 exclusion Effects 0.000 description 4
- 239000000835 fiber Substances 0.000 description 4
- 150000002430 hydrocarbons Chemical class 0.000 description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 4
- NJGCRMAPOWGWMW-UHFFFAOYSA-N octylphosphonic acid Chemical compound CCCCCCCCP(O)(O)=O NJGCRMAPOWGWMW-UHFFFAOYSA-N 0.000 description 4
- 229920003023 plastic Polymers 0.000 description 4
- 239000004033 plastic Substances 0.000 description 4
- 229920000570 polyether Polymers 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- 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 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- 239000005058 Isophorone diisocyanate Substances 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- 239000004820 Pressure-sensitive adhesive Substances 0.000 description 3
- BOTDANWDWHJENH-UHFFFAOYSA-N Tetraethyl orthosilicate Chemical compound CCO[Si](OCC)(OCC)OCC BOTDANWDWHJENH-UHFFFAOYSA-N 0.000 description 3
- 239000006229 carbon black Substances 0.000 description 3
- 235000019241 carbon black Nutrition 0.000 description 3
- 238000001704 evaporation Methods 0.000 description 3
- 230000008020 evaporation Effects 0.000 description 3
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 description 3
- 239000012528 membrane Substances 0.000 description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 3
- 230000004048 modification Effects 0.000 description 3
- 238000012986 modification Methods 0.000 description 3
- 230000035699 permeability Effects 0.000 description 3
- 239000000376 reactant Substances 0.000 description 3
- 239000012815 thermoplastic material Substances 0.000 description 3
- WYTZZXDRDKSJID-UHFFFAOYSA-N (3-aminopropyl)triethoxysilane Chemical compound CCO[Si](OCC)(OCC)CCCN WYTZZXDRDKSJID-UHFFFAOYSA-N 0.000 description 2
- PCHXZXKMYCGVFA-UHFFFAOYSA-N 1,3-diazetidine-2,4-dione Chemical compound O=C1NC(=O)N1 PCHXZXKMYCGVFA-UHFFFAOYSA-N 0.000 description 2
- AAMSQLYHKQGAEL-UHFFFAOYSA-N 1-(isocyanatomethyl)-2-(5-isocyanatopentyl)benzene Chemical compound O=C=NCCCCCC1=CC=CC=C1CN=C=O AAMSQLYHKQGAEL-UHFFFAOYSA-N 0.000 description 2
- LJKDOMVGKKPJBH-UHFFFAOYSA-N 2-ethylhexyl dihydrogen phosphate Chemical compound CCCCC(CC)COP(O)(O)=O LJKDOMVGKKPJBH-UHFFFAOYSA-N 0.000 description 2
- ZOTKGMAKADCEDH-UHFFFAOYSA-N 5-triethoxysilylpentane-1,3-diamine Chemical compound CCO[Si](OCC)(OCC)CCC(N)CCN ZOTKGMAKADCEDH-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 239000004609 Impact Modifier Substances 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 230000003373 anti-fouling effect Effects 0.000 description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
- 239000000560 biocompatible material Substances 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 238000004140 cleaning Methods 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- NKSJNEHGWDZZQF-UHFFFAOYSA-N ethenyl(trimethoxy)silane Chemical compound CO[Si](OC)(OC)C=C NKSJNEHGWDZZQF-UHFFFAOYSA-N 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 238000001125 extrusion Methods 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 230000007062 hydrolysis Effects 0.000 description 2
- 238000006460 hydrolysis reaction Methods 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N iron oxide Inorganic materials [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- 235000013980 iron oxide Nutrition 0.000 description 2
- VBMVTYDPPZVILR-UHFFFAOYSA-N iron(2+);oxygen(2-) Chemical class [O-2].[Fe+2] VBMVTYDPPZVILR-UHFFFAOYSA-N 0.000 description 2
- BFXIKLCIZHOAAZ-UHFFFAOYSA-N methyltrimethoxysilane Chemical compound CO[Si](C)(OC)OC BFXIKLCIZHOAAZ-UHFFFAOYSA-N 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- 230000003287 optical effect Effects 0.000 description 2
- 230000001590 oxidative effect Effects 0.000 description 2
- 239000003973 paint Substances 0.000 description 2
- 230000036961 partial effect Effects 0.000 description 2
- 150000003014 phosphoric acid esters Chemical class 0.000 description 2
- 229920001451 polypropylene glycol Polymers 0.000 description 2
- 229920002635 polyurethane Polymers 0.000 description 2
- 239000004814 polyurethane Substances 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000012763 reinforcing filler Substances 0.000 description 2
- 230000002441 reversible effect Effects 0.000 description 2
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- 239000000758 substrate Substances 0.000 description 2
- 230000008961 swelling Effects 0.000 description 2
- 239000004408 titanium dioxide Substances 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- 125000002030 1,2-phenylene group Chemical group [H]C1=C([H])C([*:1])=C([*:2])C([H])=C1[H] 0.000 description 1
- 125000001989 1,3-phenylene group Chemical group [H]C1=C([H])C([*:1])=C([H])C([*:2])=C1[H] 0.000 description 1
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical group CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 1
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 1
- 125000004200 2-methoxyethyl group Chemical group [H]C([H])([H])OC([H])([H])C([H])([H])* 0.000 description 1
- KHUIRIRTZCOEMK-UHFFFAOYSA-N 2-methylpropyl 3,5-diamino-4-chlorobenzoate Chemical compound CC(C)COC(=O)C1=CC(N)=C(Cl)C(N)=C1 KHUIRIRTZCOEMK-UHFFFAOYSA-N 0.000 description 1
- SLRMQYXOBQWXCR-UHFFFAOYSA-N 2154-56-5 Chemical compound [CH2]C1=CC=CC=C1 SLRMQYXOBQWXCR-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
- WECDUOXQLAIPQW-UHFFFAOYSA-N 4,4'-Methylene bis(2-methylaniline) Chemical compound C1=C(N)C(C)=CC(CC=2C=C(C)C(N)=CC=2)=C1 WECDUOXQLAIPQW-UHFFFAOYSA-N 0.000 description 1
- IBOFVQJTBBUKMU-UHFFFAOYSA-N 4,4'-methylene-bis-(2-chloroaniline) Chemical compound C1=C(Cl)C(N)=CC=C1CC1=CC=C(N)C(Cl)=C1 IBOFVQJTBBUKMU-UHFFFAOYSA-N 0.000 description 1
- 229910052582 BN Inorganic materials 0.000 description 1
- PZNSFCLAULLKQX-UHFFFAOYSA-N Boron nitride Chemical compound N#B PZNSFCLAULLKQX-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
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- 239000005909 Kieselgur Substances 0.000 description 1
- BHQZAUBWSSIHSB-UHFFFAOYSA-N N'-(silylmethyl)ethane-1,2-diamine Chemical compound NCCNC[SiH3] BHQZAUBWSSIHSB-UHFFFAOYSA-N 0.000 description 1
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- PFWCWFZWFMTGEZ-UHFFFAOYSA-N N-(dimethylsilylmethyl)-N'-methoxyethane-1,2-diamine Chemical compound CONCCNC[SiH](C)C PFWCWFZWFMTGEZ-UHFFFAOYSA-N 0.000 description 1
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- 229910052581 Si3N4 Inorganic materials 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- ISKQADXMHQSTHK-UHFFFAOYSA-N [4-(aminomethyl)phenyl]methanamine Chemical compound NCC1=CC=C(CN)C=C1 ISKQADXMHQSTHK-UHFFFAOYSA-N 0.000 description 1
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- 125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000004836 hexamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
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- 238000009413 insulation Methods 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000005340 laminated glass Substances 0.000 description 1
- 239000010985 leather Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229910000000 metal hydroxide Inorganic materials 0.000 description 1
- 150000004692 metal hydroxides Chemical class 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical compound [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 description 1
- 239000006082 mold release agent Substances 0.000 description 1
- 239000002808 molecular sieve Substances 0.000 description 1
- 229910052901 montmorillonite Inorganic materials 0.000 description 1
- ZCVJMOSHCYXMTF-UHFFFAOYSA-N n'-(dimethoxymethylsilylmethyl)ethane-1,2-diamine Chemical compound COC(OC)[SiH2]CNCCN ZCVJMOSHCYXMTF-UHFFFAOYSA-N 0.000 description 1
- CIAYYZGZMJDALI-UHFFFAOYSA-N n'-(triethoxysilylmethyl)ethane-1,2-diamine Chemical compound CCO[Si](OCC)(OCC)CNCCN CIAYYZGZMJDALI-UHFFFAOYSA-N 0.000 description 1
- CSNJSTXFSLBBPX-UHFFFAOYSA-N n'-(trimethoxysilylmethyl)ethane-1,2-diamine Chemical compound CO[Si](OC)(OC)CNCCN CSNJSTXFSLBBPX-UHFFFAOYSA-N 0.000 description 1
- MQWFLKHKWJMCEN-UHFFFAOYSA-N n'-[3-[dimethoxy(methyl)silyl]propyl]ethane-1,2-diamine Chemical compound CO[Si](C)(OC)CCCNCCN MQWFLKHKWJMCEN-UHFFFAOYSA-N 0.000 description 1
- QMIREOCYHAFOPK-UHFFFAOYSA-N n,n'-bis(3-triethoxysilylpropyl)ethane-1,2-diamine Chemical compound CCO[Si](OCC)(OCC)CCCNCCNCCC[Si](OCC)(OCC)OCC QMIREOCYHAFOPK-UHFFFAOYSA-N 0.000 description 1
- HZGIOLNCNORPKR-UHFFFAOYSA-N n,n'-bis(3-trimethoxysilylpropyl)ethane-1,2-diamine Chemical compound CO[Si](OC)(OC)CCCNCCNCCC[Si](OC)(OC)OC HZGIOLNCNORPKR-UHFFFAOYSA-N 0.000 description 1
- PLTLLUXRAYZIFK-UHFFFAOYSA-N n,n'-bis[3-(dimethoxymethylsilyl)propyl]ethane-1,2-diamine Chemical compound COC(OC)[SiH2]CCCNCCNCCC[SiH2]C(OC)OC PLTLLUXRAYZIFK-UHFFFAOYSA-N 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000003136 n-heptyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 230000006855 networking Effects 0.000 description 1
- 125000001181 organosilyl group Chemical group [SiH3]* 0.000 description 1
- 239000005022 packaging material Substances 0.000 description 1
- 239000000123 paper Substances 0.000 description 1
- 239000011087 paperboard Substances 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000004597 plastic additive Substances 0.000 description 1
- 229920005906 polyester polyol Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920002959 polymer blend Polymers 0.000 description 1
- 238000010094 polymer processing Methods 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 239000004810 polytetrafluoroethylene Substances 0.000 description 1
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 1
- 238000010944 pre-mature reactiony Methods 0.000 description 1
- 238000003672 processing method Methods 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 230000001698 pyrogenic effect Effects 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 230000002829 reductive effect Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 239000005336 safety glass Substances 0.000 description 1
- 238000005204 segregation Methods 0.000 description 1
- 150000004756 silanes Chemical class 0.000 description 1
- 125000005372 silanol group Chemical group 0.000 description 1
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 1
- 229910010271 silicon carbide Inorganic materials 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 description 1
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 125000001973 tert-pentyl group Chemical group [H]C([H])([H])C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- ZUEKXCXHTXJYAR-UHFFFAOYSA-N tetrapropan-2-yl silicate Chemical compound CC(C)O[Si](OC(C)C)(OC(C)C)OC(C)C ZUEKXCXHTXJYAR-UHFFFAOYSA-N 0.000 description 1
- ZQZCOBSUOFHDEE-UHFFFAOYSA-N tetrapropyl silicate Chemical compound CCCO[Si](OCCC)(OCCC)OCCC ZQZCOBSUOFHDEE-UHFFFAOYSA-N 0.000 description 1
- 150000003606 tin compounds Chemical class 0.000 description 1
- CPUDPFPXCZDNGI-UHFFFAOYSA-N triethoxy(methyl)silane Chemical compound CCO[Si](C)(OCC)OCC CPUDPFPXCZDNGI-UHFFFAOYSA-N 0.000 description 1
- NMEPHPOFYLLFTK-UHFFFAOYSA-N trimethoxy(octyl)silane Chemical compound CCCCCCCC[Si](OC)(OC)OC NMEPHPOFYLLFTK-UHFFFAOYSA-N 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N urea group Chemical group NC(=O)N XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- GFQYVLUOOAAOGM-UHFFFAOYSA-N zirconium(iv) silicate Chemical compound [Zr+4].[O-][Si]([O-])([O-])[O-] GFQYVLUOOAAOGM-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
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/30—Low-molecular-weight compounds
- C08G18/38—Low-molecular-weight compounds having heteroatoms other than oxygen
- C08G18/3893—Low-molecular-weight compounds having heteroatoms other than oxygen containing silicon
-
- 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
- C08G18/0895—Manufacture of polymers by continuous processes
-
- 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
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/61—Polysiloxanes
-
- 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
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/72—Polyisocyanates or polyisothiocyanates
- C08G18/74—Polyisocyanates or polyisothiocyanates cyclic
- C08G18/75—Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic
- C08G18/758—Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic containing two or more cycloaliphatic rings
-
- 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
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/72—Polyisocyanates or polyisothiocyanates
- C08G18/74—Polyisocyanates or polyisothiocyanates cyclic
- C08G18/76—Polyisocyanates or polyisothiocyanates cyclic aromatic
- C08G18/7614—Polyisocyanates or polyisothiocyanates cyclic aromatic containing only one aromatic ring
- C08G18/7628—Polyisocyanates or polyisothiocyanates cyclic aromatic containing only one aromatic ring containing at least one isocyanate or isothiocyanate group linked to the aromatic ring by means of an aliphatic group
- C08G18/765—Polyisocyanates or polyisothiocyanates cyclic aromatic containing only one aromatic ring containing at least one isocyanate or isothiocyanate group linked to the aromatic ring by means of an aliphatic group alpha, alpha, alpha', alpha', -tetraalkylxylylene diisocyanate or homologues substituted on the aromatic ring
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/42—Block-or graft-polymers containing polysiloxane sequences
- C08G77/458—Block-or graft-polymers containing polysiloxane sequences containing polyurethane sequences
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L83/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers
- C08L83/10—Block- or graft-copolymers containing polysiloxane sequences
-
- 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
- C09J183/00—Adhesives based on macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon, with or without sulfur, nitrogen, oxygen, or carbon only; Adhesives based on derivatives of such polymers
- C09J183/10—Block or graft copolymers containing polysiloxane sequences
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31551—Of polyamidoester [polyurethane, polyisocyanate, polycarbamate, etc.]
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31652—Of asbestos
- Y10T428/31663—As siloxane, silicone or silane
Definitions
- the invention relates to crosslinkable organopolysiloxane-polyurea copolymers, to a process for preparing the crosslinkable organopolysiloxane-polyurea copolymers and to their use, to crosslinkable compositions containing the crosslinkable organopolysiloxane-polyurea copolymers, to the preparation of the crosslinkable compositions, their vulcanization and the use of vulcanizates.
- Organopolysiloxane-polyurea block copolymers are known and are prepared by copolymerization of aminoalkyl-terminated siloxanes and diisocyanates (Polymer, Vol. 25 (1984), p. 1800 f.).
- these copolymers can be thermoplastic elastomers.
- such copolymers are plastic above the softening point while having elastic properties below them.
- they can be used for example as Schmelzkle ⁇ ber.
- a disadvantage of the use of such copolymers as hotmelt adhesives is that the temperature rise beyond the softening point causes the bond to be reversible again.
- moldings or adhesions produced from such copolymers are subject to a cold flow, since hydrogen bonds can constantly dissolve and re-bond even below the softening point, so that deformations and therefore failure of the desired function are possible.
- thermoplastic elastomer elastomer-based polystyrene foam
- One solution to the problem is to crosslink the individual polymer chains by additionally bonding with covalent, ie thermally non-reversible, bonds. If the thermoplastic elastomers are crosslinked during production by using, for example, trifunctional building blocks, the processing properties (eg melt viscosity) can be adversely affected. Networking after application is therefore more useful.
- EP 0 250 248 B1, EP 0 822 952 A1 and DE 101 13 980 A1 describe, for example, organopolysiloxane-polyurea block copolymers provided with moisture-crosslinkable silyl end groups. This allows crosslinking after the molten liquid application via these end groups.
- the achievable crosslinking density is low, however, especially in the long-chain block copolymers with small terminal group on the other hand is a high degree of polymerization and the block copolymer for forming the thermoplastic own ⁇ properties necessary.
- the invention relates to copolymers of the general formula
- (B) may be the same or different and is a unit of formula - [CO-NH-Z-NH-CO-NR 4 -G-NR 4 ] - (III)
- (C) may be the same or different and is a unit of formula
- X may be identical or different and is an alkylene radical having 1 to 700 carbon atoms which is unsubstituted or substituted by fluorine, chlorine, C 1 -C 6 -alkyl or C 1 -C 6 -alkyl ester, in which non-adjacent methylene units are represented by groups.
- -COO-, -OCO- or -OCOO- may be replaced, or optionally substituted arylene radical having 6 to 22 carbon atoms,
- Y may be identical or different and is a divalent hydrocarbon radical having 1 to 30 carbon atoms, in which non-adjacent methylene units may be replaced by groups -O-, or the radical - (CH 2 ) 3 -NH- SiR 2 - (CH 2 ) 3 -NH- represents,
- Z may be identical or different and is a divalent hydrocarbon radical optionally substituted by fluorine or chlorine and having 1 to 30 carbon atoms
- D may be identical or different and represents hydrogen atom or a monovalent, optionally substituted hydrocarbon radical
- E may be the same or different and represents an oxygen atom or an amino group -ND-
- R may be identical or different and a monovalent, optionally substituted by fluorine or chlorine Koh ⁇ hydrocarbon radical having 1 to 20 carbon atoms meaning tet
- R 4 may be the same or different and are a radical of the research mel -Z ⁇ SiR p (OR 1) 3 _ p with Z ⁇ equal to a top angege ⁇ for Z surrounded meaning and p is 0, 1 or 2, hydrogen atom or denotes a monovalent, optionally substituted hydrocarbon radical,
- G may be the same or different and has a meaning given for Z
- R '' is hydrogen or a radical -CO-NH-Z-NCO, preferably hydrogen atom
- R 'in the case of R' ' is hydrogen, a radical
- HND-Y-Si (OR 1) R 2 0 - 0 - (0-SiR 2) n O-Si (OR 1) 2 O R - O -Y-ND-, HNR 4 -G-NR 4 - or HE XE-, preferred
- HND-Y-Si OR 1 ) oR 2 -o ( O -SiR 2 ) n -O-Si (OR 1 ) O R 2 - O -Y-ND or HNR 4 -G-NR 4 -, means and in the case of R ", the radical -CO-NH-Z-NCO is the meaning of the radical OCN-Z-NH-CO-ND-Y-Si (OR 1 ) 0R 2 O- (O-SiR 2 ) n - 0-Si (oR 1) 2 O R O _ -Y-ND-, OCN-Z-NH-CO-NR 4 -G-NR 4 - or OCN-Z-NH-CO-EXE, preferably OCN-Z -NH-CO-ND-Y-Si (oR 1) 0R2-0- (0-SiR 2) n -0-Si (oR 1) 2 O R O _ -Y-ND or OCN-Z-NH- CO-NR 4 -
- organopolysiloxanes is intended to encompass both polymeric, oligomeric and dimeric siloxanes.
- divalent radicals Z are alkylene radicals, such as the methylene, ethylene, n-propylene, iso-propylene, n-butylene, iso-butylene, tert-butylene, n-pentylene, iso-pentylene -, neo-pentylene, tert-pentylene radical, hexylene radicals, such as the n-hexylene radical, heptylene radicals, such as the n-heptylene radical, octylene radicals, such as the n-octylene radical and iso-octylene radicals, such as 2,2,4- Trimethylpentylene radical, nonylene radicals, such as the n-nonyl radical, decyl radicals, such as the n-decylene radical, dodecylene radicals, such as the n-dodecylene radical; Alkenylene radicals, such as the vinyl
- Radical Z is preferably alkylene groups having 1 to 24 carbon atoms, more preferably hexylene, 4, 4'-methylene-biscyclohexylene and 3-methylene-3, 5, 5-trimethylcyclohexylene.
- Examples of the divalent radicals G are the examples listed for Z.
- Radicals G are preferably alkylene radicals having 1 to 6 carbon atoms, arylene radicals, such as the o-, m- or p-phenylene radical, and aralkylene radicals, such as the phenylene radical, with the radical -CH 2 CH 2 - being particularly preferred.
- Z ⁇ examples are all examples given for Z.
- Bevor ⁇ Trains t is radical Z ⁇ alkylene groups having 1 to 24 carbon atoms, more preferably alkylene groups having 1 or 3 carbon atoms.
- radicals Y are preferably alkylene radicals having 1 to 30 carbon atoms, in which non-adjacent methylene units may be replaced by groups -O-, or arylene radicals having 6 to 22 carbon atoms.
- radical Y is alkylene groups having 1 to 3 carbon atoms, in particular alkylene groups having 1 or 3 carbon atoms.
- radical X examples are the butylene radical, ethylene radical, hexylene radical, - (CH 2 ) 3- (O-CH (CH 3 ) -CH 2 ) 2-3000-O- (CH 2 ) 3, -CH (CH 3 ) -CH 2 - (O-CH (CH 3 ) -CH 2 ) 2-3000-, - (CH 2 ) 3- (O-CH 2 -CH 2 ) 2-300-O- (CH 2 ) 3 and -CH 2 -CH 2 -
- the radicals X are preferably polyether radicals, more preferably polypropyleneglycol radicals, in particular those having 2 to 600 carbon atoms.
- radical R examples include alkyl radicals, such as the methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, tert-butyl, n-pentyl, isopentyl, , neo-pentyl, tert-pentyl, hexyl, such as the n-hexyl, heptyl, such as the n-heptyl, Oc- tyl radicals, such as the n-octyl radical and iso-octyl radicals, such as the 2,2, 4-trimethylpentyl radical, nonyl radicals, such as the n-nonyl radical, decyl radicals, such as the n-decyl radical, dodecyl radicals, such as the n-dodecyl radical; Alkenyl radicals, such as the vinyl and allyl radicals; Cycloalky
- Radical R is preferably a hydrocarbon radical having 1 to 6 carbon atoms, more preferably an alkyl radical having 1 to 4 carbon atoms, in particular the methyl radical.
- radical R 1 examples are the examples given for radical R and alkoxyalkyl radicals.
- Radicals R 1 are preferably linear or branched alkyl radicals having 1 to 12 carbon atoms and alkoxyalkyl radicals such as 2-methoxyethyl, 2-ethoxyethyl and 2- (2'-methoxyethyl) ethyl, particularly preferably Alkyl radicals having 1 to 12 carbon atoms, in particular the methyl and Ethyl ⁇ rest.
- radical R 4 are the radicals specified for R, hydrogen atom and the radicals - (CH 2 ) 4 Si (OCH 3 ) 3 ,
- Radical R 4 is preferably hydrogen atom and the above-mentioned silyl-substituted alkyl radicals, more preferably hydrogen and the radicals - (CH 2 ) 3 Si (OCH 3 ) 3 , - (CH 2 ) 3 Si (OCH 2 CH 3 ) 3 , - (CH 2 ) 3 SiCH 3 (OCH 3 ) 2, - (CH 2 ) 3 SiCH 3 (OCH 2 CH 3 ) 2, -CH 2 Si (OCH 3 ) 3 , -CH 2 Si (OCH 2 CH 3 ) 3 , -CH 2 Si (OCH 2 CH 3 ) 3 , -CH 2 Si (OCH 2 CH 3 ) 3 , -CH 2 SiCH 3 (OCH 3 ) 2 and -CH 2 SiCH 3 (OCH 3 ) 2 .
- hydrocarbon radicals D are the radicals given for R above.
- the radical D is preferably an alkyl radical or hydrogen atom, particularly preferably an alkyl radical having 1 to 12 carbon atoms or hydrogen atom, in particular hydrogen atom.
- the radical E is preferably an oxygen atom.
- A preferably has the meaning of an integer from 1 to 1000, particularly preferably from 5 to 1000, in particular from 5 to 100.
- B preferably has the meaning of an integer from 1 to 1000, particularly preferably from 5 to 1000, in particular from 5 to 100.
- C preferably has the meaning of 0 or an integer from 1 to 100, particularly preferably from 0 to 10, in particular 0.
- radicals R ' are, in the case that R "is the same hydrogen atom, radicals which result from the unreacted end groups from the educts used, such as H 2 N- (CH 2 ) 3-Si (CH 3 ) 2- (O-Si (CH 3 ) 2 ) 40 -O-Si (CH 3 ) 2 - (CH 2 ) 3 -NH-, H 2 N-CH 2 -CH 2 -N- (CH 2 ) 3 Si (OCH 3 ) 3 , and HO- (CH 2 CH (CH 3 ) O) 50 -.
- radicals which result from the unreacted end groups from the educts used such as H 2 N- (CH 2 ) 3-Si (CH 3 ) 2- (O-Si (CH 3 ) 2 ) 40 -O-Si (CH 3 ) 2 - (CH 2 ) 3 -NH-, H 2 N-CH 2 -CH 2 -N- (CH 2 ) 3 Si (OCH 3 ) 3
- radicals R ' are, in the case that R "' is -CO-NH-Z-NCO, radicals which result from the unreacted end groups from the educts used, such as
- radicals R '' are hydrogen atom, -CO-NH- (CH 2) 6 -NCO, -CO-NH-C 6 H IO -CH 2 -C 6 H IO -NCO, and -CO-NH-C 6 H 3 (CH 3 ) -NCO.
- N is preferably an integer from 10 to 4000, more preferably from 30 to 1000.
- Copolymers of the invention comprising units (C) can give a harder material compared to copolymers according to the invention which contain no unit (C), since there are more hydrogen bonds in them. If the proportion of component (C) is too high, segregation phenomena occur between the organic and polysiloxane constituents, so that the transparency of the copolymers according to the invention is reduced and the copolymers become cloudy. Preference is given to polymers of the formula (I) where c is zero, since thus exclusively siloxane chains are present and thus the polymers have advantages such as, for example, high transparency and UV stability with simultaneously low surface energies.
- copolymers of the formula (I) are H [NH (CH 2 ) 3 SiMe 2 O (SiMe 2 O) 35 SiMe 2 (CH 2 ) 3 -NH-CO-NH- (CH 2 ) 6 -NH-CO-NH-CH 2 CH 2 -N ⁇ (CH 2 ) 3 -S1 (OMe) 3 ⁇ -CO-NH- (CH 2 ) 6 -NH-CO] 10 -NH (CH 2 ) 3 SiMe 2 O (SiMe 2 O) 35 SiMe 2 (CH 2 ) 3 -NH 2 ,
- copolymers of the formula (I) according to the invention have a content of units A of the formula (II) of preferably greater than 70% by weight, particularly preferably greater than 80% by weight, in each case based on the total weight of the copolymer.
- the copolymers of the formula (I) according to the invention are preferably rubber-elastic solids at room temperature with tensile strengths between preferably about 0.5 and 20 MPa and ultimate elongations between preferably about 50 to 1000%. They soften at temperatures between preferably 60 and 200 0 C and lose da ⁇ at their rubber-elastic properties. As a result of the action of moisture, the hydrolyzable radicals OR 1 can react to form OH groups, which in turn can condense with further OR 1 or OH groups to form siloxane bonds.
- These polymers additionally crosslinked according to the invention of the formula (I) preferably have a softening point which is significantly higher than the starting polymer before crosslinking. This opens up the possibility of producing polymers which can be processed at relatively low temperatures, but then can be exposed to even higher temperatures during use.
- copolymers according to the invention also have the advantage that they have very good mechanical properties without having to add fillers.
- copolymers according to the invention are distinguished by outstanding physical properties, as known from polyorganosiloxanes, such as low glass transition temperatures, transparency, good resistance to UV light, low surface energies, low hydrophobicity, good dielectric properties and high Permeability to gases. Further advantages of the copolymers according to the invention are the high thermal and oxidative stability, good resistance to swelling and decomposition by solvents containing hydrocarbons.
- the properties such as, for example, peel and peel strength, printability, tensile and break-through strength or water vapor permeability, can be set in a targeted manner.
- copolymers according to the invention can be prepared analogously to any desired processes which are already known to the person skilled in the art and are used, for example, for the synthesis of (prep) polymers for polyurethanes.
- a further subject of the present invention is a process for the preparation of the copolymers of the formula (I) according to the invention by reacting
- OCN-Z-NCO VI
- blocked diisocyanates thermalally unstable reaction products of isocyanates with, for example, phenols, ketoximes, malonic esters, nitrogen-containing heterocycles
- Formula (V) are ⁇ , ⁇ -aminopropyldimethylsilyl-terminated polydimethylsiloxanes, ⁇ , ⁇ -aminopropyldimethoxysilyl-terminated polydimethylsiloxanes, ⁇ , ⁇ -aminomethyldimethylsilyl-terminated polydimethylsiloxanes and ⁇ , ⁇ -aminomethyldimethoxysilyl-terminated polydimethylsiloxanes.
- Preferred compounds of the formula (VI) which are used in the process according to the invention are 3- (2-aminoethyl) aminopropyltrimethoxysilane, 3- (2-aminoethyl) aminopropyltriethoxysilane, 3- (2-aminoethyl) aminopropylmethyldimethoxysilane, 3- 2-aminoethyl) aminopropyldimethylmethoxysilane 3- (2-Aminoethyl) aminopropylmethyldiethoxysilane, N, N'-bis (3-trimethoxysilylpropyl) -ethylenediamine, N, N'-bis (3-triethoxysilylpropyl) ethylenediamine, N , N'-bis (3-dimethoxymethylsilylpropyl) ethylenediamine and N, N'-bis (3-diethoxymethylsilylpropyl) ethylenediamine, N-trimethoxysilylmethylethylenediamine,
- isocyanates of the formula (VII) used according to the invention are hexylene diisocyanate, 4,4'-methylenedicyclohexylene diisocyanate, 4,4'-methylenediphenylene diisocyanate, 1,3-diazetidine-2,4-dione bis (4,4 '-methylenedicyclohexyl) diisocyanate, 1,3-diazetidine-2,4-dione bis (4,4'-methylenediphenyl) diisocyanate, tetramethylenexylylene diisocyanate and isophorone diisocyanate, wherein hexylene diisocyanate, 4, 4' -methylenedicyclohexylene diisocyanate,
- 4,4'-methylenediphenylene diisocyanate, tetramethylenexylylene diisocyanate and isophorone diisocyanate are preferred, and hexylene diisocyanate, 4,4'-methylenedicyclohexylene diisocyanate and isophorone diisocyanate are particularly preferred.
- Examples of the compounds of the formula (VIII) used according to the invention are compounds known from polyurethane chemistry, such as diols, e.g. Ethylene glycol, polyethylene glycols, polypropyleneglycols, polyesterpolyols, diamines such as e.g. Ethylenediamine, 5-amino-3- (aminomethyl) -1,3,3-trimethylcyclohexane),
- the stoichiometry of the reactants for the preparation of the copolymers according to the invention is preferably selected such that the molar ratio of the isocyanate groups from the compounds of the formula (VII) to the sum of the isocyanate-reactive EH and NH groups from the compounds of the formulas (V),
- (VI) and (VIII) is in the range of preferably 0.7 to 1.3, particularly preferably 0.95 to 1.05, in particular 1.
- catalysts examples include all previously known catalysts which promote the addition of the isocyanate groups of the compounds of the general formulas (VII) to the active groups of the polymers of the formulas (V), (VI) and (VIII), such as diorganotin compounds and bismuth compounds.
- catalysts are used in the process according to the invention, these are amounts of preferably 0.0001 to 1 part by weight, particularly preferably 0.001 to 0.1 part by weight, in each case based on 100 parts by weight of the total mixture.
- solvents optionally used in the process according to the invention are tetrahydrofuran, dimethylformamide, isopropanol and methyl ethyl ketone.
- solvents are used in the process according to the invention, these are amounts of preferably from 10 to 200% by weight. parts by weight, particularly preferably 10 to 100 parts by weight, in each case based on 100 parts by weight of the total mixture.
- the reaction according to the invention can be carried out in solution or in substance, a reaction in substance being preferred.
- temperatures are preferably from 0 to 100 0 C and be ⁇ from 20 to 8O 0 C Sonders preferred.
- temperatures above the softening point of the copolymer of the formula (I) prepared are preferred.
- the process according to the invention is preferably carried out at a pressure of the surrounding atmosphere, ie between 900 and 1100 hPa.
- a pressure of the surrounding atmosphere ie between 900 and 1100 hPa.
- the mixture is operated at a pressure of preferably up to 15 MPa in some sections of the extruder and for degassing at pressures of preferably 0.1 to 1100 hPa.
- the process according to the invention is preferably carried out with the exclusion of moisture, but it is also possible to work with the presence of water.
- the preparation of the copolymers according to the invention of the general formula (I) can be carried out by methods known to the person skilled in the art, for example by means of extruders, kneaders, roll mills, dynamic or static mixers.
- the preparation of the copolymers according to the invention can be carried out continuously or batchwise. Preferably, the preparation is carried out continuously.
- the siloxane copolymers prepared according to the invention can now be freed by any, hitherto known process from reactants which may still be present or from any solvents or catalysts used, for example by distillation or extraction.
- the components used in the process according to the invention are commercially available products or can be prepared by methods customary in chemistry.
- the components used in the process according to the invention may each be a type of such a component as well as a mixture of at least two types of a respective component.
- the process according to the invention has the advantage that it is simple to carry out and that many possible copolymers with great variability can be prepared. ,
- the process according to the invention has the advantage that copolymers can be prepared in a well-defined manner.
- copolymers of the formula (I) according to the invention or prepared according to the invention can be prepared and processed by the usual processing methods for moisture-crosslinkable polymers or thermoplastic elastomers, for example by means of extrusion, injection molding, blow molding, vacuum drawing. Processing as a solution or emulsion or suspension is also possible.
- Preferred applications of the copolymers of the formula (I) according to the invention or prepared according to the invention are uses as an ingredient in adhesives and sealants, as a base material for thermoplastic elastomers such as Lucasumhüllun ⁇ gene, hoses, gaskets, keyboard mats, for membranes, such as selectively gas-permeable membranes, as additives in polymer blends, or for coating applications, for example in non-stick coatings, tissue-compatible coatings, Flammge ⁇ inhibited coatings and as biocompatible materials.
- sealants and adhesives for example hot melt adhesives, adhesives to be applied as a solution, primers for improving the adhesion of sealants and adhesives to various substrates, additives for polymer processing, anti-fouling coatings, cosmetics, personal care products, Paint additives, auxiliary in detergents and textile processing, for modifying resins or for bitumen modification.
- copolymers according to the invention or those prepared according to the invention is conceivable in many applications, for example in sealants, adhesives, as a material for the modification of fibers, as a plastic additive, for example as an impact modifier or flame retardant, as a material for antifoam formulations, as a high-performance polymer ( Thermoplastic, thermoplastic elastomer, elastomer), as a packaging material for electronic components, in insulation or shielding materials, in cable sheathing, in antifouling materials, as an additive for cleaning, cleaning or care products, as an additive for personal care products, as a coating material for wood, paper and cardboard, as mold release agents, as biocompatible material in medical applications such as contact lenses, as a coating material for textile fibers or textile fabrics, as a coating material for natural materials such as leather and furs, as a material for membrane and as a material for photoactive systems, for example for lithographic Method, optical data backup or optical Nonethelesstra ⁇ supply.
- a plastic additive for example as an impact modifier or
- copolymers according to the invention can be used wherever previously also organopolysiloxane-polyurea copolymers were used.
- copolymers of the formula (I) according to the invention are suitable for use in crosslinkable compositions, such as, for example, compositions crosslinkable at room temperature.
- a further subject of the present invention are crosslinkable compositions comprising copolymers of the formula (I) according to the invention or prepared according to the invention.
- crosslinkable compositions according to the invention are preferably compositions crosslinkable by condensation reaction.
- crosslinkable compositions comprising (i) copolymer of the formula (I), if appropriate (ii) crosslinker, optionally
- crosslinkable compositions according to the invention are preferably one-component compositions.
- the components used in each case can be mixed with one another in any desired and hitherto known manner. This mixing preferably takes place at room temperature or at a temperature which occurs when the components are combined at room temperature without additional heating or cooling, and at the pressure of the surrounding atmosphere, ie about 900 to 1100 hPa However, mixing also takes place at higher or lower pressures, for example at low pressures to avoid gas inclusions.
- compositions according to the invention and their storage are preferably carried out under substantially anhydrous conditions in order to avoid premature reaction of the compositions.
- Crosslinkers (ii) are preferably organyloxysilanes and also their partial hydrolysates, such as tetraethoxysilane, tetraisopropoxysilane, tetra-n-propoxysilane, methyltrimethoxysilane, methyltriethoxysilane, n-butyltrimethoxysilane, n-octyltrimethoxysilane, i-octyltrimethoxysilane, vinyltrimethoxysilane and Vi - nyltriethoxysilane and their Generalhydrolysate, with methyl and vinyltrimethoxysilane are particularly preferred.
- crosslinkable compositions according to the invention contain crosslinkers (ii), these are amounts of preferably 0.05 to 10 parts by weight, more preferably 0.2 to 5 parts by weight, based in each case on 100 parts by weight of crosslinkable composition.
- catalysts (iii) it is possible to use all condensation catalysts known to the person skilled in the art.
- condensation catalysts (iii) are butyl titanates and organic tin compounds, such as di-n-butyltin dilaurate and di-n-butyltin diacetate, and also reaction products thereof with the alkoxysilanes called crosslinkers or adhesion promoters, dialkyltin oxide solutions in the crosslinkers or Adverber said alkoxysilanes, wherein di-n-butyltin dilaurate and dibutyltin oxide in tetraethoxysilane is preferred and di-n-butyl tin dilaurate is particularly preferred.
- organic tin compounds such as di-n-butyltin dilaurate and di-n-butyltin diacetate
- crosslinkable compositions according to the invention comprise catalyst (ii), these are amounts of preferably 0.01 to 3 parts by weight, preferably 0.05 to 2 parts by weight, in each case based on 100 parts by weight of crosslinkable composition.
- fillers (iv) all fillers can be used, which have also been used in crosslinkable compositions.
- fillers are reinforcing fillers, ie fillers having a BET surface area of at least 30 m 2 / g, such as, for example, carbon blacks, fumed silica, precipitated silica and silicon-aluminum mixed oxides, where the fillers mentioned may be hydrophobic and non-reinforcing fillers, ie fillers having a BET surface area of less than 30 m 2 / g, such as, for example, powders of quartz, cristobalite, diatomaceous earth, calcium silicate, zirconium silicate, montmorillonites, such as benzonites, zeolites, including molecular sieves, such as Natri ⁇ umumuminiumsilikat, metal oxides such as aluminum or zinc oxide or their mixed oxides, metal hydroxides such as aluminum hydroxide, barium sulfate, calcium carbonate, gypsum, silicon nitride, silicon carbide, boron nitride, glass, carbon and plastic
- Filler (iv) is preferably pyrogenic kiesiklaren or carbon blacks or mixtures thereof, with carbon black having a BET surface area of at least 30 m 2 / g is particularly preferred.
- compositions according to the invention contain fillers (iv), these are amounts of preferably 1 to 50 parts by weight, preferably 2 to 30 parts by weight, in each case based on 100 parts by weight of crosslinkable composition.
- adhesion promoters which have hitherto been used in compositions which can be crosslinked by condensation can be used as the adhesion promoter (v), if used.
- adhesion promoters (v) are silanes with hydrolyzable groups and SiC-bonded vinyl, acryloxy, methacryloxy, epoxy, Acid anhydride, acid, ester or ether groups and their partial and mixed hydrolysates.
- Preferred adhesion promoters (v) used are 3-aminopropyltriethoxysilane, 3- (2-aminoethyl) aminopropyltrimethoxysilane, 3-aminopropyltrimethoxysilane and 3- (2-aminoethyl) aminopropyltriethoxysilane, with 3-aminopropyltriethoxysilane being particularly preferred.
- compositions according to the invention contain adhesion promoters (v), these are amounts of preferably 0.01 to 5 parts by weight, preferably 0.5 to 4 parts by weight, in each case based on 100 parts by weight of crosslinkable composition.
- plasticizers such as trimethylsilyl-terminated polydimethylsiloxanes and hydrocarbons having about 16 to 30 carbon atoms
- stabilizers such as 2-ethylhexyl phosphate, octylphosphonic acid, polyethers, antioxidants, flame retardants, such as phosphoric acid esters, light stabilizers and Pigments, such as titanium dioxide, iron oxides.
- the optionally used further substances (vi) are preferably plasticizers, such as trimethylsilyl-terminated polydimethylsiloxanes and hydrocarbons having about 16 to 30 carbon atoms, stabilizers, such as 2-ethylhexyl phosphate, octylphosphonic acid, polyethers, flame retardants, such as phosphoric acid esters and pigments, such as titanium dioxide, iron oxides, with stabilizers and pigments being particularly preferred.
- plasticizers such as trimethylsilyl-terminated polydimethylsiloxanes and hydrocarbons having about 16 to 30 carbon atoms
- stabilizers such as 2-ethylhexyl phosphate, octylphosphonic acid, polyethers
- flame retardants such as phosphoric acid esters and pigments, such as titanium dioxide, iron oxides, with stabilizers and pigments being particularly preferred.
- crosslinkable compositions according to the invention can contain crosslinkable polymers (vii), such as organopolysiloxanes having reactive end groups.
- crosslinkable siloxanes are ⁇ , ⁇ -dihydroxypolydimethylsiloxanes and ⁇ , ⁇ -bis (dimethoxymethylsilyl) -terminated polydimethylsiloxanes.
- the component (vii) optionally used in the crosslinkable compositions according to the invention is preferably polydiorganosiloxanes having at least one OH group or a hydrolyzable group at the chain ends, more preferably polydimethylsiloxanes having at least one OH group or a hydrolyzable group at the chain ends, in particular ⁇ , ⁇ -dihydroxypolydimethylsiloxanes or ⁇ , ⁇ -bis (di-methoxymethylsilyl) terminated polydimethylsiloxanes having a viscosity of 100 to 500,000 mPas.
- the crosslinkable compositions according to the invention preferably contain component (vii). This component is preferably used to adjust the processing properties, such as viscosity or pot life.
- component (vii) are amounts of preferably 1 to 50 parts by weight, more preferably 2 to 25 parts by weight, in each case based on 100 parts by weight of crosslinkable composition.
- compositions according to the invention may in each case be one type of such constituent as well as a mixture of at least two different types of such constituents.
- compositions according to the invention contain no further constituents apart from component (i), if appropriate (ii), (iii), (iv), (v), (vi) and (vii).
- the preparation of the crosslinkable compositions according to the invention is carried out by methods which are known to the person skilled in the art, for example by means of extruders, kneaders, roll mills, dynamic or static mixers.
- the preparation of the compositions according to the invention can be carried out continuously or batchwise. Preferably, the preparation is carried out continuously.
- Vulcanizates of the compositions according to the invention are obtainable by hydrolysis and subsequent condensation of the resulting silanol groups.
- the hydrolysis can be effected by atmospheric moisture or by steam, water baths or aqueous solutions in contact with the copolymer according to the invention of general formula (I).
- the usual water content of the air is preferably sufficient.
- the crosslinking of the compositions according to the invention is preferably carried out at room temperature. It can, if desired, also at higher orene ⁇ ren temperatures than room temperature, such as at -5 to 15 ° C or at 30 to 50 0 C, for example, also by means of the normal water content of the air over increasing concentrations be carried out by water.
- the crosslinking is carried out at a pressure of 100 to 1100 hPa, in particular at the pressure of the surrounding atmosphere, that is about 900 to 1100 hPa.
- a further subject of the present invention are molded articles produced by crosslinking of the compositions according to the invention.
- the vulcanizates of the copolymers according to the invention have less dependence on the mechanical properties after moisture crosslinking
- the vulcanizates of the copolymers according to the invention no longer become plastic when the temperature is raised, ie they can no longer flow and are thus more dimensionally stable. Overall, the vulcanizates according to the invention thus have better mechanical properties over a wider temperature range, so that they can be used in more diverse fields of application.
- crosslinkable compositions according to the invention are preferably used as hotmelt adhesive, adhesive, PSA (pressure sensitive adhesive), sealant, coating for example paper, textile, fibers or silicate surfaces, impregnating agent, paint, component in composite materials, additive for polymers, molding and Component used for medical purposes as well as for use in automotive or laminated glass.
- PSA pressure sensitive adhesive
- sealant coating for example paper, textile, fibers or silicate surfaces, impregnating agent, paint, component in composite materials, additive for polymers, molding and Component used for medical purposes as well as for use in automotive or laminated glass.
- compositions of the invention have the advantage that they have all of the abovementioned advantages of the copolymers of the invention used.
- compositions of the invention have the advantage that they have very good mechanical properties.
- compositions according to the invention are the high thermal and oxidative stability, good resistance to swelling and decomposition by solvents containing hydrocarbons.
- the compositions of the invention have the advantage that the properties, such as, for example, peel and peel strength, printability, tensile and tear propagation resistance or water vapor permeability, can be set in a targeted manner.
- the shaped bodies according to the invention have the advantage that they have a lower dependence of the mechanical properties on the temperature, in particular at relatively high temperatures.
- the shaped bodies according to the invention furthermore have the advantage that they have a very good adhesion to substrates.
- all viscosity data refer to a temperature of 25 ° C. Unless indicated otherwise, the examples below are at a pressure of the surrounding atmosphere, ie at about 1000 hPa, and at room temperature, that is at about 23 0 C, or at a tur Tempera ⁇ that on combining the reactants at room temperature- setting temperature without additional heating or cooling, and at a relative humidity of about 50% fürge leads. Furthermore, all statements of parts and percentages, unless otherwise stated, are by weight.
- the Shore A hardness is determined according to DIN (German Industrial Standard) 53505 (March 2000 edition).
- example 1 20 g of an ⁇ , ⁇ -aminopropyl-terminated polydimethylsiloxane having a molecular weight of 2890 g / mol (13.8 mmol NH 2 ) and a Visko ⁇ sity of 50 mPas and 5.00 g of 3- (2-aminoethyl) aminopropyltri- methoxysilane (45 , 0 mmol NH) were dissolved in 40 g of tetrahydrofuran (THF) and, with exclusion of moisture, 5.89 g of di-cyclohexylmethane-4,4-diisocyanate (HMDI) (45.0 mmol of NCO) in 10 g of THF were added. The temperature rose to 32 ° C. On closing the mixture for 2 hours, was warmed to 50 0 C. After cooling, the solvent was removed by evaporation.
- HMDI di-cyclohexylmethane-4,4-diis
- thermoplastic material A clear, colorless thermoplastic material was obtained. From this material, a 2 mm thick plate was pressed in a press at 17O 0 C and punched therefrom mold S2 according to DIN 53504. The following mechanical properties were determined: hardness 63 Shore A, tensile strength 3.1 MPa, elongation at break 118%, stress at 100% elongation 2.83 MPa.
- Example 2 18.0 g of an ⁇ , ⁇ -aminopropyl-terminated polydimethylsiloxane having a molecular weight of 2890 g / mol (12.5 mmol NH 2 ) and a
- thermoplastic material A clear, colorless thermoplastic material was obtained. From this material, a 2 mm thick plate was pressed in a press at 170 0 C and from it test specimens of the form S2 punched in accordance with DIN 53504. The following mechanical properties were determined: hardness 62 Shore A, tensile strength 4.19 MPa, elongation at break 259%, stress at 100% elongation 2.50 MPa.
- Example 6 56 g of the product prepared in Example 4 are dissolved in 150 ml of tetrahydrofuran and treated with 0.2 g of aminoethylaminopropyltrimethoxysilane, 0.1 g of a tin condensation catalyst (obtained by reacting dibutyltin diacetate and tetraethoxysilane) and 0.1 g Octylphosphonic acid mixed. The solution is poured into a dish, the solvent evaporated and from the resulting film S2-test pieces are punched. Hardness in Shore A: 68, tensile strength: 4.25 MPa, elongation at break: 151%, stress value at 100% elongation: 3.17 MPa.
- test specimens have after 2 days of storage in water (25 0 C) the following values: Hardness in Shore A 68, tensile strength: 4.24 MPa, elongation at break: 154%, modulus at 100% elongation: 3.14 MPa.
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Abstract
The invention relates to cross-linkable organopolysiloxane polyurea copolymers of formula R'-[(A)a(B)b(C)c]-R'' (I), wherein (A) is a unit of formula (II) -[CO-NH-Z-NH-CO-ND-Y-Si(OR1)oR2-o-(O-SiR2) n-O-Si(OR1)oR2-o-Y-ND]-, (B) is a unit of formula -[CO-NH-Z-NH-CO-NR4-G-NR4]- (III) and (C) is a unit of formula -[CO-NH-Z-NH-CO-E-X-E]- (IV), wherein the radicals and indices have the meaning cited in Claim 1. The invention also relates to a method for the production of cross-linkable copolymers and to the use thereof, cross-linkable compositions containing the cross-linkable copolymers, the production of cross-linkable compositions, the vulcanization thereof and use of the vulcanized products.
Description
Vernetzbare Siloxan-Harnstoff-CopolymereCrosslinkable siloxane-urea copolymers
Die Erfindung betrifft vernetzbare Organopolysiloxan-Polyharn- stoff-Copolymere, ein Verfahren zur Herstellung der vernetzba- ren Organopolysiloxan-Polyharnstoff-Copolymeren sowie deren Verwendung, vernetzbare Zusammensetzungen enthaltend die ver¬ netzbaren Organopolysiloxan-Polyharnstoff-Copolymeren, die Her¬ stellung der vernetzbaren Zusammensetzungen, deren Vulkanisati¬ on sowie die Verwendung der Vulkanisate.The invention relates to crosslinkable organopolysiloxane-polyurea copolymers, to a process for preparing the crosslinkable organopolysiloxane-polyurea copolymers and to their use, to crosslinkable compositions containing the crosslinkable organopolysiloxane-polyurea copolymers, to the preparation of the crosslinkable compositions, their vulcanization and the use of vulcanizates.
Organopolysiloxan-Polyharnstoff-Blockcopolymere sind bekannt und werden durch Copolymerisation von mit Aminoalkylgruppen terminierten Siloxanen und Diisocyanaten hergestellt (Polymer, Bd. 25 (1984) , S. 1800 f.) .Organopolysiloxane-polyurea block copolymers are known and are prepared by copolymerization of aminoalkyl-terminated siloxanes and diisocyanates (Polymer, Vol. 25 (1984), p. 1800 f.).
Durch die Ausbildung von Wasserstoffbrücken zwischen den Harn¬ stoffgruppen können diese Copolymere thermoplastische Elastome¬ re sein. Somit sind derartige Copolymere oberhalb des Erwei¬ chungspunktes plastisch, während sie darunter elastische Eigen- Schäften haben. Damit können sie beispielsweise als Schmelzkle¬ ber verwendet werden. Nachteilig für die Verwendung derartiger Copolymere als Schmelzkleber ist jedoch, dass durch Temperatur¬ erhöhung über den Erweichungspunkt hinaus die Verklebung wieder reversibel ist. Zudem unterliegen Formkörper oder Verklebungen, die aus solchen Copolymeren hergestellt wurden, einem kalten Fluss, da sich Wasserstoffbrücken auch unterhalb des Erwei¬ chungspunktes ständig lösen und neu knüpfen können, so dass Verformungen und deshalb Versagen der gewünschten Funktion mög¬ lich sind. Damit ist der Einsatzbereich limitiert auf Anwendun- gen, bei denen keine erhöhten Temperaturen bzw. Kräfte auf das thermoplastische Elastomer einwirken.
Eine Lösung des Problems besteht darin, die einzelnen Polymer¬ ketten durch zusätzlich mit kovalenten, also thermisch nicht reversiblen, Bindungen zu vernetzen. Werden die thermoplasti¬ schen Elastomere in der Herstellung durch Verwendung von bei- spielsweise trifunktionellen Bausteinen vernetzt, so können die Verarbeitungseigenschaften (z.B. Schmelzeviskosität) negativ beeinflusst werden. Eine Vernetzung nach der Applikation ist deshalb sinnvoller.By forming hydrogen bonds between the urea groups, these copolymers can be thermoplastic elastomers. Thus, such copolymers are plastic above the softening point while having elastic properties below them. Thus they can be used for example as Schmelzkle¬ ber. However, a disadvantage of the use of such copolymers as hotmelt adhesives is that the temperature rise beyond the softening point causes the bond to be reversible again. In addition, moldings or adhesions produced from such copolymers are subject to a cold flow, since hydrogen bonds can constantly dissolve and re-bond even below the softening point, so that deformations and therefore failure of the desired function are possible. Thus, the field of application is limited to applications in which no elevated temperatures or forces act on the thermoplastic elastomer. One solution to the problem is to crosslink the individual polymer chains by additionally bonding with covalent, ie thermally non-reversible, bonds. If the thermoplastic elastomers are crosslinked during production by using, for example, trifunctional building blocks, the processing properties (eg melt viscosity) can be adversely affected. Networking after application is therefore more useful.
In EP 0 250 248 Bl, EP 0 822 952 Al und DE 101 13 980 Al werden beispielsweise mit feuchtigkeitsvernetzbaren Silylendgruppen versehene Organopolysiloxan-Polyharnstoff-Blockcopolymere be¬ schrieben. Dies ermöglicht eine Vernetzung nach der schmelz¬ flüssigen Applikation über diese Endgruppen. Die erreichbare Vernetzungsdichte ist allerdings besonders bei langkettigen Blockcopolymeren mit kleiner Endgruppenkonzentration gering, andererseits ist jedoch auch ein hoher Polymerisationsgrad der Blockcopolymere für die Ausbildung der thermoplastischen Eigen¬ schaften notwendig.EP 0 250 248 B1, EP 0 822 952 A1 and DE 101 13 980 A1 describe, for example, organopolysiloxane-polyurea block copolymers provided with moisture-crosslinkable silyl end groups. This allows crosslinking after the molten liquid application via these end groups. The achievable crosslinking density is low, however, especially in the long-chain block copolymers with small terminal group on the other hand is a high degree of polymerization and the block copolymer for forming the thermoplastic own ¬ properties necessary.
Gegenstand der Erfindung sind Copolymere der allgemeinen FormelThe invention relates to copolymers of the general formula
R'-[(A)a(B)b(C)c]-R" (I),R '- [(A) a (B) b (C) c ] -R "(I),
worinwherein
(A) gleich oder verschieden sein kann und eine Einheit der For¬ mel (II)(A) may be the same or different and a unit of formula (II)
-[CO-NH-Z-NH-CO-ND-Y-Si(OR1)oR2-o~(0-SiR2)n~O-Si(OR1)oR2-o-Y-ND]-,- [CO-NH-Z-NH-CO-ND-Y-Si (OR 1) o R 2-o ~ (0-SiR 2) n ~ O-Si (OR 1) o R 2 - o -Y ND] -,
(B) gleich oder verschieden sein kann und eine Einheit der For¬ mel
- [CO-NH-Z-NH-CO-NR4-G-NR4] - (III)(B) may be the same or different and is a unit of formula - [CO-NH-Z-NH-CO-NR 4 -G-NR 4 ] - (III)
undand
(C) gleich oder verschieden sein kann und eine Einheit der For¬ mel(C) may be the same or different and is a unit of formula
-[CO-NH-Z-NH-CO-E-X-E]- (IV)- [CO-NH-Z-NH-CO-E-X-E] - (IV)
darstellen, wobeirepresent, wherein
X gleich oder verschieden sein kann und einen gegebenenfalls durch Fluor, Chlor, d-C6-Alkyl- oder Ci-C6-Alkylester sub¬ stituierten Alkylenrest mit 1 bis 700 Kohlenstoffatomen bedeutet, in dem einander nicht benachbarte Methylenein¬ heiten durch Gruppen -0-, -COO-, -OCO- oder -OCOO- ersetzt sein können, oder gegebenenfalls substituierten Arylenrest mit 6 bis 22 Kohlenstoffatomen bedeutet,X may be identical or different and is an alkylene radical having 1 to 700 carbon atoms which is unsubstituted or substituted by fluorine, chlorine, C 1 -C 6 -alkyl or C 1 -C 6 -alkyl ester, in which non-adjacent methylene units are represented by groups. , -COO-, -OCO- or -OCOO- may be replaced, or optionally substituted arylene radical having 6 to 22 carbon atoms,
Y gleich oder verschieden sein kann und einen zweiwertigen Kohlenwasserstoffrest mit 1 bis 30 Kohlenstoffatomen, in dem einander nicht benachbarte Methyleneinheiten durch Gruppen -0- ersetzt sein können, oder den Rest - (CH2) 3-NH- SiR2- (CH2) 3-NH- darstellt,Y may be identical or different and is a divalent hydrocarbon radical having 1 to 30 carbon atoms, in which non-adjacent methylene units may be replaced by groups -O-, or the radical - (CH 2 ) 3 -NH- SiR 2 - (CH 2 ) 3 -NH- represents,
Z gleich oder verschieden sein kann und einen zweiwertigen, gegebenenfalls durch Fluor oder Chlor substituierten Koh¬ lenwasserstoffrest mit 1 bis 30 Kohlenstoffatomen bedeu¬ tet, D gleich oder verschieden sein kann und Wasserstoffatom oder einen einwertigen, gegebenenfalls substituierten Kohlen- wasserstoffrest darstellt,Z may be identical or different and is a divalent hydrocarbon radical optionally substituted by fluorine or chlorine and having 1 to 30 carbon atoms, D may be identical or different and represents hydrogen atom or a monovalent, optionally substituted hydrocarbon radical,
E gleich oder verschieden sein kann und ein Sauerstoffatom oder eine Aminogruppe -ND- darstellt,
R gleich oder verschieden sein kann und einen einwertigen, gegebenenfalls durch Fluor oder Chlor substituierten Koh¬ lenwasserstoffrest mit 1 bis 20 Kohlenstoffatomen bedeu¬ tet, R1 gleich oder verschieden sein kann und Wasserstoffatom oder einen einwertigen, gegebenenfalls durch Fluor, Chlor oder Organyloxygruppen substituierten Kohlenwasserstoffrest mit 1 bis 20 Kohlenstoffatomen, -(C=O)-R oder -N=CR2 darstellt,E may be the same or different and represents an oxygen atom or an amino group -ND-, R may be identical or different and a monovalent, optionally substituted by fluorine or chlorine Koh¬ hydrocarbon radical having 1 to 20 carbon atoms meaning tet, R 1 may be identical or different and hydrogen or a monovalent, optionally substituted by fluorine, chlorine or organyloxy groups hydrocarbon radical with 1 to 20 carbon atoms, represents - (C = O) -R or -N = CR 2 ,
R4 gleich oder verschieden sein kann und einen Rest der For- mel -Z λ-SiRp (OR1) 3_p mit ZΛ gleich einer für Z oben angege¬ benen Bedeutung und p gleich 0, 1 oder 2, Wasserstoffatom oder einen einwertigen, gegebenenfalls substituierten Koh¬ lenwasserstoffrest bedeutet,R 4 may be the same or different and are a radical of the research mel -Z λ SiR p (OR 1) 3 _ p with Z Λ equal to a top angege¬ for Z surrounded meaning and p is 0, 1 or 2, hydrogen atom or denotes a monovalent, optionally substituted hydrocarbon radical,
G gleich oder verschieden sein kann und eine für Z angegebe- ne Bedeutung hat,G may be the same or different and has a meaning given for Z,
R' ' Wasserstoffatom oder einen Rest -CO-NH-Z-NCO, bevorzugt Wasserstoffatom, bedeutet,R '' is hydrogen or a radical -CO-NH-Z-NCO, preferably hydrogen atom,
R' im Fall von R' ' gleich Wasserstoffatom einen RestR 'in the case of R' 'is hydrogen, a radical
HND-Y-Si (OR1) 0R2-0- (0-SiR2)n-O-Si (OR1) OR2-O-Y-ND-, HNR4-G-NR4- oder HE-X-E-, bevorzugtHND-Y-Si (OR 1) R 2 0 - 0 - (0-SiR 2) n O-Si (OR 1) 2 O R - O -Y-ND-, HNR 4 -G-NR 4 - or HE XE-, preferred
HND-Y-Si (OR1) oR2-o- (0-SiR2) n-0-Si (OR1) OR2-O-Y-ND- oder HNR4-G-NR4-, bedeutet und im Fall von R' ' gleich Rest -CO-NH-Z-NCO die Bedeutung von Rest OCN-Z-NH-CO-ND-Y-Si (OR1) 0R2-0- (0-SiR2) n-0-Si (OR1) OR2_O-Y-ND-, OCN-Z-NH-CO-NR4-G-NR4- oder OCN-Z-NH-CO-E-X-E-, bevorzugt OCN-Z-NH-CO-ND-Y-Si (OR1) 0R2-0- (0-SiR2)n-0-Si (OR1) OR2_O-Y-ND- oder OCN-Z-NH-CO-NR4-G-NR4-, hat, n gleich oder verschieden sein kann und eine ganze Zahl von 1 bis 4000 ist, o gleich oder verschieden sein kann und 0, 1 oder 2, bevor¬ zugt 0, ist, a eine ganze Zahl von mindestens 1 ist,
b eine ganze Zahl von mindestens 1 ist, c 0 oder eine ganze Zahl von mindestens 1 ist, mit der Maßgabe, dass pro Molekül mindestens ein Rest R4 die Bedeutung von -Z Λ-SiRp(OR1) 3-p hat sowie die einzelnen Blöcke (A), (B) und (C) im Polymer statistisch verteilt sein können.HND-Y-Si (OR 1 ) oR 2 -o ( O -SiR 2 ) n -O-Si (OR 1 ) O R 2 - O -Y-ND or HNR 4 -G-NR 4 -, means and in the case of R ", the radical -CO-NH-Z-NCO is the meaning of the radical OCN-Z-NH-CO-ND-Y-Si (OR 1 ) 0R 2 O- (O-SiR 2 ) n - 0-Si (oR 1) 2 O R O _ -Y-ND-, OCN-Z-NH-CO-NR 4 -G-NR 4 - or OCN-Z-NH-CO-EXE, preferably OCN-Z -NH-CO-ND-Y-Si (oR 1) 0R2-0- (0-SiR 2) n -0-Si (oR 1) 2 O R O _ -Y-ND or OCN-Z-NH- CO-NR 4 -G-NR 4 -, n may be the same or different and is an integer from 1 to 4000, o may be the same or different and 0, 1 or 2, preferably 0, is a is an integer of at least 1, b is an integer of at least 1, c is 0 or an integer of at least 1, with the proviso that per molecule at least one radical R 4 has the meaning of -Z Λ -SiR p (OR 1 ) 3 - p and the individual blocks (A), (B) and (C) may be randomly distributed in the polymer.
Im Rahmen der vorliegenden Erfindung sollen von dem Begriff Or- ganopolysiloxane sowohl polymere, oligomere wie auch dimere Si- loxane mitumfasst werden.In the context of the present invention, the term organopolysiloxanes is intended to encompass both polymeric, oligomeric and dimeric siloxanes.
Beispiele für zweiwertige Reste Z sind Alkylenreste, wie der Methylen-, Ethylen-, n-Propylen-, iso-Propylen-, n-Butylen-, iso-Butylen-, tert.-Butylen-, n-Pentylen-, iso-Pentylen-, neo- Pentylen-, tert.-Pentylenrest, Hexylenreste, wie der n-Hexylen- rest, Heptylenreste, wie der n-Heptylenrest, Octylenreste, wie der n-Octylenrest und iso-Octylenreste, wie der 2,2,4-Trime- thylpentylenrest, Nonylenreste, wie der n-Nonylenrest, Decy- lenreste, wie der n-Decylenrest, Dodecylenreste, wie der n-Do- decylenrest; Alkenylenreste, wie der Vinylen- und der Allylen- rest; Cycloalkylenreste, wie Cyclopentylen-, Cyclohexylen-, Cy- cloheptylenreste und Methylcyclohexylenreste; Arylenreste, wie der Phenylen- und der Naphthylenrest; Alkarylenreste, wie o-, m-, p-Tolylenreste, Xylylenreste und Ethylphenylenreste; Aral- kylenreste, wie der Benzylenrest, der α- und der ß-Phenylethy- lenrest sowie der 4, 4' -Methylendiphenylenrest.Examples of divalent radicals Z are alkylene radicals, such as the methylene, ethylene, n-propylene, iso-propylene, n-butylene, iso-butylene, tert-butylene, n-pentylene, iso-pentylene -, neo-pentylene, tert-pentylene radical, hexylene radicals, such as the n-hexylene radical, heptylene radicals, such as the n-heptylene radical, octylene radicals, such as the n-octylene radical and iso-octylene radicals, such as 2,2,4- Trimethylpentylene radical, nonylene radicals, such as the n-nonyl radical, decyl radicals, such as the n-decylene radical, dodecylene radicals, such as the n-dodecylene radical; Alkenylene radicals, such as the vinylene and allylene radicals; Cycloalkylene radicals, such as cyclopentylene, cyclohexylene, cycloheptylene radicals and methylcyclohexylene radicals; Arylene radicals, such as the phenylene and the naphthylene radical; Alkarylene radicals, such as o-, m-, p-tolylene radicals, xylylene radicals and ethylphenylene radicals; Aralkylene radicals, such as the benzylene radical, the α- and the ß-Phenylethy- lenrest and the 4, 4 '-Methylendiphenylenrest.
Bevorzugt handelt es sich bei Rest Z um Alkylengruppen mit 1 bis 24 Kohlenstoffatomen, besonders bevorzugt um Hexylen-, 4, 4 '-Methylen-biscyclohexylen- und 3-Methylen-3, 5, 5-trimethyl- cyclohexylenrest.
Beispiele für die zweiwertigen Reste G sind die für Z aufge¬ führten Beispiele. Bevorzugt handelt es sich bei Rest G um Al- kylenreste mit 1 bis 6 Kohlenstoffatomen, Arylenresten wie der o-, m-, oder p-Phenylenrest und Aralkylenreste wie der Phe- nethylenrest, wobei Rest -CH2CH2- besonders bevorzugt ist.Radical Z is preferably alkylene groups having 1 to 24 carbon atoms, more preferably hexylene, 4, 4'-methylene-biscyclohexylene and 3-methylene-3, 5, 5-trimethylcyclohexylene. Examples of the divalent radicals G are the examples listed for Z. Radicals G are preferably alkylene radicals having 1 to 6 carbon atoms, arylene radicals, such as the o-, m- or p-phenylene radical, and aralkylene radicals, such as the phenylene radical, with the radical -CH 2 CH 2 - being particularly preferred.
Beispiele für ZΛ sind alle für Z angegebenen Beispiele. Bevor¬ zugt handelt es sich bei Rest Z λ um Alkylengruppen mit 1 bis 24 Kohlenstoffatomen, besonders bevorzugt um Alkylengruppen mit 1 oder 3 Kohlenstoffatomen.Examples of Z Λ are all examples given for Z. Bevor¬ Trains t is radical Z λ alkylene groups having 1 to 24 carbon atoms, more preferably alkylene groups having 1 or 3 carbon atoms.
Beispiele für Y sind alle für Z angegebenen Beispiele. Bei Rest Y handelt es sich bevorzugt um Alkylenreste mit 1 bis 30 Koh¬ lenstoffatomen, in dem einander nicht benachbarte Methylenein- heiten durch Gruppen -0- ersetzt sein können, oder um Arylen- reste mit 6 bis 22 Kohlenstoffatomen. Besonders bevorzugt han¬ delt es sich bei Rest Y um Alkylengruppen mit 1 bis 3 Kohlen¬ stoffatomen, insbesondere um Alkylengruppen mit 1 oder 3 Koh¬ lenstoffatomen.Examples of Y are all examples given for Z. The radicals Y are preferably alkylene radicals having 1 to 30 carbon atoms, in which non-adjacent methylene units may be replaced by groups -O-, or arylene radicals having 6 to 22 carbon atoms. Particularly preferably, radical Y is alkylene groups having 1 to 3 carbon atoms, in particular alkylene groups having 1 or 3 carbon atoms.
Beispiele für Rest X sind der Butylenrest, Ethylenrest, Hexy- lenrest, - (CH2) 3- (O-CH (CH3) -CH2) 2-3000-O- (CH2) 3-, -CH (CH3) -CH2- (O- CH (CH3) -CH2) 2-3000-, -(CH2) 3- (0-CH2-CH2) 2-300-O- (CH2) 3- und -CH2-CH2-Examples of radical X are the butylene radical, ethylene radical, hexylene radical, - (CH 2 ) 3- (O-CH (CH 3 ) -CH 2 ) 2-3000-O- (CH 2 ) 3, -CH (CH 3 ) -CH 2 - (O-CH (CH 3 ) -CH 2 ) 2-3000-, - (CH 2 ) 3- (O-CH 2 -CH 2 ) 2-300-O- (CH 2 ) 3 and -CH 2 -CH 2 -
(OCH2-CH2) 2-300-•(OCH 2 -CH 2 ) 2-300- •
Bei Rest X handelt es sich bevorzugt um Polyetherreste, beson¬ ders bevorzugt um Polypropylenglykolreste, insbesondere um sol¬ che mit 2 bis 600 Kohlenstoffatomen.The radicals X are preferably polyether radicals, more preferably polypropyleneglycol radicals, in particular those having 2 to 600 carbon atoms.
Beispiele für Rest R sind Alkylreste, wie der Methyl-, Ethyl-, n-Propyl-, iso-Propyl-, n-Butyl-, iso-Butyl-, tert.-Butyl-, n- Pentyl-, iso-Pentyl-, neo-Pentyl-, tert.-Pentylrest, Hexylres- te, wie der n-Hexylrest, Heptylreste, wie der n-Heptylrest, Oc-
tylreste, wie der n-Octylrest und iso-Octylreste, wie der 2,2, 4-Trimethylpentylrest, Nonylreste, wie der n-Nonylrest, De- cylreste, wie der n-Decylrest, Dodecylreste, wie der n-Dodecyl- rest; Alkenylreste, wie der Vinyl- und der Allylrest; Cycloal- kylreste, wie Cyclopentyl-, Cyclohexyl-, Cycloheptylreste und Methylcyclohexylreste; Arylreste, wie der Phenyl- und der Naphthylrest; Alkarylreste, wie o-, m-, p-Tolylreste, Xylyl- reste und Ethylphenylreste; Aralkylreste, wie der Benzylrest, der α- und der ß-Phenylethylrest.Examples of radical R are alkyl radicals, such as the methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, tert-butyl, n-pentyl, isopentyl, , neo-pentyl, tert-pentyl, hexyl, such as the n-hexyl, heptyl, such as the n-heptyl, Oc- tyl radicals, such as the n-octyl radical and iso-octyl radicals, such as the 2,2, 4-trimethylpentyl radical, nonyl radicals, such as the n-nonyl radical, decyl radicals, such as the n-decyl radical, dodecyl radicals, such as the n-dodecyl radical; Alkenyl radicals, such as the vinyl and allyl radicals; Cycloalkyl radicals, such as cyclopentyl, cyclohexyl, cycloheptyl radicals and methylcyclohexyl radicals; Aryl radicals, such as the phenyl and the naphthyl radical; Alkaryl radicals, such as o-, m-, p-tolyl radicals, xylyl radicals and ethylphenyl radicals; Aralkyl radicals, such as the benzyl radical, the α- and the ß-phenylethyl radical.
Bevorzugt handelt es sich bei Rest R um einen Kohlenwasser¬ stoffrest mit 1 bis 6 Kohlenstoffatomen, besonders bevorzugt um einen Alkylrest mit 1 bis 4 Kohlenstoffatomen, insbesondere um den Methylrest.Radical R is preferably a hydrocarbon radical having 1 to 6 carbon atoms, more preferably an alkyl radical having 1 to 4 carbon atoms, in particular the methyl radical.
Beispiele für Rest R1 sind die für Rest R angegebene Beispiele sowie Alkoxyalkylreste.Examples of radical R 1 are the examples given for radical R and alkoxyalkyl radicals.
Bevorzugt handelt es sich bei Rest R1 um lineare oder verzweig- te Alkylreste mit 1 bis 12 Kohlenstoffatomen und Alkoxyalkyl¬ reste wie der 2-Methoxyethyl-, 2-Ethoxyethyl- und 2- (2'Methoxy- ethyl) ethylrest, besonders bevorzugt um Alkylreste mit 1 bis 12 Kohlenstoffatomen, insbesondere um den Methyl- und Ethyl¬ rest.Radicals R 1 are preferably linear or branched alkyl radicals having 1 to 12 carbon atoms and alkoxyalkyl radicals such as 2-methoxyethyl, 2-ethoxyethyl and 2- (2'-methoxyethyl) ethyl, particularly preferably Alkyl radicals having 1 to 12 carbon atoms, in particular the methyl and Ethyl¬ rest.
Beispiele für Rest R4 sind die für R angegebenen Reste, Wasser¬ stoffatom sowie die Reste - (CH2) 4Si (OCH3) 3,Examples of radical R 4 are the radicals specified for R, hydrogen atom and the radicals - (CH 2 ) 4 Si (OCH 3 ) 3 ,
- (CH2CH(CH3)CH2) Si (OCH3) 3, - (CH2CH(CH3)CH2) Si (OCH2CH3) 3,- (CH 2 CH (CH 3 ) CH 2 ) Si (OCH 3 ) 3 , - (CH 2 CH (CH 3 ) CH 2 ) Si (OCH 2 CH 3 ) 3 ,
- (CH2CH (CH3) CH2) SiCH3 (OCH3) 2, - (CH2CH (CH3) CH2) SiCH3 (OCH2CH3) 3, - (CH2) 3Si (OCH3) 3/ -(CH2) 3Si(OCH2CH3) 3, - (CH2) 3SiCH3 (OCH3) 2,- (CH 2 CH (CH 3 ) CH 2 ) SiCH 3 (OCH 3 ) 2 , - (CH 2 CH (CH 3 ) CH 2 ) SiCH 3 (OCH 2 CH 3 ) 3 , - (CH 2 ) 3 Si ( OCH 3 ) 3 / - (CH 2 ) 3 Si (OCH 2 CH 3 ) 3 , - (CH 2 ) 3 SiCH 3 (OCH 3 ) 2 ,
-(CH2) 3SiCH3 (OCH2CHs)2, -CH2Si(OCH3)S, -CH2Si (OCH2CH3) 3,- (CH 2 ) 3 SiCH 3 (OCH 2 CHs) 2 , -CH 2 Si (OCH 3 ) S , -CH 2 Si (OCH 2 CH 3 ) 3 ,
-CH2SiCH3 (OCH3) 2, -CH2SiCH3 (OCH3) 2, - (CH2) 3SiCH3 (OCH2CH2OCH3) 2 und-CH 2 SiCH 3 (OCH 3 ) 2 , -CH 2 SiCH 3 (OCH 3 ) 2 , - (CH 2 ) 3 SiCH 3 (OCH 2 CH 2 OCH 3 ) 2 and
-C6H4- (CH2)2SiCH3 (OCH2CH3) 2.
Bevorzugt handelt es sich bei Rest R4 um Wasserstoffatom und die zuvor angegebenen silylsubstituierten Alkylreste, besonders bevorzugt um Wasserstoffatom und die Reste - (CH2) 3Si (OCH3) 3, -(CH2) 3Si(OCH2CH3) 3, -(CH2) 3SiCH3 (OCH3) 2, -(CH2) 3SiCH3 (OCH2CH3) 2, -CH2Si (OCH3) 3, -CH2Si (OCH2CH3) 3, -CH2SiCH3 (OCH3) 2 sowie -CH2SiCH3 (OCH3) 2.-C 6 H 4 - (CH 2 ) 2 SiCH 3 (OCH 2 CH 3 ) 2 . Radical R 4 is preferably hydrogen atom and the above-mentioned silyl-substituted alkyl radicals, more preferably hydrogen and the radicals - (CH 2 ) 3 Si (OCH 3 ) 3 , - (CH 2 ) 3 Si (OCH 2 CH 3 ) 3 , - (CH 2 ) 3 SiCH 3 (OCH 3 ) 2, - (CH 2 ) 3 SiCH 3 (OCH 2 CH 3 ) 2, -CH 2 Si (OCH 3 ) 3 , -CH 2 Si (OCH 2 CH 3 ) 3 , -CH 2 SiCH 3 (OCH 3 ) 2 and -CH 2 SiCH 3 (OCH 3 ) 2 .
Beispiele für Kohlenwasserstoffreste D sind die für R oben an- gegebenen Reste.Examples of hydrocarbon radicals D are the radicals given for R above.
Bei Rest D handelt es sich bevorzugt um einen Alkylrest oder Wasserstoffatom, besonders bevorzugt um einen Alkylrest mit 1 bis 12 Kohlenstoffatomen oder Wasserstoffatom, insbesondere um Wasserstoffatom.The radical D is preferably an alkyl radical or hydrogen atom, particularly preferably an alkyl radical having 1 to 12 carbon atoms or hydrogen atom, in particular hydrogen atom.
Bei Rest E handelt es sich bevorzugt um Sauerstoffatom.The radical E is preferably an oxygen atom.
Bevorzugt hat a die Bedeutung einer ganzen Zahl von 1 bis 1000, besonders bevorzugt von 5 bis 1000, insbesondere 5 bis 100.A preferably has the meaning of an integer from 1 to 1000, particularly preferably from 5 to 1000, in particular from 5 to 100.
Bevorzugt hat b die Bedeutung einer ganzen Zahl von 1 bis 1000, besonders bevorzugt von 5 bis 1000, insbesondere 5 bis 100.B preferably has the meaning of an integer from 1 to 1000, particularly preferably from 5 to 1000, in particular from 5 to 100.
Bevorzugt hat c die Bedeutung von 0 oder einer ganzen Zahl von 1 bis 100, besonders bevorzugt von 0 bis 10, insbesondere 0.C preferably has the meaning of 0 or an integer from 1 to 100, particularly preferably from 0 to 10, in particular 0.
Beispiele für Reste R' sind, für den Fall dass R' ' gleich Was¬ serstoffatom ist, Reste, die sich von den nicht umgesetzten Endgruppen aus den eingesetzten Edukten ergeben, wie H2N- (CH2) 3-Si (CH3) 2- (O-Si (CH3) 2) 40-O-Si (CH3) 2- (CH2) 3-NH-, H2N-CH2-CH2-N- (CH2) 3Si (OCH3) 3,
und HO- (CH2CH (CH3) O) 50- .Examples of radicals R 'are, in the case that R "is the same hydrogen atom, radicals which result from the unreacted end groups from the educts used, such as H 2 N- (CH 2 ) 3-Si (CH 3 ) 2- (O-Si (CH 3 ) 2 ) 40 -O-Si (CH 3 ) 2 - (CH 2 ) 3 -NH-, H 2 N-CH 2 -CH 2 -N- (CH 2 ) 3 Si (OCH 3 ) 3 , and HO- (CH 2 CH (CH 3 ) O) 50 -.
Beispiele für Reste R' sind, für den Fall dass R' ' gleich -CO-NH-Z-NCO ist, Reste, die sich von den nicht umgesetzten Endgruppen aus den eingesetzten Edukten ergeben, wieExamples of radicals R 'are, in the case that R "' is -CO-NH-Z-NCO, radicals which result from the unreacted end groups from the educts used, such as
OCN- (CH2) 6-NH-CO-HN- (CH2) 3-Si (CH3) 2- (O-Si (CH3) 2) 40~O-Si (CH3) 2- (CH2) 3-NH-, OCN-C6HIO-CH2-C6HIO-NH-CO-HN-CH2-CH2-N- (CH2) 3Si (OCH3) 3,OCN- (CH 2 ) 6 -NH-CO-HN- (CH 2 ) 3 -Si (CH 3 ) 2 - (O-Si (CH 3 ) 2 ) 40 -O-Si (CH 3 ) 2 - (CH 2 ) 3 -NH-, OCN-C 6 H IO -CH 2 -C 6 H IO -NH-CO-HN-CH 2 -CH 2 -N- (CH 2 ) 3 Si (OCH 3 ) 3 ,
und OCN-C6H3 (CH3) -NH-CO-O- (CH2CH(CH3) O) 50-.and OCN-C 6 H 3 (CH 3) -NH-CO-O- (CH 2 CH (CH 3) O) 50 -.
Beispiele für Reste R'' sind Wasserstoffatom, -CO-NH- (CH2) 6-NCO, -CO-NH-C6HIO-CH2-C6HIO-NCO und -CO-NH-C6H3 (CH3) -NCO.Examples of radicals R '' are hydrogen atom, -CO-NH- (CH 2) 6 -NCO, -CO-NH-C 6 H IO -CH 2 -C 6 H IO -NCO, and -CO-NH-C 6 H 3 (CH 3 ) -NCO.
Bevorzugt ist n eine ganze Zahl von 10 bis 4000, besonders be- vorzugt 30 bis 1000.N is preferably an integer from 10 to 4000, more preferably from 30 to 1000.
Index p ist bevorzugt 0.Index p is preferably 0.
Erfindungsgemäße Copolymere enthaltend Einheiten (C) können ein härteres Material ergeben im Vergleich zu erfindungsgemäßen Co- polymeren, die keine Einheit (C) enthalten, da in ihnen mehr Wasserstoffbrücken vorliegen. Wird der Anteil an Komponente (C) zu hoch, treten Entmischungserscheinungen zwischen den organi¬ schen und Polysiloxan-Bestandteilen auf, so dass die Transpa- renz der erfindungsgemäßen Copolymere reduziert wird und die Copolymere trüb werden. Bevorzugt sind Polymere der Formel (I) mit c gleich Null, da somit ausschließlich Siloxanketten vor¬ liegen und dadurch die Polymere Vorteile, wie beispielsweise hohe Transparenz und ÜV-Stabilität bei gleichzeitig niedrigen Oberflächenenergien, aufweisen.Copolymers of the invention comprising units (C) can give a harder material compared to copolymers according to the invention which contain no unit (C), since there are more hydrogen bonds in them. If the proportion of component (C) is too high, segregation phenomena occur between the organic and polysiloxane constituents, so that the transparency of the copolymers according to the invention is reduced and the copolymers become cloudy. Preference is given to polymers of the formula (I) where c is zero, since thus exclusively siloxane chains are present and thus the polymers have advantages such as, for example, high transparency and UV stability with simultaneously low surface energies.
Beispiele für Copolymere der Formel (I) sind
H [NH (CH2) 3SiMe2O (SiMe2O) 35SiMe2 (CH2) 3-NH-CO-NH- (CH2) 6-NH-CO-NH- CH2CH2-N{ (CH2) 3-S1 (OMe) 3} -CO-NH- (CH2) 6-NH-CO]10- NH (CH2) 3SiMe2O (SiMe2O) 35SiMe2 (CH2) 3-NH2,Examples of copolymers of the formula (I) are H [NH (CH 2 ) 3 SiMe 2 O (SiMe 2 O) 35 SiMe 2 (CH 2 ) 3 -NH-CO-NH- (CH 2 ) 6 -NH-CO-NH-CH 2 CH 2 -N { (CH 2 ) 3 -S1 (OMe) 3 } -CO-NH- (CH 2 ) 6 -NH-CO] 10 -NH (CH 2 ) 3 SiMe 2 O (SiMe 2 O) 35 SiMe 2 (CH 2 ) 3 -NH 2 ,
H [NH (CH2) 3Si (OMe) 20 (SiMe2O) 35Si (OMe) 2 (CH2) 3-NH-CO-NH- (CH2) 6-NH-CO- NH-CH2CH2-N{ (CH2) 3-SiMe (OMe) 2} -CO-NH- (CH2) 6-NH-CO] 10- NH (CH2) 3SiMe2O (SiMe2O) 35SiMe2 (CH2) 3-NH2,H [NH (CH 2 ) 3 Si (OMe) 2 O (SiMe 2 O) 35 Si (OMe) 2 (CH 2 ) 3 -NH-CO-NH- (CH 2 ) 6 -NH-CO-NH-CH 2 CH 2 -N {(CH 2 ) 3 -SiMe (OMe) 2 } -CO-NH- (CH 2 ) 6 -NH-CO] 10 -NH (CH 2 ) 3 SiMe 2 O (SiMe 2 O) 35 SiMe 2 (CH 2 ) 3 -NH 2 ,
H [ [NH (CH2) 3SiMe2O (SiMe2O) 35SiMe2 (CH2) 3-NH-CO-NH- (CH2) 6-NH-CO-] 5- [NH-CH2CH2-N{ (CH2) 3-Si (OEt) 3} -CO-NH- (CH2) 6-NH-CO] 5] I0-NH-CH2CH2- N{ (CH2)3-Si(OEt)3}H,H [[NH (CH 2 ) 3 SiMe 2 O (SiMe 2 O) 35 SiMe 2 (CH 2 ) 3 -NH-CO-NH- (CH 2 ) 6 -NH-CO-] 5 - [NH-CH 2 CH 2 -N {(CH 2) 3 -Si (OEt) 3} -CO-NH- (CH 2) 6 -NH-CO] 5] I0 -NH-CH 2 CH 2 - N {(CH 2) 3 -Si (OEt) 3 H,
H [NH (CH2) 3SiMe2O (SiMe2O) 35SiMe2 (CH2) 3-NH-CO-NH- (CH2) 6-NH-CO-NH- CH2CH2-Ni (CH2) 3-Si (OMe)3J-CO-NH- (CH2) 6-NH-CO-O- (CH2CH2O)5-CO-NH- (CH2) 6-NH-CO] I0-NH (CH2) 3SiMe2O (SiMe2O) 35SiMe2 (CH2) 3-NH2,H [NH (CH 2 ) 3 SiMe 2 O (SiMe 2 O) 35 SiMe 2 (CH 2 ) 3 -NH-CO-NH- (CH 2 ) 6 -NH-CO-NH-CH 2 CH 2 -Ni ( CH 2 ) 3 -Si (OMe) 3 J-CO-NH- (CH 2 ) 6 -NH-CO-O- (CH 2 CH 2 O) 5 -CO-NH- (CH 2 ) 6 -NH-CO ] I0 -NH (CH 2) 3 SiMe 2 O (SiMe 2 O) 35 SiMe 2 (CH 2) 3 -NH 2,
H [NH-CH2-SiMe2O (SiMe2O) 35SiMe2-CH2-NH-CO-NH- (CH2) 6-NH-CO-NH-CH2CH2- N{ (CH2) 3-Si (OMe) 3} -CO-NH- (CH2) 6-NH-CO-NH- (CH2CH2O) 5-CH2CH2-NH-CO- NH- (CH2) 6-NH-CO] I0-CH2-SiMe2O (SiMe2O) 35SiMe2-CH2-NH2,H [NH-CH 2 -SiMe 2 O (SiMe 2 O) 35 SiMe 2 -CH 2 -NH-CO-NH- (CH 2 ) 6 -NH-CO-NH-CH 2 CH 2 -N {(CH 2 ) 3 -Si (OMe) 3 } -CO-NH- (CH 2 ) 6 -NH-CO-NH- (CH 2 CH 2 O) 5 -CH 2 CH 2 -NH-CO-NH- (CH 2 ) 6 -NH-CO] 10 -CH 2 -SiMe 2 O (SiMe 2 O) 35 SiMe 2 -CH 2 -NH 2 ,
H [NH (CH2) 3SiMe2O (SiMe2O) 35SiMe2 (CH2) 3-NH-CO-NH-C1OH20-NH-CO-NH-H [NH (CH 2) 3 SiMe 2 O (SiMe 2 O) 35 SiMe 2 (CH 2) 3 -NH-CO-NH-C 1O H 20 -NH-CO-NH-
CH2CH2-NiCH2-SiMe(OEt)2J-CO-NH-C10H20-NH-CO]Io-CH 2 CH 2 -NiCH 2 -SiMe (OEt) 2 J-CO-NH-C 10 H 20 -NH-CO] -
NH (CH2) 3SiMe2O (SiMe2O) 35SiMe2 (CH2) 3-NH2,NH (CH 2 ) 3 SiMe 2 O (SiMe 2 O) 35 SiMe 2 (CH 2 ) 3-NH 2 ,
OCN-C7H6-NH-CO- [NH (CH2) 3SiMe2O (SiMe2O) 35SiMe2 (CH2) 3-NH-CO-NH-C7H6- NH-CO-NH-CH2CH2-Ni (CH2) 3-Si (OMe) 3} -CO-NH-C7H6-NH-CO] xo- NH (CH2) 3SiMe2O (SiMe2O) 35SiMe2 (CH2) 3-NH-CO-NH-C7H6-NCO undOCN-C 7 H 6 -NH-CO- [NH (CH 2 ) 3 SiMe 2 O (SiMe 2 O) 35 SiMe 2 (CH 2 ) 3 -NH-CO-NH-C 7 H 6 -NH-CO- NH-CH 2 CH 2 -Ni (CH 2 ) 3 -Si (OMe) 3 } -CO-NH-C 7 H 6 -NH-CO] xo - NH (CH 2 ) 3 SiMe 2 O (SiMe 2 O) 35 SiMe 2 (CH 2 ) 3 -NH-CO-NH-C 7 H 6 -NCO and
OCN-C7H6-NH-CO- [NH (CH2) 3SiMe2O (SiMe2O) 35SiMe2 (CH2) 3-NH-CO-NH-C7H6- NH-CO-NH-CH2CH2-Ni (CH2) 3-Si (OMe) 3} -CO-NH-C7H6-NH-CO] 10-NH-CH2CH2- N{ (CH2) 3-Si (OMe) 3} -CO-NH-C7H6-NCO.
Die erfindungsgemäßen Copolymere der Formel (I) haben einen Ge¬ halt an Einheiten A der Formel (II) von bevorzugt größer 70 Gew.-%, besonders bevorzugt größer 80 Gew.-%, jeweils bezogen auf das Gesamtgewicht des Copolymers .OCN-C 7 H 6 -NH-CO- [NH (CH 2) 3 SiMe 2 O (SiMe 2 O) 35 SiMe 2 (CH 2) 3-NH-CO-NH-C 7 H 6 - NH-CO- NH-CH 2 CH 2 -Ni (CH 2 ) 3 -Si (OMe) 3 } -CO-NH-C 7 H 6 -NH-CO] 10 -NH-CH 2 CH 2 -N {(CH 2 ) 3 -Si (OMe) 3 } -CO-NH-C 7 H 6 -NCO. The copolymers of the formula (I) according to the invention have a content of units A of the formula (II) of preferably greater than 70% by weight, particularly preferably greater than 80% by weight, in each case based on the total weight of the copolymer.
Die erfindungsgemäßen Copolymere der Formel (I) sind bei Raum¬ temperatur bevorzugt gummielastische Festkörper mit Zugfestig¬ keiten zwischen vorzugsweise etwa 0,5 und 20 MPa sowie Reißdeh¬ nungen zwischen bevorzugt etwa 50 bis 1000%. Sie erweichen bei Temperaturen zwischen bevorzugt 60 und 2000C und verlieren da¬ bei ihre gummielastischen Eigenschaften. Durch Einwirkung von Feuchtigkeit können die hydrolysierbaren Reste OR1 zu OH-Grup- pen reagieren, die ihrerseits wiederum mit weiteren OR1- oder OH-Gruppen unter Bildung von Siloxanbindungen kondensieren kön- nen. Diese so zusätzlich vernetzten erfindungsgemäßen Polymere der Formel (I) haben gegenüber dem Ausgangspolymer vor der Ver¬ netzung bevorzugt einen deutlich zu höheren Temperaturen ver¬ schobenen Erweichungspunkt. Damit eröffnet sich die Möglich¬ keit, Polymere herzustellen, die bei relativ niedrigen Tempera- turen verarbeitet werden können, dann aber beim Gebrauch den¬ noch höheren Temperaturen ausgesetzt werden können.The copolymers of the formula (I) according to the invention are preferably rubber-elastic solids at room temperature with tensile strengths between preferably about 0.5 and 20 MPa and ultimate elongations between preferably about 50 to 1000%. They soften at temperatures between preferably 60 and 200 0 C and lose da¬ at their rubber-elastic properties. As a result of the action of moisture, the hydrolyzable radicals OR 1 can react to form OH groups, which in turn can condense with further OR 1 or OH groups to form siloxane bonds. These polymers additionally crosslinked according to the invention of the formula (I) preferably have a softening point which is significantly higher than the starting polymer before crosslinking. This opens up the possibility of producing polymers which can be processed at relatively low temperatures, but then can be exposed to even higher temperatures during use.
Die erfindungsgemäßen Copolymere haben weiterhin den Vorteil, dass sie sehr gute mechanische Eigenschaften aufweisen ohne dass Füllstoffe zugegeben werden müssen.The copolymers according to the invention also have the advantage that they have very good mechanical properties without having to add fillers.
Weiterhin zeichnen sich die erfindungsgemäßen Copolymere durch hervorragende physikalische Eigenschaften aus, wie sie von Po- lyorganosiloxanen bekannt sind, wie beispielsweise niedrige Glasübergangstemperaturen, Transparenz, gute Beständigkeit ge¬ genüber UV-Licht, geringe Oberflächenenergien, niedrige Hydro- phobizität, gute dielektrische Eigenschaften und hohe Permeabi¬ lität gegenüber Gasen.
Weitere Vorteile der erfindungsgemäßen Copolymere sind die hohe thermische und oxidative Beständigkeit, gute Beständigkeiten gegenüber Quellung und Zersetzung durch Kohlenwasserstoffe ent- haltende Lösemitteln.Furthermore, the copolymers according to the invention are distinguished by outstanding physical properties, as known from polyorganosiloxanes, such as low glass transition temperatures, transparency, good resistance to UV light, low surface energies, low hydrophobicity, good dielectric properties and high Permeability to gases. Further advantages of the copolymers according to the invention are the high thermal and oxidative stability, good resistance to swelling and decomposition by solvents containing hydrocarbons.
Je nach der Anzahl der Einheiten (C) in den erfindungsgemäßen Copolymeren können die Eigenschaften, wie beispielsweise Schäl- und Ablösefestigkeit, Bedruckbarkeit, Zug- und Durchreißfestig- keit oder Wasserdampfdurchlässigkeit, gezielt eingestellt wer¬ den.Depending on the number of units (C) in the copolymers according to the invention, the properties, such as, for example, peel and peel strength, printability, tensile and break-through strength or water vapor permeability, can be set in a targeted manner.
Die Herstellung der erfindungsgemäßen Copolymere kann analog beliebiger Verfahren erfolgen, die dem Fachmann bereits bekannt sind und beispielsweise zur Synthese von (Prä)polymeren für Po¬ lyurethane eingesetzt werden, erfolgen.The copolymers according to the invention can be prepared analogously to any desired processes which are already known to the person skilled in the art and are used, for example, for the synthesis of (prep) polymers for polyurethanes.
Ein weiterer Gegenstand der vorliegenden Erfindung ist ein Ver¬ fahren zur Herstellung der erfindungsgemäßen Copolymere der Formel (I) durch Umsetzung vonA further subject of the present invention is a process for the preparation of the copolymers of the formula (I) according to the invention by reacting
a) mindestens einem Polymer der Formela) at least one polymer of the formula
H-ND-Y-Si(OR1)0R2-0- (0-SiR2)n"O-Si(OR1)0R2-0-Y-ND-H (V) ,H-ND-Y-Si (OR 1) 0 R2 0 - (0-SiR 2) n "O-Si (OR 1) R 2 0 - 0 -Y-ND-H (V)
b) mindestens einer Verbindung der Formelb) at least one compound of the formula
H-NR4-G-NR4-H (VI)H-NR 4 -G-NR 4 -H (VI)
c) mindestens einem Diisocyanat der Formelc) at least one diisocyanate of the formula
OCN-Z-NCO (VII)
oder blockierten Diisocyanaten (thermisch instabile Umsetzungs¬ produkten von Isocyanaten mit zum Beispiel Phenolen, Ketoximen, Malonestern, stickstoffhaltigen Heterocyclen) ,OCN-Z-NCO (VII) or blocked diisocyanates (thermally unstable reaction products of isocyanates with, for example, phenols, ketoximes, malonic esters, nitrogen-containing heterocycles),
d) gegebenenfalls Verbindungen der Formeld) optionally compounds of the formula
H-E-X-E-H (VIII) ,H-E-X-E-H (VIII),
e) gegebenenfalls einem Katalysator unde) optionally a catalyst and
f) gegebenenfalls mindestens einem Lösemittel, wobei X, Y, Z, D, E, G, R, R1, R4, und o die oben genannte Be¬ deutung aufweisen.f) optionally at least one solvent, wherein X, Y, Z, D, E, G, R, R 1 , R 4 , and o have the abovementioned Be¬ interpretation.
Beispiele der erfindungsgemäß eingesetzten Verbindungen derExamples of the compounds used according to the invention
Formel (V) sind α,ω-aminopropyldimethylsilylterminierte Polydi- methylsiloxane, α,ω-aminopropyldimethoxysilylterminierte Polydi- methylsiloxane, α,ω-aminomethyldimethylsilylterminierte Polydi- methylsiloxane und α,ω-aminomethyldimethoxysilylterminierte Po- lydimethylsiloxane .Formula (V) are α, ω-aminopropyldimethylsilyl-terminated polydimethylsiloxanes, α, ω-aminopropyldimethoxysilyl-terminated polydimethylsiloxanes, α, ω-aminomethyldimethylsilyl-terminated polydimethylsiloxanes and α, ω-aminomethyldimethoxysilyl-terminated polydimethylsiloxanes.
Bevorzugte Verbindungen der Formel (VI) , die im erfindungsgemä¬ ßen Verfahren eingesetzt werden, sind 3- (2-Aminoethyl) aminopro- pyltrimethoxysilan, 3- (2-Aminoethyl) aminopropyltriethoxysilan, 3- (2-Aminoethyl) aminopropylmethyldimethoxysilan, 3- (2-Amino- ethyl) aminopropyldimethylmethoxysilan 3- (2-Aminoethyl) aminopro- pylmethyldiethoxysilan, N,N' -Bis- (3-trimethoxysilylpropyl) -e- thylendiamin, N,N'-Bis- (3-triethoxysilylpropyl) ethylendiamin, N,N' -Bis- (3-dimethoxymethylsilylpropyl) ethylendiamin und N,N'- Bis- (3-diethoxymethylsilylpropyl) ethylendiamin, N-Trimethoxy- silylmethylethylendiamin, N-Triethoxysilylmethylethylendiamin, N-Dimethoxymethylsilylmethylethylendiamin, N-Diethoxymethyl-
silylmethylethylendiamin und N-Methoxydimethylsilylmethyl- ethylendiamin.Preferred compounds of the formula (VI) which are used in the process according to the invention are 3- (2-aminoethyl) aminopropyltrimethoxysilane, 3- (2-aminoethyl) aminopropyltriethoxysilane, 3- (2-aminoethyl) aminopropylmethyldimethoxysilane, 3- 2-aminoethyl) aminopropyldimethylmethoxysilane 3- (2-Aminoethyl) aminopropylmethyldiethoxysilane, N, N'-bis (3-trimethoxysilylpropyl) -ethylenediamine, N, N'-bis (3-triethoxysilylpropyl) ethylenediamine, N , N'-bis (3-dimethoxymethylsilylpropyl) ethylenediamine and N, N'-bis (3-diethoxymethylsilylpropyl) ethylenediamine, N-trimethoxysilylmethylethylenediamine, N-triethoxysilylmethylethylenediamine, N-dimethoxymethylsilylmethylethylenediamine, N-diethoxymethyl silylmethylethylenediamine and N-methoxydimethylsilylmethylethylenediamine.
Beispiele der erfindungsgemäß eingesetzten Isocyanate der For- mel (VII) sind Hexylendiisocyanat, 4, 4' -Methylendicyclohexylen- diisocyanat, 4, 4' -Methylendiphenylendiisocyanat, 1,3-Diazeti- dine-2, 4-dion-bis (4,4' -methylendicyclohexyl) diisocyanat, 1,3- Diazetidine-2, 4-dion-bis (4,4'-methylendiphenyl) diisocyanat, Tetramethylenxylylendiisocyanat und Isophorondiisocyanat, wobei Hexylendiisocyanat, 4, 4' -Methylendicyclohexylendiisocyanat,Examples of the isocyanates of the formula (VII) used according to the invention are hexylene diisocyanate, 4,4'-methylenedicyclohexylene diisocyanate, 4,4'-methylenediphenylene diisocyanate, 1,3-diazetidine-2,4-dione bis (4,4 '-methylenedicyclohexyl) diisocyanate, 1,3-diazetidine-2,4-dione bis (4,4'-methylenediphenyl) diisocyanate, tetramethylenexylylene diisocyanate and isophorone diisocyanate, wherein hexylene diisocyanate, 4, 4' -methylenedicyclohexylene diisocyanate,
4,4'-Methylendiphenylendiisocyanat, Tetramethylenxylylendiiso- cyanat und Isophorondiisocyanat bevorzugt sowie Hexylendiisocy¬ anat, 4, 4' -Methylendicyclohexylendiisocyanat und Isophorondii¬ socyanat besonders bevorzugt sind.4,4'-methylenediphenylene diisocyanate, tetramethylenexylylene diisocyanate and isophorone diisocyanate are preferred, and hexylene diisocyanate, 4,4'-methylenedicyclohexylene diisocyanate and isophorone diisocyanate are particularly preferred.
Beispiele der erfindungsgemäß eingesetzten Verbindungen der Formel (VIII) sindaus der Polyurethanchemie bekannte Verbindun¬ gen wie Diole wie z.B. Ethylenglycol, Polyethylenglycole, Po- lypropylenglycole, Polyesterpolyole, Diamine wie z.B. Ethylen- diamin, 5-Amino-3- (aminomethyl) -1, 3, 3-trimethylcyclohexan) ,Examples of the compounds of the formula (VIII) used according to the invention are compounds known from polyurethane chemistry, such as diols, e.g. Ethylene glycol, polyethylene glycols, polypropyleneglycols, polyesterpolyols, diamines such as e.g. Ethylenediamine, 5-amino-3- (aminomethyl) -1,3,3-trimethylcyclohexane),
Bis (4-amino-3-methylphenyl)methane, Isomerengemisch des Diami- nodiethylmethylbenzols, Bis (4-amino-3-chlorphenyl)methan, 2- Methylpropyl-4-chlor-3, 5-diaminobenzoat, und aminoterminierte Polyether (ATPE) .Bis (4-amino-3-methylphenyl) methane, isomeric mixture of diaminoethylbenzylmethylbenzene, bis (4-amino-3-chlorophenyl) methane, 2-methylpropyl-4-chloro-3,5-diaminobenzoate, and amino-terminated polyethers (ATPE) ,
Die Stöchiometrie der Reaktanden zur Herstellung der erfin¬ dungsgemäßen Copolymere wird vorzugsweise derart gewählt, dass das molare Verhältnis der Isocyanatgruppen aus den Verbindungen der Formel (VII) zur Summe der mit den Isocyanatgruppen reakti- ven EH- und NH-Gruppen aus den Verbindungen der Formeln (V) ,The stoichiometry of the reactants for the preparation of the copolymers according to the invention is preferably selected such that the molar ratio of the isocyanate groups from the compounds of the formula (VII) to the sum of the isocyanate-reactive EH and NH groups from the compounds of the formulas (V),
(VI) und (VIII) im Bereich von bevorzugt 0,7 bis 1,3, besonders bevorzugt 0,95 bis 1,05, insbesondere bei 1, liegt. Bei einem Verhältnis der Isocyanatgruppen zu den reaktiven Gruppen von
größer 1, also einem Überschuss an Isocyanatgruppen, ergeben sich erfindungsgemäße Polymere der Formel (I) mit R''= NH-CO-Z- NCO und den sich daraus ergebenden Resten R' wie oben definiert am anderen Ende der Polymerketten. Bei einem Verhältnis kleiner 1, also einem Unterschuss an Isocyanatgruppen, ergeben sich er¬ findungsgemäße Polymere der Formel (I) mit R' ' =H und den sich daraus ergebenden Resten R' wie oben definiert am anderen Ende der Polymerketten.(VI) and (VIII) is in the range of preferably 0.7 to 1.3, particularly preferably 0.95 to 1.05, in particular 1. At a ratio of the isocyanate groups to the reactive groups of greater than 1, ie an excess of isocyanate groups, polymers of the formula (I) according to the invention with R "= NH-CO-Z-NCO and the resulting radicals R 'as defined above result at the other end of the polymer chains. At a ratio of less than 1, ie a deficit in isocyanate groups, the polymers of the formula (I) according to the invention with R "= H and the resulting radicals R 'as defined above are obtained at the other end of the polymer chains.
Beispiele für die gegebenenfalls eingesetzten Katalysatoren sind alle bisher bekannten Katalysatoren, welche die Addition der Isocyanatgruppen der Verbindungen der allgemeinen Formeln (VII) an die aktiven Gruppen der Polymere gemäß den Formeln (V) , (VI) und (VIII) fördern, wie etwa Diorganozinnverbindungen und Bismutverbindungen.Examples of the optionally used catalysts are all previously known catalysts which promote the addition of the isocyanate groups of the compounds of the general formulas (VII) to the active groups of the polymers of the formulas (V), (VI) and (VIII), such as diorganotin compounds and bismuth compounds.
Besonders bevorzugt werden bei dem erfindungsgemäßen Verfahren keine Katalysatoren eingesetzt.With particular preference, no catalysts are used in the process according to the invention.
Falls im erfindungsgemäßen Verfahren Katalysatoren eingesetzt werden, handelt es sich um Mengen von vorzugsweise 0,0001 bis 1 Gewichtsteile, besonders bevorzugt 0,001 bis 0,1 Gewichtsteile, jeweils bezogen auf 100 Gewichtsteile der Gesamtmischung.If catalysts are used in the process according to the invention, these are amounts of preferably 0.0001 to 1 part by weight, particularly preferably 0.001 to 0.1 part by weight, in each case based on 100 parts by weight of the total mixture.
Beispiele für die im erfindungsgemäßen Verfahren gegebenenfalls eingesetzten Lösungsmittel sind Tetrahydrofuran, Dimethylforma- mid, Isopropanol und Methylethylketon.Examples of the solvents optionally used in the process according to the invention are tetrahydrofuran, dimethylformamide, isopropanol and methyl ethyl ketone.
Besonders bevorzugt werden bei dem erfindungsgemäßen Verfahren keine Lösungsmittel eingesetzt.With particular preference, no solvents are used in the process according to the invention.
Falls im erfindungsgemäßen Verfahren Lösungsmittel eingesetzt wird, handelt es sich um Mengen von vorzugsweise 10 bis 200 Ge-
wichtsteile, besonders bevorzugt 10 bis 100 Gewichtsteile, je¬ weils bezogen auf 100 Gewichtsteile Gesamtmischung.If solvents are used in the process according to the invention, these are amounts of preferably from 10 to 200% by weight. parts by weight, particularly preferably 10 to 100 parts by weight, in each case based on 100 parts by weight of the total mixture.
Die erfindungsgemäße Umsetzung kann in Lösung oder in Substanz erfolgen, wobei eine Umsetzung in Substanz bevorzugt ist.The reaction according to the invention can be carried out in solution or in substance, a reaction in substance being preferred.
Falls die erfindungsgemäße Umsetzung in Lösung erfolgt, sind Temperaturen von 0 bis 1000C bevorzugt und von 20 bis 8O0C be¬ sonders bevorzugt.If the reaction of the invention takes place in solution, temperatures are preferably from 0 to 100 0 C and be¬ from 20 to 8O 0 C Sonders preferred.
Falls die erfindungsgemäße Umsetzung in Substanz erfolgt, sind Temperaturen oberhalb des Erweichungspunkts des herge¬ stellten Copolymers der Formel (I) bevorzugt.If the reaction according to the invention takes place in substance, temperatures above the softening point of the copolymer of the formula (I) prepared are preferred.
Das erfindungsgemäße Verfahren wird im Falle einer diskontinu¬ ierlichen Arbeitsweise bevorzugt bei einem Druck der umgebenden Atmosphäre, also zwischen 900 und 1100 hPa, durchgeführt. Bei kontinuierlicher Herstellung, z.B. in einem Doppelschneckenex¬ truder, wird bei einem Druck von bevorzugt bis zu 15 MPa in ei- nigen Abschnitten des Extruders und zur Entgasung bei Drücken von bevorzugt 0,1 bis 1100 hPa gearbeitet.In the case of a discontinuous procedure, the process according to the invention is preferably carried out at a pressure of the surrounding atmosphere, ie between 900 and 1100 hPa. In continuous production, e.g. in a twin-screw extruder, the mixture is operated at a pressure of preferably up to 15 MPa in some sections of the extruder and for degassing at pressures of preferably 0.1 to 1100 hPa.
Das erfindungsgemäße Verfahren wird bevorzugt unter Ausschluss von Feuchtigkeit durchgeführt, es ist aber auch möglich bei An- Wesenheit von Wasser zu arbeiten.The process according to the invention is preferably carried out with the exclusion of moisture, but it is also possible to work with the presence of water.
Die Herstellung der erfindungsgemäßen Copolymeren gemäß der allgemeinen Formel (I) kann mit Methoden erfolgen, die dem Fachmann bekannt sind, wie beispielsweise mittels Extrudern, Knetern, Walzenstühlen, dynamischem oder statischen Mischern. Die Herstellung der erfindungsgemäßen Copolymere kann kontinu¬ ierlich oder diskontinuierlich erfolgen. Bevorzugt erfolgt die Herstellung kontinuierlich.
Die erfindungsgemäß hergestellten Siloxan-Copolymere können nun nach beliebigen, bisher bekannten Verfahren von gegebenenfalls noch vorhandenen Edukten bzw. gegebenenfalls eingesetzten Lö- sungsmitteln bzw. Katalysatoren befreit werden, wie z.B. durch Destillation oder Extraktion.The preparation of the copolymers according to the invention of the general formula (I) can be carried out by methods known to the person skilled in the art, for example by means of extruders, kneaders, roll mills, dynamic or static mixers. The preparation of the copolymers according to the invention can be carried out continuously or batchwise. Preferably, the preparation is carried out continuously. The siloxane copolymers prepared according to the invention can now be freed by any, hitherto known process from reactants which may still be present or from any solvents or catalysts used, for example by distillation or extraction.
Die im erfindungsgemäßen Verfahren eingesetzten Komponenten sind handelsübliche Produkte bzw. können nach in der Chemie gängigen Methoden hergestellt werden.The components used in the process according to the invention are commercially available products or can be prepared by methods customary in chemistry.
Bei den im erfindungsgemäßen Verfahren eingesetzten Komponenten kann es sich jeweils um eine Art einer solchen Komponente wie auch um ein Gemisch aus mindestens zwei Arten einer jeweiligen Komponente handeln.The components used in the process according to the invention may each be a type of such a component as well as a mixture of at least two types of a respective component.
Das erfindungsgemäße Verfahren hat den Vorteil, dass es einfach in der Durchführung ist und viele mögliche Copolymere mit gro¬ ßer Variabilität hergestellt werden können. .The process according to the invention has the advantage that it is simple to carry out and that many possible copolymers with great variability can be prepared. ,
Des Weiteren hat das erfindungsgemäße Verfahren den Vorteil, dass Copolymere wohldefiniert hergestellt werden können.Furthermore, the process according to the invention has the advantage that copolymers can be prepared in a well-defined manner.
Die erfindungsgemäßen bzw. erfindungsgemäß hergestellten Copo- lymere der Formel (I) können mit den üblichen Verarbeitungsme¬ thoden für feuchtigkeitsvernetzbare Polymere bzw. thermoplasti¬ sche Elastomere hergestellt und verarbeitet werden, beispiels¬ weise mittels Extrusion, Spritzguss, Blasverformung, Vakuum¬ tiefziehen. Eine Verarbeitung als Lösung oder Emulsion bzw. Suspension ist ebenfalls möglich.The copolymers of the formula (I) according to the invention or prepared according to the invention can be prepared and processed by the usual processing methods for moisture-crosslinkable polymers or thermoplastic elastomers, for example by means of extrusion, injection molding, blow molding, vacuum drawing. Processing as a solution or emulsion or suspension is also possible.
Bevorzugte Anwendungen der erfindungsgemäßen bzw. erfindungsge¬ mäß hergestellten Copolymere der Formel (I) sind Verwendungen
als Bestandteil in Kleb- und Dichtstoffen, als Basisstoff für thermoplastische Elastomere wie beispielsweise Kabelumhüllun¬ gen, Schläuche, Dichtungen, Tastaturmatten, für Membranen, wie selektiv gasdurchlässige Membranen, als Zusatzstoffe in PoIy- merblends, oder für Beschichtungsanwendungen beispielsweise in Antihaftbeschichtungen, gewebeverträglichen Überzügen, flammge¬ hemmten Überzügen und als biokompatible Materialien. Weitere Anwendungsmöglichkeiten sind Dicht- und Klebstoffe wie zum Bei¬ spiel Schmelzkleber, als Lösung zu applizierende Klebstoffe, Primer zur Verbesserung der Haftung von Dicht- und Klebstoffen auf verschiedenen Untergründen, Additive für die Polymerverar¬ beitung, anti-fouling Überzüge, Kosmetika, Körperpflegemittel, Lackadditive, Hilfsstoff in Waschmitteln und Textilbearbeitung, zum Modifizieren von Harzen oder zur Bitumenmodifizierung.Preferred applications of the copolymers of the formula (I) according to the invention or prepared according to the invention are uses as an ingredient in adhesives and sealants, as a base material for thermoplastic elastomers such as Kabelumhüllun¬ gene, hoses, gaskets, keyboard mats, for membranes, such as selectively gas-permeable membranes, as additives in polymer blends, or for coating applications, for example in non-stick coatings, tissue-compatible coatings, Flammge¬ inhibited coatings and as biocompatible materials. Other possible applications include sealants and adhesives, for example hot melt adhesives, adhesives to be applied as a solution, primers for improving the adhesion of sealants and adhesives to various substrates, additives for polymer processing, anti-fouling coatings, cosmetics, personal care products, Paint additives, auxiliary in detergents and textile processing, for modifying resins or for bitumen modification.
Der Einsatz der erfindungsgemäßen bzw. erfindungsgemäß herge¬ stellten Copolymere ist in vielen Anwendungen denkbar, wie bei¬ spielsweise in Dichtmassen, Klebstoffen, als Material für die Modifizierung von Fasern, als Kunststoffadditiv beispielsweise als Schlagzähverbesserer oder Flammschutzmittel, als Material für Entschäumerformulierungen, als Hochleistungspolymer (Ther¬ moplast, thermoplastisches Elastomer, Elastomer) , als Verpa¬ ckungsmaterial für elektronische Bauteile, in Isolations- oder Abschirmungsmaterialien, in Kabelummantelungen, in Antifouling- materialien, als Additiv für Putz-, Reinigungs- oder Pflegemit¬ tel, als Additiv für Körperpflegemittel, als Beschichtungsmate- rial für Holz, Papier und Pappe, als Formentrennmittel, als biokompatibles Material in medizinischen Anwendungen wie Kon¬ taktlinsen, als Beschichtungsmaterial für Textilfasern oder textile Gewebe, als Beschichtungsmaterial für Naturstoffe wie z.B. Leder und Pelze, als Material für Membranen und als Mate¬ rial für photoaktive Systeme beispielsweise für lithographische
Verfahren, optische Datensicherung oder optische Datenübertra¬ gung.The use of the copolymers according to the invention or those prepared according to the invention is conceivable in many applications, for example in sealants, adhesives, as a material for the modification of fibers, as a plastic additive, for example as an impact modifier or flame retardant, as a material for antifoam formulations, as a high-performance polymer ( Thermoplastic, thermoplastic elastomer, elastomer), as a packaging material for electronic components, in insulation or shielding materials, in cable sheathing, in antifouling materials, as an additive for cleaning, cleaning or care products, as an additive for personal care products, as a coating material for wood, paper and cardboard, as mold release agents, as biocompatible material in medical applications such as contact lenses, as a coating material for textile fibers or textile fabrics, as a coating material for natural materials such as leather and furs, as a material for membrane and as a material for photoactive systems, for example for lithographic Method, optical data backup or optical Datenübertra¬ supply.
Weiterhin bevorzugt ist die Verwendung der erfindungsgemäßen Copolymere als Trenn-Beschichtung für Klebebänder und Etiket¬ ten, Faserbeschichtung für beispielsweise Textilien, Extrusi- onshilfsmittel für Thermoplastverarbeitung, medizinische Arti¬ kel, wie beispielsweise Katheter, Infusionsbeutel oder -schlau¬ che, Schmelzkleber, PSA-Beschichtungen, überstreichbare und ü- berlackierbare Bauteile für die Automobilindustrie, Additiv für die Polymermodifizierung, wie beispielsweise Weichmacher oder Schlagzähmodifier, Folie für laminiertes Sicherheitsglas oder Fugendichtmasse für die Bauindustrie.Preference is furthermore given to using the copolymers according to the invention as a release coating for adhesive tapes and labels, fiber coating for, for example, textiles, extrusion aids for thermoplastics processing, medical articles, such as catheters, infusion bags or bags, hot melt adhesives, PSA adhesives. Coatings, overpaintable and recoatable components for the automotive industry, additive for polymer modification, such as plasticizers or impact modifiers, film for laminated safety glass or joint sealant for the construction industry.
Die erfindungsgemäßen Copolymere können überall dort eingesetzt werden, wo auch bisher Organopolysiloxan-Polyharnstoff-Copoly- mere eingesetzt wurden.The copolymers according to the invention can be used wherever previously also organopolysiloxane-polyurea copolymers were used.
Insbesondere eignen sich die erfindungsgemäßen hergestellten Copolymere der Formel (I) zur Verwendung in vernetzbaren Zusam¬ mensetzungen, wie etwa bei Raumtemperatur vernetzbaren Zusam¬ mensetzungen.In particular, the copolymers of the formula (I) according to the invention are suitable for use in crosslinkable compositions, such as, for example, compositions crosslinkable at room temperature.
Ein weiterer Gegenstand der vorliegenden Erfindung sind ver- netzbare Massen enthaltend erfindungsgemäße bzw. erfindungsge¬ mäß hergestellte Copolymere der Formel (I) .A further subject of the present invention are crosslinkable compositions comprising copolymers of the formula (I) according to the invention or prepared according to the invention.
Bevorzugt handelt es sich bei den erfindungsgemäßen vernetzba¬ ren Massen um durch Kondensationsreaktion vernetzbare Massen.The crosslinkable compositions according to the invention are preferably compositions crosslinkable by condensation reaction.
Besonders bevorzugt sind vernetzbare Massen enthaltend (i) Copolymer der Formel (I) , gegebenenfalls
(ii) Vernetzer, gegebenenfallsParticular preference is given to crosslinkable compositions comprising (i) copolymer of the formula (I), if appropriate (ii) crosslinker, optionally
(iii) Katalysator, gegebenenfalls (iv) Füllstoff, gegebenenfalls(iii) Catalyst, optionally (iv) filler, optionally
(v) Haftvermittler, gegebenenfalls(v) adhesion promoter, if appropriate
(vi) weitere Stoffe ausgewählt aus der Gruppe enthaltend Weichmacher, Stabilisatoren, Antioxidantien, Flammschutzmittel, Lichtschutzmittel und Pigmente, und gegebenenfalls(vi) other substances selected from the group consisting of plasticizers, stabilizers, antioxidants, flame retardants, light stabilizers and pigments, and optionally
(vii) vernetzbare Polymere, die unterschiedlich sind zu (i) .(vii) crosslinkable polymers other than (i).
Bei diesen erfindungsgemäßen vernetzbaren Massen handelt es sich bevorzugt um Einkomponentenmassen. Zur Bereitung dieser Einkomponentenmassen können die jeweils eingesetzten Bestand¬ teile auf beliebige und bisher bekannte Weise miteinander ver¬ mischt werden. Dieses Vermischen erfolgt bevorzugt bei Raumtem- peratur bzw. bei einer Temperatur, die sich beim Zusammengeben der Bestandteile bei Raumtemperatur ohne zusätzliche Heizung oder Kühlung einstellt, und dem Druck der umgebenden Atmosphä¬ re, also etwa 900 bis 1100 hPa. Falls erwünscht, kann dieses Vermischen aber auch bei höheren oder niedrigen Drücken erfol- gen, beispielsweise bei niedrigen Drücken zur Vermeidung von Gaseinschlüssen.These crosslinkable compositions according to the invention are preferably one-component compositions. To prepare these one-component masses, the components used in each case can be mixed with one another in any desired and hitherto known manner. This mixing preferably takes place at room temperature or at a temperature which occurs when the components are combined at room temperature without additional heating or cooling, and at the pressure of the surrounding atmosphere, ie about 900 to 1100 hPa However, mixing also takes place at higher or lower pressures, for example at low pressures to avoid gas inclusions.
Die Herstellung der erfindungsgemäßen Massen und deren Lagerung erfolgen vorzugsweise unter im Wesentlichen wasserfreien Bedin- gungen, um ein vorzeitiges Reagieren der Massen zu vermeiden.The preparation of the compositions according to the invention and their storage are preferably carried out under substantially anhydrous conditions in order to avoid premature reaction of the compositions.
Als gegebenenfalls eingesetzte Vernetzer (ii) können alle Ver¬ netzer eingesetzt werden, die auch bisher in durch Kondensation
vernetzbaren Massen eingesetzt worden sind. Bevorzugt handelt es sich bei Vernetzer (ii) um Organyloxysilane sowie deren Teilhydrolysate, wie beispielsweise Tetraethoxysilan, Tetra- isopropoxysilan, Tetra-n-propoxysilan, Methyltrimethoxysilan, Methyltriethoxysilan, n-Butyltrimethoxysilan, n-Octyltrimeth- oxysilan, i-Octyltrimethoxysilan, Vinyltrimethoxysilan und Vi- nyltriethoxysilan sowie deren Teilhydrolysate, wobei Methyl- und Vinyltrimethoxysilan besonders bevorzugt sind.As crosslinkers (ii) optionally used, it is possible to use all crosslinkers which have hitherto also been used in condensation crosslinkable compositions have been used. Crosslinkers (ii) are preferably organyloxysilanes and also their partial hydrolysates, such as tetraethoxysilane, tetraisopropoxysilane, tetra-n-propoxysilane, methyltrimethoxysilane, methyltriethoxysilane, n-butyltrimethoxysilane, n-octyltrimethoxysilane, i-octyltrimethoxysilane, vinyltrimethoxysilane and Vi - nyltriethoxysilane and their Teilhydrolysate, with methyl and vinyltrimethoxysilane are particularly preferred.
Falls die erfindungsgemäßen vernetzbaren Massen Vernetzer (ii) enthalten, handelt es sich um Mengen von vorzugsweise 0,05 bis 10 Gewichtsteilen, besonders bevorzugt 0,2 bis 5 Gewichtteilen, jeweils bezogen auf 100 Gewichtsteile vernetzbare Masse.If the crosslinkable compositions according to the invention contain crosslinkers (ii), these are amounts of preferably 0.05 to 10 parts by weight, more preferably 0.2 to 5 parts by weight, based in each case on 100 parts by weight of crosslinkable composition.
Als gegebenenfalls eingesetzte Katalysatoren (iii) können alle dem Fachmann bekannten Kondensationskatalysatoren verwendet werden.As optionally used catalysts (iii), it is possible to use all condensation catalysts known to the person skilled in the art.
Beispiele für Kondensationskatalysatoren (iii) sind Butyltita- nate und organische Zinnverbindungen, wie Di-n-butylzinndilau- rat und Di-n-butylzinndiacetat sowie dessen Umsetzungsprodukte mit den als Vernetzer bzw. Haftvermittler genannten Alkoxysila- nen, Dialkylzinnoxidlösungen in den als Vernetzer bzw. Haftver¬ mittler genannten Alkoxysilanen, wobei Di-n-butylzinndilaurat und Dibutylzinnoxid in Tetraethoxysilan bevorzugt und Di-n-bu- ylzinndilaurat besonders bevorzugt ist.Examples of condensation catalysts (iii) are butyl titanates and organic tin compounds, such as di-n-butyltin dilaurate and di-n-butyltin diacetate, and also reaction products thereof with the alkoxysilanes called crosslinkers or adhesion promoters, dialkyltin oxide solutions in the crosslinkers or Adverber said alkoxysilanes, wherein di-n-butyltin dilaurate and dibutyltin oxide in tetraethoxysilane is preferred and di-n-butyl tin dilaurate is particularly preferred.
Falls die erfindungsgemäßen vernetzbaren Massen Katalysator (i- ii) enthalten, handelt es sich um Mengen von vorzugsweise 0,01 bis 3 Gewichtsteilen, bevorzugt 0,05 bis 2 Gewichtteilen, je¬ weils bezogen auf 100 Gewichtsteile vernetzbare Masse.
Als gegebenenfalls eingesetzte Füllstoffe (iv) können alle Füllstoffe eingesetzt werden, die auch bisher in vernetzbaren Massen eingesetzt worden sind. Beispiele für Füllstoffe sind verstärkende Füllstoffe, also Füllstoffe mit einer BET-Ober- fläche von mindestens 30 m2/g, wie beispielsweise Ruße, pyrogen hergestellte Kieselsäure, gefällte Kieselsäure und Silicium- Aluminium-Mischoxide, wobei die genannten Füllstoffe hydropho- biert sein können, sowie nicht verstärkenden Füllstoffe, also Füllstoffe mit einer BET-Oberflache von weniger als 30 m2/g, wie beispielsweise Pulver aus Quarz, Cristobalit, Diatomeener¬ de, Calciumsilikat, Zirkoniumsilikat, Montmorillonite, wie Ben- tonite, Zeolithe einschließlich der Molekularsiebe, wie Natri¬ umaluminiumsilikat, Metalloxide, wie Aluminium- oder Zinkoxid bzw. deren Mischoxide, Metallhydroxide, wie Aluminiumhydroxid, Bariumsulfat, Calciumcarbonat, Gips, Siliciumnitrid, Silicium- carbid, Bornitrid, Glas-, Kohle- und Kunststoffpulver und Glas- und Kunststoffhohlkugeln.If the crosslinkable compositions according to the invention comprise catalyst (ii), these are amounts of preferably 0.01 to 3 parts by weight, preferably 0.05 to 2 parts by weight, in each case based on 100 parts by weight of crosslinkable composition. As optional fillers (iv) all fillers can be used, which have also been used in crosslinkable compositions. Examples of fillers are reinforcing fillers, ie fillers having a BET surface area of at least 30 m 2 / g, such as, for example, carbon blacks, fumed silica, precipitated silica and silicon-aluminum mixed oxides, where the fillers mentioned may be hydrophobic and non-reinforcing fillers, ie fillers having a BET surface area of less than 30 m 2 / g, such as, for example, powders of quartz, cristobalite, diatomaceous earth, calcium silicate, zirconium silicate, montmorillonites, such as benzonites, zeolites, including molecular sieves, such as Natri¬ umumuminiumsilikat, metal oxides such as aluminum or zinc oxide or their mixed oxides, metal hydroxides such as aluminum hydroxide, barium sulfate, calcium carbonate, gypsum, silicon nitride, silicon carbide, boron nitride, glass, carbon and plastic powder and glass and plastic hollow spheres.
Bevorzugt handelt es sich bei Füllstoff (iv) um pyrogene Kie- seisäuren oder Ruße oder deren Gemische, wobei Ruß mit einer BET-Oberflache von mindestens 30 m2/g besonders bevorzugt ist.Filler (iv) is preferably pyrogenic kiesisäuren or carbon blacks or mixtures thereof, with carbon black having a BET surface area of at least 30 m 2 / g is particularly preferred.
Falls die erfindungsgemäßen Massen Füllstoffe (iv) enthalten, handelt es sich um Mengen von vorzugsweise 1 bis 50 Ge- wichtsteile, bevorzugt 2 bis 30 Gewichtsteile, jeweils bezogen auf 100 Gewichtsteile vernetzbare Masse.If the compositions according to the invention contain fillers (iv), these are amounts of preferably 1 to 50 parts by weight, preferably 2 to 30 parts by weight, in each case based on 100 parts by weight of crosslinkable composition.
Als gegebenenfalls eingesetzte Haftvermittler (v) können alle Haftvermittler eingesetzt werden, die auch bisher in durch Kon- densation vernetzbaren Massen eingesetzt worden sind. Beispiele für Haftvermittler (v) sind Silane mit hydrolysierbaren Gruppen und SiC-gebundenen Vinyl-, Acryloxy-, Methacryloxy-, Epoxy-,
Säureanhydrid-, Säure-, Ester- oder Ethergruppen sowie deren Teil- und Mischhydrolysate.Any adhesion promoters which have hitherto been used in compositions which can be crosslinked by condensation can be used as the adhesion promoter (v), if used. Examples of adhesion promoters (v) are silanes with hydrolyzable groups and SiC-bonded vinyl, acryloxy, methacryloxy, epoxy, Acid anhydride, acid, ester or ether groups and their partial and mixed hydrolysates.
Bevorzugt wird als Haftvermittler (v) 3-Aminopropyltriethoxy- silan, 3- (2-Aminoethyl) aminopropyltrimethoxysilan, 3-Amino- propyltrimethoxysilan und 3- (2-Aminoethyl) aminopropyltriethoxy- silan eingesetzt, wobei 3-Aminopropyltriethoxysilan besonders bevorzugt ist.Preferred adhesion promoters (v) used are 3-aminopropyltriethoxysilane, 3- (2-aminoethyl) aminopropyltrimethoxysilane, 3-aminopropyltrimethoxysilane and 3- (2-aminoethyl) aminopropyltriethoxysilane, with 3-aminopropyltriethoxysilane being particularly preferred.
Falls die erfindungsgemäßen Massen Haftvermittler (v) enthal¬ ten, handelt es sich um Mengen von vorzugsweise 0,01 bis 5 Ge¬ wichtsteilen, bevorzugt 0,5 bis 4 Gewichtsteilen, jeweils bezo¬ gen auf 100 Gewichtsteile vernetzbare Masse.If the compositions according to the invention contain adhesion promoters (v), these are amounts of preferably 0.01 to 5 parts by weight, preferably 0.5 to 4 parts by weight, in each case based on 100 parts by weight of crosslinkable composition.
Beispiele für weitere Stoffe (vi) sind Weichmacher, wie tri- methylsilylterminierte Polydimethylsiloxane und Kohlenwasser¬ stoffe mit etwa 16 bis 30 Kohlenstoffatomen, Stabilisatoren, wie 2-Etylhexylphosphat, Octylphosphonsäure, Polyether, Antio- xidantien, Flammschutzmittel, wie Phosphorsäureester, Licht- Schutzmittel und Pigmente, wie Titandioxid, Eisenoxide.Examples of further substances (vi) are plasticizers, such as trimethylsilyl-terminated polydimethylsiloxanes and hydrocarbons having about 16 to 30 carbon atoms, stabilizers, such as 2-ethylhexyl phosphate, octylphosphonic acid, polyethers, antioxidants, flame retardants, such as phosphoric acid esters, light stabilizers and Pigments, such as titanium dioxide, iron oxides.
Bevorzugt handelt es sich bei den gegebenenfalls eingesetzten weiteren Stoffen (vi) um Weichmacher, wie trimethylsilyltermi- nierte Polydimethylsiloxane und Kohlenwasserstoffe mit etwa 16 bis 30 Kohlenstoffatomen, Stabilisatoren, wie 2-Etylhexylphos- phat, Octylphosphonsäure, Polyether, Flammschutzmittel, wie Phosphorsäureester und Pigmente, wie Titandioxid, Eisenoxide, wobei Stabilisatoren und Pigmente besonders bevorzugt sind.The optionally used further substances (vi) are preferably plasticizers, such as trimethylsilyl-terminated polydimethylsiloxanes and hydrocarbons having about 16 to 30 carbon atoms, stabilizers, such as 2-ethylhexyl phosphate, octylphosphonic acid, polyethers, flame retardants, such as phosphoric acid esters and pigments, such as titanium dioxide, iron oxides, with stabilizers and pigments being particularly preferred.
Falls Bestandteil (vi) eingesetzt wird, handelt es sich um Men¬ gen, von bevorzugt 0,01 bis 30 Gewichtsteile, besonders bevor¬ zugt 0,05 bis 25 Gewichtsteile, jeweils bezogen auf 100 Ge¬ wichtsteile vernetzbare Masse.
Gegebenenfalls können die erfindungsgemäßen vernetzbaren Massen vernetzbare Polymere (vii) , wie Organopolysiloxane mit reakti¬ ven Endgruppen, enthalten. Beispiele für solche vernetzbaren Siloxane sind α,ω-Dihydroxypolydimethylsiloxane und α,ω-bis (di- methoxymethylsilyl) terminierte Polydimethylsiloxane.If component (vi) is used, these are amounts of preferably 0.01 to 30 parts by weight, more preferably 0.05 to 25 parts by weight, in each case based on 100 parts by weight of crosslinkable composition. Optionally, the crosslinkable compositions according to the invention can contain crosslinkable polymers (vii), such as organopolysiloxanes having reactive end groups. Examples of such crosslinkable siloxanes are α, ω-dihydroxypolydimethylsiloxanes and α, ω-bis (dimethoxymethylsilyl) -terminated polydimethylsiloxanes.
Bevorzugt handelt es sich bei der gegebenenfalls in den erfin¬ dungsgemäßen vernetzbaren Massen eingesetzten Komponente (vii) um Polydiorganosiloxane mit mindestens einer OH-Gruppe oder ei¬ ner hydrolysierbaren Gruppe an den Kettenenden, besonders be¬ vorzugt um Polydimethylsiloxane mit mindestens einer OH-Gruppe oder einer hydrolysierbaren Gruppe an den Kettenenden, insbe¬ sondere um α, ω-Dihydroxypolydimethylsiloxane oder α,ω-bis(di- methoxymethylsilyl) terminierte Polydimethylsiloxane mit einer Viskosität von 100 bis 500 000 mPas .The component (vii) optionally used in the crosslinkable compositions according to the invention is preferably polydiorganosiloxanes having at least one OH group or a hydrolyzable group at the chain ends, more preferably polydimethylsiloxanes having at least one OH group or a hydrolyzable group at the chain ends, in particular α, ω-dihydroxypolydimethylsiloxanes or α, ω-bis (di-methoxymethylsilyl) terminated polydimethylsiloxanes having a viscosity of 100 to 500,000 mPas.
Bevorzugt enthalten die erfindungsgemäßen vernetzbaren Massen Komponente (vii) . Dieser Bestandteil wird bevorzugt zur Ein- Stellung der Verarbeitungseigenschaften, wie beispielsweise Viskosität oder Topfzeit, eingesetzt.The crosslinkable compositions according to the invention preferably contain component (vii). This component is preferably used to adjust the processing properties, such as viscosity or pot life.
Falls Komponente (vii) eingesetzt wird, handelt es sich um Men¬ gen von bevorzugt 1 bis 50 Gewichtsteilen, besonders bevorzugt 2 bis 25 Gewichtsteilen, jeweils bezogen auf 100 Gewichtsteile vernetzbare Masse.If component (vii) is used, these are amounts of preferably 1 to 50 parts by weight, more preferably 2 to 25 parts by weight, in each case based on 100 parts by weight of crosslinkable composition.
Bei den einzelnen Bestandteilen der erfindungsgemäßen vernetz¬ baren Massen kann es sich jeweils um eine Art eines solchen Be- standteils wie auch um ein Gemisch aus mindestens zwei ver¬ schiedenen Arten derartiger Bestandteile handeln.
Insbesondere enthalten die erfindungsgemäßen Massen außer der Komponente (i) , gegebenenfalls (ii) , (iii) , (iv) , (v) , (vi) und (vii) keine weiteren Bestandteile.The individual constituents of the crosslinkable compositions according to the invention may in each case be one type of such constituent as well as a mixture of at least two different types of such constituents. In particular, the compositions according to the invention contain no further constituents apart from component (i), if appropriate (ii), (iii), (iv), (v), (vi) and (vii).
Die Herstellung der erfindungsgemäßen vernetzbaren Massen er¬ folgt mit Methoden, die dem Fachmann bekannt sind, wie bei¬ spielsweise mittels Extrudern, Knetern, Walzenstühlen, dynami¬ schen oder statischen Mischern. Die Herstellung der erfindungs¬ gemäßen Massen kann kontinuierlich oder diskontinuierlich er- folgen. Bevorzugt erfolgt die Herstellung kontinuierlich.The preparation of the crosslinkable compositions according to the invention is carried out by methods which are known to the person skilled in the art, for example by means of extruders, kneaders, roll mills, dynamic or static mixers. The preparation of the compositions according to the invention can be carried out continuously or batchwise. Preferably, the preparation is carried out continuously.
Vulkanisate der erfindungsgemäßen Massen sind durch Hydrolyse und anschließender Kondensation der entstandenen Silanolgruppen erhältlich. Die Hydrolyse kann durch Luftfeuchtigkeit oder durch Wasserdampf, Wasserbäder oder wasserhaltige Lösungen er¬ folgen im Kontakt mit dem erfindungsgemäßen Copolymer gemäß der allgemeinen Formel (I) .Vulcanizates of the compositions according to the invention are obtainable by hydrolysis and subsequent condensation of the resulting silanol groups. The hydrolysis can be effected by atmospheric moisture or by steam, water baths or aqueous solutions in contact with the copolymer according to the invention of general formula (I).
Für die Vernetzung der erfindungsgemäßen Massen reicht vorzugs- weise der übliche Wassergehalt der Luft aus. Die Vernetzung der erfindungsgemäßen Massen erfolgt vorzugsweise bei Raumtempera¬ tur. Sie kann, falls erwünscht, auch bei höheren oder niedrige¬ ren Temperaturen als Raumtemperatur, wie beispielsweise bei -5 bis 15°C oder bei 30 bis 500C beispielsweise auch mittels den normalen Wassergehalt der Luft übersteigenden Konzentrationen von Wasser durchgeführt werden. Vorzugsweise wird die Vernet¬ zung bei einem Druck von 100 bis 1100 hPa, insbesondere beim Druck der umgebenden Atmosphäre, also etwa 900 bis 1100 hPa, durchgeführt.For the crosslinking of the compositions according to the invention, the usual water content of the air is preferably sufficient. The crosslinking of the compositions according to the invention is preferably carried out at room temperature. It can, if desired, also at higher or niedrige¬ ren temperatures than room temperature, such as at -5 to 15 ° C or at 30 to 50 0 C, for example, also by means of the normal water content of the air over increasing concentrations be carried out by water. Preferably, the crosslinking is carried out at a pressure of 100 to 1100 hPa, in particular at the pressure of the surrounding atmosphere, that is about 900 to 1100 hPa.
Ein weiterer Gegenstand der vorliegenden Erfindung sind Form¬ körper, hergestellt durch Vernetzung der erfindungsgemäßen Mas¬ sen.
Im Vergleich zu nicht vernetzten thermoplastischen Siloxan- Harnstoff-Copolymeren gemäß dem Stand der Technik weisen die Vulkanisate der erfindungsgemäßen Copolymere nach Feuchtig- keitsvernetzung eine geringere Abhängigkeit der mechanischenA further subject of the present invention are molded articles produced by crosslinking of the compositions according to the invention. In comparison with non-crosslinked thermoplastic siloxane-urea copolymers according to the prior art, the vulcanizates of the copolymers according to the invention have less dependence on the mechanical properties after moisture crosslinking
Eigenschaften von der Temperatur auf. Durch die Vernetzung wer¬ den die Vulkanisate der erfindungsgemäßen Copolymere bei Tempe¬ raturerhöhung nicht mehr plastisch, können also nicht mehr fließen und sind somit formbeständiger. Insgesamt weisen die erfindungsgemäßen Vulkanisate also bessere mechanische Eigen¬ schaften über einen weiteren Temperaturbereich auf, so dass sie in vielfältigeren Einsatzgebieten verwendet werden können.Characteristics of the temperature. As a result of the crosslinking, the vulcanizates of the copolymers according to the invention no longer become plastic when the temperature is raised, ie they can no longer flow and are thus more dimensionally stable. Overall, the vulcanizates according to the invention thus have better mechanical properties over a wider temperature range, so that they can be used in more diverse fields of application.
Die erfindungsgemäßen vernetzbaren Massen werden vorzugsweise als Schmelzkleber, Klebstoff, PSA (Pressure Sensitve Adhesive) , Dichtstoff, Beschichtung für beispielsweise Papier, Textil, Fa¬ sern oder silikatische Oberflächen, Imprägniermittel, Anstrich, Bestandteil in Verbundwerkstoffen, Additiv für Polymere, Form¬ teil und Komponente für medizinische Zwecke sowie für den Ein- satz im Automobilbau oder Laminatglas verwendet.The crosslinkable compositions according to the invention are preferably used as hotmelt adhesive, adhesive, PSA (pressure sensitive adhesive), sealant, coating for example paper, textile, fibers or silicate surfaces, impregnating agent, paint, component in composite materials, additive for polymers, molding and Component used for medical purposes as well as for use in automotive or laminated glass.
Die erfindungsgemäßen Massen haben den Vorteil, dass sie alle der obengenannten Vorteile der eingesetzten erfindungsgemäßen Copolymere besitzen.The compositions of the invention have the advantage that they have all of the abovementioned advantages of the copolymers of the invention used.
Die erfindungsgemäßen Massen haben den Vorteil, dass sie sehr gute mechanische Eigenschaften aufweisen.The compositions of the invention have the advantage that they have very good mechanical properties.
Weitere Vorteile der erfindungsgemäßen Massen sind die hohe thermische und oxidative Beständigkeit, gute Beständigkeiten gegenüber Quellung und Zersetzung durch Kohlenwasserstoffe ent¬ haltende Lösemitteln.
Die erfindungsgemäßen Massen haben den Vorteil, dass die Eigen¬ schaften, wie beispielsweise Schäl- und Ablösefestigkeit, Be- druckbarkeit, Zug- und Durchreißfestigkeit oder Wasserdampf¬ durchlässigkeit, gezielt eingestellt werden können.Further advantages of the compositions according to the invention are the high thermal and oxidative stability, good resistance to swelling and decomposition by solvents containing hydrocarbons. The compositions of the invention have the advantage that the properties, such as, for example, peel and peel strength, printability, tensile and tear propagation resistance or water vapor permeability, can be set in a targeted manner.
Die erfindungsgemäßen Formkörper haben den Vorteil, dass sie eine geringere Abhängigkeit der mechanischen Eigenschaften von der Temperatur, insbesondere bei höheren Temperaturen, besit¬ zen.The shaped bodies according to the invention have the advantage that they have a lower dependence of the mechanical properties on the temperature, in particular at relatively high temperatures.
Die erfindungsgemäßen Formkörper haben des Weiteren den Vor¬ teil, dass sie eine sehr gute Haftung auf Substraten besitzen.The shaped bodies according to the invention furthermore have the advantage that they have a very good adhesion to substrates.
In den nachstehend beschriebenen Beispielen beziehen sich alle Viskositätsangaben auf eine Temperatur von 25°C. Sofern nicht anders angegeben, werden die nachstehenden Beispiele bei einem Druck der umgebenden Atmosphäre, also etwa bei 1000 hPa, und bei Raumtemperatur, also bei etwa 230C, bzw. bei einer Tempera¬ tur, die sich beim Zusammengeben der Reaktanden bei Raumtempe- ratur ohne zusätzliche Heizung oder Kühlung einstellt, sowie bei einer relativen Luftfeuchtigkeit von etwa 50 % durchge¬ führt. Des Weiteren beziehen sich alle Angaben von Teilen und Prozentsätzen, soweit nichts anderes angegeben ist, auf das Ge¬ wicht.In the examples described below, all viscosity data refer to a temperature of 25 ° C. Unless indicated otherwise, the examples below are at a pressure of the surrounding atmosphere, ie at about 1000 hPa, and at room temperature, that is at about 23 0 C, or at a tur Tempera¬ that on combining the reactants at room temperature- setting temperature without additional heating or cooling, and at a relative humidity of about 50% durchge leads. Furthermore, all statements of parts and percentages, unless otherwise stated, are by weight.
Die Shore-A-Härte wird nach DIN (Deutsche Industrie Norm) 53505 (Ausgabe August 2000) bestimmt.The Shore A hardness is determined according to DIN (German Industrial Standard) 53505 (August 2000 edition).
Zugfestigkeit, Reißdehnung und Modul (Spannung bei 100% Dehung) wurden nach DIN 53504 (Ausgabe Mai 1994) an Probekörpern der Form S2 bestimmt.Tensile strength, elongation at break and modulus (stress at 100% strain) were determined according to DIN 53504 (May 1994 edition) on test specimens of the form S2.
Beispiel 1
20 g eines α,ω-aminopropylterminierten Polydimethylsiloxans mit einem Molgewicht von 2890 g/mol (13,8 mmol NH2) und einer Visko¬ sität von 50 mPas und 5,00 g 3- (2-Aminoethyl) aminopropyltri- methoxysilan (45,0 mmol NH) wurden in 40 g Tetrahydrofuran (THF) gelöst und unter Feuchtigkeitsausschluss mit 5,89 g Di- cyclohexylmethane-4, 4-Diisocyanate (HMDI) (45,0 mmol NCO) in 10 g THF versetzt. Die Temperatur stieg dabei auf 32°C an. An¬ schließend wurde das Gemisch für 2 Stunden auf 500C erwärmt. Nach dem Abkühlen wurde das Lösungsmittel durch Abdampfen ent- fernt.example 1 20 g of an α, ω-aminopropyl-terminated polydimethylsiloxane having a molecular weight of 2890 g / mol (13.8 mmol NH 2 ) and a Visko¬ sity of 50 mPas and 5.00 g of 3- (2-aminoethyl) aminopropyltri- methoxysilane (45 , 0 mmol NH) were dissolved in 40 g of tetrahydrofuran (THF) and, with exclusion of moisture, 5.89 g of di-cyclohexylmethane-4,4-diisocyanate (HMDI) (45.0 mmol of NCO) in 10 g of THF were added. The temperature rose to 32 ° C. On closing the mixture for 2 hours, was warmed to 50 0 C. After cooling, the solvent was removed by evaporation.
Es wurde ein glasklares farbloses thermoplastisches Material erhalten. Aus diesem Material wurde in einer Presse bei 17O0C eine 2 mm dicke Platte gepresst und daraus Prüfkörper der Form S2 gemäß DIN 53504 gestanzt. Es wurden folgende mechanischen Kennwerte ermittelt: Härte 63 Shore A, Zugfestigkeit 3,1 MPa, Reißdehnung 118%, Spannung bei 100% Dehnung 2,83 MPa.A clear, colorless thermoplastic material was obtained. From this material, a 2 mm thick plate was pressed in a press at 17O 0 C and punched therefrom mold S2 according to DIN 53504. The following mechanical properties were determined: hardness 63 Shore A, tensile strength 3.1 MPa, elongation at break 118%, stress at 100% elongation 2.83 MPa.
Beispiel 2 18,0 g eines α,ω-aminopropylterminierten Polydimethylsiloxans mit einem Molgewicht von 2890 g/mol (12,5 mmol NH2) und einerExample 2 18.0 g of an α, ω-aminopropyl-terminated polydimethylsiloxane having a molecular weight of 2890 g / mol (12.5 mmol NH 2 ) and a
Viskosität von 50 mPas und 2,0 g 3- (2-Aminoethyl) aminopropyl- trimethoxysilan (18,0 mmol NH) wurden in 40 g TetrahydrofuranViscosity of 50 mPas and 2.0 g of 3- (2-aminoethyl) aminopropyltrimethoxysilane (18.0 mmol of NH) were dissolved in 40 g of tetrahydrofuran
(THF) gelöst und unter Feuchtigkeitsausschluss mit 5,24 g Di- cyclohexylmethane-4, 4-Diisocyanate (HMDI) (40,0 mmol NCO) in 10 g THF versetzt. Die Temperatur stieg dabei auf 320C an. An¬ schließend wurde das Gemisch für 2 Stunden auf 500C erwärmt. Nach dem Abkühlen wurde das Lösungsmittel durch Abdampfen ent¬ fernt.(THF) and with exclusion of moisture with 5.24 g of di-cyclohexylmethane-4, 4-diisocyanates (HMDI) (40.0 mmol NCO) in 10 g of THF. The temperature rose to 32 0 C on. On closing the mixture for 2 hours, was warmed to 50 0 C. After cooling, the solvent was removed by evaporation.
Es wurde ein glasklares farbloses thermoplastisches Material erhalten. Aus diesem Material wurde in einer Presse bei 1700C eine 2 mm dicke Platte gepresst und daraus Prüfkörper der Form
S2 gemäß DIN 53504 gestanzt. Es wurden folgende mechanischen Kennwerte ermittelt: Härte 62 Shore A, Zugfestigkeit 4,19 MPa, Reißdehnung 259%, Spannung bei 100% Dehnung 2,50 MPa.A clear, colorless thermoplastic material was obtained. From this material, a 2 mm thick plate was pressed in a press at 170 0 C and from it test specimens of the form S2 punched in accordance with DIN 53504. The following mechanical properties were determined: hardness 62 Shore A, tensile strength 4.19 MPa, elongation at break 259%, stress at 100% elongation 2.50 MPa.
Beispiel 3Example 3
23,4 g eines α,ω-aminopropylterminierten Polydimethylsiloxans mit einem Molgewicht von 3140 g/mol (14,9 mmol NH)und einer Viskosität von 70 mPas und 1,66 g 3- (2-Aminoethyl) aminopropyl- trimethoxysilan (15,0 mmol NH) wurden in 23 ml Tetrahydrofuran (THF) gelöst und unter Feuchtigkeitsausschluss mit 3,91 g Di- cyclohexylmethane-4, 4-Diisocyanate (HMDI) (29,8 mmol NCO) in 5 ml THF versetzt. Die Temperatur stieg dabei auf 40°C an und die Lösung wurde schnell sehr viskos. Nach dem Abkühlen wurde das Lösungsmittel durch Abdampfen entfernt. Es wurde ein glas- klares farbloses thermoplastisches Material erhalten. Aus die¬ sem Material wurde in einer Presse bei 1700C eine 2 mm dicke Platte gepresst und daraus Prüfkörper der Form S2 gemäß DIN 53504 gestanzt.23.4 g of an α, ω-aminopropyl-terminated polydimethylsiloxane having a molecular weight of 3140 g / mol (14.9 mmol of NH) and a viscosity of 70 mPas and 1.66 g of 3- (2-aminoethyl) aminopropyltrimethoxysilane (15, 0 mmol of NH) were dissolved in 23 ml of tetrahydrofuran (THF) and, with exclusion of moisture, 3.93 g of di-cyclohexylmethane-4,4-diisocyanate (HMDI) (29.8 mmol of NCO) in 5 ml of THF were added. The temperature rose to 40 ° C and the solution quickly became very viscous. After cooling, the solvent was removed by evaporation. This gave a glass-clear colorless thermoplastic material. From die¬ sem material has a 2 mm thick plate was pressed in a press at 170 0 C and test specimens punched from the mold S2 according to DIN 53,504th
Beispiel 4Example 4
In den ersten Sektor eines gleichläufigen W&P-Doppelschnecken- extruders (25 mm Schneckendurchmesser, L/D = 40) wurden 12,2 kg/h eines aminopropyl-terminierten Polydimethylsiloxans (Amin- zahl 34 mg KOH/g; 7,41 mol NH/h) und 0,20 kg/h 3- (2-Amino- ethyl) aminopropyltrimethoxysilan (1,80 mol NH/h) als Gemisch dosiert. Die Temperatur betrug an dieser Stelle des Extruders 1500C. Im zweiten Sektor des Extruders wurden 1,12 kg/h Tetra- methylxylylendiisocyanat (9,21 mol NCO/h) dazudosiert. Die Tem¬ peratur des Extruders betrug an dieser Stelle 1700C. Die rest- liehen Sektoren wurden auf 1500C gehalten, im vorletzten Sektor wurde schließlich mit 100 mbar evakuiert. Am Ende des Extruders trat ein glasklarer farbloser thermoplastischer Extrudatstrang aus, der in einem sich anschließenden Granulator zerkleinert
wurde. Das so erhaltene Granulat wurde in einer Presse bei 170°C zu einer 2 mm dicken Platte gepresst und daraus Prüfkör¬ per der Form S2 gemäß DIN 53504 gestanzt. Es wurden folgende mechanischen Kennwerte ermittelt: Härte 57 Shore A, Zugfestig- keit 2,96 MPa, Reißdehnung 376%, Spannung bei 100% Dehnung 2,07 MPa.Into the first sector of a co-rotating W & P twin screw extruder (25 mm screw diameter, L / D = 40), 12.2 kg / h of an aminopropyl-terminated polydimethylsiloxane (amine number 34 mg KOH / g, 7.41 moles NH / h) and 0.20 kg / h of 3- (2-aminoethyl) aminopropyltrimethoxysilane (1.80 mol NH / h) as a mixture. The temperature of the extruder at this point was 150 0 C. In the second sector of the extruder were dosed to 1.12 kg / h tetra- methylxylylendiisocyanat (9.21 mol NCO / h). The Tem¬ temperature of the extruder at this point was 170 0 C. The remaining loan sectors were maintained at 150 0 C, in the second last sector was finally evacuated mbar by 100. At the end of the extruder emerged a crystal clear colorless thermoplastic extrudate strand, which is comminuted in a subsequent granulator has been. The granules thus obtained were pressed in a press at 170 ° C to a 2 mm thick plate and therefrom Prüfkör¬ per die S2 according to DIN 53504 punched. The following mechanical properties were determined: hardness 57 Shore A, tensile strength 2.96 MPa, elongation at break 376%, stress at 100% elongation 2.07 MPa.
Beispiel 5Example 5
30,89 g des gemäß Beispiel 1 hergestellten Polymers werden in 40 ml THF gelöst und nacheinander 0,05 g Methyltrimethoxysilan, 0,2 g 3- (2-Aminoethyl) aminopropyltrimethoxysilan, 0,10 g Dibu- tylzinndilaurat und 0,05 g Octylphosphonsäure versetzt. Diese Mischung wurde in eine 2 mm tiefe PTFE-Form gegossen und das Lösungsmittel THF verdampfen gelassen. Aus der zurückblei- benden ca. 1 mm dicken Folie wurden Probekörper der Form S2 ge¬ mäß DIN 53504 gestanzt, die anschließend 24 Stunden in Wasser gelagert wurden.30.89 g of the polymer prepared according to Example 1 are dissolved in 40 ml of THF and successively 0.05 g of methyltrimethoxysilane, 0.2 g of 3- (2-aminoethyl) aminopropyltrimethoxysilane, 0.10 g of dibutyltin dilaurate and 0.05 g of octylphosphonic acid added. This mixture was poured into a 2 mm deep PTFE mold and the solvent THF allowed to evaporate. From the remaining approx. 1 mm thick film, test specimens of the form S2 were punched in accordance with DIN 53504, which were then stored in water for 24 hours.
An den glasklaren, farblosen Probekörpern wurden die folgenden mechanischen Kennwerte gemessen: Härte 60 Shore A, Zugfestig¬ keit 5,32 MPa, Reißdehnung 390%, Spannung bei 100% Dehnung 2,31 MPa.The following mechanical properties were measured on the crystal-clear, colorless test specimens: hardness 60 Shore A, tensile strength 5.32 MPa, elongation at break 390%, stress at 100% elongation 2.31 MPa.
Beispiel 6 56 g des in Beispiel 4 hergestellten Produkts werden in 150 ml Tetrahydrofuran gelöst und mit 0,2 g Aminoethylaminopropyltri- methoxysilan, 0,1 g eines Zinnkondensationskatalysators (erhal¬ ten durch Umsetzung von Dibutylzinndiacetat und Tetraethoxysi- lan) und 0,1 g Octylphosphonsäure vermischt. Die Lösung wird in eine Schale gegossen, das Lösemittel abgedampft und aus der so erhaltenen Folie werden S2-Prüfkörper gestanzt. Härte in Sho- reA: 68, Zugfestigkeit: 4,25 MPa, Reißdehnung: 151%, Spannungs¬ wert bei 100% Dehnung: 3,17 MPa.
Die Probekörper weisen nach 2 Tagen Lagerung in Wasser (250C) folgende Werte auf: Härte in ShoreA: 68, Zugfestigkeit: 4,24 MPa, Reißdehnung: 154%, Spannungswert bei 100% Dehnung: 3,14 MPa.
Example 6 56 g of the product prepared in Example 4 are dissolved in 150 ml of tetrahydrofuran and treated with 0.2 g of aminoethylaminopropyltrimethoxysilane, 0.1 g of a tin condensation catalyst (obtained by reacting dibutyltin diacetate and tetraethoxysilane) and 0.1 g Octylphosphonic acid mixed. The solution is poured into a dish, the solvent evaporated and from the resulting film S2-test pieces are punched. Hardness in Shore A: 68, tensile strength: 4.25 MPa, elongation at break: 151%, stress value at 100% elongation: 3.17 MPa. The test specimens have after 2 days of storage in water (25 0 C) the following values: Hardness in Shore A 68, tensile strength: 4.24 MPa, elongation at break: 154%, modulus at 100% elongation: 3.14 MPa.
Claims
1. Copolymere der allgemeinen Formel1. Copolymers of the general formula
R' -[ (A)a<B)b(C)o] -R" (D ,R '- [(A) a <B) b (C) o ] -R "(D,
worinwherein
(A) gleich oder verschieden sein kann und eine Einheit der For¬ mel (II)(A) may be the same or different and a unit of formula (II)
- [CO-NH-Z-NH-CO-ND-Y-Si (OR1)0R2-0- (0-SiR2)n-O-Si (OR1)OR2-O-Y-ND] -,- [CO-NH-Z-NH-CO-ND-Y-Si (OR 1) 0 R2-0- (0-SiR 2) n -O-Si (OR 1) 2 O R - O -Y-ND ] -,
(B) gleich oder verschieden sein kann und eine Einheit der For¬ mel(B) may be the same or different and is a unit of formula
-[CO-NH-Z-NH-CO-NR4-G-NR4]- (III)- [CO-NH-Z-NH-CO-NR 4 -G-NR 4 ] - (III)
undand
(C) gleich oder verschieden sein kann und eine Einheit der For¬ mel(C) may be the same or different and is a unit of formula
- [CO-NH-Z-NH-CO-E-X-E] - (IV)- [CO-NH-Z-NH-CO-E-X-E] - (IV)
darstellen, wobeirepresent, wherein
X gleich oder verschieden sein kann und einen gegebenenfalls durch Fluor, Chlor, Ci-Cβ-Alkyl- oder Ci-Cβ-Alkylester sub- stituierten Alkylenrest mit 1 bis 700 Kohlenstoffatomen bedeutet, in dem einander nicht benachbarte Methylenein¬ heiten durch Gruppen -0-, -COO-, -OCO- oder -0C00- ersetzt sein können, oder gegebenenfalls substituierten Arylenrest mit 6 bis 22 Kohlenstoffatomen bedeutet,X may be identical or different and is an alkylene radical having 1 to 700 carbon atoms which is unsubstituted or substituted by fluorine, chlorine, C 1 -C 6 -alkyl or C 1 -C 6 -alkyl ester, in which non-adjacent methylene units are represented by groups. , -COO-, -OCO- or -0C00- replaced may be, or optionally substituted arylene radical having 6 to 22 carbon atoms,
Y gleich oder verschieden sein kann und einen zweiwertigen Kohlenwasserstoffrest mit 1 bis 30 Kohlenstoffatomen, in dem einander nicht benachbarte Methyleneinheiten durchY may be the same or different and a divalent hydrocarbon radical having 1 to 30 carbon atoms in which non-adjacent methylene units
Gruppen -0- ersetzt sein können, oder den Rest -(CH2)S-NH- SiR2- (CH2) 3-NH- darstellt,Groups -0- may be replaced, or the radical is - (CH 2 ) S -NH- SiR 2 - (CH 2 ) 3 -NH-,
Z gleich oder verschieden sein kann und einen zweiwertigen, gegebenenfalls durch Fluor oder Chlor substituierten Koh- lenwasserstoffrest mit 1 bis 30 Kohlenstoffatomen bedeu¬ tet,Z may be identical or different and denotes a bivalent hydrocarbon radical optionally substituted by fluorine or chlorine and having from 1 to 30 carbon atoms,
D gleich oder verschieden sein kann und Wasserstoffatom oder einen einwertigen, gegebenenfalls substituierten Kohlen¬ wasserstoffrest darstellt, E gleich oder verschieden sein kann und ein Sauerstoffatom oder eine Äminogruppe -ND- darstellt,D may be identical or different and represents hydrogen atom or a monovalent, optionally substituted hydrocarbon radical, E may be the same or different and represents an oxygen atom or an amino group -ND-,
R gleich oder verschieden sein kann und einen einwertigen, gegebenenfalls durch Fluor oder Chlor substituierten Koh¬ lenwasserstoffrest mit 1 bis 20 Kohlenstoffatomen bedeu- tet,R can be identical or different and denotes a monovalent hydrocarbon radical which is optionally substituted by fluorine or chlorine and has 1 to 20 carbon atoms,
R1 gleich oder verschieden sein kann und Wasserstoffatom oder einen einwertigen, gegebenenfalls durch Fluor, Chlor oder Organyloxygruppen substituierten Kohlenwasserstoffrest mit 1 bis 20 Kohlenstoffatomen, -(C=O)-R oder -N=CR2 darstellt, R4 gleich oder verschieden sein kann und einen Rest der For¬ mel -Z Λ-SiRp (OR1) 3-p mit Zλ gleich einer für Z oben angege¬ benen Bedeutung und p gleich 0, 1 oder 2, Wasserstoffatom oder einen einwertigen, gegebenenfalls substituierten Koh¬ lenwasserstoffrest bedeutet, G gleich oder verschieden sein kann und eine für Z angegebe¬ ne Bedeutung hat,R 1 may be identical or different and is hydrogen or a monovalent, optionally substituted by fluorine, chlorine or organyloxy groups hydrocarbon radical having 1 to 20 carbon atoms, - (C = O) -R or -N = CR 2 , R 4 be the same or different can be and a radical of the formula --Z Λ -SiR p (OR 1 ) 3 - p with Z λ equal to a angege¬ indicated above for Z above meaning and p is 0, 1 or 2, hydrogen atom or a monovalent, optionally substituted Koh Is hydrogen radical, G may be the same or different and has a meaning given for Z,
R' ' Wasserstoffatom oder einen Rest -CO-NH-Z-NCO bedeutet, R' im Fall von R' ' gleich Wasserstoffatom einen Rest HND-Y-Si (OR1 ) oR2-o- (0-SiR2 ) n~O-Si (OR1 ) OR2-O-Y-ND- ,R '' is hydrogen or a radical -CO-NH-Z-NCO, R 'in the case of R''is hydrogen, a radical HND-Y-Si (OR 1) o R 2 -O- (0-SiR 2) n ~ O-Si (OR 1) 2 O R - O -Y-ND-,
HNR4-G-NR4- oder HE-X-E- bedeutet und im Fall von R' ' gleich Rest -CO-NH-Z-NCO die Bedeutung vonHNR 4 -G-NR 4 - or HE-XE- and in the case of R '' is the radical -CO-NH-Z-NCO the meaning of
Rest OCN-Z-NH-CO-ND-Y-Si (OR1) OR2-O- (0-SiR2) n-0-Si (OR1) OR2-O-Y-ND-,Radical OCN-Z-NH-CO-ND-Y-Si (OR 1) 2 O R - O - (0-SiR 2) n -0-Si (OR 1) 2 O R - O -Y-ND-,
OCN-Z-NH-CO-NR4-G-NR4- oder OCN-Z-NH-CO-E-X-E- hat, n gleich oder verschieden sein kann und eine ganze Zahl vonOCN-Z-NH-CO-NR 4 -G-NR 4 - or OCN-Z-NH-CO-EXE-, n may be the same or different and an integer of
1 bis 4000 ist, o gleich oder verschieden sein kann und 0, 1 oder 2 ist, a eine ganze Zahl von mindestens 1 ist, b eine ganze Zahl von mindestens 1 ist, c 0 oder eine ganze Zahl von mindestens 1 ist, mit der Maßgabe, dass pro Molekül mindestens ein Rest R4 die Bedeutung von -Z λ-SiRp(OR1) 3-p hat sowie die einzelnen Blöcke (A), (B) und (C) im Polymer statistisch verteilt sein können.1 to 4000, o may be the same or different and is 0, 1 or 2, a is an integer of at least 1, b is an integer of at least 1, c is 0 or an integer of at least 1, with The proviso that at least one radical R 4 per molecule has the meaning of -Z λ -SiR p (OR 1 ) 3 - p and the individual blocks (A), (B) and (C) may be randomly distributed in the polymer.
2. Copolymere gemäß Anspruch 1, dadurch gekennzeichnet, dass E gleich Sauerstoffatom ist.2. Copolymers according to claim 1, characterized in that E is oxygen.
3. Verfahren zur Herstellung der Copolymere gemäß Anspruch 1 oder 2 durch Umsetzung von a) mindestens einem Polymer der Formel3. A process for the preparation of the copolymers according to claim 1 or 2 by reacting a) at least one polymer of the formula
H-ND-Y-Si (OR1)0R2-0- (0-SiR2)n"O-Si(OR1)OR2.O-Y-ND-H (V) ,H-ND-Y-Si (OR 1 ) 0 R 2 O- (O-SiR 2 ) n "O-Si (OR 1 ) O R 2 O- Y-ND-H (V)
b) mindestens einer Verbindung der Formelb) at least one compound of the formula
H-NR4-G-NR4-H (VI)H-NR 4 -G-NR 4 -H (VI)
c) mindestens einem Diisocyanat der Formelc) at least one diisocyanate of the formula
OCN-Z-NCO (VII) oder blockierten Diisocyanaten (thermisch instabile Umsetzungs¬ produkten von Isocyanaten mit zum Beispiel Phenolen, Ketoximen, Malonestern, stickstoffhaltigen Heterocyclen) ,OCN-Z-NCO (VII) or blocked diisocyanates (thermally unstable ¬ conversion products of isocyanates with, for example, phenols, ketoximes, malonic esters, nitrogen-containing heterocycles),
d) gegebenenfalls Verbindungen der Formeld) optionally compounds of the formula
H-E-X-E-H (VIII) ,H-E-X-E-H (VIII),
e) gegebenenfalls einem Katalysator unde) optionally a catalyst and
f) gegebenenfalls mindestens einem Lösemittel, wobei X, Y, Z, D, E, G, R, R1, R4, und o die oben genannte Be¬ deutung aufweisen.f) optionally at least one solvent, wherein X, Y, Z, D, E, G, R, R 1 , R 4 , and o have the abovementioned Be¬ interpretation.
4. Verfahren nach Anspruch 3, dadurch gekennzeichnet, dass die Umsetzung in Substanz erfolgt.4. The method according to claim 3, characterized in that the reaction takes place in substance.
5. Vernetzbare Massen enthaltend Copolymere gemäß Anspruch 1 oder 2 oder hergestellt nach Anspruch 3 oder 4.5. Crosslinkable compositions comprising copolymers according to claim 1 or 2 or produced according to claim 3 or 4.
6. Vernetzbare Massen gemäß Anspruch 5, dadurch gekennzeichnet, dass es sich um solche handelt enthaltend6. Crosslinkable compositions according to claim 5, characterized in that they are those containing
(i) Copolymer der Formel (I) , gegebenenfalls (ii) Vernetzer, gegebenenfalls(i) Copolymer of formula (I), optionally (ii) crosslinker, optionally
(iii) Katalysator, gegebenenfalls(iii) Catalyst, optionally
(iv) Füllstoff, gegebenenfalls(iv) filler, optionally
(v) Haftvermittler, gegebenenfalls (vi) weitere Stoffe ausgewählt aus der Gruppe enthaltend Weichmacher, Stabilisatoren, Antioxidantien, Flammschutzmittel, Lichtschutzmittel und Pigmente, und gegebenenfalls (vii) vernetzbare Polymere, die unterschiedlich sind zu (i) .(v) adhesion promoter, if appropriate (vi) other substances selected from the group consisting of plasticizers, stabilizers, antioxidants, flame retardants, light stabilizers and pigments, and optionally (vii) crosslinkable polymers other than (i).
7. Vernetzbare Massen gemäß Anspruch 5 oder 6, dadurch gekenn¬ zeichnet, dass sie Komponente (vii) enthalten.7. Crosslinkable compositions according to claim 5 or 6, characterized gekenn¬ characterized in that they contain component (vii).
8. Vernetzbare Massen gemäß einem oder mehreren der Ansprüche 5 bis 7, dadurch gekennzeichnet, dass sie außer der Komponente (i) , gegebenenfalls (ii) , (iii) , (iv) , (v) , (vi) und (vii) kei¬ ne weiteren Bestandteile enthalten.8. Crosslinkable compositions according to one or more of claims 5 to 7, characterized in that they except component (i), optionally (ii), (iii), (iv), (v), (vi) and (vii) contain no further constituents.
9. Formkörper, hergestellt durch Vernetzung der Massen gemäß einem oder mehreren der Ansprüche 5 bis 8. 9. Shaped body produced by crosslinking of the compositions according to one or more of claims 5 to 8.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE200410035710 DE102004035710A1 (en) | 2004-07-23 | 2004-07-23 | Crosslinkable siloxane-urea copolymer |
| PCT/EP2005/007685 WO2006010486A1 (en) | 2004-07-23 | 2005-07-14 | Cross-linkable siloxane urea copolymers |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| EP1771496A1 true EP1771496A1 (en) | 2007-04-11 |
Family
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP05771820A Withdrawn EP1771496A1 (en) | 2004-07-23 | 2005-07-14 | Cross-linkable siloxane urea copolymers |
Country Status (6)
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| US (1) | US7645516B2 (en) |
| EP (1) | EP1771496A1 (en) |
| KR (1) | KR20070036796A (en) |
| CN (1) | CN1989179A (en) |
| DE (1) | DE102004035710A1 (en) |
| WO (1) | WO2006010486A1 (en) |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102004041379A1 (en) | 2004-08-26 | 2006-03-02 | Wacker-Chemie Gmbh | Crosslinkable siloxane-urea copolymers |
| DE102004062353A1 (en) * | 2004-12-23 | 2006-07-06 | Wacker Chemie Ag | Organopolysiloxane-polyurea copolymers |
| EP2010588B1 (en) | 2006-04-18 | 2012-01-04 | Henkel AG & Co. KGaA | Organosilicon polyurea polymers, elastomers manufactured therefrom and their use |
| US7625978B1 (en) * | 2006-10-27 | 2009-12-01 | Henkel Corporation | Moisture curable silicone urea hot melt reinforced by organic polymers |
| US7906215B2 (en) * | 2008-04-17 | 2011-03-15 | The Boeing Company | Composition and method for corrosion protection of a structure |
| US8167363B2 (en) | 2009-04-15 | 2012-05-01 | Toyota Motor Engineering & Manufacturing North America, Inc. | Prestressed structural members and methods of making same |
| EP2289988A1 (en) * | 2009-08-24 | 2011-03-02 | Sika Technology AG | Compounds based on silane-terminated polymers |
| KR101145035B1 (en) * | 2009-08-25 | 2012-05-21 | 주식회사 삼양사 | Urethane bond-containing hydroxy-terminated siloxane, polysiloxane-polycarbonate copolymer and method of manufacturing the same |
| AU2014226366A1 (en) * | 2013-03-04 | 2015-06-25 | The Government Of The United States Of America, As Represented By The Secretary Of The Navy | Silane end capped substituted urea resins and coatings thereof |
| CN105925242A (en) * | 2016-07-06 | 2016-09-07 | 郑州中原应用技术研究开发有限公司 | Spraying type silicone flame-retardant sealant |
| WO2018022680A1 (en) | 2016-07-28 | 2018-02-01 | 3M Innovative Properties Company | Segmented silicone polyamide block copolymers and articles containing the same |
| CN109476815B (en) | 2016-07-28 | 2021-05-04 | 3M创新有限公司 | Segmented silicone polyamide block copolymers and articles comprising the same |
| CN107815055B (en) * | 2016-09-12 | 2021-02-12 | 翁秋梅 | Dynamic polymer thermoplastic elastomer and application thereof |
| CN107815169A (en) * | 2017-09-22 | 2018-03-20 | 武汉亿维登科技发展有限公司 | A kind of uvioresistant cable |
| GB201811834D0 (en) | 2018-07-19 | 2018-09-05 | Medherant Ltd | Patch |
| KR20220011924A (en) * | 2020-07-22 | 2022-02-03 | 주식회사 엘지화학 | Silicon based coating composition and silicon based release film |
| CN115295268A (en) * | 2022-08-31 | 2022-11-04 | 深圳市优宝新材料科技有限公司 | Polymer-coated magnetic powder, preparation method thereof and magnet |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA1015488A (en) * | 1972-02-17 | 1977-08-09 | Seiji Nagahisa | Polyurethane composition |
| CA1248679A (en) * | 1984-05-21 | 1989-01-10 | Peter C. Gaa | Aqueous dispersion, internally silylated and dispersed polyurethane resins, and process for producing same and surfaces containing same |
| EP0737700A3 (en) | 1986-06-20 | 1996-12-18 | Minnesota Mining & Mfg | Release agent containing a block copolymer, diamine precursors and their preparations and the products thus obtained containing the release agent |
| JP3970955B2 (en) | 1995-04-25 | 2007-09-05 | 三井化学ポリウレタン株式会社 | Aqueous polyurethane composition |
| EP0822952B1 (en) | 1995-04-25 | 2003-07-23 | Minnesota Mining And Manufacturing Company | Polydiorganosiloxane oligourea segmented copolymers and a process for making same |
| US6407195B2 (en) * | 1996-04-25 | 2002-06-18 | 3M Innovative Properties Company | Tackified polydiorganosiloxane oligourea segmented copolymers and a process for making same |
| US6641922B2 (en) * | 2001-01-17 | 2003-11-04 | A. Andrew Shores | Silicone and ionically modified isocyanate adduct |
| DE10113980A1 (en) | 2001-03-22 | 2002-10-02 | Consortium Elektrochem Ind | Silane-terminated polydiorganosiloxane-urethane copolymer |
| DE10141235A1 (en) | 2001-08-23 | 2003-03-27 | Consortium Elektrochem Ind | Moisture-curing elastic composition |
| DE10359704A1 (en) * | 2003-12-18 | 2005-07-14 | Wacker-Chemie Gmbh | Dispersions containing organopolysiloxane-polyurea copolymers |
-
2004
- 2004-07-23 DE DE200410035710 patent/DE102004035710A1/en not_active Withdrawn
-
2005
- 2005-07-14 US US11/572,281 patent/US7645516B2/en not_active Expired - Fee Related
- 2005-07-14 EP EP05771820A patent/EP1771496A1/en not_active Withdrawn
- 2005-07-14 WO PCT/EP2005/007685 patent/WO2006010486A1/en not_active Ceased
- 2005-07-14 KR KR1020077004052A patent/KR20070036796A/en not_active Ceased
- 2005-07-14 CN CNA2005800244683A patent/CN1989179A/en active Pending
Non-Patent Citations (1)
| Title |
|---|
| See references of WO2006010486A1 * |
Also Published As
| Publication number | Publication date |
|---|---|
| DE102004035710A1 (en) | 2006-03-16 |
| WO2006010486A1 (en) | 2006-02-02 |
| US20080045671A1 (en) | 2008-02-21 |
| US7645516B2 (en) | 2010-01-12 |
| KR20070036796A (en) | 2007-04-03 |
| CN1989179A (en) | 2007-06-27 |
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