CA2627006A1 - .alpha.-ethoxysilane-modified polymers, production and use thereof - Google Patents
.alpha.-ethoxysilane-modified polymers, production and use thereof Download PDFInfo
- Publication number
- CA2627006A1 CA2627006A1 CA002627006A CA2627006A CA2627006A1 CA 2627006 A1 CA2627006 A1 CA 2627006A1 CA 002627006 A CA002627006 A CA 002627006A CA 2627006 A CA2627006 A CA 2627006A CA 2627006 A1 CA2627006 A1 CA 2627006A1
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- Prior art keywords
- radicals
- polymer
- radical
- formula
- independently
- Prior art date
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- 229920000642 polymer Polymers 0.000 title claims abstract description 79
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 22
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- 239000000203 mixture Substances 0.000 claims description 57
- -1 polyethylenes Polymers 0.000 claims description 42
- 150000001875 compounds Chemical class 0.000 claims description 30
- 239000003054 catalyst Substances 0.000 claims description 25
- 239000003085 diluting agent Substances 0.000 claims description 20
- 229920001451 polypropylene glycol Polymers 0.000 claims description 15
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- 239000000463 material Substances 0.000 claims description 11
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- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 5
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- ZLGIYFNHBLSMPS-ATJNOEHPSA-N shellac Chemical compound OCCCCCC(O)C(O)CCCCCCCC(O)=O.C1C23[C@H](C(O)=O)CCC2[C@](C)(CO)[C@@H]1C(C(O)=O)=C[C@@H]3O ZLGIYFNHBLSMPS-ATJNOEHPSA-N 0.000 claims description 3
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- VOLGAXAGEUPBDM-UHFFFAOYSA-N $l^{1}-oxidanylethane Chemical group CC[O] VOLGAXAGEUPBDM-UHFFFAOYSA-N 0.000 claims description 2
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- GRVDJDISBSALJP-UHFFFAOYSA-N methyloxidanyl Chemical group [O]C GRVDJDISBSALJP-UHFFFAOYSA-N 0.000 claims description 2
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- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 16
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 15
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- 150000001298 alcohols Chemical class 0.000 description 14
- 239000012299 nitrogen atmosphere Substances 0.000 description 10
- 239000000047 product Substances 0.000 description 10
- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 8
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- 238000002360 preparation method Methods 0.000 description 8
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- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 7
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 7
- 150000004756 silanes Chemical class 0.000 description 7
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- 150000002009 diols Chemical class 0.000 description 6
- HENJUOQEQGBPSV-UHFFFAOYSA-N isocyanatomethyl-dimethoxy-methylsilane Chemical compound CO[Si](C)(OC)CN=C=O HENJUOQEQGBPSV-UHFFFAOYSA-N 0.000 description 6
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- 239000003381 stabilizer Substances 0.000 description 5
- CPUDPFPXCZDNGI-UHFFFAOYSA-N triethoxy(methyl)silane Chemical compound CCO[Si](C)(OCC)OCC CPUDPFPXCZDNGI-UHFFFAOYSA-N 0.000 description 5
- GQHTUMJGOHRCHB-UHFFFAOYSA-N 2,3,4,6,7,8,9,10-octahydropyrimido[1,2-a]azepine Chemical compound C1CCCCN2CCCN=C21 GQHTUMJGOHRCHB-UHFFFAOYSA-N 0.000 description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
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- 230000008030 elimination Effects 0.000 description 4
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- ACCCMOQWYVYDOT-UHFFFAOYSA-N hexane-1,1-diol Chemical compound CCCCCC(O)O ACCCMOQWYVYDOT-UHFFFAOYSA-N 0.000 description 4
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- VXUYXOFXAQZZMF-UHFFFAOYSA-N titanium(IV) isopropoxide Chemical compound CC(C)O[Ti](OC(C)C)(OC(C)C)OC(C)C VXUYXOFXAQZZMF-UHFFFAOYSA-N 0.000 description 4
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
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- SJRJJKPEHAURKC-UHFFFAOYSA-N N-Methylmorpholine Chemical compound CN1CCOCC1 SJRJJKPEHAURKC-UHFFFAOYSA-N 0.000 description 3
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- AYOHIQLKSOJJQH-UHFFFAOYSA-N dibutyltin Chemical compound CCCC[Sn]CCCC AYOHIQLKSOJJQH-UHFFFAOYSA-N 0.000 description 3
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- YCZJVRCZIPDYHH-UHFFFAOYSA-N ditridecyl benzene-1,2-dicarboxylate Chemical compound CCCCCCCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCCCCCCC YCZJVRCZIPDYHH-UHFFFAOYSA-N 0.000 description 1
- JRBPAEWTRLWTQC-UHFFFAOYSA-N dodecylamine Chemical compound CCCCCCCCCCCCN JRBPAEWTRLWTQC-UHFFFAOYSA-N 0.000 description 1
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- 239000003822 epoxy resin Substances 0.000 description 1
- NKSJNEHGWDZZQF-UHFFFAOYSA-N ethenyl(trimethoxy)silane Chemical compound CO[Si](OC)(OC)C=C NKSJNEHGWDZZQF-UHFFFAOYSA-N 0.000 description 1
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- ZZUFCTLCJUWOSV-UHFFFAOYSA-N furosemide Chemical compound C1=C(Cl)C(S(=O)(=O)N)=CC(C(O)=O)=C1NCC1=CC=CO1 ZZUFCTLCJUWOSV-UHFFFAOYSA-N 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 239000005337 ground glass Substances 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 229910001385 heavy metal Inorganic materials 0.000 description 1
- 125000005842 heteroatom Chemical group 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- SYECJBOWSGTPLU-UHFFFAOYSA-N hexane-1,1-diamine Chemical compound CCCCCC(N)N SYECJBOWSGTPLU-UHFFFAOYSA-N 0.000 description 1
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 229920001477 hydrophilic polymer Polymers 0.000 description 1
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
- 239000001863 hydroxypropyl cellulose Substances 0.000 description 1
- 235000010977 hydroxypropyl cellulose Nutrition 0.000 description 1
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- 239000011256 inorganic filler Substances 0.000 description 1
- 229910003475 inorganic filler Inorganic materials 0.000 description 1
- LZKLAOYSENRNKR-LNTINUHCSA-N iron;(z)-4-oxoniumylidenepent-2-en-2-olate Chemical compound [Fe].C\C(O)=C\C(C)=O.C\C(O)=C\C(C)=O.C\C(O)=C\C(C)=O LZKLAOYSENRNKR-LNTINUHCSA-N 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
- QRFPECUQGPJPMV-UHFFFAOYSA-N isocyanatomethyl(trimethoxy)silane Chemical compound CO[Si](OC)(OC)CN=C=O QRFPECUQGPJPMV-UHFFFAOYSA-N 0.000 description 1
- 229940102253 isopropanolamine Drugs 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000004611 light stabiliser Substances 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 239000000944 linseed oil Substances 0.000 description 1
- 235000021388 linseed oil Nutrition 0.000 description 1
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
- 239000001095 magnesium carbonate Substances 0.000 description 1
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 150000002734 metacrylic acid derivatives Chemical class 0.000 description 1
- 150000002736 metal compounds Chemical class 0.000 description 1
- ARYZCSRUUPFYMY-UHFFFAOYSA-N methoxysilane Chemical group CO[SiH3] ARYZCSRUUPFYMY-UHFFFAOYSA-N 0.000 description 1
- VOFZZZOHJMJYKC-UHFFFAOYSA-N methyl n-(trimethoxysilylmethyl)carbamate Chemical class COC(=O)NC[Si](OC)(OC)OC VOFZZZOHJMJYKC-UHFFFAOYSA-N 0.000 description 1
- OCDZSSJEBQKKJI-UHFFFAOYSA-N methyl(triethoxysilylmethoxy)carbamic acid Chemical compound CCO[Si](CON(C)C(=O)O)(OCC)OCC OCDZSSJEBQKKJI-UHFFFAOYSA-N 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- QOHMWDJIBGVPIF-UHFFFAOYSA-N n',n'-diethylpropane-1,3-diamine Chemical compound CCN(CC)CCCN QOHMWDJIBGVPIF-UHFFFAOYSA-N 0.000 description 1
- GEMHFKXPOCTAIP-UHFFFAOYSA-N n,n-dimethyl-n'-phenylcarbamimidoyl chloride Chemical compound CN(C)C(Cl)=NC1=CC=CC=C1 GEMHFKXPOCTAIP-UHFFFAOYSA-N 0.000 description 1
- KOVKEDGZABFDPF-UHFFFAOYSA-N n-(triethoxysilylmethyl)aniline Chemical compound CCO[Si](OCC)(OCC)CNC1=CC=CC=C1 KOVKEDGZABFDPF-UHFFFAOYSA-N 0.000 description 1
- WUFHQGLVNNOXMP-UHFFFAOYSA-N n-(triethoxysilylmethyl)cyclohexanamine Chemical compound CCO[Si](OCC)(OCC)CNC1CCCCC1 WUFHQGLVNNOXMP-UHFFFAOYSA-N 0.000 description 1
- REODOQPOCJZARG-UHFFFAOYSA-N n-[[diethoxy(methyl)silyl]methyl]cyclohexanamine Chemical compound CCO[Si](C)(OCC)CNC1CCCCC1 REODOQPOCJZARG-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
- WIBFFTLQMKKBLZ-SEYXRHQNSA-N n-butyl oleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCCCC WIBFFTLQMKKBLZ-SEYXRHQNSA-N 0.000 description 1
- SZVGMOIRUYZMMW-UHFFFAOYSA-N n-silylbenzamide Chemical class [SiH3]NC(=O)C1=CC=CC=C1 SZVGMOIRUYZMMW-UHFFFAOYSA-N 0.000 description 1
- BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical class OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 1
- KHLCTMQBMINUNT-UHFFFAOYSA-N octadecane-1,12-diol Chemical compound CCCCCCC(O)CCCCCCCCCCCO KHLCTMQBMINUNT-UHFFFAOYSA-N 0.000 description 1
- JFOJYGMDZRCSPA-UHFFFAOYSA-J octadecanoate;tin(4+) Chemical compound [Sn+4].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O JFOJYGMDZRCSPA-UHFFFAOYSA-J 0.000 description 1
- XHLCCKLLXUAKCM-UHFFFAOYSA-N octadecyl 2-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)C(C)C1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 XHLCCKLLXUAKCM-UHFFFAOYSA-N 0.000 description 1
- IOQPZZOEVPZRBK-UHFFFAOYSA-N octan-1-amine Chemical compound CCCCCCCCN IOQPZZOEVPZRBK-UHFFFAOYSA-N 0.000 description 1
- OEIJHBUUFURJLI-UHFFFAOYSA-N octane-1,8-diol Chemical compound OCCCCCCCCO OEIJHBUUFURJLI-UHFFFAOYSA-N 0.000 description 1
- BARWIPMJPCRCTP-CLFAGFIQSA-N oleyl oleate Chemical compound CCCCCCCC\C=C/CCCCCCCCOC(=O)CCCCCCC\C=C/CCCCCCCC BARWIPMJPCRCTP-CLFAGFIQSA-N 0.000 description 1
- 239000012766 organic filler Substances 0.000 description 1
- 125000005375 organosiloxane group Chemical group 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- UKODFQOELJFMII-UHFFFAOYSA-N pentamethyldiethylenetriamine Chemical compound CN(C)CCN(C)CCN(C)C UKODFQOELJFMII-UHFFFAOYSA-N 0.000 description 1
- DGTNSSLYPYDJGL-UHFFFAOYSA-N phenyl isocyanate Chemical compound O=C=NC1=CC=CC=C1 DGTNSSLYPYDJGL-UHFFFAOYSA-N 0.000 description 1
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 150000003018 phosphorus compounds Chemical class 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 229920002432 poly(vinyl methyl ether) polymer Polymers 0.000 description 1
- 229920001515 polyalkylene glycol Polymers 0.000 description 1
- 229920001521 polyalkylene glycol ether Polymers 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 229920001707 polybutylene terephthalate Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229920000909 polytetrahydrofuran Polymers 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical class CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 125000002572 propoxy group Chemical group [*]OC([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- SCPYDCQAZCOKTP-UHFFFAOYSA-N silanol Chemical compound [SiH3]O SCPYDCQAZCOKTP-UHFFFAOYSA-N 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- XJKVPKYVPCWHFO-UHFFFAOYSA-N silicon;hydrate Chemical compound O.[Si] XJKVPKYVPCWHFO-UHFFFAOYSA-N 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 235000011150 stannous chloride Nutrition 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 150000003459 sulfonic acid esters Chemical class 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000003784 tall oil Substances 0.000 description 1
- FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 description 1
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 125000003396 thiol group Chemical group [H]S* 0.000 description 1
- 239000012974 tin catalyst Substances 0.000 description 1
- 150000003606 tin compounds Chemical class 0.000 description 1
- AXZWODMDQAVCJE-UHFFFAOYSA-L tin(II) chloride (anhydrous) Chemical compound [Cl-].[Cl-].[Sn+2] AXZWODMDQAVCJE-UHFFFAOYSA-L 0.000 description 1
- KSBAEPSJVUENNK-UHFFFAOYSA-L tin(ii) 2-ethylhexanoate Chemical compound [Sn+2].CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O KSBAEPSJVUENNK-UHFFFAOYSA-L 0.000 description 1
- 150000003609 titanium compounds Chemical class 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 230000002110 toxicologic effect Effects 0.000 description 1
- 231100000027 toxicology Toxicity 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 150000003624 transition metals Chemical class 0.000 description 1
- 150000003628 tricarboxylic acids Chemical class 0.000 description 1
- HXOGQBSDPSMHJK-UHFFFAOYSA-N triethoxy(6-methylheptyl)silane Chemical compound CCO[Si](OCC)(OCC)CCCCCC(C)C HXOGQBSDPSMHJK-UHFFFAOYSA-N 0.000 description 1
- DENFJSAFJTVPJR-UHFFFAOYSA-N triethoxy(ethyl)silane Chemical compound CCO[Si](CC)(OCC)OCC DENFJSAFJTVPJR-UHFFFAOYSA-N 0.000 description 1
- OCANZHUXNZTABW-UHFFFAOYSA-N triethoxy(pent-4-enyl)silane Chemical compound CCO[Si](OCC)(OCC)CCCC=C OCANZHUXNZTABW-UHFFFAOYSA-N 0.000 description 1
- DQWPFSLDHJDLRL-UHFFFAOYSA-N triethyl phosphate Chemical compound CCOP(=O)(OCC)OCC DQWPFSLDHJDLRL-UHFFFAOYSA-N 0.000 description 1
- XZZNDPSIHUTMOC-UHFFFAOYSA-N triphenyl phosphate Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)(=O)OC1=CC=CC=C1 XZZNDPSIHUTMOC-UHFFFAOYSA-N 0.000 description 1
- 239000002383 tung oil Substances 0.000 description 1
- UKRDPEFKFJNXQM-UHFFFAOYSA-N vinylsilane Chemical class [SiH3]C=C UKRDPEFKFJNXQM-UHFFFAOYSA-N 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- PAPBSGBWRJIAAV-UHFFFAOYSA-N ε-Caprolactone Chemical compound O=C1CCCCCO1 PAPBSGBWRJIAAV-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/32—Polymers modified by chemical after-treatment
- C08G65/329—Polymers modified by chemical after-treatment with organic compounds
- C08G65/336—Polymers modified by chemical after-treatment with organic compounds containing silicon
-
- C—CHEMISTRY; METALLURGY
- 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
- C08G18/71—Monoisocyanates or monoisothiocyanates
- C08G18/718—Monoisocyanates or monoisothiocyanates containing silicon
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Sealing Material Composition (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Polyurethanes Or Polyureas (AREA)
- Polyethers (AREA)
- Other Resins Obtained By Reactions Not Involving Carbon-To-Carbon Unsaturated Bonds (AREA)
- Paints Or Removers (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102005051921A DE102005051921A1 (de) | 2005-10-29 | 2005-10-29 | α-Ethoxysilan modifizierte Polymere, deren Herstellung und Verwendung |
| DE102005051921.0 | 2005-10-29 | ||
| PCT/EP2006/010082 WO2007048538A1 (de) | 2005-10-29 | 2006-10-19 | α-ETHOXYSILAN MODIFIZIERTE POLYMERE, DEREN HERSTELLUNG UND VERWENDUNG |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2627006A1 true CA2627006A1 (en) | 2007-05-03 |
Family
ID=37769385
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002627006A Abandoned CA2627006A1 (en) | 2005-10-29 | 2006-10-19 | .alpha.-ethoxysilane-modified polymers, production and use thereof |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US8003745B2 (https=) |
| EP (1) | EP1940993A1 (https=) |
| JP (1) | JP2009513806A (https=) |
| CN (1) | CN101300319B (https=) |
| BR (1) | BRPI0617946A2 (https=) |
| CA (1) | CA2627006A1 (https=) |
| DE (1) | DE102005051921A1 (https=) |
| WO (1) | WO2007048538A1 (https=) |
Families Citing this family (36)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2007204502A (ja) * | 2006-01-05 | 2007-08-16 | Konishi Co Ltd | 硬化性シリコーン系樹脂組成物 |
| US8415444B2 (en) * | 2007-01-12 | 2013-04-09 | Kaneka Corporation | Curable composition |
| DE102007038030B4 (de) * | 2007-08-10 | 2009-07-09 | Henkel Ag & Co. Kgaa | Härtbare Zusammensetzungen aus Dimethoxysilanen |
| EP2212365B1 (de) * | 2007-11-21 | 2019-03-06 | Sika Technology AG | Feuchtigkeitshärtende zusammensetzung umfassend mindestens zwei silangruppen-aufweisende polymere |
| WO2010008154A2 (en) * | 2008-07-15 | 2010-01-21 | Korea Bio-Gen Co., Ltd | Room temperature moisture curable hybrid resin, method of preparing the same and application thereof |
| DE102008038488A1 (de) | 2008-08-20 | 2010-02-25 | Henkel Ag & Co. Kgaa | Feuchtigkeitshärtende wasserfeste Beschichtung |
| DE102008042632A1 (de) | 2008-10-06 | 2010-04-08 | Wacker Chemie Ag | Vernetzbare Massen auf der Basis von Organosiliciumverbindungen |
| DE102008043825A1 (de) * | 2008-11-18 | 2010-05-20 | Wacker Chemie Ag | Verfahren zum Abdichten von Oberflächen |
| DE102009016195A1 (de) | 2009-04-03 | 2010-10-07 | Basf Coatings Ag | Feuchtigkeitshärtende Beschichtungsmittel auf der Basis aprotischer Lösemittel enthaltend Bindemittel mit Alkoxysilangruppen und deren Verwendung |
| DE102009027357A1 (de) * | 2009-06-30 | 2011-01-05 | Wacker Chemie Ag | Alkoxysilanterminierte Polymere enthaltende Kleb- oder Dichtstoffmassen |
| JP5447284B2 (ja) * | 2009-08-19 | 2014-03-19 | 旭硝子株式会社 | 硬化性組成物、粘着体、粘着積層体および粘着体の製造方法 |
| DE102010001588A1 (de) | 2010-02-04 | 2011-08-04 | Henkel AG & Co. KGaA, 40589 | Härtbare Zusammensetzungen mit verbesserten Brandeigenschaften |
| DE102010043853A1 (de) * | 2010-11-12 | 2012-05-16 | Tesa Se | Haft- oder Schmelzklebmassen für feuchtigkeitsunempfindliche Verklebungen |
| JP2013056954A (ja) * | 2011-09-07 | 2013-03-28 | Sunstar Engineering Inc | 硬化性組成物 |
| US9593271B2 (en) | 2011-09-22 | 2017-03-14 | Kaneka Corporation | Curable composition and cured product thereof |
| FR2982156B1 (fr) | 2011-11-09 | 2014-07-04 | Oreal | Composition cosmetique ou dermatologique comprenant un alpha-alcoxysilane obtenu a partir d'un acrylate |
| FR2982154B1 (fr) | 2011-11-09 | 2015-07-17 | Oreal | Composition cosmetique ou dermatologique comprenant un compose modifie alpha-alcoxysilane |
| FR2982158B1 (fr) | 2011-11-09 | 2014-06-20 | Oreal | Composition cosmetique ou dermatologique comprenant un alpha-alcoxysilane obtenu a partir d'un epoxyde |
| FR2982157B1 (fr) | 2011-11-09 | 2016-08-19 | Oreal | Composition cosmetique ou dermatologique comprenant un alpha-alcoxysilane a base uree ou amide |
| FR2982149B1 (fr) | 2011-11-09 | 2016-08-26 | Oreal | Composition comprenant un alpha-alcoxysilane obtenu a partir d'une polyamine |
| EP2641935A1 (de) * | 2012-03-19 | 2013-09-25 | Sika Technology AG | Zusammensetzung auf Basis von silanterminierten Polymeren |
| WO2014009557A1 (de) * | 2012-07-13 | 2014-01-16 | Sika Technology Ag | Hochgefüllte zusammensetzung auf basis von silanterminierten polymeren |
| DE102013206266A1 (de) * | 2013-04-10 | 2014-10-16 | Wacker Chemie Ag | Vernetzbare Massen auf der Basis von Organosiliciumverbindungen |
| FR3005052B1 (fr) | 2013-04-30 | 2015-04-17 | Oreal | Compose adapte au maquillage et/ou soin des ongles |
| JP6161510B2 (ja) * | 2013-10-25 | 2017-07-12 | 東洋ゴム工業株式会社 | ゴム組成物及び空気入りタイヤ |
| KR101664948B1 (ko) | 2014-01-09 | 2016-10-13 | 한국생산기술연구원 | 알콕시실릴기를 갖는 새로운 노볼락 경화제, 이의 제조 방법, 이를 포함하는 조성물, 경화물 및 이의 용도 |
| DE102014101949A1 (de) | 2014-02-17 | 2015-08-20 | Franken Systems Gmbh | Verfahren zur druckwasserfesten Abdichtung von Bauwerken |
| CN104004488B (zh) * | 2014-04-14 | 2017-01-04 | 江苏矽时代材料科技有限公司 | 一种环保型端硅烷基丙烯酸酯改性聚氨酯电子密封胶 |
| DE202015009122U1 (de) * | 2015-03-17 | 2016-11-07 | Henkel Ag & Co. Kgaa | Silane und härtbare Zusammensetzungen, die diese Silane als Vernetzer enthalten |
| ES2707979T3 (es) | 2015-04-09 | 2019-04-08 | Evonik Degussa Gmbh | Aductos de isocianatoalquiltrimetoxisilanos y agentes ignífugos reactivos con éstos |
| CN105131380A (zh) * | 2015-08-18 | 2015-12-09 | 合肥市再德高分子材料有限公司 | 一种高性能改性羧基丁腈橡胶复合材料 |
| EP3362491B1 (de) * | 2015-10-15 | 2020-07-29 | Sika Technology AG | Katalysatorsystem für härtbare zusammensetzungen auf basis von silangruppen-haltigen polymeren |
| CN105219337B (zh) * | 2015-11-16 | 2018-08-14 | 广州市白云化工实业有限公司 | 双组份硅烷改性聚醚密封材料及其制备方法 |
| CN112920783B (zh) * | 2019-12-05 | 2022-08-02 | 中国石油化工股份有限公司 | 一种钻井液用润湿反转抑制剂及其制备方法 |
| CN112680164A (zh) * | 2020-12-29 | 2021-04-20 | 苏州添易朗科技有限公司 | 一种光学贴合用多功能密封胶的制备 |
| CN119978943B (zh) * | 2025-02-11 | 2025-08-22 | 广东中科新能源科技有限公司 | 提高热轧机组带钢质量的高分子重防腐材料及其制备工艺 |
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| JPS5924771A (ja) | 1982-08-02 | 1984-02-08 | Semedain Kk | 一液型室温硬化性シ−ラント組成物 |
| US5068304A (en) | 1988-12-09 | 1991-11-26 | Asahi Glass Company, Ltd. | Moisture-curable resin composition |
| JPH0649348A (ja) * | 1992-08-04 | 1994-02-22 | Shin Etsu Chem Co Ltd | 常温硬化性ポリエーテル組成物 |
| US5424384A (en) * | 1994-05-10 | 1995-06-13 | Dow Corning Corporation | Curable organosiloxane compositions containing low temperature reactive adhesion additives |
| DE19727029B4 (de) | 1997-06-25 | 2006-11-09 | Henkel Kgaa | Einkomponentige Reaktivsystem-Zusammensetzung, Verfahren zu ihrer Herstellung und ihre Verwendung |
| DE19908562A1 (de) * | 1998-03-25 | 1999-10-07 | Henkel Kgaa | Polyurethan und polyurethanhaltige Zubereitung |
| DE10053545A1 (de) * | 2000-10-27 | 2002-05-08 | Henkel Kgaa | Polymere mit Harnstoffgruppen und Silylgruppen, deren Herstellung und Verwendung |
| ES2292747T5 (es) | 2001-02-23 | 2014-04-10 | Henkel Ag & Co. Kgaa | Polímeros alcoxisililfuncionales mixtos |
| JP4099451B2 (ja) * | 2001-08-28 | 2008-06-11 | ワッカー ケミー アクチエンゲゼルシャフト | アルコキシシラン末端のポリマーを含有する速硬性１成分混合物 |
| US7307134B2 (en) * | 2002-02-22 | 2007-12-11 | Henkel Corporation | Mixed alkoxysilyl functional polymers |
| DE10237270A1 (de) * | 2002-08-14 | 2004-03-04 | Consortium für elektrochemische Industrie GmbH | Silanvernetzbare Beschichtungsformulierungen |
| DE10237271A1 (de) | 2002-08-14 | 2004-03-04 | Consortium für elektrochemische Industrie GmbH | Polymermassen auf Basis alkoxysilanterminierter Polymere mit regulierbarer Härtungsgeschwindigkeit |
| JP4101632B2 (ja) * | 2002-11-01 | 2008-06-18 | 株式会社カネカ | 硬化性組成物および復元性、クリープ性改善方法 |
| DE10327624B3 (de) * | 2003-06-20 | 2004-12-30 | Degussa Ag | Organosiliciumverbindungen, Verfahren zu ihrer Herstellung, sowie ihre Verwendung |
| US8003744B2 (en) * | 2003-08-25 | 2011-08-23 | Kaneka Corporation | Curing composition with improved heat resistance |
| US7009022B2 (en) * | 2003-12-15 | 2006-03-07 | Henkel Corporation | Moisture curable high strength, flexible RTV organic copolymer compositions and methods of preparation |
| US7294665B1 (en) * | 2004-03-15 | 2007-11-13 | Henkel Corporation | Moisture curable compositions with enhanced adhesion to polyolefins |
| US7307314B2 (en) * | 2004-06-16 | 2007-12-11 | Cree Microwave Llc | LDMOS transistor with improved gate shield |
-
2005
- 2005-10-29 DE DE102005051921A patent/DE102005051921A1/de not_active Ceased
-
2006
- 2006-10-19 JP JP2008538276A patent/JP2009513806A/ja not_active Ceased
- 2006-10-19 WO PCT/EP2006/010082 patent/WO2007048538A1/de not_active Ceased
- 2006-10-19 EP EP06806391A patent/EP1940993A1/de not_active Withdrawn
- 2006-10-19 CN CN2006800404831A patent/CN101300319B/zh not_active Expired - Fee Related
- 2006-10-19 CA CA002627006A patent/CA2627006A1/en not_active Abandoned
- 2006-10-19 BR BRPI0617946-0A patent/BRPI0617946A2/pt not_active IP Right Cessation
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2008
- 2008-04-18 US US12/105,487 patent/US8003745B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| JP2009513806A (ja) | 2009-04-02 |
| DE102005051921A1 (de) | 2007-05-03 |
| US8003745B2 (en) | 2011-08-23 |
| WO2007048538A1 (de) | 2007-05-03 |
| US20080269406A1 (en) | 2008-10-30 |
| BRPI0617946A2 (pt) | 2011-08-09 |
| CN101300319A (zh) | 2008-11-05 |
| EP1940993A1 (de) | 2008-07-09 |
| CN101300319B (zh) | 2013-03-13 |
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