CN101711259A - 厌氧可固化组合物 - Google Patents
厌氧可固化组合物 Download PDFInfo
- Publication number
- CN101711259A CN101711259A CN200880020288A CN200880020288A CN101711259A CN 101711259 A CN101711259 A CN 101711259A CN 200880020288 A CN200880020288 A CN 200880020288A CN 200880020288 A CN200880020288 A CN 200880020288A CN 101711259 A CN101711259 A CN 101711259A
- Authority
- CN
- China
- Prior art keywords
- component
- composition
- polyol
- polyamines
- vulcabond
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 218
- 239000000463 material Substances 0.000 claims description 49
- 229920005862 polyol Polymers 0.000 claims description 34
- 150000003077 polyols Chemical class 0.000 claims description 33
- 229920000768 polyamine Polymers 0.000 claims description 26
- 229920006295 polythiol Polymers 0.000 claims description 23
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 claims description 22
- 239000000126 substance Substances 0.000 claims description 21
- 239000011248 coating agent Substances 0.000 claims description 17
- 238000000576 coating method Methods 0.000 claims description 17
- 238000004519 manufacturing process Methods 0.000 claims description 11
- 239000007795 chemical reaction product Substances 0.000 claims description 9
- 238000007789 sealing Methods 0.000 claims description 9
- 238000012856 packing Methods 0.000 claims description 7
- OUUQCZGPVNCOIJ-UHFFFAOYSA-M Superoxide Chemical compound [O-][O] OUUQCZGPVNCOIJ-UHFFFAOYSA-M 0.000 claims description 6
- 238000000034 method Methods 0.000 claims description 5
- 238000002156 mixing Methods 0.000 claims description 4
- 230000003068 static effect Effects 0.000 claims description 2
- 238000007493 shaping process Methods 0.000 claims 1
- 239000011159 matrix material Substances 0.000 abstract description 46
- 230000009969 flowable effect Effects 0.000 abstract description 10
- 239000002904 solvent Substances 0.000 abstract description 7
- 238000001723 curing Methods 0.000 description 37
- 239000000758 substrate Substances 0.000 description 23
- -1 isocyanatomethyl Chemical group 0.000 description 19
- 239000000853 adhesive Substances 0.000 description 18
- 230000001070 adhesive effect Effects 0.000 description 18
- WTFAGPBUAGFMQX-UHFFFAOYSA-N 1-[2-[2-(2-aminopropoxy)propoxy]propoxy]propan-2-amine Chemical compound CC(N)COCC(C)OCC(C)OCC(C)N WTFAGPBUAGFMQX-UHFFFAOYSA-N 0.000 description 17
- 239000000047 product Substances 0.000 description 15
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 14
- 239000003795 chemical substances by application Substances 0.000 description 14
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 13
- 239000002390 adhesive tape Substances 0.000 description 12
- 229920000642 polymer Polymers 0.000 description 12
- 239000007788 liquid Substances 0.000 description 11
- 229920001228 polyisocyanate Polymers 0.000 description 11
- 239000005056 polyisocyanate Substances 0.000 description 11
- 238000012360 testing method Methods 0.000 description 10
- 239000004215 Carbon black (E152) Substances 0.000 description 9
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 9
- 150000002148 esters Chemical class 0.000 description 9
- 229920003226 polyurethane urea Polymers 0.000 description 9
- 238000002360 preparation method Methods 0.000 description 9
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 8
- 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
- 238000006243 chemical reaction Methods 0.000 description 8
- 239000012975 dibutyltin dilaurate Substances 0.000 description 8
- 229930195733 hydrocarbon Natural products 0.000 description 8
- 150000002430 hydrocarbons Chemical class 0.000 description 8
- ZEMPKEQAKRGZGQ-AAKVHIHISA-N 2,3-bis[[(z)-12-hydroxyoctadec-9-enoyl]oxy]propyl (z)-12-hydroxyoctadec-9-enoate Chemical compound CCCCCCC(O)C\C=C/CCCCCCCC(=O)OCC(OC(=O)CCCCCCC\C=C/CC(O)CCCCCC)COC(=O)CCCCCCC\C=C/CC(O)CCCCCC ZEMPKEQAKRGZGQ-AAKVHIHISA-N 0.000 description 7
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 7
- 229910000831 Steel Inorganic materials 0.000 description 7
- 238000004140 cleaning Methods 0.000 description 7
- 239000013530 defoamer Substances 0.000 description 7
- 239000000178 monomer Substances 0.000 description 7
- 229910052757 nitrogen Inorganic materials 0.000 description 7
- 239000010959 steel Substances 0.000 description 7
- JOYRKODLDBILNP-UHFFFAOYSA-N urethane group Chemical group NC(=O)OCC JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 7
- LRXTYHSAJDENHV-UHFFFAOYSA-H zinc phosphate Chemical compound [Zn+2].[Zn+2].[Zn+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O LRXTYHSAJDENHV-UHFFFAOYSA-H 0.000 description 7
- 229910000165 zinc phosphate Inorganic materials 0.000 description 7
- 229920002396 Polyurea Polymers 0.000 description 6
- 125000000217 alkyl group Chemical group 0.000 description 6
- 238000007872 degassing Methods 0.000 description 6
- FRIBMENBGGCKPD-UHFFFAOYSA-N 3-(2,3-dimethoxyphenyl)prop-2-enal Chemical compound COC1=CC=CC(C=CC=O)=C1OC FRIBMENBGGCKPD-UHFFFAOYSA-N 0.000 description 5
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 5
- 150000001412 amines Chemical class 0.000 description 5
- 125000004432 carbon atom Chemical group C* 0.000 description 5
- 239000000975 dye Substances 0.000 description 5
- 239000003921 oil Substances 0.000 description 5
- 230000008719 thickening Effects 0.000 description 5
- 229910052718 tin Inorganic materials 0.000 description 5
- LDHQCZJRKDOVOX-UHFFFAOYSA-N 2-butenoic acid Chemical compound CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 4
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 4
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 4
- 230000008901 benefit Effects 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 235000011187 glycerol Nutrition 0.000 description 4
- 239000001257 hydrogen Substances 0.000 description 4
- 229910052739 hydrogen Inorganic materials 0.000 description 4
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 4
- 239000012948 isocyanate Substances 0.000 description 4
- 238000012423 maintenance Methods 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 150000003254 radicals Chemical class 0.000 description 4
- 229960004418 trolamine Drugs 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- 229920000742 Cotton Polymers 0.000 description 3
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 3
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- GNVMUORYQLCPJZ-UHFFFAOYSA-M Thiocarbamate Chemical compound NC([S-])=O GNVMUORYQLCPJZ-UHFFFAOYSA-M 0.000 description 3
- 125000001931 aliphatic group Chemical group 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 150000004985 diamines Chemical class 0.000 description 3
- 239000008393 encapsulating agent Substances 0.000 description 3
- 239000007888 film coating Substances 0.000 description 3
- 238000009501 film coating Methods 0.000 description 3
- 229910052736 halogen Inorganic materials 0.000 description 3
- 150000002367 halogens Chemical class 0.000 description 3
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 3
- 239000003999 initiator Substances 0.000 description 3
- 150000002513 isocyanates Chemical class 0.000 description 3
- 230000005012 migration Effects 0.000 description 3
- 238000013508 migration Methods 0.000 description 3
- 229920000151 polyglycol Polymers 0.000 description 3
- 239000010695 polyglycol Substances 0.000 description 3
- 230000000717 retained effect Effects 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- 229920002554 vinyl polymer Polymers 0.000 description 3
- QEQBMZQFDDDTPN-UHFFFAOYSA-N (2-methylpropan-2-yl)oxy benzenecarboperoxoate Chemical compound CC(C)(C)OOOC(=O)C1=CC=CC=C1 QEQBMZQFDDDTPN-UHFFFAOYSA-N 0.000 description 2
- MTZUIIAIAKMWLI-UHFFFAOYSA-N 1,2-diisocyanatobenzene Chemical compound O=C=NC1=CC=CC=C1N=C=O MTZUIIAIAKMWLI-UHFFFAOYSA-N 0.000 description 2
- MNAHQWDCXOHBHK-UHFFFAOYSA-N 1-phenylpropane-1,1-diol Chemical compound CCC(O)(O)C1=CC=CC=C1 MNAHQWDCXOHBHK-UHFFFAOYSA-N 0.000 description 2
- 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 2
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 2
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 description 2
- 241000196324 Embryophyta Species 0.000 description 2
- 239000002202 Polyethylene glycol Substances 0.000 description 2
- 239000004721 Polyphenylene oxide Substances 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 238000013006 addition curing Methods 0.000 description 2
- 150000001335 aliphatic alkanes Chemical class 0.000 description 2
- 125000003342 alkenyl group Chemical group 0.000 description 2
- 150000004982 aromatic amines Chemical class 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 229920002678 cellulose Polymers 0.000 description 2
- 239000001913 cellulose Substances 0.000 description 2
- KIQKWYUGPPFMBV-UHFFFAOYSA-N diisocyanatomethane Chemical compound O=C=NCN=C=O KIQKWYUGPPFMBV-UHFFFAOYSA-N 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- STVZJERGLQHEKB-UHFFFAOYSA-N ethylene glycol dimethacrylate Chemical compound CC(=C)C(=O)OCCOC(=O)C(C)=C STVZJERGLQHEKB-UHFFFAOYSA-N 0.000 description 2
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 2
- 229920001903 high density polyethylene Polymers 0.000 description 2
- 239000004700 high-density polyethylene Substances 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 230000007246 mechanism Effects 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- CFJYNSNXFXLKNS-UHFFFAOYSA-N p-menthane Chemical compound CC(C)C1CCC(C)CC1 CFJYNSNXFXLKNS-UHFFFAOYSA-N 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 229920000570 polyether Polymers 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- 239000000376 reactant Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 239000000565 sealant Substances 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 239000003352 sequestering agent Substances 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- CIHOLLKRGTVIJN-UHFFFAOYSA-N tert‐butyl hydroperoxide Chemical compound CC(C)(C)OO CIHOLLKRGTVIJN-UHFFFAOYSA-N 0.000 description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
- 239000012207 thread-locking agent Substances 0.000 description 2
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 2
- 238000012546 transfer Methods 0.000 description 2
- XFNJVJPLKCPIBV-UHFFFAOYSA-N trimethylenediamine Chemical compound NCCCN XFNJVJPLKCPIBV-UHFFFAOYSA-N 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- JHPBZFOKBAGZBL-UHFFFAOYSA-N (3-hydroxy-2,2,4-trimethylpentyl) 2-methylprop-2-enoate Chemical compound CC(C)C(O)C(C)(C)COC(=O)C(C)=C JHPBZFOKBAGZBL-UHFFFAOYSA-N 0.000 description 1
- JCZPOYAMKJFOLA-IMJSIDKUSA-N (3s,4s)-pyrrolidine-3,4-diol Chemical compound O[C@H]1CNC[C@@H]1O JCZPOYAMKJFOLA-IMJSIDKUSA-N 0.000 description 1
- ZBBLRPRYYSJUCZ-GRHBHMESSA-L (z)-but-2-enedioate;dibutyltin(2+) Chemical compound [O-]C(=O)\C=C/C([O-])=O.CCCC[Sn+2]CCCC ZBBLRPRYYSJUCZ-GRHBHMESSA-L 0.000 description 1
- GBDZXPJXOMHESU-UHFFFAOYSA-N 1,2,3,4-tetrachlorobenzene Chemical compound ClC1=CC=C(Cl)C(Cl)=C1Cl GBDZXPJXOMHESU-UHFFFAOYSA-N 0.000 description 1
- OKIRBHVFJGXOIS-UHFFFAOYSA-N 1,2-di(propan-2-yl)benzene Chemical compound CC(C)C1=CC=CC=C1C(C)C OKIRBHVFJGXOIS-UHFFFAOYSA-N 0.000 description 1
- ALQLPWJFHRMHIU-UHFFFAOYSA-N 1,4-diisocyanatobenzene Chemical compound O=C=NC1=CC=C(N=C=O)C=C1 ALQLPWJFHRMHIU-UHFFFAOYSA-N 0.000 description 1
- YHCVYAHUIMOIGE-UHFFFAOYSA-N 2,3-dihydroxypropyl but-2-enoate Chemical compound CC=CC(=O)OCC(O)CO YHCVYAHUIMOIGE-UHFFFAOYSA-N 0.000 description 1
- KKSVEWVQRUFYIN-UHFFFAOYSA-N C(C=C)(=O)OC.C(C=C)(=O)OCCCO Chemical compound C(C=C)(=O)OC.C(C=C)(=O)OCCCO KKSVEWVQRUFYIN-UHFFFAOYSA-N 0.000 description 1
- IPJWNWFUOHMNCS-UHFFFAOYSA-N C(C=C)(=O)OC.OC(CC)(C1=CC=CC=C1)O Chemical compound C(C=C)(=O)OC.OC(CC)(C1=CC=CC=C1)O IPJWNWFUOHMNCS-UHFFFAOYSA-N 0.000 description 1
- WSNMPAVSZJSIMT-UHFFFAOYSA-N COc1c(C)c2COC(=O)c2c(O)c1CC(O)C1(C)CCC(=O)O1 Chemical compound COc1c(C)c2COC(=O)c2c(O)c1CC(O)C1(C)CCC(=O)O1 WSNMPAVSZJSIMT-UHFFFAOYSA-N 0.000 description 1
- 239000009261 D 400 Substances 0.000 description 1
- 239000004258 Ethoxyquin Substances 0.000 description 1
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 1
- AXISYYRBXTVTFY-UHFFFAOYSA-N Isopropyl tetradecanoate Chemical compound CCCCCCCCCCCCCC(=O)OC(C)C AXISYYRBXTVTFY-UHFFFAOYSA-N 0.000 description 1
- 239000005639 Lauric acid Substances 0.000 description 1
- RDFXCMMSWDVURH-UHFFFAOYSA-N O1CCOCC1.[Sn] Chemical compound O1CCOCC1.[Sn] RDFXCMMSWDVURH-UHFFFAOYSA-N 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- 239000004823 Reactive adhesive Substances 0.000 description 1
- 235000004443 Ricinus communis Nutrition 0.000 description 1
- 240000000528 Ricinus communis Species 0.000 description 1
- 239000004902 Softening Agent Substances 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 239000005864 Sulphur Substances 0.000 description 1
- 239000004809 Teflon Substances 0.000 description 1
- 229920006362 Teflon® Polymers 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical group [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- DAKWPKUUDNSNPN-UHFFFAOYSA-N Trimethylolpropane triacrylate Chemical compound C=CC(=O)OCC(CC)(COC(=O)C=C)COC(=O)C=C DAKWPKUUDNSNPN-UHFFFAOYSA-N 0.000 description 1
- 239000007983 Tris buffer Substances 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- XECAHXYUAAWDEL-UHFFFAOYSA-N acrylonitrile butadiene styrene Chemical compound C=CC=C.C=CC#N.C=CC1=CC=CC=C1 XECAHXYUAAWDEL-UHFFFAOYSA-N 0.000 description 1
- 239000004676 acrylonitrile butadiene styrene Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 125000001118 alkylidene group Chemical group 0.000 description 1
- 239000004411 aluminium Substances 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 125000003368 amide group Chemical group 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 125000003710 aryl alkyl group Chemical group 0.000 description 1
- 150000004646 arylidenes Chemical group 0.000 description 1
- 230000000712 assembly Effects 0.000 description 1
- 238000000429 assembly Methods 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229940106691 bisphenol a Drugs 0.000 description 1
- YHWCPXVTRSHPNY-UHFFFAOYSA-N butan-1-olate;titanium(4+) Chemical compound [Ti+4].CCCC[O-].CCCC[O-].CCCC[O-].CCCC[O-] YHWCPXVTRSHPNY-UHFFFAOYSA-N 0.000 description 1
- 125000004106 butoxy group Chemical group [*]OC([H])([H])C([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 150000007942 carboxylates Chemical class 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- RWGFKTVRMDUZSP-UHFFFAOYSA-N cumene Chemical compound CC(C)C1=CC=CC=C1 RWGFKTVRMDUZSP-UHFFFAOYSA-N 0.000 description 1
- 125000000392 cycloalkenyl group Chemical group 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- 238000005238 degreasing Methods 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- 125000005442 diisocyanate group Chemical group 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 238000003912 environmental pollution Methods 0.000 description 1
- 229920006332 epoxy adhesive Polymers 0.000 description 1
- 125000001033 ether group Chemical group 0.000 description 1
- DECIPOUIJURFOJ-UHFFFAOYSA-N ethoxyquin Chemical compound N1C(C)(C)C=C(C)C2=CC(OCC)=CC=C21 DECIPOUIJURFOJ-UHFFFAOYSA-N 0.000 description 1
- 229940093500 ethoxyquin Drugs 0.000 description 1
- 235000019285 ethoxyquin Nutrition 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- SFNALCNOMXIBKG-UHFFFAOYSA-N ethylene glycol monododecyl ether Chemical compound CCCCCCCCCCCCOCCO SFNALCNOMXIBKG-UHFFFAOYSA-N 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 238000010438 heat treatment Methods 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
- 238000006459 hydrosilylation reaction Methods 0.000 description 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- VQPKAMAVKYTPLB-UHFFFAOYSA-N lead;octanoic acid Chemical compound [Pb].CCCCCCCC(O)=O VQPKAMAVKYTPLB-UHFFFAOYSA-N 0.000 description 1
- 230000013011 mating Effects 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- UICBCXONCUFSOI-UHFFFAOYSA-N n'-phenylacetohydrazide Chemical compound CC(=O)NNC1=CC=CC=C1 UICBCXONCUFSOI-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
- NSBIQPJIWUJBBX-UHFFFAOYSA-N n-methoxyaniline Chemical compound CONC1=CC=CC=C1 NSBIQPJIWUJBBX-UHFFFAOYSA-N 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 229930004008 p-menthane Natural products 0.000 description 1
- 229940059574 pentaerithrityl Drugs 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- RGSFGYAAUTVSQA-UHFFFAOYSA-N pentamethylene Natural products C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 description 1
- 238000000016 photochemical curing Methods 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 229920001515 polyalkylene glycol Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920006264 polyurethane film Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000010944 pre-mature reactiony Methods 0.000 description 1
- 230000002028 premature Effects 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 125000006239 protecting group Chemical group 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 150000003333 secondary alcohols Chemical class 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229960001866 silicon dioxide Drugs 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- FDDDEECHVMSUSB-UHFFFAOYSA-N sulfanilamide Chemical compound NC1=CC=C(S(N)(=O)=O)C=C1 FDDDEECHVMSUSB-UHFFFAOYSA-N 0.000 description 1
- 229940124530 sulfonamide Drugs 0.000 description 1
- 150000003457 sulfones Chemical class 0.000 description 1
- 239000013008 thixotropic agent Substances 0.000 description 1
- 230000009974 thixotropic effect Effects 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- AUTOISGCBLBLBA-UHFFFAOYSA-N trizinc;diphosphite Chemical compound [Zn+2].[Zn+2].[Zn+2].[O-]P([O-])[O-].[O-]P([O-])[O-] AUTOISGCBLBLBA-UHFFFAOYSA-N 0.000 description 1
- CHJMFFKHPHCQIJ-UHFFFAOYSA-L zinc;octanoate Chemical compound [Zn+2].CCCCCCCC([O-])=O.CCCCCCCC([O-])=O CHJMFFKHPHCQIJ-UHFFFAOYSA-L 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J4/00—Adhesives based on organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond ; adhesives, based on monomers of macromolecular compounds of groups C09J183/00 - C09J183/16
- C09J4/06—Organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond in combination with a macromolecular compound other than an unsaturated polymer of groups C09J159/00 - C09J187/00
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F20/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride, ester, amide, imide or nitrile thereof
- C08F20/02—Monocarboxylic acids having less than ten carbon atoms, Derivatives thereof
- C08F20/10—Esters
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B7/00—Layered products characterised by the relation between layers; Layered products characterised by the relative orientation of features between layers, or by the relative values of a measurable parameter between layers, i.e. products comprising layers having different physical, chemical or physicochemical properties; Layered products characterised by the interconnection of layers
- B32B7/04—Interconnection of layers
- B32B7/10—Interconnection of layers at least one layer having inter-reactive properties
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/08—Processes
- C08G18/10—Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/2805—Compounds having only one group containing active hydrogen
- C08G18/288—Compounds containing at least one heteroatom other than oxygen or nitrogen
-
- 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
- C08G18/32—Polyhydroxy compounds; Polyamines; Hydroxyamines
- C08G18/3203—Polyhydroxy compounds
- C08G18/3206—Polyhydroxy compounds aliphatic
-
- 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
- C08G18/36—Hydroxylated esters of higher fatty acids
-
- 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
- C08G18/48—Polyethers
- C08G18/50—Polyethers having heteroatoms other than oxygen
- C08G18/5021—Polyethers having heteroatoms other than oxygen having nitrogen
- C08G18/5024—Polyethers having heteroatoms other than oxygen having nitrogen containing primary and/or secondary amino groups
-
- 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
- C08G18/67—Unsaturated compounds having active hydrogen
- C08G18/671—Unsaturated compounds having only one group containing active hydrogen
- C08G18/672—Esters of acrylic or alkyl acrylic acid having only one group containing active hydrogen
-
- 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
- C08G71/00—Macromolecular compounds obtained by reactions forming a ureide or urethane link, otherwise, than from isocyanate radicals in the main chain of the macromolecule
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J175/00—Adhesives based on polyureas or polyurethanes; Adhesives based on derivatives of such polymers
- C09J175/04—Polyurethanes
- C09J175/14—Polyurethanes having carbon-to-carbon unsaturated bonds
- C09J175/16—Polyurethanes having carbon-to-carbon unsaturated bonds having terminal carbon-to-carbon unsaturated bonds
-
- 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
- C09J4/00—Adhesives based on organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond ; adhesives, based on monomers of macromolecular compounds of groups C09J183/00 - C09J183/16
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/04—Homopolymers or copolymers of ethene
- C08L23/06—Polyethene
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2666/00—Composition of polymers characterized by a further compound in the blend, being organic macromolecular compounds, natural resins, waxes or and bituminous materials, non-macromolecular organic substances, inorganic substances or characterized by their function in the composition
- C08L2666/02—Organic macromolecular compounds, natural resins, waxes or and bituminous materials
- C08L2666/04—Macromolecular compounds according to groups C08L7/00 - C08L49/00, or C08L55/00 - C08L57/00; Derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L55/00—Compositions of homopolymers or copolymers, obtained by polymerisation reactions only involving carbon-to-carbon unsaturated bonds, not provided for in groups C08L23/00 - C08L53/00
- C08L55/02—ABS [Acrylonitrile-Butadiene-Styrene] polymers
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Sealing Material Composition (AREA)
- Polyurethanes Or Polyureas (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Macromonomer-Based Addition Polymer (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Abstract
Description
组分 | WT% |
EBIPMA | 72.00 |
PEGMA | 22.50 |
糖精 | 1.000 |
稳定剂 | 0.500 |
染料 | 0.500 |
促进剂(乙酰基苯基肼(APH)) | 0.500 |
增稠剂(二氧化硅) | 2.000 |
CHP(氢过氧化枯烯) | 1.000 |
组分 | WT% |
100.000 |
组分 | WT% |
Baytec*MP 020 | 100.00 |
所使用的产品 | 试验类型 | 基底 | 螺帽和螺栓 | In-lbs |
无 | 松动 | 无 | 磷酸锌+油的钢 | 41 |
本发明组合物A | 松动 | 无 | 磷酸锌+油的钢 | 237 |
2760 | 松动 | 无 | 磷酸锌+油的钢 | 451 |
组分 | %wt | CAS No. |
单体4,4`-MDI | 70-100 | 26447-40-5 |
聚乙二醇二甲基丙烯酸酯(PEGMA) | 0-30 | 110-82-7,123-31-9 |
组分 | %wt | CAS No. |
聚乙二醇二甲基丙烯酸酯 | 1-30 | 110-82-7,123-31-9 |
蓖麻基有机触变剂 | 1-3 | 8001-78-3 |
蓖麻油 | 20-40 | 8001-78-3 |
1,4-丁二醇 | 5-15 | 110-63-4 |
聚(丙烯腈-丁二烯-苯乙烯) | 5-20 | 100-42-5,9003-56-9 |
糖精 | 1-2 | 81-07-2 |
聚乙烯粉末 | 0.1-0.5 | 9002-88-4 |
氢过氧化枯烯 | 0.5-2.0 | 80-15-9 |
甘油 | 1-6 | 56-81-5 |
聚氧亚丙基二胺 | 5-10 | 9046-10-0 |
组分 | %wt |
Lupranate MP102* | 78.65 |
Lupranate M20S* | 10.00 |
厌氧催化剂(糖精) | 0.30 |
组分 | %wt |
增塑剂(三醋精) | 10.00 |
过苯甲酸叔丁酯(TBPB) | 1.00 |
消泡剂 | 0.05 |
总计 | 100.00 |
组分 | %wt |
PEGMA | 25.00 |
HPMA | 1.00 |
增稠剂 | 0.50 |
四官能的聚醚多羟基化合物 | 48.00 |
蓖麻油(低湿度多羟基化合物) | 24.39 |
染料 | 0.04 |
消泡剂 | 0.05 |
二月桂酸二丁锡(DBTDL) | 0.02 |
厌氧催化剂(三乙醇胺) | 1.00 |
总计 | 100.00 |
组分 | %wt |
厌氧催化剂(糖精) | 0.30 |
二醇三酯增塑剂(三醋精) | 10.00 |
Lupranate MP 102 | 65.36 |
蓖麻油(低湿多羟基化合物) | 8.28 |
DBTDL | 0.01 |
Lupranate M20S | 15.00 |
TBPB | 1.00 |
消泡剂 | 0.05 |
总计 | 100.00 |
组分 | %wt |
PEGMA | 25.00 |
HPMA | 1.00 |
增稠剂 | 1.50 |
多羟基化合物 | 38.54 |
蓖麻油(低湿多羟基化合物) | 32.85 |
三乙醇胺 | 1.00 |
染料 | 0.04 |
消泡剂 | 0.05 |
DBTDL | 0.02 |
总计 | 100.00 |
组分 | %wt |
三醋精 | 13.00 |
Lupranate MP102 | 86.95 |
消泡剂 | 0.05 |
总计 | 100.00 |
组分 | %wt |
PEGMA | 25.00 |
蓖麻油(低湿多羟基化合物) | 32.85 |
糖精 | 0.30 |
增稠剂 | 1.00 |
三乙醇胺 | 1.50 |
多羟基化合物 | 43.85 |
自由基稳定剂 | 0.75 |
螯合剂 | 1.00 |
染料 | 0.04 |
消泡剂 | 0.04 |
DBTDL | 0.02 |
组分 | %wt |
TBPB | 0.05 |
总计 | 100.00 |
组分 | %wt |
Lupranate MP102 | 100.00 |
总计 | 100.00 |
组分 | %wt |
PEGMA | 25.00 |
三醋精 | 10.00 |
糖精 | 0.30 |
增稠剂 | 1.00 |
蓖麻油(低湿多羟基化合物) | 12.50 |
三乙醇胺 | 1.50 |
多羟基化合物 | 47.35 |
自由基稳定剂 | 0.75 |
螯合剂 | 1.00 |
染料 | 0.04 |
组分 | %wt |
消泡剂 | 0.04 |
TBPB | 0.50 |
DBTDL | 0.02 |
总计 | 100.00 |
Claims (14)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US93953407P | 2007-05-22 | 2007-05-22 | |
US60/939,534 | 2007-05-22 | ||
PCT/US2008/006343 WO2008153673A1 (en) | 2007-05-22 | 2008-05-16 | Anaerobically curable compositions |
Publications (2)
Publication Number | Publication Date |
---|---|
CN101711259A true CN101711259A (zh) | 2010-05-19 |
CN101711259B CN101711259B (zh) | 2015-12-02 |
Family
ID=40130011
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN200880020288.1A Expired - Fee Related CN101711259B (zh) | 2007-05-22 | 2008-05-16 | 厌氧可固化组合物 |
Country Status (8)
Country | Link |
---|---|
US (1) | US8835593B2 (zh) |
EP (1) | EP2148893A4 (zh) |
JP (1) | JP5566882B2 (zh) |
KR (1) | KR101524684B1 (zh) |
CN (1) | CN101711259B (zh) |
CA (1) | CA2687601C (zh) |
MX (1) | MX2009012542A (zh) |
WO (1) | WO2008153673A1 (zh) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN108368384A (zh) * | 2015-10-22 | 2018-08-03 | 汉高知识产权控股有限责任公司 | 可厌氧固化的组合物 |
CN110128994A (zh) * | 2019-04-09 | 2019-08-16 | 中海油常州涂料化工研究院有限公司 | 一种可湿固化的厌氧胶及其制备方法 |
CN113840852A (zh) * | 2019-04-05 | 2021-12-24 | 汉高知识产权控股有限责任公司 | 可厌氧固化的组合物 |
CN117165248A (zh) * | 2023-10-31 | 2023-12-05 | 南京艾布纳新材料股份有限公司 | 一种多重固化型聚氨酯可陶瓷化密封胶及其制备方法 |
Families Citing this family (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA2738910C (en) * | 2008-09-30 | 2016-02-02 | Henkel Corporation | Dry-to-the-touch moisture-curable compositions and products made therefrom |
CN103502297A (zh) * | 2011-05-03 | 2014-01-08 | 陶氏环球技术有限责任公司 | 包含异氰酸酯官能预聚物的加速固化组合物 |
JP5655770B2 (ja) * | 2011-12-13 | 2015-01-21 | トヨタ自動車株式会社 | 電子部品及び当該電子部品の製造方法 |
US9416301B2 (en) | 2012-11-08 | 2016-08-16 | Dow Global Technologies Llc | Ultrafast dual cure adhesive useful for bonding to glass |
US8945338B2 (en) * | 2013-03-15 | 2015-02-03 | Henkel US IP LLC | Anaerobic curable compositions |
EP2995663A1 (en) * | 2014-09-12 | 2016-03-16 | Afinitica Technologies, S. L. | Fast and elastic adhesive |
CN117164812A (zh) * | 2015-01-26 | 2023-12-05 | 汉高股份有限及两合公司 | 由可再生材料制备的官能化聚氨酯 |
EP3250655B1 (en) * | 2015-01-26 | 2024-05-15 | Henkel AG & Co. KGaA | Anaerobic curable compositions |
US10246565B2 (en) * | 2015-03-24 | 2019-04-02 | The Boeing Company | Rapidly curing adhesives using encapsulated catalyst and focused ultrasound |
WO2016160135A1 (en) * | 2015-04-03 | 2016-10-06 | Henkel IP & Holding GmbH | (meth)acrylate-functionalized extended isosorbide |
WO2017066539A1 (en) * | 2015-10-16 | 2017-04-20 | Henkel IP & Holding GmbH | Reactive resins made from renewable sources |
GB201617938D0 (en) * | 2016-10-24 | 2016-12-07 | Henkel IP & Holding GmbH | Sealant material |
Family Cites Families (22)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1594037A1 (de) * | 1966-04-15 | 1969-12-04 | Henkel & Cie Gmbh | Verfahren zur Beschleunigung der Haertung von bei Sauerstoffausschluss erhaertenden Klebstoffen oder Dichtungsmitteln |
CA1065536A (en) * | 1975-03-12 | 1979-10-30 | Louis J. Baccei | Curable acrylate compositions having improved thermal properties |
US4287330A (en) * | 1975-05-23 | 1981-09-01 | Loctite Corporation | Accelerator for curable compositions |
US4111890A (en) | 1977-12-19 | 1978-09-05 | Sws Silicones Corporation | Curable organopolysiloxane compositions containing titanium esters |
US4320221A (en) * | 1980-12-12 | 1982-03-16 | The Dow Chemical Company | Addition polymerizable isocyanate-polyol anaerobic adhesives |
JPS6140388A (ja) * | 1984-07-31 | 1986-02-26 | Sunstar Giken Kk | 二液性接着剤 |
FR2624872B1 (fr) * | 1987-12-22 | 1991-10-18 | Elf Aquitaine | Formulation adhesive acrylique anaerobie stable chimiquement et susceptible de fournir un joint adhesif durci presentant des resistances ameliorees au choc et au cisaillement ou/et une bonne tenue thermique |
JP2949893B2 (ja) * | 1991-02-14 | 1999-09-20 | 株式会社スリーボンド | 速硬性を有する嫌気性接着剤組成物 |
US5426166A (en) * | 1994-01-26 | 1995-06-20 | Caschem, Inc. | Urethane adhesive compositions |
JPH08120247A (ja) * | 1994-10-26 | 1996-05-14 | Nippon Synthetic Chem Ind Co Ltd:The | 粘着剤組成物 |
JPH10237420A (ja) * | 1997-02-20 | 1998-09-08 | Three Bond Co Ltd | 嫌気硬化性シール剤組成物 |
JPH10279888A (ja) * | 1997-04-09 | 1998-10-20 | Okura Ind Co Ltd | 接着剤組成物 |
JPH11302347A (ja) * | 1998-04-24 | 1999-11-02 | Nippon Synthetic Chem Ind Co Ltd:The | 硬化型樹脂組成物 |
US6727320B2 (en) * | 1998-11-02 | 2004-04-27 | Henkel Loctite Corporation | Polymerizable compositions in non-flowable forms |
US7144956B2 (en) * | 1998-11-02 | 2006-12-05 | Henkel Corporation | Polymerizable compositions in non-flowable forms |
US6673875B2 (en) * | 2000-03-29 | 2004-01-06 | Henkel Loctite Corporation | Anaerobic compositions with enhanced toughness and crack resistance |
US7250466B2 (en) * | 2000-09-25 | 2007-07-31 | Henkel Corporation | Rapid curing anaerobic compositions |
JP2003013027A (ja) * | 2001-06-28 | 2003-01-15 | Sekisui Chem Co Ltd | アクリル系粘着剤組成物及び粘着テープ |
US6723763B2 (en) * | 2002-03-15 | 2004-04-20 | Henkel Loctite Corporation | Cure accelerators for anaerobic adhesive compositions |
US6750309B1 (en) * | 2002-05-17 | 2004-06-15 | Henkel Corporation | Methacrylated polyurethane copolymers with silicone segments containing alkoxysilyl groups |
US7271227B1 (en) * | 2004-04-20 | 2007-09-18 | Henkel Corporation | Adhesive compositions free of metallic catalyst |
WO2008153668A2 (en) * | 2007-05-22 | 2008-12-18 | Henkel Corporation | Dry-to-the-touch anaerobically curable compositions and products made therefrom |
-
2008
- 2008-05-16 CN CN200880020288.1A patent/CN101711259B/zh not_active Expired - Fee Related
- 2008-05-16 WO PCT/US2008/006343 patent/WO2008153673A1/en active Application Filing
- 2008-05-16 MX MX2009012542A patent/MX2009012542A/es active IP Right Grant
- 2008-05-16 CA CA2687601A patent/CA2687601C/en not_active Expired - Fee Related
- 2008-05-16 EP EP08767780A patent/EP2148893A4/en not_active Withdrawn
- 2008-05-16 KR KR1020097026626A patent/KR101524684B1/ko not_active IP Right Cessation
- 2008-05-16 JP JP2010509351A patent/JP5566882B2/ja not_active Expired - Fee Related
-
2009
- 2009-09-18 US US12/562,603 patent/US8835593B2/en active Active
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN108368384A (zh) * | 2015-10-22 | 2018-08-03 | 汉高知识产权控股有限责任公司 | 可厌氧固化的组合物 |
CN113840852A (zh) * | 2019-04-05 | 2021-12-24 | 汉高知识产权控股有限责任公司 | 可厌氧固化的组合物 |
CN110128994A (zh) * | 2019-04-09 | 2019-08-16 | 中海油常州涂料化工研究院有限公司 | 一种可湿固化的厌氧胶及其制备方法 |
CN117165248A (zh) * | 2023-10-31 | 2023-12-05 | 南京艾布纳新材料股份有限公司 | 一种多重固化型聚氨酯可陶瓷化密封胶及其制备方法 |
CN117165248B (zh) * | 2023-10-31 | 2024-02-23 | 南京艾布纳新材料股份有限公司 | 一种多重固化型聚氨酯可陶瓷化密封胶及其制备方法 |
Also Published As
Publication number | Publication date |
---|---|
CN101711259B (zh) | 2015-12-02 |
MX2009012542A (es) | 2010-02-12 |
CA2687601C (en) | 2015-07-07 |
EP2148893A1 (en) | 2010-02-03 |
WO2008153673A1 (en) | 2008-12-18 |
US8835593B2 (en) | 2014-09-16 |
JP2010529218A (ja) | 2010-08-26 |
KR101524684B1 (ko) | 2015-06-03 |
CA2687601A1 (en) | 2008-12-18 |
JP5566882B2 (ja) | 2014-08-06 |
US20100006208A1 (en) | 2010-01-14 |
KR20100021619A (ko) | 2010-02-25 |
EP2148893A4 (en) | 2011-12-21 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN101711259B (zh) | 厌氧可固化组合物 | |
US9181457B2 (en) | Dry-to-the-touch anaerobically curable compositions and products made therefrom | |
JP6753870B2 (ja) | 赤外線で硬化する潜在性2液型ポリウレタン接着剤 | |
CN100480279C (zh) | 稳定的有机硼烷聚合反应引发剂和可聚合的组合物 | |
US8410229B2 (en) | Polyurethane-modified acrylic resin and preparing method thereof | |
CN102604583A (zh) | 一种耐蒸煮无溶剂型复膜胶及其制备方法 | |
CN102015806A (zh) | 两部分杂化粘合剂 | |
JP6027006B2 (ja) | 超分岐ポリマーを基剤とする二成分形ポリウレタン | |
CN107660218A (zh) | 使用基于聚(环氧丁烷)的异氰酸酯封端的准预聚物制备的双组分聚氨基甲酸酯粘合剂 | |
CN101597470A (zh) | 一种无溶剂型双组分聚氨酯胶粘剂及其制备方法 | |
SK9462002A3 (en) | Adhesion promoters for monomer-free reactive polyurethanes | |
KR20050040833A (ko) | 유기보란 아민 착체 중합 개시제 및 중합성 조성물 | |
CN105542702B (zh) | 一种紫外光固化聚氨酯胶粘剂及其制备方法 | |
CA2783716C (en) | Solvent borne two-component polyurethane coating composition | |
KR20210082192A (ko) | 폴리우레탄 또는 폴리우레아의 연속 제조 | |
CN107384293A (zh) | 一种热塑性聚氨酯热熔胶的制备方法 | |
CN102101967A (zh) | 单组分聚脲型聚氨酯涂料及其制备方法 | |
US20050129955A1 (en) | Binding agent component for surface coating agents with improved adhesive properties | |
CN104837941B (zh) | 固体可自粘的含异氰酸酯有机聚合物和其使用方法 | |
CN102203207B (zh) | 指触干燥的可湿气固化的组合物及由其制备的产品 | |
CN114437662B (zh) | 工业用环保型聚氨酯胶黏剂及其制备方法和应用 | |
CN116987475B (zh) | 一种免保压且快速固化的聚氨酯胶及其制备方法 | |
FR2582661A1 (fr) | Composition de revetement durcissable par penetration de vapeur comprenant des resines de poly(nitro-alcools) et des gents de durcissement de type multi-isocyanate et procede pour la durcir | |
CN111320947A (zh) | 一种太阳能背板复膜胶及其膜制备方法 | |
CN112771132A (zh) | 包含茂金属和乙酰苯肼固化体系的可厌氧固化的组合物 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
ASS | Succession or assignment of patent right |
Owner name: HENKEL US IP LLC Free format text: FORMER OWNER: HENKEL CORP. Effective date: 20140827 |
|
C41 | Transfer of patent application or patent right or utility model | ||
TA01 | Transfer of patent application right |
Effective date of registration: 20140827 Address after: American Connecticut Applicant after: Henkel American Intellectual Property LLC Address before: American Connecticut Applicant before: Henkel Corp. |
|
C41 | Transfer of patent application or patent right or utility model | ||
TA01 | Transfer of patent application right |
Effective date of registration: 20150930 Address after: Dusseldorf Applicant after: THE DIAL Corp. Address before: American Connecticut Applicant before: Henkel American Intellectual Property LLC |
|
C14 | Grant of patent or utility model | ||
GR01 | Patent grant | ||
CF01 | Termination of patent right due to non-payment of annual fee | ||
CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20151202 |