RU2012130294A - Катализаторы для полиольных премиксов для получения полиуретановой пены, содержащих в качестве пенообразующих агентов галогенизированные олефины - Google Patents
Катализаторы для полиольных премиксов для получения полиуретановой пены, содержащих в качестве пенообразующих агентов галогенизированные олефины Download PDFInfo
- Publication number
- RU2012130294A RU2012130294A RU2012130294/04A RU2012130294A RU2012130294A RU 2012130294 A RU2012130294 A RU 2012130294A RU 2012130294/04 A RU2012130294/04 A RU 2012130294/04A RU 2012130294 A RU2012130294 A RU 2012130294A RU 2012130294 A RU2012130294 A RU 2012130294A
- Authority
- RU
- Russia
- Prior art keywords
- salts
- composition according
- potassium
- foaming composition
- group
- Prior art date
Links
- 239000003054 catalyst Substances 0.000 title claims abstract 14
- 239000003795 chemical substances by application Substances 0.000 title claims 2
- 239000006260 foam Substances 0.000 title abstract 2
- 229920005830 Polyurethane Foam Polymers 0.000 title 1
- 150000001336 alkenes Chemical class 0.000 title 1
- 239000011496 polyurethane foam Substances 0.000 title 1
- 239000000203 mixture Substances 0.000 claims abstract 17
- 238000005187 foaming Methods 0.000 claims abstract 15
- 150000001412 amines Chemical class 0.000 claims abstract 14
- -1 quaternary ammonium carboxylate Chemical class 0.000 claims abstract 9
- 150000001735 carboxylic acids Chemical class 0.000 claims abstract 7
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims abstract 6
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims abstract 6
- 229910052700 potassium Inorganic materials 0.000 claims abstract 6
- 239000011591 potassium Substances 0.000 claims abstract 6
- 150000003839 salts Chemical class 0.000 claims abstract 6
- 239000004088 foaming agent Substances 0.000 claims abstract 5
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims abstract 4
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims abstract 4
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims abstract 4
- RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 claims abstract 4
- 150000002736 metal compounds Chemical class 0.000 claims abstract 4
- 150000002902 organometallic compounds Chemical class 0.000 claims abstract 4
- SCVFZCLFOSHCOH-UHFFFAOYSA-M potassium acetate Chemical compound [K+].CC([O-])=O SCVFZCLFOSHCOH-UHFFFAOYSA-M 0.000 claims abstract 4
- 229910052725 zinc Inorganic materials 0.000 claims abstract 4
- 239000011701 zinc Substances 0.000 claims abstract 4
- 229910052718 tin Inorganic materials 0.000 claims abstract 3
- ZSLUVFAKFWKJRC-IGMARMGPSA-N 232Th Chemical compound [232Th] ZSLUVFAKFWKJRC-IGMARMGPSA-N 0.000 claims abstract 2
- 229910052684 Cerium Inorganic materials 0.000 claims abstract 2
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 claims abstract 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims abstract 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims abstract 2
- 229910021578 Iron(III) chloride Inorganic materials 0.000 claims abstract 2
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims abstract 2
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 claims abstract 2
- 229910052776 Thorium Inorganic materials 0.000 claims abstract 2
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims abstract 2
- 229910052770 Uranium Inorganic materials 0.000 claims abstract 2
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 claims abstract 2
- WYOFTXWVYIGTCT-UHFFFAOYSA-K [OH-].[Sb+3].OCC([O-])=O.OCC([O-])=O Chemical compound [OH-].[Sb+3].OCC([O-])=O.OCC([O-])=O WYOFTXWVYIGTCT-UHFFFAOYSA-K 0.000 claims abstract 2
- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 claims abstract 2
- 229910052783 alkali metal Inorganic materials 0.000 claims abstract 2
- 229910052782 aluminium Inorganic materials 0.000 claims abstract 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims abstract 2
- 229910052787 antimony Inorganic materials 0.000 claims abstract 2
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 claims abstract 2
- FAPDDOBMIUGHIN-UHFFFAOYSA-K antimony trichloride Chemical compound Cl[Sb](Cl)Cl FAPDDOBMIUGHIN-UHFFFAOYSA-K 0.000 claims abstract 2
- 229910052797 bismuth Inorganic materials 0.000 claims abstract 2
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 claims abstract 2
- 229910052793 cadmium Inorganic materials 0.000 claims abstract 2
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 claims abstract 2
- GWXLDORMOJMVQZ-UHFFFAOYSA-N cerium Chemical compound [Ce] GWXLDORMOJMVQZ-UHFFFAOYSA-N 0.000 claims abstract 2
- 229910052804 chromium Inorganic materials 0.000 claims abstract 2
- 239000011651 chromium Substances 0.000 claims abstract 2
- 229910017052 cobalt Inorganic materials 0.000 claims abstract 2
- 239000010941 cobalt Substances 0.000 claims abstract 2
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims abstract 2
- 229910052802 copper Inorganic materials 0.000 claims abstract 2
- 239000010949 copper Substances 0.000 claims abstract 2
- 239000012975 dibutyltin dilaurate Substances 0.000 claims abstract 2
- 125000003630 glycyl group Chemical class [H]N([H])C([H])([H])C(*)=O 0.000 claims abstract 2
- RXPAJWPEYBDXOG-UHFFFAOYSA-N hydron;methyl 4-methoxypyridine-2-carboxylate;chloride Chemical compound Cl.COC(=O)C1=CC(OC)=CC=N1 RXPAJWPEYBDXOG-UHFFFAOYSA-N 0.000 claims abstract 2
- 229910052742 iron Inorganic materials 0.000 claims abstract 2
- 239000011133 lead Substances 0.000 claims abstract 2
- 229910052749 magnesium Inorganic materials 0.000 claims abstract 2
- 239000011777 magnesium Substances 0.000 claims abstract 2
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 claims abstract 2
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 claims abstract 2
- 229910052753 mercury Inorganic materials 0.000 claims abstract 2
- 229910052751 metal Inorganic materials 0.000 claims abstract 2
- 239000002184 metal Substances 0.000 claims abstract 2
- 229910052750 molybdenum Inorganic materials 0.000 claims abstract 2
- 239000011733 molybdenum Substances 0.000 claims abstract 2
- 229910052759 nickel Inorganic materials 0.000 claims abstract 2
- 229920005862 polyol Polymers 0.000 claims abstract 2
- 150000003077 polyols Chemical class 0.000 claims abstract 2
- ZUFQCVZBBNZMKD-UHFFFAOYSA-M potassium 2-ethylhexanoate Chemical compound [K+].CCCCC(CC)C([O-])=O ZUFQCVZBBNZMKD-UHFFFAOYSA-M 0.000 claims abstract 2
- 235000011056 potassium acetate Nutrition 0.000 claims abstract 2
- 229910052708 sodium Inorganic materials 0.000 claims abstract 2
- 239000011734 sodium Substances 0.000 claims abstract 2
- 239000004094 surface-active agent Substances 0.000 claims abstract 2
- 239000011135 tin Substances 0.000 claims abstract 2
- 229910052719 titanium Inorganic materials 0.000 claims abstract 2
- 239000010936 titanium Substances 0.000 claims abstract 2
- JFALSRSLKYAFGM-UHFFFAOYSA-N uranium(0) Chemical compound [U] JFALSRSLKYAFGM-UHFFFAOYSA-N 0.000 claims abstract 2
- 229910052720 vanadium Inorganic materials 0.000 claims abstract 2
- LEONUFNNVUYDNQ-UHFFFAOYSA-N vanadium atom Chemical compound [V] LEONUFNNVUYDNQ-UHFFFAOYSA-N 0.000 claims abstract 2
- 150000003751 zinc Chemical class 0.000 claims abstract 2
- IFNXAMCERSVZCV-UHFFFAOYSA-L zinc;2-ethylhexanoate Chemical class [Zn+2].CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O IFNXAMCERSVZCV-UHFFFAOYSA-L 0.000 claims abstract 2
- 229910052726 zirconium Inorganic materials 0.000 claims abstract 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims 4
- DMUPYMORYHFFCT-UPHRSURJSA-N (z)-1,2,3,3,3-pentafluoroprop-1-ene Chemical compound F\C=C(/F)C(F)(F)F DMUPYMORYHFFCT-UPHRSURJSA-N 0.000 claims 3
- SJRJJKPEHAURKC-UHFFFAOYSA-N N-Methylmorpholine Chemical compound CN1CCOCC1 SJRJJKPEHAURKC-UHFFFAOYSA-N 0.000 claims 3
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 claims 3
- CDOOAUSHHFGWSA-OWOJBTEDSA-N (e)-1,3,3,3-tetrafluoroprop-1-ene Chemical compound F\C=C\C(F)(F)F CDOOAUSHHFGWSA-OWOJBTEDSA-N 0.000 claims 2
- LDTMPQQAWUMPKS-OWOJBTEDSA-N (e)-1-chloro-3,3,3-trifluoroprop-1-ene Chemical compound FC(F)(F)\C=C\Cl LDTMPQQAWUMPKS-OWOJBTEDSA-N 0.000 claims 2
- NDMMKOCNFSTXRU-UHFFFAOYSA-N 1,1,2,3,3-pentafluoroprop-1-ene Chemical compound FC(F)C(F)=C(F)F NDMMKOCNFSTXRU-UHFFFAOYSA-N 0.000 claims 2
- QAERDLQYXMEHEB-UHFFFAOYSA-N 1,1,3,3,3-pentafluoroprop-1-ene Chemical compound FC(F)=CC(F)(F)F QAERDLQYXMEHEB-UHFFFAOYSA-N 0.000 claims 2
- LDTMPQQAWUMPKS-UHFFFAOYSA-N 1-chloro-3,3,3-trifluoroprop-1-ene Chemical compound FC(F)(F)C=CCl LDTMPQQAWUMPKS-UHFFFAOYSA-N 0.000 claims 2
- FDMFUZHCIRHGRG-UHFFFAOYSA-N 3,3,3-trifluoroprop-1-ene Chemical compound FC(F)(F)C=C FDMFUZHCIRHGRG-UHFFFAOYSA-N 0.000 claims 2
- NLOLSXYRJFEOTA-UHFFFAOYSA-N 1,1,1,4,4,4-hexafluorobut-2-ene Chemical compound FC(F)(F)C=CC(F)(F)F NLOLSXYRJFEOTA-UHFFFAOYSA-N 0.000 claims 1
- PGJHURKAWUJHLJ-UHFFFAOYSA-N 1,1,2,3-tetrafluoroprop-1-ene Chemical compound FCC(F)=C(F)F PGJHURKAWUJHLJ-UHFFFAOYSA-N 0.000 claims 1
- BNYODXFAOQCIIO-UHFFFAOYSA-N 1,1,3,3-tetrafluoroprop-1-ene Chemical compound FC(F)C=C(F)F BNYODXFAOQCIIO-UHFFFAOYSA-N 0.000 claims 1
- GIWQSPITLQVMSG-UHFFFAOYSA-N 1,2-dimethylimidazole Chemical compound CC1=NC=CN1C GIWQSPITLQVMSG-UHFFFAOYSA-N 0.000 claims 1
- MCTWTZJPVLRJOU-UHFFFAOYSA-N 1-methyl-1H-imidazole Chemical compound CN1C=CN=C1 MCTWTZJPVLRJOU-UHFFFAOYSA-N 0.000 claims 1
- OHMHBGPWCHTMQE-UHFFFAOYSA-N 2,2-dichloro-1,1,1-trifluoroethane Chemical compound FC(F)(F)C(Cl)Cl OHMHBGPWCHTMQE-UHFFFAOYSA-N 0.000 claims 1
- MELCWEWUZODSIS-UHFFFAOYSA-N 2-[2-(diethylamino)ethoxy]-n,n-diethylethanamine Chemical compound CCN(CC)CCOCCN(CC)CC MELCWEWUZODSIS-UHFFFAOYSA-N 0.000 claims 1
- GTEXIOINCJRBIO-UHFFFAOYSA-N 2-[2-(dimethylamino)ethoxy]-n,n-dimethylethanamine Chemical compound CN(C)CCOCCN(C)C GTEXIOINCJRBIO-UHFFFAOYSA-N 0.000 claims 1
- SBICOSJPCBAFED-UHFFFAOYSA-N 2-chloro-1,1-difluoroprop-1-ene Chemical class CC(Cl)=C(F)F SBICOSJPCBAFED-UHFFFAOYSA-N 0.000 claims 1
- HLFNUPJVFUAPLD-UHFFFAOYSA-M 2-ethylhexanoate;2-hydroxypropyl(trimethyl)azanium Chemical group CC(O)C[N+](C)(C)C.CCCCC(CC)C([O-])=O HLFNUPJVFUAPLD-UHFFFAOYSA-M 0.000 claims 1
- OTOLFQXGRCJFQN-UHFFFAOYSA-M 2-hydroxypropyl(trimethyl)azanium;formate Chemical compound [O-]C=O.CC(O)C[N+](C)(C)C OTOLFQXGRCJFQN-UHFFFAOYSA-M 0.000 claims 1
- ZWXQPERWRDHCMZ-UHFFFAOYSA-N 2-methyl-n-propan-2-ylpropan-2-amine Chemical compound CC(C)NC(C)(C)C ZWXQPERWRDHCMZ-UHFFFAOYSA-N 0.000 claims 1
- NGRYSBPZIYVTHZ-UHFFFAOYSA-N 3-[3-(dimethylamino)propoxy]-n,n-dimethylpropan-1-amine Chemical compound CN(C)CCCOCCCN(C)C NGRYSBPZIYVTHZ-UHFFFAOYSA-N 0.000 claims 1
- HXNJCCYKKHPFIO-UHFFFAOYSA-N 3-chloro-1,1,2,3-tetrafluoroprop-1-ene Chemical compound FC(Cl)C(F)=C(F)F HXNJCCYKKHPFIO-UHFFFAOYSA-N 0.000 claims 1
- JLEIRAYWBMNMKU-UHFFFAOYSA-N 3-ethylpentan-3-amine Chemical compound CCC(N)(CC)CC JLEIRAYWBMNMKU-UHFFFAOYSA-N 0.000 claims 1
- ZMSQJSMSLXVTKN-UHFFFAOYSA-N 4-[2-(2-morpholin-4-ylethoxy)ethyl]morpholine Chemical compound C1COCCN1CCOCCN1CCOCC1 ZMSQJSMSLXVTKN-UHFFFAOYSA-N 0.000 claims 1
- HVCNXQOWACZAFN-UHFFFAOYSA-N 4-ethylmorpholine Chemical compound CCN1CCOCC1 HVCNXQOWACZAFN-UHFFFAOYSA-N 0.000 claims 1
- 239000004215 Carbon black (E152) Substances 0.000 claims 1
- XBPCUCUWBYBCDP-UHFFFAOYSA-N Dicyclohexylamine Chemical compound C1CCCCC1NC1CCCCC1 XBPCUCUWBYBCDP-UHFFFAOYSA-N 0.000 claims 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 1
- JGFZNNIVVJXRND-UHFFFAOYSA-N N,N-Diisopropylethylamine (DIPEA) Chemical compound CCN(C(C)C)C(C)C JGFZNNIVVJXRND-UHFFFAOYSA-N 0.000 claims 1
- SVYKKECYCPFKGB-UHFFFAOYSA-N N,N-dimethylcyclohexylamine Chemical compound CN(C)C1CCCCC1 SVYKKECYCPFKGB-UHFFFAOYSA-N 0.000 claims 1
- GSCCALZHGUWNJW-UHFFFAOYSA-N N-Cyclohexyl-N-methylcyclohexanamine Chemical compound C1CCCCC1N(C)C1CCCCC1 GSCCALZHGUWNJW-UHFFFAOYSA-N 0.000 claims 1
- 150000001299 aldehydes Chemical class 0.000 claims 1
- 150000001340 alkali metals Chemical class 0.000 claims 1
- NEHMKBQYUWJMIP-UHFFFAOYSA-N chloromethane Chemical compound ClC NEHMKBQYUWJMIP-UHFFFAOYSA-N 0.000 claims 1
- HEYYNPBHZQPMJJ-UHFFFAOYSA-L dibenzoyloxylead Chemical compound C=1C=CC=CC=1C(=O)O[Pb]OC(=O)C1=CC=CC=C1 HEYYNPBHZQPMJJ-UHFFFAOYSA-L 0.000 claims 1
- 150000002148 esters Chemical class 0.000 claims 1
- NBVXSUQYWXRMNV-UHFFFAOYSA-N fluoromethane Chemical compound FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 claims 1
- 150000008282 halocarbons Chemical class 0.000 claims 1
- 229930195733 hydrocarbon Natural products 0.000 claims 1
- 150000002430 hydrocarbons Chemical class 0.000 claims 1
- 150000002576 ketones Chemical class 0.000 claims 1
- VMOWKUTXPNPTEN-UHFFFAOYSA-N n,n-dimethylpropan-2-amine Chemical compound CC(C)N(C)C VMOWKUTXPNPTEN-UHFFFAOYSA-N 0.000 claims 1
- ASKYIFBXGFWCBG-UHFFFAOYSA-N n-benzyl-n-methylcyclopentanamine Chemical compound C1CCCC1N(C)CC1=CC=CC=C1 ASKYIFBXGFWCBG-UHFFFAOYSA-N 0.000 claims 1
- WFMUJLWWGDJDBF-UHFFFAOYSA-N n-benzyl-n-methylpropan-2-amine Chemical compound CC(C)N(C)CC1=CC=CC=C1 WFMUJLWWGDJDBF-UHFFFAOYSA-N 0.000 claims 1
- OBYVIBDTOCAXSN-UHFFFAOYSA-N n-butan-2-ylbutan-2-amine Chemical compound CCC(C)NC(C)CC OBYVIBDTOCAXSN-UHFFFAOYSA-N 0.000 claims 1
- FUUUBHCENZGYJA-UHFFFAOYSA-N n-cyclopentylcyclopentanamine Chemical compound C1CCCC1NC1CCCC1 FUUUBHCENZGYJA-UHFFFAOYSA-N 0.000 claims 1
- BBPKSHICVYBPRR-UHFFFAOYSA-N n-propan-2-yl-n-(2,2,2-trifluoroethyl)butan-2-amine Chemical compound CCC(C)N(C(C)C)CC(F)(F)F BBPKSHICVYBPRR-UHFFFAOYSA-N 0.000 claims 1
- CATWEXRJGNBIJD-UHFFFAOYSA-N n-tert-butyl-2-methylpropan-2-amine Chemical compound CC(C)(C)NC(C)(C)C CATWEXRJGNBIJD-UHFFFAOYSA-N 0.000 claims 1
- MTEWAFVECQBILW-UHFFFAOYSA-N n-tert-butylcyclohexanamine Chemical compound CC(C)(C)NC1CCCCC1 MTEWAFVECQBILW-UHFFFAOYSA-N 0.000 claims 1
- 150000007524 organic acids Chemical class 0.000 claims 1
- MSSNHSVIGIHOJA-UHFFFAOYSA-N pentafluoropropane Chemical compound FC(F)CC(F)(F)F MSSNHSVIGIHOJA-UHFFFAOYSA-N 0.000 claims 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 claims 1
- BZVJOYBTLHNRDW-UHFFFAOYSA-N triphenylmethanamine Chemical compound C=1C=CC=CC=1C(C=1C=CC=CC=1)(N)C1=CC=CC=C1 BZVJOYBTLHNRDW-UHFFFAOYSA-N 0.000 claims 1
- YFTHZRPMJXBUME-UHFFFAOYSA-N tripropylamine Chemical compound CCCN(CCC)CCC YFTHZRPMJXBUME-UHFFFAOYSA-N 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 1
- BOZRCGLDOHDZBP-UHFFFAOYSA-N 2-ethylhexanoic acid;tin Chemical compound [Sn].CCCCC(CC)C(O)=O BOZRCGLDOHDZBP-UHFFFAOYSA-N 0.000 abstract 1
- KRJUSWXDFZSJQD-UHFFFAOYSA-N benzoic acid;lead Chemical compound [Pb].OC(=O)C1=CC=CC=C1 KRJUSWXDFZSJQD-UHFFFAOYSA-N 0.000 abstract 1
Classifications
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- 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
- C08G18/16—Catalysts
- C08G18/18—Catalysts containing secondary or tertiary amines or salts thereof
- C08G18/1875—Catalysts containing secondary or tertiary amines or salts thereof containing ammonium salts or mixtures of secondary of tertiary amines and 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
- C08G18/08—Processes
- C08G18/16—Catalysts
- C08G18/22—Catalysts containing metal compounds
- C08G18/227—Catalysts containing metal compounds of antimony, bismuth or arsenic
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
- B01J31/12—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing organo-metallic compounds or metal hydrides
- B01J31/128—Mixtures of organometallic compounds
-
- 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
- C08G18/16—Catalysts
- C08G18/161—Catalysts containing two or more components to be covered by at least two of the groups C08G18/166, C08G18/18 or C08G18/22
- C08G18/163—Catalysts containing two or more components to be covered by at least two of the groups C08G18/166, C08G18/18 or C08G18/22 covered by C08G18/18 and C08G18/22
-
- 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
- C08G18/16—Catalysts
- C08G18/18—Catalysts containing secondary or tertiary amines or salts thereof
- C08G18/1816—Catalysts containing secondary or tertiary amines or salts thereof having carbocyclic groups
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Abstract
1. Пенообразующая композиция, содержащаяa. гидрогалогенолефиновый пенообразующий агент,b. один или более чем один полиол,c. одно или более чем одно поверхностно-активное вещество иd. неаминовый катализатор, выбранный из группы, состоящей из неорганометаллического соединения, органометаллического соединения, катализатора на основе карбоксилата четвертичного аммония и их комбинаций, где указанное неорганометаллическое соединение или органометаллическое соединение независимо содержат органическую соль металла, выбранного из группы, состоящей из висмута, свинца, олова, цинка, хрома, кобальта, меди, железа, марганца, магния, калия, натрия, титана, ртути, цинка, сурьмы, урана, кадмия, тория, алюминия, никеля, церия, молибдена, ванадия, циркония и их комбинаций.2. Пенообразующая композиция по п.1, отличающаяся тем, что указанный неаминовый катализатор выбран из группы, состоящей из нитрата висмута, 2-этилгексоата свинца, бензоата свинца, нафтаната свинца, хлорида железа (III), хлорида сурьмы (III), гликолята сурьмы, солей олова с карбоновыми кислотами, солей диалкилолова с карбоновыми кислотами, ацетата калия, октоата калия, 2-этилгексоата калия, калиевых солей карбоновых кислот, цинковых солей карбоновых кислот, 2-этилгексаноата цинка, солей глицина, солей карбоновых кислот со щелочными металлами и N-(2-гидрокси-5-нонилфенол)метил-N-метилглицината натрия, 2-этилгексаноата олова (II), дилаурата дибутилолова и их комбинаций.3. Пенообразующая композиция по п.2, отличающаяся тем, что указанный неаминовый катализатор присутствует в количестве от приблизительно 0,25% (по массе) до приблизительно 3,0% (по массе) от массы композиции.4. Пенообра
Claims (11)
1. Пенообразующая композиция, содержащая
a. гидрогалогенолефиновый пенообразующий агент,
b. один или более чем один полиол,
c. одно или более чем одно поверхностно-активное вещество и
d. неаминовый катализатор, выбранный из группы, состоящей из неорганометаллического соединения, органометаллического соединения, катализатора на основе карбоксилата четвертичного аммония и их комбинаций, где указанное неорганометаллическое соединение или органометаллическое соединение независимо содержат органическую соль металла, выбранного из группы, состоящей из висмута, свинца, олова, цинка, хрома, кобальта, меди, железа, марганца, магния, калия, натрия, титана, ртути, цинка, сурьмы, урана, кадмия, тория, алюминия, никеля, церия, молибдена, ванадия, циркония и их комбинаций.
2. Пенообразующая композиция по п.1, отличающаяся тем, что указанный неаминовый катализатор выбран из группы, состоящей из нитрата висмута, 2-этилгексоата свинца, бензоата свинца, нафтаната свинца, хлорида железа (III), хлорида сурьмы (III), гликолята сурьмы, солей олова с карбоновыми кислотами, солей диалкилолова с карбоновыми кислотами, ацетата калия, октоата калия, 2-этилгексоата калия, калиевых солей карбоновых кислот, цинковых солей карбоновых кислот, 2-этилгексаноата цинка, солей глицина, солей карбоновых кислот со щелочными металлами и N-(2-гидрокси-5-нонилфенол)метил-N-метилглицината натрия, 2-этилгексаноата олова (II), дилаурата дибутилолова и их комбинаций.
3. Пенообразующая композиция по п.2, отличающаяся тем, что указанный неаминовый катализатор присутствует в количестве от приблизительно 0,25% (по массе) до приблизительно 3,0% (по массе) от массы композиции.
4. Пенообразующая композиция по п.1, отличающаяся тем, что указанный неаминовый катализатор представляет собой карбоксилат четвертичного аммония.
5. Пенообразующая композиция по п.4, отличающаяся тем, что указанный неаминовый катализатор представляет собой (2-гидроксипропил)триметиламмония 2-этилгексаноат или (2-гидроксипропил)триметиламмония формиат.
6. Пенообразующая композиция по п.5, отличающаяся тем, что указанный неаминовый катализатор присутствует в количестве от приблизительно 0,25% (по массе) до приблизительно 3,0% (по массе) от массы композиции.
7. Пенообразующая композиция по п.1, отличающаяся тем, что указанный пенообразующий агент дополнительно включает пенообразующий соагент, выбранный из группы, состоящей из воды, углеводорода, фторуглерода, хлоруглерода, гидрохлорфторуглерода, гидрофторуглерода, галогенизированного углеводорода, простого эфира, сложного эфира, спирта, альдегида, кетона, органической кислоты, газообразующего вещества и их комбинаций.
8. Пенообразующая композиция по п.1, отличающаяся тем, что указанный пенообразующий агент включает гидрогалогенолефин, выбранный из группы, состоящей из трифторпропена, тетрафторпропена, пентафторпропана, хлортрифторпропена, хлордифторпропенов, хлортрифторпропена, хлортетрафторпропена, гексафторбутена и их комбинаций.
9. Пенообразующая композиция по п.8, отличающаяся тем, что указанный пенообразующий агент выбран из группы, состоящей из 1,3,3,3-тетрафторпропена (1234ze); 1,1,3,3-тетрафторпропена; 1,2,3,3,3-пентафторпропена (1225уе); 1,1,1-трифторпропена; 1,1,1,3,3-пентафторпропена (1225zc); 1,1,2,3,3-пентафторпропена (1225ус); (Z)-1,1,1,2,3-пентафторпропена (1225yez); 1-хлор-3,3,3-трифторпропена (1233zd); 1,1,1,4,4,4гексафторбут-2-ена (1336mzzm) и их комбинаций.
10. Пенообразующая композиция по п.1, дополнительно содержащая аминовый катализатор.
11. Пенообразующая композиция по п.10, отличающаяся тем, что аминовый катализатор выбран из группы, состоящей из N,N,N',N'',N''-пентаметилдиэтилтриамина, N,N-дициклогексилметиламина; N,N-этилдиизопропиламина; N,N-диметилциклогексиламина; N,N-диметилизопропиламина; N-метил-N-изопропилбензиламина; N-метил-N-циклопентилбензиламина; N-изопропил-N-втор-бутил-трифторэтиламина; N,N-диэтил-(α-фенилэтил)амина, N,N,N-три-н-пропиламина, дициклогексиламина; трет-бутилизопропиламина; ди-трет-бутиламина; циклогексил-трет-бутиламина; ди-втор-бутиламина, дициклопентиламина; ди-(α-трифторметилэтил)амина; ди-(α-фенилэтил)амина; трифенилметиламина; 1,1-диэтил-н-пропиламина; диморфолинодиэтилового эфира; N-этилморфолина; N-метилморфолина; бис(диметиламиноэтил)эфира; имидазола; н-метилимидазола; 1,2-диметилимидазола; диморфолинодиметилового эфира; N,N,N',N',N'',N''-пентаметилдиэтилентриамина; N,N,N',N',N'',N''-пентаэтилдиэтилентриамина; N,N,N',N',N'',N''-пентаметилдипропилентриамина; бис(диэтиламиноэтил)эфира; бис(диметиламинопропил)эфира и их комбинаций.
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| US12/967,345 US20110152392A1 (en) | 2009-12-17 | 2010-12-14 | Catalysts For Polyurethane Foam Polyol Premixes Containing Halogenated Olefin Blowing Agents |
| PCT/US2010/060678 WO2011084563A2 (en) | 2009-12-17 | 2010-12-16 | Catalysts for polyurethane foam polyol premixes containing halogenated olefin blowing agents |
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| RU2015144564A Division RU2015144564A (ru) | 2009-12-17 | 2010-12-16 | Катализаторы для полиольных премиксов для получения полиуретановой пены, содержащих в качестве пенообразующих агентов галогенизированные олефины |
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| RU2015144564A RU2015144564A (ru) | 2009-12-17 | 2010-12-16 | Катализаторы для полиольных премиксов для получения полиуретановой пены, содержащих в качестве пенообразующих агентов галогенизированные олефины |
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| US20110152392A1 (en) * | 2009-12-17 | 2011-06-23 | Honeywell International Inc. | Catalysts For Polyurethane Foam Polyol Premixes Containing Halogenated Olefin Blowing Agents |
| JP6134470B2 (ja) | 2008-03-07 | 2017-05-24 | アーケマ・インコーポレイテッド | クロロ−3,3,3−トリフルオロプロペンによる安定した処方系 |
| US9145480B2 (en) | 2010-10-28 | 2015-09-29 | Honeywell International Inc. | Mixtures containing 1,1,1,3,3,3-hexafluorobutene and 1-chloro-3,3,3-trifluoropropene |
| US9556303B2 (en) * | 2011-02-21 | 2017-01-31 | Honeywell International Inc. | Catalysts for polyurethane foam polyol premixes containing halogenated olefin blowing agents |
| EP2678391B1 (en) * | 2011-02-21 | 2019-07-31 | Honeywell International Inc. | Polyurethane foam premixes containing halogenated olefin blowing agents and foams made from same |
| BR112013023254B1 (pt) * | 2011-03-11 | 2020-12-15 | Arkema Inc | Composição pré-mistura de poliol e método para estabilizar uma mistura de espuma termofixa |
| EP2702088B1 (en) * | 2011-04-15 | 2018-05-16 | Arkema, Inc. | Improved stability of polyurethane polyol blends containing halogenated olefin blowing agent |
| CA2843012A1 (en) * | 2011-07-28 | 2013-01-31 | Honeywell International Inc. | Foams and flame resistant articles made from foams containing 1-chloro-3,3,3-trifluoropropene (1233zd) |
| US9896558B2 (en) * | 2011-08-01 | 2018-02-20 | Basf Se | HFO/water-blown rigid foam systems |
| TR201906669T4 (tr) * | 2011-09-21 | 2019-05-21 | Dow Global Technologies Llc | Tersiyer amin bileşiklerinin karışımlarını ve katalist olarak lewis asitlerini kullanarak yapılan poliüretanlar. |
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- 2010-12-16 RU RU2012130294/04A patent/RU2012130294A/ru not_active Application Discontinuation
- 2010-12-16 CA CA2784583A patent/CA2784583A1/en not_active Abandoned
- 2010-12-16 CN CN201510000562.0A patent/CN104592468A/zh active Pending
- 2010-12-16 MX MX2012006804A patent/MX2012006804A/es unknown
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| RU2015144564A (ru) | 2018-12-28 |
| CN102753624A (zh) | 2012-10-24 |
| JP2017071781A (ja) | 2017-04-13 |
| EP2513227A2 (en) | 2012-10-24 |
| CN104592468A (zh) | 2015-05-06 |
| RU2015144564A3 (ru) | 2019-01-30 |
| KR20120115982A (ko) | 2012-10-19 |
| MX2012006804A (es) | 2012-08-31 |
| JP2013514452A (ja) | 2013-04-25 |
| US20110152392A1 (en) | 2011-06-23 |
| US20200048397A1 (en) | 2020-02-13 |
| JP6072157B2 (ja) | 2017-02-01 |
| BR112012014267A2 (pt) | 2020-08-25 |
| EP2513227A4 (en) | 2014-12-03 |
| WO2011084563A2 (en) | 2011-07-14 |
| US11746180B2 (en) | 2023-09-05 |
| JP2016000820A (ja) | 2016-01-07 |
| US20220298288A9 (en) | 2022-09-22 |
| CA2784583A1 (en) | 2011-07-14 |
| CN106084163A (zh) | 2016-11-09 |
| JP5810096B2 (ja) | 2015-11-11 |
| WO2011084563A3 (en) | 2011-10-20 |
| US20220195106A1 (en) | 2022-06-23 |
| US20180105633A1 (en) | 2018-04-19 |
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