BR0008107B1 - processos para a produção de espumas de poliuretana rìgida finamente celular e/ou de poliisocianurato, uso da espuma produzida pelos referidos processos e espuma de poliuretana ou poliisocianurato produzida no molde. - Google Patents
processos para a produção de espumas de poliuretana rìgida finamente celular e/ou de poliisocianurato, uso da espuma produzida pelos referidos processos e espuma de poliuretana ou poliisocianurato produzida no molde. Download PDFInfo
- Publication number
- BR0008107B1 BR0008107B1 BRPI0008107-8A BR0008107A BR0008107B1 BR 0008107 B1 BR0008107 B1 BR 0008107B1 BR 0008107 A BR0008107 A BR 0008107A BR 0008107 B1 BR0008107 B1 BR 0008107B1
- Authority
- BR
- Brazil
- Prior art keywords
- polyol
- foam
- mol
- weight
- polyisocyanurate
- Prior art date
Links
- 239000006260 foam Substances 0.000 title claims abstract description 34
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 10
- 238000000034 method Methods 0.000 title claims description 21
- 229920002635 polyurethane Polymers 0.000 title claims description 12
- 239000004814 polyurethane Substances 0.000 title claims description 12
- 229920000582 polyisocyanurate Polymers 0.000 title claims description 8
- 239000011495 polyisocyanurate Substances 0.000 title claims description 8
- 230000001413 cellular effect Effects 0.000 title claims 3
- 229920005862 polyol Polymers 0.000 claims abstract description 44
- 150000003077 polyols Chemical class 0.000 claims abstract description 43
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 16
- 229920001228 polyisocyanate Polymers 0.000 claims abstract description 15
- 239000005056 polyisocyanate Substances 0.000 claims abstract description 15
- 239000000839 emulsion Substances 0.000 claims abstract description 12
- 239000003054 catalyst Substances 0.000 claims description 16
- -1 polyol ester Chemical class 0.000 claims description 9
- 239000000126 substance Substances 0.000 claims description 9
- 239000004721 Polyphenylene oxide Substances 0.000 claims description 7
- 239000000654 additive Substances 0.000 claims description 7
- 229920000570 polyether Polymers 0.000 claims description 7
- 238000007906 compression Methods 0.000 claims description 4
- 230000006835 compression Effects 0.000 claims description 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 4
- 238000009413 insulation Methods 0.000 claims description 4
- 229920000728 polyester Polymers 0.000 claims description 4
- 229920000642 polymer Polymers 0.000 claims description 4
- 150000002148 esters Chemical class 0.000 claims description 3
- 238000006243 chemical reaction Methods 0.000 claims description 2
- 239000002131 composite material Substances 0.000 claims description 2
- 125000000524 functional group Chemical group 0.000 claims description 2
- 239000011810 insulating material Substances 0.000 claims description 2
- 239000000758 substrate Substances 0.000 claims description 2
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 claims 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- 125000004429 atom Chemical group 0.000 claims 1
- 229910052739 hydrogen Inorganic materials 0.000 claims 1
- 239000001257 hydrogen Substances 0.000 claims 1
- 238000005057 refrigeration Methods 0.000 claims 1
- 229920005830 Polyurethane Foam Polymers 0.000 abstract description 11
- 239000011496 polyurethane foam Substances 0.000 abstract description 11
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 abstract description 3
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical group OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 abstract description 3
- 210000004027 cell Anatomy 0.000 description 38
- 239000000203 mixture Substances 0.000 description 25
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 12
- 238000009472 formulation Methods 0.000 description 11
- 239000012948 isocyanate Substances 0.000 description 11
- 150000002513 isocyanates Chemical class 0.000 description 11
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 9
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 6
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 6
- 238000001000 micrograph Methods 0.000 description 6
- 239000003381 stabilizer Substances 0.000 description 6
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 4
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 4
- 150000001991 dicarboxylic acids Chemical class 0.000 description 4
- 239000003995 emulsifying agent Substances 0.000 description 4
- SCVFZCLFOSHCOH-UHFFFAOYSA-M potassium acetate Chemical compound [K+].CC([O-])=O SCVFZCLFOSHCOH-UHFFFAOYSA-M 0.000 description 4
- SJRJJKPEHAURKC-UHFFFAOYSA-N N-Methylmorpholine Chemical compound CN1CCOCC1 SJRJJKPEHAURKC-UHFFFAOYSA-N 0.000 description 3
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- 239000004359 castor oil Substances 0.000 description 3
- 235000019438 castor oil Nutrition 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 239000000945 filler Substances 0.000 description 3
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 3
- KIDHWZJUCRJVML-UHFFFAOYSA-N putrescine Chemical compound NCCCCN KIDHWZJUCRJVML-UHFFFAOYSA-N 0.000 description 3
- 239000007858 starting material Substances 0.000 description 3
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- SVYKKECYCPFKGB-UHFFFAOYSA-N N,N-dimethylcyclohexylamine Chemical compound CN(C)C1CCCCC1 SVYKKECYCPFKGB-UHFFFAOYSA-N 0.000 description 2
- AKNUHUCEWALCOI-UHFFFAOYSA-N N-ethyldiethanolamine Chemical compound OCCN(CC)CCO AKNUHUCEWALCOI-UHFFFAOYSA-N 0.000 description 2
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 2
- 239000007983 Tris buffer Substances 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 230000000844 anti-bacterial effect Effects 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 238000005187 foaming Methods 0.000 description 2
- 230000000855 fungicidal effect Effects 0.000 description 2
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
- CRVGTESFCCXCTH-UHFFFAOYSA-N methyl diethanolamine Chemical group OCCN(C)CCO CRVGTESFCCXCTH-UHFFFAOYSA-N 0.000 description 2
- BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
- 229920005906 polyester polyol Polymers 0.000 description 2
- 229920005903 polyol mixture Polymers 0.000 description 2
- 229920000098 polyolefin Polymers 0.000 description 2
- 229920006389 polyphenyl polymer Polymers 0.000 description 2
- 235000011056 potassium acetate Nutrition 0.000 description 2
- 235000013772 propylene glycol Nutrition 0.000 description 2
- TYFQFVWCELRYAO-UHFFFAOYSA-N suberic acid Chemical compound OC(=O)CCCCCCC(O)=O TYFQFVWCELRYAO-UHFFFAOYSA-N 0.000 description 2
- KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 2
- 150000005846 sugar alcohols Polymers 0.000 description 2
- WGTYBPLFGIVFAS-UHFFFAOYSA-M tetramethylammonium hydroxide Chemical compound [OH-].C[N+](C)(C)C WGTYBPLFGIVFAS-UHFFFAOYSA-M 0.000 description 2
- 125000005628 tolylene group Chemical group 0.000 description 2
- VOZKAJLKRJDJLL-UHFFFAOYSA-N tolylenediamine group Chemical group CC1=C(C=C(C=C1)N)N VOZKAJLKRJDJLL-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
- IMNIMPAHZVJRPE-UHFFFAOYSA-N triethylenediamine Chemical compound C1CN2CCN1CC2 IMNIMPAHZVJRPE-UHFFFAOYSA-N 0.000 description 2
- XFNJVJPLKCPIBV-UHFFFAOYSA-N trimethylenediamine Chemical compound NCCCN XFNJVJPLKCPIBV-UHFFFAOYSA-N 0.000 description 2
- DNIAPMSPPWPWGF-VKHMYHEASA-N (+)-propylene glycol Chemical compound C[C@H](O)CO DNIAPMSPPWPWGF-VKHMYHEASA-N 0.000 description 1
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-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
- ZFDWWDZLRKHULH-UHFFFAOYSA-N 1,2-dimethyl-5,6-dihydro-4h-pyrimidine Chemical compound CN1CCCN=C1C ZFDWWDZLRKHULH-UHFFFAOYSA-N 0.000 description 1
- FCQPNTOQFPJCMF-UHFFFAOYSA-N 1,3-bis[3-(dimethylamino)propyl]urea Chemical compound CN(C)CCCNC(=O)NCCCN(C)C FCQPNTOQFPJCMF-UHFFFAOYSA-N 0.000 description 1
- YPFDHNVEDLHUCE-UHFFFAOYSA-N 1,3-propanediol Substances OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 1
- RTBFRGCFXZNCOE-UHFFFAOYSA-N 1-methylsulfonylpiperidin-4-one Chemical compound CS(=O)(=O)N1CCC(=O)CC1 RTBFRGCFXZNCOE-UHFFFAOYSA-N 0.000 description 1
- VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 description 1
- RLYCRLGLCUXUPO-UHFFFAOYSA-N 2,6-diaminotoluene Chemical compound CC1=C(N)C=CC=C1N RLYCRLGLCUXUPO-UHFFFAOYSA-N 0.000 description 1
- OHKOAJUTRVTYSW-UHFFFAOYSA-N 2-[(2-aminophenyl)methyl]aniline Chemical compound NC1=CC=CC=C1CC1=CC=CC=C1N OHKOAJUTRVTYSW-UHFFFAOYSA-N 0.000 description 1
- UTNMPUFESIRPQP-UHFFFAOYSA-N 2-[(4-aminophenyl)methyl]aniline Chemical compound C1=CC(N)=CC=C1CC1=CC=CC=C1N UTNMPUFESIRPQP-UHFFFAOYSA-N 0.000 description 1
- OBCSAIDCZQSFQH-UHFFFAOYSA-N 2-methyl-1,4-phenylenediamine Chemical compound CC1=CC(N)=CC=C1N OBCSAIDCZQSFQH-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- AXNUJYHFQHQZBE-UHFFFAOYSA-N 3-methylbenzene-1,2-diamine Chemical compound CC1=CC=CC(N)=C1N AXNUJYHFQHQZBE-UHFFFAOYSA-N 0.000 description 1
- 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 1
- YBRVSVVVWCFQMG-UHFFFAOYSA-N 4,4'-diaminodiphenylmethane Chemical compound C1=CC(N)=CC=C1CC1=CC=C(N)C=C1 YBRVSVVVWCFQMG-UHFFFAOYSA-N 0.000 description 1
- BRKHZWFIIVVNTA-UHFFFAOYSA-N 4-cyclohexylmorpholine Chemical compound C1CCCCC1N1CCOCC1 BRKHZWFIIVVNTA-UHFFFAOYSA-N 0.000 description 1
- HVCNXQOWACZAFN-UHFFFAOYSA-N 4-ethylmorpholine Chemical compound CCN1CCOCC1 HVCNXQOWACZAFN-UHFFFAOYSA-N 0.000 description 1
- DGRGLKZMKWPMOH-UHFFFAOYSA-N 4-methylbenzene-1,2-diamine Chemical compound CC1=CC=C(N)C(N)=C1 DGRGLKZMKWPMOH-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 239000004604 Blowing Agent Substances 0.000 description 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 1
- 238000005684 Liebig rearrangement reaction Methods 0.000 description 1
- OYHQOLUKZRVURQ-HZJYTTRNSA-N Linoleic acid Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(O)=O OYHQOLUKZRVURQ-HZJYTTRNSA-N 0.000 description 1
- UEEJHVSXFDXPFK-UHFFFAOYSA-N N-dimethylaminoethanol Chemical compound CN(C)CCO UEEJHVSXFDXPFK-UHFFFAOYSA-N 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- ALQSHHUCVQOPAS-UHFFFAOYSA-N Pentane-1,5-diol Chemical compound OCCCCCO ALQSHHUCVQOPAS-UHFFFAOYSA-N 0.000 description 1
- LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- AWMVMTVKBNGEAK-UHFFFAOYSA-N Styrene oxide Chemical compound C1OC1C1=CC=CC=C1 AWMVMTVKBNGEAK-UHFFFAOYSA-N 0.000 description 1
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 1
- 229930006000 Sucrose Natural products 0.000 description 1
- UWHCKJMYHZGTIT-UHFFFAOYSA-N Tetraethylene glycol, Natural products OCCOCCOCCOCCO UWHCKJMYHZGTIT-UHFFFAOYSA-N 0.000 description 1
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 1
- SLINHMUFWFWBMU-UHFFFAOYSA-N Triisopropanolamine Chemical compound CC(O)CN(CC(C)O)CC(C)O SLINHMUFWFWBMU-UHFFFAOYSA-N 0.000 description 1
- ISKQADXMHQSTHK-UHFFFAOYSA-N [4-(aminomethyl)phenyl]methanamine Chemical compound NCC1=CC=C(CN)C=C1 ISKQADXMHQSTHK-UHFFFAOYSA-N 0.000 description 1
- CQQXCSFSYHAZOO-UHFFFAOYSA-L [acetyloxy(dioctyl)stannyl] acetate Chemical compound CCCCCCCC[Sn](OC(C)=O)(OC(C)=O)CCCCCCCC CQQXCSFSYHAZOO-UHFFFAOYSA-L 0.000 description 1
- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 238000007112 amidation reaction Methods 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- JFCQEDHGNNZCLN-UHFFFAOYSA-N anhydrous glutaric acid Natural products OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 description 1
- 150000004982 aromatic amines Chemical class 0.000 description 1
- 125000002029 aromatic hydrocarbon group Chemical group 0.000 description 1
- 238000005422 blasting Methods 0.000 description 1
- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 1
- VPKDCDLSJZCGKE-UHFFFAOYSA-N carbodiimide group Chemical group N=C=N VPKDCDLSJZCGKE-UHFFFAOYSA-N 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 229960002887 deanol Drugs 0.000 description 1
- FOTKYAAJKYLFFN-UHFFFAOYSA-N decane-1,10-diol Chemical compound OCCCCCCCCCCO FOTKYAAJKYLFFN-UHFFFAOYSA-N 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- JQZRVMZHTADUSY-UHFFFAOYSA-L di(octanoyloxy)tin Chemical compound [Sn+2].CCCCCCCC([O-])=O.CCCCCCCC([O-])=O JQZRVMZHTADUSY-UHFFFAOYSA-L 0.000 description 1
- PNOXNTGLSKTMQO-UHFFFAOYSA-L diacetyloxytin Chemical compound CC(=O)O[Sn]OC(C)=O PNOXNTGLSKTMQO-UHFFFAOYSA-L 0.000 description 1
- 239000012975 dibutyltin dilaurate Substances 0.000 description 1
- 150000001990 dicarboxylic acid derivatives Chemical class 0.000 description 1
- 235000013870 dimethyl polysiloxane Nutrition 0.000 description 1
- XXBDWLFCJWSEKW-UHFFFAOYSA-N dimethylbenzylamine Chemical compound CN(C)CC1=CC=CC=C1 XXBDWLFCJWSEKW-UHFFFAOYSA-N 0.000 description 1
- 239000012972 dimethylethanolamine Substances 0.000 description 1
- PYBNTRWJKQJDRE-UHFFFAOYSA-L dodecanoate;tin(2+) Chemical compound [Sn+2].CCCCCCCCCCCC([O-])=O.CCCCCCCCCCCC([O-])=O PYBNTRWJKQJDRE-UHFFFAOYSA-L 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- PLONEVHFXDFSLA-UHFFFAOYSA-N ethyl hexanoate;tin(2+) Chemical compound [Sn+2].CCCCCC(=O)OCC PLONEVHFXDFSLA-UHFFFAOYSA-N 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 210000000497 foam cell Anatomy 0.000 description 1
- 239000004872 foam stabilizing agent Substances 0.000 description 1
- DYDNPESBYVVLBO-UHFFFAOYSA-N formanilide Chemical compound O=CNC1=CC=CC=C1 DYDNPESBYVVLBO-UHFFFAOYSA-N 0.000 description 1
- 238000007710 freezing Methods 0.000 description 1
- 230000008014 freezing Effects 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 1
- 150000002430 hydrocarbons Chemical group 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 235000020778 linoleic acid Nutrition 0.000 description 1
- OYHQOLUKZRVURQ-IXWMQOLASA-N linoleic acid Natural products CCCCC\C=C/C\C=C\CCCCCCCC(O)=O OYHQOLUKZRVURQ-IXWMQOLASA-N 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 150000004668 long chain fatty acids Chemical class 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
- 239000013518 molded foam Substances 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- LSHROXHEILXKHM-UHFFFAOYSA-N n'-[2-[2-[2-(2-aminoethylamino)ethylamino]ethylamino]ethyl]ethane-1,2-diamine Chemical compound NCCNCCNCCNCCNCCN LSHROXHEILXKHM-UHFFFAOYSA-N 0.000 description 1
- XFLSMWXCZBIXLV-UHFFFAOYSA-N n,n-dimethyl-2-(4-methylpiperazin-1-yl)ethanamine Chemical compound CN(C)CCN1CCN(C)CC1 XFLSMWXCZBIXLV-UHFFFAOYSA-N 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 235000021313 oleic acid Nutrition 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
- 150000004986 phenylenediamines Chemical class 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920000166 polytrimethylene carbonate Polymers 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000002683 reaction inhibitor Substances 0.000 description 1
- WBHHMMIMDMUBKC-XLNAKTSKSA-N ricinelaidic acid Chemical compound CCCCCC[C@@H](O)C\C=C\CCCCCCCC(O)=O WBHHMMIMDMUBKC-XLNAKTSKSA-N 0.000 description 1
- 229960003656 ricinoleic acid Drugs 0.000 description 1
- FEUQNCSVHBHROZ-UHFFFAOYSA-N ricinoleic acid Natural products CCCCCCC(O[Si](C)(C)C)CC=CCCCCCCCC(=O)OC FEUQNCSVHBHROZ-UHFFFAOYSA-N 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 1
- 125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 description 1
- 239000000779 smoke Substances 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- 235000011121 sodium hydroxide Nutrition 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 239000001384 succinic acid Substances 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 125000001302 tertiary amino group Chemical group 0.000 description 1
- 238000005809 transesterification reaction Methods 0.000 description 1
- 150000003626 triacylglycerols Chemical class 0.000 description 1
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N urea group Chemical group NC(=O)N XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- AVWRKZWQTYIKIY-UHFFFAOYSA-N urea-1-carboxylic acid Chemical group NC(=O)NC(O)=O AVWRKZWQTYIKIY-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/4009—Two or more macromolecular compounds not provided for in one single group of groups C08G18/42 - C08G18/64
- C08G18/4018—Mixtures of compounds of group C08G18/42 with compounds of group C08G18/48
-
- 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
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F16—ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
- F16L—PIPES; JOINTS OR FITTINGS FOR PIPES; SUPPORTS FOR PIPES, CABLES OR PROTECTIVE TUBING; MEANS FOR THERMAL INSULATION IN GENERAL
- F16L59/00—Thermal insulation in general
- F16L59/02—Shape or form of insulating materials, with or without coverings integral with the insulating materials
-
- 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
- C08G2110/00—Foam properties
- C08G2110/0025—Foam properties rigid
-
- 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
- C08G2110/00—Foam properties
- C08G2110/0083—Foam properties prepared using water as the sole blowing agent
Landscapes
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Mechanical Engineering (AREA)
- Polyurethanes Or Polyureas (AREA)
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
- Cleaning Implements For Floors, Carpets, Furniture, Walls, And The Like (AREA)
- Thermal Insulation (AREA)
- Materials For Medical Uses (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19905989.6 | 1999-02-13 | ||
| DE19905989A DE19905989A1 (de) | 1999-02-13 | 1999-02-13 | Feinzellige, wassergetriebene Polyurethanhartschaumstoffe |
| PCT/EP2000/000783 WO2000047647A1 (de) | 1999-02-13 | 2000-02-01 | Feinzellige, wassergetriebene polyurethanhartschaumstoffe |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| BR0008107A BR0008107A (pt) | 2001-11-06 |
| BR0008107B1 true BR0008107B1 (pt) | 2010-11-30 |
Family
ID=7897368
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BRPI0008107-8A BR0008107B1 (pt) | 1999-02-13 | 2000-02-01 | processos para a produção de espumas de poliuretana rìgida finamente celular e/ou de poliisocianurato, uso da espuma produzida pelos referidos processos e espuma de poliuretana ou poliisocianurato produzida no molde. |
Country Status (17)
| Country | Link |
|---|---|
| EP (1) | EP1161474B1 (https=) |
| JP (1) | JP2002536516A (https=) |
| CN (1) | CN1176965C (https=) |
| AT (1) | ATE265478T1 (https=) |
| AU (1) | AU2800600A (https=) |
| BR (1) | BR0008107B1 (https=) |
| CA (1) | CA2362505A1 (https=) |
| DE (2) | DE19905989A1 (https=) |
| DK (1) | DK1161474T3 (https=) |
| ES (1) | ES2216863T3 (https=) |
| HK (1) | HK1044787B (https=) |
| HU (1) | HU226761B1 (https=) |
| PL (1) | PL207099B1 (https=) |
| RU (1) | RU2237678C2 (https=) |
| TR (1) | TR200102312T2 (https=) |
| TW (1) | TWI227245B (https=) |
| WO (1) | WO2000047647A1 (https=) |
Families Citing this family (87)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE10060817A1 (de) * | 2000-12-07 | 2002-06-20 | Henkel Kgaa | Steinverbundplatten zur Isolierung |
| US6833431B2 (en) * | 2001-05-02 | 2004-12-21 | Bayer Aktiengesellschaft | Double-metal cyanide catalysts for preparing polyether polyols |
| DE102004062540A1 (de) * | 2004-12-24 | 2006-07-06 | Bayer Materialscience Ag | Polyurethan-Hartschaumstoffe, ein Verfahren zu ihrer Herstellung sowie ihre Verwendung |
| DE602006017354D1 (de) * | 2005-04-29 | 2010-11-18 | Dow Global Technologies Inc | Polyesterpolyole mit sekundären alkoholgruppen und ihre verwendung bei der herstellung von polyurethanen wie polyurethanweichschaumstoffen |
| DE102005021994A1 (de) * | 2005-05-09 | 2006-11-23 | Basf Ag | Verfahren zur Herstellung von Vakuumisolations-Paneelen |
| CN101374877B (zh) * | 2006-01-27 | 2011-05-04 | 巴斯夫欧洲公司 | 生产开孔粘弹性软质聚氨酯泡沫的方法 |
| CN101631810B (zh) | 2006-12-29 | 2013-07-24 | 江森自控科技公司 | 聚氨酯泡沫组成、产品及方法 |
| JP2009040916A (ja) * | 2007-08-09 | 2009-02-26 | Nippon Polyurethane Ind Co Ltd | 水発泡硬質ポリイソシアヌレートフォーム形成用組成物、該組成物を用いた水発泡硬質ポリイソシアヌレートフォームの製造方法、及び該製造方法により得られる水発泡硬質ポリイソシアヌレートフォーム |
| ES2625883T3 (es) * | 2007-12-19 | 2017-07-20 | Basf Se | Procedimiento para la preparación de espumas rígidas que contienen grupos uretano y grupos isocianurato |
| DE102008000243A1 (de) | 2008-02-06 | 2009-08-13 | Evonik Goldschmidt Gmbh | Neuartige Kompatibilisierungsmittel zur Verbesserung der Lagerstabilität von Polyolmischungen |
| DE102008000255A1 (de) | 2008-02-08 | 2009-08-20 | Evonik Goldschmidt Gmbh | Siloxanzusammensetzungen |
| DE102009001595A1 (de) | 2009-03-17 | 2010-09-23 | Evonik Goldschmidt Gmbh | Kompatibilisierungsmittel zur Verbesserung der Lagerstabilität von Polyolmischungen |
| CA2805017C (en) | 2010-07-13 | 2018-06-05 | Bayer Intellectual Property Gmbh | Slightly modified prepolymers and their uses |
| DE102010060390A1 (de) * | 2010-11-05 | 2012-05-10 | Bayer Materialscience Aktiengesellschaft | Emulsionsförmige Reaktionsmischung und Verfahren zur Herstellung von Polyurethanschäumen aus einer solchen Reaktionsmischung |
| DE102010063241A1 (de) | 2010-12-16 | 2012-06-21 | Evonik Goldschmidt Gmbh | Siliconstabilisatoren für Polyurethan- oder Polyisocyanurat-Hartschaumstoffe |
| DE102011007468A1 (de) | 2011-04-15 | 2012-10-18 | Evonik Goldschmidt Gmbh | Zusammensetzung, enthaltend spezielle Carbamat-artige Verbindungen, geeignet zur Herstellung von Polyurethanschäumen |
| DE102011007479A1 (de) | 2011-04-15 | 2012-10-18 | Evonik Goldschmidt Gmbh | Zusammensetzung, enthaltend spezielle Amide und organomodifizierte Siloxane, geeignet zur Herstellung von Polyurethanschäumen |
| US20130030073A1 (en) * | 2011-07-26 | 2013-01-31 | Bayer Materialscience Llc | Amine-initiated polyols from renewable resources and processes for their production and use |
| DE102011109541A1 (de) | 2011-08-03 | 2013-02-07 | Evonik Goldschmidt Gmbh | Verwendung von Polysiloxanen enthaltend verzweigte Polyetherreste zur Herstellung von Polyurethanschäumen |
| PL2748218T3 (pl) * | 2011-08-23 | 2017-08-31 | Basf Se | Zastosowanie mikroemulsji i sposób wytwarzania tworzyw piankowych |
| DE102013201829A1 (de) | 2013-02-05 | 2014-08-07 | Evonik Industries Ag | Amine, geeignet zur Verwendung bei der Herstellung von Polyurethanen |
| WO2015022273A1 (de) * | 2013-08-13 | 2015-02-19 | Bayer Materialscience Ag | Polyurethanschaumstoffe und ihre verwendung |
| DE102013217395A1 (de) | 2013-09-02 | 2015-03-05 | Evonik Industries Ag | Verwendung von Mischungen organofunktionell modifizierter Polysiloxane mit Amiden bei der Herstellung von Polyurethanweichschäumen |
| EP2886591A1 (de) | 2013-12-19 | 2015-06-24 | Evonik Industries AG | Zusammensetzung, geeignet zur Herstellung von Polyurethanschäumen, enthaltend mindestens ein Nukleierungsmittel |
| DE102013226575B4 (de) | 2013-12-19 | 2021-06-24 | Evonik Operations Gmbh | Zusammensetzung, geeignet zur Herstellung von Polyurethanschäumen, enthaltend mindestens einen ungesättigten Fluorkohlenwasserstoff oder ungesättigten Fluorkohlenwasserstoff als Treibmittel, Polyurethanschäume, Verfahren zu deren Herstellung und deren Verwendung |
| DE102014215388A1 (de) | 2014-08-05 | 2016-02-11 | Evonik Degussa Gmbh | Stickstoffhaltige Verbindungen, geeignet zur Verwendung bei der Herstellung von Polyurethanen |
| DE102014215381B4 (de) | 2014-08-05 | 2020-06-10 | Evonik Operations Gmbh | Stickstoffhaltige Verbindungen, geeignet zur Verwendung bei der Herstellung von Polyurethanen |
| DE102014215384A1 (de) | 2014-08-05 | 2016-02-11 | Evonik Degussa Gmbh | Stickstoffhaltige Verbindungen, geeignet zur Verwendung bei der Herstellung von Polyurethanen |
| DE102014215382A1 (de) | 2014-08-05 | 2016-02-11 | Evonik Degussa Gmbh | Stickstoffhaltige Verbindungen, geeignet zur Verwendung bei der Herstellung von Polyurethanen |
| DE102014215380B4 (de) | 2014-08-05 | 2022-04-28 | Evonik Operations Gmbh | Stickstoffhaltige Verbindungen, geeignet zur Verwendung bei der Herstellung von Polyurethanen |
| DE102014215383B4 (de) | 2014-08-05 | 2020-06-10 | Evonik Operations Gmbh | Stickstoffhaltige Verbindungen, geeignet zur Verwendung bei der Herstellung von Polyurethanen |
| DE102014215387B4 (de) | 2014-08-05 | 2020-06-10 | Evonik Operations Gmbh | Stickstoffhaltige Verbindungen, geeignet zur Verwendung bei der Herstellung von Polyurethanen |
| ES2845608T3 (es) | 2015-03-03 | 2021-07-27 | Evonik Operations Gmbh | Producción de capas de poliuretano porosas |
| EP3078696A1 (de) | 2015-04-08 | 2016-10-12 | Evonik Degussa GmbH | Herstellung emissionsarmer polyurethane |
| EP3115389B1 (de) | 2015-07-07 | 2020-04-01 | Evonik Operations GmbH | Herstellung von polyurethanschaum |
| EP3176206A1 (de) | 2015-12-01 | 2017-06-07 | Evonik Degussa GmbH | Verfahren zur herstellung feinzelliger schaumstoffe unter verwendung eines zellalterungshemmers |
| EP3205678A1 (de) | 2016-02-10 | 2017-08-16 | Evonik Degussa GmbH | Alterungsbeständige und emissionsarme matratzen und/oder kissen |
| EP3459984A1 (de) | 2017-09-25 | 2019-03-27 | Evonik Degussa GmbH | Herstellung von polyurethanschaum |
| ES2910300T3 (es) | 2017-12-05 | 2022-05-12 | Basf Se | Procedimiento para la fabricación de espumas rígidas de celdas abiertas, que contienen grupos uretano y grupos isocianurato |
| CN112867743B (zh) | 2018-10-15 | 2023-05-02 | 陶氏环球技术有限责任公司 | 配制的多元醇组合物 |
| FI3908617T3 (fi) | 2019-01-07 | 2024-09-17 | Evonik Operations Gmbh | Kovan polyuretaanivaahtomuovin valmistus |
| ES2898877T3 (es) | 2019-01-07 | 2022-03-09 | Evonik Operations Gmbh | Producción de espuma dura de poliuretano |
| EP3744745A1 (de) | 2019-05-28 | 2020-12-02 | Evonik Operations GmbH | Herstellung von pu-schaumstoffen |
| US12458150B2 (en) | 2019-07-19 | 2025-11-04 | Evonik Operations Gmbh | Shaped PU foam articles |
| WO2021013607A1 (de) | 2019-07-24 | 2021-01-28 | Evonik Operations Gmbh | Herstellung von polyurethansystemen |
| EP3805285B1 (de) | 2019-10-08 | 2024-07-10 | Evonik Operations GmbH | Herstellung von polyurethanhartschaum |
| RS67445B1 (sr) | 2019-11-07 | 2025-12-31 | Evonik Operations Gmbh | Trajna deformacija sabijanjem |
| EP3865527A1 (de) | 2020-02-14 | 2021-08-18 | Evonik Operations GmbH | Herstellung von pu-schaumstoffen |
| DE102020202057A1 (de) | 2020-02-19 | 2021-08-19 | Evonik Operations Gmbh | Polyurethan-Isolierschaumstoffe und ihre Herstellung |
| EP3919539A1 (de) | 2020-06-04 | 2021-12-08 | Evonik Operations GmbH | Herstellung von polyurethanschaum |
| EP3940012A1 (de) | 2020-07-16 | 2022-01-19 | Evonik Operations GmbH | Stickstofffreie und stickstoffarme vernetzende additive für kaltblockweichschaum mit verbesserten kompressions- und alterungseigenschaften |
| US12122890B2 (en) | 2020-08-20 | 2024-10-22 | Evonik Operations Gmbh | Production of polyurethane foam |
| US20220106432A1 (en) | 2020-10-07 | 2022-04-07 | Evonik Operations Gmbh | Shaped flexible pu foam articles |
| KR20230117741A (ko) | 2020-12-08 | 2023-08-09 | 에보니크 오퍼레이션즈 게엠베하 | 폴리우레탄 발포체의 제조 |
| US20240182660A1 (en) | 2021-03-02 | 2024-06-06 | Evonik Operations Gmbh | Production of polyurethane foam |
| CN117120500A (zh) | 2021-04-14 | 2023-11-24 | 赢创运营有限公司 | 硬质聚氨酯或聚异氰脲酸酯泡沫的生产 |
| CN117529512A (zh) | 2021-06-17 | 2024-02-06 | 赢创运营有限公司 | 成型软质聚氨酯泡沫制品 |
| US20240368334A1 (en) | 2021-07-01 | 2024-11-07 | Evonik Operations Gmbh | Production of rigid polyurethane or polyisocyanurate foam |
| MX2023014998A (es) | 2021-07-02 | 2024-02-16 | Evonik Operations Gmbh | Produccion de espumas de pu con polioles reciclados. |
| WO2023275031A1 (de) | 2021-07-02 | 2023-01-05 | Evonik Operations Gmbh | Herstellung von pu-schaumstoffen unter einsatz von recycling-polyolen |
| CA3224253A1 (en) | 2021-07-02 | 2023-01-05 | Ralph Marquardt | Production of pu foams using recycled polyols |
| US20240294724A1 (en) | 2021-07-02 | 2024-09-05 | Evonik Operations Gmbh | Recovering di- and/or polyisocyanates from pu-depolymerisation processes |
| EP4363478A1 (de) | 2021-07-02 | 2024-05-08 | Evonik Operations GmbH | Herstellung von pu-schaumstoffen unter einsatz von recycling-polyolen |
| CA3224261A1 (en) | 2021-07-02 | 2023-01-05 | Annegret Terheiden | Production of pu foams |
| CN118742583A (zh) | 2022-02-22 | 2024-10-01 | 赢创运营有限公司 | 使用来自基于胺的水解过程的回收多元醇生产pu泡沫 |
| EP4257323A1 (en) | 2022-04-08 | 2023-10-11 | Evonik Operations GmbH | System and method for determining parameters for foam production |
| EP4257326A1 (en) | 2022-04-08 | 2023-10-11 | Evonik Operations GmbH | Optical determination of a control signal in response to detection of macroscopic polyurethane foam defects |
| EP4257325A1 (en) | 2022-04-08 | 2023-10-11 | Evonik Operations GmbH | Optical prediction of polyurethane foam parameters |
| EP4257324A1 (en) | 2022-04-08 | 2023-10-11 | Evonik Operations GmbH | System and method for automatically setting parameters for foam production |
| EP4257327A1 (en) | 2022-04-08 | 2023-10-11 | Evonik Operations GmbH | Optical determination of a control signal for slabstock polyurethane foam production |
| EP4526372A1 (de) | 2022-05-17 | 2025-03-26 | Evonik Operations GmbH | Herstellung von polyurethanschaum |
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| EP4282892A1 (de) | 2022-05-25 | 2023-11-29 | Evonik Operations GmbH | Herstellung von polyurethanschaum unter verwendung von katalysatoren auf basis ionischer flüssigkeiten |
| EP4536723A1 (de) | 2022-06-08 | 2025-04-16 | Evonik Operations GmbH | Herstellung von flammwidrigem polyurethanschaum |
| CN119343389A (zh) | 2022-06-08 | 2025-01-21 | 赢创运营有限公司 | 用于生产聚氨酯泡沫的聚醚-硅氧烷嵌段共聚物 |
| EP4299656A1 (de) | 2022-07-01 | 2024-01-03 | Evonik Operations GmbH | Herstellung von propoxylierten benzoldicarbonsäureamiden und dem entsprechenden polyurethanschaum |
| JP2025528473A (ja) | 2022-08-31 | 2025-08-28 | エボニック オペレーションズ ゲーエムベーハー | ポリウレタンフォームの製造 |
| WO2024068268A1 (de) | 2022-09-28 | 2024-04-04 | Evonik Operations Gmbh | Verfahren zur herstellung von sioc-verknüpften, linearen polydialkylsiloxan-polyether-blockcopolymeren und ihre verwendung |
| EP4372024A1 (en) | 2022-11-15 | 2024-05-22 | Evonik Operations GmbH | New method for recycling of polyisocyanurates |
| EP4372036A1 (en) | 2022-11-15 | 2024-05-22 | Evonik Operations GmbH | Depolymerization of polyisocyanurate with organic amine bases |
| WO2024170429A1 (de) | 2023-02-17 | 2024-08-22 | Evonik Operations Gmbh | Stabilisatoren für polyurethanschaumstoffe enthaltend recycling-polyol |
| JP2026504596A (ja) | 2023-02-17 | 2026-02-05 | エボニック オペレーションズ ゲーエムベーハー | 固形物を含有するポリウレタンフォーム材のための安定剤 |
| WO2025082815A1 (de) | 2023-10-19 | 2025-04-24 | Evonik Operations Gmbh | Stabilisatoren für polyurethanschaumstoffe |
| CN120424304A (zh) | 2024-02-02 | 2025-08-05 | 赢创运营有限公司 | 聚氨酯或聚异氰脲酸酯泡沫的生产 |
| CN120424305A (zh) | 2024-02-02 | 2025-08-05 | 赢创运营有限公司 | 聚氨酯或聚异氰脲酸酯泡沫的生产 |
| EP4606832A1 (de) | 2024-02-22 | 2025-08-27 | Evonik Operations GmbH | Stabilisatoren für polyurethanschaumstoffe enthaltend recycling-polyol |
| CA3279246A1 (en) | 2024-07-12 | 2026-03-01 | Evonik Operations Gmbh | Production of polyurethane foam |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3621039A1 (de) * | 1986-06-24 | 1988-01-07 | Bayer Ag | Verfahren zur herstellung von hydroxylgruppen aufweisenden oligoestern und deren verwendung |
| JPH02180916A (ja) * | 1989-01-06 | 1990-07-13 | M D Kasei Kk | 硬質ポリウレタンフォームの製造方法 |
| JPH03195718A (ja) * | 1989-12-25 | 1991-08-27 | Mitsui Toatsu Chem Inc | 硬質ウレタンフォームの製造方法 |
| DE4303556C1 (de) * | 1993-02-08 | 1994-10-27 | Bayer Ag | Harte Polyurethane oder Polyurethanschaumstoffe |
| ES2118987T3 (es) * | 1993-02-10 | 1998-10-01 | Bayer Ag | Procedimiento para la obtencion de plasticos celulares a base de isocianato. |
| GB9314556D0 (en) * | 1993-07-14 | 1993-08-25 | Ici Plc | Rigid polyurethane foams |
| EP0672697A1 (de) * | 1994-03-17 | 1995-09-20 | Bayer Ag | Verfahren zur Herstellung von Urethan-, Harnstoff- und Biuretgruppen aufweisenden Hartschaumstoffen und deren Verwendung |
| JP3425816B2 (ja) * | 1995-01-19 | 2003-07-14 | 三井化学株式会社 | 硬質ポリウレタンフォーム |
| BR9608507A (pt) * | 1995-05-12 | 1999-06-08 | Ici Plc | Processo para a preparação de espuma rigida de poliuretano processo para preparar uma espuma flexível de poliuretano sistema de reação e espuma flexível de poliuretano |
| DE19634392A1 (de) * | 1996-08-26 | 1998-03-05 | Bayer Ag | Schäumfähige Polyurethanzubereitungen mit gutem Fließverhalten sowie ein Verfahren zur Herstellung geschäumter Polyurethan-Formteile |
| GB2324798B (en) * | 1997-05-01 | 1999-08-18 | Ici Plc | Open celled cellular polyurethane products |
| DE19742010A1 (de) * | 1997-09-24 | 1999-03-25 | Basf Ag | Lagerstabile Emulsionen zur Herstellung von feinzelligen Hartschaumstoffen auf Isocyanatbasis |
-
1999
- 1999-02-13 DE DE19905989A patent/DE19905989A1/de not_active Withdrawn
-
2000
- 2000-02-01 CA CA002362505A patent/CA2362505A1/en not_active Abandoned
- 2000-02-01 HU HU0200140A patent/HU226761B1/hu not_active IP Right Cessation
- 2000-02-01 BR BRPI0008107-8A patent/BR0008107B1/pt not_active IP Right Cessation
- 2000-02-01 AU AU28006/00A patent/AU2800600A/en not_active Abandoned
- 2000-02-01 HK HK02106473.1A patent/HK1044787B/zh not_active IP Right Cessation
- 2000-02-01 RU RU2001125433/04A patent/RU2237678C2/ru not_active IP Right Cessation
- 2000-02-01 JP JP2000598561A patent/JP2002536516A/ja active Pending
- 2000-02-01 EP EP00906260A patent/EP1161474B1/de not_active Expired - Lifetime
- 2000-02-01 AT AT00906260T patent/ATE265478T1/de not_active IP Right Cessation
- 2000-02-01 ES ES00906260T patent/ES2216863T3/es not_active Expired - Lifetime
- 2000-02-01 CN CNB00803737XA patent/CN1176965C/zh not_active Expired - Fee Related
- 2000-02-01 TR TR2001/02312T patent/TR200102312T2/xx unknown
- 2000-02-01 DK DK00906260T patent/DK1161474T3/da active
- 2000-02-01 WO PCT/EP2000/000783 patent/WO2000047647A1/de not_active Ceased
- 2000-02-01 DE DE50006255T patent/DE50006255D1/de not_active Expired - Lifetime
- 2000-02-01 PL PL350076A patent/PL207099B1/pl unknown
- 2000-02-03 TW TW089101871A patent/TWI227245B/zh not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| HUP0200140A2 (hu) | 2002-05-29 |
| JP2002536516A (ja) | 2002-10-29 |
| TR200102312T2 (tr) | 2002-01-21 |
| AU2800600A (en) | 2000-08-29 |
| TWI227245B (en) | 2005-02-01 |
| PL207099B1 (pl) | 2010-11-30 |
| HK1044787A1 (en) | 2002-11-01 |
| HUP0200140A3 (en) | 2002-06-28 |
| HK1044787B (zh) | 2005-09-09 |
| CN1340069A (zh) | 2002-03-13 |
| WO2000047647A1 (de) | 2000-08-17 |
| BR0008107A (pt) | 2001-11-06 |
| DE19905989A1 (de) | 2000-08-17 |
| DK1161474T3 (da) | 2004-08-16 |
| PL350076A1 (en) | 2002-11-04 |
| HU226761B1 (en) | 2009-09-28 |
| ATE265478T1 (de) | 2004-05-15 |
| EP1161474A1 (de) | 2001-12-12 |
| CA2362505A1 (en) | 2000-08-17 |
| ES2216863T3 (es) | 2004-11-01 |
| CN1176965C (zh) | 2004-11-24 |
| DE50006255D1 (de) | 2004-06-03 |
| EP1161474B1 (de) | 2004-04-28 |
| RU2237678C2 (ru) | 2004-10-10 |
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