JP2009520067A - アロファネート変性イソシアネートを含んでなるポリウレタンエラストマー - Google Patents
アロファネート変性イソシアネートを含んでなるポリウレタンエラストマー Download PDFInfo
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- JP2009520067A JP2009520067A JP2008545738A JP2008545738A JP2009520067A JP 2009520067 A JP2009520067 A JP 2009520067A JP 2008545738 A JP2008545738 A JP 2008545738A JP 2008545738 A JP2008545738 A JP 2008545738A JP 2009520067 A JP2009520067 A JP 2009520067A
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- Japan
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- molecular weight
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- polyisocyanate
- isocyanate
- Prior art date
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- 239000012948 isocyanate Substances 0.000 title claims abstract description 24
- 229920003225 polyurethane elastomer Polymers 0.000 title claims abstract description 8
- 150000002513 isocyanates Chemical class 0.000 title claims description 18
- -1 aliphatic isocyanate Chemical class 0.000 claims abstract description 67
- 239000005056 polyisocyanate Substances 0.000 claims abstract description 63
- 229920001228 polyisocyanate Polymers 0.000 claims abstract description 63
- 150000003077 polyols Chemical class 0.000 claims abstract description 46
- 229920005862 polyol Polymers 0.000 claims abstract description 45
- 229920000570 polyether Polymers 0.000 claims abstract description 26
- 239000004721 Polyphenylene oxide Substances 0.000 claims abstract description 23
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 22
- 150000001412 amines Chemical class 0.000 claims abstract description 21
- 229920001971 elastomer Polymers 0.000 claims abstract description 18
- 239000000806 elastomer Substances 0.000 claims abstract description 18
- 239000007795 chemical reaction product Substances 0.000 claims abstract description 13
- 150000002894 organic compounds Chemical class 0.000 claims abstract description 13
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- 238000000034 method Methods 0.000 claims description 35
- 125000001931 aliphatic group Chemical group 0.000 claims description 23
- 239000000049 pigment Substances 0.000 claims description 23
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- 125000004432 carbon atom Chemical group C* 0.000 claims description 16
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- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 claims description 14
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 claims description 14
- 229910052799 carbon Inorganic materials 0.000 claims description 7
- KORSJDCBLAPZEQ-UHFFFAOYSA-N dicyclohexylmethane-4,4'-diisocyanate Chemical compound C1CC(N=C=O)CCC1CC1CCC(N=C=O)CC1 KORSJDCBLAPZEQ-UHFFFAOYSA-N 0.000 claims description 7
- 239000011541 reaction mixture Substances 0.000 claims description 7
- 229940008841 1,6-hexamethylene diisocyanate Drugs 0.000 claims description 6
- 125000003158 alcohol group Chemical group 0.000 claims description 6
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 claims description 6
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- 239000012974 tin catalyst Substances 0.000 claims description 3
- 125000004122 cyclic group Chemical group 0.000 claims 2
- 125000001302 tertiary amino group Chemical group 0.000 claims 2
- 238000004519 manufacturing process Methods 0.000 abstract description 8
- 125000003277 amino group Chemical group 0.000 abstract description 4
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- 229910052751 metal Inorganic materials 0.000 description 13
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- 239000006229 carbon black Substances 0.000 description 8
- 235000019241 carbon black Nutrition 0.000 description 8
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 8
- XFXPMWWXUTWYJX-UHFFFAOYSA-N Cyanide Chemical compound N#[C-] XFXPMWWXUTWYJX-UHFFFAOYSA-N 0.000 description 7
- 239000005058 Isophorone diisocyanate Substances 0.000 description 7
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 7
- 125000002947 alkylene group Chemical group 0.000 description 7
- 229920001451 polypropylene glycol Polymers 0.000 description 7
- 238000006243 chemical reaction Methods 0.000 description 6
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- 238000002360 preparation method Methods 0.000 description 6
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- 150000003512 tertiary amines Chemical group 0.000 description 6
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 5
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 5
- 239000002253 acid Substances 0.000 description 5
- 239000003963 antioxidant agent Substances 0.000 description 5
- 150000007942 carboxylates Chemical class 0.000 description 5
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 5
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical group OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 5
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 4
- 239000007983 Tris buffer Substances 0.000 description 4
- 150000001298 alcohols Chemical class 0.000 description 4
- 229910052797 bismuth Inorganic materials 0.000 description 4
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 description 4
- 239000000975 dye Substances 0.000 description 4
- 239000001257 hydrogen Substances 0.000 description 4
- 229910052739 hydrogen Inorganic materials 0.000 description 4
- 125000001841 imino group Chemical group [H]N=* 0.000 description 4
- 238000000465 moulding Methods 0.000 description 4
- 125000006353 oxyethylene group Chemical group 0.000 description 4
- AVWRKZWQTYIKIY-UHFFFAOYSA-N urea-1-carboxylic acid Chemical group NC(=O)NC(O)=O AVWRKZWQTYIKIY-UHFFFAOYSA-N 0.000 description 4
- JCTXKRPTIMZBJT-UHFFFAOYSA-N 2,2,4-trimethylpentane-1,3-diol Chemical compound CC(C)C(O)C(C)(C)CO JCTXKRPTIMZBJT-UHFFFAOYSA-N 0.000 description 3
- LCZVSXRMYJUNFX-UHFFFAOYSA-N 2-[2-(2-hydroxypropoxy)propoxy]propan-1-ol Chemical compound CC(O)COC(C)COC(C)CO LCZVSXRMYJUNFX-UHFFFAOYSA-N 0.000 description 3
- QWGRWMMWNDWRQN-UHFFFAOYSA-N 2-methylpropane-1,3-diol Chemical compound OCC(C)CO QWGRWMMWNDWRQN-UHFFFAOYSA-N 0.000 description 3
- ZRWNRAJCPNLYAK-UHFFFAOYSA-N 4-bromobenzamide Chemical compound NC(=O)C1=CC=C(Br)C=C1 ZRWNRAJCPNLYAK-UHFFFAOYSA-N 0.000 description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- SJRJJKPEHAURKC-UHFFFAOYSA-N N-Methylmorpholine Chemical compound CN1CCOCC1 SJRJJKPEHAURKC-UHFFFAOYSA-N 0.000 description 3
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- UWHCKJMYHZGTIT-UHFFFAOYSA-N Tetraethylene glycol, Natural products OCCOCCOCCOCCO UWHCKJMYHZGTIT-UHFFFAOYSA-N 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
- ORLQHILJRHBSAY-UHFFFAOYSA-N [1-(hydroxymethyl)cyclohexyl]methanol Chemical compound OCC1(CO)CCCCC1 ORLQHILJRHBSAY-UHFFFAOYSA-N 0.000 description 3
- KXBFLNPZHXDQLV-UHFFFAOYSA-N [cyclohexyl(diisocyanato)methyl]cyclohexane Chemical compound C1CCCCC1C(N=C=O)(N=C=O)C1CCCCC1 KXBFLNPZHXDQLV-UHFFFAOYSA-N 0.000 description 3
- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 3
- 229910052782 aluminium Inorganic materials 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 3
- 239000012975 dibutyltin dilaurate Substances 0.000 description 3
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 3
- 238000005516 engineering process Methods 0.000 description 3
- 238000002347 injection Methods 0.000 description 3
- 239000007924 injection Substances 0.000 description 3
- 239000000178 monomer Substances 0.000 description 3
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 3
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- 150000003141 primary amines Chemical group 0.000 description 3
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- IMNIMPAHZVJRPE-UHFFFAOYSA-N triethylenediamine Chemical compound C1CN2CCN1CC2 IMNIMPAHZVJRPE-UHFFFAOYSA-N 0.000 description 3
- 150000004072 triols Chemical class 0.000 description 3
- DNIAPMSPPWPWGF-VKHMYHEASA-N (+)-propylene glycol Chemical compound C[C@H](O)CO DNIAPMSPPWPWGF-VKHMYHEASA-N 0.000 description 2
- ARXKVVRQIIOZGF-UHFFFAOYSA-N 1,2,4-butanetriol Chemical compound OCCC(O)CO ARXKVVRQIIOZGF-UHFFFAOYSA-N 0.000 description 2
- YPFDHNVEDLHUCE-UHFFFAOYSA-N 1,3-propanediol Substances OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 2
- MJBGJRXHOQIARE-UHFFFAOYSA-N 1-(diethylamino)-3-[4-[[4-(diethylaminocarbamoylamino)phenyl]methyl]phenyl]urea Chemical compound C1=CC(NC(=O)NN(CC)CC)=CC=C1CC1=CC=C(NC(=O)NN(CC)CC)C=C1 MJBGJRXHOQIARE-UHFFFAOYSA-N 0.000 description 2
- KGRVJHAUYBGFFP-UHFFFAOYSA-N 2,2'-Methylenebis(4-methyl-6-tert-butylphenol) Chemical compound CC(C)(C)C1=CC(C)=CC(CC=2C(=C(C=C(C)C=2)C(C)(C)C)O)=C1O KGRVJHAUYBGFFP-UHFFFAOYSA-N 0.000 description 2
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 2
- XUQNLOIVFHUMTR-UHFFFAOYSA-N 2-[[2-hydroxy-5-nonyl-3-(1-phenylethyl)phenyl]methyl]-4-nonyl-6-(1-phenylethyl)phenol Chemical compound OC=1C(C(C)C=2C=CC=CC=2)=CC(CCCCCCCCC)=CC=1CC(C=1O)=CC(CCCCCCCCC)=CC=1C(C)C1=CC=CC=C1 XUQNLOIVFHUMTR-UHFFFAOYSA-N 0.000 description 2
- JWAZRIHNYRIHIV-UHFFFAOYSA-N 2-naphthol Chemical compound C1=CC=CC2=CC(O)=CC=C21 JWAZRIHNYRIHIV-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
- VSAWBBYYMBQKIK-UHFFFAOYSA-N 4-[[3,5-bis[(3,5-ditert-butyl-4-hydroxyphenyl)methyl]-2,4,6-trimethylphenyl]methyl]-2,6-ditert-butylphenol Chemical compound CC1=C(CC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)C(C)=C(CC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)C(C)=C1CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 VSAWBBYYMBQKIK-UHFFFAOYSA-N 0.000 description 2
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- IRIAEXORFWYRCZ-UHFFFAOYSA-N Butylbenzyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCC1=CC=CC=C1 IRIAEXORFWYRCZ-UHFFFAOYSA-N 0.000 description 2
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- 150000001414 amino alcohols Chemical class 0.000 description 2
- RSOILICUEWXSLA-UHFFFAOYSA-N bis(1,2,2,6,6-pentamethylpiperidin-4-yl) decanedioate Chemical compound C1C(C)(C)N(C)C(C)(C)CC1OC(=O)CCCCCCCCC(=O)OC1CC(C)(C)N(C)C(C)(C)C1 RSOILICUEWXSLA-UHFFFAOYSA-N 0.000 description 2
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- 238000010189 synthetic method Methods 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- KKEYFWRCBNTPAC-UHFFFAOYSA-L terephthalate(2-) Chemical compound [O-]C(=O)C1=CC=C(C([O-])=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-L 0.000 description 1
- NZNAAUDJKMURFU-UHFFFAOYSA-N tetrakis(2,2,6,6-tetramethylpiperidin-4-yl) butane-1,2,3,4-tetracarboxylate Chemical compound C1C(C)(C)NC(C)(C)CC1OC(=O)CC(C(=O)OC1CC(C)(C)NC(C)(C)C1)C(C(=O)OC1CC(C)(C)NC(C)(C)C1)CC(=O)OC1CC(C)(C)NC(C)(C)C1 NZNAAUDJKMURFU-UHFFFAOYSA-N 0.000 description 1
- JOUDBUYBGJYFFP-FOCLMDBBSA-N thioindigo Chemical compound S\1C2=CC=CC=C2C(=O)C/1=C1/C(=O)C2=CC=CC=C2S1 JOUDBUYBGJYFFP-FOCLMDBBSA-N 0.000 description 1
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 description 1
- 229910001887 tin oxide Inorganic materials 0.000 description 1
- HPGGPRDJHPYFRM-UHFFFAOYSA-J tin(iv) chloride Chemical class Cl[Sn](Cl)(Cl)Cl HPGGPRDJHPYFRM-UHFFFAOYSA-J 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
- 239000013638 trimer Substances 0.000 description 1
- QXJQHYBHAIHNGG-UHFFFAOYSA-N trimethylolethane Chemical compound OCC(C)(CO)CO QXJQHYBHAIHNGG-UHFFFAOYSA-N 0.000 description 1
- PHYFQTYBJUILEZ-IUPFWZBJSA-N triolein Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(OC(=O)CCCCCCC\C=C/CCCCCCCC)COC(=O)CCCCCCC\C=C/CCCCCCCC PHYFQTYBJUILEZ-IUPFWZBJSA-N 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N urethane group Chemical group NC(=O)OCC JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- LSGOVYNHVSXFFJ-UHFFFAOYSA-N vanadate(3-) Chemical compound [O-][V]([O-])([O-])=O LSGOVYNHVSXFFJ-UHFFFAOYSA-N 0.000 description 1
- 238000004383 yellowing Methods 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052984 zinc sulfide Inorganic materials 0.000 description 1
- IFNXAMCERSVZCV-UHFFFAOYSA-L zinc;2-ethylhexanoate Chemical compound [Zn+2].CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O IFNXAMCERSVZCV-UHFFFAOYSA-L 0.000 description 1
- NHXVNEDMKGDNPR-UHFFFAOYSA-N zinc;pentane-2,4-dione Chemical compound [Zn+2].CC(=O)[CH-]C(C)=O.CC(=O)[CH-]C(C)=O NHXVNEDMKGDNPR-UHFFFAOYSA-N 0.000 description 1
- DRDVZXDWVBGGMH-UHFFFAOYSA-N zinc;sulfide Chemical compound [S-2].[Zn+2] DRDVZXDWVBGGMH-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
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/72—Polyisocyanates or polyisothiocyanates
- C08G18/77—Polyisocyanates or polyisothiocyanates having heteroatoms in addition to the isocyanate or isothiocyanate nitrogen and oxygen or sulfur
- C08G18/78—Nitrogen
- C08G18/7806—Nitrogen containing -N-C=0 groups
- C08G18/7818—Nitrogen containing -N-C=0 groups containing ureum or ureum derivative groups
- C08G18/7837—Nitrogen containing -N-C=0 groups containing ureum or ureum derivative groups containing allophanate 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
- C08G18/08—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
- C08G18/08—Processes
- C08G18/16—Catalysts
- C08G18/18—Catalysts containing secondary or tertiary amines or salts thereof
-
- 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
- C08G18/1858—Catalysts containing secondary or tertiary amines or salts thereof having carbon-to-nitrogen double bonds
-
- 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
- C08G18/20—Heterocyclic amines; Salts thereof
- C08G18/2045—Heterocyclic amines; Salts thereof containing condensed heterocyclic rings
- C08G18/2063—Heterocyclic amines; Salts thereof containing condensed heterocyclic rings having two nitrogen atoms in the condensed ring system
-
- 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
-
- 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
- C08G18/4866—Polyethers having a low unsaturation value
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/72—Polyisocyanates or polyisothiocyanates
- C08G18/77—Polyisocyanates or polyisothiocyanates having heteroatoms in addition to the isocyanate or isothiocyanate nitrogen and oxygen or sulfur
- C08G18/78—Nitrogen
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Polyurethanes Or Polyureas (AREA)
- Injection Moulding Of Plastics Or The Like (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US11/300,957 US20070142610A1 (en) | 2005-12-15 | 2005-12-15 | Polyurethane elastomers comprising allophanate modified isocyanates |
| PCT/US2006/047381 WO2007075330A1 (en) | 2005-12-15 | 2006-12-12 | Polyurethane elastomers comprising allophanate modified isocyanates |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2009520067A true JP2009520067A (ja) | 2009-05-21 |
| JP2009520067A5 JP2009520067A5 (enExample) | 2010-02-12 |
Family
ID=37882437
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2008545738A Pending JP2009520067A (ja) | 2005-12-15 | 2006-12-12 | アロファネート変性イソシアネートを含んでなるポリウレタンエラストマー |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US20070142610A1 (enExample) |
| EP (1) | EP1963388A1 (enExample) |
| JP (1) | JP2009520067A (enExample) |
| KR (1) | KR20080080535A (enExample) |
| CN (1) | CN101321792B (enExample) |
| BR (1) | BRPI0619836A2 (enExample) |
| CA (1) | CA2633041A1 (enExample) |
| MX (1) | MX2008007214A (enExample) |
| RU (1) | RU2433145C2 (enExample) |
| WO (1) | WO2007075330A1 (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2010516886A (ja) * | 2007-01-30 | 2010-05-20 | ダウ グローバル テクノロジーズ インコーポレイティド | アミン開始ポリオール及びアミン開始ポリオールから作製される硬質ポリウレタンフォーム |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20070185302A1 (en) * | 2006-02-08 | 2007-08-09 | Bayer Materialscience Llc | Polyurethane elastomers comprising allophanate modified isocyanates |
| DE102007005960A1 (de) * | 2007-02-07 | 2008-08-14 | Bayer Materialscience Ag | Ruß-gefüllte Polyurethane mit hoher Dielektrizitätskonstante und Durchschlagsfestigkeit |
| US9550857B2 (en) | 2010-07-13 | 2017-01-24 | Basf Se | High-functionality polyisocyanates containing urethane groups |
| EP2593490B1 (de) * | 2010-07-13 | 2015-09-09 | Basf Se | Hochfunktionelle urethangruppen aufweisende polyisocyanate |
| CN103140530A (zh) * | 2010-07-30 | 2013-06-05 | 巴斯夫欧洲公司 | 包含氨基甲酸酯基的高官能度多异氰酸酯 |
| EP2803684A1 (de) * | 2013-05-13 | 2014-11-19 | Basf Se | Isocyanat-Epoxid-Hybridharze |
| JP7539991B2 (ja) * | 2020-09-30 | 2024-08-26 | 三井化学株式会社 | 水分散型ポリイソシアネート、水性ポリウレタン樹脂組成物および物品 |
Citations (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH05239170A (ja) * | 1991-12-05 | 1993-09-17 | Imperial Chem Ind Plc <Ici> | ポリウレタン／ポリウレアを調製するための反応システム |
| JPH07206977A (ja) * | 1993-12-21 | 1995-08-08 | Miles Inc | 脂肪族ｒｉｍエラストマー |
| JPH093152A (ja) * | 1995-06-15 | 1997-01-07 | Arco Chem Technol Lp | ポリウレタンエラストマーとその製造に適したポリオキシアルキレンポリオール |
| JP2001501241A (ja) * | 1996-10-01 | 2001-01-30 | レクティセル | 光安定性エラストマー性ポリウレタン成形品及びその製法 |
| JP2001525465A (ja) * | 1997-12-05 | 2001-12-11 | バイエル・アクチエンゲゼルシヤフト | 向上した物理的特性を有する、ポリウレタンおよびポリウレタン／ウレア熱硬化および湿分硬化エラストマー |
| JP2003292564A (ja) * | 2002-03-29 | 2003-10-15 | Nippon Polyurethane Ind Co Ltd | ゴルフボール用熱可塑性ポリウレタン樹脂及びそれを用いたゴルフボール |
| JP2003342340A (ja) * | 2002-05-29 | 2003-12-03 | Sumika Bayer Urethane Kk | 意匠面に使用されるインストルメントパネル用インテグラルスキンポリウレタンフォームの製造方法 |
| JP2004148554A (ja) * | 2002-10-29 | 2004-05-27 | Nippon Polyurethane Ind Co Ltd | 自動車内装材の製造方法 |
| JP2004237643A (ja) * | 2003-02-07 | 2004-08-26 | Nippon Polyurethane Ind Co Ltd | 自動車内装材の製造方法 |
| JP2005290324A (ja) * | 2004-04-05 | 2005-10-20 | Sumika Bayer Urethane Kk | 低硬度熱硬化性ポリウレタンエラストマーおよびその製造方法 |
| JP2009526122A (ja) * | 2006-02-08 | 2009-07-16 | バイエル・マテリアルサイエンス・リミテッド・ライアビリティ・カンパニー | アロファネート変性イソシアネートを含んでなるポリウレタンエラストマー |
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|---|---|---|---|---|
| US4218543A (en) * | 1976-05-21 | 1980-08-19 | Bayer Aktiengesellschaft | Rim process for the production of elastic moldings |
| US4269945A (en) * | 1980-01-24 | 1981-05-26 | The Dow Chemical Company | Reaction injection molded polyurethanes employing aliphatic amine chain extenders |
| US4642320A (en) * | 1983-11-02 | 1987-02-10 | The Dow Chemical Company | Reaction injection molded polyureas employing high molecular weight amine-terminated polyethers |
| EP0275010B1 (de) * | 1987-01-14 | 1991-11-21 | Bayer Ag | Verfahren zur Herstellung von Polyurethan-Formteilen |
| US4764543A (en) * | 1987-08-03 | 1988-08-16 | The Dow Chemical Company | Microcellular foamed or reaction injection molded polyurethane/polyureas employing amine terminated polymers and diamine chain extenders |
| US5656677A (en) * | 1989-01-20 | 1997-08-12 | Recticel | Method for preparing and applying a sprayable, light stable polyurethane |
| US5470813A (en) * | 1993-11-23 | 1995-11-28 | Arco Chemical Technology, L.P. | Double metal cyanide complex catalysts |
| US5502150A (en) * | 1994-06-29 | 1996-03-26 | Bayer Corporation | Linear HDI urethane prepolymers for rim application |
| CA2174305C (en) * | 1995-06-07 | 2007-07-03 | Ronald A. Cageao | Method of producing gaskets from polyurethane/urea compositions and gaskets produced therefrom |
| KR100562814B1 (ko) * | 1999-03-17 | 2006-03-21 | 헌트스만 인터내셔날,엘엘씨 | 성형 폴리우레탄 재료의 제조 방법 |
| US6765080B2 (en) * | 2002-06-06 | 2004-07-20 | Bayer Corporation | High performance RIM elastomers and a process for their production |
-
2005
- 2005-12-15 US US11/300,957 patent/US20070142610A1/en not_active Abandoned
-
2006
- 2006-12-12 BR BRPI0619836-8A patent/BRPI0619836A2/pt not_active IP Right Cessation
- 2006-12-12 WO PCT/US2006/047381 patent/WO2007075330A1/en not_active Ceased
- 2006-12-12 CN CN200680045284XA patent/CN101321792B/zh not_active Expired - Fee Related
- 2006-12-12 JP JP2008545738A patent/JP2009520067A/ja active Pending
- 2006-12-12 RU RU2008128301/04A patent/RU2433145C2/ru not_active IP Right Cessation
- 2006-12-12 CA CA002633041A patent/CA2633041A1/en not_active Abandoned
- 2006-12-12 EP EP06845291A patent/EP1963388A1/en not_active Withdrawn
- 2006-12-12 MX MX2008007214A patent/MX2008007214A/es active IP Right Grant
- 2006-12-12 KR KR1020087014124A patent/KR20080080535A/ko not_active Ceased
Patent Citations (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH05239170A (ja) * | 1991-12-05 | 1993-09-17 | Imperial Chem Ind Plc <Ici> | ポリウレタン／ポリウレアを調製するための反応システム |
| JPH07206977A (ja) * | 1993-12-21 | 1995-08-08 | Miles Inc | 脂肪族ｒｉｍエラストマー |
| JPH093152A (ja) * | 1995-06-15 | 1997-01-07 | Arco Chem Technol Lp | ポリウレタンエラストマーとその製造に適したポリオキシアルキレンポリオール |
| JP2001501241A (ja) * | 1996-10-01 | 2001-01-30 | レクティセル | 光安定性エラストマー性ポリウレタン成形品及びその製法 |
| JP2001525465A (ja) * | 1997-12-05 | 2001-12-11 | バイエル・アクチエンゲゼルシヤフト | 向上した物理的特性を有する、ポリウレタンおよびポリウレタン／ウレア熱硬化および湿分硬化エラストマー |
| JP2003292564A (ja) * | 2002-03-29 | 2003-10-15 | Nippon Polyurethane Ind Co Ltd | ゴルフボール用熱可塑性ポリウレタン樹脂及びそれを用いたゴルフボール |
| JP2003342340A (ja) * | 2002-05-29 | 2003-12-03 | Sumika Bayer Urethane Kk | 意匠面に使用されるインストルメントパネル用インテグラルスキンポリウレタンフォームの製造方法 |
| JP2004148554A (ja) * | 2002-10-29 | 2004-05-27 | Nippon Polyurethane Ind Co Ltd | 自動車内装材の製造方法 |
| JP2004237643A (ja) * | 2003-02-07 | 2004-08-26 | Nippon Polyurethane Ind Co Ltd | 自動車内装材の製造方法 |
| JP2005290324A (ja) * | 2004-04-05 | 2005-10-20 | Sumika Bayer Urethane Kk | 低硬度熱硬化性ポリウレタンエラストマーおよびその製造方法 |
| JP2009526122A (ja) * | 2006-02-08 | 2009-07-16 | バイエル・マテリアルサイエンス・リミテッド・ライアビリティ・カンパニー | アロファネート変性イソシアネートを含んでなるポリウレタンエラストマー |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2010516886A (ja) * | 2007-01-30 | 2010-05-20 | ダウ グローバル テクノロジーズ インコーポレイティド | アミン開始ポリオール及びアミン開始ポリオールから作製される硬質ポリウレタンフォーム |
Also Published As
| Publication number | Publication date |
|---|---|
| RU2433145C2 (ru) | 2011-11-10 |
| RU2008128301A (ru) | 2010-01-20 |
| EP1963388A1 (en) | 2008-09-03 |
| KR20080080535A (ko) | 2008-09-04 |
| BRPI0619836A2 (pt) | 2011-10-18 |
| CA2633041A1 (en) | 2007-07-05 |
| MX2008007214A (es) | 2009-03-04 |
| CN101321792B (zh) | 2011-04-13 |
| CN101321792A (zh) | 2008-12-10 |
| US20070142610A1 (en) | 2007-06-21 |
| WO2007075330A1 (en) | 2007-07-05 |
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| WO2007075329A1 (en) | Rim elastomers based on isocyanurates of isophorone diisocyanate and prepolymers thereof | |
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| US7772353B2 (en) | Fast curing aliphatic RIM elastomers | |
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