JP2009508979A - オキサゾリドン基を含む付着、高反応性硬質ポリウレタンフォーム - Google Patents
オキサゾリドン基を含む付着、高反応性硬質ポリウレタンフォーム Download PDFInfo
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- JP2009508979A JP2009508979A JP2008531080A JP2008531080A JP2009508979A JP 2009508979 A JP2009508979 A JP 2009508979A JP 2008531080 A JP2008531080 A JP 2008531080A JP 2008531080 A JP2008531080 A JP 2008531080A JP 2009508979 A JP2009508979 A JP 2009508979A
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- JP
- Japan
- Prior art keywords
- isocyanate
- groups
- polyisocyanate
- mixture
- polyol
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
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- 229920005830 Polyurethane Foam Polymers 0.000 title claims abstract description 18
- 239000011496 polyurethane foam Substances 0.000 title claims abstract description 18
- WDGCBNTXZHJTHJ-UHFFFAOYSA-N 2h-1,3-oxazol-2-id-4-one Chemical group O=C1CO[C-]=N1 WDGCBNTXZHJTHJ-UHFFFAOYSA-N 0.000 title claims description 12
- 239000000853 adhesive Substances 0.000 title description 2
- 230000001070 adhesive effect Effects 0.000 title description 2
- 229920005862 polyol Polymers 0.000 claims abstract description 87
- 150000003077 polyols Chemical class 0.000 claims abstract description 87
- 229920001228 polyisocyanate Polymers 0.000 claims abstract description 69
- 239000005056 polyisocyanate Substances 0.000 claims abstract description 69
- 239000006260 foam Substances 0.000 claims abstract description 52
- 239000012948 isocyanate Substances 0.000 claims abstract description 26
- 150000002513 isocyanates Chemical class 0.000 claims abstract description 26
- 239000004604 Blowing Agent Substances 0.000 claims abstract description 24
- 238000000034 method Methods 0.000 claims abstract description 16
- 239000000758 substrate Substances 0.000 claims abstract description 12
- IZXIZTKNFFYFOF-UHFFFAOYSA-N 2-Oxazolidone Chemical compound O=C1NCCO1 IZXIZTKNFFYFOF-UHFFFAOYSA-N 0.000 claims abstract description 10
- 239000000203 mixture Substances 0.000 claims description 51
- 238000006243 chemical reaction Methods 0.000 claims description 34
- 150000001875 compounds Chemical class 0.000 claims description 31
- 239000003054 catalyst Substances 0.000 claims description 27
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 claims description 27
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 claims description 18
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical group OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 claims description 13
- 239000000463 material Substances 0.000 claims description 12
- 230000015572 biosynthetic process Effects 0.000 claims description 7
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- 150000003512 tertiary amines Chemical class 0.000 claims description 7
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- 125000000524 functional group Chemical group 0.000 claims description 4
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- 230000001464 adherent effect Effects 0.000 abstract 1
- 229920000647 polyepoxide Polymers 0.000 description 27
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 25
- -1 diisocyanate compound Chemical class 0.000 description 25
- 239000007788 liquid Substances 0.000 description 17
- 239000000126 substance Substances 0.000 description 17
- 238000009472 formulation Methods 0.000 description 15
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 12
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- 150000001412 amines Chemical class 0.000 description 12
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 12
- 229920000570 polyether Polymers 0.000 description 11
- 229920000642 polymer Polymers 0.000 description 11
- 239000004094 surface-active agent Substances 0.000 description 11
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 10
- 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 9
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 9
- 239000000047 product Substances 0.000 description 9
- PXKLMJQFEQBVLD-UHFFFAOYSA-N bisphenol F Chemical compound C1=CC(O)=CC=C1CC1=CC=C(O)C=C1 PXKLMJQFEQBVLD-UHFFFAOYSA-N 0.000 description 8
- 238000005187 foaming Methods 0.000 description 8
- 239000004014 plasticizer Substances 0.000 description 8
- 239000007787 solid Substances 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 7
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 7
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 7
- 229910052751 metal Inorganic materials 0.000 description 7
- 239000002184 metal Substances 0.000 description 7
- 239000003981 vehicle Substances 0.000 description 7
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 6
- XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical compound ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 6
- 239000002253 acid Substances 0.000 description 6
- 239000001569 carbon dioxide Substances 0.000 description 6
- 229910002092 carbon dioxide Inorganic materials 0.000 description 6
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 6
- 229910052757 nitrogen Inorganic materials 0.000 description 6
- 239000002245 particle Substances 0.000 description 6
- 239000004593 Epoxy Substances 0.000 description 5
- 239000004721 Polyphenylene oxide Substances 0.000 description 5
- 150000002009 diols Chemical class 0.000 description 5
- 125000001931 aliphatic group Chemical group 0.000 description 4
- 238000013459 approach Methods 0.000 description 4
- 125000003118 aryl group Chemical group 0.000 description 4
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 4
- 229920001577 copolymer Polymers 0.000 description 4
- 239000006071 cream Substances 0.000 description 4
- 125000003700 epoxy group Chemical group 0.000 description 4
- 239000003822 epoxy resin Substances 0.000 description 4
- 150000002739 metals Chemical class 0.000 description 4
- 229920005906 polyester polyol Polymers 0.000 description 4
- 150000003335 secondary amines Chemical class 0.000 description 4
- IMNIMPAHZVJRPE-UHFFFAOYSA-N triethylenediamine Chemical compound C1CN2CCN1CC2 IMNIMPAHZVJRPE-UHFFFAOYSA-N 0.000 description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- SJRJJKPEHAURKC-UHFFFAOYSA-N N-Methylmorpholine Chemical compound CN1CCOCC1 SJRJJKPEHAURKC-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 150000007513 acids Chemical class 0.000 description 3
- 125000003277 amino group Chemical group 0.000 description 3
- 150000008064 anhydrides Chemical class 0.000 description 3
- 239000012298 atmosphere Substances 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- 150000004657 carbamic acid derivatives Chemical class 0.000 description 3
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 3
- 150000002170 ethers Chemical class 0.000 description 3
- 235000011187 glycerol Nutrition 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 3
- 230000000704 physical effect Effects 0.000 description 3
- 229920001451 polypropylene glycol Polymers 0.000 description 3
- 229920001296 polysiloxane Polymers 0.000 description 3
- YPFDHNVEDLHUCE-UHFFFAOYSA-N propane-1,3-diol Chemical compound OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 3
- 239000000376 reactant Substances 0.000 description 3
- 229910052718 tin Inorganic materials 0.000 description 3
- 125000006527 (C1-C5) alkyl group Chemical group 0.000 description 2
- ARXKVVRQIIOZGF-UHFFFAOYSA-N 1,2,4-butanetriol Chemical compound OCCC(O)CO ARXKVVRQIIOZGF-UHFFFAOYSA-N 0.000 description 2
- VOZKAJLKRJDJLL-UHFFFAOYSA-N 2,4-diaminotoluene Chemical compound CC1=CC=C(N)C=C1N VOZKAJLKRJDJLL-UHFFFAOYSA-N 0.000 description 2
- GTEXIOINCJRBIO-UHFFFAOYSA-N 2-[2-(dimethylamino)ethoxy]-n,n-dimethylethanamine Chemical compound CN(C)CCOCCN(C)C GTEXIOINCJRBIO-UHFFFAOYSA-N 0.000 description 2
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- NIQCNGHVCWTJSM-UHFFFAOYSA-N Dimethyl phthalate Chemical compound COC(=O)C1=CC=CC=C1C(=O)OC NIQCNGHVCWTJSM-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
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- 239000002841 Lewis acid Substances 0.000 description 2
- 239000002879 Lewis base Substances 0.000 description 2
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-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
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 2
- SLINHMUFWFWBMU-UHFFFAOYSA-N Triisopropanolamine Chemical compound CC(O)CN(CC(C)O)CC(C)O SLINHMUFWFWBMU-UHFFFAOYSA-N 0.000 description 2
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 2
- 239000012963 UV stabilizer Substances 0.000 description 2
- 229920013701 VORANOL™ Polymers 0.000 description 2
- YRKCREAYFQTBPV-UHFFFAOYSA-N acetylacetone Chemical compound CC(=O)CC(C)=O YRKCREAYFQTBPV-UHFFFAOYSA-N 0.000 description 2
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- 150000001298 alcohols Chemical class 0.000 description 2
- 125000002723 alicyclic group Chemical group 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 125000002947 alkylene group Chemical group 0.000 description 2
- IMUDHTPIFIBORV-UHFFFAOYSA-N aminoethylpiperazine Chemical compound NCCN1CCNCC1 IMUDHTPIFIBORV-UHFFFAOYSA-N 0.000 description 2
- 229910052785 arsenic Inorganic materials 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 2
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical class C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
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- 229910052742 iron Inorganic materials 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
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- VEAZEPMQWHPHAG-UHFFFAOYSA-N n,n,n',n'-tetramethylbutane-1,4-diamine Chemical compound CN(C)CCCCN(C)C VEAZEPMQWHPHAG-UHFFFAOYSA-N 0.000 description 2
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- GFIWSSUBVYLTRF-UHFFFAOYSA-N 2-[2-(2-hydroxyethylamino)ethylamino]ethanol Chemical compound OCCNCCNCCO GFIWSSUBVYLTRF-UHFFFAOYSA-N 0.000 description 1
- DLBIJSSPZNMGAU-UHFFFAOYSA-N 2-[2-(2-hydroxyethylamino)propylamino]ethanol Chemical compound OCCNC(C)CNCCO DLBIJSSPZNMGAU-UHFFFAOYSA-N 0.000 description 1
- GOJUJUVQIVIZAV-UHFFFAOYSA-N 2-amino-4,6-dichloropyrimidine-5-carbaldehyde Chemical group NC1=NC(Cl)=C(C=O)C(Cl)=N1 GOJUJUVQIVIZAV-UHFFFAOYSA-N 0.000 description 1
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- QWGRWMMWNDWRQN-UHFFFAOYSA-N 2-methylpropane-1,3-diol Chemical compound OCC(C)CO QWGRWMMWNDWRQN-UHFFFAOYSA-N 0.000 description 1
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- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical class OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 1
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- AXNUJYHFQHQZBE-UHFFFAOYSA-N toluenediamine group Chemical group C1(=C(C(=CC=C1)N)N)C AXNUJYHFQHQZBE-UHFFFAOYSA-N 0.000 description 1
- STCOOQWBFONSKY-UHFFFAOYSA-N tributyl phosphate Chemical compound CCCCOP(=O)(OCCCC)OCCCC STCOOQWBFONSKY-UHFFFAOYSA-N 0.000 description 1
- SRPWOOOHEPICQU-UHFFFAOYSA-N trimellitic anhydride Chemical compound OC(=O)C1=CC=C2C(=O)OC(=O)C2=C1 SRPWOOOHEPICQU-UHFFFAOYSA-N 0.000 description 1
- QXJQHYBHAIHNGG-UHFFFAOYSA-N trimethylolethane Chemical compound OCC(C)(CO)CO QXJQHYBHAIHNGG-UHFFFAOYSA-N 0.000 description 1
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- XZZNDPSIHUTMOC-UHFFFAOYSA-N triphenyl phosphate Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)(=O)OC1=CC=CC=C1 XZZNDPSIHUTMOC-UHFFFAOYSA-N 0.000 description 1
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- SQOXTAJBVHQIOO-UHFFFAOYSA-L zinc;dicarbamothioate Chemical compound [Zn+2].NC([O-])=S.NC([O-])=S SQOXTAJBVHQIOO-UHFFFAOYSA-L 0.000 description 1
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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
- C08G18/02—Polymeric products of isocyanates or isothiocyanates of isocyanates or isothiocyanates only
- C08G18/025—Polymeric products of isocyanates or isothiocyanates of isocyanates or isothiocyanates only the polymeric products containing carbodiimide 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
-
- 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
- C08G18/003—Polymeric products of isocyanates or isothiocyanates with epoxy compounds having no active hydrogen
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- C—CHEMISTRY; METALLURGY
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- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L83/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
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Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
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- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Polyurethanes Or Polyureas (AREA)
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| PCT/US2006/013781 WO2007040617A1 (en) | 2005-09-15 | 2006-04-12 | Attached, high reactivity rigid polyurethane foams containing oxazolidone groups |
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| JP2009508979A true JP2009508979A (ja) | 2009-03-05 |
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| JP (1) | JP2009508979A (enExample) |
| KR (1) | KR101284934B1 (enExample) |
| CN (1) | CN101268110B (enExample) |
| WO (1) | WO2007040617A1 (enExample) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2020537702A (ja) * | 2017-10-19 | 2020-12-24 | 山▲東▼理工大学 | 有機アミン塩発泡剤 |
| JP2022536640A (ja) * | 2019-06-12 | 2022-08-18 | コベストロ・インテレクチュアル・プロパティ・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツング・アンド・コー・カーゲー | イソシアネート基末端ポリオキサゾリジノンを作製する方法 |
Families Citing this family (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE602005009505D1 (de) * | 2004-03-11 | 2008-10-16 | Dow Global Technologies Inc | Gebundene, hochreaktive polyurethan-hartschaumstoffe |
| US20100096173A1 (en) * | 2007-02-23 | 2010-04-22 | Kentaro Fujino | Epoxy resin composition, prepreg, and laminate and printed wiring board |
| DE102008008391A1 (de) * | 2008-02-09 | 2009-08-13 | Bayer Materialscience Ag | Geschäumte, lichtechte Polyurethanformteile |
| CN102164978A (zh) * | 2008-07-30 | 2011-08-24 | 陶氏环球技术有限责任公司 | 基于邻-环己烷二胺引发的多元醇的硬质聚氨酯泡沫体系统 |
| RU2011107249A (ru) * | 2008-07-30 | 2012-09-10 | ДАУ ГЛОБАЛ ТЕКНОЛОДЖИЗ ЭлЭлСи (US) | Полиольные смеси, содержащие инициированные ортоциклогександиамином полиолы, для жестких полиуретановых пен |
| WO2011109335A1 (en) | 2010-03-03 | 2011-09-09 | Dow Global Technologies Llc | Process for insulating a vehicle cabin |
| CN103003324B (zh) | 2010-07-08 | 2015-02-25 | 陶氏环球技术有限责任公司 | 用脂肪酸酯增塑的改进的聚氨酯密封泡沫组合物 |
| EP2736694B1 (en) | 2011-07-26 | 2019-07-10 | Dow Global Technologies LLC | Method for filling hollow cavities with polymer foam |
| US20150375428A1 (en) * | 2012-10-11 | 2015-12-31 | Douglas E. Reeves | Closed-cell polyurethane structure method and system |
| EP3154929B1 (en) | 2014-04-21 | 2020-09-16 | Firestone Building Products Company, LLC | Method of preparing a foam |
| CN107434846A (zh) * | 2017-09-20 | 2017-12-05 | 贵州航天天马机电科技有限公司 | 一种耐高温聚氨酯硬质泡沫材料及其制备方法 |
| KR20200075869A (ko) | 2017-11-10 | 2020-06-26 | 다우 글로벌 테크놀로지스 엘엘씨 | 폴리우레탄 발포체 시스템 |
| JP7286678B2 (ja) | 2018-05-18 | 2023-06-05 | ダウ グローバル テクノロジーズ エルエルシー | ポリイソシアネート成分、ポリウレタン発泡系、およびそれから製造される物品 |
| EP3802659A1 (en) | 2018-05-29 | 2021-04-14 | Dow Global Technologies LLC | Composite structure |
| EP3827038A1 (en) | 2018-07-23 | 2021-06-02 | Dow Global Technologies, LLC | A foam composition and a foam composite made therefrom |
| MX2021011431A (es) * | 2019-03-20 | 2021-10-13 | Ppg Ind Ohio Inc | Composiciones de recubrimiento de dos componentes. |
| CN110028646B (zh) * | 2019-04-30 | 2021-04-27 | 青岛国工高新材料有限公司 | 一种适用于高压喷涂的遇水膨胀材料及其制备方法 |
| CN111440435A (zh) * | 2020-04-27 | 2020-07-24 | 北京茂华聚氨酯建材有限公司 | 一种高阻燃性聚氨酯保温板及其制备方法 |
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| JPS62500730A (ja) * | 1985-05-07 | 1987-03-26 | ザ ダウ ケミカル カンパニ− | ポリオキサゾリドンの製造方法 |
| JPH07241858A (ja) * | 1994-02-17 | 1995-09-19 | Bayer Ag | 回転注型法によるポリウレタン硬質フォームを用いるパイプの断熱法 |
| JP2000515893A (ja) * | 1996-07-29 | 2000-11-28 | ザ ダウ ケミカル カンパニー | アルカノールアミン／二酸化炭素付加物及びポリウレタンフォーム |
| WO2004081075A1 (en) * | 2003-03-11 | 2004-09-23 | Dow Global Technologies, Inc. | Low amine emission polyutethane foam |
| JP4824670B2 (ja) * | 2004-03-11 | 2011-11-30 | ダウ グローバル テクノロジーズ エルエルシー | 結合された高反応性硬質ポリウレタンフォーム |
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| FR2291996A1 (fr) * | 1974-11-20 | 1976-06-18 | Rhone Poulenc Ind | Polymeres nouveaux prepares a partir de polyisocyanates et de polyepoxydes |
| US4129695A (en) | 1974-11-20 | 1978-12-12 | Rhone-Poulenc Industries | Process for preparing foams from polyisocyanates and polyepoxides |
| US4568703A (en) | 1984-07-27 | 1986-02-04 | Bp Chemicals Limited | Process for the production of polymers containing isocyanurate and or oxazolidone linkages |
| US4699931A (en) | 1986-04-25 | 1987-10-13 | Olin Corporation | Oxazolidone-modified isocyanurate foams and a composition and method for their production |
| FR2616792B1 (fr) | 1987-06-17 | 1991-10-04 | Alsthom | Materiau a structure mousse resistant a la chaleur, constitue a partir de polymeres d'oxazolidones et d'isocyanurates |
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| DE3938062A1 (de) | 1989-11-16 | 1991-05-23 | Bayer Ag | Hochtemperaturbestaendige schaumstoffe |
| DE19742012A1 (de) * | 1997-09-24 | 1999-03-25 | Basf Ag | Temperaturstabile Hartschaumstoffe auf Isocyanatbasis mit geringer Sprödigkeit und niedriger Wärmeleitfähigkeit |
| US5817860A (en) | 1998-03-20 | 1998-10-06 | Essex Specialty Products, Inc. | Polyurethane prepolymer compositions, foams made therefrom and methods of making each thereof |
| US6423755B1 (en) | 2000-02-25 | 2002-07-23 | Essex Specialty Products, Inc | Rigid polyurethane foams |
| BR0208765A (pt) * | 2001-04-01 | 2005-01-04 | Dow Global Technologies Inc | Espuma de poliuretano rìgidas |
| US6699916B2 (en) | 2001-10-29 | 2004-03-02 | Dow Global Technologies Inc. | Rigid hybrid polyurethane foams |
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2006
- 2006-04-12 WO PCT/US2006/013781 patent/WO2007040617A1/en not_active Ceased
- 2006-04-12 CN CN2006800340628A patent/CN101268110B/zh not_active Expired - Fee Related
- 2006-04-12 JP JP2008531080A patent/JP2009508979A/ja active Pending
- 2006-04-12 KR KR1020087008831A patent/KR101284934B1/ko not_active Expired - Fee Related
- 2006-04-12 EP EP20060740919 patent/EP1924619B1/en not_active Expired - Lifetime
- 2006-04-12 US US11/403,658 patent/US7714030B2/en active Active
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| Publication number | Priority date | Publication date | Assignee | Title |
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| JPS62500730A (ja) * | 1985-05-07 | 1987-03-26 | ザ ダウ ケミカル カンパニ− | ポリオキサゾリドンの製造方法 |
| JPH07241858A (ja) * | 1994-02-17 | 1995-09-19 | Bayer Ag | 回転注型法によるポリウレタン硬質フォームを用いるパイプの断熱法 |
| JP2000515893A (ja) * | 1996-07-29 | 2000-11-28 | ザ ダウ ケミカル カンパニー | アルカノールアミン／二酸化炭素付加物及びポリウレタンフォーム |
| WO2004081075A1 (en) * | 2003-03-11 | 2004-09-23 | Dow Global Technologies, Inc. | Low amine emission polyutethane foam |
| JP4824670B2 (ja) * | 2004-03-11 | 2011-11-30 | ダウ グローバル テクノロジーズ エルエルシー | 結合された高反応性硬質ポリウレタンフォーム |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2020537702A (ja) * | 2017-10-19 | 2020-12-24 | 山▲東▼理工大学 | 有機アミン塩発泡剤 |
| JP7036913B2 (ja) | 2017-10-19 | 2022-03-15 | 山▲東▼理工大学 | 有機アミン塩発泡剤 |
| JP2022536640A (ja) * | 2019-06-12 | 2022-08-18 | コベストロ・インテレクチュアル・プロパティ・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツング・アンド・コー・カーゲー | イソシアネート基末端ポリオキサゾリジノンを作製する方法 |
| JP7725372B2 (ja) | 2019-06-12 | 2025-08-19 | コベストロ、ドイチュラント、アクチエンゲゼルシャフト | イソシアネート基末端ポリオキサゾリジノンを作製する方法 |
Also Published As
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| WO2007040617A1 (en) | 2007-04-12 |
| KR20080058387A (ko) | 2008-06-25 |
| US7714030B2 (en) | 2010-05-11 |
| EP1924619B1 (en) | 2014-11-19 |
| KR101284934B1 (ko) | 2013-07-10 |
| CN101268110B (zh) | 2011-01-26 |
| CN101268110A (zh) | 2008-09-17 |
| EP1924619A1 (en) | 2008-05-28 |
| US20070059512A1 (en) | 2007-03-15 |
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