JP2017509738A5 - - Google Patents
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- JP2017509738A5 JP2017509738A5 JP2016549432A JP2016549432A JP2017509738A5 JP 2017509738 A5 JP2017509738 A5 JP 2017509738A5 JP 2016549432 A JP2016549432 A JP 2016549432A JP 2016549432 A JP2016549432 A JP 2016549432A JP 2017509738 A5 JP2017509738 A5 JP 2017509738A5
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- JP
- Japan
- Prior art keywords
- component
- polyol
- mol
- polyester polyol
- mass
- 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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- 229920005862 polyol Polymers 0.000 claims description 48
- 150000003077 polyols Chemical class 0.000 claims description 47
- WOZVHXUHUFLZGK-UHFFFAOYSA-N dimethyl terephthalate Chemical compound COC(=O)C1=CC=C(C(=O)OC)C=C1 WOZVHXUHUFLZGK-UHFFFAOYSA-N 0.000 claims description 42
- 229920005906 polyester polyol Polymers 0.000 claims description 41
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 claims description 40
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 claims description 18
- 238000000034 method Methods 0.000 claims description 18
- 229920000139 polyethylene terephthalate Polymers 0.000 claims description 18
- 239000005020 polyethylene terephthalate Substances 0.000 claims description 18
- 239000004604 Blowing Agent Substances 0.000 claims description 14
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical class CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 claims description 14
- LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 claims description 14
- 239000004721 Polyphenylene oxide Substances 0.000 claims description 14
- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 claims description 14
- 239000000203 mixture Substances 0.000 claims description 14
- 229920000570 polyether Polymers 0.000 claims description 14
- -1 polyethylene terephthalate Polymers 0.000 claims description 14
- 239000004088 foaming agent Substances 0.000 claims description 13
- 150000001875 compounds Chemical class 0.000 claims description 12
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 claims description 12
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 claims description 12
- 239000003063 flame retardant Substances 0.000 claims description 10
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 claims description 9
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 claims description 9
- 239000003054 catalyst Substances 0.000 claims description 9
- 239000002666 chemical blowing agent Substances 0.000 claims description 9
- 235000019253 formic acid Nutrition 0.000 claims description 9
- 239000006260 foam Substances 0.000 claims description 7
- 229920000582 polyisocyanurate Polymers 0.000 claims description 7
- 239000011495 polyisocyanurate Substances 0.000 claims description 7
- 125000003118 aryl group Chemical group 0.000 claims description 6
- HQVFCQRVQFYGRJ-UHFFFAOYSA-N formic acid;hydrate Chemical compound O.OC=O HQVFCQRVQFYGRJ-UHFFFAOYSA-N 0.000 claims description 6
- 229920005830 Polyurethane Foam Polymers 0.000 claims description 5
- 125000001931 aliphatic group Chemical group 0.000 claims description 5
- 229940053200 antiepileptics fatty acid derivative Drugs 0.000 claims description 5
- 125000004432 carbon atom Chemical group C* 0.000 claims description 5
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 5
- 150000002009 diols Chemical class 0.000 claims description 5
- 229930195729 fatty acid Natural products 0.000 claims description 5
- 239000000194 fatty acid Substances 0.000 claims description 5
- 150000004665 fatty acids Chemical class 0.000 claims description 5
- 239000011496 polyurethane foam Substances 0.000 claims description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 5
- 230000032050 esterification Effects 0.000 claims description 4
- 238000005886 esterification reaction Methods 0.000 claims description 4
- 229920002635 polyurethane Polymers 0.000 claims description 4
- 239000004814 polyurethane Substances 0.000 claims description 4
- 238000006243 chemical reaction Methods 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 229920000728 polyester Polymers 0.000 claims description 3
- 239000002671 adjuvant Substances 0.000 claims description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims 2
- 125000005442 diisocyanate group Chemical group 0.000 claims 2
- 238000007046 ethoxylation reaction Methods 0.000 claims 2
- 229920001228 polyisocyanate Polymers 0.000 claims 2
- 239000005056 polyisocyanate Substances 0.000 claims 2
- VOZKAJLKRJDJLL-UHFFFAOYSA-N tolylenediamine group Chemical group CC1=C(C=C(C=C1)N)N VOZKAJLKRJDJLL-UHFFFAOYSA-N 0.000 claims 2
- GTRSAMFYSUBAGN-UHFFFAOYSA-N tris(2-chloropropyl) phosphate Chemical compound CC(Cl)COP(=O)(OCC(C)Cl)OCC(C)Cl GTRSAMFYSUBAGN-UHFFFAOYSA-N 0.000 claims 2
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 claims 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 claims 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 claims 1
- 239000004970 Chain extender Substances 0.000 claims 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 claims 1
- 239000005642 Oleic acid Substances 0.000 claims 1
- 239000002202 Polyethylene glycol Substances 0.000 claims 1
- 235000019484 Rapeseed oil Nutrition 0.000 claims 1
- 125000003277 amino group Chemical group 0.000 claims 1
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 claims 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 claims 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 claims 1
- 235000021313 oleic acid Nutrition 0.000 claims 1
- 229920001223 polyethylene glycol Polymers 0.000 claims 1
- 235000012424 soybean oil Nutrition 0.000 claims 1
- 239000003549 soybean oil Substances 0.000 claims 1
- 239000003760 tallow Substances 0.000 claims 1
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- QWTDNUCVQCZILF-UHFFFAOYSA-N isopentane Chemical compound CCC(C)C QWTDNUCVQCZILF-UHFFFAOYSA-N 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- 238000009835 boiling Methods 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- RGSFGYAAUTVSQA-UHFFFAOYSA-N Cyclopentane Chemical compound C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 description 2
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 2
- XPDWGBQVDMORPB-UHFFFAOYSA-N Fluoroform Chemical compound FC(F)F XPDWGBQVDMORPB-UHFFFAOYSA-N 0.000 description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical compound C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- 239000001569 carbon dioxide Substances 0.000 description 2
- 229910002092 carbon dioxide Inorganic materials 0.000 description 2
- RWRIWBAIICGTTQ-UHFFFAOYSA-N difluoromethane Chemical compound FCF RWRIWBAIICGTTQ-UHFFFAOYSA-N 0.000 description 2
- AFABGHUZZDYHJO-UHFFFAOYSA-N dimethyl butane Natural products CCCC(C)C AFABGHUZZDYHJO-UHFFFAOYSA-N 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- NNPPMTNAJDCUHE-UHFFFAOYSA-N isobutane Chemical compound CC(C)C NNPPMTNAJDCUHE-UHFFFAOYSA-N 0.000 description 2
- 239000012948 isocyanate Substances 0.000 description 2
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 2
- 150000002513 isocyanates Chemical class 0.000 description 2
- TZIHFWKZFHZASV-UHFFFAOYSA-N methyl formate Chemical compound COC=O TZIHFWKZFHZASV-UHFFFAOYSA-N 0.000 description 2
- 229920001707 polybutylene terephthalate Polymers 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 238000005809 transesterification reaction Methods 0.000 description 2
- LVGUZGTVOIAKKC-UHFFFAOYSA-N 1,1,1,2-tetrafluoroethane Chemical compound FCC(F)(F)F LVGUZGTVOIAKKC-UHFFFAOYSA-N 0.000 description 1
- FRCHKSNAZZFGCA-UHFFFAOYSA-N 1,1-dichloro-1-fluoroethane Chemical compound CC(F)(Cl)Cl FRCHKSNAZZFGCA-UHFFFAOYSA-N 0.000 description 1
- NPNPZTNLOVBDOC-UHFFFAOYSA-N 1,1-difluoroethane Chemical compound CC(F)F NPNPZTNLOVBDOC-UHFFFAOYSA-N 0.000 description 1
- ATEBGNALLCMSGS-UHFFFAOYSA-N 2-chloro-1,1-difluoroethane Chemical compound FC(F)CCl ATEBGNALLCMSGS-UHFFFAOYSA-N 0.000 description 1
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- LOMVENUNSWAXEN-UHFFFAOYSA-N Methyl oxalate Chemical compound COC(=O)C(=O)OC LOMVENUNSWAXEN-UHFFFAOYSA-N 0.000 description 1
- 235000011054 acetic acid Nutrition 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 150000001335 aliphatic alkanes Chemical class 0.000 description 1
- 125000005599 alkyl carboxylate group Chemical group 0.000 description 1
- 229910002091 carbon monoxide Inorganic materials 0.000 description 1
- 238000003763 carbonization Methods 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 150000001924 cycloalkanes Chemical class 0.000 description 1
- UMNKXPULIDJLSU-UHFFFAOYSA-N dichlorofluoromethane Chemical compound FC(Cl)Cl UMNKXPULIDJLSU-UHFFFAOYSA-N 0.000 description 1
- 229940099364 dichlorofluoromethane Drugs 0.000 description 1
- 150000005690 diesters Chemical class 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- UHCBBWUQDAVSMS-UHFFFAOYSA-N fluoroethane Chemical compound CCF UHCBBWUQDAVSMS-UHFFFAOYSA-N 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- UKACHOXRXFQJFN-UHFFFAOYSA-N heptafluoropropane Chemical compound FC(F)C(F)(F)C(F)(F)F UKACHOXRXFQJFN-UHFFFAOYSA-N 0.000 description 1
- DMEGYFMYUHOHGS-UHFFFAOYSA-N heptamethylene Natural products C1CCCCCC1 DMEGYFMYUHOHGS-UHFFFAOYSA-N 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001282 iso-butane Substances 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 description 1
- 229920005903 polyol mixture Polymers 0.000 description 1
- 239000001294 propane 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
- 239000007858 starting material Substances 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP14154645 | 2014-02-11 | ||
| EP14154645.7 | 2014-02-11 | ||
| PCT/EP2015/051569 WO2015121057A1 (de) | 2014-02-11 | 2015-01-27 | Verfahren zur herstellung von polyurethan-hartschäumen und polyisocyanurat-hartschäumen |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2017509738A JP2017509738A (ja) | 2017-04-06 |
| JP2017509738A5 true JP2017509738A5 (https=) | 2018-03-08 |
Family
ID=50071499
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2016549432A Pending JP2017509738A (ja) | 2014-02-11 | 2015-01-27 | ポリウレタン硬質フォーム及びポリイソシアヌレート硬質フォームの製造方法 |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US10259906B2 (https=) |
| EP (1) | EP3105274B1 (https=) |
| JP (1) | JP2017509738A (https=) |
| KR (1) | KR102338624B1 (https=) |
| CN (1) | CN105980438A (https=) |
| BR (1) | BR112016017431A8 (https=) |
| CA (1) | CA2938060A1 (https=) |
| ES (1) | ES2673860T3 (https=) |
| MX (1) | MX367477B (https=) |
| PL (1) | PL3105274T3 (https=) |
| RU (1) | RU2016136382A (https=) |
| WO (1) | WO2015121057A1 (https=) |
Families Citing this family (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US11114719B2 (en) | 2018-02-16 | 2021-09-07 | H.B. Fuller Company | Electric cell potting compound and method of making |
| BR112020020776B1 (pt) | 2018-04-10 | 2024-02-06 | Stepan Company | Mistura, espuma de pu ou pu-pir rígida e placa de isolamento para uma aplicação em telhado ou parede |
| KR102867102B1 (ko) * | 2018-08-16 | 2025-10-01 | 바스프 에스이 | 환경 친화적으로 유도된 폴리우레탄 분무 폼 시스템 |
| WO2020089439A1 (en) * | 2018-11-02 | 2020-05-07 | Covestro Deutschland Ag | A rigid polyurethane precast panel |
| CN111138618A (zh) * | 2018-11-02 | 2020-05-12 | 科思创德国股份有限公司 | 聚氨酯硬质预制板 |
| CA3201872A1 (en) * | 2020-12-10 | 2022-06-16 | Jian Feng XU | Polyetherester polyol and use thereof for producing polyurethane rigid foam materials |
| CN114213797A (zh) * | 2022-01-11 | 2022-03-22 | 陈小云 | 一种耐磨防刮smc模塑料及其制备方法 |
| CA3251176A1 (en) | 2022-04-04 | 2023-10-12 | Basf Se | A METHOD FOR RETURNING TO THE VALUE CHAIN TO RECOVERY OF PHOSPHORO ACID ESTER-BASED FLAME REFRIGERANTS FROM RIGID POLYURETHANE FOAM |
| EP4612224A1 (en) | 2022-11-03 | 2025-09-10 | Basf Se | Value chain return process for the recovery of not bonded additives by extraction from polyurethane or polyisocyanurate rigid foams and depolymerization of the polyurethane rigid foams |
| CN120153019A (zh) | 2022-11-03 | 2025-06-13 | 巴斯夫欧洲公司 | 用于从废聚氨酯和聚异氰脲酸酯硬质泡沫的解聚中回收聚合亚甲基亚苯基胺（pMDA）作为其HCl盐的价值链返回方法 |
| CN121487992A (zh) | 2023-07-14 | 2026-02-06 | 巴斯夫欧洲公司 | 具有接枝多元醇内容物的pu-软泡沫的回收利用 |
| CN121487991A (zh) | 2023-07-14 | 2026-02-06 | 巴斯夫欧洲公司 | 用于回收利用聚氨酯泡沫的方法 |
| KR20260040032A (ko) | 2023-07-14 | 2026-03-23 | 바스프 에스이 | 하나 이상의 폼 조각을 포함하는 폼 혼합물로부터 타겟 폼 조각을 선택하기 위한 방법, 재활용 공정의 반응기에 공급하기 위해 폼 혼합물을 전처리하기 위한 방법 및 전처리 장치, 및 각각의 컴퓨터 프로그램 |
| CN121843800A (zh) | 2023-07-14 | 2026-04-10 | 巴斯夫欧洲公司 | 用于对来自废物流的聚氨酯物体进行分类的方法和系统 |
| WO2025016920A1 (en) | 2023-07-14 | 2025-01-23 | Basf Se | Process for autocatalytic hydroglycolytic or hydrolytic cleavage of waste streams containing polyurethane |
| EP4491364A1 (en) | 2023-07-14 | 2025-01-15 | Basf Se | Method and pre-processing arrangement for pre-processing a foam mix for feeding a reactor |
| WO2025016900A1 (en) | 2023-07-14 | 2025-01-23 | Basf Se | Process for recycling polyurethane waste through remonomerization by hydro ammonolysis |
| CN121666421A (zh) | 2023-07-14 | 2026-03-13 | 巴斯夫欧洲公司 | 通过水解和再缩合从基于聚酯醇的聚氨酯中回收聚酯醇 |
| WO2025016861A1 (en) | 2023-07-14 | 2025-01-23 | Basf Se | Method and pre-processing arrangement for pre-processing a foam mix for feeding a reactor of a recycling process for recovering raw materials and respective computer program |
| WO2025190719A1 (en) | 2024-03-13 | 2025-09-18 | Basf Se | Method for selecting and pre-processing target foam elements from a vehicle scrap material |
| WO2025190721A1 (en) | 2024-03-13 | 2025-09-18 | Basf Se | Method for recycling a polymer material from a vehicle scrap material |
| WO2025190718A1 (en) | 2024-03-13 | 2025-09-18 | Basf Se | Method for selecting target foam pieces from a vehicle scrap material |
| WO2025262151A2 (en) | 2024-06-19 | 2025-12-26 | Basf Se | Process for recycling polyurethane waste through remonomerization by hydroaminolysis |
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| DE1003714B (de) | 1956-01-25 | 1957-03-07 | Glanzstoff Ag | Verfahren zum Abbau von Polyaethylenterephthalat zu Terephthalsaeuredimethylester |
| US4529744A (en) * | 1982-10-25 | 1985-07-16 | Stepan Company | Compatibilized aromatic polyester polyols |
| US5051528A (en) | 1990-04-24 | 1991-09-24 | Eastman Kodak Company | Recovery process for ethylene glycol and dimethylterephthalate |
| US6461536B2 (en) * | 1998-02-09 | 2002-10-08 | Basf Corporation | Stable polyester polyol composition |
| WO2006100756A1 (ja) | 2005-03-22 | 2006-09-28 | Kawasaki Kasei Chemicals Ltd. | ポリエステルポリオールの製造方法 |
| KR101398244B1 (ko) * | 2005-11-14 | 2014-05-22 | 다우 글로벌 테크놀로지스 엘엘씨 | 향상된 열 전도성을 갖는 강성 폴리우레탄 발포체의 성형방법 |
| SI2340269T1 (sl) | 2008-10-15 | 2013-01-31 | Basf Se | Poliesterski polioli na bazi terefthalične kisline |
| SG190728A1 (en) * | 2010-12-02 | 2013-07-31 | Basf Se | Polyester polyols based on aromatic dicarboxylic acids |
| US20120214891A1 (en) * | 2011-02-23 | 2012-08-23 | Basf Se | Polyester polyols based on aromatic dicarboxylic acids |
| KR101903816B1 (ko) * | 2011-03-22 | 2018-10-02 | 바스프 에스이 | 낮은 열 전도율 및 우수한 열 안정성을 갖는 pu 경질 폼 |
| EP2800769B1 (de) * | 2012-01-02 | 2015-12-09 | Basf Se | Verfahren zur herstellung von polyurethan-hartschäumen und polyisocyanurat-hartschäumen |
| US20130251975A1 (en) * | 2012-03-23 | 2013-09-26 | Basf Se | Producing rigid polyurethane foams and rigid polyisocyanurate foams |
-
2015
- 2015-01-27 EP EP15702428.2A patent/EP3105274B1/de active Active
- 2015-01-27 BR BR112016017431A patent/BR112016017431A8/pt not_active Application Discontinuation
- 2015-01-27 US US15/117,960 patent/US10259906B2/en not_active Expired - Fee Related
- 2015-01-27 KR KR1020167024871A patent/KR102338624B1/ko active Active
- 2015-01-27 PL PL15702428T patent/PL3105274T3/pl unknown
- 2015-01-27 CN CN201580007973.0A patent/CN105980438A/zh active Pending
- 2015-01-27 JP JP2016549432A patent/JP2017509738A/ja active Pending
- 2015-01-27 CA CA2938060A patent/CA2938060A1/en not_active Abandoned
- 2015-01-27 WO PCT/EP2015/051569 patent/WO2015121057A1/de not_active Ceased
- 2015-01-27 RU RU2016136382A patent/RU2016136382A/ru not_active Application Discontinuation
- 2015-01-27 ES ES15702428.2T patent/ES2673860T3/es active Active
- 2015-01-27 MX MX2016009946A patent/MX367477B/es active IP Right Grant
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