JP2007308696A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2007308696A5 JP2007308696A5 JP2007120630A JP2007120630A JP2007308696A5 JP 2007308696 A5 JP2007308696 A5 JP 2007308696A5 JP 2007120630 A JP2007120630 A JP 2007120630A JP 2007120630 A JP2007120630 A JP 2007120630A JP 2007308696 A5 JP2007308696 A5 JP 2007308696A5
- Authority
- JP
- Japan
- Prior art keywords
- ammonium
- pivalate
- potassium
- jimechirujia
- neodecanoate
- 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.)
- Granted
Links
- -1 Quaternary ammonium ions Chemical class 0.000 description 10
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 6
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 5
- 239000003054 catalyst Substances 0.000 description 4
- IUGYQRQAERSCNH-UHFFFAOYSA-N pivalic acid Chemical compound CC(C)(C)C(O)=O IUGYQRQAERSCNH-UHFFFAOYSA-N 0.000 description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- WFMNHCSATCWAAQ-UHFFFAOYSA-M potassium;2,2-dimethylpropanoate Chemical compound [K+].CC(C)(C)C([O-])=O WFMNHCSATCWAAQ-UHFFFAOYSA-M 0.000 description 3
- QEMXHQIAXOOASZ-UHFFFAOYSA-N tetramethylammonium Chemical compound C[N+](C)(C)C QEMXHQIAXOOASZ-UHFFFAOYSA-N 0.000 description 3
- VQLNWBFHYYUMGE-UHFFFAOYSA-M 2,2-dimethylpropanoate;tetramethylazanium Chemical compound C[N+](C)(C)C.CC(C)(C)C([O-])=O VQLNWBFHYYUMGE-UHFFFAOYSA-M 0.000 description 2
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
- KNWIDSLTUVLFSP-UHFFFAOYSA-N azanium;2,2-dimethylpropanoate Chemical compound [NH4+].CC(C)(C)C([O-])=O KNWIDSLTUVLFSP-UHFFFAOYSA-N 0.000 description 2
- 150000007942 carboxylates Chemical class 0.000 description 2
- 238000006386 neutralization reaction Methods 0.000 description 2
- SCVFZCLFOSHCOH-UHFFFAOYSA-M potassium acetate Chemical compound [K+].CC([O-])=O SCVFZCLFOSHCOH-UHFFFAOYSA-M 0.000 description 2
- 229910001414 potassium ion Inorganic materials 0.000 description 2
- QCVVTFGMXQFNJW-UHFFFAOYSA-M potassium;7,7-dimethyloctanoate Chemical compound [K+].CC(C)(C)CCCCCC([O-])=O QCVVTFGMXQFNJW-UHFFFAOYSA-M 0.000 description 2
- OSBSFAARYOCBHB-UHFFFAOYSA-N tetrapropylammonium Chemical compound CCC[N+](CCC)(CCC)CCC OSBSFAARYOCBHB-UHFFFAOYSA-N 0.000 description 2
- OXICUYPQJJOLTJ-UHFFFAOYSA-M 2,2-diethylbutanoate;tetrabutylazanium Chemical compound CCC(CC)(CC)C([O-])=O.CCCC[N+](CCCC)(CCCC)CCCC OXICUYPQJJOLTJ-UHFFFAOYSA-M 0.000 description 1
- BGQAXVATHIXCDS-UHFFFAOYSA-M 2,2-dimethylpropanoate;2-hydroxypropyl(trimethyl)azanium Chemical compound CC(C)(C)C([O-])=O.CC(O)C[N+](C)(C)C BGQAXVATHIXCDS-UHFFFAOYSA-M 0.000 description 1
- WMDLGLNAIPCRPO-UHFFFAOYSA-M 2,2-dimethylpropanoate;tetrabutylazanium Chemical compound CC(C)(C)C([O-])=O.CCCC[N+](CCCC)(CCCC)CCCC WMDLGLNAIPCRPO-UHFFFAOYSA-M 0.000 description 1
- DZBCYSCTDNOYGW-UHFFFAOYSA-M 2,2-dimethylpropanoate;tetraethylazanium Chemical compound CC(C)(C)C([O-])=O.CC[N+](CC)(CC)CC DZBCYSCTDNOYGW-UHFFFAOYSA-M 0.000 description 1
- OPRNESZUKSRODH-UHFFFAOYSA-M 2,2-dimethylpropanoate;triethyl(2-hydroxypropyl)azanium Chemical compound CC(C)(C)C([O-])=O.CC[N+](CC)(CC)CC(C)O OPRNESZUKSRODH-UHFFFAOYSA-M 0.000 description 1
- ZWRMFEQRSUWLKC-UHFFFAOYSA-N 2-hydroxyethyl(tripropyl)azanium Chemical compound CCC[N+](CCC)(CCC)CCO ZWRMFEQRSUWLKC-UHFFFAOYSA-N 0.000 description 1
- FKJCCFRFRZONNO-UHFFFAOYSA-N 2-hydroxypropyl 7,7-dimethyloctanoate Chemical compound CC(O)COC(=O)CCCCCC(C)(C)C FKJCCFRFRZONNO-UHFFFAOYSA-N 0.000 description 1
- YTLUDYJZQJMFKO-UHFFFAOYSA-M 2-hydroxypropyl(trimethyl)azanium;acetate Chemical compound CC([O-])=O.CC(O)C[N+](C)(C)C YTLUDYJZQJMFKO-UHFFFAOYSA-M 0.000 description 1
- WIEZPMIEWPJAOF-UHFFFAOYSA-N 2-hydroxypropyl(tripropyl)azanium Chemical compound CCC[N+](CCC)(CCC)CC(C)O WIEZPMIEWPJAOF-UHFFFAOYSA-N 0.000 description 1
- JPKKMFOXWKNEEN-UHFFFAOYSA-N 2-methylcholine Chemical compound CC(O)C[N+](C)(C)C JPKKMFOXWKNEEN-UHFFFAOYSA-N 0.000 description 1
- BBXMJUVLTRNHNL-UHFFFAOYSA-M 4,4-dimethylpentanoate 2-hydroxypropyl(trimethyl)azanium Chemical compound CC(O)C[N+](C)(C)C.CC(C)(C)CCC([O-])=O BBXMJUVLTRNHNL-UHFFFAOYSA-M 0.000 description 1
- DBSXLUUKLBPMOD-UHFFFAOYSA-M 4,4-dimethylpentanoate tetrabutylazanium Chemical compound CC(C)(C)CCC([O-])=O.CCCC[N+](CCCC)(CCCC)CCCC DBSXLUUKLBPMOD-UHFFFAOYSA-M 0.000 description 1
- XHXUDPQEOSCVMR-UHFFFAOYSA-M 4,4-dimethylpentanoate tetraethylazanium Chemical compound CC[N+](CC)(CC)CC.CC(C)(C)CCC([O-])=O XHXUDPQEOSCVMR-UHFFFAOYSA-M 0.000 description 1
- MAEVVHNWLDPOJU-UHFFFAOYSA-M 4,4-dimethylpentanoate tetrapropylazanium Chemical compound CC(C)(C)CCC([O-])=O.CCC[N+](CCC)(CCC)CCC MAEVVHNWLDPOJU-UHFFFAOYSA-M 0.000 description 1
- BULJKZVNYCGORB-UHFFFAOYSA-M 4,4-dimethylpentanoate triethyl(2-hydroxypropyl)azanium Chemical compound CC(C)(C)CCC([O-])=O.CC[N+](CC)(CC)CC(C)O BULJKZVNYCGORB-UHFFFAOYSA-M 0.000 description 1
- XKTMMFRRPGCHAB-UHFFFAOYSA-M 5,5-dimethylhexanoate 2-hydroxypropyl(trimethyl)azanium Chemical compound CC(O)C[N+](C)(C)C.CC(C)(C)CCCC([O-])=O XKTMMFRRPGCHAB-UHFFFAOYSA-M 0.000 description 1
- GIWNUIUAZASMPW-UHFFFAOYSA-M 5,5-dimethylhexanoate tetrabutylazanium Chemical compound CC(C)(C)CCCC([O-])=O.CCCC[N+](CCCC)(CCCC)CCCC GIWNUIUAZASMPW-UHFFFAOYSA-M 0.000 description 1
- BEMNPJSJBMDCMB-UHFFFAOYSA-M 5,5-dimethylhexanoate tetraethylazanium Chemical compound CC[N+](CC)(CC)CC.CC(C)(C)CCCC([O-])=O BEMNPJSJBMDCMB-UHFFFAOYSA-M 0.000 description 1
- TZJZZAIOYZDILR-UHFFFAOYSA-M 5,5-dimethylhexanoate tetrapropylazanium Chemical compound CC(C)(C)CCCC([O-])=O.CCC[N+](CCC)(CCC)CCC TZJZZAIOYZDILR-UHFFFAOYSA-M 0.000 description 1
- CEUZAIYZBKHMDP-UHFFFAOYSA-M 5,5-dimethylhexanoate triethyl(2-hydroxypropyl)azanium Chemical compound CC(C)(C)CCCC([O-])=O.CC[N+](CC)(CC)CC(C)O CEUZAIYZBKHMDP-UHFFFAOYSA-M 0.000 description 1
- YPIFGDQKSSMYHQ-UHFFFAOYSA-M 7,7-dimethyloctanoate Chemical compound CC(C)(C)CCCCCC([O-])=O YPIFGDQKSSMYHQ-UHFFFAOYSA-M 0.000 description 1
- YDMDCVPQHIJHGV-UHFFFAOYSA-M 7,7-dimethyloctanoate tetrabutylazanium Chemical compound CC(C)(C)CCCCCC([O-])=O.CCCC[N+](CCCC)(CCCC)CCCC YDMDCVPQHIJHGV-UHFFFAOYSA-M 0.000 description 1
- CBMMNVUMIHGVQG-UHFFFAOYSA-M 7,7-dimethyloctanoate tetraethylazanium Chemical compound CC[N+](CC)(CC)CC.CC(C)(C)CCCCCC([O-])=O CBMMNVUMIHGVQG-UHFFFAOYSA-M 0.000 description 1
- ZHRWWTRLAOBACK-UHFFFAOYSA-M 7,7-dimethyloctanoate tetrapropylazanium Chemical compound CC(C)(C)CCCCCC([O-])=O.CCC[N+](CCC)(CCC)CCC ZHRWWTRLAOBACK-UHFFFAOYSA-M 0.000 description 1
- OSXQNJYCHFJYPS-UHFFFAOYSA-M 7,7-dimethyloctanoate triethyl(2-hydroxypropyl)azanium Chemical compound CC[N+](CC)(CC)CC(C)O.CC(C)(C)CCCCCC([O-])=O OSXQNJYCHFJYPS-UHFFFAOYSA-M 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- NPYPAHLBTDXSSS-UHFFFAOYSA-N Potassium ion Chemical compound [K+] NPYPAHLBTDXSSS-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 235000019270 ammonium chloride Nutrition 0.000 description 1
- 239000000908 ammonium hydroxide Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- YDPYPPXSVLZBNR-UHFFFAOYSA-N benzyl-(2-hydroxypropyl)-dimethylazanium Chemical compound CC(O)C[N+](C)(C)CC1=CC=CC=C1 YDPYPPXSVLZBNR-UHFFFAOYSA-N 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- OEYIOHPDSNJKLS-UHFFFAOYSA-N choline Chemical compound C[N+](C)(C)CCO OEYIOHPDSNJKLS-UHFFFAOYSA-N 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- QHZOCFVYIBVNMJ-UHFFFAOYSA-M heptanoate;tetramethylazanium Chemical compound C[N+](C)(C)C.CCCCCCC([O-])=O QHZOCFVYIBVNMJ-UHFFFAOYSA-M 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- 229910001416 lithium ion Inorganic materials 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 235000011056 potassium acetate Nutrition 0.000 description 1
- STOWNEZDFATGDW-UHFFFAOYSA-M potassium;4,4-dimethylpentanoate Chemical compound [K+].CC(C)(C)CCC([O-])=O STOWNEZDFATGDW-UHFFFAOYSA-M 0.000 description 1
- GDSFVWFHSCZYGQ-UHFFFAOYSA-M potassium;5,5-dimethylhexanoate Chemical compound [K+].CC(C)(C)CCCC([O-])=O GDSFVWFHSCZYGQ-UHFFFAOYSA-M 0.000 description 1
- YOSXTSJZQNTKKX-UHFFFAOYSA-M potassium;heptanoate Chemical compound [K+].CCCCCCC([O-])=O YOSXTSJZQNTKKX-UHFFFAOYSA-M 0.000 description 1
- 229910001419 rubidium ion Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910001415 sodium ion Inorganic materials 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- DZLFLBLQUQXARW-UHFFFAOYSA-N tetrabutylammonium Chemical compound CCCC[N+](CCCC)(CCCC)CCCC DZLFLBLQUQXARW-UHFFFAOYSA-N 0.000 description 1
- CBXCPBUEXACCNR-UHFFFAOYSA-N tetraethylammonium Chemical compound CC[N+](CC)(CC)CC CBXCPBUEXACCNR-UHFFFAOYSA-N 0.000 description 1
- UCVGPWMKVFBRMN-UHFFFAOYSA-N tributyl(2-hydroxyethyl)azanium Chemical compound CCCC[N+](CCO)(CCCC)CCCC UCVGPWMKVFBRMN-UHFFFAOYSA-N 0.000 description 1
- PPOMHYHIAFOMRU-UHFFFAOYSA-N tributyl(2-hydroxypropyl)azanium Chemical compound CCCC[N+](CCCC)(CCCC)CC(C)O PPOMHYHIAFOMRU-UHFFFAOYSA-N 0.000 description 1
- ZSPDDMXDEWGOCE-UHFFFAOYSA-N triethyl(2-hydroxypropyl)azanium Chemical compound CC[N+](CC)(CC)CC(C)O ZSPDDMXDEWGOCE-UHFFFAOYSA-N 0.000 description 1
- GZBUMTPCIKCWFW-UHFFFAOYSA-N triethylcholine Chemical compound CC[N+](CC)(CC)CCO GZBUMTPCIKCWFW-UHFFFAOYSA-N 0.000 description 1
- 238000005292 vacuum distillation Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US11/418,287 US8530534B2 (en) | 2006-05-04 | 2006-05-04 | Trimerization catalysts from sterically hindered salts |
| US11/418,287 | 2006-05-04 |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2010226866A Division JP5722585B2 (ja) | 2006-05-04 | 2010-10-06 | 立体的に込み合った塩類からの新規な三量化触媒 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2007308696A JP2007308696A (ja) | 2007-11-29 |
| JP2007308696A5 true JP2007308696A5 (enExample) | 2010-11-25 |
| JP4898541B2 JP4898541B2 (ja) | 2012-03-14 |
Family
ID=38229993
Family Applications (3)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2007120630A Active JP4898541B2 (ja) | 2006-05-04 | 2007-05-01 | 立体的に込み合った塩類からの新規な三量化触媒 |
| JP2010226866A Active JP5722585B2 (ja) | 2006-05-04 | 2010-10-06 | 立体的に込み合った塩類からの新規な三量化触媒 |
| JP2014242975A Active JP6006283B2 (ja) | 2006-05-04 | 2014-12-01 | 立体的に込み合った塩類からの新規な三量化触媒 |
Family Applications After (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2010226866A Active JP5722585B2 (ja) | 2006-05-04 | 2010-10-06 | 立体的に込み合った塩類からの新規な三量化触媒 |
| JP2014242975A Active JP6006283B2 (ja) | 2006-05-04 | 2014-12-01 | 立体的に込み合った塩類からの新規な三量化触媒 |
Country Status (8)
| Country | Link |
|---|---|
| US (2) | US8530534B2 (enExample) |
| EP (1) | EP1852448B1 (enExample) |
| JP (3) | JP4898541B2 (enExample) |
| KR (2) | KR100909643B1 (enExample) |
| CN (1) | CN101067018B (enExample) |
| AT (1) | ATE522558T1 (enExample) |
| BR (1) | BRPI0702265B1 (enExample) |
| MX (1) | MX2007005295A (enExample) |
Families Citing this family (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8552077B2 (en) * | 2006-05-04 | 2013-10-08 | Air Products And Chemicals, Inc. | Trimer catalyst additives for improving foam processability |
| US8580864B2 (en) * | 2006-05-04 | 2013-11-12 | Air Products And Chemicals, Inc. | Trimer catalysts with improved processability and surface cure |
| EP2291425A1 (en) * | 2008-05-22 | 2011-03-09 | Dow Global Technologies Inc. | Thermoset polyurethanes comprising cis, trans-1, 3- and 1, 4-cyclohexanedimethylether groups |
| ES2437604T3 (es) * | 2008-11-10 | 2014-01-13 | Dow Global Technologies Llc | Un sistema catalítico de trimerización de isocianato, una formulación precursora, un procedimiento para trimerizar isocianatos, espumas rígidas de poliisocianurato/poliuretano hechas a partir de los mismos y un procedimiento para hacer dichas espumas |
| JP2012508301A (ja) * | 2008-11-10 | 2012-04-05 | ダウ グローバル テクノロジーズ エルエルシー | イソシアネート三量化触媒系、前駆体配合物、イソシアネートを三量化する方法、それより作製された硬質ポリイソシアヌレート／ポリウレタンフォーム（発泡体）、及びそのようなフォームを作製する方法 |
| ES2436013T3 (es) * | 2008-11-10 | 2013-12-26 | Dow Global Technologies Llc | Sistema catalítico de trimerización de isocianato, una formulación precursora, un procedimiento para trimerizar isocianatos, espumas rígidas de poliisocianurato/poliuretano hechas a partir de los mismos y un procedimiento para hacer dichas espumas |
| KR101064208B1 (ko) * | 2009-02-11 | 2011-09-14 | 주식회사 세호테크 | 무주석, 무독성 유기금속촉매 및 그 제조방법 |
| WO2013024107A1 (de) * | 2011-08-16 | 2013-02-21 | Bayer Intellectual Property Gmbh | Verfahren zur herstellung eines polyurethan-polyisocyanurat-hartschaums |
| PL3110546T3 (pl) | 2014-02-26 | 2022-07-11 | Evonik Operations Gmbh | Sposób wytwarzania pianki poliizocyjanuranowej/poliuretanowej |
| KR102199218B1 (ko) * | 2014-09-05 | 2021-01-07 | 삼성디스플레이 주식회사 | 표시 장치, 표시 제어 장치 및 표시 방법 |
| JP2016124912A (ja) * | 2014-12-26 | 2016-07-11 | 三洋化成工業株式会社 | 樹脂製造用活性水素含有組成物およびフォームの製造方法 |
| CN104558468B (zh) * | 2014-12-31 | 2018-02-23 | 江苏奥斯佳材料科技有限公司 | 一种聚氨酯催化剂在合成硬质聚氨酯材料中的应用 |
| CN104558467B (zh) * | 2014-12-31 | 2018-02-23 | 江苏奥斯佳材料科技有限公司 | 一种聚氨酯催化剂及其应用 |
| CN104558469B (zh) * | 2014-12-31 | 2018-02-23 | 江苏奥斯佳材料科技有限公司 | 一种聚氨酯催化剂在合成软质聚氨酯泡沫塑料中的应用 |
| US10889681B2 (en) | 2014-12-31 | 2021-01-12 | Jiangsu Osic Performance Materials Co. Ltd. | Polyurethane catalyst and application thereof |
| ES2854355T3 (es) * | 2015-06-18 | 2021-09-21 | Evonik Operations Gmbh | Catalizadores de trimerización de sales estéricamente impedidas y aminas terciarias que tienen grupos reactivos con isocianatos |
| US11370875B2 (en) * | 2016-12-08 | 2022-06-28 | Sekisui Chemical Co., Ltd. | Urethane resin composition |
| EP3609925A4 (en) | 2017-04-14 | 2021-01-06 | Videojet Technologies Inc. | FAST DRY COMPOSITION FOR CONTINUOUS INKJET APPLICATIONS |
| CN107913730B (zh) * | 2017-11-30 | 2020-04-10 | 万华化学集团股份有限公司 | 亚胺型季铵盐催化剂、其制备方法及多异氰酸酯组合物 |
| AU2019323594A1 (en) * | 2018-08-21 | 2021-02-11 | Huntsman International Llc | Catalyst for PIR/PUR foam production |
| CN114040934A (zh) * | 2019-07-08 | 2022-02-11 | 科思创知识产权两合公司 | 具有延长的适用期的用于生产聚异氰脲酸酯基塑料的可聚合组合物 |
| CN110560159B (zh) * | 2019-08-13 | 2020-10-20 | 清华大学 | 一种用于叔碳酸缩水甘油酯制备的催化剂及其制备方法 |
| US12258435B1 (en) | 2024-02-06 | 2025-03-25 | Patcham Usa Llc | Method for preparing low density polyurethanes using catalysts that are free from tertiary amines and tin |
Family Cites Families (42)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3686225A (en) * | 1969-04-01 | 1972-08-22 | Du Pont | Complexes of polyether compounds and ionic compounds |
| GB1258357A (enExample) | 1970-04-23 | 1971-12-30 | ||
| US3940517A (en) | 1973-01-11 | 1976-02-24 | The Celotex Corporation | Polyisocyanurate foam, catalyst composition and process for producing such |
| US3993652A (en) | 1973-07-09 | 1976-11-23 | Air Products And Chemicals, Inc. | Cyclic quaternary hydroxyalkyl phenoxide catalysts for isocyanate reactions |
| US3892687A (en) | 1973-07-09 | 1975-07-01 | Air Prod & Chem | Quaternary hydroxyalkyl tertiary amine bases as poluyrethane catalysts |
| US3988267A (en) | 1973-07-09 | 1976-10-26 | Air Products And Chemicals, Inc. | Quaternary hydroxyalkyl tertiary amine bases as polyurethane catalysts |
| US4003859A (en) * | 1974-01-30 | 1977-01-18 | The Upjohn Company | Novel process for trimerizing polyisocyanates |
| US3954684A (en) | 1974-07-09 | 1976-05-04 | The Upjohn Company | Foam process using tertiary amine/quaternary ammonium salt catalyst |
| US3989651A (en) | 1974-07-09 | 1976-11-02 | The Upjohn Company | Catalyst for sprayable polyisocyanurate foam composition |
| US4026840A (en) | 1975-06-09 | 1977-05-31 | Air Products And Chemicals, Inc. | Hydroxyalkyl tertiary amine catalysts for isocyanate reactions |
| US4148980A (en) | 1977-05-03 | 1979-04-10 | Basf Wyandotte Corporation | Novel carboxylate catalysts for the preparation of foams characterized by polyisocyanurate, polyurethane and poly (urethane-isocyanurate) linkages |
| DE2916201A1 (de) | 1979-04-21 | 1980-10-30 | Huels Chemische Werke Ag | Verfahren zur trimerisierung von diisocyanaten |
| US4393148A (en) | 1982-09-30 | 1983-07-12 | Pennwalt Corporation | Reaction of t-alkylhydrazinium salts and ogranic peroxides to foam unsaturated polyester resins |
| US4460714A (en) | 1983-12-01 | 1984-07-17 | Pennwalt Corporation | Unsaturated polyester resin foams using inorganic iron salts |
| US4489177A (en) * | 1983-12-29 | 1984-12-18 | Olin Corporation | Isocyanate-reactive compounds from TDI distillation residue and polyurethanes prepared therefrom |
| DE3403277A1 (de) * | 1984-01-31 | 1985-08-01 | Bayer Ag, 5090 Leverkusen | Verfahren zur herstellung von polyisocyanaten mit biuretstruktur |
| US4503226A (en) | 1984-04-30 | 1985-03-05 | Olin Corporation | Process for trimerizing organic polyisocyanates |
| US4623673A (en) * | 1985-10-24 | 1986-11-18 | The Dow Chemical Company | Urethane-modified polyisocyanurate rigid foam |
| US4698398A (en) | 1985-11-14 | 1987-10-06 | E. I. Du Pont De Nemours And Company | Coating composition of a hydroxy functional epoxy polyester graft copolymer |
| GB8531180D0 (en) | 1985-12-18 | 1986-01-29 | Ici Plc | Cocatalyst systems |
| GB8712363D0 (en) | 1987-05-26 | 1987-07-01 | Ici Plc | Polyisocyanurate rigid foams |
| US5321050A (en) | 1992-08-06 | 1994-06-14 | Nisshinbo Industries, Inc. | Method for producing modified polyisocyanurate foams |
| US5296516A (en) * | 1992-12-09 | 1994-03-22 | Basf Corporation | Polyurethane and polyisocyanurate rigid foams prepared using ternary blowing agent mixtures |
| JPH06200069A (ja) | 1993-01-05 | 1994-07-19 | Mitsui Toatsu Chem Inc | 硬質ポリウレタンフォーム |
| JPH0797429A (ja) | 1993-08-06 | 1995-04-11 | Takeda Chem Ind Ltd | 新規なポリオール組成物及びそれを用いる硬質ポリウレタンフオームの製造方法 |
| US5691440A (en) * | 1995-10-05 | 1997-11-25 | Arco Chemical Technonogy, L.P. | Catalyst and process for producing isocyanate trimers |
| JPH10139697A (ja) | 1996-09-09 | 1998-05-26 | Asahi Glass Co Ltd | 含フッ素炭化水素系組成物 |
| DE19813107A1 (de) * | 1998-03-25 | 1999-09-30 | Basf Ag | Verfahren zur Herstellung von Polyurethanschaumstoffen |
| US5902835A (en) | 1998-05-28 | 1999-05-11 | Air Products And Chemicals, Inc. | Group IVB metal blowing catalyst compositions for the production of polyurethane foams |
| JP2000063475A (ja) * | 1998-08-26 | 2000-02-29 | Mitsui Chemicals Inc | 硬質ポリウレタンフォーム |
| JP2002080552A (ja) * | 2000-09-06 | 2002-03-19 | Canon Chemicals Inc | イソシアネート組成物、ウレタンゴム組成物の製造方法、クリーニングブレード |
| DE10142296C1 (de) | 2001-08-29 | 2003-02-13 | Bayer Ag | Polyurethanelastomere, Verfahren zu ihrer Herstellung und ihre Verwendung |
| JP3953353B2 (ja) * | 2002-04-11 | 2007-08-08 | アキレス株式会社 | 硬質ポリウレタンフォームの製造方法 |
| ES2282640T3 (es) | 2002-05-27 | 2007-10-16 | Huntsman International Llc | Polimeros supramoleculares espumados. |
| EP1375546A1 (en) | 2002-06-21 | 2004-01-02 | Crompton GmbH | Low emission tin catalysts |
| US6846850B2 (en) * | 2003-01-22 | 2005-01-25 | Bayer Materialscience Llc | Rigid polyurethane foams with improved properties |
| US6825238B2 (en) * | 2003-01-29 | 2004-11-30 | Air Products And Chemicals, Inc. | Low acid organometallic catalyst for the production of flexible, semi-flexible and rigid polyurethane foams |
| JP4104539B2 (ja) * | 2003-04-22 | 2008-06-18 | 花王株式会社 | ポリイソシアヌレートフォームの製造法 |
| JP2005307143A (ja) * | 2003-06-30 | 2005-11-04 | Bridgestone Corp | 硬質ポリウレタンフォーム |
| DE102004009740A1 (de) | 2004-02-25 | 2005-09-15 | Basf Ag | Zinn- und Übergangsmetallfreie Polyurethanschaumstoffe |
| US8729146B2 (en) * | 2005-06-14 | 2014-05-20 | Momentive Performance Materials Inc. | Catalyst composition and process using same |
| US8552077B2 (en) * | 2006-05-04 | 2013-10-08 | Air Products And Chemicals, Inc. | Trimer catalyst additives for improving foam processability |
-
2006
- 2006-05-04 US US11/418,287 patent/US8530534B2/en active Active
-
2007
- 2007-04-27 AT AT07008702T patent/ATE522558T1/de not_active IP Right Cessation
- 2007-04-27 EP EP07008702A patent/EP1852448B1/en active Active
- 2007-05-01 JP JP2007120630A patent/JP4898541B2/ja active Active
- 2007-05-02 MX MX2007005295A patent/MX2007005295A/es active IP Right Grant
- 2007-05-03 BR BRPI0702265A patent/BRPI0702265B1/pt active IP Right Grant
- 2007-05-04 KR KR1020070043581A patent/KR100909643B1/ko active Active
- 2007-05-08 CN CN2007101024145A patent/CN101067018B/zh active Active
-
2008
- 2008-12-31 KR KR1020080138665A patent/KR20090026242A/ko not_active Withdrawn
-
2010
- 2010-10-06 JP JP2010226866A patent/JP5722585B2/ja active Active
-
2013
- 2013-08-28 US US14/012,155 patent/US9890236B2/en active Active
-
2014
- 2014-12-01 JP JP2014242975A patent/JP6006283B2/ja active Active
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2007308696A5 (enExample) | ||
| JP2013501100A5 (enExample) | ||
| CO6310992A2 (es) | Metodo para preparar chalconas de 3-trifluorometilo | |
| EA201790306A1 (ru) | 2-(морфолин-4-ил)-1,7-нафтиридины | |
| EP2631253A3 (en) | Preparation of polymer, resulting polymer, resist composition, and patterning process | |
| JP2019511923A5 (enExample) | ||
| JP2016510019A5 (enExample) | ||
| CA2862755A1 (en) | Antiviral compounds with a dibenzooxaheterocycle moiety | |
| JP2014507477A5 (enExample) | ||
| JP2016536324A5 (enExample) | ||
| NZ609191A (en) | Methods of making l-ornithine phenyl acetate | |
| JP2016534199A5 (enExample) | ||
| JP2013542261A5 (enExample) | ||
| JP2011105732A5 (enExample) | ||
| BR112016010080A8 (pt) | compostos de pirazolopirimidina, composição farmacêutica e seu uso | |
| MY167395A (en) | Method for producing glufosinate p free acid | |
| RU2011139325A (ru) | Аморфная соль макроциклического ингибитора hcv | |
| JP2015531613A5 (enExample) | ||
| JP2016520038A5 (enExample) | ||
| JP2014515432A5 (enExample) | ||
| JP2014520901A5 (enExample) | ||
| RU2015112009A (ru) | Бактерицидные композиции | |
| JP2013517320A5 (enExample) | ||
| WO2010100470A3 (en) | Biocidal compositions comprising a phosphonium salt and a polymeric quaternary ammonium compound | |
| RU2015102160A (ru) | Твердая детергентная композиция |