ES2122703T3 - Poli(eter glicoles) y alcoholes obtenidos a partir de 3,4-epoxi-1-buteno, tetrahidrofurano y un iniciador. - Google Patents
Poli(eter glicoles) y alcoholes obtenidos a partir de 3,4-epoxi-1-buteno, tetrahidrofurano y un iniciador.Info
- Publication number
- ES2122703T3 ES2122703T3 ES95941421T ES95941421T ES2122703T3 ES 2122703 T3 ES2122703 T3 ES 2122703T3 ES 95941421 T ES95941421 T ES 95941421T ES 95941421 T ES95941421 T ES 95941421T ES 2122703 T3 ES2122703 T3 ES 2122703T3
- Authority
- ES
- Spain
- Prior art keywords
- sub
- waste
- tetrahydrofuran
- epoxy
- butene
- 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.)
- Expired - Lifetime
Links
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 title abstract 4
- GXBYFVGCMPJVJX-UHFFFAOYSA-N Epoxybutene Chemical compound C=CC1CO1 GXBYFVGCMPJVJX-UHFFFAOYSA-N 0.000 title abstract 2
- 239000003999 initiator Substances 0.000 title abstract 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 title abstract 2
- -1 POLY (ETHER GLYCOLS Chemical class 0.000 title 1
- 150000001298 alcohols Chemical class 0.000 title 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 title 1
- 239000002699 waste material Substances 0.000 abstract 5
- 150000001875 compounds Chemical class 0.000 abstract 3
- 239000003377 acid catalyst Substances 0.000 abstract 1
- 230000000269 nucleophilic effect Effects 0.000 abstract 1
- 238000006116 polymerization reaction Methods 0.000 abstract 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
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/04—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers only
- C08G65/06—Cyclic ethers having no atoms other than carbon and hydrogen outside the ring
- C08G65/14—Unsaturated oxiranes
-
- 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
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/04—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers only
- C08G65/06—Cyclic ethers having no atoms other than carbon and hydrogen outside the ring
- C08G65/16—Cyclic ethers having four or more ring atoms
- C08G65/20—Tetrahydrofuran
-
- 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
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/32—Polymers modified by chemical after-treatment
- C08G65/321—Polymers modified by chemical after-treatment with inorganic compounds
- C08G65/322—Polymers modified by chemical after-treatment with inorganic compounds containing hydrogen
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Polyethers (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US08/344,905 US5502137A (en) | 1994-11-25 | 1994-11-25 | Polyether glycols and alcohols derived from 3,4-epoxy-1-butene, tetrahydrofuran and an initiator |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2122703T3 true ES2122703T3 (es) | 1998-12-16 |
Family
ID=23352598
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES95941421T Expired - Lifetime ES2122703T3 (es) | 1994-11-25 | 1995-11-13 | Poli(eter glicoles) y alcoholes obtenidos a partir de 3,4-epoxi-1-buteno, tetrahidrofurano y un iniciador. |
Country Status (10)
| Country | Link |
|---|---|
| US (2) | US5502137A (enExample) |
| EP (1) | EP0793682B1 (enExample) |
| JP (1) | JPH10510315A (enExample) |
| CN (1) | CN1166842A (enExample) |
| CA (1) | CA2205813A1 (enExample) |
| DE (1) | DE69505270T2 (enExample) |
| ES (1) | ES2122703T3 (enExample) |
| MY (1) | MY132065A (enExample) |
| TW (1) | TW311917B (enExample) |
| WO (1) | WO1996017001A1 (enExample) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6090900A (en) * | 1997-02-25 | 2000-07-18 | Eastman Chemical Company | Polymers containing functionalized olefin monomers |
| MXPA01011111A (es) | 1999-05-04 | 2002-06-04 | Eastman Chem Co | Composiciones de recubrimiento basadas en alcoholes de polieter preparado de 3-4-epoxi-1-buteno. |
| US6608156B1 (en) | 2000-10-05 | 2003-08-19 | Eastman Chemical Company | Process for preparing interpolymers of ethylene and 2,3-dihydrofuran, or a heteroatom substituted olefin monomer and ethylene interpolymers |
| US6472491B1 (en) | 2000-10-05 | 2002-10-29 | Eastman Chemical Company | Process for preparing ethylene interpolymers and ethylene interpolymers |
| US6555595B1 (en) * | 2001-10-10 | 2003-04-29 | Rensselaer Polytechnic Institute | Photopolymerizable compositions |
| JP5125834B2 (ja) * | 2002-08-30 | 2013-01-23 | 三菱化学株式会社 | 縮合系共重合体 |
| WO2004022062A1 (en) | 2002-09-04 | 2004-03-18 | Schering Corporation | Pyrazolopyrimidines as cyclin dependent kinase inhibitors |
| BRPI0923998A2 (pt) * | 2009-04-15 | 2016-01-26 | Invista Tech Sarl | método para tratar resina de ácido perfluorosulfônico, resina de ácido perfluorosulfônico e processo para fabricar poliéter glicol ou copoliéter glicol |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1027400B (de) * | 1956-11-02 | 1958-04-03 | Bayer Ag | Verfahren zur Herstellung von ungesaettigten Mischpolymerisaten des Tetrahydrofurans |
| US3287330A (en) * | 1958-02-06 | 1966-11-22 | Du Pont | Polyether polymers having unsaturated side chains |
| US3133905A (en) * | 1960-05-23 | 1964-05-19 | Goodyear Tire & Rubber | Polyhydroxyl terminated polyethers |
| US3385913A (en) * | 1965-03-24 | 1968-05-28 | Allied Chem | Thermosetting copolymers based upon propylene oxide-butadiene monoxide copolymers |
| US4500705A (en) * | 1984-01-09 | 1985-02-19 | E. I. Du Pont De Nemours And Company | Method for reducing oligomeric cyclic ether content of a polymerizate |
| US5118869A (en) * | 1991-02-13 | 1992-06-02 | E. I. Du Pont De Nemours And Company | Polymerizing tetrahydrofuran to produce polytetramethylene ether glycol using a modified fluorinated resin catalyst containing sulfonic acid groups |
| US5434314A (en) * | 1994-01-18 | 1995-07-18 | Eastman Chemical Company | Polyether glycols and alcohols derived from 3,4-epoxy-1-butene |
-
1994
- 1994-11-25 US US08/344,905 patent/US5502137A/en not_active Expired - Fee Related
-
1995
- 1995-10-04 TW TW084110366A patent/TW311917B/zh active
- 1995-11-02 MY MYPI95003306A patent/MY132065A/en unknown
- 1995-11-13 EP EP95941421A patent/EP0793682B1/en not_active Expired - Lifetime
- 1995-11-13 WO PCT/US1995/015026 patent/WO1996017001A1/en not_active Ceased
- 1995-11-13 CA CA002205813A patent/CA2205813A1/en not_active Abandoned
- 1995-11-13 CN CN95196445A patent/CN1166842A/zh active Pending
- 1995-11-13 DE DE69505270T patent/DE69505270T2/de not_active Expired - Fee Related
- 1995-11-13 US US08/554,999 patent/US5536809A/en not_active Expired - Fee Related
- 1995-11-13 JP JP8518875A patent/JPH10510315A/ja active Pending
- 1995-11-13 ES ES95941421T patent/ES2122703T3/es not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| WO1996017001A1 (en) | 1996-06-06 |
| EP0793682B1 (en) | 1998-10-07 |
| CN1166842A (zh) | 1997-12-03 |
| US5502137A (en) | 1996-03-26 |
| MY132065A (en) | 2007-09-28 |
| TW311917B (enExample) | 1997-08-01 |
| JPH10510315A (ja) | 1998-10-06 |
| US5536809A (en) | 1996-07-16 |
| DE69505270T2 (de) | 1999-03-04 |
| DE69505270D1 (de) | 1998-11-12 |
| EP0793682A1 (en) | 1997-09-10 |
| CA2205813A1 (en) | 1996-06-06 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FG2A | Definitive protection |
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