GB736991A - The manufacture of polyoxyalkylene glycols and their mono-ethers - Google Patents
The manufacture of polyoxyalkylene glycols and their mono-ethersInfo
- Publication number
- GB736991A GB736991A GB823851A GB823851A GB736991A GB 736991 A GB736991 A GB 736991A GB 823851 A GB823851 A GB 823851A GB 823851 A GB823851 A GB 823851A GB 736991 A GB736991 A GB 736991A
- Authority
- GB
- United Kingdom
- Prior art keywords
- ethylene oxide
- pipe
- ethylene
- ethylene glycol
- catalyst
- 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
Links
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
- C08G65/26—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 and other compounds
- C08G65/2696—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 and other compounds characterised by the process or apparatus used
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Polyethers (AREA)
Abstract
<PICT:0736991/IV (a)/1> Polyoxyalkylene glycols or monoethers thereof containing at least four oxyethylene groups per molecule and having molecular weights up to 10,000 are formed by continuously passing a homogeneous liquid mixture of ethylene oxide, an alkali metal catalyst and an organic hydroxy compound through a reactor with an internal temperature of 50-190 DEG C. and a pressure sufficient to maintain the reactants in the liquid phase (e.g. 7-130 atmospheres), the contact time in the reactor being 5-60 minutes so that 25-97 per cent of the ethylene oxide reacts. Organic hydroxy compounds mentioned are ethylene glycol, propylene glycol, diethylene glycol and dipropylene glycol, polyoxyethylene and polyoxypropylene glycols with 3 or more oxyalkylene groups, n-butyl alcohol, lauryl alcohol, 2-ethyl hexanol, benzyl alcohol, ethylene glycol monomethyl ether, phenol, b -naphthol, di-isobutyl cresol, octyl phenol, oleyl alcohol, cresol and 2,21-thiodiethanol. The catalyst is sodium, potassium or lithium generally dissolved as hydroxide or alkoxide. The catalyst concentration is preferably 0.005-0.1 gram mols./litre of reactants. Impurities such as carbon dioxide, ethylene dichloride, acetaldehyde or acetic acid are removed from the reactants; thus the ethylene oxide may be passed to the reaction zone through a bed of solid caustic soda or potash. In a preferred embodiment, the hydroxy body is mixed with the catalyst, traces of water or methanol are removed by vacuum and the mixture fed by pump 11 and supply line 13 to join the ethylene oxide fed by pump 12 and supply line 14 in orifice mixer 17. The reaction mixture passes to stainless steel reactor coil 19 surrounded in vessel 20 by liquid 21 maintained boiling by heater 23 in reboiler 22 under reflux condenser 24. Inert gas, e.g. nitrogen, may be fed through pipe 33 and vent pipe 34 into vessel 20. The boiling liquid may be water, ethylene glycol, or ethylene glycol monobutyl ether or blends thereof. The reacted mixture leaves coil 19 by pipe 25 and needle let-down valve 26 and passes by pipe 27 to stripping still 28 whence unreacted ethylene oxide is removed for recycling, and the product is pumped by pump 29 and pipe 30 to cooler 31 for storage or further treatment, viz. neutralization of alkali, and filtration. Products which are monoethers may be esterified, e.g. the product from ethylene glycol monomethyl ether and ethylene oxide was esterified with lauric or palmitic acid. The Specification includes a number of specified examples of the preparation of particular polymers.ALSO:<PICT:0736991/IV (b)/1> Polyoxyalkylene glycols or monoethers thereof containing at least four oxyethylene groups and having molecular weights up to 10,000 are formed by continuously passing a homogeneous liquid mixture of ethylene oxide, an alkali metal catalyst and an organic hydroxy compound through a reactor with an internal temperature of 50-190 DEG C. and a pressure sufficient to maintain the reactants in the liquid phase (e.g. 7-130 atmosphere) the contact time in the reactor being 5-60 minutes so that 25-97 per cent of the ethylene oxide reacts. Organic hydroxy compounds mentioned are ethylene glycol, propylene glycol, diethylene glycol and dipropylene glycol, polyoxyethylene and poloxypropylene glycols with 3 or more oxyalkylene groups, n-butyl alcohol, lauryl alcohol, 2-ethyl hexanol, benzyl alcohol, ethylene glycol monomethyl ether, phenol, b -naphthol, diisobutyl cresol, octyl phenol, oleyl alcohol, cresol and 2,21-thiodiethanol. The catalyst is sodium, potassium or lithium generally dissolved as hydroxide or alkoxide. The catalyst concentration is preferably 0.005-0.1 gram mols/litre of reactants. Impurities such as carbon dioxide, ethylene dichloride, acetaldehyde or acetic acid are removed from the reactants; thus the ethylene oxide may be passed to the reaction zone through a bed of solid caustic soda or potash. In a preferred embodiment, the hydroxy body is mixed with the catalyst, traces of water or methanol are removed by vacuum and the mixture fed by pump 11 and supply line 13 to join the ethylene oxide, fed by pump 12 and supply line 14, in orifice mixer 17. The reaction mixture passes to stainless steel reactor coil 19 surrounded in vessel 20 by liquid 21 maintained boiling by heater 23 in reboiler 22 under reflux condenser 24. Inert gas, e.g. nitrogen may be fed through pipe 33 and vent pipe 34 into vessel 20. The boiling liquid may be water, ethylene glycol or ethylene glycol monobutyl ether, or blends thereof. The reacted mixture leaves coil 19 by pipe 25 and needle let-down valve 26 and passes by pipe 27 to stripping still 28 whence unreacted ethylene oxide is removed for recycling, and the product is pumped by pump 29 and pipe 30 to cooler 31 for storage or further treatment, viz. neutralization of alkali, and filtration. Products which are monoethers may be esterified, e.g. the product from ethylene glycol monomethyl ether and ethylene oxide was esterified with lauric or palmitic acid. The Specification includes a number of specific examples of the preparation of particular polymers.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB823851A GB736991A (en) | 1951-04-09 | 1951-04-09 | The manufacture of polyoxyalkylene glycols and their mono-ethers |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB823851A GB736991A (en) | 1951-04-09 | 1951-04-09 | The manufacture of polyoxyalkylene glycols and their mono-ethers |
Publications (1)
Publication Number | Publication Date |
---|---|
GB736991A true GB736991A (en) | 1955-09-21 |
Family
ID=9848636
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB823851A Expired GB736991A (en) | 1951-04-09 | 1951-04-09 | The manufacture of polyoxyalkylene glycols and their mono-ethers |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB736991A (en) |
Cited By (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2988572A (en) * | 1958-03-07 | 1961-06-13 | Union Carbide Corp | Process for the manufacture of polyoxyalkylene compounds |
US3117998A (en) * | 1959-04-14 | 1964-01-14 | Allied Chem | Propylene oxide polyethers |
US3190927A (en) * | 1960-04-13 | 1965-06-22 | Wyandotte Chemicals Corp | Process for oxyalkylating solid polyols |
US3364267A (en) * | 1965-11-08 | 1968-01-16 | Dow Chemical Co | Process for preparation of glycol ethers of phenols |
US3406208A (en) * | 1962-05-17 | 1968-10-15 | Henkel & Compagnie G M B H | Polyglycol ethers suitable for detergent preparations, and process for preparing the same |
US3452103A (en) * | 1966-12-30 | 1969-06-24 | Whittaker Corp | Fluorohydroxy ethers |
US3475499A (en) * | 1967-03-23 | 1969-10-28 | Halcon International Inc | Preparation of glycols and glycol ethers |
US4385173A (en) | 1980-04-21 | 1983-05-24 | Shell Oil Company | Polyol polyether preparation process |
EP0850954A1 (en) * | 1996-12-27 | 1998-07-01 | CP TECH S.r.l. | A method for the production of polyadducts of alkylene oxides with a liquid in a gas dispersion reactor |
WO2001036513A1 (en) * | 1999-11-18 | 2001-05-25 | Basf Corporation | Continuous process for the production of sucrose based polyether polyols |
WO2001036514A1 (en) * | 1999-11-18 | 2001-05-25 | Basf Corporation | Continuous process for the production of polyether polyols |
WO2004056904A1 (en) * | 2002-12-20 | 2004-07-08 | Basf Aktiengesellschaft | Method for producing polyoxyalkylene glycols |
CN100554310C (en) * | 2006-01-17 | 2009-10-28 | 中国科学院过程工程研究所 | Monoalkoxy polyoxyethylene glycol and preparation method thereof |
WO2013010971A1 (en) * | 2011-07-19 | 2013-01-24 | Basf Se | Process for a continuous production of polyetherols |
US8957257B2 (en) | 2011-07-19 | 2015-02-17 | Basf Se | Process for a continuous production of polyetherols |
EP3339350A1 (en) * | 2016-12-23 | 2018-06-27 | Universite De Liege | Continuous flow process for the polymerization of an alkylene oxide |
-
1951
- 1951-04-09 GB GB823851A patent/GB736991A/en not_active Expired
Cited By (24)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2988572A (en) * | 1958-03-07 | 1961-06-13 | Union Carbide Corp | Process for the manufacture of polyoxyalkylene compounds |
US3117998A (en) * | 1959-04-14 | 1964-01-14 | Allied Chem | Propylene oxide polyethers |
US3190927A (en) * | 1960-04-13 | 1965-06-22 | Wyandotte Chemicals Corp | Process for oxyalkylating solid polyols |
US3406208A (en) * | 1962-05-17 | 1968-10-15 | Henkel & Compagnie G M B H | Polyglycol ethers suitable for detergent preparations, and process for preparing the same |
US3364267A (en) * | 1965-11-08 | 1968-01-16 | Dow Chemical Co | Process for preparation of glycol ethers of phenols |
US3452103A (en) * | 1966-12-30 | 1969-06-24 | Whittaker Corp | Fluorohydroxy ethers |
US3475499A (en) * | 1967-03-23 | 1969-10-28 | Halcon International Inc | Preparation of glycols and glycol ethers |
US4385173A (en) | 1980-04-21 | 1983-05-24 | Shell Oil Company | Polyol polyether preparation process |
EP0850954A1 (en) * | 1996-12-27 | 1998-07-01 | CP TECH S.r.l. | A method for the production of polyadducts of alkylene oxides with a liquid in a gas dispersion reactor |
WO1998029458A1 (en) * | 1996-12-27 | 1998-07-09 | Linde Ag | A method for the production of polyadducts of alkylene oxides with a liquid in gas dispersion reactor |
AU720858B2 (en) * | 1996-12-27 | 2000-06-15 | Linde Ag | A method for the production of polyadducts of alkylene oxides with a liquid in gas dispersion reactor |
CN1111543C (en) * | 1996-12-27 | 2003-06-18 | 林德股份公司 | Utilize the gas phase dispersion reactor to produce the method for oxyalkylene addition polymer |
US6319999B1 (en) | 1996-12-27 | 2001-11-20 | Linde Aktiengesellschaft | Method for the production of polyadducts of alkylene oxides with a liquid in gas dispersion reactor |
WO2001036514A1 (en) * | 1999-11-18 | 2001-05-25 | Basf Corporation | Continuous process for the production of polyether polyols |
US6380367B1 (en) | 1999-11-18 | 2002-04-30 | Basf Corporation | Continuous process for the production of sucrose based polyether polyols |
US6410801B1 (en) | 1999-11-18 | 2002-06-25 | Basf Corporation | Continuous process for the production of polyether polyols |
WO2001036513A1 (en) * | 1999-11-18 | 2001-05-25 | Basf Corporation | Continuous process for the production of sucrose based polyether polyols |
WO2004056904A1 (en) * | 2002-12-20 | 2004-07-08 | Basf Aktiengesellschaft | Method for producing polyoxyalkylene glycols |
CN100554310C (en) * | 2006-01-17 | 2009-10-28 | 中国科学院过程工程研究所 | Monoalkoxy polyoxyethylene glycol and preparation method thereof |
WO2013010971A1 (en) * | 2011-07-19 | 2013-01-24 | Basf Se | Process for a continuous production of polyetherols |
US8957257B2 (en) | 2011-07-19 | 2015-02-17 | Basf Se | Process for a continuous production of polyetherols |
EP3339350A1 (en) * | 2016-12-23 | 2018-06-27 | Universite De Liege | Continuous flow process for the polymerization of an alkylene oxide |
WO2018114416A1 (en) * | 2016-12-23 | 2018-06-28 | Université de Liège | Continuous flow process for the polymerization of an alkylene oxide |
CN110036055A (en) * | 2016-12-23 | 2019-07-19 | 列日大学 | The continuous current method of polymerization for alkylene oxide |
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