GB736991A - The manufacture of polyoxyalkylene glycols and their mono-ethers - Google Patents

The manufacture of polyoxyalkylene glycols and their mono-ethers

Info

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
Application number
GB823851A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Oxirane Ltd
Original Assignee
Oxirane Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Oxirane Ltd filed Critical Oxirane Ltd
Priority to GB823851A priority Critical patent/GB736991A/en
Publication of GB736991A publication Critical patent/GB736991A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G65/00Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
    • C08G65/02Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
    • C08G65/26Macromolecular 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
    • C08G65/2696Macromolecular 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.
GB823851A 1951-04-09 1951-04-09 The manufacture of polyoxyalkylene glycols and their mono-ethers Expired GB736991A (en)

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)

* Cited by examiner, † Cited by third party
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

Cited By (24)

* Cited by examiner, † Cited by third party
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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