GB892557A - Purification process - Google Patents

Purification process

Info

Publication number
GB892557A
GB892557A GB4439559A GB4439559A GB892557A GB 892557 A GB892557 A GB 892557A GB 4439559 A GB4439559 A GB 4439559A GB 4439559 A GB4439559 A GB 4439559A GB 892557 A GB892557 A GB 892557A
Authority
GB
United Kingdom
Prior art keywords
polyethers
acid
propylene oxide
acids
examples
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
GB4439559A
Inventor
Robert Paul Gentles
Arthur Ibbotson
Harry James Twitchett
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.)
Imperial Chemical Industries Ltd
Original Assignee
Imperial Chemical Industries 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 Imperial Chemical Industries Ltd filed Critical Imperial Chemical Industries Ltd
Priority to GB4439559A priority Critical patent/GB892557A/en
Publication of GB892557A publication Critical patent/GB892557A/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
    • C08G65/30Post-polymerisation treatment, e.g. recovery, purification, drying

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Polyethers (AREA)

Abstract

Polyethers contaminated with basic inorganic materials are purified by treating with an acid of the formula HxMFy where M is an element of Group 3 or 4 of the Periodic Table, x is 1 to 3 and y is 4 to 6. The polyethers are particularly those obtained by polymerizing a b -alkylene oxides, optionally in the presence of a compound containing reactive hydrogen, and in the presence of an alkaline catalyst, e.g. KOH and NaOH. Examples of the fluoro-acids are fluoroboric, fluorosilicic, fluorotitanic and fluoroaluminic acids. They may be added as aqueous solutions or as solutions or suspensions of metal fluoride, e.g.titanium tetrafluoride or aluminium trifluoride, in hydrofluoric acid. The amount of acid is preferably sufficient to produce a pH of 3 to 5. The temperature may be from 25 DEG to 150 DEG C., preferably 90 DEG to 110 DEG C. where the polyether is liquid. The resultant insoluble matter is removed by filtration. Prior to this, a further treatment with an acid-acceptor is preferably effected. Suitable acceptors are basic compounds insoluble in polyethers, e.g. silicates and carbonates of alkaline earth metals. In the examples, the polyethers are prepared from: (1) glycerol and propylene oxide; (2) trimethylolpropane and propylene oxide and then with ethylene oxide; (3) ethylene oxide and isooctanol; (4) trimethylolpropane and propylene oxide. These polyethers have hydroxyl values ranging from 59 to 542 mg. KOH per gm., the upper limit corresponding to a molecular weight of 310.ALSO:Polyethers contaminated with basic inorganic materials are purified by treating with an acid of the formula HxMFy where M is an element of Group 3 or 4 of the Periodic Table, x is 1 to 3 and y is 4 to 6. The polyethers are particularly those obtained by polymerising a b -alkylene oxides, optionally in the presence of a compound containing reactive hydrogen, such as water, monohydric alcohols, e.g. butanol, diols, pentaerythritol, sorbitol, sucrose and others mentioned hereinafter, and in the presence of an alkaline catalyst, e.g. KOH and NaOH. Examples of the fluoro-acids are fluoroboric, flourosilicic, fluorotitanic and fluoroaluminic acids. They may be added as aqueous solutions or as solutions or suspensions of metal fluoride, e.g. titanium tetrafluoride or aluminium trifluoride, in hydrofluoric acid. The amount of acid is preferably sufficient to produce a pH of 3 to 5. The temperature may be from 25 DEG to 150 DEG , preferably 90 DEG to 110 DEG C. where the polyether is liquid. The resultant insoluble matter is removed by filtration. Prior to this, a further treatment with an acid-acceptor is preferably effected, suitable acceptors being basic compounds insoluble in polyethers, e.g. silicates and carbonates of alkaline earth metals. In the examples, the polyethers are prepared from (1) glycerol and propylene oxide; (2) trimethyl propane and propylene oxide and then with ethylene oxide; (3) ethylene oxide and isooctanol; (4) trimethylpropane and propylene oxide. These polyethers have hydroxyl values ranging from 59 to 542 mg.K.O.H. per gm., the upper limit corresponding to a molecular weight of 310.
GB4439559A 1959-12-31 1959-12-31 Purification process Expired GB892557A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB4439559A GB892557A (en) 1959-12-31 1959-12-31 Purification process

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB4439559A GB892557A (en) 1959-12-31 1959-12-31 Purification process

Publications (1)

Publication Number Publication Date
GB892557A true GB892557A (en) 1962-03-28

Family

ID=10433096

Family Applications (1)

Application Number Title Priority Date Filing Date
GB4439559A Expired GB892557A (en) 1959-12-31 1959-12-31 Purification process

Country Status (1)

Country Link
GB (1) GB892557A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2173108A1 (en) * 1972-02-24 1973-10-05 Basf Ag
EP0094014A1 (en) * 1982-05-06 1983-11-16 The B.F. GOODRICH Company Process for preparing colorless hydroxyl epihalohydrin polymers
GB2135322A (en) * 1983-01-21 1984-08-30 Vyzk Ustav Petrochem A process for purifying at least partially water-soluble polyethers and/or copolymers

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2173108A1 (en) * 1972-02-24 1973-10-05 Basf Ag
EP0094014A1 (en) * 1982-05-06 1983-11-16 The B.F. GOODRICH Company Process for preparing colorless hydroxyl epihalohydrin polymers
GB2135322A (en) * 1983-01-21 1984-08-30 Vyzk Ustav Petrochem A process for purifying at least partially water-soluble polyethers and/or copolymers

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