GB1147791A - Polyethers - Google Patents

Polyethers

Info

Publication number
GB1147791A
GB1147791A GB3492165A GB3492165A GB1147791A GB 1147791 A GB1147791 A GB 1147791A GB 3492165 A GB3492165 A GB 3492165A GB 3492165 A GB3492165 A GB 3492165A GB 1147791 A GB1147791 A GB 1147791A
Authority
GB
United Kingdom
Prior art keywords
butylene oxide
trans
optionally
polymers
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
GB3492165A
Inventor
Anthony Joseph Burgess
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 GB3492165A priority Critical patent/GB1147791A/en
Publication of GB1147791A publication Critical patent/GB1147791A/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
    • C08G65/04Macromolecular 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
    • C08G65/06Cyclic ethers having no atoms other than carbon and hydrogen outside the ring
    • C08G65/08Saturated oxiranes

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)

Abstract

1,147,791. Polymers of trans-2,3-butylene oxide; polyurethenes. IMPERIAL CHEMICAL INDUSTRIES Ltd. 5 Aug., 1966 [16 Aug., 1965], No. 34921/65. Headings C3C and C3R. Partially crystalline polymers of trans-2,3- butylene oxide having at least 80% hydroxyl end groups and molecular weights in the range of from 300 to 3000 are prepared by polymerizing trans-2,3-butylene oxide in the presence of an acidic catalyst, which may be a protonic acid, such as sulphuric, fluorosulphonic or perchloric acid, or a Lewis acid, such as boron trifluoride or its addition products or aluminium chloride, the latter being used together with a co-catalyst that is water or a polyhydroxy compound, such as a glycol. One or more other alkylene oxides, such as propylene oxide, 1,2- butylene oxide and cis-2,3-butylene oxide, may optionally be copolymerized with the trans- 2-3-butylene oxide in a random or block form, but the trans-2,3-butylene oxide preferably constitutes at least 25%, on a molar basis, of the total oxides used. After polymerization the catalyst residues can be removed from the polyether by washing with an aqueous solution or suspension of an alkaline material or by treating with active carbon or absorbent earth. An antioxidant, such as a sterically hindered phenol, may be incorporated in the polyether during manufacture or purification. The polyethers may be reacted with organic polyisocyanates to form polyurethanes, optionally in the presence of gas-generating agents such as water or inert liquids of low boiling point. Catalysts, e.g. tertiary amines and organo-metallic compounds, and surface active agents, e.g. siloxane polymers and siloxane-oxyalkylene block copolymers may optionally be added to the reaction mixture.
GB3492165A 1965-08-16 1965-08-16 Polyethers Expired GB1147791A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB3492165A GB1147791A (en) 1965-08-16 1965-08-16 Polyethers

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB3492165A GB1147791A (en) 1965-08-16 1965-08-16 Polyethers

Publications (1)

Publication Number Publication Date
GB1147791A true GB1147791A (en) 1969-04-10

Family

ID=10371580

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3492165A Expired GB1147791A (en) 1965-08-16 1965-08-16 Polyethers

Country Status (1)

Country Link
GB (1) GB1147791A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4393199A (en) 1981-05-12 1983-07-12 S R I International Cationic polymerization
EP0687699A3 (en) * 1994-06-10 1996-01-17 Arco Chem Tech
WO2022200087A1 (en) 2021-03-26 2022-09-29 Evonik Operations Gmbh Novel polyethers on the basis of 2,3-epoxybutane and process for the preparation thereof

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4393199A (en) 1981-05-12 1983-07-12 S R I International Cationic polymerization
EP0687699A3 (en) * 1994-06-10 1996-01-17 Arco Chem Tech
WO2022200087A1 (en) 2021-03-26 2022-09-29 Evonik Operations Gmbh Novel polyethers on the basis of 2,3-epoxybutane and process for the preparation thereof

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