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GB1105620A - New polyesters - Google Patents

New polyesters

Info

Publication number
GB1105620A
GB1105620A GB1484866A GB1484866A GB1105620A GB 1105620 A GB1105620 A GB 1105620A GB 1484866 A GB1484866 A GB 1484866A GB 1484866 A GB1484866 A GB 1484866A GB 1105620 A GB1105620 A GB 1105620A
Authority
GB
United Kingdom
Prior art keywords
glycols
butylene
per cent
mol per
mixture
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
GB1484866A
Inventor
Roxburgh Richmond Aitken
Peter Richmond Grindley
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 GB1484866A priority Critical patent/GB1105620A/en
Publication of GB1105620A publication Critical patent/GB1105620A/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
    • C08G63/00Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
    • C08G63/02Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
    • C08G63/12Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from polycarboxylic acids and polyhydroxy compounds
    • C08G63/16Dicarboxylic acids and dihydroxy compounds
    • C08G63/20Polyesters having been prepared in the presence of compounds having one reactive group or more than two reactive groups
    • 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
    • C08G63/00Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
    • C08G63/02Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
    • C08G63/12Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from polycarboxylic acids and polyhydroxy compounds
    • C08G63/16Dicarboxylic acids and dihydroxy compounds
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L27/00Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers
    • C08L27/02Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L27/04Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment containing chlorine atoms
    • C08L27/06Homopolymers or copolymers of vinyl chloride
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L67/00Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
    • C08L67/02Polyesters derived from dicarboxylic acids and dihydroxy compounds

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

Polyesters are made by reacting (a) adipic acid or an alkyl ester thereof with (b) a mixture of glycols comprising 10 to 50 mol per cent 1:6-hexanediol and 10 to 90 mol per cent 1,2-propylene glycol or 1,3-butylene glycol or a mixture thereof. The reaction mixture may also contain (c) a monocarboxylic acid, e.g. caproic, lauric, stearic, palm kernel or coconut acids and/or (d) a monohydric alcohol, e.g. n-hexanol, 2-ethylhexanol, n-decanol, n-dodecanol or various alcohols obtained by the carboxylation of olefins. Up to 17.5 mol per cent of the adipic acid may be replaced by other dicarboxylic acids, e.g. succinic, glutaric, suberic, azelaic, sebacic, 3-methyladipic, 2:4-diethyladipic, 2-ethylsuberic, phthalic, isophthalic or 4:41-diphenyldicarboxylic acid. Similarly up to 17.5 mol per cent of the glycols (b) may be replaced by other glycols, e.g. ethylene-, 1:2-butylene-, 2:3-butylene-, 1:4-butylene-, 1:5-pentylene-, neopentylene-, 1,10-decylene-, diethylene- or dipropylene glycols. The polyesters are primarily used for plasticizing polyvinyl chloride and copolymers of vinyl chloride with vinyl acetate, unsym. dichloroethylene, styrene and esters, nitriles and amides of acrylic, methacrylic, fumaric and maleic acids. They may also be used for plasticizing chlorobutadiene and butadieneacrylonitrile polymers, chlorinated vinyl chloride polymers, chlorinated rubber, nitrocellulose, ethyl cellulose and cellulose acetate. The plasticized polyvinyl chloride composition may also contain a liquid barium-cadmium complex as a heat stabilizer or a polyisocyanate to assist in good adhesion of the composition to a substrate.
GB1484866A 1966-04-04 1966-04-04 New polyesters Expired GB1105620A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB1484866A GB1105620A (en) 1966-04-04 1966-04-04 New polyesters

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB1484866A GB1105620A (en) 1966-04-04 1966-04-04 New polyesters

Publications (1)

Publication Number Publication Date
GB1105620A true GB1105620A (en) 1968-03-06

Family

ID=10048556

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1484866A Expired GB1105620A (en) 1966-04-04 1966-04-04 New polyesters

Country Status (1)

Country Link
GB (1) GB1105620A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3699189A (en) * 1969-11-10 1972-10-17 Goodyear Tire & Rubber Polyester-vinyl chloride copolymer adhesive
US4317760A (en) 1979-07-31 1982-03-02 Dainippon Ink And Chemicals, Inc. Halogen-containing resin composition
FR2526029A1 (en) * 1982-04-30 1983-11-04 Mitsubishi Monsanto Chem POLYESTER IN WHICH THE MONOMERIC POLYATOMIC ALCOHOL COMPONENT IS AT LEAST PARTIALLY 1.2 BUTANEDIOL
EP1782966A1 (en) * 2005-10-28 2007-05-09 Sumtiomo Rubber Industries Ltd Rubber composition for tire and pneumatic tire using the same
CN115612076A (en) * 2022-10-14 2023-01-17 金华市龙达塑胶助剂有限公司 Medical PVC sheet lubricant and preparation process thereof

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3699189A (en) * 1969-11-10 1972-10-17 Goodyear Tire & Rubber Polyester-vinyl chloride copolymer adhesive
US4317760A (en) 1979-07-31 1982-03-02 Dainippon Ink And Chemicals, Inc. Halogen-containing resin composition
US4421885A (en) 1979-07-31 1983-12-20 Dainippon Ink And Chemicals, Inc. Halogen-containing resin composition containing ester plasticizer
FR2526029A1 (en) * 1982-04-30 1983-11-04 Mitsubishi Monsanto Chem POLYESTER IN WHICH THE MONOMERIC POLYATOMIC ALCOHOL COMPONENT IS AT LEAST PARTIALLY 1.2 BUTANEDIOL
GB2120262A (en) * 1982-04-30 1983-11-30 Mitsubishi Monsanto Chem Polyester
US4596886A (en) * 1982-04-30 1986-06-24 Mitsubishi Monsanto Chemical Company Polyester containing impure 1,2-butanediol
EP1782966A1 (en) * 2005-10-28 2007-05-09 Sumtiomo Rubber Industries Ltd Rubber composition for tire and pneumatic tire using the same
CN1958669B (en) * 2005-10-28 2011-06-15 住友橡胶工业株式会社 Rubber composition for tire and pneumatic tire using the same
US8100157B2 (en) 2005-10-28 2012-01-24 Sumitomo Rubber Industries, Ltd. Rubber composition for tire and pneumatic tire using the same
CN115612076A (en) * 2022-10-14 2023-01-17 金华市龙达塑胶助剂有限公司 Medical PVC sheet lubricant and preparation process thereof

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