GB1012003A - Method for aiding processing of polymers - Google Patents

Method for aiding processing of polymers

Info

Publication number
GB1012003A
GB1012003A GB2254863A GB2254863A GB1012003A GB 1012003 A GB1012003 A GB 1012003A GB 2254863 A GB2254863 A GB 2254863A GB 2254863 A GB2254863 A GB 2254863A GB 1012003 A GB1012003 A GB 1012003A
Authority
GB
United Kingdom
Prior art keywords
formula
reaction
ester
glycol
ester acid
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
GB2254863A
Inventor
Alan Sydney Anthony
Geoffrey Goldberg
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.)
A Boake Roberts and Co Ltd
Original Assignee
A Boake Roberts and Co 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 A Boake Roberts and Co Ltd filed Critical A Boake Roberts and Co Ltd
Priority to GB2254863A priority Critical patent/GB1012003A/en
Publication of GB1012003A publication Critical patent/GB1012003A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/04Oxygen-containing compounds
    • C08K5/10Esters; Ether-esters
    • C08K5/101Esters; Ether-esters of monocarboxylic acids
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/04Oxygen-containing compounds
    • C08K5/10Esters; Ether-esters
    • C08K5/12Esters; Ether-esters of cyclic polycarboxylic acids

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)

Abstract

A polymer composition comprises a synthetic thermoplastic polymer and from 1 to 50% by weight of said polymer of a complete or partial benzyl ester of a glycol ester acid of the formula HO2C.R.CO.OZO.OC.R.CO2H, wherein each R is the residue of an internal anhydride of an aliphatic or mono-benzenoid di- or tri-carboxylic acid having a 5 or 6 membered anhydride ring system and of the formula <FORM:1012003/C3/1> and Z is the residue of an alkylene or polyalkylene ether glycol having the formula HOZOH. Preferred benzyl esters are those derived from polyalkylene ether glycols of the formula HO(CxH2xO)pH, wherein x has a value of 2, 3 or 4 and p has an average value of 2 to 45. Specified synthetic thermoplastic polymers are polyethylene, polypropylene, polystyrene, plasticized and unplasticized vinyl chloride polymers and copolymers, and acrylate and methacrylate polymers and copolymers. The polymer compositions may also contain conventional additives, e.g. pigments, anti-oxidants, plasticizers, stabilizers and fillers. The benzyl esters are prepared by the reaction of benzyl chloride with substantially the stoichiometric amount of the appropriate ester acid in the presence of sufficient of a tertiary amine to act as an acceptor for the theoretical amount of hydrogen chloride liberated during the reaction. The ester acid reactants are prepared by the reaction of the required proportions of the appropriate anhydride and glycol under substantially anhydrous conditions and, preferably, in the presence of an amine which stabilizes the ester acid as it is formed.ALSO:Benzyl esters of glycol ester acids of the formula HO2C.RCO.OZO.OC.R.CO2H, wherein each R is the residue of an internal anhydride of an aliphatic or mono-benzenoid di- or tricarboxylic acid having a 5 or 6-membered anhydride ring system and of the formula <FORM:1012003/C2/1> and Z is the residue of an alkylene or polyalkylene ether glycol of the formula HOZOH, are prepared by the reaction of benzyl chloride with substantially the stoichiometric amount of the appropriate ester acid in the presence of sufficient of a tertiary amine to act as an acceptor for the theoretical amount of hydrogen chloride liberated during the reaction. Complete or partial esters may be prepared by this process. The ester acid reactants are prepared by the reaction of the required proportions of the appropriate anhydride and glycol under substantially anhydrous conditions and, preferably, in the presence of an amine which stabilizes the ester acid as it is formed. An example describes the preparation of diethylene glycol bis-phthalate ester acid and subsequently of dibenzyl diethylene bis-phthalate mixed ester.
GB2254863A 1963-06-06 1963-06-06 Method for aiding processing of polymers Expired GB1012003A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB2254863A GB1012003A (en) 1963-06-06 1963-06-06 Method for aiding processing of polymers

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB2254863A GB1012003A (en) 1963-06-06 1963-06-06 Method for aiding processing of polymers

Publications (1)

Publication Number Publication Date
GB1012003A true GB1012003A (en) 1965-12-01

Family

ID=10181190

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2254863A Expired GB1012003A (en) 1963-06-06 1963-06-06 Method for aiding processing of polymers

Country Status (1)

Country Link
GB (1) GB1012003A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2454235A1 (en) * 1974-11-15 1976-05-20 Teroson Gmbh Plastisols of methyl methacrylate polymers - contg organic plasticiser as coatings for metals, textiles or cables
DE2529732A1 (en) * 1975-07-03 1977-01-13 Teroson Gmbh Acrylic, pref methyl methacrylate copolymer plastisols - contg pref phthalate plasticisers used eg as sealants and corrosion inhibitors
US4210567A (en) 1974-11-15 1980-07-01 Teroson G.M.B.H. Plastisol of an acrylate polymer and a plasticizer

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2454235A1 (en) * 1974-11-15 1976-05-20 Teroson Gmbh Plastisols of methyl methacrylate polymers - contg organic plasticiser as coatings for metals, textiles or cables
US4210567A (en) 1974-11-15 1980-07-01 Teroson G.M.B.H. Plastisol of an acrylate polymer and a plasticizer
DE2529732A1 (en) * 1975-07-03 1977-01-13 Teroson Gmbh Acrylic, pref methyl methacrylate copolymer plastisols - contg pref phthalate plasticisers used eg as sealants and corrosion inhibitors

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