GB1090932A - Acrylonitrile/butadiene/styrene resin compositions - Google Patents

Acrylonitrile/butadiene/styrene resin compositions

Info

Publication number
GB1090932A
GB1090932A GB568165A GB568165A GB1090932A GB 1090932 A GB1090932 A GB 1090932A GB 568165 A GB568165 A GB 568165A GB 568165 A GB568165 A GB 568165A GB 1090932 A GB1090932 A GB 1090932A
Authority
GB
United Kingdom
Prior art keywords
esters
iso
octyl
tri
decyl
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
GB568165A
Inventor
Samuel Howard Coulson
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.)
Geigy Co Ltd
Original Assignee
Geigy 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 Geigy Co Ltd filed Critical Geigy Co Ltd
Priority to GB568165A priority Critical patent/GB1090932A/en
Priority to CH140566A priority patent/CH457843A/en
Priority to NL6601650A priority patent/NL6601650A/xx
Priority to BE676264D priority patent/BE676264A/xx
Priority to FR49117A priority patent/FR1467778A/en
Publication of GB1090932A publication Critical patent/GB1090932A/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

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

A thermoplastic composition comprises an ABS resin and (a) an alkyl ester of a carboxylic acid having a solubility parameter of from 8.5 to 9.2, or (b) a mixture of two or more esters, the mean solubility parameter of the esters being from 8.5 to 9.2. The preferred alkyl esters of aspect (a) of the invention are dialkyl esters of an aliphatic or aromatic dicarboxylic acid, the alkyl groups being straight- or branched-chain and preferably containing from 6 to 20 carbon atoms, e.g. di-n-heptyl, di-n-octyl-, di-iso-octyl-, di-tertiary-octyl-, di-2-ethylhexyl-, di-1-methyl-heptyl-, di-n-nonyl-, di-3,5,5-trimethyl-hexyl-, di-n-decyl- and di-iso-decyl adipates, pimelates, azelates and sebacates, di-n-heptyl-, di-n-octyl-, di-iso-octyl-, di-tertiary-octyl-, di-2-ethylhexyl-, di-1-methyl-heptyl-, di-3,5,5-trimethyl-hexyl-, di-n-decyl-, di-iso-decyl-, and di-tridecyl-o-phthalates, iso-phthalates and terephthalates. The mixture of esters of aspect (b) of the invention may comprise organic esters and/or inorganic esters. The preferred organic esters are as for aspect (a) of the invention, but including the succinates and glutarates. Inorganic esters include alkyl and aryl phosphates, preferably trialkyl and triaryl phosphates, and the C15 alkyl sulphonic esters of phenol and cresol, e.g. tri-iso-octyl-, tri-phenyl-, tri-tolyl-, and tri-xylyl phosphates. The esters are preferably present in amount from 2% to 20% by weight based on the ABS resin. In examples are used di-isooctyl phthalate, di-tridecyl phthalate, di-isooctyl azelate, iso-decyl ester of a mixture of succinic, glutaric and adipic acids, di-isodecyl phthalate, an equimola mixture of di-iso-octyl azelate and tri-tolyl phosphate, mixtures of tritolyl phosphate and tri-iso-octyl phosphate, 1:1 by weight mixture of di-iso-octyl azelate and di-tridecyl-phthalate. Comparative examples are given using polybutylene adipate, tri-tolyl phosphate, chlorinated paraffin and tri-isoctyl phosphate. Fillers, e.g. calcium carbonate, china clay, silica or mica, inorganic or organic pigments and anti-oxidants, e.g. phenothiazine or a substituted phenol may be added.
GB568165A 1965-02-10 1965-02-10 Acrylonitrile/butadiene/styrene resin compositions Expired GB1090932A (en)

Priority Applications (5)

Application Number Priority Date Filing Date Title
GB568165A GB1090932A (en) 1965-02-10 1965-02-10 Acrylonitrile/butadiene/styrene resin compositions
CH140566A CH457843A (en) 1965-02-10 1966-02-01 Molding compounds
NL6601650A NL6601650A (en) 1965-02-10 1966-02-09
BE676264D BE676264A (en) 1965-02-10 1966-02-09
FR49117A FR1467778A (en) 1965-02-10 1966-02-10 New thermoplastic materials, in particular based on acrylonitrile, butadiene and styrene resins

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB568165A GB1090932A (en) 1965-02-10 1965-02-10 Acrylonitrile/butadiene/styrene resin compositions

Publications (1)

Publication Number Publication Date
GB1090932A true GB1090932A (en) 1967-11-15

Family

ID=9800654

Family Applications (1)

Application Number Title Priority Date Filing Date
GB568165A Expired GB1090932A (en) 1965-02-10 1965-02-10 Acrylonitrile/butadiene/styrene resin compositions

Country Status (4)

Country Link
BE (1) BE676264A (en)
CH (1) CH457843A (en)
GB (1) GB1090932A (en)
NL (1) NL6601650A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0183112A1 (en) * 1984-11-12 1986-06-04 The Dow Chemical Company Rubber-reinforced styrenic polymer resins exhibiting increased elongation
US5376717A (en) * 1992-02-18 1994-12-27 Ips Corporation Low VOC (volatile organic compounds), solvent-based ABS adhesives
US5817708A (en) * 1996-07-19 1998-10-06 The B. F. Goodrich Company Low volatile organic solvent based adhesive
US5821289A (en) * 1996-07-19 1998-10-13 The B.F. Goodrich Company Low volatile organic solvent based adhesive

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0183112A1 (en) * 1984-11-12 1986-06-04 The Dow Chemical Company Rubber-reinforced styrenic polymer resins exhibiting increased elongation
US4652601A (en) * 1984-11-12 1987-03-24 The Dow Chemical Company Rubber-reinforced styrenic polymer resins exhibiting increased elongation
AU592774B2 (en) * 1984-11-12 1990-01-25 Dow Chemical Company, The Rubber-reinforce styrenic polymer resins exhibiting increased elongation
US5376717A (en) * 1992-02-18 1994-12-27 Ips Corporation Low VOC (volatile organic compounds), solvent-based ABS adhesives
US5495040A (en) * 1992-02-18 1996-02-27 Ips Corporation Low VOC (volatile organic compound) primer for joining acrylonitrile-butadiene-styrene terpolymer articles
US5817708A (en) * 1996-07-19 1998-10-06 The B. F. Goodrich Company Low volatile organic solvent based adhesive
US5821289A (en) * 1996-07-19 1998-10-13 The B.F. Goodrich Company Low volatile organic solvent based adhesive
US5859103A (en) * 1996-07-19 1999-01-12 B. F. Goodrich Company Low volatile organic solvent based adhesive
US5962560A (en) * 1996-07-19 1999-10-05 The B.F. Goodrich Company Low volatile organic solvent based adhesive

Also Published As

Publication number Publication date
BE676264A (en) 1966-08-09
NL6601650A (en) 1966-08-11
CH457843A (en) 1968-06-15

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