GB1106367A - Oriented polyarylsulphone film - Google Patents

Oriented polyarylsulphone film

Info

Publication number
GB1106367A
GB1106367A GB1822864A GB1822864A GB1106367A GB 1106367 A GB1106367 A GB 1106367A GB 1822864 A GB1822864 A GB 1822864A GB 1822864 A GB1822864 A GB 1822864A GB 1106367 A GB1106367 A GB 1106367A
Authority
GB
United Kingdom
Prior art keywords
film
polyarylsulphone
diphenyl
stretching
extrusion
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
GB1822864A
Inventor
Brian Edmund Jennings
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 GB1822864A priority Critical patent/GB1106367A/en
Priority to FR15463A priority patent/FR1441766A/en
Priority to DE19651569060 priority patent/DE1569060A1/en
Publication of GB1106367A publication Critical patent/GB1106367A/en
Expired legal-status Critical Current

Links

Classifications

    • 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
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L81/00Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing sulfur with or without nitrogen, oxygen or carbon only; Compositions of polysulfones; Compositions of derivatives of such polymers
    • C08L81/06Polysulfones; Polyethersulfones

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Manufacture Of Macromolecular Shaped Articles (AREA)
  • Shaping By String And By Release Of Stress In Plastics And The Like (AREA)

Abstract

1,106,367. Polyarylsulphone films. IMPERIAL CHEMICAL INDUSTRIES Ltd. 26 April, 1965 [1 May, 1964], No. 18228/64. Heading B5B. An oriented film of a polyarylsulphone is formed of repeating units of the formula -Ar-SO 2 - where Ar is a divalent aromatic residue which may vary from unit to unit in the polymer chain, and in at least some of the units Ar is derived from a compound of formula (where Z is -O-, -S-, or the residue of a 4,4<SP>1</SP>-bisphenol) and in any other units Ar is similarly derived from benzene, diphenyl, or a polynuclear aromatic hydrocarbon containing not more than two aromatic nuclei so that in the divalent aromatic residues containing two benzene rings each benzene ring bears one of the valencies and one or more of the hydrogen atoms bound to aromatic rings may be replaced by halogen atoms or alkyl or alkoxy groups and a minor proportion of the -SO 2 - links may be replaced by -CO- links. The residues Ar may be derived from diphenyl ether or diphenyl sulphide, and optionally also in minor proportion from diphenyl. Films may be made by compression-moulding, melt-extrusion, calendering, or casting from a solution of the polymer in a suitable solvent e.g. nitrobenzene or dimethyl formamide. In moulding or extrusion, temperatures of at least 300‹ C. are required to obtain the material in a sufficiently mobile form, but temperatures above 330‹ C. may cause thermal degradation. Orientation may be effected by stretching, suitably at 240-260‹ C. A preferred oriented film is made from a polyarylsulphone in which the benzene rings in the polymer chain are essentially all -para. The stretching method used depends largely on the process used for forming the film. Longitudinal stretching may be effected by the use of feed and draw rolls, and the film may then be transversely stretched by tentering. Alternatively tentering alone may be employed using a tenter in which the pairs of clamps diverge laterally while the distance between adjacent pairs is also increased, thus simultaneously stretching the film both laterally and longitudinally. Alternatively, tubular films may be made by melt-extrusion and drawn by passage between two pairs of nip rolls while simultaneously inflated, in known manner.
GB1822864A 1964-05-01 1964-05-01 Oriented polyarylsulphone film Expired GB1106367A (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
GB1822864A GB1106367A (en) 1964-05-01 1964-05-01 Oriented polyarylsulphone film
FR15463A FR1441766A (en) 1964-05-01 1965-04-30 Polyarylsulfone Oriented Sheet and Method of Manufacture
DE19651569060 DE1569060A1 (en) 1964-05-01 1965-04-30 Use of polyarylsulfones to produce oriented thermoplastic films

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB1822864A GB1106367A (en) 1964-05-01 1964-05-01 Oriented polyarylsulphone film

Publications (1)

Publication Number Publication Date
GB1106367A true GB1106367A (en) 1968-03-13

Family

ID=10108849

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1822864A Expired GB1106367A (en) 1964-05-01 1964-05-01 Oriented polyarylsulphone film

Country Status (2)

Country Link
DE (1) DE1569060A1 (en)
GB (1) GB1106367A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4120931A (en) * 1976-05-27 1978-10-17 Sumitomo Chemical Company, Limited Method of manufacturing oriented amorphous aromatic polymeric films
RU2562651C2 (en) * 2012-10-23 2015-09-10 Открытое акционерное общество "Научно-исследовательский институт электронных материалов", (ОАО "НИИЭМ") Nanocomposite polyarylsulphonic film material

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4120931A (en) * 1976-05-27 1978-10-17 Sumitomo Chemical Company, Limited Method of manufacturing oriented amorphous aromatic polymeric films
RU2562651C2 (en) * 2012-10-23 2015-09-10 Открытое акционерное общество "Научно-исследовательский институт электронных материалов", (ОАО "НИИЭМ") Nanocomposite polyarylsulphonic film material

Also Published As

Publication number Publication date
DE1569060A1 (en) 1969-11-06

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