GB1430867A - Infusible and insoluble styrene fibres - Google Patents

Infusible and insoluble styrene fibres

Info

Publication number
GB1430867A
GB1430867A GB1829973A GB1829973A GB1430867A GB 1430867 A GB1430867 A GB 1430867A GB 1829973 A GB1829973 A GB 1829973A GB 1829973 A GB1829973 A GB 1829973A GB 1430867 A GB1430867 A GB 1430867A
Authority
GB
United Kingdom
Prior art keywords
cross
ethylene
styrene
group
fibres
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
GB1829973A
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.)
Kanebo Ltd
Original Assignee
Kanebo 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 Kanebo Ltd filed Critical Kanebo Ltd
Publication of GB1430867A publication Critical patent/GB1430867A/en
Expired legal-status Critical Current

Links

Classifications

    • D—TEXTILES; PAPER
    • D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F6/00—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
    • D01F6/28—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from copolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D01F6/42—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from copolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds comprising cyclic compounds containing one carbon-to-carbon double bond in the side chain as major constituent
    • D—TEXTILES; PAPER
    • D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F11/00—Chemical after-treatment of artificial filaments or the like during manufacture
    • D01F11/04—Chemical after-treatment of artificial filaments or the like during manufacture of synthetic polymers
    • D01F11/06—Chemical after-treatment of artificial filaments or the like during manufacture of synthetic polymers of macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Artificial Filaments (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
  • Optical Fibers, Optical Fiber Cores, And Optical Fiber Bundles (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

1430867 Cross - linked polymer fibres KANEBO KK 16 April 1973 [14 April 1972] 18299/73 Heading B5B [Also in Division C3] Insoluble, infusible fibres are produced by melt-spinning under a non-oxidizing atmosphere a copolymer of molecular weight 4000 to 500,000 of styrene and an olefinically unsaturated compound in which the molar ratio of styrene to the unsaturated compound is from 99 : 1 to 20 : 80, and then cross-linking the fibres. The olefinically unsaturated compound has at least one functional group which is a halogen atom or a haloalkyl, amino, carboxyl, esterified carboxyl, haloformyl, hydroxyl, amido (ineluding sulphonamido and n-methylamido) or nitrile group. The preferred compounds have either the formula or the formula where R<SP>1</SP> is a hydrogen or halogen atom, a C 1 -C 4 alkyl group, a carboxyl or an esterified carboxyl group; R<SP>2</SP> is a hydrogen atom, a C 1 -C 4 alkyl group or phenyl; X is a functional group as defined above; n is 0 or 1 and m is 1, 2 or 3. The cross-linking agent is applied from a solution which contains from 0À5 to 60% by weight. Its exact nature is selected to accord with the nature of the functional group, and lists of suitable types of agent are given for each group. In the examples the comonomers are mixed o- and p-chioromethylstyrene (cross-linked by pyridine, ethylene diamine and hydroxylamine hydrochloride, diethylamine, disodium ethylene glycol, tetrakis (hydroxy methyl) phosphonium chloride, sodium oxalate, sodium sulphide and hexamethylene diamine), acrylamide (crosslinked by formaldehyde and oxalic acid), paminomethyl styrene (cross-linked by ethylene dibromide, formaldehyde, tolylene diisocyanate and terephthalic acid dichloride), methacrylic acid (ethylene glycol bisglycidyl ether, ethylene dibromide and ethylene diamine), p-hydroxymethyl styrene (xylylene diisocyanate, adipic acid dichloride), allyl alcohol (diphenylmethane diisocyanate), acrylic acid chloride (ethylene diamine, disodium ethylene glycol), methyl methacrylate (disodium ethylene glycol and ethylene diamine), vinyl chloride (ethylene diamine) and vinylidene chloride (ethylene dithioglycol). After spinning the polymer is drawn, if required, then cross-linked, by immersion in a bath of the appropriate reagent, which bath may optionally contain a swelling agent.
GB1829973A 1972-04-14 1973-04-16 Infusible and insoluble styrene fibres Expired GB1430867A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP47037898A JPS5119047B2 (en) 1972-04-14 1972-04-14

Publications (1)

Publication Number Publication Date
GB1430867A true GB1430867A (en) 1976-04-07

Family

ID=12510346

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1829973A Expired GB1430867A (en) 1972-04-14 1973-04-16 Infusible and insoluble styrene fibres

Country Status (4)

Country Link
JP (1) JPS5119047B2 (en)
DE (1) DE2318851C3 (en)
FR (1) FR2180118B1 (en)
GB (1) GB1430867A (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1500541A (en) * 1975-03-20 1978-02-08 Mullard Ltd Method of producing positive-working electron resist coatings
JPS53112845U (en) * 1977-02-17 1978-09-08
JPH0275186A (en) * 1988-09-09 1990-03-14 Hitachi Ltd Sheath heater fitting structure

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IT649942A (en) * 1960-05-11

Also Published As

Publication number Publication date
JPS5119047B2 (en) 1976-06-15
DE2318851C3 (en) 1975-08-14
FR2180118B1 (en) 1977-12-30
JPS49524A (en) 1974-01-07
FR2180118A1 (en) 1973-11-23
DE2318851A1 (en) 1973-10-25
DE2318851B2 (en) 1975-01-02

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Legal Events

Date Code Title Description
PS Patent sealed
PCNP Patent ceased through non-payment of renewal fee