GB1455667A - Insoluble and infusible cured phenol-aldehyde resin fibres and production thereof - Google Patents

Insoluble and infusible cured phenol-aldehyde resin fibres and production thereof

Info

Publication number
GB1455667A
GB1455667A GB2387274A GB2387274A GB1455667A GB 1455667 A GB1455667 A GB 1455667A GB 2387274 A GB2387274 A GB 2387274A GB 2387274 A GB2387274 A GB 2387274A GB 1455667 A GB1455667 A GB 1455667A
Authority
GB
United Kingdom
Prior art keywords
fibres
aqueous
phenol
pva
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
GB2387274A
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.)
Japan Exlan Co Ltd
Original Assignee
Japan Exlan 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
Priority claimed from JP6010373A external-priority patent/JPS5634648B2/ja
Priority claimed from JP13149773A external-priority patent/JPS5082314A/ja
Priority claimed from JP13291673A external-priority patent/JPS5127776B2/ja
Priority claimed from JP13291573A external-priority patent/JPS5127775B2/ja
Priority claimed from JP13911673A external-priority patent/JPS5088327A/ja
Priority claimed from JP13911573A external-priority patent/JPS5128732B2/ja
Application filed by Japan Exlan Co Ltd filed Critical Japan Exlan Co Ltd
Publication of GB1455667A publication Critical patent/GB1455667A/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
    • C08G8/00Condensation polymers of aldehydes or ketones with phenols only
    • C08G8/38Block or graft polymers prepared by polycondensation of aldehydes or ketones onto macromolecular compounds
    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01FCHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F6/00Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
    • D01F6/88Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from mixtures of polycondensation products as major constituent with other polymers or low-molecular-weight compounds
    • D01F6/94Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from mixtures of polycondensation products as major constituent with other polymers or low-molecular-weight compounds of other polycondensation products

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Chemical Or Physical Treatment Of Fibers (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
  • Artificial Filaments (AREA)

Abstract

1455667 Phenol-aldehyde resin fibres JAPAN EXLAN CO Ltd 29 May 1974 [29 May 1973 22 Nov 1973 26 Nov 1973 (2) 11 Dec 1973 (2)] 23872/74 Heading B5B [Also in Division C3] Insoluble and infusible, flame retardant phenol-aldehyde resin fibres are produced by curing fibres comprising 30-98% wt. of a crosslinkable phenol-aldehyde resin and 70-2% wt. of a water-soluble polymer (PVA) containing at least 50 mol. per cent of vinyl alcohol units. The phenol-aldehyde resin may be a resol or a mixture of a resol and a novolac resin. The PVA polymer preferably has a degree of polymerization of 500-2500 and may be prepared by hydrolysis of polyvinyl acetate or a copolymer of vinyl acetate, or by etherification, esterification or formalization of a part of the hydroxyl groups of the vinyl alcohol polymer thus obtained. The fibres are produced by first preparing an aqueous solution consisting of the cross-linkable phenol-aldehyde resin and PVA in the above percentage amounts, wet-spinning the aqueous solution and then curing the wetspun fibres, generally by heating above 60‹ C. and/or by acid treatment and/or by treatment with an acid and aldehyde. The aqueous solution is spun into an aqueous coagulating bath preferably containing at least one of the following coagulants: (NH 4 ) 2 SO 4 , Na 2 SO 4 , K 2 SO 4 , ZnSO 4 , CuSO 4 , FeSO 4 , MgSO 4 , (Al) 2 (SO 4 ) 3 , NH 4 NO 3 , NaNO 3 , KNO 3 , Al(NO 3 ) 3 , NaCl, KCl, Na 3 PO 4 , aluminium potassium sulphate, potassium bichromate and potassium citrate; and optionally at least one boron compound capable of forming boric ester bonds with the hydroxyl groups of the phenol/aldehyde resin and/or PVA, e.g. boric acid, metaboric acid, boron oxide, borates and metaborates; and optionally at least one reducing compound, e.g. sulphites, bisulphites, hydrosulphite, thiosulphate, bisulphite addition compounds of HCHO, hydroxylamine and stannous chloride. The coagulating bath is preferably made acid by addition of an inorganic and/or organic acid. In general the wet-spun fibres may be treated before or after curing with an inorganic and/or organic acid, or with an aqueous acidic solution containing either a boron compound or a reducing compound, which improves the colour of the fibres. In Examples 1-7 aqueous solutions of PVA having a degree of saponification of 78-99À9 mol. per cent and a degree of polymerization of 1750 and phenol-HCHO resol resin alone or in admixture with a phenol- HCHO novolac are wet-spun into aqueous coagulating baths containing Na 2 SO 4 and either boric acid or borax or potassium metaborate and optionally H 2 SO 4 . The fibres obtained are cold-drawn, heat-treated, washed and dried, and then cured by heating. In Examples 8, 9 aqueous solutions of the resol and PVA are wet spun into aqueous baths containing Na 2 SO 4 , H 2 SO 4 and either sodium hydrogen sulphite or hydrosulphite. In Examples 10, 11 and 14 aqueous solutions of the resol resin and PVA are wet spun into aqueous baths of NaS 2 O 4 , H 2 SO 4 and boric acid and the resulting fibres are cold-drawn and then crosslinked by heating. The cured fibres are then either treated with any of the following acids: H 2 SO 4 , benzoic, acetic, succinic, lactic, oxalic, maleic, malonic, H 3 PO 4 , or HCl, or are treated with an aqueous solution of boric acid or sodium borate. In Examples 12, 13 the uncured fibres of Example 10 are either treated with an aqueous solution of Na 2 SO 4 and H 2 SO 4 and then cured or are first cured by heating and then treated with aqueous p-toluene sulphonic acid. In Example 17 the crosslinked fibres of Example 10 are treated with aqueous solutions of any of the following reducing compounds: NaHSO 3 , Na 2 S 2 O 4 , SnCl 2 or with aqueous HCl alone and together with NaHSO 3 .
GB2387274A 1973-05-29 1974-05-29 Insoluble and infusible cured phenol-aldehyde resin fibres and production thereof Expired GB1455667A (en)

Applications Claiming Priority (6)

Application Number Priority Date Filing Date Title
JP6010373A JPS5634648B2 (en) 1973-05-29 1973-05-29
JP13149773A JPS5082314A (en) 1973-11-22 1973-11-22
JP13291673A JPS5127776B2 (en) 1973-11-26 1973-11-26
JP13291573A JPS5127775B2 (en) 1973-11-26 1973-11-26
JP13911673A JPS5088327A (en) 1973-12-11 1973-12-11
JP13911573A JPS5128732B2 (en) 1973-12-11 1973-12-11

Publications (1)

Publication Number Publication Date
GB1455667A true GB1455667A (en) 1976-11-17

Family

ID=27550773

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2387274A Expired GB1455667A (en) 1973-05-29 1974-05-29 Insoluble and infusible cured phenol-aldehyde resin fibres and production thereof

Country Status (1)

Country Link
GB (1) GB1455667A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103409841A (en) * 2013-07-30 2013-11-27 中原工学院 Preparation method of boric acid modified high-ortho phenolic fiber
US8765829B2 (en) 2005-09-08 2014-07-01 Kingspan Holdings (Irl) Limited Phenolic foam
CN109183187A (en) * 2018-07-27 2019-01-11 中原工学院 A method of the high ortho phenolic fiber of boron modification is prepared using wet spinning
CN109208115A (en) * 2018-07-27 2019-01-15 中原工学院 A method of epoxy-modified high ortho position thermosetting phenolic fiber is prepared using wet spinning
CN109208116A (en) * 2018-07-27 2019-01-15 中原工学院 A method of high ortho position thermosetting phenolic fiber is prepared using wet spinning

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8765829B2 (en) 2005-09-08 2014-07-01 Kingspan Holdings (Irl) Limited Phenolic foam
CN103409841A (en) * 2013-07-30 2013-11-27 中原工学院 Preparation method of boric acid modified high-ortho phenolic fiber
CN103409841B (en) * 2013-07-30 2015-11-04 中原工学院 The preparation method of boric acid modified high ortho phenolic fiber
CN109183187A (en) * 2018-07-27 2019-01-11 中原工学院 A method of the high ortho phenolic fiber of boron modification is prepared using wet spinning
CN109208115A (en) * 2018-07-27 2019-01-15 中原工学院 A method of epoxy-modified high ortho position thermosetting phenolic fiber is prepared using wet spinning
CN109208116A (en) * 2018-07-27 2019-01-15 中原工学院 A method of high ortho position thermosetting phenolic fiber is prepared using wet spinning
CN109208116B (en) * 2018-07-27 2021-03-16 中原工学院 Method for preparing high-ortho thermosetting phenolic fiber by adopting wet spinning

Also Published As

Publication number Publication date
DE2425558B2 (en) 1976-07-15
DE2425558A1 (en) 1974-12-19

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Legal Events

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