GB911485A - Textile treatment - Google Patents

Textile treatment

Info

Publication number
GB911485A
GB911485A GB382060A GB382060A GB911485A GB 911485 A GB911485 A GB 911485A GB 382060 A GB382060 A GB 382060A GB 382060 A GB382060 A GB 382060A GB 911485 A GB911485 A GB 911485A
Authority
GB
United Kingdom
Prior art keywords
groups
oxide
glycol
sulphonates
condensation
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
GB382060A
Inventor
William Baird
John Earnshaw
Gwilym Thomas Jones
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
Priority to NL260799D priority Critical patent/NL260799A/xx
Application filed by Imperial Chemical Industries Ltd filed Critical Imperial Chemical Industries Ltd
Priority to GB382060A priority patent/GB911485A/en
Publication of GB911485A publication Critical patent/GB911485A/en
Expired legal-status Critical Current

Links

Classifications

    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M13/00Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/322Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing nitrogen
    • D06M13/372Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing nitrogen containing etherified or esterified hydroxy groups ; Polyethers of low molecular weight

Landscapes

  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
  • Polyethers (AREA)

Abstract

Condensation products suitable for the antistatic treatment of textiles are produced by reacting a water-soluble polyamine, prepared from an alkylene oxide condensate of molecular weight within the range 200-1,000 and containing at least two primary amino groups and at least one polyalkylene oxide chain, with an organic compound containing two or more nitrogen alkylating groups attached to an organic radical which may be substituted by other groups and the main chain of which may be interrupted by not more than three ether oxygen atoms. The polyamines may be prepared by reacting alkylene oxide condensates having molecular weights of 200-1,000, e.g. polyethylene glycols, ethylene oxide condensates of polyhydroxy compounds such as glycerol, sorbitol or pentaerythritol, amines such as methylamines, ethylamine or cetylamine or amides or mixed ethylene oxide/propylene oxide or mixed ethylene oxide/butylene oxide condensates, with thionyl chloride and replacing the chlorine atoms by reaction with ammonia or with acrylonitrile and converting the products to amines by catalytic hydrogenation. The organic compounds containing two or more nitrogen-alkylating groups may be chlorides, bromides, iodides, sulphates, methane sulphonates, benzene sulphonates or p-toluene sulphonates of aliphatic polyhydroxy compounds, e.g. ethylene glycol, diethylene glycol, propylene glycol, hexamethylene glycol, glycerol or pentaerythritol.ALSO:Textiles, e.g. cellulose acetate, polyamides, polyethylene terephthalate and polyacrylonitrile fibres are rendered antistatic by treating them with a condensation product obtained from a water-soluble polyamine, prepared from an alkylene oxide condensate of molecular weight within the range 200-1000 and containing at least two primary amino groups and at least one polyalkylene oxide chain, by interaction of the polyamine with an organic compound containing two or more nitrogen-alkylating groups attached to an organic radical, which may be substituted by other groups and the main chain of which may be interrupted by not more than three ether oxygen atoms and then heating the textiles to a temperature of from 130 DEG to 210 DEG C. The polyamines may be prepared by reacting alkylene oxide condensates having molecular weights of 200-1000, e.g. polyethylene glycols, ethylene oxide condensates of polyhydroxy compounds such as glycerol, sorbitol or pentaerythritol, amines such as methylamine, ethylamine or cetylamine or amides or mixed ethylene oxide/propylene oxide or mixed ethylene oxide/butylene oxide condensates, with thionyl chloride and replacing the chlorine atoms by reaction with ammonia or with acrylonitrile and converting the products to amines by catalytic hydrogenation. The organic compounds containing two or more nitrogenalkylating groups may be chlorides, bromides, iodides, sulphates, methane sulphonates, benzene sulphonates or p-toluene sulphonates of aliphatic polyhydroxy compounds, e.g. ethylene glycol, diethylene glycol, propylene glycol, hexamethylene glycol, glycerol or pentaerythritol. The reaction between the polyamine and the alkylating agent may be effected in two stages, in the first stage partial condensation being achieved by reacting at a low temperature, by partially neutralising the amine before condensation with a volatile weak acid, e.g. acetic acid, or by using an alkylating agent in which the two alkylating groups are of different reactivities, e.g. 1-bromo-3-chloropropane or 2-chloroethyl-p-toluene sulphonate. The partially condensed material may then be applied to the textile material from aqueous or aqueousalcoholic solution or dispersion and the final stage of condensation carried out on the textile material itself. After application of the condensation product the textile material is dried and then heated to 130 DEG -210 DEG C. From 0.1 to 5% by weight of the condensation product is preferably applied to the textile material.
GB382060A 1960-02-03 1960-02-03 Textile treatment Expired GB911485A (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
NL260799D NL260799A (en) 1960-02-03
GB382060A GB911485A (en) 1960-02-03 1960-02-03 Textile treatment

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB382060A GB911485A (en) 1960-02-03 1960-02-03 Textile treatment

Publications (1)

Publication Number Publication Date
GB911485A true GB911485A (en) 1962-11-28

Family

ID=9765539

Family Applications (1)

Application Number Title Priority Date Filing Date
GB382060A Expired GB911485A (en) 1960-02-03 1960-02-03 Textile treatment

Country Status (2)

Country Link
GB (1) GB911485A (en)
NL (1) NL260799A (en)

Also Published As

Publication number Publication date
NL260799A (en)

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