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GB1118876A - Improvements in the treatment of synthetic polyester shaped articles - Google Patents

Improvements in the treatment of synthetic polyester shaped articles

Info

Publication number
GB1118876A
GB1118876A GB3160564A GB3160564A GB1118876A GB 1118876 A GB1118876 A GB 1118876A GB 3160564 A GB3160564 A GB 3160564A GB 3160564 A GB3160564 A GB 3160564A GB 1118876 A GB1118876 A GB 1118876A
Authority
GB
United Kingdom
Prior art keywords
polymeric compound
weight
polyoxyalkylene
bis
polyester
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
GB3160564A
Inventor
William Michael Corbett
Joan Lesley Carrington
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 GB3160564A priority Critical patent/GB1118876A/en
Publication of GB1118876A publication Critical patent/GB1118876A/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
    • D06M13/244Treating 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 sulfur or phosphorus
    • D06M13/282Treating 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 sulfur or phosphorus with compounds containing phosphorus
    • D06M13/292Mono-, di- or triesters of phosphoric or phosphorous acids; Salts thereof

Landscapes

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

Abstract

A composition suitable for treating filaments, fibres, fabrics and films made from a synthetic, essentially linear, crystalline polyester containing an optical brightener, comprises an aqueous dispersion containing a water-insoluble, cocrystallizable polymeric compound which is a copolyester containing at least one polyoxyalkylene group and sufficient repeat units identical with those forming the crystalline portions of the polyester from which the treated materials are made to confer crystallizability on the copolymer, 0.2-1% by weight based on the weight of the polymeric compound of a hindered phenol antioxidant and 0.2-2% by weight base on the weight of the polymeric compound of a compound A having the formula <FORM:1118876/C3/1> , <FORM:1118876/C3/2> , <FORM:1118876/C3/3> and <FORM:1118876/C3/4> in which R, R1, R2, R3 and R4 are alkyl or aryl groups or are such that RH, R1H, R2H, R3H groups or are such that RH, R1H, R2H, R3H and R4H are plyalkylene glycols, or being dipropylene glycol pentol triphosphite having the formula <FORM:1118876/C3/5> The hindered phenol may be 2,4-dimethyl - 6-a -methylcyclohexylphenol, 2,6-ditertiarybutyl 2,6-ditertiarybutyl 4 - methylphenol, bis - (2 - hydroxy - 3 - a - methylcyclohexyl - 5 - methyl phenyl) - methane or bis - (3 - methyl - 6 - tert. - butylphenol) 4,41disulphide and suitable phosphorus compounds are di-isodecylphenyl phosphite, dioctadecylpentaerythritol disphosphite, tris-dipropyleneglycol phosphate, dipropylene glycolpentol triphosphite and tris-dipropylene glycol phosphite. The polyoxyalkylene glycol group of the co-crystallizable polymeric compound may be derived from a polyoxyalkylene glycol having an average molecular weight of 300 or above and the relative viscosity of the co-crystallizable polymeric compound containing at least one polyoxyalkylene as measured in a 1% by weight solution in orthochlorophenol at 25 DEG C. may be not less than 1.1.ALSO:Filaments, fibres and fabrics made from a synthetic, essentially linear, crystalline polyester containing an optical brightener are rendered hydrophilic and antistatic by treating them with an aqueous dispersion containing a water insoluble, co-crystallisable polymeric compound which is a copolymer containing at least one polyoxyalkylene group and sufficient repeat units identical with those forming the crystalline portions of the polyester from which the treated materials are made to confer crystallisability on the copolymer, 0.2-1% by weight based on the weight of the polymeric compound of a hindered phenol antioxidant and 1.2-2% by weight based on the weight of the polymeric compound of a compound A having the formula <FORM:1118876/D1-D2/1> <FORM:1118876/D1-D2/2> <FORM:1118876/D1-D2/3> in which R, R1, R2, R3 and R4 are alkyl or aryl groups or are such that RH, R1H, R2H, R3H and R4H are polyalkylene glycols, or being dipropylene glycol pentol triphosphite having the formula <FORM:1118876/D1-D2/4> and then heating them at a temperature above 90 DEG C. The optical brightener, e.g. 1:2-bis (6 - methyl benzoxazol - 2 - yl) ethylene, 2:5 - bis (tert. butyl - benzoxazol - 2 - yl) thiophene, 2 - cyano - 4 - naphthotriazoyl - 41 - chloro stilbene and 3\sv - methylpyrazol - 1\sv - yl - 3 - phenylcoumarin, may be added to the starting materials or to the final polyester or may be applied to the materials treated during or after formation. The hindered phenol may be 2, 4 - dimethyl - 6 - a - methylcyclohexylphenol, 2, 6 - ditertiarybutyl - 4 - methylphenol, bis (2 - hydroxy - 3 - a - methylcyclohexyl - 5 -methyl phenyl) - methane or bis (3 - methyl - 6 - tert. butylphenol) - 4 4\sv - disulphide and suitable phosphorus compounds are di-isodecylphenyl phosphite, dioctadecyl pentaerythritol disphosphite, tris - dipropyleneglycol phosphite, dipropylene glycolpentol triphosphite and tris - dipropylene glycol phosphite. The polyoxyalkylene glycol group of the co-crystallisable polymeric compound may be derived from a polyoxyalkylene glycol having an average molecular weight of 300 or above and the viscosity ratio of the cocrystallisable polymeric compound containing at least one polyoxyalkylene as measured in a 1% by weight solution in orthochlorophenol at 25 DEG C may be not less than 1.1. Polyester fibres alone or in admixture with cotton, wool or regenerated cellulose fibres may be treated.
GB3160564A 1964-08-04 1964-08-04 Improvements in the treatment of synthetic polyester shaped articles Expired GB1118876A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB3160564A GB1118876A (en) 1964-08-04 1964-08-04 Improvements in the treatment of synthetic polyester shaped articles

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB3160564A GB1118876A (en) 1964-08-04 1964-08-04 Improvements in the treatment of synthetic polyester shaped articles

Publications (1)

Publication Number Publication Date
GB1118876A true GB1118876A (en) 1968-07-03

Family

ID=10325645

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3160564A Expired GB1118876A (en) 1964-08-04 1964-08-04 Improvements in the treatment of synthetic polyester shaped articles

Country Status (1)

Country Link
GB (1) GB1118876A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2058329A1 (en) * 1969-08-16 1971-05-28 Toho Chem Ind Co Ltd
EP0475907A3 (en) * 1990-09-14 1992-04-22 Ciba-Geigy Ag Compound and process for the production of good quality moulded articles
WO2005097810A1 (en) * 2004-03-26 2005-10-20 E.I. Dupont De Nemours And Company Alkoxylated phosphite ester and process therefor

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2058329A1 (en) * 1969-08-16 1971-05-28 Toho Chem Ind Co Ltd
EP0475907A3 (en) * 1990-09-14 1992-04-22 Ciba-Geigy Ag Compound and process for the production of good quality moulded articles
WO2005097810A1 (en) * 2004-03-26 2005-10-20 E.I. Dupont De Nemours And Company Alkoxylated phosphite ester and process therefor
US7138356B2 (en) 2004-03-26 2006-11-21 E. I. Du Pont De Nemours And Company Alkoxylated phosphite ester and process therefor

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