GB565675A - Improvements in and relating to the manufacture and use of new textile assistants - Google Patents

Improvements in and relating to the manufacture and use of new textile assistants

Info

Publication number
GB565675A
GB565675A GB706/43A GB70643A GB565675A GB 565675 A GB565675 A GB 565675A GB 706/43 A GB706/43 A GB 706/43A GB 70643 A GB70643 A GB 70643A GB 565675 A GB565675 A GB 565675A
Authority
GB
United Kingdom
Prior art keywords
guanidinium
sulpho
salts
bis
treated
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
GB706/43A
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.)
Akzo Nobel UK PLC
Original Assignee
Courtaulds PLC
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 Courtaulds PLC filed Critical Courtaulds PLC
Priority to GB706/43A priority Critical patent/GB565675A/en
Publication of GB565675A publication Critical patent/GB565675A/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
    • D06M13/402Amides imides, sulfamic acids
    • D06M13/432Urea, thiourea or derivatives thereof, e.g. biurets; Urea-inclusion compounds; Dicyanamides; Carbodiimides; Guanidines, e.g. dicyandiamides
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C303/00Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides
    • C07C303/32Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of salts of sulfonic acids
    • 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
    • D06M13/248Treating 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 sulfur
    • D06M13/256Sulfonated compounds esters thereof, e.g. sultones
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06PDYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
    • D06P1/00General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
    • D06P1/44General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders
    • D06P1/62General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders using compositions containing low-molecular-weight organic compounds with sulfate, sulfonate, sulfenic or sulfinic groups

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Coloring (AREA)
  • Artificial Filaments (AREA)

Abstract

Guanidine or amino guanidine salts of sulphonated aliphatic dicarboxylic acids are prepared by reacting an alkali metal sulphonate of a dialkyl ester of an aliphatic dicarboxylic acid with guanidine or amino guanidine carbonate or bicarbonate. According to the proportions of reactants used, three salts are obtainable: guanidinium dialkyl-, bis-(guanidinium) mono-alkyl, or tris-(guanidinium)-sulpho dicarboxylate. The mono-guanidinium salts are readily soluble in water, alcohols, benzene, cyclohexanone, etc.; the bis-salts are more soluble in water and alcohols, but insoluble in the other solvents, whilst the tris-salts are only soluble in water. These compounds are wetting, dispersing, emulsifying and detergent agents. The mono- and bis-, and to a lesser extent, the tris-guanidinium salts are useful in producing soft finishes on textile materials; admixed with water-soluble urea-, thiourea- and melamine-formaldehyde condensates and applied to cellulosic textiles, they impart an improved soft resilient handle. In conjunction with formaldehyde, they impart wool-like dyeing properties to cellulosic textile material, the formaldehyde mixture or soluble condensate of the guanidinium salt being insolubilised in the fabric by heating to (say) 140 DEG C.; dyestuffs specified in this connection are acid wool, direct cotton, chrome, sulphur and vat (including solubilised vat dyestuffs, i.e. sulphuric ester salts of the leuco vat dyestuffs), aqueous dispersions of insoluble amino- and hydroxy-azo compounds and of insoluble amino- and acylamino-anthraquinones. Treatment of cellulosic textiles, dyed with direct cotton dyestuffs, with water-soluble condensates of the guanidinium salts and formaldehyde, followed by insolubisation improves the wash fastness of the dyeing. The mono- and bis-compounds also have good foaming properties. In examples: (1) the following salts are prepared: guanidinium dioctyl-, and dicetyl-sulpho succinates, and bis-(guanidinium) mono-butyl-, hexyl- and bis - (amino guanidinium) - octyl - sulpho succinates. (2) The treatment of all viscose satin fabric with an aqueous solution of bis-(guanidinium) octyl sulpho succinate results in fabric of a soft handle. (3) Viscose fabric is treated with a solution of guanidinium dicetyl sulpho dicarboxylate, a water-soluble urea-formaldehyde condensate, and ammonium sulphate, the fabric then being dried and heated at 140 DEG C. which renders it crease-resistant and of soft handle. (4) Viscose staple fibre treated with a solution of bis-(guanidinium) butyl sulpho succinate and formaldehyde, dried and heated at 140 DEG C., is dyed in a bath containing Solway blue BS and formic acid. (5) Viscose staple fibre is treated as in (4), but using the hexyl sulpho succinate and dyeing with Coomassie navy blue 2RNS, the dye solution also containing acetic acid and potassium dichromate. (6) All-viscose fabric is treated as in example (4), and dyed with Diphenyl fast red 7BL. (7) Viscose staple fibre is treated with the solution described in example (4) to which is added ammonium thiocyanate and after drying and heating, is dyed with a solution containing Eriochrome Azurol B (Geigy), potassium chromate and ammonium sulphate. (8) Viscose fibre treated as in example (7) is entered into a solution of Eriochrome black T and acetic acid, to which is added during dyeing, formic acid and then sodium dichromate. (9) Viscose fabric dyed with chlorazol fast red KS is treated with the solution described in example (4), and after drying and heating to 140 DEG C. has a soft handle and dye wash-fastness. (10) Viscose fabric dyed with Rigan sky blue 9 (Soc. Chem. Ind., Basle) is treated with a solution of the bis-(amino guanidinium) octyl sulpho succinate and formaldehyde dried and heated at 140 DEG C. (11) All viscose fabric dyed with Chlorantine fast blue 3GLL and treated with a solution of guanidinium dioctyl sulpho succinate, formaldehyde and ammonium sulphate is dried and heated; the fabric is soft, resilient and the dyeing is wash-fast. Other guanidinium salts mentioned are guanidinium dibutyl- and tris-(guanidinium)-sulpho succinates. Other dialkyl aliphatic sulpho dicarboxylates specified are the dialkyl esters of sulpho glutaric-, adipic-, pimelic-, suberic-, azelaic- and sebacic-acids.
GB706/43A 1943-01-14 1943-01-14 Improvements in and relating to the manufacture and use of new textile assistants Expired GB565675A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB706/43A GB565675A (en) 1943-01-14 1943-01-14 Improvements in and relating to the manufacture and use of new textile assistants

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB706/43A GB565675A (en) 1943-01-14 1943-01-14 Improvements in and relating to the manufacture and use of new textile assistants

Publications (1)

Publication Number Publication Date
GB565675A true GB565675A (en) 1944-11-22

Family

ID=9709116

Family Applications (1)

Application Number Title Priority Date Filing Date
GB706/43A Expired GB565675A (en) 1943-01-14 1943-01-14 Improvements in and relating to the manufacture and use of new textile assistants

Country Status (1)

Country Link
GB (1) GB565675A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2652348A (en) * 1950-07-21 1953-09-15 American Cyanamid Co Antistatic treatment of shaped articles comprising a vinyl resin and treated articles
US2675320A (en) * 1951-06-12 1954-04-13 American Cyanamid Co Coated pigment and mineral oil ink containing same
WO2002059382A1 (en) * 2001-01-26 2002-08-01 Clariant International Ltd Production of tanned leather and products suitable therefore
WO2016196555A1 (en) 2015-06-02 2016-12-08 Stepan Company Cold-water cleaning method
WO2017100051A2 (en) 2015-12-07 2017-06-15 Stepan Comapny Cold-water cleaning compositions and methods

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2652348A (en) * 1950-07-21 1953-09-15 American Cyanamid Co Antistatic treatment of shaped articles comprising a vinyl resin and treated articles
US2675320A (en) * 1951-06-12 1954-04-13 American Cyanamid Co Coated pigment and mineral oil ink containing same
WO2002059382A1 (en) * 2001-01-26 2002-08-01 Clariant International Ltd Production of tanned leather and products suitable therefore
US6991659B2 (en) 2001-01-26 2006-01-31 Clariant Finance (Bvi) Limited Production of tanned leather and products suitable therefore
KR100854236B1 (en) * 2001-01-26 2008-08-25 클라리언트 파이넌스 (비브이아이)리미티드 Production of tanned leather and salts and treatment agents therefor
WO2016196555A1 (en) 2015-06-02 2016-12-08 Stepan Company Cold-water cleaning method
WO2017100051A2 (en) 2015-12-07 2017-06-15 Stepan Comapny Cold-water cleaning compositions and methods

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