GB571919A - Processes for waterproofing cellulose fibres and the resulting products - Google Patents

Processes for waterproofing cellulose fibres and the resulting products

Info

Publication number
GB571919A
GB571919A GB10048/43A GB1004843A GB571919A GB 571919 A GB571919 A GB 571919A GB 10048/43 A GB10048/43 A GB 10048/43A GB 1004843 A GB1004843 A GB 1004843A GB 571919 A GB571919 A GB 571919A
Authority
GB
United Kingdom
Prior art keywords
acid
solution
chloromethyl
formaldehyde
acetate
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
GB10048/43A
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.)
Novartis AG
National Starch and Chemical Investment Holding Corp
Original Assignee
JR Geigy AG
National Starch and Chemical Investment Holding Corp
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 JR Geigy AG, National Starch and Chemical Investment Holding Corp filed Critical JR Geigy AG
Publication of GB571919A publication Critical patent/GB571919A/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
    • D06M15/00Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/37Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/39Aldehyde resins; Ketone resins; Polyacetals
    • D06M15/423Amino-aldehyde resins
    • 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
    • D06M15/00Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/37Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/39Aldehyde resins; Ketone resins; Polyacetals

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)

Abstract

Cellulose fibres or textile materials formed thereof are waterproofed by treatment in an acid solution of a water-soluble condensation product of a compound of the urea or guanidine group which contains either the group =N-CO-N= or =N-C(NH)-N= and formaldehyde, the acid solution also containing a salt of a metal of the 2nd, 3rd or 4th group of the periodic system, rendering the resin insoluble on the fibre by heating to a high temperature, and after-treating with a water-soluble salt of a carboxylic acid containing a high molecular aliphatic or alicyclic residue with more than 11 carbon atoms. The salt of the carboxylic acid may be included in the impregnating bath. A carboxylic acid or a derivative thereof may be added. Compounds of the urea or guanidine group specified are dicyandiamide, cyanurea, dicyandiamidine, biguanides, biurets, and melamine. High-molecular carboxylic acids specified are lauric, stearic, cocoanut fatty acids, tallow-grease, 4-stearoylamino-l-hydroxybenzene-2-carboxylic acid, 4-stearoylamino-l-mercaptobenzene-2-carboxylic acid, 1-hydroxy-2-carboxylic acid stearophenone, 5-octadecylhydroxy-methyl-2-hydroxybenzoic acid, 5 - octadecylhydroxy - methyl-o-cresotinic acid, 3 : 5-di-(octadecylhydroxymethyl) - 2 - hydroxybenzoic acid, the reaction products of ethyloctadecyl aniline and chloromethylene salicylic acid, of p-hydroxy-methyl-o-cresotinic acid and ethyloctadecyl aniline, of o-chloromethyl-p-cresotinic acid and ethyloctadecylaniline, of o:p-di-(chloromethyl)-salicylic acid and ethyloctadecyl aniline, of p-chloromethyl-o-cresotinic acid and octadecyl-anthranilic acid, of o:p-di-(chloromethyl)-salicylic acid and octadecylanthranilic acid, of chloromethylsalicylic acid and as - diethyl - stearoyl-p-phenylenediamine, of chloromethyl-salicylic acid and p-dimethylamino-benzyl-N-stearoylamine, of chloromethyl-salicylic acid and p - ethylbenzylamino - benzyl - N - stearoylamine, and of chloromethyl-salicylic acid and 2 - heptadecyl - benzimidazole. Aluminium, barium, zirconium, copper, lead, tin, zinc, and mercury salts may be used. Carboxylic acids specified are benzoic, o- and p-chlorobenzoic, toluylic, o - benzoylbenzoic, o - (p1 - chloro - or methyl - benzoyl) - benzoic, sulphobenzoic, sulphosalicylic, sulphophthalic, resorcylic, cresotinic, maleic, and phthalic acids. In example 1, dicyandiamine or cyanurea is heated with formaldehyde, acetic acid, and water for 4-5 hours on a water bath, and regenerated cellulose fibre is treated with an aqueous solution of this condensation product and aluminium acetate, thoroughly squeezed, dried, and after-treated with a soap solution. In example 2, dicyandiamidine sulphate is refluxed with formaldehyde and sodium acetate, aluminium acetate solution is added, and regenerated cellulose fibre is foularded twice cold in the solution, dried, rinsed, treated with a soap solution, centrifuged and dried. Aluminium acetate may be replaced by calcium chloride, strontium nitrate, barium chloride, magnesium chloride, or zinc chloride, and the soap solution by a solution of the sodium salt of 4-stearoylamino-l-of one of the high-molecular carboxylic acids previously specified. In example 3, biguanide sulphate is refluxed with formaldehyde and sodium acetate, aluminium acetate (or zirconium oxychloride, copper acetate, or tin chloride) solution is added, and regenerated cellulose fibre is foularded twice cold in the solution, hot dried, soaked, soaped and finished. Alternatively, the soap solution or a solution of the sodium salt of the high-molecular carboxylic acid may be added to the impregnation bath. In example 4, dicyandiamide is refluxed with formaldehyde, formic acid, and benzoic acid, aluminium acetate solution is added, and cotton fabric is soaked in the solution, rinsed, centrifuged, soaped, rinsed, centrifuged, and dried. Specifications 511,102, 517,337 and 526,550 are referred to.
GB10048/43A 1942-06-23 1943-06-22 Processes for waterproofing cellulose fibres and the resulting products Expired GB571919A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH571919X 1942-06-23

Publications (1)

Publication Number Publication Date
GB571919A true GB571919A (en) 1945-09-14

Family

ID=4520965

Family Applications (1)

Application Number Title Priority Date Filing Date
GB10048/43A Expired GB571919A (en) 1942-06-23 1943-06-22 Processes for waterproofing cellulose fibres and the resulting products

Country Status (3)

Country Link
CH (4) CH231697A (en)
FR (2) FR895776A (en)
GB (1) GB571919A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE967187C (en) * 1942-07-31 1957-10-17 American Cyanamid Co Process for making paper with improved wet strength
DE3500408A1 (en) * 1985-01-08 1986-07-10 Skw Trostberg Ag, 8223 Trostberg METHOD FOR THE PRODUCTION OF PAPER, CARDBOARD, PAPERBOARDS AND OTHER MATERIALS CONTAINING CELLULOSE UNDER NEUTRAL TO LOW BASIC PH CONDITIONS

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1034858B (en) * 1952-03-18 1958-07-24 Jacques Wolf & Co Process for the production of a resin from dicyandiamide and formaldehyde which is stable in aqueous solution and does not gel
DE1040236B (en) * 1952-11-14 1958-10-02 Lucien Sellet Process for the production of water-soluble, modified aminoplast resins

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE967187C (en) * 1942-07-31 1957-10-17 American Cyanamid Co Process for making paper with improved wet strength
DE3500408A1 (en) * 1985-01-08 1986-07-10 Skw Trostberg Ag, 8223 Trostberg METHOD FOR THE PRODUCTION OF PAPER, CARDBOARD, PAPERBOARDS AND OTHER MATERIALS CONTAINING CELLULOSE UNDER NEUTRAL TO LOW BASIC PH CONDITIONS

Also Published As

Publication number Publication date
CH231697A (en) 1944-04-15
CH237722A (en) 1945-05-15
CH233160A (en) 1944-07-15
CH236680A (en) 1945-02-28
FR895775A (en) 1945-02-02
FR895776A (en) 1945-02-02

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