GB517631A - New water repellent agents - Google Patents

New water repellent agents

Info

Publication number
GB517631A
GB517631A GB2285038A GB2285038A GB517631A GB 517631 A GB517631 A GB 517631A GB 2285038 A GB2285038 A GB 2285038A GB 2285038 A GB2285038 A GB 2285038A GB 517631 A GB517631 A GB 517631A
Authority
GB
United Kingdom
Prior art keywords
phenylene
alcohols
compounds
dicarbamate
quaternary
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
GB2285038A
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 GB2285038A priority Critical patent/GB517631A/en
Priority to GB22852/38A priority patent/GB517632A/en
Priority to US28805939 priority patent/US2386141A/en
Publication of GB517631A publication Critical patent/GB517631A/en
Priority to US331189A priority patent/US2386142A/en
Priority to US609480A priority patent/US2431140A/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
    • D06M13/46Compounds containing quaternary nitrogen atoms
    • D06M13/461Quaternised amin-amides from polyamines or heterocyclic compounds or polyamino-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
    • D06M13/322Treating 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
    • D06M13/425Carbamic or thiocarbamic acids or derivatives thereof, e.g. urethanes

Landscapes

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

Abstract

517,631. Quaternary ammonium compounds; softening, waterproofing and anti-crease treatments for textiles. ROGERS, M. A. T., and IMPERIAL CHEMICAL INDUSTRIES, Ltd. Aug. 2, 1938, Nos. 22850/38, 22851/38, 7097/39 and 7099/39. [Classes 2 (iii) and 15 (ii)] [Also in Group VIII] Quaternary ammonium salts are made by combining with aliphatic or beterocyclic tertiary amines halogenmethyl compounds of the formula where R is an aliphatic radicle of at least 7 carbon atoms, A is a divalent organic radicle, and X is halogen- The halogenethyl compounds are made by causing the chloroformic ester of an alcohol R.OH (2 mols.) to react with a diamine NH2.A.NH 2 (1 mol.), whereby a dicarbamate of the formula RO.CO.NH.A.NH.CO.OR is formed which is then treated with a hydrogen halide or phosgene and formaldehyde or a polymer thereof, or with a dihalogenodimethyl ether, Alcohols of the formula R.OH include octyl, decyl, dodecyl, myristyl, cetyl, octadecenyl, octadecyl and ceryl alcohols, and mixtures of alcohols obtained by reduction of the acids of natural fats and oils, e.g. coconut oil, palm kernel oil or wool fat, alcohols obtainable by reduction of the esters of montanic acid or by hydrolysis of the mixed sulphuric esters obtained by sulphonation of polymerized lower olefines, and also alcohols which are likewise esters, e.g. #-hydroxyethyl stearate. A large number of suitable halogenomethyl compounds is specified, including those in which X=Cl or Br, and A=-CH2-, -CH2-CH2-, or a hexamethylene, o-, m- or p-phenylene,2-chloro- or 2-methoxy-1:4-phenylene, 6-methyl-1:3- phenylene, 1:5-naphthylene residue, or is two phenylene residues linked by an -S-, -SO-, or -CH2- group. The aliphatic or heterocyclic tertiary amines specified are trimethylamine, triethylamine, N:N<1>-tetramethylethylenediamine, dimethyl (or ethyl) cyclohexylamine, N-methylpiperidine, pyridine and alphapicoline. In examples : (1) di-octodecyl-pphenylene dicarbamate (made from octadecyl chloroformate and p-phenylenediamine) is treated with paraformaldehyde and hydrogen chloride, and the dichlormethyl compound obtained is combined with pyridine to form di-octodecyl-N:-Wdi-(N<1>-chloropyridinomethyl) p-phenylene dicarbamate ; similarly dipyridinium dichlorides may be made in which A is o- or m-phenylene, ethylene, hexamethylene, etc., or in which R is dodecyl, amd (2) the dichlormethyl compounds made from diocatadecyl - m - phenylenedicarbamate or dioctadecyl-ethylene-dicarbamate are combined with triethylamine, trimethylamine, or dimethylcyclohexylamine. The products may be used for softening or waterproofing textile materials of animal or vegetable origin, or composed of regenerated cellulose or cellulose esters or ethers, by impregnating the materials with the quaternary salts in solution or suspension in water or an organic liquid, the impregnated material being subsequently subjected to a short heat treatment to decompose the quaternary salt. Examples are given of the application of this process to calico, viscose, cellulose acetate and wool delaine fabrics. The quaternary salts may also be applied to natural or regenerated cellulose textile materials in conjunction with anti-creasing treatments, by treating the materials with a solution or suspension of the quaternary salt in water or an organic liquid before, simultaneously with, or after a treatment with a medium comprising a partly condensed resinous condensation product derived from an aldehyde and urea, thiourea or derivative thereof, or a phenol or an amino-1:35- triazine under neutral, acid or alkaline conditions, or with the components of such a resinous condensation product, followed by drying and finally by a short heat treatment to decompose the quaternary salt and insolubilize the resin. Examples are given of the application of this treatment to viscose and mercerized cotton fabrics. Specifications 291,473, 291,474, 304,900, [all in Class 2 (iii)], 431,703, 449,243, 458,877, 466,015, 466,817, 477,991, 485,198, 493,920, 495,025, 497,856, and 498,287 are referred to.
GB2285038A 1938-08-02 1938-08-02 New water repellent agents Expired GB517631A (en)

Priority Applications (5)

Application Number Priority Date Filing Date Title
GB2285038A GB517631A (en) 1938-08-02 1938-08-02 New water repellent agents
GB22852/38A GB517632A (en) 1938-08-02 1938-08-02 New organic nitrogen compounds
US28805939 US2386141A (en) 1938-08-02 1939-08-02 Process of treating textile materials
US331189A US2386142A (en) 1938-08-02 1940-04-23 Quaternary ammonium salts and process of making the same
US609480A US2431140A (en) 1938-08-02 1945-08-04 Dicarbamates and process of making the same

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB2285038A GB517631A (en) 1938-08-02 1938-08-02 New water repellent agents

Publications (1)

Publication Number Publication Date
GB517631A true GB517631A (en) 1940-02-05

Family

ID=10186047

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2285038A Expired GB517631A (en) 1938-08-02 1938-08-02 New water repellent agents

Country Status (1)

Country Link
GB (1) GB517631A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE943944C (en) * 1940-07-20 1956-06-07 Ciba Geigy Process for the production of new condensation products

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE943944C (en) * 1940-07-20 1956-06-07 Ciba Geigy Process for the production of new condensation products

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