GB758937A - Method for rendering polyacrylonitrile filaments and other articles readily dyeable - Google Patents

Method for rendering polyacrylonitrile filaments and other articles readily dyeable

Info

Publication number
GB758937A
GB758937A GB31158/53A GB3115853A GB758937A GB 758937 A GB758937 A GB 758937A GB 31158/53 A GB31158/53 A GB 31158/53A GB 3115853 A GB3115853 A GB 3115853A GB 758937 A GB758937 A GB 758937A
Authority
GB
United Kingdom
Prior art keywords
chloride
dyes
dye
vinyl
phosphonium
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
GB31158/53A
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.)
Dow Chemical Co
Original Assignee
Dow Chemical Co
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 Dow Chemical Co filed Critical Dow Chemical Co
Publication of GB758937A publication Critical patent/GB758937A/en
Expired legal-status Critical Current

Links

Classifications

    • 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
    • D06P3/00Special processes of dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form, classified according to the material treated
    • D06P3/70Material containing nitrile groups
    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01FCHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F6/00Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
    • D01F6/02Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D01F6/18Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds from polymers of unsaturated nitriles, e.g. polyacrylonitrile, polyvinylidene cyanide
    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01FCHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F6/00Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
    • D01F6/28Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from copolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D01F6/38Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from copolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds comprising unsaturated nitriles as the major constituent

Landscapes

  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Toxicology (AREA)
  • Artificial Filaments (AREA)
  • Coloring (AREA)

Abstract

Filaments, films, rods, tubes, and similar articles of acrylonitrile polymers containing at least 85 per cent of acrylonitrile in the polymer molecule are obtained with good dyeing affinities by spinning an aqueous saline solution of the polymer into an aqueous coagulant, stretching the formed articles, freeing them from salts, and incorporating in them while they are in the aquagel condition at any stage before drying, at least 1 per cent of their dry weight of a dye assistant which is soluble in water and is either an amine salt, a quaternary ammonium salt, a sulphonium salt, a phosphonium halide, or a polymer of a N-vinyl derivative of a carboxylic acid amide or lactam. The dye assistant may be introduced into the coagulated and still swollen spun product before or after partial orientation. The products may be dyed with various kinds of dyes, e.g. with dyes commonly used for dyeing wool, cotton, silk, viscose or acetate rayon, or nylon. Numerous examples of suitable dye assistants are specified, including as water-soluble amine salts: octadecyl ammonium chloride, N - 2 - [2 - (2,2,3,3 - tetramethylbutyl phenoxy) - ethoxy]ethyl - N,N - dimethyl ammonium chloride, 2-n-nonyl pyridine hydrochloride, and 2-heptadecyl-3-butyl glyoxalidine hydrochloride; as quaternary ammonium salts: n-dodecylbenzyl trimethyl ammonium chloride, 2 - hydroxyethyl - n - octadecyl - dimethyl ammonium bromide, benzyl-2-[2-(2,3,4,6-tetrachlorophenoxy) - ethoxy] ethyl morpholinium chloride, n-hexadecyl pyridinium chloride, n-dodecyl isoquinolinium bromide, bis-(polyoxyethylene oleate)-ethyl methyl ammonium ethosulphate, pentamethylene bis-(n-dodecyl dimethyl ammonium chloride), and dimethyl 2-hydroxyethyl stearamidopropyl ammonium chloride; as water-soluble sulphonium salts: n-dodecyl dimethyl sulphonium chloride, bromide, or methosulphate, di-(2-hydroxyethyl)-methyl sulphonium methosulphate di-capric ester, and n-dodecyl 2-chloroethyl methyl sulphonium 2-chloroethyl sulphate; as phosphonium halides: cetyl trimethyl phosphonium chloride, benzyl n-dodecyl dimethyl phosphonium bromide, benzyl cetyl dimethyl phosphonium iodide, and dichlorobenzyl triphenyl phosphonium chloride; and as water-soluble polymers of N-vinyl derivatives of carboxylic acid amides or lactams: N-vinyl a -pyrrolidone, N-vinyl N-methyl (or ethyl) formamide (or acetamide), and N-vinyl capro (or valero) lactam. The undried fibres or other articlse may be soaked in a solution of the dye assistant at a pH of 1-8 at temperatures below 10 DEG C. up to 100 DEG C. The treated and subsequently dried materials may be dyed with direct cotton dyes, azoic dyes, vat dyes, soluble vat dyes; acid, acid-mordant, and basic dyes; and acetate dyes. In an example, a water-swollen unstretched tow, formed by extrusion of a saline solution of polyacrylonitrile into an aqueous coagulating bath, is soaked in a solution of dodecyl trimethyl ammonium chloride and then stretched and dried. The tow is dyed in a hot bath containing Pontamine Green and sodium sulphate. In another example, the tow is impregnated with the dye assistant after the stretching and before drying. It is then dyed in a bath containing Sulphanthrene Red, caustic soda, and sodium hydrosulphite, the dye being developed by treatment of the impregnated tow with a solution of hydrogen peroxide.ALSO:For improving the dyeing affinities of filaments, films, rods, tubes, and similar articles of acrylonitrile polymers containing at least 85 per cent of acrylonitrile in the polymer into an aqueous coagulant and spinning an aqueous saline solution of the polymer into an aqueous coagulate and which are stretched, washed, and subsequently dried, there is applied to the articles while they are in an aquagel condition at any stage before drying, at least 1 per cent of their dry weight of a dye assistant which is soluble in water and is either an amine salt, a quaternary ammonium salt, a sulphonium salt, a phosphonium halide, or a polymer of a N-vinyl derivative of a carboxylic acid amide or lactam. The articles may be dyed with various kinds of dyes, e.g. with dyes commonly used for dyeing cotton, wool, silk, viscose or acetate rayon, or nylon. Numerous examples of suitable dye assistants are specified, including as amine salts:-octadecyl ammonium chloride, N-2-[2-(2, 2, 3, 3, -tetramethyl butyl phenoxy)-ethoxy] ethyl-N, N-dimethyl ammonium chloride, and 2-n-nonyl pyridine hydrochloride; as quaternary ammonium salts:-n-dodecylbenzyl trimethyl ammonium chloride, benzyl -2- [2-(2, 3, 4, 6-tetrachlorophenoxy)ethoxy] ethyl morpholinium chloride, and n hexadecyl pyridinium chloride; as sulphonium salts:-n-dodecyl dimethyl sulphonium chloride, bromide, or methosulphate, and di-(2-hydroxyethyl) methyl sulphonium methosulphate dicapric ester; as phosphonium halides: -cetyl trimethyl phosphonium chloride, benzyl cetyl dimethyl phosphonium iodide, and dichlorobenzyl triphenyl phosphonium chloride; and as polymers of N-vinyl derivatives of carboxylic amides or lactams:-N-vinyl-a -pyrrolidone, N-vinyl-N-methyl (or ethyl) formamide (or acetamide), and N-vinyl capro (or valero) lactam. The aquagel fibres or other articles may be soaked in a solution of the dye assistant at a pH of 1-8 at below 10 DEG C up to 100 DEG C. The treated and subsequently dried materials may be dyed with direct cotton dyes, azoic, vat, soluble vat, acid, mordantacid, basic, and acetic dyes. When dyeing with a soluble vat dye, e.g. Indigosol Green, the dye bath may be prepared by dissolving the dyestuff in hot water containing sodium carbonate and then adding sodium hydrosulphite and sodium sulphate. The goods may be entered at 40 DEG C. and the temperature gradually raised to 90 DEG C. The goods are subsequently placed in a developing bath containing ammonium thiocyanate and potassium dichromate at 30 DEG C. Dilute sulphuric acid is added and the temperature raised to 85 DEG C. The goods are then washed and neutralized. In an example, a tow of polyacrylonitrile after leaving the coagulating bath is soaked with a solution of dodecyl trimethyl ammonium chloride and then stretched, dried, and subsequently dyed in a hot bath containing Pontamine Green and sodium sulphate. A similar tow is stretched before the impregnation with the dye assistant, and after drying is dyed in a bath containing Sulphanthrene Red, caustic soda, and sodium hydrosulphite and the dye is developed by treatment with hydrogen peroxide. A similar tow is impregnated with polyvinyl pyrrolidone, padded with Naphtholate A.S. and then entered into a bath containing diazotized 2-chloro-4-nitraniline at 95-100 DEG C. The tow is passed into a developing bath containing formic acid, acetic acid, and sodium sulphate.
GB31158/53A 1953-01-26 1953-11-10 Method for rendering polyacrylonitrile filaments and other articles readily dyeable Expired GB758937A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US758937XA 1953-01-26 1953-01-26

Publications (1)

Publication Number Publication Date
GB758937A true GB758937A (en) 1956-10-10

Family

ID=22128608

Family Applications (1)

Application Number Title Priority Date Filing Date
GB31158/53A Expired GB758937A (en) 1953-01-26 1953-11-10 Method for rendering polyacrylonitrile filaments and other articles readily dyeable

Country Status (5)

Country Link
BE (1) BE524317A (en)
DE (1) DE1115406B (en)
FR (1) FR1102483A (en)
GB (1) GB758937A (en)
NL (2) NL96192C (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1068859B (en) * 1956-09-10
US3104933A (en) * 1960-07-11 1963-09-24 Yardney International Corp Method of dyeing with polyvinyl alcohol ester and quaternary ammonium compounds
WO2018067092A3 (en) * 2016-08-09 2018-06-21 Aksa Akri̇li̇k Ki̇mya Sanayi̇i̇ Anoni̇m Şi̇rketi̇ Fibre dyeing method

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NL229439A (en) * 1957-07-10
US3105732A (en) * 1961-01-10 1963-10-01 Burlington Industries Inc Process for dyeing blends of nylon 6 and nylon 66

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BE446308A (en) * 1941-07-04
US2558781A (en) * 1947-09-04 1951-07-03 American Cyanamid Co Method of treating water-swollen polymers
DE848687C (en) * 1949-07-27 1952-09-08 Bayer Ag Process for upgrading polyacrylonitrile or molded structures made of polyacrylonitrile
NL87382C (en) * 1950-06-22

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1068859B (en) * 1956-09-10
US3104933A (en) * 1960-07-11 1963-09-24 Yardney International Corp Method of dyeing with polyvinyl alcohol ester and quaternary ammonium compounds
WO2018067092A3 (en) * 2016-08-09 2018-06-21 Aksa Akri̇li̇k Ki̇mya Sanayi̇i̇ Anoni̇m Şi̇rketi̇ Fibre dyeing method

Also Published As

Publication number Publication date
FR1102483A (en) 1955-10-21
NL182627B (en)
DE1115406B (en) 1961-10-19
NL96192C (en)
BE524317A (en)

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