US681117A - Process of dyeing thiosulfate colors. - Google Patents
Process of dyeing thiosulfate colors. Download PDFInfo
- Publication number
- US681117A US681117A US4571001A US1901045710A US681117A US 681117 A US681117 A US 681117A US 4571001 A US4571001 A US 4571001A US 1901045710 A US1901045710 A US 1901045710A US 681117 A US681117 A US 681117A
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- United States
- Prior art keywords
- dyeing
- colors
- sodium
- thiosulfate
- sulfur
- 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.)
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Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P1/00—General 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
- D06P1/30—General 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 sulfur dyes
- D06P1/305—SO3H-groups containing dyes
Definitions
- the sulfid colors are produced by fusion of various organic compounds with sodium sulfid and sulfur and are usually put upon the market in a form containing the coloringmatter mixed with sodium sulfid, polysulfids, and other inorganic sulfur compounds.
- the dyeing is effected by the agency of the sodium sulfid which they contain or which may
- the rotting or tendering of the cotton above referred to has been observed more particularly with the black coloring-matters of this class, (see Dr.
- the following example illustrates the general method of procedure: Six pounds of Clayton fast black 13, M. or Clayton fast black B cone are dissolved, with the addition'of six pounds of neutral sodium-sulfite crystals, in about two gallons of boiling wet The solution is added to forty gallons of boiling water containing three pounds of calcined soda and ten to twenty pounds of salt.
- the bath thus prepared is used, for instance, for dyeing cotton piece goods on the ordinaryjigger in the following manner: The goods are passed twice through the boiling bath, and then while stillrunning a solution of two pounds of glucose and six pounds of caustic-soda lye, (65 Twaddell,) mixed cold, is added in portions of one-fifth every ten minutes.
- the dyeing is complete in about one hour, and the goods are then caused to pass direct from the dye liquor between squeezing-rollers into another jigger containing warm water for washing. I'fa high de-' gree of fastness be required, the color is subsequently fixed' by passingthe goods through a hot solution containing three per cent. of copper sulfate one per cent. of-sodium bichromate, and three per cent. of acetic acid, all calculated on the weight of the cotton. A perfectly even dyeing throughout the piece is thus obtained, and the cotton retains undiminished its original strength.
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- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Coloring (AREA)
Description
40 be added for the purpose.
UNITED STATES PATENT OFFICE.
ARTHUR GEORGE GREEN, OFHEATON MOOR, AND ALEXANDER MEYENEERG, OF MANCHESTER, ENGLAND, ASSIGNORS TO THE CLAYTON ANILINE COMPANY, LIMITED, OF CLAYTON, MANCHESTER, ENGLAND.
PROCESS OF DYEING THlOSULFATE COLORS.
SPECIFICATION forming part of Letters Patent No. 681,117, dated August 20, 1901.
Application filed February 2, 1901. Serial No. 45,710. (No specimens.)
IO lowing to be a full, clear, and exact description of the invention, such as will enable others skilled in the art to which it appertains to i make and use the same.
Although the coloring matters of the Vidal or sultid class have acquired a constantly-increasing importance, especially for black dyeing, their general employment has been greatly retarded by several grave disadvantages. These are (a) a tendency to 2o render the cotton-fiber rotten or tender,
more particularly after the goods have been stored for some time or when undergoing subsequent steaming or .hot pressing; (b) a tendency to give uneven or bronzy dyeings in conv sequence of precipitation of insoluble color on the surface of the fiber, necessitating great care to avoid exposure to air during dyeing;
(a) necessity for excluding copper pipes, rollers, and the like from the dyejvessels; (d)
unpleasant odors arising from the waste liquors when run off.
The sulfid colors are produced by fusion of various organic compounds with sodium sulfid and sulfur and are usually put upon the market in a form containing the coloringmatter mixed with sodium sulfid, polysulfids, and other inorganic sulfur compounds. The dyeing is effected by the agency of the sodium sulfid which they contain or which may The rotting or tendering of the cotton above referred to has been observed more particularly with the black coloring-matters of this class, (see Dr. Chapuis, Journal of the Society of Dyers and OoZom'isi-s, 1900, page 84,) and investigation has led to the conclusion that the do structive effect is due to the deposition of finely-divided sulfur upon the cotton fiber during the process of dyeing, which sulfur 5o subsequently becomes oxidized to sulfuric or sulfurous acid, which tenders or rots the cotton. The sulfur thus deposited must either arise from free sulfur or polysulfids contained in the dyestuff or be produced during the dyeing operation by oxidation of the 5 5 sulfid of sodium present. The tendering or rotting action, together with the other disadvantages above mentioned, which are also at tributable to the presence of sodium sulfid, should therefore be avoidable if the color could be used in a form free from admixture with inorganic sulfur compounds and if the sodium sulfid required for dyeing could be replaced by another reducing agent. The use of glucose and caustic soda has long ago been suggested for this purpose, (see German Pat-- ent, No. 113,195, of April 10, 1897;) but attempts made to replace sodium sulfid by this agent have so far proved unsuccessful in practice, probably because the sodium sulfid in the ordinary dyeing process fulfils a double role, and in addition to acting as a reducing agent serves also as a solvent for the coloring-matter. When such sulfid colors are freed from sodium sulfid'as, for instance, by precipitation by carbonic acid or air-they are in general insoluble in water, and when brought into solution as leuco compounds by means of glucose and caustic soda they do not give even dyeings, but upon reoxiidation are completely precipitated, owing to want of a substance capable of combining with the reformed coloring-matter and rendering it soluble. After much experiment We havesolved these problems in thefollowing manner: First, in order to avoid the presence of inorganic sulfur or sulfids in the dye-bath we makeuse of i the particular class of sulfur coloring-matters which are prepared in aqueous solution by means of sodium thiosulfate without the employment of sulfur or sulfids and which, although presenting close relationship with the melt colors, are chemically distinct therefrom. These coloring-matters as, for example, Clayton fast black, Clayton fast brown, drov -are put upon the market in a pure form entirely free from inorganic sulfur compounds. They are insoluble in water, and in order to bring them into solution we heat them with neutral sodium sulfate. With this 1 .ter.
salt they combine to form easily-soluble sta ble compounds (probably salts of thiosulfonic acids) which, although themselves possessing no dyeing properties, are readily converted by reducing agents into dyeingleuco compounds, (probably sulfhydryl derivatives,) sodium sulfite being re-formed. The dyeing takes place as t-heleuco compound is oxidized by the air, and the sodium sulfite present plays the further important role of combining again with that portion of the re-formed coloring-matter which is not taken up by the fiber, thus holding it in solution for later use and preventing uneven dyeing. For effecting the necessary reduction various reducing agents may be employed; but we have at present obtained the best results by means of glucose and an alkali. These materials we prefer to add to the dye-bath in portions throughout the dyeing and in quantity sufficient to maintain the color in a satisfactorilyreduced condition.
The following example illustrates the general method of procedure: Six pounds of Clayton fast black 13, M. or Clayton fast black B cone are dissolved, with the addition'of six pounds of neutral sodium-sulfite crystals, in about two gallons of boiling wet The solution is added to forty gallons of boiling water containing three pounds of calcined soda and ten to twenty pounds of salt. The bath thus prepared is used, for instance, for dyeing cotton piece goods on the ordinaryjigger in the following manner: The goods are passed twice through the boiling bath, and then while stillrunning a solution of two pounds of glucose and six pounds of caustic-soda lye, (65 Twaddell,) mixed cold, is added in portions of one-fifth every ten minutes. The dyeing is complete in about one hour, and the goods are then caused to pass direct from the dye liquor between squeezing-rollers into another jigger containing warm water for washing. I'fa high de-' gree of fastness be required, the color is subsequently fixed' by passingthe goods through a hot solution containing three per cent. of copper sulfate one per cent. of-sodium bichromate, and three per cent. of acetic acid, all calculated on the weight of the cotton. A perfectly even dyeing throughout the piece is thus obtained, and the cotton retains undiminished its original strength.
Having now particularly described and ascertained the nature of our said invention and in what manner the same is to be performed, we declare that what we claim is-- 1. The new and improved process of dyeing, such process consisting in first rendering soluble thiosulfate colors free from sulfids, polysulfids or 'free sulfur, then effecting the dyeing by conversion of the coloring-matter, by solution in aqueous neutral sodium sulfite, into its soluble sulfite compound, and reducing the latter in the dye-bath by means of an alkaline reducing agent.
2. The new and improved processof dyein g, such process consisting in first rendering a thiosulfate color soluble by means of so-
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US4571001A US681117A (en) | 1901-02-02 | 1901-02-02 | Process of dyeing thiosulfate colors. |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US4571001A US681117A (en) | 1901-02-02 | 1901-02-02 | Process of dyeing thiosulfate colors. |
Publications (1)
Publication Number | Publication Date |
---|---|
US681117A true US681117A (en) | 1901-08-20 |
Family
ID=2749661
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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US4571001A Expired - Lifetime US681117A (en) | 1901-02-02 | 1901-02-02 | Process of dyeing thiosulfate colors. |
Country Status (1)
Country | Link |
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US (1) | US681117A (en) |
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1901
- 1901-02-02 US US4571001A patent/US681117A/en not_active Expired - Lifetime
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