US972066A - Process of dyeing and product thereof. - Google Patents

Process of dyeing and product thereof. Download PDF

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Publication number
US972066A
US972066A US49298909A US1909492989A US972066A US 972066 A US972066 A US 972066A US 49298909 A US49298909 A US 49298909A US 1909492989 A US1909492989 A US 1909492989A US 972066 A US972066 A US 972066A
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dyeing
fiber
liters
kilos
product
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US49298909A
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Joseph Deinet
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Bayer AG
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Individual
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    • 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
    • D06P1/22General 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 vat dyestuffs including indigo
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S8/00Bleaching and dyeing; fluid treatment and chemical modification of textiles and fibers
    • Y10S8/916Natural fiber dyeing
    • Y10S8/917Wool or silk

Definitions

  • JOSEPH DEINET OF ELBERFELD, GERMANY, ASSIGNOR TO FARBENFABRIKEN VORM.
  • FRIEDR BAYER & C0,, 013 ELBERFELD, GERMANY, A CORPORA'E ION OF GERMANY.
  • lVool is dyed in an analogous way: Stir up 10 kilos dibenzoyl-l.fi-diaminoanthraqninone (10 per cent.) with 9-10 kilos causti soda lye 30" PM. and 30 liters of a hydrosultite solution 17 Be. lVhcn all the color is thormighly dissolved, add this solution to the dye bath which consists of 1200-1500 liters of water of 30 1., to which liter caustic soda lye 30 He. and 2 liters of a hydrosulfite solution 17 and 20-40 kilos Glaubers salt has previously been added. llnter 50 kilos wool, work for K; to 1 hour Specification of Letters Patent.
  • I claim 1 The process of dyeing textile fiber which consists in reacting on dibcnzoyl-LS- diaminoanthraquinone with suitable reducing agents to form leuco compounds which are then applied to the fiber and finally oxidized, thus producing on the fiber a yellow shade of extreme fastness.
  • yellow colored textile fiber impregnated with the oxidation products of the leuco compound oft dihenzoyl-1.5diaminoanthraquinone whic treated fiber remains unchanged upon boiling with 10% inuriatic acid, and also re mains unchanged when touched with cold concentrated sulfuric acid and dilute caustic potash; and which upon being touched with a watery solution coi'itaining 0.4 of anhydrous lrydrosulfite ofsodium and ().S'/ of caustic soda changes its color of yellow to olive brown which on exposure to air assumes again its original appearance.

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  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Coloring (AREA)

Description

UNITED s'rATEs PATENT oFFIGE.
JOSEPH DEINET, OF ELBERFELD, GERMANY, ASSIGNOR TO FARBENFABRIKEN VORM. FRIEDR. BAYER & C0,, 013 ELBERFELD, GERMANY, A CORPORA'E ION OF GERMANY.
, PROCESS OF DYEING AND PRODUCT THEREOF.
No Drawing.
To all whom it may concern:
Be it: known that I, Josnrn Dl-ZINE'L, citizen of the German Empire, residing at Elberfeld, Germany, have invented new and useful l mprovements in Processes of Dyeing and Products Thereof, of which the tel- 'sulfite solution 20 Be. and 6 liters caustic lowing is a specification.
I have made the surprising discovery that the dibenzoyl1.5-diaminoanthraquinone can be used as a valuable Vtlt dye. It yields with alkalinereducing agents .a vat which dyes the textile .tiber a yellow shade of excellent fastness.
In order to illustrate my new process more fully the following example is given, the parts being by weight: Stir up 20 kilos. of dibenzoyl-l.ii-diaminoanthraquinone (10 per cent. paste) -with liters of warm water, add. to this mixture 40 liters of a hydrosoda lye 30 136. After a short time the color is completely dissolved.
. Prepare a dye bath which should contain 2000 liters *ateir, one-half liter caustic soda lye 30 1%. and 2' liters hydrosul tite solution and 80 parts of common salt and add to this cold bath the dye solution prepared as above indicated, through a sieve. Stir the loath well, let stand during some minutes, enter 100 kilos well wetted out cotton and work for 1 hour in the cold bath. After dyeing, squeeze out well, rinse, and acidulate the goods in a hath containing 2 ccm. sult'urie acid of 66 136. per liter, rinse and finally soap. A very fast clear yellow shade is thus obtained. a
lVool is dyed in an analogous way: Stir up 10 kilos dibenzoyl-l.fi-diaminoanthraqninone (10 per cent.) with 9-10 kilos causti soda lye 30" PM. and 30 liters of a hydrosultite solution 17 Be. lVhcn all the color is thormighly dissolved, add this solution to the dye bath which consists of 1200-1500 liters of water of 30 1., to which liter caustic soda lye 30 He. and 2 liters of a hydrosulfite solution 17 and 20-40 kilos Glaubers salt has previously been added. llnter 50 kilos wool, work for K; to 1 hour Specification of Letters Patent.
Application filed April 29, 1909. Serial No. 492,989.
.mersed in the liquor.
at 13p (3., the goods being continually in1 v I Patented Oct. 4, 1910.
After dyeing, squeeze out well, oxidize by exposure" to air, rinse, acidulate, wash and dry. very fast yellow shade is thus obtained.
\ Silk and charged silk is dyed in an analogous way.
I claim 1. The process of dyeing textile fiber which consists in reacting on dibcnzoyl-LS- diaminoanthraquinone with suitable reducing agents to form leuco compounds which are then applied to the fiber and finally oxidized, thus producing on the fiber a yellow shade of extreme fastness.
2. The process of dyeing textile fiber which consists in reacting on dibenzoyl ljdiaminoanthraquinone with alkaline reduc ing agents to form leuco compounds which are then applied to the fiber-and finally oxidized, thus producing on the fiber a yellow shade of extreme fastness.
3. The process of dyeing textile fiber which consists inreacting on dibenz0yl-1.5- diaminoanthraquinone with hydrosulfite and caustic soda lye to form leuco compounds which are then applied to the fiber and finally oxidized, thus producing on the fiber a yellow shade of extreme fastness.
4.. As a new article of manufacture, yellow colored textile fiber impregnated with the oxidation products of the leuco compound oft dihenzoyl-1.5diaminoanthraquinone whic treated fiber remains unchanged upon boiling with 10% inuriatic acid, and also re mains unchanged when touched with cold concentrated sulfuric acid and dilute caustic potash; and which upon being touched with a watery solution coi'itaining 0.4 of anhydrous lrydrosulfite ofsodium and ().S'/ of caustic soda changes its color of yellow to olive brown which on exposure to air assumes again its original appearance.
In testimony whereof I have hereunto set my hand in the presence oftwo subscribing witnesses.
, JOSEPH DETN GT. [1,. s.] lVitnesscs:
OTTO Kenn C. J. VVRIGH'L,
US49298909A 1909-04-29 1909-04-29 Process of dyeing and product thereof. Expired - Lifetime US972066A (en)

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2450773A (en) * 1944-03-30 1948-10-05 Allied Chem & Dye Corp Dyeing of wool with indigo dyestuffs

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2450773A (en) * 1944-03-30 1948-10-05 Allied Chem & Dye Corp Dyeing of wool with indigo dyestuffs

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