US2145580A - Spinning solutions containing organic dyes and products thereof - Google Patents
Spinning solutions containing organic dyes and products thereof Download PDFInfo
- Publication number
- US2145580A US2145580A US748259A US74825934A US2145580A US 2145580 A US2145580 A US 2145580A US 748259 A US748259 A US 748259A US 74825934 A US74825934 A US 74825934A US 2145580 A US2145580 A US 2145580A
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- United States
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- products
- spinning
- organic dyes
- spinning solutions
- griesheim
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- 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
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- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F1/00—General methods for the manufacture of artificial filaments or the like
- D01F1/02—Addition of substances to the spinning solution or to the melt
- D01F1/10—Other agents for modifying properties
Definitions
- the present invention relates to a process of producing dyed rayon products, such. as filaments, yarns, ribbons, films, etc., by admixing suitable organic dyes with the spinning solutions prior to 5 the extrusion thereof.
- the primary object of my invention has to do with the addition of such organic dyes to strongly alkaline spinning solutions, such as viscose, cuprammonium cellulose, silk fibroin, alkali metal alginates, gelatine, etc., which will not be deleteriously affected by alkali or acids, desulphurizing agents and bleaching compounds used in the manufacture of artificial products from said spinning solutions.
- strongly alkaline spinning solutions such as viscose, cuprammonium cellulose, silk fibroin, alkali metal alginates, gelatine, etc.
- Another object of this invention has to do with the incorporation of Triazol-Echtrot C (Griesheim), Toluylenrot (Griesheim), Triazol- Reinblau R, etc., into strongly alkaline spinning solutions.
- Viscose rayon for example, is produced by treating cellulose with strong caustic alkali to form alkali cellulose which, subsequently, is transformed into cellulose xanthogenate (viscose) with the assistance of carbon bisulphide. After 1 ripening the viscose solution, it is spun into a sulphuric acid bath, etc., to form regenerated cellulose. The sulphur is removed from the regenerated cellulose with alkaline sulphides, such as ammonium sulphide, etc. Finally the viscose 40 products are bleached with sodium hypochlorite solutions, etc.
- Cuprammonium cellulose is produced by dissolving cellulose in copper hydroxide-ammonia solution and spinning the dissolved cellulose into acid or alkaline spinning baths. The products are then freed from copper and bleached. In a similar manner, artificial products are made from alkaline solutions of alginates, silk fibroin, gelatine, etc. From the above, it will readily be recog- 50 nized that only such organic dyes can be incorporated into alkaline spinning baths which are resistant to acids, desulphurizing agents and bleaching compounds, otherwise satisfactory products cannot be obtained. It is for this reason that rayon products have, heretofore, been exclusively dyed in finished form, i. e., after removal of sulphur, bleaching agents, etc. Unexpectedly,
- Triazol-Echtrot C (Grieslieim): O2eHinNn01SNai C 0 0 Na ITIH:
- a spinning solution for the manufacture of dyed artificial products comprising a viscose solution and a dye of the group consisting of Triazol- Echtrot C (Griesheim) having the formula C29H19N5O7SNa2, Toluylenrot (Griesheim) ,having the formula Cs2I-IisNeO12S4Na4Cl2 and Triazol-Reinblau R having the formula 2.
- a spinning solution for the manufacture of dyed artificial products comprising a cellulosic solution of the group consisting of viscose and cuprammonium cellulose and an organic dyestufi of the group consisting of Triazol-Echtrot C (Griesheim) having the formula C2sH19N5O7SNa2, Toluylenrot (Griesheim) having the formula C32H1sNsOi2S4Na4C'l2 and Triazol-Reinblau RlGriesheim) having the formula C34H24N5O11SsNa3.
- a spinning solution for the manufacture of dyed artificial products comprising a cuproammonium cellulose solution and a dye of the group consisting of Triazol-Echtrot C (Griesheim) having the formula C29H19N5O7SNa2, Toluylenrot (Griesheim) having the formula C32H18N6012S4N3AC12 and Triazol-Reinblau R having the formula C34H24N5O11S3Na3.
Description
Patented Jan. 31, 1939 UNITED STATES SPINNING SOLUTIONS ooNTAININo. ORGAN- 1o DYES AND PRODUCTS THEREOF Rudolph S. Bley, Milligan College, Tenn., assignor to North American Rayon Corporation, New York, N. Y., a corporation of Delaware No Drawing. Application October 13, 1934, Se-
rial No. 748,259. Renewed June 7, 1938 3 Claims.
The present invention relates to a process of producing dyed rayon products, such. as filaments, yarns, ribbons, films, etc., by admixing suitable organic dyes with the spinning solutions prior to 5 the extrusion thereof.
The primary object of my invention has to do with the addition of such organic dyes to strongly alkaline spinning solutions, such as viscose, cuprammonium cellulose, silk fibroin, alkali metal alginates, gelatine, etc., which will not be deleteriously affected by alkali or acids, desulphurizing agents and bleaching compounds used in the manufacture of artificial products from said spinning solutions.
Another object of this invention has to do with the incorporation of Triazol-Echtrot C (Griesheim), Toluylenrot (Griesheim), Triazol- Reinblau R, etc., into strongly alkaline spinning solutions.
Other objects of my invention will become apparent to those skilled in the art after a study of the following specification.
I am well aware that it has, heretofore, been proposed to add inorganic pigments to cellulosic spinning solutions with a view of forming therefrom dyed products. However, until the present time, it has been impossible to incorporate organic dyes into strongly alkaline spinning solutions without impairing the colors of the finished products. Viscose rayon, for example, is produced by treating cellulose with strong caustic alkali to form alkali cellulose which, subsequently, is transformed into cellulose xanthogenate (viscose) with the assistance of carbon bisulphide. After 1 ripening the viscose solution, it is spun into a sulphuric acid bath, etc., to form regenerated cellulose. The sulphur is removed from the regenerated cellulose with alkaline sulphides, such as ammonium sulphide, etc. Finally the viscose 40 products are bleached with sodium hypochlorite solutions, etc.
Cuprammonium cellulose is produced by dissolving cellulose in copper hydroxide-ammonia solution and spinning the dissolved cellulose into acid or alkaline spinning baths. The products are then freed from copper and bleached. In a similar manner, artificial products are made from alkaline solutions of alginates, silk fibroin, gelatine, etc. From the above, it will readily be recog- 50 nized that only such organic dyes can be incorporated into alkaline spinning baths which are resistant to acids, desulphurizing agents and bleaching compounds, otherwise satisfactory products cannot be obtained. It is for this reason that rayon products have, heretofore, been exclusively dyed in finished form, i. e., after removal of sulphur, bleaching agents, etc. Unexpectedly,
I have found that a number of organic dyes, for
example Triazol-Echtrot C (Griesheim), To-
luylenrot (Griesheim) Triazol-Reinblau R,
etc. can be admixed with strongly alkaline spin ning solutions without being decomposed by the same. These dyes are manufactured by the Chemische Fabrik Griesheim-Elektron in Germany and. sold under the aforementioned tradenames.
These dyestuffs have the following chemical structures:
(1) Triazol-Echtrot C (Grieslieim): O2eHinNn01SNai C 0 0 Na ITIH:
G. Schultz Farbstoiftabellen, VII edition, Vol. pp. 171, No. 410.
(2) Toluylenrot (Griesheim): Ca1H aNgOnS4Na4Clz OaNa Cl 1 G HzN S oaNB HaN S OaNfl Qnag S OaNa G Schultz arbstofftabellen", VII edition, Vol. I,
pp. '177, No. 425
(3) 'lriazol-Reinblau R (Grleshoim): o n monsmas G. Schultz Farbstoiftabellefl, VII edition, Vol. I, pp. 193, No. 469.
They may be dissolved and/or dispersed in alkaline spinning solutions to form therewith after extrusion uniformly dyed products. The proportions of dye, added to the spinning solutions, may
be varied at will in order to produce any desired color-shade, and it is possible to admix a plurality of different dyes with a single batch of spinning solution. Instead of admixing the dyes with the whole bulk of spinning solution before entering the spinning machines, it is advisable to strongly dye a portion of the spinning solution and to mix it with the rest of spinning solution just before entering the spinning machines.
Modifications of my invention will readily be recognized by those skilled in the art, and I wish to include all modifications falling within the scope of the appended claims.
I claim:
1. A spinning solution for the manufacture of dyed artificial products comprising a viscose solution and a dye of the group consisting of Triazol- Echtrot C (Griesheim) having the formula C29H19N5O7SNa2, Toluylenrot (Griesheim) ,having the formula Cs2I-IisNeO12S4Na4Cl2 and Triazol-Reinblau R having the formula 2. A spinning solution for the manufacture of dyed artificial products comprising a cellulosic solution of the group consisting of viscose and cuprammonium cellulose and an organic dyestufi of the group consisting of Triazol-Echtrot C (Griesheim) having the formula C2sH19N5O7SNa2, Toluylenrot (Griesheim) having the formula C32H1sNsOi2S4Na4C'l2 and Triazol-Reinblau RlGriesheim) having the formula C34H24N5O11SsNa3.
3. A spinning solution for the manufacture of dyed artificial products comprising a cuproammonium cellulose solution and a dye of the group consisting of Triazol-Echtrot C (Griesheim) having the formula C29H19N5O7SNa2, Toluylenrot (Griesheim) having the formula C32H18N6012S4N3AC12 and Triazol-Reinblau R having the formula C34H24N5O11S3Na3.
RUDOLPH S. BLEY.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US748259A US2145580A (en) | 1934-10-13 | 1934-10-13 | Spinning solutions containing organic dyes and products thereof |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US748259A US2145580A (en) | 1934-10-13 | 1934-10-13 | Spinning solutions containing organic dyes and products thereof |
Publications (1)
Publication Number | Publication Date |
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US2145580A true US2145580A (en) | 1939-01-31 |
Family
ID=25008688
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US748259A Expired - Lifetime US2145580A (en) | 1934-10-13 | 1934-10-13 | Spinning solutions containing organic dyes and products thereof |
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Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2559787A (en) * | 1945-07-20 | 1951-07-10 | Celanese Corp | Colored cellulose esters and ethers |
US2690398A (en) * | 1949-06-16 | 1954-09-28 | Ciba Ltd | Pigment preparations and process of making same |
US2884332A (en) * | 1953-04-30 | 1959-04-28 | Saul & Co | Printing of textile materials and preparations therefor |
US2927035A (en) * | 1957-03-26 | 1960-03-01 | Ciba Ltd | Colored shaped structures from viscose and process for their manufacture |
DE1116390B (en) * | 1959-02-14 | 1961-11-02 | Dynamit Nobel Ag | Process for the production of colored vulcanized fiber boards |
US3020166A (en) * | 1957-08-28 | 1962-02-06 | Ciba Company Inc | Process for the manufacture of dyed structures from regenerated cuprammonium cellulose |
DE1147752B (en) * | 1957-08-28 | 1963-04-25 | Ciba Geigy | Process for the production of colored structures, in particular fibers and foils, from regenerated cellulose |
US3252816A (en) * | 1962-05-28 | 1966-05-24 | Allied Chem | Pigmented extrudable viscose solutions |
DE1220964B (en) * | 1957-03-26 | 1966-07-14 | Ciba Geigy | Process for producing colored fibers or films from viscose |
US3386841A (en) * | 1963-05-11 | 1968-06-04 | Hoechst Ag | Process for the manufacture of plastic articles dyed in the mass |
-
1934
- 1934-10-13 US US748259A patent/US2145580A/en not_active Expired - Lifetime
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2559787A (en) * | 1945-07-20 | 1951-07-10 | Celanese Corp | Colored cellulose esters and ethers |
US2690398A (en) * | 1949-06-16 | 1954-09-28 | Ciba Ltd | Pigment preparations and process of making same |
US2884332A (en) * | 1953-04-30 | 1959-04-28 | Saul & Co | Printing of textile materials and preparations therefor |
US2927035A (en) * | 1957-03-26 | 1960-03-01 | Ciba Ltd | Colored shaped structures from viscose and process for their manufacture |
DE1220964B (en) * | 1957-03-26 | 1966-07-14 | Ciba Geigy | Process for producing colored fibers or films from viscose |
US3020166A (en) * | 1957-08-28 | 1962-02-06 | Ciba Company Inc | Process for the manufacture of dyed structures from regenerated cuprammonium cellulose |
DE1147752B (en) * | 1957-08-28 | 1963-04-25 | Ciba Geigy | Process for the production of colored structures, in particular fibers and foils, from regenerated cellulose |
DE1116390B (en) * | 1959-02-14 | 1961-11-02 | Dynamit Nobel Ag | Process for the production of colored vulcanized fiber boards |
US3252816A (en) * | 1962-05-28 | 1966-05-24 | Allied Chem | Pigmented extrudable viscose solutions |
US3386841A (en) * | 1963-05-11 | 1968-06-04 | Hoechst Ag | Process for the manufacture of plastic articles dyed in the mass |
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