US452324A - Heinrich thies - Google Patents
Heinrich thies Download PDFInfo
- Publication number
- US452324A US452324A US452324DA US452324A US 452324 A US452324 A US 452324A US 452324D A US452324D A US 452324DA US 452324 A US452324 A US 452324A
- Authority
- US
- United States
- Prior art keywords
- acid
- grams
- aniline
- black
- acids
- 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 - Lifetime
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- KRHYYFGTRYWZRS-UHFFFAOYSA-N HF Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 38
- 239000002253 acid Substances 0.000 description 34
- 239000004744 fabric Substances 0.000 description 32
- 239000000203 mixture Substances 0.000 description 22
- VEXZGXHMUGYJMC-UHFFFAOYSA-N HCl Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 20
- 229960002050 Hydrofluoric Acid Drugs 0.000 description 20
- 150000007513 acids Chemical class 0.000 description 20
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 20
- 238000000034 method Methods 0.000 description 20
- XTEGARKTQYYJKE-UHFFFAOYSA-M chlorate Chemical compound [O-]Cl(=O)=O XTEGARKTQYYJKE-UHFFFAOYSA-M 0.000 description 14
- 239000004753 textile Substances 0.000 description 14
- 238000006243 chemical reaction Methods 0.000 description 12
- 239000000835 fiber Substances 0.000 description 10
- 229920000767 polyaniline Polymers 0.000 description 10
- 238000004043 dyeing Methods 0.000 description 8
- -1 yarn Substances 0.000 description 8
- AQMRBJNRFUQADD-UHFFFAOYSA-N Copper(I) sulfide Chemical compound [S-2].[Cu+].[Cu+] AQMRBJNRFUQADD-UHFFFAOYSA-N 0.000 description 6
- VKJKEPKFPUWCAS-UHFFFAOYSA-M Potassium chlorate Chemical compound [K+].[O-]Cl(=O)=O VKJKEPKFPUWCAS-UHFFFAOYSA-M 0.000 description 6
- QTBSBXVTEAMEQO-UHFFFAOYSA-N acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 6
- 239000000460 chlorine Substances 0.000 description 6
- 229910052801 chlorine Inorganic materials 0.000 description 6
- ZAMOUSCENKQFHK-UHFFFAOYSA-N chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 6
- 239000003086 colorant Substances 0.000 description 6
- 229910052802 copper Inorganic materials 0.000 description 6
- RYGMFSIKBFXOCR-UHFFFAOYSA-N copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 6
- 239000010949 copper Substances 0.000 description 6
- 238000000354 decomposition reaction Methods 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- 238000005755 formation reaction Methods 0.000 description 6
- MUBZPKHOEPUJKR-UHFFFAOYSA-N oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 6
- 150000003839 salts Chemical class 0.000 description 6
- 239000011780 sodium chloride Substances 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonium chloride Substances [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 4
- FEWJPZIEWOKRBE-XIXRPRMCSA-N Mesotartaric acid Chemical compound OC(=O)[C@@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-XIXRPRMCSA-N 0.000 description 4
- QGZKDVFQNNGYKY-UHFFFAOYSA-O ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 4
- 235000019270 ammonium chloride Nutrition 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-M chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 230000003647 oxidation Effects 0.000 description 4
- 238000007254 oxidation reaction Methods 0.000 description 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-N phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 4
- KEAYESYHFKHZAL-UHFFFAOYSA-N sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 4
- 239000011734 sodium Substances 0.000 description 4
- 229910052708 sodium Inorganic materials 0.000 description 4
- 238000006467 substitution reaction Methods 0.000 description 4
- 235000013311 vegetables Nutrition 0.000 description 4
- RUFPHBVGCFYCNW-UHFFFAOYSA-N 1-Naphthylamine Chemical compound C1=CC=C2C(N)=CC=CC2=C1 RUFPHBVGCFYCNW-UHFFFAOYSA-N 0.000 description 2
- UXJVWJGDHIZPLD-UHFFFAOYSA-O Ammonium vanadate Chemical compound [NH4+].O=[V-](=O)=O UXJVWJGDHIZPLD-UHFFFAOYSA-O 0.000 description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate dianion Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 2
- 239000005749 Copper compound Substances 0.000 description 2
- 229920000742 Cotton Polymers 0.000 description 2
- 229920001353 Dextrin Polymers 0.000 description 2
- FYGDTMLNYKFZSV-MRCIVHHJSA-N Dextrin Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)OC1O[C@@H]1[C@@H](CO)OC(O[C@@H]2[C@H](O[C@H](O)[C@H](O)[C@H]2O)CO)[C@H](O)[C@H]1O FYGDTMLNYKFZSV-MRCIVHHJSA-N 0.000 description 2
- 229920002472 Starch Polymers 0.000 description 2
- 210000002268 Wool Anatomy 0.000 description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 2
- RHGQHPKUDOFZPE-UHFFFAOYSA-Q ammonium hexacyanoferrate(3-) Chemical compound [NH4+].[NH4+].[NH4+].N#C[Fe-3](C#N)(C#N)(C#N)(C#N)C#N RHGQHPKUDOFZPE-UHFFFAOYSA-Q 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 150000001785 cerium compounds Chemical class 0.000 description 2
- 230000005591 charge neutralization Effects 0.000 description 2
- 150000001845 chromium compounds Chemical class 0.000 description 2
- 239000004020 conductor Substances 0.000 description 2
- 150000001879 copper Chemical class 0.000 description 2
- 150000001880 copper compounds Chemical class 0.000 description 2
- 230000000875 corresponding Effects 0.000 description 2
- 238000010494 dissociation reaction Methods 0.000 description 2
- 230000005593 dissociations Effects 0.000 description 2
- 230000005484 gravity Effects 0.000 description 2
- 159000000011 group IA salts Chemical class 0.000 description 2
- 150000002506 iron compounds Chemical class 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000002932 luster Substances 0.000 description 2
- QDHHCQZDFGDHMP-UHFFFAOYSA-N monochloramine Chemical compound ClN QDHHCQZDFGDHMP-UHFFFAOYSA-N 0.000 description 2
- 230000001264 neutralization Effects 0.000 description 2
- 238000006386 neutralization reaction Methods 0.000 description 2
- GRYLNZFGIOXLOG-UHFFFAOYSA-N nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 2
- 235000006408 oxalic acid Nutrition 0.000 description 2
- 239000007800 oxidant agent Substances 0.000 description 2
- 230000001590 oxidative Effects 0.000 description 2
- MIMJFNVDBPUTPB-UHFFFAOYSA-N potassium hexacyanoferrate(3-) Chemical compound [K+].[K+].[K+].N#C[Fe-3](C#N)(C#N)(C#N)(C#N)C#N MIMJFNVDBPUTPB-UHFFFAOYSA-N 0.000 description 2
- 238000009738 saturating Methods 0.000 description 2
- 235000019698 starch Nutrition 0.000 description 2
- 239000008107 starch Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- LSNNMFCWUKXFEE-UHFFFAOYSA-N sulfonic acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 2
- 235000002906 tartaric acid Nutrition 0.000 description 2
- 239000011975 tartaric acid Substances 0.000 description 2
- 229960001367 tartaric acid Drugs 0.000 description 2
- 229940095064 tartrate Drugs 0.000 description 2
- 150000003681 vanadium Chemical class 0.000 description 2
- 229910052720 vanadium Inorganic materials 0.000 description 2
- 150000003682 vanadium compounds Chemical class 0.000 description 2
- LEONUFNNVUYDNQ-UHFFFAOYSA-N vanadium(0) Chemical compound [V] LEONUFNNVUYDNQ-UHFFFAOYSA-N 0.000 description 2
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
- D06P1/32—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 oxidation dyes
Definitions
- My invention is based on the discovery that by the employment of hydrofluoric acid (I-IF) or its salts in addition to the means heretofore used in producing aniline-black in or upon textile fabrics, yarn, or cloth, superior results are produced, as fully pointed out in the following specification and claim.
- I-IF hydrofluoric acid
- the printed fabrics are brought into a weak alkaline bath, by which a beautiful blue-black hue is obtained.
- This process produces a beautiful black, but the mixture attacks the metallic parts of the printing-machine, and, furthermore, it injures and weakens the textile fabric.
- Lauth introduced in place of the soluble chloride of copper the insoluble sulphide of copper.
- a mixture of eight hundred grams of hydrochloratc of aniline, three hundred and fifty grams of chlorate of potassium, three hundred grams of sulphide of copper, and three hundred grams of sal-amrnoniac is thickened with ten liters of starch-paste.
- the textile fabric is printed and left in the oxidizing-chamber until a beautiful blackish-green hue appears, when the fabric is washed and finally exposed to the action of a weak alkaline bath.
- vanadium salts such as ammonium vanadate and vanadium chloride-have been used in addition to chlorate of potassium.
- nitric acid, phosphoric acid, oxalic acid, or hydrobromio acid or their salts in place of the acids or salts above named; but the acids heretofore proposed partly act with insufficient energy and partly with too much energy, partly they volatilize with great difficulty, and the reaction toward its end becomes excessively acid and vehement.
- hydrochloric acid when applied according to my invention, produces entirely different effects from those above named. Its action consists, chiefly, in thermo-chemical effects and depends, principally, upon its quality of not being liable to decomposition. acids hydrofluoric acid has the largest neutralization heat-that is to say, it develops the largest amount of heat in forming combinations. Its avidity for bases as compared with hydrochloric acid is as one hundred to five. It absorbs on being liberated and on being volatilized a large amount of heat,which paralyzes the increasing energy of the oxidation heat on the fiber, which is a bad conductor of.heat. By the reaction and decomposition of the alkaline chlorates hydrofluoric acid does not become decomposed, like the acids heretofore used. As a weak and partly Of all.
- volatizable acid it assumes in the formation of the black coloring-matter its proportionate share in the reaction.
- the progress of oxidation therefore does not alternate an y more between substitution products of the acid and the products of decomposition produced by the increasing energy of a free acid upon the chlorates.
- Particularly the formation of a suflicient quantity of chlorine in stain. wascendi is avoided, and in consequence thereof no substitution products of chlorine are formed, which, according to our present knowledge,- produce the well-known greening of aniline-black--that is to say, a greenish hue in the color.
- the aniline-black produced according to my invention with the acid of hydrofluoric acid is deep black. in looking down, but brown in looking overhand. It is not changed by sulphurous acid or by any other acid. It does not show the basic qualities of the ordinary anilineblaek, and for this reason it combines more readily with tar colors, which can be used for shading.
- the principal advantage of my invention is that the fiber retains its natural qualities. The luster of the silk is not dimmed, wool remains soft, and vegetable fibers are scarcely affected.
- My invention is also of advantage in the process of producing black, brown, or gray colors from aniline or its homologucs and from naphthylamine.
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Coloring (AREA)
Description
UNITED STATES PATENT OFFICE.
HEINRICH THIES, OF BARMEN, GERMANY, ASSIGNOR OF ONE-HALF TO FRIEDRICH OLEFF, OF SAME PLACE.
PROCESS OF DYEING ANlLlNE-BLACK.
SPECIFICATION forming part of Letters Patent No. 452,324, dated May 12, 1891.
Application filed February 5 1891. Serial No. 3 80,295. (No specimens.)
To all whom it may concern.-
Be it known that I, HEINRICH THIEs,asubject of the King of Prussia, residing at Barmen Rittershausen, Province of Rhenish Prussia, in the Kingdom of Prussia and Gen man Empire, have invented new and useful Improvements in Printing and Dyeing Aniline-Black, of which the following is a specification.
My invention is based on the discovery that by the employment of hydrofluoric acid (I-IF) or its salts in addition to the means heretofore used in producing aniline-black in or upon textile fabrics, yarn, or cloth, superior results are produced, as fully pointed out in the following specification and claim.
A large quantity of processes for producing aniline-black in or upon textile fabrics, yarn, or cloth have been proposed such, for instance, as that proposed by Lightfoot, (Pinkney, Chem. News 33, p. 116,) according to which a mixture of fifty grams aniline, fifty grams hydrochloric acid, fifty grams of a solution of chloride of copper of 1.44 specific gravity, twenty-five grams of chlorate of potassium, twenty-five grams of ammonium chloride, and twelve grams of acetic acid is thickened with a liter of starch-paste, and the product thus obtained is printed'upon the textile material, and then the printed material is hung up for two or three days in an oxidizing-chamber at a temperature of 30 centigrade, during which time the printed surface, which at the beginning shows no color, assumes a dark-green color. If this color has sufficiently developed, the printed fabrics are brought into a weak alkaline bath, by which a beautiful blue-black hue is obtained. This process produces a beautiful black, but the mixture attacks the metallic parts of the printing-machine, and, furthermore, it injures and weakens the textile fabric. In order to obviate these disadvantages Lauth introduced in place of the soluble chloride of copper the insoluble sulphide of copper. According to his process a mixture of eight hundred grams of hydrochloratc of aniline, three hundred and fifty grams of chlorate of potassium, three hundred grams of sulphide of copper, and three hundred grams of sal-amrnoniac is thickened with ten liters of starch-paste. The textile fabric is printed and left in the oxidizing-chamber until a beautiful blackish-green hue appears, when the fabric is washed and finally exposed to the action of a weak alkaline bath.
In order to obviate the harmful effect of the above mixture upon the textile fabric, Koechlin used in place of hydrochlorate of aniline the tartrate of aniline, in the follow ing manner: Two kilograms starch and two kilograms dextrine are boiled in ten liters of water, and two kilograms of aniline, two kilograms of tartaric acid, one kilogram of salammoniac, one kilogram of chlorate of sodium, and immediately before using the mixture one kilogram of sulphide of copper is added, and the mixture thus produced is used for printing, the printed fabric being finally treated as above stated. In place of the copper salts, potassium ferri-cyanide or ammonium ferri-cyanide, and also vanadium salts such as ammonium vanadate and vanadium chloride-have been used in addition to chlorate of potassium. It has also been proposed to use nitric acid, phosphoric acid, oxalic acid, or hydrobromio acid or their salts in place of the acids or salts above named; but the acids heretofore proposed partly act with insufficient energy and partly with too much energy, partly they volatilize with great difficulty, and the reaction toward its end becomes excessively acid and vehement.
'The hydrochloric acid, when applied according to my invention, produces entirely different effects from those above named. Its action consists, chiefly, in thermo-chemical effects and depends, principally, upon its quality of not being liable to decomposition. acids hydrofluoric acid has the largest neutralization heat-that is to say, it develops the largest amount of heat in forming combinations. Its avidity for bases as compared with hydrochloric acid is as one hundred to five. It absorbs on being liberated and on being volatilized a large amount of heat,which paralyzes the increasing energy of the oxidation heat on the fiber, which is a bad conductor of.heat. By the reaction and decomposition of the alkaline chlorates hydrofluoric acid does not become decomposed, like the acids heretofore used. As a weak and partly Of all.
volatizable acid it assumes in the formation of the black coloring-matter its proportionate share in the reaction. The progress of oxidation therefore does not alternate an y more between substitution products of the acid and the products of decomposition produced by the increasing energy of a free acid upon the chlorates. Particularly the formation of a suflicient quantity of chlorine in stain. wascendi is avoided, and in consequence thereof no substitution products of chlorine are formed, which, according to our present knowledge,- produce the well-known greening of aniline-black--that is to say, a greenish hue in the color.
In order to compensate for the weakness of the hydrofluoric acid, I retain a portion of the acids which are at present used in the process, but I limit the energy of these acids to a fixed degree by combining the same for the most part with strong stable metallic bases and eventually with ammonium, whereby the reaction is accelerated by contact and dissociation. By the employment of hydrofluoric acid in the process of oxidizing the aniline the appearance of a surplus of free acids, with theconsequent obnoxioussecondary reactions, is avoided. The saturating capacity of the aniline at the points of entrance and exit is therefore assumed by the hydrofluoric acid. It produces, even with great latitude in the quantity, a uniform black in the reaction from beginning to end.
By the simultaneous employment of the acids heretofore used in the process it is possible either to avoid or to produce the formation of chlorine, and consequently the process can be carried out so as to produce at once either a stable black or a black the greening of which can be exactly gaged, as business may demand.
The following is an example of the mixture, which can be used successively for dyeing mixed fabrics of cotton and silk: carbonate of copper, two grams; bicarbonate of ammonium, four grams; hydrochloric acid of thirty per eentum in solution, twenty-five grams. To this solution is added hydrofluoric acid of sixty per centum, fifty-five grams, diluted with two hundred grams water. To this mixture are added one hundred and forty grams of aniline oil and sixty grams of chlorate of sodium dissolved in a sufficient quantity of water so that the entire mixture fills aliter. A corresponding quantity of the textile fabric is saturated with this liquid, and after having become saturated the fabric is dried and oxidized and finally washed.
For woolen fabrics the proportion of the acids and oxidizing agents in the mixture must be changed. For printing with anilineblack I use the well-known vanadium, cerium, iron, chromium, or copper compounds with the chlorates; but for a portion of the acids I substitute fluoric acid.
The aniline-black produced according to my invention with the acid of hydrofluoric acid is deep black. in looking down, but brown in looking overhand. It is not changed by sulphurous acid or by any other acid. It does not show the basic qualities of the ordinary anilineblaek, and for this reason it combines more readily with tar colors, which can be used for shading. The principal advantage of my invention, however, is that the fiber retains its natural qualities. The luster of the silk is not dimmed, wool remains soft, and vegetable fibers are scarcely affected.
My invention is also of advantage in the process of producing black, brown, or gray colors from aniline or its homologucs and from naphthylamine.
\Vhat I claim as new, and desire to secure by Letters Patent, is
The within-described process for dyeing or printing animal or vegetable fiber, yarn, or cloth in black and analogous colors, which consists in exposing such fiber, yarn,or cloth to the action of aniline oil in the presence of hydrochloric acid, an alkaline salt, and hydrofluoric acid, substantially as described.
In testimony whereof I have hereunto set my hand in presence of two subscribing witnesses.
HEINRICH THIES. \Yitnesscs:
WM. ESSEMREIN, RUDOLPH FRICKE.
Publications (1)
Publication Number | Publication Date |
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US452324A true US452324A (en) | 1891-05-12 |
Family
ID=2521204
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US452324D Expired - Lifetime US452324A (en) | Heinrich thies |
Country Status (1)
Country | Link |
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US (1) | US452324A (en) |
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0
- US US452324D patent/US452324A/en not_active Expired - Lifetime
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