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Part 181

Henley's Twentieth Century Formulas, Recipes and Processes · Gardner Dexter Hiscox — chapter 181 of 563 · ~1,584 words · public domain

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Here are some recipes:

Parts Color Dyestuff by Cit. Dextrin Weight Acid Blue Marine blue B. N. 3.5 35.0 60.0 Brown Vesuvin S. 30.0 37.5 30.0 Green Brilliant green O. 13.5 18.0 67.5 Orange Orange II. 9.0 18.0 75.0 Red Diamond fuchsine I. 3.5 18.0 75.0 Pink Eosin A. 4.5 — 90.0 Violet Methyl violet 6 B. 3.6 18.0 75.0 Yellow Naphthol yellow S. 13.5 36.0 67.5

Very little of these mixtures suffices for dyeing five eggs. The coloring matter is dissolved in 600 parts by weight of boiling water, while the eggs to be dyed are boiled hard, whereupon they are placed in the dye solution until they seem sufficiently colored. The dyes should be put up in waxed paper.

«Fast Stamping Color.»—Rub up separately, 20 parts of cupric sulphate and 20 parts of anilic hydrochlorate, then mix carefully together, after adding 10 parts of dextrin. The mixture is next ground with 5 parts of glycerine and sufficient water until a thick, uniform, paste-like mass results, adapted for use by means of stencil and bristle-brush. Aniline black is formed thereby in and upon the fiber, which is not destroyed by boiling.

«New Mordanting Process.»—The ordinary method of mordanting wool with a bichromate and a reducing agent always makes the fiber more or less tender, and Amend proposed to substitute the use of a solution of chromic acid containing 1 to 2 per cent of the weight of the wool, at a temperature not exceeding 148° F., and to treat it afterwards with a solution of sodium bisulphite. According to a recent French patent, better results are obtained with neutral or slightly basic chromium sulphocyanide. This salt, if neutral or only slightly basic, will mordant wool at 148° F. The double sulphocyanide of chromium and ammonium, got by dissolving chromic oxide in ammonium sulphocyanide, can also be used. Nevertheless, in order to precipitate chromium chromate on the fiber, it is advisable to have a soluble chromate and a nitrate present, as well as a soluble copper salt and a free acid. One example of the process is as follows: Make the bath with 2 to 3 per cent of ammonio-chromium sulphocyanide, one-half of 1 per cent sodium bichromate, one-third of 1 per cent sodium nitrite, one-third of 1 per cent sulphate of copper, and 1.5 per cent sulphuric acid—percentages based on the weight of the wool. Enter cold and slowly heat to about 140° to 150° F. Then work for half an hour, lift and rinse. The bath does not exhaust and can be reinforced and used again.

«Process for Dyeing in Khaki Colors.»—Bichromate of potash or of soda, chloride of manganese, and a solution of acetate of soda or formiate of soda (15° Bé.) are dissolved successively in equal quantities.

The solution thus composed of these three salts is afterwards diluted at will, according to the color desired, constituting a range from a dark brown to a light olive green shade. The proportions of the three salts may be increased or diminished, in order to obtain shades more or less bister.

Cotton freed from its impurities by the usual methods, then fulled as ordinarily, is immersed in the bath. After a period, varying according to the results desired, the cotton, threads, or fabrics of cotton, are washed thoroughly and plunged, still wet, into an alkaline solution, of which the concentration ought never to be less than 14° Bé. This degree of concentration is necessary to take hold of the fiber when the cotton comes in contact with the alkaline bath, and by the contraction which takes place the oxides of chrome and of manganese remain fixed in the fibers.

This second operation is followed by washing in plenty of water, and then the cotton is dried in the open air. If the color is judged to be too pale, the threads or fabrics are immersed again in the initial bath, left the necessary time for obtaining the desired shade, and then {277} washed, but without passing them through an alkaline bath. This process furnishes a series of khaki colors, solid to light, to fulling and to chlorine.

«LAKES:»

Scarlet Lake.—In a vat holding 120 gallons provided with good agitating apparatus, dissolve 8 pounds potash alum in 10 gallons hot water and add 50 gallons cold water. Prepare a solution of 2 pounds ammonia soda and add slowly to the alum solution, stirring all the time. In a second vessel dissolve 5 pounds of brilliant scarlet aniline, by first making it into a paste with cold water and afterwards pouring boiling water over it; now let out steam into the vat until a temperature of 150° to 165° F. is obtained. Next dissolve 10 pounds barium chloride in 10 gallons hot water in a separate vessel, add this very slowly, stir at least 3 hours, keeping up temperature to the same figures. Fill up vat with cold water and leave the preparation for the night. Next morning the liquor (which should be of a bright red color) is drawn off, and cold water again added. Wash by decantation 3 times, filter, press gently, and make into pulp.

It is very important to precipitate the aluminum cold, and heat up before adding the dyestuff. The chemicals used for precipitating must be added very slowly and while constantly stirring. The quantity used for the three washings is required each time to be double the quantity originally used.

I.—Madder Lakes.—Prepare from the root 1 pound best madder, alum water (1 pound alum with 1 1⁠/⁠2 gallons of water), saturated solution of carbonate of potash (3⁠/⁠4 pound carbonate of potash to 1⁠/⁠2 gallon of water).

The madder root is inclosed in a linen bag of fine texture, and bruised with a pestle in a large mortar with 2 gallons of water (free from lime) added in small quantities at a time, until all the coloring matter is extracted. Make this liquor boil, and gradually pour into the boiling water solution. Add the carbonate of potash solution gradually, stirring all the time. Let the mixture stand for 12 hours and drop and dry as required.

II.—Garancine Process.—This is the method usually employed in preference to that from the root. Garancine is prepared by steeping madder root in sulphate of soda and washing.

Garancine 2 pounds Alum (dissolved in a little water) 2 pounds Chloride of tin 1⁠/⁠2 ounce Sufficient carbonate of potash or soda to precipitate the alum.

Boil the garancine in 4 gallons of pure water; add the alum, and continue boiling from 1 to 2 hours. Allow the product to partially settle and filter through flannel before cooling. Add to the filtrate the chloride of tin, and sufficient of the potash or soda solution to precipitate the alum; filter through flannel and wash well. The first filtrate may be used for lake of an inferior quality, and the garancine originally employed may also be treated as above, when a lake slightly inferior to the first may be obtained.

Maroon Lake.—Take of a mixture made of:

2⁠/⁠3 Sapan wood, 1⁠/⁠3 Lima wood 56 parts Soda crystals 42 parts Alum 56 parts

Extract the color from the woods as for rose pink, and next boil the soda and alum together and add to the woods solution cold. This must be washed clean before adding to the wood liquor.

Carnation Lake.—

Water 42 gallons Cochineal 12 pounds Salts of tartar 1 1⁠/⁠2 pounds Potash alum 3⁠/⁠4 pound Nitrous acid, nitromuriate of tin 44 pounds Muriatic acid, nitromuriate of tin 60 pounds Pure block tin, nitromuriate of tin 22 pounds

Should give specific gravity 1.310.

Boil the water with close steam, taking care that no iron touches it; add the cochineal and boil for not more than five minutes; then turn off the steam and add salts of tartar and afterwards carefully add the alum. If it should not rise, put on steam until it does, pass through a 120-mesh sieve into a settling vat, and let it stand for 48 hours (not for precipitation). Add gradually nitromuriate of tin until the test on blotting paper (given below) shows that the separation is complete. Draw off clear water after it has settled, and filter. To test, rub a little of the paste on blotting paper, then dry on steam chest or on the hand, and if on bending it cracks, too much tin has been used.

To Test the Color to See if it is Precipitating.—Put a drop of color on white blotting paper, and if the color spreads, it is not precipitating. If there is a {278} colorless ring around the spot of color it shows that precipitation is taking place; if the white ring is too strong, too much has been used.

«BLACK LAKES FOR WALL-PAPER MANUFACTURE:»

Bluish-Black Lake.—Boil well 220 parts of Domingo logwood in 1,000 parts of water to which 2 parts of ammonia soda have been added; to the boiling logwood add next 25 parts of green vitriol and then 3.5 parts of sodium bichromate. The precipitated logwood lake is washed out well twice and then filtered.

Black Lake AI.—Logwood extract, Sanford, 120 parts; green vitriol, 30 parts; acetic acid, 7° Bé., 10 parts; sodium bichromate, 16 parts; powdered alum, 20 parts. The logwood extract is first dissolved in boiling water and brought to 25° Bé. by the addition of cold water. Then the remaining ingredients are added in rotation, the salts in substance, finely powdered, with constant stirring. After the precipitation, wash twice and filter.

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