Henley’s Twentieth Century Book of Recipes, Formulas and Processes (1914); edited by Gardner Dexter Hiscox, 1822?

Testing Body Colors For Gritty Admixtures.

—The fineness of the powdered pigment is not a guarantee of the absence of gritty admixtures. The latter differ from the pigment proper in their specific gravity. If consisting of metallic oxides or metallic sulphides the sandy admixtures are lighter than the pigments and rise to the surface upon a systematic shaking of the sample. In the case of other pigments, e. g., aluminas and iron varnish colors, they collect at the bottom. For carrying out the test, a smoothly bored metallic tube about ¹/₂ to ³/₄ inch in diameter and 6 to 7 inches long is used. Both ends are closed with screw caps and at one side of the tube some holes about ¹/₆ of an inch in diameter are bored, closed by pieces of a rubber hose pushed on. The tube is filled with the pigment powder, screwed up and feebly shaken for some time in a vertical position (the length of time varying according to the fineness of the powder). Samples may now be taken from all parts of the tube. Perhaps glass tubes would be preferable, but lateral apertures cannot be so readily made. After the necessary samples have been collected in this manner, they must be prepared with a standard sample, which is accomplished either by feeling the powder between the fingers or by inspecting it under a microscope, or else by means of the scratching test, which last named is the usual way. The requisites for these scratch tests consist of two soft, well-polished glass plates (2 ¹/₂ x 2 ¹/₄ inches) which are fixed by means of cement in two stronger plates of hard wood suitably hollowed out. The surface of the glass must project about ¹/₂ inch over the wooden frame. If a sample of the pigment powder is placed on such a glass plate, another plate is laid on top and both are rubbed slowly together; this motion will retain a soft, velvety character in case the pigment is free from gritty admixtures; if otherwise, the glass is injured and a corresponding sound becomes audible. Next the powder is removed from the plate, rubbing the latter with a soft rag, and examining the surface with a microscope. From the nature of the scratches on the plate the kind of gritty ingredients can be readily determined. The human finger is sufficiently sensitive to detect the presence of gritty substances, yet it is not capable of distinguishing whether they consist of imperfectly reduced or badly sifted grains of pigment or real gritty admixtures.

To Determine The Covering Power Of Pigments.

—To determine the covering power of white lead, or any other pigment, take equal quantities of several varieties of white lead and mix them with a darker pigment, black, blue, etc., the latter also in equal proportions. The white lead which retains the lightest color is naturally the most opaque. In a similar manner, on the other hand, the mixing power of the dark pigments can be ascertained. If experiments are made with a variety of white lead or zinc white, by the admixture of dark pigments, the color which tints the white lead or zinc white most, also possesses the greatest covering or mixing power.

To Detect The Presence Of Aniline In A Pigment.

—Lay a little of the color upon letter paper and pour a drop of spirit on it. If it is mixed with aniline the paper is colored right through thereby, while a pure pigment does not alter the shade of the paper and will never penetrate it.

Vehicle For Oil Colors.

—Petroleum, 20 to 30 pounds; tallow, 3 to 5 pounds; cotton-seed oil, 5 to 7 pounds; colophony, 5 to 7 pounds. The pigments {561} having been ground up with this mixture, the mixed paint can be made still better by adding to it about a sixth of its weight of the following mixture: Vegetable oil, 8 to 20 pounds; saponified rosin, 6 to 16 pounds; turpentine, 4 to 30 ounces.

Frankfort Black.

—Frankfort black, also known as German black, is a name applied to a superior grade of lampblack. In some districts of Germany it is said to be made by calcining wine lees and tartar. The material is heated in large cylindrical vessels having a vent in the cover for the escape of smoke and vapors that are evolved during the process. When no more smoke is observed, the operation is finished. The residuum in the vessels is then washed several times in boiling water to extract the salts contained therein and finally is reduced to the proper degree of fineness by grinding on a porphyry.

Paris Green.

—Emerald or Paris green is rather permanent to light, but must not be mixed with pigments containing sulphur, because of the tendency to blacken when so mixed. It will not resist acids, ammonia, and caustics.

PILE OINTMENTS.

PLANTS:

I.—	“Extract” witch-hazel	2 fluidounces
Lanum	2 ounces
Petrolatum	6 ounces
Glycerine	4 fluidounces
Tannic acid	1 drachm
Powdered opium	1 drachm
II.—	Tannic acid	20 grains
Bismuth subnitrate	1 drachm
Powdered opium	10 grains
Lanum	3 drachms
Petrolatum	5 drachms

Temperature Of Water For Watering Plants.

—Experiments were made several years ago at the Wisconsin Agricultural Experiment Station to determine whether cold water was detrimental to plants. Plants were grown under glass and in the open field, and in all cases the results were similar. Thus, coleus planted in lots of equal size and vigor were watered with water at 35°, 50°, 65°, and 86° F. At the end of 60 days it was impossible to note any difference, and when the experiment was repeated with water at 32°, 40°, 70°, and 100° F., the result was the same. Beans watered with water at 32°, 40°, 70°, and 100° F., were equally vigorous; in fact, water at 32° and 40° F. gave the best results. Lettuce watered with water at 32° F. yielded slightly more than the other lots. From these experiments it was concluded that for vegetable and flowering plants commonly grown under glass, ordinary well or spring water may be used freely at any time of the year without warming.

PLASTER

Therapeutic Grouping Of Medicinal Plasters.

—The vehicle for medicated plasters requires some other attribute than simply adhesiveness. From a study of the therapy of plasters they may be put in three groups, similarly to the ointments with reference to their general therapeutic uses, which also governs the selection of the respective vehicles.

1.—Epidermatic: Supportive, protective, antiseptic, counter-irritant, vesicant. Vehicle: Rubber or any suitable {562} adhesive. Official plasters: Emp. adhesivum, E. capsici.

2.—Endermatic: Anodyne, astringent, alterative, resolvent, sedative, stimulant. Vehicle: Oleates or lead plaster, sometimes with rosins or gum rosins. Official plasters: Emp. Belladonnæ, E. opii, E. plumbi, E. saponis.

3.—Diadermatic: For constitutional or systemic effects. Vehicle: Lanolin or plaster-mull. Official plasters: Emp. hydrargyri.

Methods Of Preparing Rubber Plasters.—mechanic Roller Pressure Method.

—This method of incorporating the rubber with certain substances to give it the necessary body to serve as a vehicle is at present the only one employed. But since it requires the use of the heaviest machinery—some of the apparatus weighing many tons—and enormous steam power, its application for pharmaceutical purposes is out of the question.

As is well known, the process consists in: 1. Purification of the rubber by mascerating and pressing it and removing foreign impurities by elutriating it with water. 2. Forming a homogeneous mass of the dried purified rubber by working it on heated revolving rollers and incorporating sufficient quantities of orris powder and oleoresins. 3. Incorporating the medicinal agent, i. e., belladonna extract, with the rubber mass by working it on warmed revolving rollers. 4. Spreading the prepared piaster.

Solution in Volatile Solvents.—This process has been recommended from time to time, the principal objection being the use of so relatively large quantities of inflammable solvents.

The German Pharmacopœia Method.

—The following is the formula of “Arzneibuch fur das Deutsche Reich,” 1900: Emplastrum adhesivum: Lead plaster, waterfree, 40 parts; petrolatum, 2.5 parts; liquid petrolatum, 2.5 parts, are melted together, and to the mixture add rosin, 35 parts; dammar, 10 parts, previously melted. To the warm mixture is added caoutchouc, 10 parts; dissolved in benzine, 75 parts, and the mixture stirred on the water-bath until all the benzine is lost by evaporation.

The Coleplastrum adhesivum of the Austrian Society is still more complex, the formula containing the following: Rosin oil, empyreumatic, 150 parts; copaiba, 100 parts; rosin, 100 parts; lard, 50 parts; wax, 30 parts; dissolved in ether, 1,200 parts, in which caoutchouc, 250 parts, has been previously dissolved; to this is then added orris powder, 220 parts; sandarac, 50 parts; ether, 400 parts. The mixture, when uniform, is spread on cloth.

Solution Of Rubber In Fixed Solvent: Petrolatum And Incorporation With Lead Acetate.

—India rubber dissolves, though with difficulty, in petrolatum. The heat required to melt the rubber being comparatively high, usually considerably more than 212° F., as stated in the U. S. P., it is necessary to melt the rubber first and then add the petrolatum, in order to avoid subjecting the latter to the higher temperature. The mixture of equal parts of rubber and petrolatum is of a soft jelly consistence, not especially adhesive, but when incorporated with the lead oleate furnishes a very adhesive plaster. While at first 5 per cent of each rubber and petrolatum was used, it has been found that the petrolatum would melt and exude around the edges of the plaster when applied to the skin, and the quantity was therefore reduced to 2 per cent of each. This mass affords a plaster which is readily adhesive to the body, does not run nor become too soft. Plasters spread on cloth have been kept for months exposed to the sun in the summer weather without losing their stability or permanency.

The lead oleate made by the interaction of hot solution of soap and lead acetate, thoroughly washed with hot water, and freed from water by working the precipitated oleate on a hot tile, is much to be preferred to the lead plaster made by the present official process. The time-honored method of boiling litharge, olive oil, and water is for the requirements of the pharmacists most tedious and unsatisfactory. Since in the beginning of the process, at least, a temperature higher than that of 212° F. is required, the water bath cannot be employed, and in the absence of this limiting device the product is usually “scorched.” When the steam bath under pressure can be used this objection does not apply. But the boiling process requires from 3 to 4 hours, with more or less attention, while the precipitation method does not take over half an hour. Besides, true litharge is difficult to obtain, and any other kind will produce unsatisfactory results.

Dissolve the soap in 350 parts hot distilled water and strain the solution. Dissolve the lead acetate in 250 parts hot distilled water and filter the solution while hot into the warm soap solution, stirring constantly. When the precipitate which has formed has separated, decant the liquid and wash the precipitate thoroughly with hot water. Remove the precipitate, let it drain, free from water completely by kneading it on a warm slab, form it into rolls, wrap in paraffine paper, and preserve in tightly closed containers.

Melt the rubber at a temperature not exceeding 302° F., add the petrolatum, and continue the heat until the rubber is dissolved. Add the lead plaster to the hot mixture, continue the heat until it becomes liquid; then let it cool and stir until it stiffens.

Court Plaster Or Sticking Plaster.

—I.—Brush silk over with a solution of isinglass, in spirits or warm water, dry and repeat several times. For the last application apply several coats of balsam of Peru. This is used to close cuts or wounds, by warming and applying it. It does not wash off until the skin partially heals.

II.—Isinglass, 1 part; water, 10 parts; dissolve, strain the solution, and gradually add to it of tincture of benzoin, 2 parts; apply this mixture gently warmed, by means of a camel’s-hair brush, to the surface of silk or sarcenet, stretched on a frame, and allow each coating to dry before applying the next one, the application being repeated as often as necessary; lastly, give the prepared surface a coating of tincture of benzoin or tincture of balsam of Peru. Some manufacturers apply this to the unprepared side of the plaster, and others add to the tincture a few drops of essence of ambergris or essence of musk.

III. (Deschamps).—A piece of fine muslin, linen, or silk is fastened to a flat board, and a thin coating of smooth, strained flour paste is given to it; over this, when dry, two coats of colorless gelatin, made into size with water, quantity sufficient, are applied warm. Said to be superior to the ordinary court plaster.

Coloring Of Modeling Plaster.

—I.—If burnt gypsum is stirred up with water containing formaldehyde and with a little alkali, and the quantity of water necessary for the induration of the plaster containing in solution a reducible metallic salt is added thereto, a plaster mass of perfectly uniform coloring is obtained. The hardening of the plaster is not affected thereby. According to the concentration of the metallic salt solutions and the choice of the salts, the most varying shades of color, as black, red, brown, violet, pearl gray, and bronze may be produced. The color effect may be enhanced by the addition of certain colors. For the production of a gray-colored gypsum mass, for example, the mode of procedure is as follows: Stir 15 drachms of plaster with one-fourth its weight of water, containing a few drops of formaldehyde and a little soda lye and add 10 drops of a one-tenth normal silver solution, which has previously been mixed with the amount of water necessary for hardening the gypsum. The mass will immediately upon mixing assume a pearl-gray shade, uniform throughout. In order to produce red or copper-like, black or bronze-like shades, gold salts, copper salts or silver salts, bismuth salts or lead salts, singly or mixed, are used. Naturally, these colorings admit of a large number of modifications. In lieu of formaldehyde other reducing agents may be employed, such as solutions of sulphurous acid or hydrogen peroxide with a little alkali. Metals in the elementary state may likewise be made use of, e. g., iron, which, stirred with a little copper solution and plaster, produces a brown mass excelling in special hardness, etc. This process of coloring plaster is distinguished from the former methods in that the coloration is caused by metals in the nascent state and that a very fine division is obtained. The advantage of the dyeing method consists in that colorings can be produced with slight quantities of a salt; besides, the fine contours of the figures are in no way affected by this manner of coloring, and another notable advantage lies in the mass being colored throughout, whereby a great durability of the color against outside actions is assured. Thus a peeling off of the color or other way of becoming detached, such as by rubbing off, is entirely excluded.

II.—Frequently, in order to obtain colored plaster objects, ocher or powdered colors are mixed with the plaster. This method leaves much to be desired, because the mixture is not always perfect, and instead of the expected uniform color, blotches appear. Here is a more {564} certain recipe: Boil brazil wood, logwood, or yellow wood, in water, according to the desired color, or use extracts of the woods. When the dye is cold mix it with the plaster. The dye must be passed through a cloth before use. One may also immerse the plaster articles, medals, etc., in this dye, but in this case they must be left for some time and the operation repeated several times.

Treatment Of Fresh Plaster.

—Freshly plastered cement surfaces on walls may be treated as follows:

The freshly plastered surface first remains without any coating for about 14 days; then it is coated with a mixture of 50 parts water and 10 parts ammonia carbonate dissolved in hot water; leave this coat alone for a day, paint it again and wait until the cement has taken on a uniform gray color, which takes place as a rule in 12 to 14 days. Then prime the surface thus obtained with pure varnish and finish the coating, after drying, with ordinary varnish paint or turpentine paint.

Plaster For Foundry Models.

—Gum lac, 1 part; wood spirit, 2 parts; lampblack in sufficient quantity to dye.

Plaster from Spent Gas Lime.—Spent lime from gas purifiers, in which the sulphur has been converted into calcium sulphate, by exposure to weather, if necessary, is mixed with clay rich in alumina. The mixture is powdered, formed into balls or blocks with water, and calcined at a temperature below that at which the setting qualities of calcium sulphate are destroyed. Slaked lime, clay, and sand are added to the calcined product, and the whole is finely powdered.

Plaster Mold.

—Nearly all fine grades of metals can be cast in plaster molds, provided only a few pieces of the castings are wanted. Dental plaster should be used, with about one-half of short asbestos. Mix the two well together, and when the mold is complete let it dry in a warm place for several days, or until all the moisture is excluded. If the mold is of considerable thickness it will answer the purpose better. When ready for casting, the plaster mold should be warmed, and smoked over a gas light; then the metal should be poured in, in as cool a state as it will run.

Cleaning Of Statuettes And Other Plaster Objects.

—Nothing takes the dust more freely than plaster objects, more or less artistic, which are the modest ornaments of our dwellings. They rapidly contract a yellow-gray color, of unpleasant appearance. Here is a practical method for restoring the whiteness: Take finely powdered starch, quite white, and make a thick paste with hot water. Apply, when still hot, with a flexible spatula or a brush on the plaster object. The layer should be quite thick. Let it dry slowly. On drying, the starch will split and scale off. All the soiled parts of the plaster will adhere, and be drawn off with the scales. This method of cleaning does not detract from the fineness of the model.

Hardening And Toughening Plaster Of Paris.

—I.—Plaster of Paris at times sets too rapidly; therefore the following recipe for toughening and delaying drying will be useful. To calcined plaster of Paris add 4 per cent of its weight of powdered marshmallow root, which will keep it from setting for about an hour, and augment its hardness when set, or double the quantity of marshmallow root powder, and the plaster will become very firm, and may be worked 2 or 3 hours after mixing, and may be carved and polished when hard. It is essential that these powders, which are of different densities and specific gravities, should be thoroughly mixed, and the plaster of Paris be quite fresh, and it must be passed through fine hair sieves to ensure its being an impalpable powder. To ensure thorough mixing, pass the combined powders through the hair sieve three times. Make up with water sufficient for the required model or models. Should any of the powder be left over it may be kept by being put in an air-tight box and placed in a warm room.

The marshmallow root powder may be replaced by dextrin, gum arabic, or glue. The material treated is suitable while yet in a soft state, for rolling, glass-tube developing, making plates, etc.

II.—Plaster of Paris may be caused to set more quickly if some alum be dissolved in the water used for rendering it plastic. If the gypsum is first moistened with a solution of alum and then again burned, the resulting compound sets very quickly and becomes as hard as marble. Borax may be similarly employed. The objects may also be be treated with a solution of caustic baryta. But it has been found that no matter how deep this penetrates, the baryta is again drawn toward the surface when the water evaporates, a portion efflorescing on the outside, and only a thin layer remaining in the outer shell, where it is converted into carbonate. This at the same time {565} stops up the pores, rendering it impossible to repeat the operation. It was later found that the whole mass of the cast might be hardened by applying to it with a brush made of glass bristles, a hot solution of baryta. To prevent separation of the crystallized baryta at the surface, the object must be raised to a temperature of 140° to 175° F. To produce good results, however, it is necessary to add to the plaster before casting certain substances with which the baryta can combine. These are silicic acid in some form, or the sulphates of zinc, magnesium, copper, iron, aluminum, etc. With some of these the resulting object may be colored. As it is, however, difficult to insure the production of uniform tint, it is better when employing salts producing color, to mix the plaster with about 5 per cent of quicklime, or, better, to render it plastic with milk of lime, and then to soak the object in a solution of metallic sulphate.

Preservation Of Plaster Casts.

—Upon complete drying, small objects are laid for a short while in celluloid varnish of 4 per cent, while large articles are painted with it, from the top downward, using a soft brush. Articles set up outside and exposed to the weather are not protected by this treatment, while others can be readily washed off and cleaned with water. To cover 100 square feet of surface, 1 ³/₄ pints of celluloid varnish are required.

To Arrest The Setting Of Plaster Of Paris.

—Citric acid will delay the setting of plaster of Paris for several hours. One ounce of acid, at a cost of about 5 cents, will be sufficient to delay the setting of 100 pounds of plaster of Paris for 2 or 3 hours. Dissolve the acid in the water before mixing the plaster.

Weatherproofing Casts.

—I.—Brethauer’s method of preparing plaster of Paris casts for resisting the action of the weather is as follows: Slake 1 part of finely pulverized lime to a paste, then mix gypsum with limewater and intimately mix both. From the compound thus prepared the figures are cast. When perfectly dry they are painted with hot linseed oil, repeating the operation several times, then with linseed-oil varnish, and finally with white oil paint. Statues, etc., prepared in this way have been constantly exposed to the action of the weather for 4 years without suffering any change.

II.—Jacobsen prepares casts which retain no dust, and can be washed with lukewarm soap water by immersing them or throwing upon them in a fine spray a hot solution of a soap prepared from stearic acid and soda lye in ten times its quantity, by weight, of hot water.

Reproduction Of Plaster Originals.

—This new process consists in making a plaster mold over the original in the usual manner. After the solidification of the plaster the mass of the original is removed, as usual, by cutting out and rinsing out. The casting mold thus obtained is next filled out with a ceramic mass consisting of gypsum, 1 part; powdered porcelain, 5 parts; and flux, 1 part. After the mass has hardened it is baked in the mold. This renders the latter brittle and it falls apart on moistening with water while the infusion remains as a firm body, which presents all the details of the original in a true manner.

PLATING

The plating of metal surfaces is accomplished in four different ways: (1) By oxidation, usually involving dipping in an acid bath; (2) by electrodeposition, involving suspension in a metallic solution, through which an electric current is passed; (3) by applying a paste that is fixed, as by burning in; (4) by pouring on molten plating metal and rolling. For convenience the methods of plating are arbitrarily classified below under the following headings:

Bronzing:

Art Bronzes.

—These are bronzes of different tints, showing a great variety according to the taste and fancy of the operator.

I.—After imparting to an object a coating of vert antique, it is brushed to remove the verdigris, and another coat is applied with the following mixture: Vinegar, 1,000 parts, by weight; powdered bloodstone, 125 parts, by weight; plumbago, 25 parts, by weight. Finish with a waxed brush and a coat of white varnish.

II.—Cover the object with a mixture of vinegar, 1,000 parts, by weight; powdered bloodstone, 125 parts, by weight; plumbago, 25 parts, by weight; sal ammoniac, 32 parts, by weight; ammonia, 32 parts, by weight; sea salt, 32 parts, by weight. Finish as above.

Antique Bronzes.

—In order to give new bronze castings the appearance and patina of old bronze, various compositions are employed, of which the following are the principal ones:

I.—Vert Antique: Vinegar, 1,000 parts, by weight; copper sulphate, 16 parts, by weight; sea salt, 32 parts, by weight; sal ammoniac, 32 parts, by weight; mountain green (Sanders green), 70 parts, by weight; chrome yellow, 30 parts, by weight; ammonia, 32 parts, by weight.

II.—Vert Antique: Vinegar, 1,000 parts, by weight; copper sulphate, 16 parts, by weight; sea salt, 32 parts, by weight; sal ammoniac, 32 parts, by weight; mountain green, 70 parts, by weight; ammonia, 32 parts, by weight.

III.—Dark Vert Antique: To obtain darker vert antique, add a little plumbago to the preceding mixtures.

IV.—Vinegar, 1,000 parts, by weight; sal ammoniac, 8 parts, by weight; potassium bioxalate, 1 part, by weight.

Brass Bronzing.

—I.—Immerse the articles, freed from dirt and grease, into a cold solution of 10 parts of potassium permanganate, 50 parts of iron sulphate, 5 parts of hydrochloric acid, in 1,000 parts of water. Let remain 30 seconds; then withdraw, rinse off, and dry in fine, soft sawdust. If the articles have become too dark, or if a reddish-brown color be desired, immerse for about 1 minute into a warm (60° C. or 140° F.) solution of chromic acid, 10 parts; hydrochloric acid, 10 parts; potassium permanganate, 10 parts; iron sulphate, 50 parts; water, 1,000 parts. Treat as before. If the latter solution alone be used the product will be a brighter dark yellow or reddish-brown color. By heating in a drying oven the tone of the colors is improved.

II.—Rouge, with a little chloride of platinum and water, will form a chocolate brown of considerable depth of tone and is exceedingly applicable to brass surfaces which are to resemble a copper bronze.

Copper Bronzing.

—I.—After cleaning the pieces, a mixture made as follows is passed over them with a brush: Castor oil, 20 parts; alcohol, 80 parts; soft soap, 40 parts; water, 40 parts. The day after application, the piece has become bronzed; and if the time is prolonged, the tint will change. Thus, an affinity of shades agreeable to the eye can be procured. The piece is dried in hot sawdust, and colorless varnish with large addition of alcohol is passed over it. This formula for bronzing galvanic apparatus imparts any shade desired, from Barbodienne bronze to antique green, provided the liquid remains for some time in contact with the copper.

II.—Acetate of copper, 6 parts; sal ammoniac, 7 parts; acetic acid, 1 part; distilled water, 100 parts. Dissolve all in water in an earthen or porcelain vessel. Place on the fire and heat slightly; next, with a brush give the objects to be bronzed 2 or 3 coats, according to the shade desired. It is necessary that each coat be thoroughly dry before applying another.

Bronzing Of Gas Fixtures.

—Gas fixtures which have become dirty or tarnished from use may be improved in appearance by painting with bronze paint and then, if a still better finish is required, varnishing after the paint is thoroughly dry with some light-colored varnish that will give a hard and brilliant coating.

If the bronze paint is made up with ordinary varnish it is liable to become discolored from acid which may be present in the varnish. One method proposed for obviating this is to mix the varnish with about 5 times its volume of spirit of turpentine, add to the mixture dried slaked lime in the proportion of about 40 grains to the pint, agitate well, {567} repeating the agitation several times, and finally allowing the suspended matter to settle and decanting the clear liquid. The object of this is, of course, to neutralize any acid which may be present. To determine how effectively this has been done, the varnish may be chemically tested.

Iron Bronzing.

—I.—The surface of a casting previously cleaned and polished is evenly painted with a vegetable oil, e. g., olive oil, and then well heated, care being taken that the temperature does not rise to a point at which the oil will burn. The cast iron absorbs oxygen at the moment when the decomposition of the oil begins, and a brown layer of oxide is formed which adheres firmly to the surface and which may be vigorously polished, giving a bronze-like appearance to the surface of the iron.

II.—To give polished iron the appearance of bronze commence by cleaning the objects, then subject them for about 5 minutes to the vapor of a mixture of concentrated hydrochloric and nitric acids; then smear them with Vaseline and heat them until the vaseline begins to decompose. The result is a fine bronzing.

Liquid For Bronze Powder.

—Take 2 ounces gum animi and dissolve in ¹/₂ pint linseed oil by adding gradually while the oil is being heated. Boil, strain, and dilute with turpentine.

Bronzing Metals.

—I.—The following composition is recommended for bronzing metal objects exposed to the air: Mix about equal parts of siccative, rectified oil of turpentine, caoutchouc oil, and dammar varnish, and apply this composition on the objects, using a brush. This bronze has been found to resist the influences of the weather.

II.—Cover the objects with a light layer of linseed oil, and then heat over a coal fire, prolonging the heat until the desired shade is reached.

III.—Expose the objects to be bronzed for about 5 minutes to the vapors of a bath composed of 50 parts of nitric acid and 50 parts of concentrated hydrochloric acid. Then rub the articles with vaseline and heat until the vaseline is decomposed. The objects to be bronzed must always be perfectly polished.

IV.—To bronze iron articles they should be laid in highly heated coal dust; the articles must be covered up in the glowing dust, and the heat must be the same throughout. The iron turns at first yellow, then blue, and finally rather black. Withdraw the objects when they have attained the blue shade or the black color; then while they are still hot, rub them with a wad charged with tallow.

V.—For electrolytic bronzing of metals the baths employed differ from the brass baths only in that they contain tin in solution instead of zinc. According to Elsner, dissolve 70 parts, by weight, of cupric sulphate in 1,000 parts of water and add a solution of 8 parts of stannic chloride in caustic lye. For a positive pole plate put in a bronze plate. The bath works at ordinary temperature.

VI.—A good bath consists of 10 parts of potash, 2 parts of cupric chloride, 1 part of tin salt, 1 part of cyanide of potassium dissolved in 100 parts of water.

VII.—Mix a solution of 32 parts of copper sulphate in 500 parts of water with 64 parts of cyanide of potassium. After the solution has become clear, add 4 to 5 parts of stannic chloride dissolved in potash lye.

VIII.—Precipitate all soda from a solution of blue vitriol by phosphate of sodium, wash the precipitate well, and dissolve in a concentrated solution of pyrophosphate of copper. Also, saturate a solution of the same salt with tin salt. Of both solutions add enough in such proportion to a solution of 50 parts, by weight, of pyrophosphate of sodium in 1,000 parts of water until the solution appears clear and of the desired color. A cast bronze plate serves as an anode. From time to time a little soda, or if the precipitate turns out too pale, copper solution should be added.

Tin Bronzing.

—The pieces are well washed and all grease removed; next plunged into a solution of copperas (green vitriol), 1 part; sulphate, 1 part; water, 20 parts. When dry they are plunged again into a bath composed of verdigris, 4 parts; dissolved in distilled wine vinegar, 11 parts. Wash, dry, and polish with English red.

Zinc Bronzing.

—The zinc article must be first electro-coppered before proceeding to the bronzing. The process used is always the same; the different shades are, however, too numerous to cover all of them in one explanation. The bronzing of zinc clocks is most frequently done on a brown ground, by mixing graphite, lampblack, and sanguine stirred in water in which a little Flanders Dutch glue is dissolved. The application is made by means of a brush. When it is dry a {568} spirit varnish is applied; next, before the varnish is perfectly dry, a little powdered bronze or sanguine or powdered bronze mixed with sanguine or with graphite, according to the desired shades. For green bronze, mix green sanders with chrome yellow stirred with spirit in which a little varnish is put. When the bronzing is dry, put on the varnish and the powdered bronze as above described. After all has dried, pass the brush over a piece of wax, then over the bronzed article, being careful to charge the brush frequently with wax.

Coloring Of Metals:

Direct Coloration Of Iron And Steel By Cupric Selenite.

—Iron precipitates copper and selenium from their salts. Immersed in a solution of cupric selenite, acidulated with a few drops of nitric acid, it precipitates these two metals on its surface in the form of a dull black deposit, but slightly adherent. But, if the object is washed with water, then with alcohol, and rapidly dried over a gas burner, the deposit becomes adherent. If rubbed with a cloth, this deposit turns a blue black or a brilliant black, according to the composition of the bath.

The selenite of copper is a greenish salt insoluble in water, and but slightly soluble in water acidulated with nitric or sulphuric acid. It is preferable to mix a solution of cupric sulphate with a solution of selenious acid, and to acidulate with nitric acid, in order to prevent the precipitation of the selenite of copper.

This process, originated by Paul Malherbe, is quite convenient for blackening or bluing small objects of iron or steel, such as metallic pens or other small pieces. It does not succeed so well for objects of cast iron; and the selenious acid is costly, which is an obstacle to its employment on large metallic surfaces.

The baths are quickly impoverished, for insoluble yellow selenite of iron is deposited.

Brilliant Black Coloration.—Selenious acid, 6 parts; cupric sulphate, 10 parts; water, 1,000 parts; nitric acid, 4 to 6 parts.

Blue-Black Coloration.—Selenious acid, 10 parts; cupric sulphate, 10 parts; water, 1,000 parts; nitric acid, 4 to 6 parts.

By immersing the object for a short time the surface of the metal can be colored in succession yellow, rose, purple, violet and blue.

Coloration Of Copper And Brass With Cupric Selenite.

—When an object of copper or brass is immersed in a solution of selenite of copper acidulated with nitric acid, the following colors are obtained, according to the time of the immersion: Yellow, orange, rose, purple, violet, and blue, which is the last color which can be obtained. In general, the solution should be slightly acid; otherwise the color is fugacious and punctate.

	a.	b.
Selenious acid	6.5	2.9 parts
Sulphate of copper	12.5	20.0 parts
Nitric acid	2.0	2.5 parts
Water	1,000.0	1,000.0 parts

Production Of Rainbow Colors On Metals

(iron, copper, brass, zinc, etc.)—I.—The following process of irisation is due to Puscher. It allows of covering the metals with a thick layer of metallic sulphide, similar to that met with in nature—in galena, for example.

These compounds are quite solid and are not attacked by concentrated acids and alkalies, while dilute reagents are without action. In 5 minutes thousands of objects of brass can be colored with the brightest hues. If they have been previously cleaned chemically, the colors deposited on the surface adhere with such strength that they can be worked with the burnisher.

Forty-five parts of sodium hyposulphite are dissolved in 500 parts of water; a solution of 15 parts of neutral acetate of lead in 500 parts of water is poured in. The clear mixture, which is composed of a double salt of hyposulphite of lead and of sodium, possesses, when heated to 212° F., the property of decomposing slowly and of depositing brown flakes of lead sulphide. If an article of gold, silver, copper, brass, tombac, iron, or zinc is put into this bath while the precipitation is taking place, the object will be covered with a film of lead sulphide, which will give varied and brilliant colors, according to its thickness. For a uniform coloration, it is necessary that the pieces should be heated quite uniformly. However, iron assumes under this treatment only a blue color, and zinc a bronze color. On articles of copper the first gold color which appears is defective. Lead and tin are not colored.

By substituting for the neutral acetate of lead an equal quantity of cupric sulphate and proceeding in a similar way, brass or imitation gold is covered with a very beautiful red, succeeded by an imperfect green, and finally a magnificent brown, with iridescent points of greenish red. The latter coating is fairly permanent.

Zinc is not colored in this solution, and {569} precipitates in it a quantity of flakes of greenish brown (cupric sulphide), but if about one-third of the preceding solution of lead acetate is added, a solid black color is developed, which, when covered with a light coating of wax, gains much in intensity and solidity. It is also useful to apply a slight coating of wax to the other colors.

II.—Beautiful designs may be obtained, imitating marble, with sheets of copper plunged into a solution of lead, thickened by the addition of gum tragacanth, and heated to 212° F. Afterwards they are treated with the ordinary lead solution. The compounds of antimony, for example the tartrate of antimony and potash, afford similar colorations, but require a longer time for their development. The solutions mentioned do not change, even after a long period, and may be employed several times.

III.—By mixing a solution of cupric sulphate with a solution of sodium hyposulphite, a double hyposulphite of sodium and of copper is obtained.

If in the solution of this double salt an article of nickel or of copper, cleaned with nitric acid, then with soda, is immersed, the following colors will appear in a few seconds: Brilliant red, green, rose, blue, and violet. To isolate a color, it is sufficient to take out the object and wash it with water. The colors obtained on nickel present a moiré appearance, similar to that of silk fabrics.

IV.—Tin sulphate affords with sodium hyposulphite a double salt, which is reduced by heat, with production of tin sulphide. The action of this double salt on metallic surfaces is the same as that of the double salts of copper and lead. Mixed with a solution of cupric sulphate, all the colors of the spectrum will be readily obtained.

V.—Coloration of Silver.—The objects of copper or brass are first covered with a layer of silver, when they are dipped in the following solution at the temperature of 205° to 212° F.: Water, 3,000 parts; sodium hyposulphite, 300 parts; lead acetate, 100 parts.

VI.—Iron precipitates bismuth from its chlorhydric solution. On heating this deposit, the colors of the rainbow are obtained.

Soap, granular and dried	100 parts
Lead acetate	60 parts
Distilled water, a sufficient quantity.

Rubber, cut in small pieces	20 parts
Petrolatum	20 parts
Lead plaster	960 parts