Dynamite.

—Dynamite is ordinarily made up of 75 per cent nitro-glycerine, 25 per cent infusorial earth; dualine contains 80 per cent nitro-glycerine, 20 per cent nitro-cellulose; rend-rock has 40 per cent nitro-glycerine, 40 per cent nitrate of potash, 13 per cent cellulose, 7 per cent paraffine; giant powder, 36 per cent nitro-glycerine, 48 per cent nitrate of potash, 8 per cent sulphur, 8 per cent rosin or charcoal.

Smokeless Powder.

—The base of smokeless powders is nitrated cellulose, {330} which has been treated in one of various ways to make it burn slower than gun cotton, and also to render it less sensitive to heat and shocks. As a rule, these powders are not only less inflammable than gun cotton, but require stronger detonators. As metallic salts cause smoke, they are not used in these powders. The smokeless powders now in use may be divided into three groups: (1) Those consisting of mixtures of nitro-glycerine and nitrated cellulose, which have been converted into a hard, hornlike mass, either with or without the aid of a solvent. To this group belongs ballistite, containing 50 per cent of nitro-glycerine, 49 per cent of nitrated cellulose, and 1 per cent of diphenylamin; also cordite (see further on), Lenord’s powder, and amberite. This last contains 40 parts of nitro-glycerine and 56 parts of nitrated cellulose. (2) Those consisting mainly of nitrated cellulose of any kind, which has been rendered hard and horny by treatment with some solvent which is afterwards evaporated. These are prepared by treating nitrated cellulose with ether or benzine, which dissolves the collodion, and when evaporated leaves a hard film of collodion on the surface of each grain. Sometimes a little camphor is added to the solvent, and, remaining in the powder, greatly retards its combustion. (3) Those consisting of nitro-derivatives of the aromatic hydrocarbons, either with or without the admixture of nitrated cellulose; to this group belong Dupont’s powder, consisting of nitrated cellulose dissolved in nitro-benzine; indurite, consisting of cellulose hexanitrate (freed from collodion by extraction with methyl alcohol), made into a paste with nitro-benzine, and hardened by treatment with steam until the excess of nitro-benzine is removed; and plastomeite, consisting of dinitrotoluene and nitrated wood pulp.

Cordite is the specific name of a smokeless powder which has been adopted by the English government as a military explosive. It contains nitro-glycerine, 58 parts; gun cotton, 37 parts; and petrolatum, 5 parts. The nitro-glycerine and gun cotton are first mixed, 19.2 parts of acetone added, and the pasty mass kneaded for several hours. The petrolatum is then added and the mixture again kneaded. The paste is then forced through fine openings to form threads, which are dried at about 105° F. until the acetone evaporates. The threads, which resemble brown twine, are then cut into short lengths for use.

Another process for the manufacture of smokeless powder is as follows: Straw, preferably oat-straw, is treated in the usual way with a mixture of nitric acid and concentrated sulphuric acid, and then washed in water to free it from these, then boiled with water, and again with a solution of potassium carbonate. It is next subjected, for 2 to 6 hours, to the action of a solution composed of 1,000 parts of water, 12.5 parts of potassium nitrate, 3.5 parts of potassium chlorate, 12.5 parts of zinc sulphate, and 12.5 parts of potassium permanganate. The excess of solution is pressed out, and the mass is then pulverized, granulated, and finally dried.

The warning as to the danger of experimenting with the manufacture of ordinary gunpowder applies with renewed force when nitro-glycerine is the subject of the experiment.

Berge’s Blasting Powder.

—This is composed of chlorate of potash, 1 part; chromate of potash, 0.1 part; sugar, 0.45 parts; yellow wax, 0.09 parts. The proportions indicated may vary within certain limits, according to the force desired. For the preparation, the chlorate and the chromate of potash, as well as the sugar, are ground separately and very finely, and sifted so that the grains of the different substances may have the same size. At first any two of the substances are mixed as thoroughly as possible, then the third is added. The yellow wax, cut in small pieces, is finally added, and all the substances are worked together to produce a homogeneous product. The sugar may be replaced with charcoal or any other combustible body. For commercial needs, the compound may be colored with any inert matter, also pulverized.

Safety In Explosives

.—Ammoniacal salts have been used in the manufacture of explosives to render them proof against firedamp, but not with the full success desired. Ammonium chloride has been utilized, but inconveniences are met with, and the vapor is quite disagreeable. In coöperation with equivalent quantities of soda and potash, its action is regarded as favorable. Tests employing benzine vapor and coal dust were made, and the comparative security calculated to be as given below.

I.—Donarite, composed as follows: 80 per cent of nitrate of ammonia, 12 of trinitrotoluol, 4 of flour, 3.8 of nitro-glycerine, and 0.2 per cent of cotton collodion. Security: Donarite alone, 87 parts; 95 per cent of donarite and 5 per {331} cent of ammonium chloride, 125 parts; 90 per cent of donarite and 10 per cent of ammonium chloride, 250 parts; 86 per cent of donarite and 5.5 per cent of ammonium chloride, with 8.5 per cent of nitrate of soda, 425 parts. The force of the explosion is decreased about 8 per cent, while the security is quintupled.

II.—Roburite, with the following composition: 72.5 per cent nitrate of ammonia; 12 binitro-benzol; 10 nitrate of potash; 5 sulphate of ammonia; 0.5 per cent permanganate of potash. Security: Roburite only, 325 parts; ammonium chloride, taking the place of sulphate of ammonia, 400 parts. Here an intensification of the explosive force is simultaneously produced.

III.—Ammon carbonite I, composed thus: 4 per cent nitro-glycerine; 75.5 nitrate of ammonia; 9.5 nitrate of potash; 9.5 coal dust; 10.5 flour. Security: Ammon carbonite I only, 250 parts; 95 per cent A. C. I. and 5 per cent ammonium chloride, 400 parts; 92 per cent A. C. I. and 8 per cent ammonium chloride, 500 parts. The addition of 5 per cent ammonium chloride diminishes the explosive force only 3 per cent.

IV.—An explosive of nitro-glycerine base composed thus: 30 per cent nitro-glycerine; 1 per cent cotton collodion; 52.6 nitrate of ammonia; 13 nitrate of potash; 3 to 4 per cent starch. Security of this mixture, 150 parts.

V.—Thirty per cent nitro-glycerine; 1 per cent cotton collodion; 47.3 nitrate of ammonia; 11.6 nitrate of potash; 3.1 starch; 7 per cent ammonium chloride. This mixture has a security of 350 parts.

Inflammable Explosive With Chlorate Of Potash.

—Take as an agent promoting combustion, potassium chlorate; as a combustible agent, an oxidized, nitrated, or natural rosin. If, to such a mixture, another body is added in order to render it soft and plastic, such as oil, nitro-benzine, glucose, glycerine, the benefit of the discovery is lost, for the mixture is rendered combustible with nitro-benzine, fecula, sulphur, etc., and inexplosive with glycerine, glucose, and the oil.

Of all the chlorates and perchlorates, potassium chlorate (KClO3) responds the best to what is desired. As to the rosins, they may be varied, or even mixed. To obtain the oxidation or nitration of the rosins, they are heated with nitric acid, more or less concentrated, and with or without the addition of sulphuric acid. An oxidation, sufficient and without danger, can be secured by a simple and practical means. This is boiling them for several hours in water containing nitric acid, which is renewed from time to time in correspondence with its decomposition. The rosins recommended by M. Turpin are of the terebinthine group, having for average formula C20H30O2. Colophony is the type.

The products, thus nitrated, are washed with boiling water, and, on occasion, by a solution slightly alkaline, with a final washing with pure water, and dried at a temperature of 230° F. or in the open air.

The mixing of the constituents of this explosive is preferably cold. For this purpose they are used in the state of fine powder, and when mixed in the tub, 2 1/2 to 5 per cent of a volatile dissolvent is added, as alcohol, carbon sulphide, ether, or benzine. As soon as thoroughly mingled, the mass is put either in an ordinary grainer, or in a cylinder of wire cloth revolving horizontally on its axis, with glass gobilles forming a screen, by the aid of which the graining is rapidly accomplished. Thus a powder more or less finely granulated is produced free from dust.

The proportions preferably employed are:

1. Potassium chlorate 85 parts
   Natural rosin 15 parts
2. Potassium chlorate 80 parts
   Nitrated rosin 20 parts

For employment in firedamp mines, there is added to these compounds from 20 to 40 per cent of one of the following substances: Ammonium oxalate, ammonium carbonate, oxalic acid, sodium bicarbonate, calcium fluoride, or other substance of the nature to lower sufficiently the temperature of the explosive flame.

Gun Cotton.

—For the production of a high-grade gun cotton, it is important that the cotton used should approach as near as possible pure cellulose. The waste from cotton mills, thoroughly purified, is usually employed. After careful chemical examination has been made to ascertain its freedom from grease and other impurities, the cotton waste is picked over by hand to remove such impurities as wood, cardboard, string, etc. The cotton is then passed through the “teasing machine,” which opens out all knots and lumps, thereby reducing it to a state more suitable for the acid treatment and exposing to view any foreign substances which may have escaped notice in the previous picking. The cotton is then dried. When {332} perfectly dry, it is removed to air-tight iron cases, in which it is allowed to cool. The iron cases are taken to the dipping houses, and the cotton waste weighed into small portions, which are then transferred as rapidly as possible to the mixed acids, allowed to remain a few minutes, then removed to the grating and the excess of acid squeezed out. The cotton now containing about ten times its weight of acid is placed in an earthenware pot and transferred to the steeping pits, where it is allowed to remain for 24 hours, a low temperature being maintained by a stream of cold water.

The cotton is now wholly converted into nitro-cellulose. The superfluous acid is next removed by a centrifugal extractor, after which the gun cotton is taken out of the machine and immediately immersed in a large volume of water, and thoroughly washed until it shows no acid reaction. The moisture is then run out and the gun cotton is conveyed by tramway to the boiling vats, where it undergoes several boilings by means of steam. When the “heat test” shows that a sufficient degree of stability has been obtained, the gun cotton is removed to a beating engine, and reduced to a very fine state of division. When this process is completed the pulp is run by gravity along wooden shoots, provided with “grit traps” and electromagnets, which catch any traces of sand, iron, etc., into large “poachers,” in which the gun cotton is continuously agitated, together with a large quantity of water. In this way it is thoroughly washed and a blend made of a large quantity of gun cotton.

Soluble Gun Cotton.

—Soluble gun cotton is made on the same lines, except that greater attention has to be paid to the physical condition of the cotton used, and to the temperature and strength of acid mixture, etc.

The term “soluble” usually implies that the gun cotton is dissolved by a mixture of ethyl-ether and ethyl-alcohol, 2 parts of the former to 1 of the latter being the proportions which yield the best solvent action. The classification of nitro-celluloses according to their solubility in ether-alcohol is misleading, except when the nitrogen contents are also quoted.

The number of solvents for gun cotton which have at various times been proposed is very large. Among the more important may be mentioned the following: Alcohols (used chiefly in conjunction with other solvents), methyl, ethyl, propyl, and amyl, methyl-amyl ether, acetic ether, di-ethyl-ketone, methyl-ethyl ketone, amyl nitrate and acetate, nitro-benzole, nitro-toluol, nitrated oils, glacial acetic acid, camphor dissolved in alcohol, etc.

Some of the above may be called selective solvents, i. e., they dissolve one particular variety of gun cotton better than others, so that solubility in any given solvent must not be used to indicate solubility in another. No nitro-cotton is entirely soluble in any solvent. The solution, after standing some time, always deposits a small amount of insoluble matter. Therefore, in making collodion solutions, care should be taken to place the containing bottles in a place free from vibration and shock. After standing a few weeks the clear supernatant liquid may be decanted off. On a larger scale collodion solutions are filtered under pressure through layers of tightly packed cotton wool. The state of division is important. When the end in view is the production of a strong film or thread, it is advisable to use unpulped or only slightly pulped nitro-cellulose. In this condition it also dissolves more easily than the finely pulped material.

Fulminates:

Fulminating Antimony.
—Tartar emetic (dried), 100 parts; lampblack or charcoal powder, 3 parts. Triturate together, put into a crucible that it will three-fourths fill (previously rubbed inside with charcoal powder). Cover it with a layer of dry charcoal powder, and lute on the cover. After 3 hours’ exposure to a strong heat in a reverberatory furnace, and 6 or 7 hours’ cooling, cautiously transfer the solid contents of the crucible, as quickly as possible, without breaking, to a wide-mouthed stoppered phial, where, after some time, it will spontaneously crumble to a powder. When the above process is properly conducted, the resulting powder contains potassium, and fulminates violently on contact with water. A piece the size of a pea introduced into a mass of gunpowder explodes it on being thrown into water, or on its being moistened in any other manner.
Fulminating Bismuth.
—Take bismuth, 120 parts; carbureted cream of tartar, 60 parts; niter, 1 part.
Fulminating Copper.
—Digest copper (in powder of filings) with fulminate of mercury or of silver, and a little water. {333} It forms soluble green crystals that explode with a green flame.
Fulminating Mercury.
—Take mercury, 100 parts; nitric acid (specific gravity, 1.4), 1,000 parts (or 740 parts, by measure). Dissolve by a gentle heat, and when the solution has acquired the temperature of 130° F., slowly pour it through a glass funnel tube into alcohol (specific gravity, .830), 830 parts (or 1,000 parts, by measure). As soon as the effervescence is over, and white fumes cease to be evolved, filter through double paper, wash with cold water, and dry by steam (not hotter than 212° F.) or hot water. The fulminate is then to be packed in 100-grain paper parcels, and these stored in a tight box or corked bottle. Product 130 per cent of the weight of mercury employed.
Fulminating Powder.
—I.—Niter, 3 parts; carbonate of potash (dry), 2 parts; flowers of sulphur, 1 part; reduce them separately to fine powder, before mixing them. A little of this compound (20 to 30 grains), slowly heated on a shovel over the fire, first fuses and becomes brown, and then explodes with a deafening report.

II.—Sulphur, 1 part; chlorate of potassa, 3 parts. When triturated, with strong pressure, in a marble or wedgwood-ware mortar, it produces a series of loud reports. It also fulminates by percussion.

III.—Chlorate of potassa, 6 parts; pure lampblack, 4 parts; sulphur, 1 part. A little placed on an anvil detonates with a loud report when struck with a hammer.

EYE LOTIONS:

“Black Eye” Lotion.

—“Black eyes” or other temporary discolorations of the skin may be disguised by the application of pink grease paint, or collodion colored by means of a little carmine. As lotions the following have been recommended:
I.— Ammonium chloride  1 part
Alcohol  1 part
Water 10 parts

Diluted acetic acid may be substituted for half of the water, and the alcohol may be replaced by tincture of arnica, with advantage.

II.— Potassium nitrate 15 grains
Ammonium chloride 30 grains
Aromatic vinegar  4 drachms
Water to make 8 ounces.

III.—The following is to be applied with camel’s-hair pencil every 1, 2, or 3 hours. Be careful not to get it in the eyes, as it smarts. It will remove the black discoloration overnight:

Oxalic acid 15 grains
Distilled water  1 ounce

Foreign Matter In The Eye.

—If a piece of iron or other foreign matter in the eye irritates it, and there is no way of removing it until morning, take a raw Irish potato, grate it, and use as a poultice on the eye. It will ease the eye so one can sleep, and sometimes draws the piece out.

Drops Of Lime In The Eye.

—If lime has dropped in the eye, the pouring-in of or the wiping-out with a few drops of oil is the best remedy, as the causticity of the lime is Arrested thereby. Poppy-seed oil or olive oil is prescribed, but pure linseed oil ought to render the same service, as it is also used in the household. Subsequently, the eye may be rinsed out with syrup, as the saccharine substance will harden any remaining particles of lime and destroy all causticity entirely.

FATS

Bear Fat.

—Fresh bears’ fat is white and very similar to lard in appearance. The flank fat is softer and more transparent than the kidney fat, and its odor recalls that of fresh bacon. Bears’ fat differs from the fats of the dog, fox, and cat in having a lower specific gravity, a very low melting point, and a fairly high iodine value.

Bleaching Bone Fat.

—Bone fat, which is principally obtained from horse bones, is very dark colored in the crude state, and of an extremely disagreeable smell. To remedy these defects it may be bleached by the air or chemicals, the former method only giving good results {334} when the fat has been recovered by means of steam. It consists in cutting up the fat into small fragments and exposing it to the air for several days, the mass being turned over at intervals with a shovel. When sufficiently bleached in this manner, the fat is boiled with half its own weight of water, which done, about 3 or 4 per cent of salt is added, and the whole is boiled over again. This treatment, which takes 2 or 3 weeks, sweetens the fat, makes it of the consistency of butter, and reduces the color to a pale yellow. Light seems to play no part in the operation, the change being effected solely by the oxygen of the air. The chemical treatment has the advantage of being more rapid, sufficient decoloration being produced in a few hours. The fat, which should be free from gelatin, phosphate of lime, and water, is placed in an iron pan along with an equal weight of brine of 14° to 15° Bé. strength, with which it is boiled for 3 hours and left to rest overnight. Next day the fat is drawn off into a wooden vessel, where it is treated by degrees with a mixture of 2 parts of potassium bichromate, dissolved in 6 of boiling water, and 8 parts of hydrochloric acid (density 22° Bé.), this quantity being sufficient for 400 parts of fat. Decoloration proceeds gradually, and when complete the fat is washed with hot water.

Bleaching Tallows And Fats.

—Instead of exposing to the sun, which is always attended with danger of rendering fats rancid, it is better to liquefy these at a gentle heat, and then add 1/5 in weight of a mixture of equal parts of kaolin and water. The fatty matter should be worked up for a time and then left to separate. Kaolin has the advantage of cheapness in price and of being readily procured.

Freshly burned animal charcoal would perhaps be a more satisfactory decolorizer than kaolin, but it is more expensive to start with, and not so easy to regenerate.

Exposure of tallow to the action of steam under high pressure (a temperature of 250° or 260° F.) is also said to render it whiter and harder.

Coloring Matter In Fats.

—A simple method for the detection of the addition of coloring matter to fats is here described. Ten parts, by measure, of the melted fat are put into a small separating funnel and dissolved in 10 parts, by measure, of petroleum ether. The solution is then treated with 15 parts, by measure, of glacial acetic acid and the whole shaken thoroughly. The addition of coloring matter is known by the red or yellow coloration which appears in the lower layer of acetic acid after the contents of the funnel have been allowed to settle. If only a slight addition of coloring matter is suspected, the acetic acid solution is run off into a porcelain basin and the latter heated on a water bath, when the coloration will be seen more readily. This test is intended for butter and margarine, but is also suitable for tallow, lard, etc.

Fatty Acid Fermentation Process.

—The production of fatty acids from fats and oils by fermentation is growing in importance. These particulars, which are the actual results from recent experiments on a somewhat extended scale, are given: Seven hundred and fifty pounds of cottonseed oil are mixed with 45 gallons of water and 3 1/2 pounds of acetic acid; this mixture is heated to a temperature of 85° F. Castor-oil seeds, 53 pounds, decorticated and ground, are mixed thoroughly with 3 gallons of water and 4 1/2 gallons of the oil, and this mixture is stirred into the oil and water; the whole mass is then kept mixed for 12 hours by blowing air through, after which it is allowed to stand for another 12 hours, being given a gentle stir by hand at the end of every hour. After 24 hours the mass is heated to a temperature of 180° F., which stops the fermentation and at the same time allows the fatty acids to separate more freely. To assist in this effect there is added 1 gallon of sulphuric acid (1 in 3) solution.

After 2 hours’ standing, the mass will have separated into three layers—fatty acids on the top, glycerine water below, and a middle, undefined layer. The glycerine water is run away, and the whole mass left to stand for 2 hours. The middle portion is run off from the separated fatty acids into another vessel, where it is mixed with 10 gallons of hot water, thoroughly stirred, and allowed to stand for 16 hours or more. The watery layer at the bottom, which contains some glycerine, is then run off, while the residue is mixed with a further quantity of 10 gallons of water, and again allowed to stand. The water which separates out, also the layer of fatty acids that forms on the top, are run off and mixed with the portions previously obtained. The various glycerine waters are treated to recover the glycerine, while the fatty acids are made marketable in any convenient way. {335}

Preservation Of Fats.

—To produce fats and oils containing both iodine and sulphur, whereby they are preserved from going rancid, and consequently can be utilized to more advantage for the usual purposes, such as the manufacture of soaps, candles, etc., following is the Loebell method:

The essential feature of the process is that the iodine is not merely held in solution by the oil or fat, but enters into chemical combination with the same; the sulphur also combines chemically with the oil or fat, and from their reactions the preserving properties are derived.

The process consists of heating, for example, 6 parts of oil with 1 part of sulphur to a temperature varying between 300° and 400° F., then, when at about 195° F., a solution of iodine and oil is added to the mixture, which is constantly agitated until cool to prevent lumps forming. A product is thus obtained which acquires the consistency of butter, and contains both iodine and sulphur in combination.

Purifying Oils And Fats.

—In purifying fatty oils and fats for edible purposes the chief thing is to remove the free fatty acids, which is done by the aid of solutions of alkalies and alkaline earths. The subsequent precipitation of the resulting soapy emulsions, especially when lime is used, entails prolonged heating to temperatures sometimes as high as the boiling point of water. Furthermore, the amount of alkalies taken is always greater than is chemically necessary, the consequence being that some of the organic substances present are attacked, and malodorous products are formed, a condition necessitating the employment of animal charcoal, etc., as deodorizer.

To prevent the formation of these untoward products, which must injuriously affect the quality of edible oils, C. Fresenius proposes to accelerate the dispersion of the said emulsions by subjecting the mixtures to an excess pressure of 1 to 1 1/2 atmospheres and a corresponding temperature of about 220° F., for a short time, the formation of decomposition products, and any injurious influence on the taste and smell of the substance being prevented by the addition of fresh charcoal, etc., beforehand. Charcoal may, and must in certain cases, be replaced for this purpose by infusorial earth or fuller’s earth. When this process is applied to cottonseed oil, 100 parts of the oil are mixed with 1/10 part of fresh, pure charcoal, and 1/2 part of pure fuller’s earth. The mixture is next neutralized with lime-water, and placed in an autoclave, where it is kept for an hour under pressure, and at a temperature of 220° F. Under these conditions the emulsion soon separates, and when this is accomplished the whole is left to cool down in a closed vessel.

FEATHER BLEACHING AND COLORING:

See also Dyes.

Bleaching And Coloring Feathers.

—Feathers, in their natural state, are not adapted to undergo the processes of dyeing and bleaching; they must be prepared by removing their oil and dirt. This is usually done by washing them in moderately warm soap and water, and rinsing in warm and cold water; or the oil may be chemically removed by the use of benzine. To remove it entirely, the feathers must be left in the cleansing fluid from a half hour to an hour, when they may be subjected to the process of bleaching.

Bleaching Plumes.

—Plumes may be almost entirely bleached by the use of hydrogen peroxide, without injuring their texture.

In specially constructed glass troughs, made the length of an average ostrich feather, 15 or 20 of these feathers can be treated at a time. The bleaching fluid is made from a 30 per cent solution of hydrogen peroxide, with enough ammonia added to make it neutral; in other words when neutral, blue litmus paper will not turn red, and red will take a pale violet tinge. The previously cleansed feathers are entirely immersed in this bleaching bath, which may be diluted if desired. The trough is covered with a glass plate and put in a dark place. From time to time the feathers are stirred and turned, adding more hydrogen peroxide. This process requires 10 to 12 hours and if necessary should be repeated. After bleaching they are rinsed in distilled water or rain water, dried in the air, and kept in motion while drying.

To insure success in coloring feathers in delicate tints, they must be free from all impurities, and evenly white. It has been found of advantage to rub the quill of heavy ostrich plumes while still moist with carbonate of ammonia before the dyeing is begun.

Methods Of Dyeing Feathers.

—I.—A boiling hot neutral solution, the feathers to be dried in a rotating apparatus. Suitable dyes for this method are chrysoidin, {336} A, C; crystal vesuvin, 4 B C; phosphin extra, leather yellow, O H; leather red, O, G B; leather brown, O; morocco red, O; azophocphine, G O, B R O; fuchsine, cerise, G R; grenadine, O; safranine, O; methylene violet, malachite green, crystal brilliant green, methylene green, methylene gray, coal black II.

II.—A boiling hot sulphuric solution. Dyes, acid fuchsine, orseilline, R B; acid cerise, O; acid maroon, O; opal blue, blue de lyon, R B; cotton blue, No. 2, China blue No. 2, naphthalene green, O; patent blue, V A; fast blue, O R; fast blue black, O; deep black, G; azo yellow, victorine yellow, orange No. 2, fast brown O, ponceau G R R R, fast red O, Bordeaux, G B R.

III.—An acetic solution. Dyes, Bengal pink G B, phloxine G O, rosolan O B O F, rhodamine O 4 G, eosine A G, erythrosine.

By appropriate mixtures of the dyes of any one class, plumes can be dyed every possible color. After dyeing they are rinsed, and dried in a rotating apparatus. The final process is that of curling, which is done by turning them round and round over a gentle heat. For white feathers a little sulphur may be burned in the fire; for black or colored ones a little sugar.

IV.—The spray method. The solution of the dye to be used is put into an atomizer, and the spray directed to that part of the feather which it is desired to color. By using different colors the most marvelous effects and most delicate transitions from one color to another are obtained. Any kind of an atomizer can be used, the rubber bulb, pump, or bellows; the result is the same.

FERTILIZERS

(See also Phosphate, Artificial.)

Plant Fertilizers.

—Plants are as sensitive to excessively minute quantities of nutrient substances, such as salts of potassium, in the soil, as they are to minute quantities of poisonous substances. Poisons are said to be infinitely more sensitive reagents for the presence of certain metallic salts than the most delicate chemical, the statement having been made that a trace of copper which might be obtained by distilling in a copper retort is fatal to the white and yellow lupin, the castor-oil plant, and spirogyra. Coupin has found salts of silver, mercury, copper, and cadmium especially fatal to plants. With copper sulphate the limit of sensitiveness is placed at 1 in 700,000,000. Devaux asserts that both phanerogams and cryptogams are poisoned by solutions of salts of lead or copper diluted to the extent of 1 in 10,000,000, or less.

As a result of a series of experiments, Schloesing stated that the nitrification of ammonium salts is not for all plants a necessary preliminary to the absorption of nitrogen by the plant. While for some plants, as for example buckwheat, the preferable form of the food material is that of a nitrate, others, for instance, tropeolum, thrive even better when the nitrogen is presented to them in an ammoniacal form.

Artificial Fertilizers For Pot Plants.

—Experiments on vegetation have shown that a plant will thrive when the lacking substances are supplied in a suitable form, e. g., in the following combinations:

I.—Calcium nitrate, potassium nitrate, potassium phosphate, magnesium phosphate, ferric phosphate (sodium chloride).

II.—Calcium nitrate, ammonium nitrate, potassium sulphate, magnesium phosphate, iron chloride (or sulphate) (sodium silicate).

It is well known that in nature nitrates are formed wherever decomposition of organic nitrogenous substances takes place in the air, the ammonia formed by the decomposition being oxidized to nitric acid. These conditions for the formation of nitrates are present in nearly every cornfield, and they are also the cause of the presence of nitrates in water that has its source near stables, etc. In Peruvian guano nitrogen is present partly in the form of potassium nitrate, partly as ammonium phosphate and sulphate. As a nitrate it acts more rapidly than in the form of ammonia, but in the latter case the effect is more lasting. Phosphoric acid occurs in guano combined with ammonia, potash, and chiefly with lime, the last being slower and more lasting in action than the others. {337}

Nearly all artificial fertilizers conform, more or less, to one of the following general formulas:

I.—Artificial Flower Fertilizer.—

1 2 3
Ammonium nitrate 0.40 1.60  40.0 parts
Ammonium phosphate 0.20 0.80  20.0 parts
Potassium nitrate 0.25 1.00  25.0 parts
Ammonium chloride 0.05 0.20   5.0 parts
Calcium sulphate 0.06 0.24   6.0 parts
Ferrous sulphate 0.04 0.16   4.0 parts
1.00 4.00 100.0 parts

Dissolve 1 part in 1,000 parts water, and water the flowers with it 2 or 3 times weekly. Dissolve 4 parts in 1,000 parts water, and water with this quantity 10 or 12 pots of medium size.

II.—Compost for Indoor Plants.—

1 2 3
Ammonium sulphate 0.30 1.20  30.0 parts
Sodium chloride 0.30 1.20  30.0 parts
Potassium nitrate 0.15 0.60  15.0 parts
Magnesium sulphate 0.15 0.60  15.0 parts
Magnesium phosphate 0.04 0.20   4.0 parts
Sodium phosphate 0.06 0.24   6.0 parts
1.00 4.00 100.0 parts

One part to be dissolved in 1,000 parts water and the flowers watered up to 3 times daily. Dissolve 4 parts in 1,000 parts water, and water with this solution daily:

III.—Plant Food Solution.—

1 2
Potassium chloride 0.16 or  12.5 parts
Calcium nitrate 0.71 or  58.0 parts
Magnesium sulphate 0.125 or  12.0 parts
Potassium phosphate 0.133 or  15.0 parts
Iron phosphate, recently precipitated 0.032 or   2.5 parts
1.160 or 100.0 parts

This turbid mixture (1 part in 1,000 parts) is used alternately with water for watering a pot of about 1 quart capacity; for smaller or larger pots in proportion. After using the amount indicated, the watering is continued with water alone.

IV.—Fertilizer with Organic Matter, for Pot Flowers.—

Potassium nitrate   100.0 parts
Ammonium phosphate   100.0 parts
Phosphoric acid     2.5 parts
Simple syrup 1,000 parts

Add not more than 10 parts to 1,000 parts water, and water alternately with this and with water alone. For cactaceæ, crassulaceæ, and similar plants, which do not assimilate organic matter directly, use distilled water instead of syrup.

Chlorotic plants are painted with a dilute iron solution or iron is added to the soil, which causes them to assume their natural green color. The iron is used in form of ferric chloride or ferrous sulphate.

V.— Sodium phosphate 4 ounces
Sodium nitrate 4 ounces
Ammonium sulphate 2 ounces
Sugar 1 ounce

Use 2 teaspoonfuls to a gallon of water.

VI.— Ammonium phosphate      30 parts
Sodium nitrate      25 parts
Potassium nitrate      25 parts
Ammonium sulphate      20 parts
Water 100,000 parts

One application of this a week is enough for the slower growing plants, and 2 for the more rapid growing herbaceous ones.

VII.— Calcium phosphate   4 ounces
Potassium nitrate   1 ounce
Potassium phosphate   1 ounce
Magnesium sulphate   1 ounce
Iron (ferric) phosphate 100 grains

VIII.—Pot plants, especially flowering plants kept around the house, should be treated to an occasional dose of the following:

Ammonium chloride  2 parts
Sodium phosphate  4 parts
Sodium nitrate  3 parts
Water 80 parts

Mix and dissolve. To use, add 25 drops to the quart of water, and use as in ordinary watering.

IX.— Sugar 1 part
Potassium nitrate 2 parts
Ammonium sulphate 4 parts
X.— Ferric phosphate 1 part
Magnesium sulphate 2 parts
Potassium phosphate 2 parts
Potassium nitrate 2 parts
Calcium acid phosphate 8 parts

About a teaspoonful of either of these mixtures is added to a gallon of water, and the plants sprinkled with the liquid.

For hastening the growth of flowers, the following fertilizer is recommended: {338}

XI.— Potassium nitrate 30 parts
Potassium phosphate 25 parts
Ammonium sulphate 10 parts
Ammonium nitrate 35 parts

The following five are especially recommended for indoor use:

XII.— Sodium chloride 10 parts
Potassium nitrate  5 parts
Magnesium sulphate  5 parts
Magnesia  1 part
Sodium phosphate  2 parts

Mixed and bottled. Dissolve a teaspoonful daily in a quart of water and water the plants with the solution.