BROMINE.

Fig. 139.Fig. 139.

a b.Glass tube, bent as in picture.c.Piece of damp sponge squeezed into the head of the tube. Any liquid poured in atbwill flow through the sponge until it has attained the same level ina.

a b.Glass tube, bent as in picture.c.Piece of damp sponge squeezed into the head of the tube. Any liquid poured in atbwill flow through the sponge until it has attained the same level ina.

Having poured the albumen on a perfectly clean glass plate, taking care to have sufficient to run freely over the surface of the glass, the excess is then gently drained off and the plate turned so as to have the coated side downwards; it is then fixed in a sling made by taking a stout bit of string about three feet long, which is doubled and knotted at the fold, leaving the two ends free; two small triangles or stirrups of silver wire looped at one corner are now tied on to the ends of the string, and these form a support for the opposite edges of the glass plate to rest on; the two strings are knotted together at aconvenient distance from the stirrups to prevent the glass slipping out, and the plate is now rotated rapidly over a heated metallic surface, such as an iron box containing some burning charcoal or thewarming pan, care being taken to avoid dust as much as possible, and to use only the whites of new-laid eggs. (Fig. 140.) The glass plate, covered with dry albumen, is now iodized to a straw colour by exposure over a box containing iodine, as in the Daguerreotype process, and is sensitized by immersion for three or four minutes in a bath containing a solution of nitrate of silver (twenty-five grains to an ounce of water); the plate is afterwards washed in distilled water and left to dry spontaneously, of course in a darkened room. The plates may then be placed ready for use in a very ingenious tin box devised by Mr. Crookes, which keeps them perfectly light-tight even in the sun, and at the same time is less bulky than the ordinary wooden ones. It is made of tin plate, the cover sliding tight over the top, and more than half way down the sides; light is further excluded by means of an outer jacket of tin, which is soldered to the box a little below the centre. The cover thus slides between the case and the jacket, and renders injury to the plates by the entrance of light an impossibility. (Fig. 141.)

Fig. 140.Fig. 140.

a.Loop for finger.b.The knot which prevents the stirrups of silver wire,c c, slipping off the corners of the glass plate.d d.The opposite corners of the glass plate on which the stirrups are placed.

a.Loop for finger.b.The knot which prevents the stirrups of silver wire,c c, slipping off the corners of the glass plate.d d.The opposite corners of the glass plate on which the stirrups are placed.

Fig. 141.

a a.Tin box, with partitions to hold glass plates,b b.The outer jacket, between which and the box,a, the lid or cover,c, slides.

a a.Tin box, with partitions to hold glass plates,b b.The outer jacket, between which and the box,a, the lid or cover,c, slides.

The sensitive albumenized glass plate is exposed in the camera from fifteen to thirty minutes, and developed (much in the same way as the paper pictures) with one ounce of a saturatedsolution of gallic acid containing ten or fifteen drops of the sensitizing solution. The plate is usually placed on a levelling stand, and the solution poured on the glass plate; the development is slow, and may be quickened sometimes by the application of heat.

The picture is fixed by immersion for a short time in a bath containing one part of a saturated solution of hyposulphite of soda in eight of water. The pictures produced by this process are exquisitely defined, provided always the camera is well focussed, and to assist this operation a magnifying glass may be employed. After removal from the hyposulphite of soda the plate is well washed with water, and being allowed to dry spontaneously, is now ready to print from.

The glass plates for this, as well as the albumen on glass process, should be cleaned by rubbing them over first with a mixture of Tripoli powder and ammonia, which is washed off under a tap, and the glass being drained is rubbed dry and polished with a clean calico duster kept exclusively for this purpose.

The iodized collodion is now poured on, and the excess returned to the bottle. Collodion can be made very easily, but if prepared without due precautions, it cannot be used afterwards, and reminds one of the old story of the enthusiastic son, who, when asking his father's permission to espouse the beloved, enumerated amongst her other accomplishments, the fact that shecouldmake a pudding, and was answered by the bluff question, "But can you eat it afterwards?" So it is with collodion: a great deal of messing and loss of time is saved by purchasing it of the various makers, amongst whom may be specially noticed Mr. Richard Thomas, of 10, Pall Mall, who has devoted the whole of his attention to the preparation of this important photographic chemical, and with a success which his numerous patrons can well testify. The collodion is sold either mixed with the iodizing solution, or the two can be obtained separately, with directions on the bottles as to the quantities to be mixed together.

The plate covered with the iodized collodion is quickly transferred to a bath containing a solution prepared in the following manner:—Dissolve four ounces of nitrate of silver in eight ounces of water, and to this add twenty grains of iodide of potassium in one ounce of water; shake them together, and then pour the whole into fifty-six ounces of distilled water, and in half an hour add one ounce of alcohol and half an ounce of ether; agitate the whole and filter the next morning. The collodion plate is kept in this solution for a certain period, only learnt by experience, and should be occasionally lifted out to see if a uniform transparency is obtained; say that the immersion may be continued for five minutes, it is now ready for the camera, and may be exposed from about one to two minutes, or more if the light is deficient; the time of exposure is also a matter ofpractice, mere directions can be of no use in this stage of the process.

The picture is developed on a levelled stand, with a solution of threegrains of pyrogallic acid in three ounces of water, to which sixty drops of glacial acetic acid have been added. When fully developed the plate is washed with water and fixed with a solution of hyposulphite of soda, consisting of one part of the saturated solution to eight of water, again thoroughly but gently washed, so as not to endanger the separation of the film from the glass; it is allowed to dry spontaneously, and being coated with amber varnish (a solution of amber in chloroform) is now ready to print from. It is, perhaps, hardly necessary to add, that the sensitizing and developing processes must be performed in a dark room.

Fig. 142.Fig. 142.

a.Glass or gutta-percha bath to hold the sensitizing solution.b.Glass, with piece cemented on the end to hold the prepared glass plate,c, whilst dipped in the bath,a. The platechas a cross in one corner to show prepared side.

a.Glass or gutta-percha bath to hold the sensitizing solution.b.Glass, with piece cemented on the end to hold the prepared glass plate,c, whilst dipped in the bath,a. The platechas a cross in one corner to show prepared side.

Fig. 143.Fig. 143.

First effect of peripatetic photography on the rural population.

Bromine (βρωμος, a bad odour). Symbol, Br. Combining proportion, 80. Specific gravity, 2.966.

In a previous portion of this work, the connexion between chlorine, iodine, and bromine has been pointed out; and as we have to notice the colour of the element bromine, the chromatic union of the triad may be alluded to. These elements present very nearly all the colours of the spectrum:

Brominered to orange.Chlorineyellow to green.Iodineblue, indigo, violet.

These three elements also furnish examples of the three conditions of matter; iodine being a solid, bromine a fluid, chlorine a gas; the relation of their combining proportions is also curious: as might be expected, the fluid bromine takes an intermediate position, and (according to the axiom that half the sum of the extremes is equal to the mean) by dividing the combining proportions of iodine and chlorine, and adding them together, we have, as nearly as possible, the combining proportion of bromine:

Chlorine35÷2=17.75Iodine126÷2=63————80.75

The combining proportion of bromine is 80, but 80.75 is so near, that it may reasonably be conjectured future experiments will reduce the number of the three elements, and may prove that they are only modifications of a single one. This is the only kind of alchemy which is tolerated in the nineteenth century, and any philosopher who will reduce the number of elements, and prove that some of them are only modifications of others, will achieve a renown that must transcend theéclatof all previous discoverers.

Bromine was discovered by Balard, in 1826, and, like chlorine and iodine, is a constituent of sea water. The chief source of bromine is a mineral spring at Kreutznach, in Germany. The process by which it is obtained offers a good example of chemical affinity; the water of the mineral spring is evaporated, all crystallizable salts removed, and a current of chlorine gas passed through the remaining solution, which changes to a yellow colour, in consequence of the liberation of the bromine by the combinations of chlorine with the bases previously united with the former; the liquid is then shaken with ether, which dissolves out the bromine. In the next place, the etherial solution is agitated with strong solution of potassa, and is thus obliged to part with the bromine which is converted into bromate of potassa; this is ultimately changed by fusion to bromide of potassium; and by distillation with black oxide of manganese and sulphuric acid, the bromine is finally obtained. Sixprocesses are therefore necessary before the small quantity of bromine contained in the mineral spring-water, is separated.

Bromine is a very heavy fluid, which should be preserved by keeping it in a bottle covered with water; when required, a few drops may be removed by means of a small tube, and dropped into a warm bottle, which is quickly filled with the orange-red vapour. If some phosphorus is placed in a deflagrating spoon, and exposed to the action of bromine vapour, it takes fire spontaneously.

Powdered antimony sprinkled into the vapour of bromine immediately takes fire.

A burning taper immersed in a bottle containing the vapour of bromine is gradually extinguished.

Liquid bromine exposed to a freezing mixture of ice and salt, or reduced to a temperature of about eight degrees below zero, solidifies into a yellowish-brown, brittle, crystalline mass.

A solution of indigo shaken with a small quantity of the vapour of bromine is quickly bleached. Many substances, when brought in contact with liquid bromine, combine with explosive violence, and therefore experiments with liquid bromine are not recommended, as all the most instructive and conclusive results can be obtained by the use of the vapour of bromine, which is easily procured by allowing a few drops to fall into a warm, dry bottle.

Bromine, as already mentioned, is used in the art of photography.

Symbol, F. Combining proportion, 19.

This singular element seems almost to embody the ancient idea of the alchemists, being a sort ofalkahest, or universal solvent; or in plainer language, its affinities for other bodies are so powerful, that it attacks every substance (not even excepting gold), at the moment of its liberation, and combines therewith, so that its isolation has not yet been effected. Chemists who assert that they have been able to obtain fluorine in the elementary condition, pronounce it to be a gas which possesses the colour of chlorine; but the experiments, as hitherto conducted, render that statement extremely doubtful.

The only interesting fact connected with fluorine, is the remarkable property of attacking glass and other silicious bodies, belonging to its combination with hydrogen gas, called hydrofluoric acid. This acid is easily obtained and used by placing some powdered fluorspar in a leaden tray six inches square and two inches deep. If sulphuric acid is now mixed with the powdered spar, so as to form a thin paste, and heat applied, the vapour of the hydrofluoric acid quickly rises, and can be employed to etch a glass plate upon which a drawing may have been previously traced by scratching away the wax, with which it is first coated. By heating the glass plate before a fire, a sufficient quantity of wax is soon melted on to it by merely rubbing the wax against the glass plate; any excess should be avoided, if a well-executed drawing is required to be etched on its surface. (Fig. 144.)

Fig. 144.Fig. 144.

a a a.The glass plate, with the waxed side downwards, placed on the leaden tray containing the fluorspar and sulphuric acid.b.Spirit lamp.

a a a.The glass plate, with the waxed side downwards, placed on the leaden tray containing the fluorspar and sulphuric acid.b.Spirit lamp.

The wax plate must not remain too long over the leaden tray, as the heat is apt to melt the wax, when the acid not only attacks those parts from which the wax has been removed by the etching needle, but also the surface of the glass generally, and thus the clearness of the design is spoilt. After exposure—and it is as well to prepare two or three glass plates for the experiment—the wax is quickly removed by rubbing and washing with oil of turpentine, and the design (beautifully etched into the glass) is then apparent.

This group of non-metallic elements has been frequently styled "Metalloids," meaning substances allied to, but not possessing, all the properties belonging to a metallic substance; and therefore perhaps the expression, non-metallic solids, is the best that can be adopted. They may be subdivided into two classes of three each, which have properties more or less allied to each other—viz.,

Carbon, Boron, Silicon; andSelenium, Sulphur, Phosphorus.

Symbol, C; Combining Proportion, 6.

This element has almost the property of ubiquity, and is to be found not only in all animal and vegetable substances, in common air, sea, and fresh water, but also in various stones and minerals, and especially in chalk and limestone.

There is, perhaps, no element which offers a greater variety of amusing experiments and elementary facts than carbon, whether it be considered either in its simple or combined state.

A piece of carbon, in the shape of the Koh-i-Noor, was one of the chief attractions at the first Exhibition in Hyde Park. The diamond is the hardest and most beautiful form of charcoal; how it was made in the great laboratory of nature, or how its particles came together, seems to be a mystery which up to the present time has not yet been solved, at all events no artificial process has yet produced the diamond.

Sir D. Brewster, speaking of the Koh-i-Noor, remarks that on placing it under a microscope, he observed several minute cavities surrounded with sectors of polarized light, which could only have been produced by the expansive action of acompressed gas or fluid, that had existed in the cavities when the diamond was in thesoftstate.

Now it is known that bamboo, which is of a highly silicious nature, has the property of depositing in its joints a peculiar form of silica, called tabasheer. Silicon is one of the triad with carbon—i.e., it is allied to carbon on account of certain analogies; may it not then be supposed that, in times gone by, ages past, when the atmosphere was known to be highly charged with carbonic acid gas, there might possibly have existed some peculiar tree which had not only the power of decomposing carbonic acid (possessed by all plants at the present period), but was enabled, like the bamboo, to deposit, not silica, which is the oxide of silicium, but carbon, the purest form of charcoal—viz., the diamond? Speculation in these matters is ever more rife than stern proof, and it may be stated, that all attempts to manufacture this precious gem (like those of the alchemists with gold and silver) have most signally failed.

Box and various woods, dried bones, and different organic matters, placed in a nearly close iron or other vessel, and heated red hot, so that all volatile matter may escape, leave behind a solid black substance called charcoal. If that kind obtained from bones, and termed bone black or ivory black, is roughly powdered, and placed in a flask with some solution of indigo or some vinegar, or syrup obtained by dissolving common moist sugar in water, and boiled for a short period, the colour is removed, and on filtering the liquid it is found to be as clear and colourless as water, provided sufficient ivory black has been employed.

Charcoal is a disinfectant, and is used for respirators; it has even been recommended medically, and charcoal lozenges can be bought at various chemists' shops. If a few drops of a strong solution of hydrosulphuret of ammonia (which has the agreeable odour belonging to putrid eggs) is mixed with half a pint of water, it will of course smell strongly, and likewise precipitate Goulard water, or a solution of acetate of lead black; but on shaking the water with a few ounces of charcoal, it no longer smells of sulphuretted hydrogen, and if filtered and poured into a solution of lead does not turn it black. This chemical action of charcoal, independent of its seeming mechanical attraction for colouring matter, would appear to show that the pores of charcoal contain oxygen, which in that peculiar condensed state destroys colouring matter, and oxidizes other bodies.

A very satisfactory experiment, proving that the diamond and plumbago or black lead are identical with charcoal, although differing in outward form and purity, can be made at a little cost, by purchasing a fragment of refuse diamond, called "boart," of Mr. Tennant of the Strand. A small piece costs about five shillings. The fragment should be carefully supported by winding somethinplatinum wire round it, as, if the wire is too thick, it cools down the heat of the bit of diamond and prevents it kindling in the oxygen gas. A difficulty may arise in preparing the fragment, in consequence of the wire continually slipping off. The "boart" should therefore be grasped by the thumb and first finger, and the wire wound round; then it must be carefully turned and again wound across with the platinum wire, as in the sketch below. (Fig. 145.)

Fig. 145.Fig. 145.

a.The platinum wire.b.The fragment of "boart" or refuse diamond.

A piece of black lead (so called) may now be taken from a lead pencil and also supported by platinum wire; likewise a bit of common bark charcoal or hard coke. Three bottles of oxygen should now be prepared from chlorate of potash and oxide of manganese, an extra bottle being provided for the diamond in case there should be any failure in its ignition. The bark charcoal can be first ignited by holding a corner in the spirit lamp for a few seconds; when plunged into oxygen it immediately kindles and burns with rapidity, and if the cork is well fitted, the product of combustion—viz., carbonic acid gas—is retained for future examination. The small piece of black lead is next heated red hot in the flame of the spirit lamp, and being attached by its platinum support to a stiff copper wire thrust through a cork, which fits the bottle of oxygen, is placed whilst red hot in the gas, and continues to glow until consumed. The fragment of diamond is by no means, however, soeasily ignited, the flame of the spirit lamp must be urged upon it with the blowpipe; when quite red hot, an assistant may remove the stopper from the bottle of oxygen, and the person heating the diamond should plunge it instantly into the gas; if this is dexterously managed, the fragment ofboartglows like a little star, and the combustion frequently continues till the piece diminishes so much that it falls out of its platinum support.

Sometimes the diamond cools down without igniting, the same process must therefore be repeated, and a few extra bottles of oxygen will prevent disappointment, as every failure destroys the purity of the gas by admixture with atmospheric air when the stopper is removed. (Fig. 146.)

Fig. 146.Fig. 146.

a.Bottle containing bark charcoal.b.Ditto the plumbago or black lead.c.Ditto the diamond.

a.Bottle containing bark charcoal.b.Ditto the plumbago or black lead.c.Ditto the diamond.

The combustion having ceased in the three bottles, the corks are removed, and the glass stoppers again fitted for the purpose of testing theproducts, which offer no apparent indication of any change, as oxygen and carbonic acid gas are both invisible. In each bottle a new combination has been produced; the charcoal, the black lead, the diamond have united with the oxygen, in the proportion of six parts of carbon to sixteen parts of oxygen, to form twenty-two parts of carbonic acid gas, which may be easily detected by pouring into each bottle a small quantity of a solution of slacked lime in water, called lime water. This test is easily made by shaking up common slacked lime with rain or distilled water for about an hour, and then passing it through a calico or paper filter. The test, though perfectly clear when poured in, becomes immediately clouded with a white precipitate, usually termed amilkiness, no doubt in allusion to the London milk, which is supposed to contain a notable proportion of chalk and water, for in this case the precipitate is chalk, the carbonic acid from the diamond and the charcoal having united with the lime held in solution by the water and formed carbonate of lime, or chalk, a substance similar in composition to marble, limestone, Iceland or double refracting spar, these three being nearly similar in composition, and differing only, like carbon and the diamond, in external appearance.

The milkiness, however, must not be held as conclusive of the presence of carbonic acid gas until a little vinegar or other acid, such as hydrochloric or nitric, has been finally added; if it now disappears with effervescence (like the admixture of tartaric acid, water, and carbonate of soda), the little bubbles of carbonic acid gas again escaping slowly upwards, leaving the liquid in the three bottles quite clear, then the experimentalist may sum up his labours with these effects, which prove in the most decisive manner that common charcoal, black lead, and the diamond, are formed of one and the same element—viz., carbon.

Having effected the synthesis (or combining together) of the diamond and oxygen, it is no longer possible to recover it in its brilliant and beautiful form. If the product of combustion is retained in a flask made of thin, hard glass, and two or three pellets of the metal potassium are placed in directly after the diamond has ceased to burn, and the flame of a spirit lamp applied till the potassium ignites, then the metal, by its great affinity for oxygen, takes away and separates it again from that which was formerly the diamond; but instead of the jewel being deposited, there is nothing butblack, shapeless, and minute particles of carbon obtained, if the potash produced is dissolved in water, and the charcoal separated by a filter.

Chalk is made by uniting carbonic acid gas with lime; it may therefore be employed as a source of the gas, by placing a few lumps of chalk, or marble, or limestone, in a bottle such as was used in the generation of hydrogen gas; on the addition of some water and hydrochloric acid, effervescence takes place from the escape of carbonic acid gas, and the cork and pewter pipe being adapted, it may be conveyed by its own gravity into glasses, jugs, or any other vessels, and a pneumatic trough will not be required. Carbonic acid gas has a specific gravity of 1.529, and is therefore rather more than half as heavy again as atmospheric air.

In order to satisfy the mind of the operator that the gas obtained from chalk is similar to theproduct of combustion from the diamond, some lime-water may be placed in a glass, and the gas from the bottle allowed to bubble through it; instantly the same milkiness is apparent, which again vanishes on the addition of acid. And this experiment is rendered still more striking if a lighted taper be placed in the glass just after the addition of the acid, when it will be immediately extinguished.

If a lady's muff-box, supported by threads or chains, is hung on one end of a scale-beam, and counterbalanced by a scale pan and a few shot, it isimmediately depressed on pouring into the muff-box a quantity of carbonic acid gas, which may have been previously collected in a large tin vessel. After showing the weight of the gas, the box is detached from the scale-beam, and the contents poured upon a series of lighted candles, which are all extinguished in succession. (Fig. 147.)

Fig. 147.Fig. 147.

a.Carbonic acid gas poured out of the tin box intob, the muff-box.b b.Detached muff-box, and candles extinguished by the carbonic acid gas poured from it.

a.Carbonic acid gas poured out of the tin box intob, the muff-box.b b.Detached muff-box, and candles extinguished by the carbonic acid gas poured from it.

The property of carbonic acid gas of extinguishing flame, as compared with the contrary property of oxygen, is nicely shown by first passing into a large and tall gas jar one half of its volume of oxygen gas; a large cork perforated with holes may be introduced, so as to float upon the surface of the water in the gas jar, and is usefully employed to break the violence with which the carbonic acid enters the gas jar, as it is passed in to fill up the remaining half volume of the gas jar, which now contains oxygen at the top, and carbonic acid gas at the bottom. On testing the contents of the jar with a lighted taper, it burns fiercely in the oxygen, but is immediately extinguished in thecarbonic acid gas, being alternately lighted and put out as it is raised or depressed in the gas jar.

A little treacle, water, and a minute portion of size, may be placed with some yeast in a quart bottle, to which a cork and pewter or glass pipe is attached; directly the fermentation begins, quantities of carbonic acid gas may be collected, and tested either with lime-water or the lighted taper.

Some clear lime-water placed in a convenient glass is quickly rendered milky on passing through it the air from the lungs by means of a glass tube; thus proving that respiration and (as shown by the ninth experiment) fermentation, as well as the combustion of charcoal, produce carbonic acid gas.

Carbonic acid gas is not only generated by the above processes, but is liberated naturally in enormous quantities from volcanoes, and from certain soils: hence the peculiar nature of the air in the Grotto del Cane. Dogs thrust into this cave drop down immediately, and are immediately revived by the tender mercies of the guides, who throw them into the adjoining lake. This natural phenomenon is well imitated by taking a box, open at the top, and nailing on to it a frame of cardboard,which may be painted to represent rocks, taking care that a portion (about three inches deep) at the lower part is well pasted to the box at the edges, so that the gas may be retained; a hole is perforated at the top side to admit a lighted taper, and another at the side for the pipe from the carbonic acid bottle; when the bottom is filled with gas, a taper is applied, which is found to burn in the upper part, but is immediately extinguished when it reaches the lower division, where the three inches of pasteboard prevent it falling out: thus showing in a simple manner why a guide may enter the cave with impunity, whilst the dog is rendered insensible because immersed in the gas. (Fig. 148.)

Fig. 148.Fig. 148.

a a.The box model of the Grotto del Cane.b b.Cardboard fixed in front of box, and painted to imitate rocks.c.Carbonic acid gas bottle, with bent tube passing through hole in the side of the box. A taper introduced atdburns in the upper, and is extinguished in the lower, part of the model.

a a.The box model of the Grotto del Cane.b b.Cardboard fixed in front of box, and painted to imitate rocks.c.Carbonic acid gas bottle, with bent tube passing through hole in the side of the box. A taper introduced atdburns in the upper, and is extinguished in the lower, part of the model.

Many fatal accidents have occurred in consequence of the air in deep pits, graves, &c., becoming unfit for respiration by the accumulation of carbonic acid gas, which may arise either from cavities in the soil, where animal matter has undergone decomposition, or it may happen from the depth and narrowness of the hole or well preventing a proper draught or current of air, so that it becomes foul by the breathing of the man who is digging the pit. Air which contains one or two per cent. of carbonic acid will support the respiration of man, or maintain the flame of a candle; but it produces the most serious results if inhaled for any length of time; a lighted candle let down into a well (suspected to contain foul air) before the descent of the person who is to work in it, may burn, but does not indicate the presence of the small percentage of the poison, carbonic acid. Frequently no trouble is taken to test the air with a lighted candle; a man is lowered by his companions, who see him suddenly become insensible, another is then lowered quickly to rescue him, and he shares the same fate; and indeed cases have occurred where even a third and a fourth have blindly and ignorantly rushed to their death in the humane attempt to rescue their fellow creatures. What is to be done in these cases? Are the living to remain idle whilst the unfortunate man is suffocating rapidly at the bottom of the pit? No; provided they do not venture themselves into the pit, they may try every known expedient to alter the condition of the foul air, so as to enable them to descend to the rescue. One should be despatched to any neighbouring house or cottage for a pan of burning coals; if any slacked lime is to be had, it may be rapidly mixed with water, and poured down the side of the pit; a bundle of shavings set on fire and let down, keeping it to one side, so as to establish a current; or even the empty buckets constantly let down empty and pulled up full of the noxious air, may appear a somewhat absurd step to take, but under the circumstances any plan that will change the air sufficiently to enable another person to descend must be adopted; in proof of which the following experiments may be adduced:

Fill a deep glass jar with carbonic acid, and ascertain its presence with a lighted taper; if a beaker glass to which a string is attached is let down into the vessel and drawn up, and then inverted over a lightedtaper, the utility of this simple plan is at once rendered apparent; the beaker glass represents the empty bucket, and can be let down and pulled up full of carbonic acid until a sensible change in the condition of the atmosphere is produced. The best plan, however, is to set the air in motion by heat obtained from burning matter, or even a kettle of boiling water, lowered by a cord, and this fact is well shown by putting a small flask full of boiling water, and corked, at the bottom of the deep glass jar containing the carbonic acid gas, which rises like other gases when sufficiently heated, and passing away, mixes with the surrounding air. (Fig. 149.)

Fig. 149.Fig. 149.

a.Deep jar containing carbonic acid gas, which is being removed by the little glass bucket.b.Jar containing corked flask of boiling water on a pad; the heated gas rises and the cold air descends to take its place.

a.Deep jar containing carbonic acid gas, which is being removed by the little glass bucket.b.Jar containing corked flask of boiling water on a pad; the heated gas rises and the cold air descends to take its place.

Carbonic acid gas dissolved in water under considerable pressure, forms that most agreeable drink called soda-water; the gas is not only useful in this respect, but has been applied most successfully by Mr. Gurney to extinguish a fire on a gigantic scale, which had been burning for years in the waste of a coal mine in Scotland. The same gas, generated suddenly by the combustion of a mixture of nitre, coke dust, and clay, or plaster of Paris, in vessels of a peculiar construction, has formed the subject of a patent by Phillips, since merged into the Fire Annihilator Company. The instrument is peculiarly adapted for shipping, and might, if properly used, be the means of saving many ships and valuable lives. (Fig. 150.)

Its practical value is established by the test of actual use: in the streets, by the Leeds Fire Brigade, and by firemen of the Fire Annihilator Company, temporarily stationed at Liverpool and Manchester.

The Fire Annihilator has been formally recognised by the Government Emigration Commissioners, who introduced into the Passengers' Act, 1852, in §24, the alternative, "Or other apparatus for extinguishing fire," with distinct reference to this invention, and subsequently by formal order authorized their officers to pass ships carrying Fire Annihilators.

Fig. 150.Fig. 150.

a.A carriage with six fire annihilators, No. 5 size, fitted with moveable pipes. The body of the carriage forms a tank for forty gallons of water; the tank is filled at a bunghole in the platform; a patent tap is fitted to the rear of the carriage; a spigot is placed near the end upright of the rail; a hand-pump is placed in the box at rear of carriage; a leather bucket with foot-holds and three canvas buckets are hung on the carriage; a hammer for removing and driving on the cover of the fire annihilator, and a nut wrench for the No. 10 truck, are placed in the box.b.A fire annihilator, No. 10 size, with moveable pipe, on a spring truck, is attached to the carriage.The battery is fitted with shafts for one horse. A pole is also provided to fix across the shafts, so that the battery may be drawn by hand.

a.A carriage with six fire annihilators, No. 5 size, fitted with moveable pipes. The body of the carriage forms a tank for forty gallons of water; the tank is filled at a bunghole in the platform; a patent tap is fitted to the rear of the carriage; a spigot is placed near the end upright of the rail; a hand-pump is placed in the box at rear of carriage; a leather bucket with foot-holds and three canvas buckets are hung on the carriage; a hammer for removing and driving on the cover of the fire annihilator, and a nut wrench for the No. 10 truck, are placed in the box.b.A fire annihilator, No. 10 size, with moveable pipe, on a spring truck, is attached to the carriage.

The battery is fitted with shafts for one horse. A pole is also provided to fix across the shafts, so that the battery may be drawn by hand.

Monsieur Adolphe Girard has proposed that all houses should be provided with an apparatus for the generation of carbonic acid gas,placed outside the building, which is to be conveyed along the ceiling by means of pipes perforated with numerous holes, and to be put in operation directly a fire breaks out. This plan, however ingenious, could hardly supply the carbonic acid gas with sufficient rapidity, and it is to be feared would utterly fail in practice. (Fig. 151.)

Fig. 151.Fig. 151.

a.Tank containing acid, communicating by a pipe withb, half filled with chalk and water.c c C C.Pipes conveying carbonic acid from the generatorb, to the ceiling, where it is discharged from numerous holes on the fire beneath.

a.Tank containing acid, communicating by a pipe withb, half filled with chalk and water.c c C C.Pipes conveying carbonic acid from the generatorb, to the ceiling, where it is discharged from numerous holes on the fire beneath.

Symbol, B; combining proportion, 10.9.

Discovered by Homberg, in 1702, in borax, which is a biborate of soda (NaO,2BO3), and is used very extensively in the manufacture of glass; also for glazing stoneware and soldering metals; it is also a valuable flux in various crucible operations, whilst in testing minerals with the blowpipe it is invaluable. Borax is made either from tincal, a substance that occurs naturally in some parts of India, China, and Persia, or by the addition of carbonate of soda to boracic acid, a substance obtained from the volcanic districts of Tuscany, whence it is imported to this country, and used in the manufacture of borax.

The element boron may be obtained by placing some pure boracic acid and some small bits of potassium in a tube together, and applying the flame of a spirit-lamp, a glow of heat takes place, and when the tube is cold the potash may be washed away, and the boron remains as a dark brownish powder somewhat resembling carbon. M. St. Claire Deville and Wöhler have lately made some important discoveries with respect to this element, and disproved the statement that it is uncrystallizable. Their researches prove it to be producible under three forms and of various colours, such as honey-yellow and garnet-red, the crystals in some cases being like diamonds of the purest water—i.e., limpid and transparent. A new combination of aluminium and boron is stated to possess the most remarkable properties. It is harder than the diamond, and in the state of powder will cut and drill rubies, and even the diamond itself, with more facility than diamond powder. Deville and Wöhler incline to the belief that the diamond is dimorphous, and capable (in conditions yet to be described) of assuming the same forms as boron. At a high temperature, boron, like titanium, absorbsnitrogenonly from the atmosphere, and rejects the oxygen. (Query, may not some of those remarkably hard black diamonds prove to be boron?)

Symbol, Si; combining proportion, 21.3.

The great Berzelius was the first to obtain this element in 1823. Silicon in the pure state is a dark brown powder; if ignited at a very high temperature it assumes a chocolate colour, which is supposed to be the allotropic condition, because it no longer burns when heated moderately in oxygen or air, and is not attacked by hydrofluoric acid.The most interesting combination of silicon is the teroxide called silicic acid, silica (SiO3). Silicon is next to oxygen so far as regards its plentifulness, and is found in the state of silica in nearly every mineral, but especially in rock crystal, quartz, flint, sand, jasper, agate, and tripoli. It is largely used in the manufacture of glass, and a most useful "soluble glass" is obtained by melting together in a crucible fifteen parts of sand, ten parts of carbonate of potash, and one part of charcoal.

Cold water merely washes away the excess of alkali, and after this is done the powdered soluble glass may be boiled with water in the proportion of one of the former with five of the latter, when it gradually dissolves; the solution may be evaporated to a thick pasty fluid, which looks like jelly when cool, and on exposure to the air in thin films changes to a transparent, colourless, brittle, but not hard glass. Wood, cotton, and linen fabrics are rendered less combustible when coated with this glass, which excludes the oxygen of the air, and it has lately been employed to fill up the porous and capillary openings in stone exposed to the atmosphere, and is stated to be very efficacious as a preservative of the stone in some cases.

Symbol, S; combining proportion, 16.

Sulphur, like charcoal, is of common occurrence in nature, and is chiefly supplied from the volcanic districts of Tuscany and Sicily: there is an abundance of this element in the United Kingdom, but then it is locked up in combination with iron, copper, and lead, under the name of iron pyrites, copper pyrites, galena; and whilst Sicily and Tuscany supply thousands of tons weight in the uncombined state, it is not, of course, worth while to go through expensive operations at home for the separation of sulphur from the ores. During the dispute between Sicily and England, several patents were secured for new and economical processes by which sulphur was obtained from various minerals; and had this country been excluded from a supply of native sulphur, no doubt some of these patents would now be in active operation.

It is almost possible to estimate the commercial prosperity of a country by the sulphur it consumes, not, happily, by their warlike operations, but in the manufacture of oil of vitriol or sulphuric acid, which is the starting point of a great number of useful arts and manufactures.

Some very curious results may be obtained by heating sulphur at certain temperatures; in the ordinary state it is a pale yellow solid, and when subjected to a temperature of 226° Fahr. it melts to a brownish-yellow, transparent, thin fluid; according to all preconceived notions of the properties of substances which liquify by an increase of heat, it might be imagined that every additional degree of heat would onlyrender the melted sulphur still more liquid, but strange to say, when it reaches a temperature of about 320° Fahr. it changes red, and thick like treacle; and as the heat rises it becomes so tenacious, that the ladle in which it is contained may be inverted, and the sulphur will hardly flow out: at about 482° Fahr. it again becomes liquid, but not so fluid as at the lower temperature. If allowed to cool from 482° Fahr., the above results are simply inverted; the sulphur becomes thick, again liquid, and finally crystallizes in long, thin, rhombic prisms, which are seen most perfectly by first allowing a crust of sulphur to form on the liquid portion, and then having made two holes in this crust, the sulphur is poured out, when the remainder is found in the interior of the crucible crystallized in the form already mentioned. Sulphur takes fire in the air when exposed to a heat of about 560° Fahr., and burns with a pale blue flame; and, as already stated, it may be poured from a considerable height on a still dark night, and produces a continuous column of blue fire, just like an unbroken current of electricity. If the melted and burning sulphur is received into a vessel containing boiling water, it is no longer yellow, but assumes a curiousallotropicstate, in which it is a reddish-brown, transparent, shapeless mass, that may be easily kneaded and used for the purpose of taking casts of seals, which become yellow in a few days, and are found then to be hard and crystallized.

Sulphur vapour, in one sense, may be regarded as a supporter of combustion: if a clean Florence oil-flask is filled with copper turnings, and a little roughly-powdered sulphur sprinkled in, and heat applied, the copper glows with an intense heat, and burning in the vapour of the sulphur, produces a sulphuret of copper; from this compound the sulphur may be again obtained by boiling the powdered sulphuret with weak nitric acid, which oxidizes and dissolves the copper, leaving the greater part of the sulphur behind, which may be collected, melted, and burnt, and will be found to display all the properties belonging to that element. This experiment is a very good example of simple analysis; and if the copper is weighed and likewise the combined sulphur, a good notion may be formed of the principles of combining proportions.

A little sulphur burnt under a gas jar, or in any convenient box (a hat-box, for instance), produces sulphurous acid (SO2), which will bleach a wetted red rose or dahlia, and many other flowers. This gas is employed most extensively in bleaching straw, and sundry woollen goods, such as blankets and flannel, and likewise silk, and is perhaps one of the best disinfectants that can be employed; when fever has been raging in the dwellings of the poor, as in cottages, &c., all metallic substances should be removed, the doors and windows closed, the bedding, &c., well exposed, and then a quantity of sulphur should be burnt in an old frying-panplaced on a brick, taking care to avoid the chance of setting the place on fire; after a few hours the doors and windows may be opened, and the disinfectant will be found to have done its work cheaply and surely.

The presence of sulphur in various organic substances, such as hair, the white of egg, and fibrine, is easily detected by heating them in a solution of potash, and adding acetate of lead as long as the precipitate formed is redissolved; finally the solution must be heated to the boiling point, when it instantly becomes black by the separation of sulphuret of lead.

Sulphuric acid, HO,SO3, or oil of vitriol, is made in such enormous quantities that it is never worth while to attempt its preparation on a small scale. In consequence of its great affinity for water, many energetic changes are produced by its action. Oil of vitriol poured on some loaf sugar placed in a breakfast-cup with the addition of a dessert-spoonful of boiling water, rapidly boils and deposits an enormous quantity of black charcoal. If a word be written on a piece of white calico with dilute sulphuric acid, and then rapidly and thoroughly washed out, no visible change occurs; but if the calico is exposed to heat, so that the excess of water is driven off, the remaining and now concentrated oil of vitriol attacks the calico, and the word is indelibly printed in black by the decomposition of the fabric of cotton. A very remarkable process has lately been introduced by Mr. Warren de la Rue, by which paper is converted into a sort of tough parchment-like material, called ametastine, by the action of oil of vitriol and water of a certain fixed strength; and any departure from the exact proportions destroys the toughness of the paper. After the paper has been acted upon by the acid, it becomes extremely tenacious, and will support a considerable weight without breaking. Mr. Smee has used this ametastine in the construction of an hygrometer, and states that it may save many a traveller from catching a severe rheumatism in a damp bed.

When the vapour of sulphur is passed over red-hot charcoal and the product carefully condensed, a peculiar liquid is obtained, called bisulphide of carbon (CS2), which possesses a peculiar odour, is extremely transparent and brilliant-looking, and enjoys a high refractive power. This liquid is used as a solvent for phosphorus and other substances, and is extremely volatile and combustible, and burns silently with a pale blue flame. The combustion of its vapour, mixed with certain gases, offers a good example of the fact that slow burning may be a peaceful experiment, whilst very rapid combustion often resolves itself into an explosion. Thus, if a few drops of bisulphide of carbon are dropped into a narrow-mouthed dry quart bottle containing common air, and flame applied, the combustion takes place with rapidity, a rushing orroaring sound being audible, in consequence of the diffused vapour being supplied with more oxygen, and burning more rapidly than it would do if simply consumed from a stick or glass rod wetted with the fluid. A still greater rapidity of combustion is ensured by dropping some bisulphide of carbon into a long stout cylindrical jar, fifteen inches long and three inches in diameter, containing nitric oxide gas (NO2); when flame is applied the mixture burns with a bright flash and some noise, and if burnt in a narrow mouthed bottle would most likely blow it to atoms.

The greatest rapidity of combustion, and of course the loudest noise, is obtained by shaking some bisulphide of carbon in a similar stout and strong cylindrical jar filled with oxygen gas, but in this case the jar must be protected with a double cylinder of stout wire gauze; it does not always break, but if it is blown to fragments each particle becomes a lancet-shaped piece of glass, which is capable of producing the most dangerous wounds. (Fig. 152.)


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