Supposing, now, that acetylene contained in a closed vessel, either as compressed gas, as a solution in acetone, or as a liquid, were brought to explosion by spark or shock, the effects capable of production have to be considered. Berthelot and Vieille have shown that if gaseous acetylene is stored at a pressure of 11.23 kilogrammes per square centimetre, [Footnote: 1 kilo. per sq. cm. is almost identical with 1 atmosphere, or 15 lb. per sq. inch.] the pressure after explosion reaches 92.33 atmospheres on an average, which is an increase of 8.37 times the original figure; if the gas is stored at 21.13 atmospheres, the mean pressure after explosion is 213.15 atmospheres, or 10.13 times the original amount. If liquid acetylene is tested similarly, the original pressure, which must clearly be more than 21.53 atmospheres (Ansdell) at 0° C., may rise to 5564 kilos, per square centimetre, as Berthelot and Vieille observed when a steel bomb having a capacity of 49 c.c. was charged with 18 grammes of liquefied acetylene. In the case of the solution in acetone, the magnitudes of the pressures set up are of two entirely different orders according as the original pressure 20 atmospheres or somewhat less; but apart from this, they vary considerably with the extent to which the vessel is filled with the liquid, and they also depend on whether the explosion is produced in the solution or in the gas space above. Taking the lower original pressure first, viz., 10 atmospheres, when a vessel was filled with solution to 33 per cent. of its capacity, the pressure after explosion reached about 95 atmospheres if the spark was applied to the gas space; but attained 117.4 atmospheres when the spark was applied to the acetone. When the vessel was filled 56 per cent. full, the pressures after explosion reached about 89, or 155 atmospheres, according as the gas or the liquid was treated with the spark. But when the original pressure was 20 atmospheres, and the vessel was filled to 35 per cent. of its actual capacity with solution, the final pressures ranged from 303 to 568 atmospheres when the gas was fired, and from 2000 to 5100 when the spark was applied to the acetone. Examining these figures carefully, it will be seen that the phenomena accompanying the explosion of a solution of acetylene in acetone resemble those of the explosion of compressed gaseous acetylene when the original pressure under which the solution is stored is about 10 atmospheres; but resemble those of the explosion of liquefied acetylene when the original pressure of the solution reaches 20 atmospheres, this being due to the fact that at an original pressure of 10 atmospheres the acetone itself does not explode, but, being exothermic, rather tends to decrease the severity of the explosion; whereas at an original pressure of 20 atmospheres the acetone does explode (or burn), and adds its heat of combustion to the heat evolved by the acetylene. Thus at 10 atmospheres the presence of the acetone is a source of safety; but at 20 atmospheres it becomes an extra danger.

Since sound steel cylinders may easily be constructed to boar a pressure of 250 atmospheres, but would be burst by a pressure considerably less than 5000 atmospheres, it appears that liquefied acetylene and its solution in acetone at a pressure of 20 atmospheres are quite unsafe; and it might also seem that both the solution at a pressure of 10 atmospheres and the simple gas compressed to the same limit should be safe. But there is an important difference here, in degree if not in kind, because, given a cylinder of known capacity containing (1) gaseous acetylene compressed to 10 atmospheres, or (2) containing the solution at the same pressure, if an explosion were to occur, in case (1) the whole contents would participate in the decomposition, whereas in case (2), as mentioned already, only the small quantity of gaseous acetylene above the solution would be dissociated.

It is manifest that of the three varieties of compressed acetylene now under consideration, the solution in acetone is the only one fit for general employment; but it exhibits the grave defects (a) that the pressure under which it is prepared must be so small that the pressure in the cylinders can never approach 20 atmospheres in the hottest weather or in the hottest situation to which they may be exposed, (b) that the gas does not escape smoothly enough to be convenient from large vessels unless those vessels are agitated, and (c) that the cylinders must always be used in a certain position with the valve at the top, lest part of the liquid should run out into the pipes. For these reasons the simple solution of acetylene in acetone has not become of industrial importance; but the processes of absorbing either the gas, or better still its solution in acetone, in porous matter have already achieved considerable success. Both methods have proved perfectly safe and trustworthy; but the combination of the acetone process with the porous matter makes the cylinders smaller per unit volume of acetylene they contain. Several varieties of solid matter appear to work satisfactorily, the only essential feature in their composition being that they shall possess a proper amount of porosity and be perfectly free from action upon the acetylene or the acetone (if present). Lime does attack acetone in time, and therefore it is not a suitable ingredient of the solid substance whenever acetylene is to be compressed in conjunction with the solvent; so that at present either a light brick earth which has a specific gravity of 0.5 is employed, or a mixture of charcoal with certain inorganic salts which has a density of 0.3, and can be introduced through a small aperture into the cylinder in a semi-fluid condition. Both materials possess a porosity of 80 per cent., that is to say, when a cylinder is apparently filled quite full, only 20 per cent, of the space is really occupied by the solid body, the remaining 80 per cent, being available for holding the liquid or the compressed gas. If all comparisons as to degree of explosibility and effects of explosion are omitted, an analogy may be drawn between liquefied acetylene or its compressed solution in acetone and nitroglycerin, while the gas or solution of the gas absorbed in porous matter resembles dynamite. Nitroglycerin is almost too treacherous a material to handle, but as an explosive (which in reason absorbed or dissolved acetylene is not) dynamite is safe, and even requires special arrangements to explode it.

In Paris, where the acetone process first found employment on a large scale, the company supplying portable cylinders to consumers uses large storage vessels filled, as above mentioned, apparently full of porous solid matter, and also charged to about 43 per cent, of their capacity with acetone, thus leaving about 37 per cent. of the apace for the expansion which occurs as the liquid takes up the gas. Acetylene is generated, purified, and thoroughly dried according to the usual methods; and it is then run through a double-action pump which compresses it first to a pressure of 3.5 kilos., next to a pressure of 3.5 x 3.5 = 12 kilos, per square centimetre, and finally drives it into the storage vessels. Compression is effected in two stages, because the process is accompanied by an evolution of much heat, which might cause the gas to explode during the operation; but since the pump is fitted with two cylinders, the acetylene can be cooled after the first compression. The storage vessels then contain 100 times their apparent volume of acetylene; for as the solubility of acetylene in acetone at ordinary temperature and pressure is about 25 volumes of gas in 1 of liquid, a vessel holding 100 volumes when empty takes up 25 x 43 = 1000 volumes of acetylene roughly at atmospheric pressure; which, as the pressure is approximately 10 atmospheres, becomes 1000 x 10 = 10,000 volumes per 100 normal capacity, or 100 times the capacity of the vessel in terms of water. From these large vessels, portable cylinders of various useful dimensions, similarly loaded with porous matter and acetone, are charged simply by placing them in mutual contact, thus allowing the pressure and the surplus gas to enter the small one; a process which has the advantage of renewing the small quantity of acetone vaporised from the consumers' cylinders as the acetylene is burnt (for acetone is somewhat volatile, cf. Chapter X.), so that only the storage vessels ever need to have fresh solvent introduced.

Where it is procurable, the use of acetylene compressed in this fashion is simplicity itself; for the cylinders have only to be connected with the house service-pipes through a reducing valve of ordinary construction, set to give the pressure which the burners require. When exhausted, the bottle is simply replaced by another. Manifestly, however, the cost of compression, the interest on the value of the cylinders, and the carriage, &c., make the compressed gas more expensive per unit of volume (or light) than acetylene locally generated from carbide and water; and indeed the value of the process does not lie so much in the direction of domestic illumination as in that of the lighting, and possibly driving, of vehicles and motor-cars--more especially in the illumination of such vehicles as travel constantly, or for business purposes, over rough road surfaces and perform mostly out-and-home journeys. Nevertheless, absorbed acetylene may claim close attention for one department of household illumination, viz., the portable table-lamp; for the base of such an apparatus might easily be constructed to imitate the acetone cylinder, and it could be charged by simple connexion with a larger one at intervals. In this way the size of the lamp for a given number of candle-hours would be reduced below that of any type of actual generator, and the troubles of after-generation, always more or less experienced in holderless generators, would be entirely done away with. Dissolved acetylene is also very useful for acetylene welding or autogenous soldering.

The advantages of compressed and absorbed acetylene depend on the small bulk and weight of the apparatus per unit of light, on the fact that no amount of agitation can affect the evolution of gas (as may happen with an ordinary acetylene generator), on the absence of any liquid which may freeze in winter, and on there being no need for skilled attention except when the cylinders are being changed. These vessels weigh between 2.5 and 3 kilos, per 1 litre capacity (normal) and since they are charged with 100 times their apparent volume of acetylene, they may be said to weigh 1 kilo, per 33 litres of available acetylene, or roughly 2 lb. per cubic foot, or, again, if half-foot burners are used, 2 lb. per 36 candle- hours. According to Fouché, if electricity obtained from lead accumulators is compared with acetylene on the basis of the weight of apparatus needed to evolve a certain quantify of light, 1 kilo, of acetylene cylinder is equal to 1.33 kilos, of lead accumulator with arc lamps, or to 4 kilos. of accumulator with glow lamps; and moreover the acetylene cylinder can be charged and discharged, broadly speaking, as quickly or as slowly as may be desired; while, it may be added, the same cylinder will serve one or more self-luminous jets, one or more incandescent burners, any number and variety of heating apparatus, simultaneously or consecutively, at any pressure which may be required. From the aspect of space occupied, dissolved acetylene is not so concentrated a source of artificial light as calcium carbide; for 1 volume of granulated carbide is capable of omitting as much light as 4 volumes of compressed gas; although, in practice, to the 1 volume of carbide must be added that of the apparatus in which it is decomposed.

LIQUEFIED ACETYLENE.--In most civilised countries the importation, manufacture, storage, and use of liquefied acetylene, or of the gas compressed to more than a fraction of one effective atmosphere, is quite properly prohibited by law. In Great Britain this has been done by an Order in Council dated November 26, 1897, which specifies 100 inches of water column as the maximum to which compression may be pushed. Power being retained, however, to exempt from the order any method of compressing acetylene that might be proved safe, the Home Secretary issued a subsequent Order on March 28, 1898, permitting oil-gas containing not more than 20 per cent, by volume of acetylene (see below) to be compressed to a degree not exceeding 150 lb. per square inch, i.e., to about 10 atmospheres, provided the gases are mixed together before compression; while a third Order, dated April 10, 1901, allows the compression of acetylene into cylinders filled as completely as possible with porous matter, with or without the presence of acetone, to a pressure not exceeding 150 lb. per square inch provided the cylinders themselves have been tested by hydraulic pressure for at least ten minutes to a pressure not less than double [Footnote: In France the cylinders are tested to six times and in Russia to five times their working pressure.] that which it is intended to use, provided the solid substance is similar in every respect to the samples deposited at the Home Office, provided its porosity does not exceed 80 per cent., provided air is excluded from every part of the apparatus before the gas is compressed, provided the quantity of acetone used (if used at all) is not sufficient to fill the porosity of the solid, provided the temperature is not permitted to rise during compression, and provided compression only takes place in premises approved by H.M.'s Inspectors of Explosives.

DILUTED ACETYLENE.--Acetylene is naturally capable of admixture or dilution with any other gas or vapour; and the operation may be regarded in either of two ways; (1) as a, means of improving the burning qualities of the acetylene itself, or (2) as a means of conferring upon some other gas increased luminosity. In the early days of the acetylene industry, generation was performed in so haphazard a fashion, purification so generally omitted, and the burners were so inefficient, that it was proposed to add to the gas a comparatively small proportion of some other gaseous fluid which should be capable of making it burn without deposition of carbon while not seriously impairing its latent illuminating power. One of the first diluents suggested was carbon dioxide (carbonic acid gas), because this gas is very easy and cheap to prepare; and because it was stated that acetylene would bear an addition of 5 or even 8 per cent, of carbon dioxide and yet develop its full degree of luminosity. This last assertion requires substantiation; for it is at least a grave theoretical error to add a non-inflammable gas to a combustible one, as is seen in the lower efficiency of all flames when burning in common air in comparison with that which they exhibit in oxygen; while from the practical aspect, so harmful is carbon dioxide in an illuminating gas, that coal-gas and carburetted water-gas are frequently most rigorously freed from it, because a certain gain in illuminating power may often thus be achieved more cheaply than by direct enrichment of the gas by addition of hydrocarbons. Being prepared from chalk and any cheap mineral acid, hydrochloric by preference, in the cold, carbon dioxide is so cheap that its price in comparison with that of acetylene is almost nil; and therefore, on the above assumption, 105 volumes of diluted acetylene might be made essentially for the same price as 100 volumes of neat acetylene, and according to supposition emit 5 per cent. more light per unit of volume.

It is reported that several railway trains in Austria are regularly lighted with acetylene containing 0.4 to 1.0 per cent. of carbon dioxide in order to prevent deposition of carbon at the burners. The gas is prepared according to a patent process which consists in adding a certain proportion of a "carbonate" to the generator water. In the United Kingdom, also, there are several installations supplying an acetylene diluted with carbon dioxide, the gas being produced by putting into that portion of a water-to-carbide generator which lies nearest to the water- supply some solid carbonate like chalk, and using a dilute acid to attack the material. Other inventors have proposed placing a solid acid, like oxalic, in the former part of a generator and decomposing it with a carbonate solution; or they have suggested putting into the generator a mixture of a solid acid and a solid soluble carbonate, and decomposing it with plain water.

Clearly, unless the apparatus in which such mixtures as these are intended to be prepared is designed with considerable care, the amount of carbon dioxide in the gas will be liable to vary, and may fall to zero. If any quantity of carbide present has been decomposed in the ordinary way, there will be free calcium hydroxide in the generator; and if the carbon dioxide comes into contact with this, it will be absorbed, unless sufficient acid is employed to convert the calcium carbonate (or hydroxide) into the corresponding normal salt of calcium. Similarly, during purification, a material containing any free lime would tend to remove the carbon dioxide, as would any substance which became alkaline by retaining the ammonia of the crude gas.