heat energy[1] is due to some form of potential energy in the compound which becomes actual heat energy at the moment of dissolution of the chemical union. The manner in which a substance is endothermic is of importance as regards the practical employment of explosives. Some particular endothermic state or form results from the mode of formation and the consequent internal structure of the molecule. Physical structure alone can be the cause of a relative endothermic state, as in the glass bulbs known as Rupert’s drops, &c., or even in chilled steel. Rupert’s drops fly in pieces on being scratched or cut to a certain depth. The cause is undoubtedly to be ascribed to the molecular state of the glass brought about by chilling from the melted state. The molecules have not had time to separate or arrange themselves in easy positions. In steel when melted the carbide of iron is no doubt diffused equally throughout the liquid. When cooled slowly some carbide separates out more or less, and the steel is soft or annealed. When chilled the carbides are retained in solid solution. The volume of chilled glass or steel differs slightly from that in the annealed state.
Superfused substances are probably in a similar state of physical potential or strain. Many metallic salts, and organic compounds especially, will exhibit this state when completely melted and then allowed to cool in a clean atmosphere. On touching with a little of the same substance in a solid state the liquids will begin to crystallize, at the same time becoming heated almost up to their melting-points. The metal gallium shows this excellently well, keeping liquid for years until touched with the solid metal, when there is a considerable rise of temperature as solidification takes place.
All carbon compounds, excepting carbon dioxide, and many if not all compounds of nitrogen, are endothermic. Most of the explosives in common use contain nitrogen in some form.
Exothermic compounds are in a certain sense the reverse of endothermic; they are relatively inert and react but slowly or not at all, unless energy be expended upon them from outside. Water, carbon dioxide and most of the common minerals belong to this class.
The explosives actually employed at the present time include mixtures, such as gunpowders and some chlorate compositions, the ingredients of which separately may be non-explosive; compounds used singly, as guncotton, nitroglycerin (in the form of dynamite), picric acid (as lyddite or melinite), trinitrotoluene, nitrocresols, mercury fulminate, &c. ; combinations of some explosive compounds, such as cordite and the smokeless propellants in general use for military purposes; and, finally, blasting and detonating or igniting compositions, some of which contain inert diluting materials as well as one or more high explosives. Many igniting compositions are examples of the last type, consisting of a high explosive diluted with a neutral substance, and frequently containing in addition a composition which is inflamed by the explosion of the diluted high explosive, the flame in turn igniting the actual propellant.
Explosive Mixtures.—The explosive mixture longest known is undoubtedly gunpowder (q.v.) in some form—that is, a mixture of charcoal with sulphur and nitre, the last being the oxygen provider. Besides the nitrates of metals and ammonium nitrate, there is a limited number of other substances capable of serving in a sufficiently energetic manner as oxygen providers. A few chlorates, perchlorates, permanganates and chromates almost complete the list. Of these the sodium, potassium and barium chlorates are best known and have been actually tried, in admixture with some combustible substances, as practical explosives. Most other metallic chlorates are barred from practical employment owing to instability, deliquescence or other property.
Of the chlorates those of potassium and sodium are the most stable, and mixtures of either of these salts with sulphur or sulphides, phosphorus, charcoal, sugar, starch, finely-ground cellulose, coal or almost any kind of organic, i.e. carbon, compound, in certain proportions, yield an explosive mixture. In many cases these mixtures are not only fired or exploded by heating to a certain temperature, but also by quite moderate friction or percussion. Consequently there is much danger in manufacture and storage, and however these mixtures have been made up, they are quite out of the question as propellants on account of their great tendency to explode in the manner of a detonator. In addition they are not smokeless, and leave a considerable residue which in a gun would produce serious fouling.
Mixtures of chlorates with aromatic compounds such as the nitro- or dinitro-benzenes or even naphthalene make very powerful blasting agents. The violent action of a chlorate mixture is due first to the rapid evolution of oxygen, and also to the fact that a chlorate can be detonated when alone. A drop of sulphuric acid will start the combustion of a chlorate mixture. In admixture with sulphur, sulphides and especially phosphorus, chlorates give extremely sensitive compositions, some of which form the basis of friction tube and firing mixtures.
Potassium and sodium perchlorates and permanganates make similar but slightly less sensitive explosive mixtures with the above-mentioned substances. Finely divided metals such as aluminium or magnesium give also with permanganates, chlorates or perchlorates sensitive and powerful explosives. Bichromates, although containing much available oxygen, form but feeble explosive mixtures, but some compounds of chromic acid with diazo compounds and some acetylides are extremely powerful as well as sensitive. Ammonium bichromate is a self-combustible after the type of ammonium nitrate, but scarcely an explosive.
Explosive Compounds.—Nearly all the explosive compounds in actual use either for blasting purposes or as propellants are nitrogen compounds, and are obtained more or less directly from nitric acid. Most of the propellants at present employed consist essentially of nitrates of some organic compound, and may be viewed theoretically as nitric acid, the hydrogen of which has been replaced by a carbon complex; such compounds are expressed by M·O·NO2, which indicates that the carbon group is in some manner united by means of oxygen to the nitrogen group. Guncotton and nitroglycerin are of this class. Another large class of explosives is formed by a more direct attachment of nitrogen to the carbon complex, as represented by M·NO2. A number of explosives of the detonating type are of this class. They contain the same proportions of oxygen and nitrogen as nitrites, but are not nitrites. They have been termed nitro-derivatives for distinction. One of the simplest and longest-known members of this group is nitrobenzene, C6H5NO2, which is employed to some extent as an explosive, being one ingredient in rack-a-rock and other blasting compositions. The dinitro-benzenes, C6H4(NO2)2, made from it are solids which are somewhat extensively employed as constituents of some sporting powders, and in admixture with ammonium nitrate form a blasting powder of a “flameless” variety which is comparatively safe in dusty or “gassy” coal seams.
Picric acid or trinitrophenol, C6H2·OH·(NO2)3 is employed as a high explosive for shell, &c. It requires, however, either to be enclosed and heated, or to be started by a powerful detonator to develop its full effect. Its compounds with metals, such as the potassium salt, C6H2·OK·(NO2)3, are when dry very easily detonated by friction or percussion and always on heating, whereas picric acid itself will burn very quietly when set fire to under ordinary conditions. Trinitrotoluene, C6H2·CH3·(NO2)3, is a high explosive resembling picric acid in the manner of its explosion (to which in fact it is a rival), but differs therefrom in not forming salts with metals. The nitronaphthols, C10H6·OH·NO2, and higher nitration products may be counted in the list. Their salts with metals behave much like the picrates.
All these nitro compounds can be reduced by the action of nascent hydrogen to substances called amines (q.v.), which are not always explosive in themselves, but in some cases can form nitrates of a self-combustible nature. Aminoacetic acid, for instance, will form a nitrate which burns rapidly but quietly, and might be employed as an explosive. By the action of nitrous acid at low temperatures on aromatic amines, e.g. aniline, C6H5NH2, diazo compounds are produced. These are all highly explosive, and when in a dry state are for the most part also extremely sensitive to friction, percussion or heat. As many of these diazo compounds contain no oxygen their explosive nature must be ascribed to the peculiar state of union of the nitrogen. This state is attempted to be shown by the formulae such as, for
- ↑ Not necessarily heat energy entirely. A number of substances—acetylides and some nitrogen compounds, such as nitrogen chloride—decompose with extreme violence, but little heat is produced.
