Hydrate of lime4·625
Chlorine4·5

Or nearly equal weights of the chlorine and the base; indicating a surprising degree of excellence in the preparation. The average commercial samples of bleaching powder from different factories which I examined some years ago, did not possess nearly that strength; but varied in their quantity of chlorine from 20 to 28 per cent. In my synthetic experiments related above, the greatest quantity of chlorine that would combine with the atomic hydrate of lime, was in the proportion of 130 to 200; but there is no doubt that if the lime contains additional water, it will condense more gas. I have never seen a chloride of lime of the strength mentioned by Dr. Thomson, and I should think there must be some fallacy in his statements. I have recorded in the paper above quoted an experiment which proves that with additional moisture, a chloride of lime may be obtained of the following composition:—

Chlorine39·5
Lime39·9
Water20·6
100·0

In the article Bleaching, of the Encyclopædia Britannica, Dr. Thomson deduces from a test trial of Mr. Crum, that the best bleaching powder is a compound of 1 atom chlorite of lime = 11, 3 atoms chloride of calcium = 21, and 8 atoms of water = 9. “But,” adds he, “in general the whole lime is not accurately saturated with chlorine. Accordingly, when the bleaching powder is dissolved in water a small residue almost always remains undissolved. Unless the powder be fresh made, a portion of chlorite is always converted into chloride of calcium. It is probable therefore that the best bleaching powder, as it comes into the hands of the bleachers, consists of

1atom chlorite of lime11
3atoms chloride of calcium21
6atoms water6·75
Impurity2·25
41·00

“If we consider the bleaching powder as a compound of chlorine and lime, our mode of calculating will not be altered. Instead of 1 atom chlorite of lime, and 3 atoms chloride of calcium, we shall have 4 atoms chloride of lime, 6 atoms water, and 2·25 of impurity as before.” In such ambiguity does this able chemist place this interesting compound, for theoretical reasons, of which I cannot see the value. Surely there is no difficulty in conceiving chlorine to exercise a direct attractive force towards the hydrate of lime, as it is known to do towards each of its elementary constituents, the oxygen and the calcium. Such refinements as the preceding tend merely to mystify a plain matter. Even the chlorous acid here brought into play to form the ideal chlorite, is by his own admission a hypothetical being. “When chlorate of potash” says Dr. Thomson, “is mixed with sulphuric acid, and made into small balls the size of a pea, if we expose these balls to a heat somewhat lower than that of boiling water, a bright yellowish green gas separates, which may be received over mercury. Its smell is peculiar and aromatic. Water absorbs at least seven times its volume of it. It destroys vegetable blues. Its constituents are,

1 volume chlorine2·5 or 4·5
2 volumes oxygen2·222or4.

Thus this compound consists in weight of chlorine 4·5, oxygen 4 = 8·5. It has been called quarteroxide of chlorine, but it is more probably a teroxide. It has been supposed by some to possess acid properties, and has therefore been called chlorous acid. But this is only as yet a hypothesis.”

Surely this by the Doctor’s own showing is very slender authority for renouncing our long-received doctrines concerning the constitution of bleaching powder. I shall conclude by remarking that the ultra-atomists are now in a dilemma about this substance; M. Welter, and many French chemists calling it a sub-chloride, of 1 atom of chlorine to 2 atoms of lime, and Dr. Thomson showing that Mr. Tennant, the greatest and best manufacturer of it, has produced it in the state of a chloride, or 1 atom of each. The fact is, in chloride of lime, as in water of ammonia, alcohol, and muriatic acid, there is no sufficient reason for definite proportion in any term short of saturation, and therefore we shall find that chloride in every gradation of strength from 1 per cent. of chlorine up to 40 per cent.—the strongest which I succeeded in preparing, though I passed a constant stream of chlorine in great excess over a pure hydrate of lime for upwards of 24 hours, with frequent renewal of the surface; indeed, till it refused to absorb any more gas, as indicated by its remaining stationary in weight.

CHLOROMETRY; Chlorometrie, is the name given by the French to the process for testing the decolouring power of any combination of chlorine, but especially of the commercial articles, the chlorides of lime, potash, and soda. M. Gay Lussac proposed many years ago the following graduated method of applying indigo to this purpose. As indigo varies much in its dyeing quality, and of consequence in the proportion of chlorine required for its decoloration, he assumes as the unity of blanching power, one litre of chlorine gas, measured at the mean pressure of 29·6 inches, and at the temperature of melting ice. This volume of gas, when combined with a determinate quantity of water, is employed to test the standard solution of indigo. For this purpose a solution in sulphuric acid of any sample of indigo is taken, and diluted with water to such a degree that 10 measures of it, in a graduated tube, are decoloured by that one measure of combined chlorine gas. Each measure of indigo solution so destroyed is called a degree, and this measure being divided into five parts, the real test of chlorine is given to fiftieths, which is sufficiently nice. For the standard of the assays, a chloride of lime as pure and fully saturated as possible is taken, and dissolved in such a quantity of water, that the solution shall contain, or be equivalent to, one volume of chlorine gas. Calculation proves that this condition is exactly fulfilled by dissolving 4938 grammes of the said chloride in half a litre of water; or in English measures, 5 gr. very nearly in 500 grain measures of water. This solution, which serves for a type, indicates 10° in the assay, or proof; that is to say, each single volume destroys the colour of 10 volumes of the dilute indigo solution. It may be remarked, that a greater degree of precision is in general attainable with a weak solution of chlorine or a chloride, for example at 4° or 5°, than with one much stronger; consequently if, after a preliminary trial, the standard considerably exceeds 10°, a given volume of water must be added to the solution, and then the above proof must be taken. If the volume of water added was double, the number of degrees afterwards found must be tripled, to obtain the true title of the chloride. It is, however, to be observed that the degree of decoloration varies with the time taken in making the mixture; the more slowly the chlorine is added to the indigo, the less of it escapes into the atmosphere, and the more effective it becomes in destroying the colour. The best mode of obtaining comparable results, is to pour suddenly into the test quantity of chlorine the whole volume of the indigo solution likely to be decoloured; but it is requisite to find approximately beforehand, what quantity of indigo-blue will probably be destroyed. When it comes to the verge of destruction, it is green; but yellowish-brown when entirely decomposed.