Coloriasto on väriaiheisten tekstien (ja kuvien) verkkoarkisto
(Archive for colour themed articles and images)
INDEX: coloriasto.net
12.3.11
A Dictionary of Arts: Chlorometry
A Dictionary of Arts, Manufactures, and Mines; containing A Clear Exposition of Their Principles and Practice
by Andrew Ure, M. D.;
F. R. S. M. G. S. Lond.: M. Acad. M. S. Philad.; S. PH. DOC. N. GERM. Ranow.; Mulh. Etc. Etc.
Illustrated with nearly fifteen hundred engravings on wood
Eleventh American, From The Last London Edition.
To which is appended, a Supplement of Recent Improvements to The Present Time.
New York: D Appleton & company, 200 Broadway. Philadelphia: George S. Appleton, 148 Chestnut St.
MDCCCXLVII
1847
CHLOROMETRY; Chlorometrie, is the name given by the French to the process for testing the decoloring 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 afterward 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 color. 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.
I have tried the indigo test in many ways, but never could confide in it. The sulphuric solution of indigo is very liable to change by keeping, and thus to lead to erroneous results. The method of testing the chlorides by green sulphate of iron, described under bleaching, is in my opinion preferable to the above.
M. Gay Lussac has recently proposed another proof of chlorine, founded on the same principle as that by green vitriol, namely, the quantity of it requisite to raise a metallic substance from a lower to a higher stage of oxidizement. He now prescribes as the preferable plan of chlorometry, to pour very slowly from a graduated glass tube, a standard solution of the chloride, to be tested upon a determinate quantity of arsenious acid dissolved in muriatic acid, till the whole arsenious be converted into the arsenic acid. The value of the chloride is greater the less of it is required to produce this effect. It is easy to recognize, by a few drops of solution of indigo, the instant when all the arsenious acid has disappeared; for then the blue tint is immediately effaced, and cannot be restored by the addition of a fresh drop of the indigo solutions.
In graduating the arsenical chlorometer, M. Gay Lussac takes for his unity the decoloring power of one volume of chlorine at 32° Fahr., and divides it into 100 parts. Suppose that we prepare a solution of chlorine containing its own volume of the gas, and an arsenious solution, such, that under a like volume, the two solutions shall reciprocally destroy each other. Let us call the first, the normal solution of chlorine, and the second, the normal arsenious solution. We shall fix at 10 grammes the weight of chloride of lime subjected to trial; and dissolve it in water, so that the total volume of the solution shall be a litre (1000 grammes measure), including the sediment. If we take a constant volume of this solution, 10 centimetres cube (10 gramme measures), for example, divided into 100 equal parts, and pour into it gradually the arsenious solution (measured by like portions), till the chlorine be destroyed, the bleaching power will be proportional to the number of portions of the arsenious solution, which the chloride shall have required. If the chloride has destroyed 100 portions of the arsenious solution, its title will be 100; if it has destroyed 80 portions, its title will be 80, &c., and so forth.
On pouring the acidulous arsenious solution into the chloride of lime, this will become very acid; the chlorine will be emitted abundantly, and the proof will be quite incorrect. If, on the contrary, we pour the solution of the chloride of lime into the arsenious solution, this evil will not occur, since the chlorine will always find plenty of arsenious acid to set upon, whatever be the dilution of the one or the other; but in this case, the standard of the chlorine is not given directly, as it is in the inverse ratio of the number of portions which are required to destroy the measures of the arsenious solution. If 50 portions of the chloride have been required, the proof will be 100x100/50=200°; if 200 have been required, the proof will be 100x100/200=50°, &c. This evil is not, however, very serious, since we have merely to consult a table, in which we can find the proof corresponding to each volume of the chloride employed for destroying the constant measure of the arsenious solution. The arsenious solution should be slightly tinged with sulphate of indigo, so as to show, by the disappearance of the color, the precise point or instant of its saturation with chlorine, that is, its conversion into arsenic acid. If the arsenious acid be pure, the normal solution may be made directly by dissolving 4.439 grammes of it in muriatic acid (free from sulphurous acid), and diluting the solution till it occupies one litre, or 1000 grammes measure. Annales de Chimie et Physique, I.X. 225.
Ei kommentteja:
Lähetä kommentti