Selenium And Tellurium
acid metallic sulphur elementary temperature heat
SELENIUM AND TELLURIUM I are two rather rare chemical elements discovered, the latter by Muller von Reichenstein in 1782, the former by Berzelius in 1817. Both occur only in the mineral kingdom as components of very rare minerals, most of which are compounds of one or the other or of both and sulphur with silver, lead, bismuth, antimony, gold, and other metals.
Elementary Selenium. - This, like elementary sulphur, exists in a variety of forms, which are conveniently considered as modifications of the two genera now to be described. (1) A-on-metallic selenium includes the flocculent scarlet precipitate produced by the reduction of solution of selenium by sulphurous acid in the cold. The scarlet flocks when dried without the aid of heat assume the form of a brown-red powder of sp. gr. 4.26, which dissolves in 1000 times its weight of boiling bisulphide of carbon (at 46°•6 C.). The solution on cooling deposits most of its selenium in the form of minute monoclinic crystals of sp.
gr. 4.5 (isomorphous with monoclinic sulphur), which retain their solubility in bisulphide of carbon up to 100° C. At 110° C. or higher temperatures they pass into the metallic modification (see below) with evolution of heat. With the amorphous kind a similar change sets in at or above 80° C. and attains its maximum of rapidity at a point be-tween 125° and 180° C. Fused selenium when cooled down suddenly hardens into a very dark-coloured glass of 4.28 sp. gr., soluble in bisulphide of carbon ; on gradual cool-ing it becomes more or less completely " metallic." (2) Metallic selenium is a dark grey or black solid of 4.8 sp. gr. ; it exhibits metallic lustre, stretches perceptibly under the hammer, and its fracture is similar to that of grey cast iron. It is insoluble in bisulphide of carbon. Its fusing point is sharply defined and lies at 217° C. At the ordi-nary temperature it conducts electricity, while the non-metallic modification does not ; at higher temperatures, or after temporary exposure to higher temperatures, the con-ductivity on either side becomes an eminently variable quantity. According to Draper and Moss, glassy selenium begins to conduct electricity at 165° to 175° C., and the conductivity increases regularly as the temperature rises to near the boiling-point. With metallic seleniura, which behaves similarly, the increase of conductivity is propor-tional to the increase of temperature to near the fusing point (217° C.); but from this point upwards it decreases mpidly and attains its minimum at 250° C. According to W. Siemens, however, selenium by long exposure to 200° C. becomes what one may call electrically metallic ; the conductivity then decreases when the tempemture rises, just as it does with ordinary metals. But this electro-metallicity is not permanent ; orr continued exposure to a lower temperature it vanishes gradually, until the propor-tion of quasi-metal has fallen to a limit-value depending on that temperature. Very surprising is the observation of Sale that the electric conductivity of metallic selenium increases on exposure to the light ; the red and ultra-red rays, as he found, act most powerfully. The effect of insolation is almost instantaneous, but on re-exposure to darkness the original condition is re-established only very gradually. W. Siemens found that his electro-metallic selenium (as produced at 200° C.) is more sensitive to light than any other kind. The conductivity of such selenium starting from darkness is raised twofold by dif-fuse and tenfold by direct sunlight. The specific heat of selenium, according to Regnault, is 0.0746 both in the glassy and in the metallic modification. Selenium (of any kind) boils at 700° C. (Mitscherlich). The vapour has an intense colour intermediate between that of chlorine and that of sulphur. According to Deville and Troost, at 880° C. it is 7.67 times, and at 1420° is 5.68 times, as heavy as air ; theory, for Se2= 1 molecule, demands 5.47.
Elementary Tellurium. - This, the compact form, is a silver-white resplendent metal of markedly crystalline structure ; the crystals are rhombohedra, and the ingot consequently is very brittle. Specific gravity 6.2. The metal fuses at about 500° C., and is distillable at very high temperatures. Its vapour is golden yellow and has a very brilliant absorption-spectrum. The vapour density, accord-ing to Deville and Troost, is 9.08 at 1439° C. (air =1), corresponding to Te2= 1 molecule. A bar of tellurium be-comes feebly electrical when rubbed with a woollen cloth. The electric conductivity, like that of selenium, is largely influenced by the temperature and previous exposure to heat, and it increases after exposure to light, though not to the same extent as selenium does. Starting from the ordinary temperature the conductivity decreases up to some point between 90° and 145° C. ; it then increases up to 200° C. (the highest tempemture tried) ; on cooling it de-creases steadily, and finally is only one-fifth or one-sixth of what it was at 200°. The numerical value at 200° (silver = 100) was found equal to 0.0035 to 0.0031 (F. Exncr).
Extraction of the Elementary Substances. - If seleniferous sulphur or pyrites is used for the rnanufacture of oil of vitriol by the chamber process, most of the selenium accumulates as such iu the " chamber mud," from which it may be extracted by the following method of Wohler's. The mud, after having been thoroughly washed and dried, is fused with alkaline nitrate and carbonate, to convert the selenium into selenate (Se04K2 or Na2), which is ex-tracted by means of water. The Mtered solution is boiled with hydrochloric acid to convert the selenic into selenium acid (Se03 + 2HCl= C12+ H20 + Se02), and this last is then reduced by addi-tion of sulphurous acid and heating, when the selenium comes down as a red precipitate (Se0, + 2SO2= 2S02 + Se). A richer material than chamber mud is seleniferous ore-smoke as produced in Mansfeld, Nvhich likewise contains free selenium. Its extraction, according to O. Pettersen and F. Nilson, is best effected by digestion with con-centrated solution of cyanide of potassium at 80°C., which converts the selenium into selenocyauide (SeNCK), easily extractable by water. The filtered solution is acidified with hydrochlmic acid and allowed to stand, when the selenium (through the spontaneous decomposi-tion of the SeNC. II into NCH and Se) comes down as a precipitate.
Tellurium is generally prepared from Transylvanian gold ore. The powdered ore is oxidized by rneans of hot nitric acid and the least sufficiency of hydrochloric acid, the excess of nitric acid being chased away by evaporation, and the residue mixed Nvith sulphuric acid (to convert the lead into insoluble sulphate), and with some tartaric acid to prevent precipitation of tellurious acid (Te02) in the subsequent treatment with water. From the filtered aqueous solution the gold is removed by addition of ferrous sulphate and by filtration. The filtrate is treated with sulphurous acid to reduce the tellurious acid to tellurium, which separates out as a black precipitate. The precipitated metal is fused down and then sublimed at a. very high temperature, in a porcelain tube, in a current of hydrogen, to remove non-volatile impurities and eliminate the last trace of selenium (SeH2).
Che9nical Relations. - Selenium and tellurium aro siznilar in their chemical character to sulphur ; the gradation of properties within the triad is iu the order of the atomic weights, which are S=32.06, Se =79.07, To= 128 (0=16). In oxygen or air the elementary sub-stances burn readily into (solid) dioxides (Se02, Te02), in the case of selenium with production of a charactaistie stench of putrid radish, owing probably to the formation of a trace of hydride, Se112. Nitric acid, in the heat, converts sulphur directly into sulphuric acid. In the case of the two rare elements the oxidation stops at the stage corresponding to sulphurous acid. The acids Se0,1I, and Te031-12 are not liable to further oxidation by any of the wet-way reagents (HNO3, H20 and C12, Br2, 12, &c.) which convert sulphur-ous into sulphuric acid.
By fusion with nitre and alkaline carbonate the three elements, in their elementary or less oxygenated forms, are readily converted into salts, R2Z04 (sulphates, &c., =S, Se, or Te). Selenic and telluric acids (H2Z04), unlike sulphuric, when boiled with aqueous hydrochloric acid, are gradually reduced to the lower acids (Se or Te)03112, with evolution of chlorine ; and the lower acids are readily reduced to (precipitates of) elementary selenium and tellurium re-spectively by the action of sulphurous acid in the heat. Chlorine combines readily with elementary selenium and tellurium into dichlorides (Se or Te)C1.2, which, however, on continued chlorina-tion aro at last completely converted into the tetrachlorides (Se or To)C14. These last, unlike the corresponding sulphur compound, are distillable without decomposition. Metals capable of uniting directly with sulphur as a nile unite also with selenium and tellurium into corresponding compounds. Hydrogen unites with elementary selenium and tellurium in the heat into gaseous hydrides (Se or Te)H2 closely similar to sulphuretted hydrogen. But, as these hydrides are liable to dissociation, the pure compounds must bo prepared by the decomposition of the zinc compounds Zn17., with hydrochloric acid. For the description of individual compounds reference must be made to the handbooks of chemistry. (NV. D. )