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See also:CADMIUM (See also:symbol Cd, atomic See also:weight 112.4 (0=16)) , a metallic See also:element, showing a See also:close relationship to See also:zinc, with which it is very frequently associated. It was discovered in 1817 by F. Stromeyer in a See also:sample of zinc carbonate from which a specimen of zinc See also:oxide was obtained, having a yellow See also:colour, although quite See also:free from See also:iron; Stromeyer showing that this coloration was due to the presence of the oxide of a new See also:metal. Simultaneously See also:Hermann, a See also:German chemical manufacturer, discovered the new metal in a specimen of zinc oxide which had been thought to contain See also:arsenic, since it gave a yellow precipitate, in See also:acid See also:solution, on the addition of sulphuretted See also:hydrogen. This supposition was shown to be incorrect, and the nature of the new element was ascertained.
Cadmium does not occur naturally in the uncombined See also:condition, and only one See also:mineral is known which contains it in any appreciable quantity, namely, See also:greenockite, or cadmium sulphide, found at See also:Greenock and at Bishopton in See also:Scotland, and in Bohemia and See also:Pennsylvania. It is, however, nearly always found associated with zinc See also:blende, and with See also:calamine, although only in small quantities.
The metal is usually obtained from the flue-dust (produced during the first three or four See also:hours working of a zinc See also:distillation) which is collected in the See also:sheet iron cones or adapters of the zinc retorts. This is mixed with small See also:coal, and when redistilled gives an enriched dust, and by repeating the See also:process and distilling from See also:cast iron retorts the metal is obtained. It can be purified by solution in hydrochloric acid and subsequent precipitation by metallic zinc.
Cadmium is a See also: It is malleable and can he rolled out into sheets. The specific gravity of the metal is 8.564, this value being slightly increased after hammering; its specific See also:heat is 0.0548 (R. See also:Bunsen), it melts at 310-320° C. and boils between 763-772° C. (T. Carnelley), forming a deep yellow vapour. The cadmium See also:molecule, as shown by determinations of the See also:density of its vapour, is monatomic. The metal unites with the See also:majority of the heavy metals to form See also:alloys; some of these, the so-called fusible alloys, find a useful application from the fact that they possess a See also:low melting-point. It also
See also:teeth. The metal is quite permanent in dry See also:air, but in moist air it becomes coated with a superficial layer of the oxide; it See also:burns on See also:heating to redness, forming a See also: It is a basic oxide, dissolving readily in acids, with the formation of salts, somewhat analogous to those of zinc. Cadmium hydroxide, Cd(OH)2, is obtained as a white precipitate by adding See also:potassium hydroxide to a solution of any soluble cadmium See also:salt. It is decomposed by heat into the oxide and water, and is soluble in See also:ammonia but not in excess of dilute potassium hydroxide; this latter See also:property serves to distinguish it from zinc hydroxide. The chloride,CdCl2,bromide,CdBr2,and iodide,Cdl2,arealsoknown, cadmium iodide being sometimes used in See also:photography, as it is one of the few iodides which are soluble in See also:alcohol. Cadmium chloride and iodide have been shown to behave in an anomalous way in aqueous solution (W. Hittorf, Pogg. See also:Ann., 1859, 106, 513), probably owing to the formation of complex ions; the abnormal behaviour apparently diminishing as the solution becomes more and more dilute, until, at very high dilutions the salts are ionized in the normal manner. Cadmium sulphate, CdSO4, is known in several hydrated forms; being deposited, on spontaneous evaporation of a concentrated aqueous solution, in the form of large monosymmetric crystals of See also:composition 3CdSO4.8H20, whilst a boiling saturated solution, to which concentrated sulphuric acid has been added, deposits crystals of composition CdSO4•H2O. It is largely used for the purpose of making See also:standard electric cells, such for example as the See also:Weston See also:cell. Cadmium sulphide, CdS, occurs naturally as greenockite (q.v.), and can be artificially prepared by passing sulphuretted hydrogen through acid solutions of soluble cadmium salts, when it is precipitated as a See also:pale yellow amorphous solid. It is used as a pigment (cadmium yellow), for it retains its colour in an See also:atmosphere containing sulphuretted hydrogen; it melts at a white heat, and on cooling solidifies to a See also:lemon-yellow micaceous See also:mass. Normal cadmium See also:carbonates are unknown, a white precipitate of variable composition being obtained on the addition of solutions of the alkaline carbonates to soluble cadmium salts. Cadmium nitrate, Cd(NO3)2.4H20, is a deliquescent salt, which may be obtained by dissolving either the metal, or its oxide or carbonate in dilute nitric acid. It crystallizes in needles and is soluble in alcohol. Cadmium salts can be recognized by the brown incrustation which is formed when they are heated on See also:charcoal in the oxidizing See also:flame of the See also:blowpipe; and also by the yellow precipitate formed when sulphuretted hydrogen is passed though their acidified solutions. This precipitate is insoluble in See also:cold dilute acids, in ammonium sulphide, and in solutions of the See also:caustic alkalis, a behaviour which distinguishes it from the yellow sulphides of arsenic and tin. Cadmium is estimated quantitatively by See also:conversion into the oxide, being precipitated from boiling solutions by the addition of See also:sodium carbonate, the carbonate thus formed passing into the oxide on ignition. It can also be determined as sulphide, by precipitation with sulphuretted hydrogen, the precipitated sulphide being dried at too° C. and weighed. The atomic weight of cadmium was found by 0. W. See also:Huntington (Berichte, 1882, 15, p. 8o), from an See also:analysis of the pure bromide, to be 111.9. H. N. See also:Morse and H. C. See also: The atomic weight of cadmium has been revised by G. P. See also:Baxter and M. A. Hines (Journ. Amer. Chem. See also:Soc., 1905, 27, p. 222), by determinations of the ratio of cadmium chloride to See also:silver chloride, and of the amount of silver required to precipitate cadmium chloride. The mean value obtained was 112.469 (Ag=107.93). The mean value 112.467 was obtained by Baxter, Hines and Frevert (ibid., 1906, 28, p. 770) by analysing cadmium bromide. Additional information and CommentsThere are no comments yet for this article.
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