CADMIUM (symbol Cd, atomic weight I12.4 (0=16)), a metallic element, showing a close relationship to zinc, with which it is very frequently associated.
The cadmium molecule, as shown by determinations of the density of its vapour, is monatomic. The metal unites with the majority of the heavy metals to form alloys; some of these, the so-called fusible alloys, find a useful application from the fact that they possess a low melting-point.
Cadmium vapour decomposes water at a red heat, with liberation of hydrogen, and formation of the oxide of the metal.
Cadmium oxide, CdO, is a brown powder of specific gravity 6.5, which can be prepared by heating the metal in air or in oxygen; or by ignition of the nitrate or carbonate; by heating the metal to a white heat in a current of oxygen it is obtained as a dark red crystalline sublimate.
Cadmium hydroxide, Cd(OH) 2, is obtained as a white precipitate by adding potassium hydroxide to a solution of any soluble cadmium salt.
The chloride,CdC1 2, bromide,CdBr 2, and iodide,Cdl2,arealsoknown, cadmium iodide being sometimes used in photography, as it is one of the few iodides which are soluble in alcohol.
Cadmium chloride and iodide have been shown to behave in an anomalous way in aqueous solution (W.
Cadmium sulphate, CdSO 4, is known in several hydrated forms; being deposited, on spontaneous evaporation of a concentrated aqueous solution, in the form of large monosymmetric crystals of composition 3CdSO 4.8H 2 O, whilst a boiling saturated solution, to which concentrated sulphuric acid has been added, deposits crystals of composition CdSO 4 4H 2 0.
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 pale yellow amorphous solid.
It is used as a pigment (cadmium yellow), for it retains its colour in an atmosphere containing sulphuretted hydrogen; it melts at a white heat, and on cooling solidifies to a lemon-yellow micaceous mass.
Normal cadmium 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(N03)2.4H20, is a deliquescent salt, which may be obtained by dissolving either the metal, or its oxide or carbonate in dilute nitric acid.
Cadmium salts can be recognized by the brown incrustation which is formed when they are heated on charcoal in the oxidizing flame of the blowpipe; and also by the yellow precipitate formed when sulphuretted hydrogen is passed though their acidified solutions.
The atomic weight of cadmium was found by 0.
Chem., 1891, I, p. 364), by the electrolytic reduction of cadmium oxide in potassium cyanide solution, obtained as a mean value 112.055.
The atomic weight of cadmium has been revised by G.
Soc., 1905, 27, p. 222), by determinations of the ratio of cadmium chloride to silver chloride, and of the amount of silver required to precipitate cadmium chloride.
The mean value 112.467 was obtained by Baxter, Hines and Frevert (ibid., 1906, 28, p. 770) by analysing cadmium bromide.
Stromeyer detected a new metallic element, cadmium, in certain zinc ores; it was rediscovered at subsequent dates by other observers and its chemical resemblance to zinc noticed.
If the substance does not melt but changes colour, we may have present: zinc oxide - from white to yellow, becoming white on cooling; stannic oxide - white to yellowish brown, dirty white on cooling; lead oxide - from white or yellowish-red to brownish-red, yellow on cooling; bismuth oxide - from white or pale yellow to orange-yellow or reddish-brown, pale yellow on cooling; manganese oxide - from white or yellowish white to dark brown, remaining dark brown on cooling (if it changes on cooling to a bright reddishbrown, it indicates cadmium oxide); copper oxide - from bright blue or green to black; ferrous oxide - from greyish-white to black; ferric oxide - from brownish-red to black, brownish-red on cooling; potassium chromate - yellow to dark orange, fusing at a red heat.
If the hot bead is colourless and remains clear on cooling, we may suspect the presence of antimony, aluminium, zinc, cadmium, lead, calcium and magnesium.
The oxide films of antimony, arsenic, tin and bismuth are white, that of bismuth slightly yellowish; lead yields a very pale yellow film, and cadmium a brown one; mercury yields no oxide film.
The solution is filtered and treated with an excess of sulphuretted hydrogen, either in solution or by passing in the gas; this precipitates mercury (mercuric), any lead left over from the first group, copper, bismuth, cadmium, arsenic, antimony and tin as sulphides.
The precipitate formed by sulphuretted hydrogen may contain the black mercuric, lead, and copper sulphides, dark-brown bismuth sulphide, yellow cadmium and arsenious sulphides, orange-red antimony sulphide, brown stannous sulphide, dull-yellow stannic sulphide, and whitish sulphur, the last resulting from the oxidation of sulphuretted hydrogen by ferric salts, chromates, &c. Warming with ammonium sulphide dissolves out the arsenic, antimony and tin salts, which are reprecipitated by the addition of hydrochloric acid to the ammonium sulphide solution.
Filter from the bismuth hydrate, and if copper is present, add potassium cyanide till the colour is destroyed, then pass sulphuretted hydrogen, and cadmium is precipitated as the yellow sulphide.
For certain concentrated solutions the transport number is found to be greater than unity; thus for a normal solution of cadmium iodide its value is I 12.
If some of the anions, instead of being simple iodine ions represented chemically by the symbol I, are complex structures formed by the union of iodine with unaltered cadmium iodide - structures represented by some such chemical formula as I(CdI 2), the concentration of the solution round the anode would be increased by the passage of an electric current, and the phenomena observed would be explained.
Thus, diminishing the concentration of the cadmium iodine solution from normal to one-twentieth normal changes the transport number from I 12 to o 64.
An alloy of 15 parts of bismuth, 8 of lead, 4 of tin and 3 of cadmium (Wood's alloy) melts below 70° C.
Gold, silver, copper, lead, aluminium, cadmium, iron (pure), nickel and cobalt are practically amorphous, the crystals (where they exist) being so closely packed as to produce a virtually homogeneous mass.
Distillable at red heats: cadmium, alkali metals, zinc, magnesium.
Of the rest, the following are readily oxidized by steam at a red heat, with formation of hydrogen gas - zinc, iron, cadmium, cobalt, nickel, tin.
Iron, zinc, cadmium, also tin under certain conditions, reduce the dilute acid, partially at least, to nitrous oxide, N 2 0, or ammonium nitrate, NH4N03.
Potassium, for example, yields peroxide, K202 or K204; sodium gives Na202; the barium-group metals, as well as magnesium, cadmium, zinc, lead, copper, are converted into their monoxides MeO.
Second in importance is the carbonate, calamine (q.v.) or zinc spar, which at one time was the principal ore; it almost invariably contains the carbonates of cadmium, iron, manganese, magnesium and calcium, and may be contaminated with clay, oxides of iron, galena and calcite; "white calamine" owes its colour to much clay; "red calamine" to admixed iron and manganese oxides.
It is chemically related to cadmium and mercury, the resemblance to cadmium being especially well marked; one distinction is that zinc is less basigenic. Zinc is capable of isomorphously replacing many of the bivalent metals - magnesium, manganese, iron, nickel, cobalt and cadmium.
For the metallurgy see Walter Renton Ingalls, The Metallurgy of Zinc and Cadmium; Production and Properties of Zinc; A.
At a red heat rutile is produced, at the boiling point of zinc brookite, and of cadmium anatase.
For example, if vapours of the volatile metals cadmium, zinc and magnesium are allowed to act on platinum or palladium, alloys are produced.
Fromm have shown that alloys may be precipitated from dilute solutions by zinc, cadmium, tin, lead and copper.
Spring has shown that by compressing a finely divided mixture of i 5 parts of bismuth, 8 parts of lead, 4 parts of tin and 3 parts of cadmium, an alloy is pro duced which melts at ioo C., that is, much below the meltingpoint of any of the four metals.
In the curve for sodium-cadmium, the compound NaCd 2 is plainly shown.
The presence of minute quantities of cadmium, lead, bismuth, antimony, arsenic, tin, tellurium and zinc renders gold brittle, 2 ' 0 15th part of one of the three metals first named being sufficient to produce that quality.
The metal can be reduced by magnesium, zinc, cadmium, iron, tin, copper and substances like hypophosphorous acid from acid solutions or from alkaline ones by formaldehyde.
Tin amalgam is used for "silvering" mirrors, gold and silver amalgam in gilding and silvering, cadmium and copper amalgam in dentistry, and an amalgam of zinc and tin for the rubbers of electrical machines; the zinc plates of electric batteries are amalgamated in order to reduce polarization.
Troost made it available for specially high temperatures by employing porcelain vessels, sealing them with the oxyhydrogen blow-pipe, and maintaining a constant temperature by a vapour bath of mercury (3500), sulphur (4400), cadmium (860°) and zinc (1040°).
The alloy used is composed of 15 parts of bismuth, 8 of lead, 4 of tin and 3 of cadmium; it melts at 70°, and can be experimented with as readily as mercury.
Klein's solution, an aqueous solution of cadmium borotungstate, 2Cd(OH)2-B203.9W03.16H20, introduced by D.
Mourlot has shown that aluminium sulphide, zinc sulphide and cadmium sulphide are the only sulphur compounds which can resist the heat of the electric furnace without decomposition or volatilization, and of these aluminium sulphide is the only one which is decomposed by water with the evolution of sulphuretted hydrogen.
The anhydrous chlorides of nickel, cobalt, cadmium, barium, iron and lead act in the same way as catalysts at about 300° C., and the bromides of lead, cadmium, nickel and barium at about 320° C.