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See also:CERIUM (See also:symbol Ce, atomic See also:weight 140.25) , a metallic chemical See also:element which occurs with the rare earths in the minerals cerite, samarskite, euxenite, See also:monazite, See also:parisite and many See also:yttrium minerals . The particular See also:earth containing See also:cerium was discovered by M . H . See also:Klaproth in 1803, whilst J . See also:Berzelius at about the same See also:time also examined it and came to the conclusion ' So See also:Irenaeus . According to See also:Hippolytus and See also:Epiphanius it was the See also:Holy See also:Ghost that thus descended.that it was the See also:oxide of a new See also:metal, which he termed cerium . The crude oxide of the metal is obtained from cerite, by evaporating the See also:mineral with strong sulphuric See also:acid, removing excess of acid and dissolving the See also:residue in See also:ice-See also:cold See also:water; sulphuretted See also:hydrogen is passed through the See also:solution, which is then filtered, acidified with hydrochloric acid, and precipitated as oxalate by oxalic acid; the oxalate is then converted into oxide by ignition . From the crude oxide so obtained (which contains lanthanum and See also:didymium oxides) the cerium may be separated by See also:conversion into its See also:double sulphate on the addition of See also:potassium sulphate, the sulphates of the cerium See also:group being insoluble in a saturated solution of potassium sulphate . The sulphate is subsequently boiled with water, when a basic sulphate is precipitated . For the preparation of pure cerium compounds see Auer v . Welsbach, Monatshefte, 1884, v . 508 . The metal was first obtained, in an impure See also:state, by C . G . Mosander, by fusing its chloride with See also:sodium . W . F . See also:Hillebrand and T . See also:Norton have prepared it by the See also:electrolysis of the melted chloride (Pogg . See also:Ann., 1875, 156, p . 466) ; and C . Winkler (Berichte, 1891, See also:xxiv . 884) obtained it by See also:heating the dioxide with See also:magnesium See also:powder . The metal has somewhat the See also:appearance of See also:iron, and has a specific gravity of 6.628, which, after melting, is increased to 6.728 . Its specific See also:heat is 0.04479 (W . F . Hine-See also:brand) . It is permanent in dry See also:air, but tarnishes in moist air; it can be hammered and rolled; it melts at 623° C . It See also:burns readily on heating, with a brilliant See also:flame; and it also combines with See also:chlorine,See also:bromine, See also:iodine, See also:sulphur, See also:phosphorus and See also:cyanogen . In the See also:case of the two former elements the See also:combination is accompanied by See also:combustion of the metal . With water it is slowly converted into the dioxide . Cold concentrated nitric and sulphuric acids are without See also:action on the metal, but it reacts rapidly with dilute nitric and hydrochloric acids . The dioxide is used in incandescent See also:gas mantles (see See also:LIGHTING) . Three oxides of cerium are known . The sesquioxide, Ce2O3, is obtained by heating the carbonate in a current of hydrogen . It is a bluish-See also:green powder, which on exposure rapidly combines with the See also:oxygen of the air .
By the addition of See also:caustic soda to cerous salts, a See also: Double salts of cerous chloride with stannic chloride, mercuric chloride, and platinic chloride are also known . Cerous bromide, 2CeBr3 3H2O, and iodide, CeI,•9H2O, are known . Cerous sulphide, Ce2S3, results on heating cerium with sulphur or cerium oxide in carbon bisulphide vapour . It is a red infusible See also:mass of specific gravity 5.1, and is slowly decomposed by warm water . The sulphate, Cez(SO4)3, is formed on dissolving the carbonate in sulphuric acid, or on dissolving the basic sulphate in sulphuric acid, in the presence of sulphur dioxide, evaporating the solution, and drying the product obtained, at high temperature (B . Brauner, Monatshefte, 1885, vi . 793) . It is a white powder of specific gravity 3.912, easily soluble in cold water . Many hydrated forms of the sulphate are known, as are also double salts of the sulphate with potassium, sodium, ammonium, See also:thallium and See also:cadmium sulphates . Ceric fluoride, CeFeH2O, is obtained when the hydrated dioxide is dissolved in hydrofluoric acid and the solution evaporated on the water See also:bath (B . Brauner) . The sulphate, Ce(SO4)2.4H2O, is formed when the basic sulphate is dissolved in sulphuric acid; or when the dioxide is dissolved in dilute sulphuric acid, and evaporated in vaeuo over sulphuric acid . It forms yellow crystals soluble in water; the aqueous solution on See also:standing gradually depositing a basic See also:salt . Double sulphates of composition2Ce(SO4)2.2K2SO4.2H20, Ce(SO4),.3(NH4)4SOe4H2OSre 762 known . Nitrates of cerium have been described, as have also See also:phosphates, See also:carbonates and a See also:carbide . Cerium compounds may be recognized by the red precipitate of ceric hydroxide, which is formed when sodium hypochlorite is added to a colourless cerous salt . For the quantitative determination of the metal, the salts are precipitated by caustic potash, the precipitate washed, dried and heated, and finally weighed as the dioxide . The atomic See also:weight of cerium has been determined by B . Brauner (Chem . See also:News, 1895, lxxi . 283) from the See also:analysis of the oxalate; the values obtained varying from 140.07 to 140.35 . |
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