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Bismuthates

The actual structure at a vapor-liquid interface can be probed with x-rays. Rice and co-workers [72,73,117] use x-ray reflection to determine the composition perpendicular to the surface and grazing incidence x-ray diffraction to study the transverse structure of an interface. In a study of bismuth gallium mixtures. [Pg.78]

Getting I 1998 New determination of the bismuth l-ll equilibrium pressure—a proposed modification to the practical pressure scale Metroiogica 35 119... [Pg.1963]

France M R, Buchanan J W, Robinson J C, Pullins S FI, Tucker J T, King R B and Duncan M A 1997 Antimony and bismuth oxide clusters growth and decomposition of new magic number clusters J. Phys. Chem. A 101 6214... [Pg.2407]

Peppiat S J 1975 The melting of small particles II. Bismuth Proc. R. Soc. 354 401... [Pg.2923]

Blackman M, Peppiat S J and Sambles J R 1972 Superheating of bismuth Nature Phys. Sc/. 239 61... [Pg.2923]

Crude lead contains traces of a number of metals. The desilvering of lead is considered later under silver (Chapter 14). Other metallic impurities are removed by remelting under controlled conditions when arsenic and antimony form a scum of lead(II) arsenate and antimonate on the surface while copper forms an infusible alloy which also takes up any sulphur, and also appears on the surface. The removal of bismuth, a valuable by-product, from lead is accomplished by making the crude lead the anode in an electrolytic bath consisting of a solution of lead in fluorosilicic acid. Gelatin is added so that a smooth coherent deposit of lead is obtained on the pure lead cathode when the current is passed. The impurities here (i.e. all other metals) form a sludge in the electrolytic bath and are not deposited on the cathode. [Pg.168]

Each of these elements occurs naturally as a sulphide ore arsenic as realgar As S,, orpiment As, Sg and arsenical pyrites with approximate formula FeAsS antimony as stibnite Sb2S3 and bismuth as B12S3. [Pg.209]

Arsenic and antimony resemble phosphorus in having several allotropic modifications. Both have an unstable yellow allotrope. These allotropes can be obtained by rapid condensation of the vapours which presumably, like phosphorus vapour, contain AS4 and Sb4 molecules respectively. No such yellow allotrope is known for bismuth. The ordinary form of arsenic, stable at room temperature, is a grey metallic-looking brittle solid which has some power to conduct. Under ordinary conditions antimony and bismuth are silvery white and reddish white metallic elements respectively. [Pg.210]

Arsenic dissolves in concentrated nitric acid forming arsenicfV) acid, H3ASO4, but in dilute nitric acid and concentrated sulphuric acid the main product is the arsenic(III) acid, HjAsOj. The more metallic element, antimony, dissolves to form the (III) oxide Sb O, with moderately concentrated nitric acid, but the (V) oxide Sb205 (structure unknown) with the more concentrated acid. Bismuth, however, forms the salt bismulh(lll) nitrate Bi(N03)3. 5H,0. [Pg.212]

Antimony and bismuth do not react with sodium hydroxide. [Pg.213]

A complete set of trihalides for arsenic, antimony and bismuth can be prepared by the direct combination of the elements although other methods of preparation can sometimes be used. The vigour of the direct combination reaction for a given metal decreases from fluorine to iodine (except in the case of bismuth which does not react readily with fluorine) and for a given halogen, from arsenic to bismuth. [Pg.213]

These stability changes are in accordance with the change from a non-metal to a weak metal for the Group V elements nitrogen to bismuth. [Pg.214]

Very small quantities of bismuthine are obtained when a bismuth-magnesium alloy, BijMgj, is dissolved in hydrochloric acid. As would be expected, it is extremely unstable, decomposing at room temperature to bismuth and hydrogen. Alkyl and aryl derivatives, for example trimethylbismuthine, Bi(CHj)3, are more stable. [Pg.227]

Nitrogen is unusual in forming so many oxides. The acidity of the Group V oxides falls from phosphorus, whose oxides are acidic, through arsenic and antimony whose oxides are amphoteric, to the basic oxide ofbismuth. This change is in accordance with the change from the non-metallic element, phosphorus, to the essentially metallic element, bismuth. The +5 oxides are found, in each case, to be more acidic than the corresponding + 3 oxides. [Pg.228]

Bismuth forms both -l-3 and -l-5 oxides. The -1-3 oxide, unlike the corresponding oxides of the other Group V elements, is insoluble... [Pg.237]


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