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A Comprehensive Treatise on Inorganic and Theoretical Chemistry

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PLATINUM 253<br />

<strong>and</strong> L. T. Bourl<strong>and</strong> found the susceptibility to be independent of temp. D. M. Bose<br />

<strong>and</strong> H. G. Bhar also studied the magnetic properties.<br />

V. Ipateeff <strong>and</strong> A. Andreevsky observed that hydrogen, at elevated temp, <strong>and</strong><br />

press., acting <strong>on</strong> 3 to 30 per cent. soln. of platinous chloride, precipitates the platinum,<br />

<strong>and</strong> the proporti<strong>on</strong> of platinum precipitated is the greater, the greater is the initial<br />

c<strong>on</strong>e, of the soln. The additi<strong>on</strong> of acids, <strong>and</strong> of ferric chloride inhibits the reacti<strong>on</strong>,<br />

but without affecting the influence of the other factors. With 0-01 to 1 per cent,<br />

soln., in the presence of ir<strong>on</strong> <strong>and</strong> nickel salts, the reducti<strong>on</strong> is complicated <strong>and</strong> slow,<br />

particularly if mineral acids are present. W. J. Russell found that hydrogen precipitates<br />

the metal from platinum salts at ordinary temp, <strong>and</strong> press. J. J. Berzelius<br />

said that the greenish-grey powder behaves like a fatty substance in that it is<br />

scarcely wetted by water ; <strong>and</strong> that the salt is not affected by water ; G. Magnus<br />

also noted that the brown powder is insoluble in "water, but is soluble in the motherliquor.<br />

E. Knoevenagal <strong>and</strong> E. Ebler observed that no precipitate is formed with<br />

hydrogen dioxide. J. J. Berzelius, <strong>and</strong> G. Magnus noted that the salt is soluble<br />

in hot hydrochloric acid, <strong>and</strong>, "with access of air, some hydrochloroplatinic acid<br />

is formed—L. F. Nils<strong>on</strong> added that some hydrochloroplatinic acid may be<br />

formed with the separati<strong>on</strong> of platinum—vide infra. Potassium iodide colours<br />

soln. of platinous salts a dark reddish-brown, <strong>and</strong> after a time the soln. is<br />

decolorized as a precipitate of platinous iodide is formed. O. Stelling estimated<br />

platinum by the potentiometric titrati<strong>on</strong> of platinous salts with a OliV-soln. of<br />

potassium bromate. H. Rose observed that hydrogen sulphide, <strong>and</strong> amm<strong>on</strong>ium<br />

sulphide give a brown soln. with a hydrochloric acid soln. of platinous chloride,<br />

<strong>and</strong> later platinous sulphide is precipitated, <strong>and</strong> the precipitate dissolves in a large<br />

excess of amm<strong>on</strong>ium sulphide. J. J. Berzelius observed that the dichloride is not<br />

changed by sulphuric acid or by nitric acid ; <strong>and</strong> that boiling aqua regia c<strong>on</strong>verts<br />

it into hydrochloroplatinic acid. H. Rose observed that stannous chloride colours<br />

soln. of platinous salts reddish-brown without forming a precipitate. P. Schottl<strong>and</strong>er<br />

found that a soln. of amm<strong>on</strong>ium chloroplatinite <strong>and</strong> sodium thiosulphate<br />

furnish platinous thiosulphate, as a white precipitate, when treated with alcohol.<br />

W. Peters observed that in an atm. of amm<strong>on</strong>ia, additive compounds are formed—<br />

vide infra—M. Delepine noted that an ammine is precipitated -when amm<strong>on</strong>ia is<br />

added to the aq. soln. H. Rose observed no precipitate is formed by additi<strong>on</strong> of a<br />

soln. of sodium phosphate. G. Gore said that platinous chloride is insoluble in<br />

liquid amm<strong>on</strong>ia, <strong>and</strong> E. Divers, that it is insoluble in an amm<strong>on</strong>ia soln. of amm<strong>on</strong>ium<br />

nitrate. P. Schutzenberger prepared the compounds with carb<strong>on</strong> m<strong>on</strong>oxide<br />

indicated below, <strong>and</strong> the results were c<strong>on</strong>firmed by W. Manchot. W. Manchot<br />

<strong>and</strong> E. Enk found that at 140°, platinum dichloride <strong>and</strong> tetrachloride with carb<strong>on</strong><br />

m<strong>on</strong>oxide form platinum dicarb<strong>on</strong>yldichloride, PtCl2(CO)2 ; <strong>and</strong> W. Manchot<br />

<strong>and</strong> G. Lehmann observed that the carb<strong>on</strong>yl, 2PtCl2.3CO, is also formed.<br />

P. Schutzenberger <strong>and</strong> C. F<strong>on</strong>taine, <strong>and</strong> A.Rosenheim <strong>and</strong> W. Lowenstamm prepared<br />

from phosphorus trichloride the complex platinous dichlorobisphosphorotrichloride,<br />

[Pt(PCIa)2Cl2], <strong>and</strong> platinous dichlorobisphosphorotrihydroxde, [Pt(P(OH)3}2C12] ;<br />

platinous dichlorophosphorotrihydroxide, [Pt(P(OH)3)Cl2], platinous chlorophosphorotrihydroxidodihydrophosphite,<br />

[Pt(P(OH)3)Cl(H2PO3)], <strong>and</strong> P. Schutzenberger,<br />

platinous dichlorosilverphosphite, [Pt(P(OAg)3)2Cl2J. P. Schutzenberger,<br />

P. Schutzenberger <strong>and</strong> C. F<strong>on</strong>taine, E. Baudrim<strong>on</strong>t, A. Werner, G. Quesneville,<br />

A. Rosenheim <strong>and</strong> W. Lowenstamm, A. Rosenheim <strong>and</strong> W. Levy, <strong>and</strong> D. Cochin<br />

described platinous dichlorophosphorotrichloride, [Pt(PCl3)Cl2J2, <strong>and</strong> platinous<br />

dichlorophosphorotrichloroplatinite, [Pt(PCl3)Cl2]2.PtCl2.<br />

H. Rose observed that mercuric cyanide does not react immediately with soln.<br />

of platinous chloride ; nor has potassium ferrocyanide or ferricyanide any acti<strong>on</strong>.<br />

M. S. Kharasch <strong>and</strong> T. A. Ashford prepared complex salts with ethylene.<br />

K. A. Hofmann <strong>and</strong> H. Kirmreuther found that the ethylene halides gradually<br />

reduce soln. of platinous chloride. L. Tschugaeff observed that when platinous<br />

chloride is heated On a water-bath, the tertiary amines precipitate platinum.

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