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A Comprehensive Treatise on Inorganic and Theoretical Chemistry

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248 INORGANIC AND THEORETICAL, CHEMISTRY<br />

baryta water, or sod a-lye ; it is soluble in acids, but cold acetic acid has no acti<strong>on</strong>,<br />

whilst the hot acid forms barium acetate <strong>and</strong> hydrated platinum dioxide.<br />

For the tin platirtcU.es, vide 7. 46, 14 ; the vanadium platinates, 9. 54, 6 ; chromium<br />

platinates, 11. 60, 15 <strong>and</strong> 16; the molybdenum platinates, 11. 61, 11 ; <strong>and</strong> the tungsten<br />

platinates, 11. 62, 12.<br />

According to E. Prost, 3 an oxide, Pt5O1I-IlH2O, is obtained by boiling a soln.<br />

of hydrated platinum dioxide in c<strong>on</strong>e, nitric acid. "Lt. Wohler could not prepare<br />

this product, <strong>and</strong> c<strong>on</strong>sidered it to be a mixture of different hydrated oxides.<br />

Ja. Wohler 4 <strong>and</strong> co-workers, C. Marie, M. Ie Blanc, <strong>and</strong> R. Ruer showed that<br />

the oxide film which was observed by F. Kohlrausch to form <strong>on</strong> the anode during<br />

the electrolysis of a soln. of platinic chloride is possibly platinum trioxide, PtO3 ;<br />

<strong>and</strong> that the same film is formed when the metal becomes passive. E. Haber <strong>and</strong><br />

S. Grinberg showed that it liberates iodine from potassium iodide. According to<br />

Li. Wohler <strong>and</strong> F. Martin, when the yellow soln. of hydrated platinum dioxide in<br />

2iV-KOH is oxidized anodically whilst the soln. is well-cooled, the anode so<strong>on</strong><br />

becomes covered with a golden yellow, amorphous deposit, which peels off in thin,<br />

silky plates. It is potassium platinic decoxide, K20.3Pt03. The trioxide can be<br />

obtained from this salt by treatment with ice-cold 0-5iV-acetic acid. The reddishbrown<br />

product c<strong>on</strong>tained slightly less oxygen than that necessary for the trioxide,<br />

owing to the fact that it readily parts with some of its oxygen as so<strong>on</strong> as<br />

all the alkali has been removed. On keeping, the percentage of oxygen gradually<br />

decreases, but it never falls to that necessary for the dioxide, probably because a<br />

solid soluti<strong>on</strong> of the trioxide in the dioxide is formed. Platinum trioxide is not<br />

acted <strong>on</strong> by dil. sulphuric, nitric, or acetic acids. It slowly liberates chlorine from<br />

dil. hydrochloric acid. Sulphurous acid dissolves it with the formati<strong>on</strong> of a colourless<br />

complex. C<strong>on</strong>e, sulphuric <strong>and</strong> nitric acids slowly decomposed it with the formati<strong>on</strong><br />

of the dioxide. On gently heating, it gives the dioxide. In the cold it has no<br />

acti<strong>on</strong> <strong>on</strong> alcohol or acetic acid. The oxidati<strong>on</strong> which takes place <strong>on</strong> warming is<br />

due to the dioxide which is formed. It does not decompose into hydrogen dioxide,<br />

<strong>and</strong> must therefore be classed as a polyoxide or peroxide of platinum of the<br />

c<strong>on</strong>stituti<strong>on</strong><br />

G. Grube, 5 in his study of the behaviour of the oxygen electrode, found that<br />

potentials from 1*5 volts downwards are due to solid soln. of platinum trioxide<br />

in platinum dioxide, or of platinum dioxide in platinum m<strong>on</strong>oxide. Since, however,<br />

platinum electrodes can be polarized up to potentials of 2 volts, G. Grube suggested<br />

that an unknown platinum tetroxide, PtO4, is formed.<br />

REFERENCES.<br />

1 R. Adams <strong>and</strong> R. L.. Shriuer, Journ. Amer. Chem. Soc., 45. 2171, 1923 ; R. Adams,<br />

V. Voorhees <strong>and</strong> R. L. Shriner, Organic Syntheses, 8. 92, 1928 ; F. D. Aguirroche, Anal. Fis.<br />

Quint., 25. 411, 1927 ; A. Bar<strong>on</strong>i, AtH Accad. Lincei, (7), 21. 756, 1936; F. Becker, Ueber die<br />

Dissoziati<strong>on</strong> der Oxyde des Iridiums und des Platins, l>armstadt, 1927 ; I. Bellucci, Zeit. anorg.<br />

Chem., 44. 182, 1905 ; AtH Accad. JLincei, (5), 12. ii, 635, 1904 ; Gazz. Chirn. Ital., 35. i, 163,<br />

1905 ; W. Bersch, Zeit. phys. Chem., 8. 394, 1891 ; J. J. Berzolius, Schweigger's Journ., 7. 58,<br />

1813 ; M. Bl<strong>on</strong>del, Recherches sur quelques combinati<strong>on</strong>s du platine, Paris, 1905 ; Ann. Chim.<br />

Phys., (S), 6. 103, 1905; W. F. Bruce, Journ. Amer. Chem. 8oc., 58. 687, 1936; O. Brunck,<br />

Zett. anorg. Chem., 10. 247, 1895; P. T. Cleve, Svenska Vet. A/cad. H<strong>and</strong>l., 10. 9, 1872 ; B. E. Dix<strong>on</strong>,<br />

Journ. Chem. Soc., 2948, 1932 ; J. W. Dobereiner, Fogg. Ann., 28. 181, 1833 ; N. W. Fischer,<br />

Das VerhaUniss der chemischen Vertv<strong>and</strong>schaft zur galvanischen Electrizitat in Versuchen dargestellt,<br />

Berlin, J830 ; E. Fremy, Compt. Rend., 81. 893, 1850; Ann. Chim. Phys., (3), 81. 478, 1850;<br />

B. Gerdes, Ueber die bei Klehtrolyse des carbaminsauren und kohlensauren Amm<strong>on</strong>s mit Wechselstromen<br />

und Platinelektroden entstehenden Platinbasen, Leipzig, 1882 ; C. Oerhardt, Compt.<br />

Rend. Trav. Chim., 273, 1850 ; Liebig's Ann., 76. 311, 1850 ; Journ. prakt. Chem., (1), 51. 351,<br />

185O; (1), 58. 345, 1851 ; P. Gr<strong>and</strong>adam, Ann. Chim. Phys., (11), 4. 83, 1935; C. Grimm,<br />

ib., (1), 69. 420, 1856 ; Phil. Mag., (4), 12. 301, 1856 ; Liebig's Ann., 99. 67, 1856 ; W. Hittorf,

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