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atomic weight 145.0 PLATINUM [symbol ...

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Originally appearing in Volume V21, Page 808 of the 1911 Encyclopedia Britannica.
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atomic See also:

weight 145.0 See also:PLATINUM [See also:symbol Pt (0=16)]  , a metallic chemical See also:element . The name, derived from platina, the diminutive of Span. plena (See also:silver), was first given to a See also:mineral, See also:platinum ore or native platinum, originally discovered in See also:South See also:America, from the resemblance to silver . See also:Russia furnishes about 95% of the See also:world's See also:annual See also:supply of platinum . Native platinum occurs usually in small metallic scales or See also:flat grains, sometimes in the See also:form of irregular nuggets, and occasionally, though rarely, in small crystals belonging to the cubic See also:system . Grains of platinum have been found embedded, with See also:chromite, in See also:serpentine derived from an See also:olivine-See also:rock, the See also:metal having probably separated out from an See also:original basic magma . It is said to occur also in See also:veins in syenitic and other rocks . Usually, however, platinum is found in detrital deposits, especially in auriferous sands, where it is associated with osmiridium (known also as iridosmine), chromite, See also:magnetite, See also:corundum, See also:zircon, &c . The platinum has a See also:steel See also:grey or silver-See also:white See also:colour and a metallic lustre; is often magnetic, sometimes with See also:polarity; has a hardness of about 4.5 and a specific gravity varying with its See also:composition from 14 to 19 . Native platinum usually contains more or less See also:iron and See also:copper, often See also:gold, and invariably a small proportion of some of the allied metals—See also:iridium, See also:osmium, See also:ruthenium, See also:rhodium and See also:palladium . From the associated metals it was named by J . F . L .

See also:

Hausmann polyxene (Gr. iroXbs, many, and Evoc, a See also:guest), whilst from its occurrence as a white metal in auriferous alluvia it is sometimes known to miners as " white gold." Platina del See also:Pinto was the name by which native platinum was first introduced into See also:Europe from South America about the See also:middle of the 18th See also:century . Although it appears to have been known locally much earlier, the See also:attention of scientific men in Europe was first directed to it by See also:Antonio de Ulloa y See also:Garcia de La Torre, a Spaniard who joined a See also:French scientific expedition to See also:Peru in 1735, and published in 1748 an See also:account of his See also:journey, in which he refers to platinum, though not under that name, as occurring with gold in New See also:Granada (now See also:Colombia) . See also:Sir See also:William See also:Watson, an See also:English physicist, had, however, in 1741 received some grains of the mineral, probably from the ' Reproduced by J . F . Riano, in Studies of See also:Early See also:Spanish See also:Music (See also:London, 1887) . ' See facsimile edited by Dr See also:George See also:Warner, pl. See also:xxviii. fol . 51 . 3 See F . J . See also:Furnivall, See also:Captain See also:Cox, his See also:ballads and Books, or See also:Robert Laneham's See also:Letter A.D . 1575 (London, 1871), clx . 86 .

re-melted in a reverberatory See also:

furnace with See also:galena or litharge, the See also:lead platinum alloy being then cupelod, and the platinum fused into an See also:ingot by re-smelting in a See also:lime furnace (see Dingler's Polytech . Journ . 1859, 153, p . 38; 1859, 154, p . 383, 1862, 165, p . 205) . The platinum so obtained is not pure . In See also:Wollaston's wet method the ore is dissolved in aqua regia, the osmiridium, ruthenium and rhodium being See also:left unattacked, and the platinum precipitated as ammonium platinochloride by adding ammonium chloride in the presence of an excess of See also:acid . The See also:double chloride is then washed, dried and ignited, leaving a See also:residue of metal . G . Matthey (Chem . See also:News, 1879, 39, p .

175) obtains pure platinum from the commercial metal by fusing the latter with a large excess of lead . The lead alloy is then treated with a dilute nitric acid and the insoluble portion taken up in dilute aqua regia, From the See also:

solution so obtained lead is precipitated as sulphate, and platinum and rhodium as double ammonium chlorides . The rhodium ammonium chloride is converted by fusing with See also:potassium and ammonium bisulphates into rhodium sulphate, which is then removed by extraction with See also:water, when a residue of finely divided platinum remains . The See also:German See also:firm of Heraus (in See also:Hanover) See also:heat the raw ore with aqua regia and water under pressure, evaporate the solution to dryness, and heat the residue to 125° C . A clear aqueous See also:extract of the residue is then acidified with hydrochloric acid and precipitated with ammonium chloride . The double chloride is ignited and the finely divided platinum so obtained is fused in the oxyhydrogen See also:blowpipe . same locality, though brought by way of See also:Jamaica; and it was he who first described it in 1750 as a new metal . Native platinum was discovered in 1819 in the gold washings of Verkhniy-Isetsk, in the Urals, but it was not until 1822 that its true nature was recognized . The See also:chief See also:Russian localities are in the districts of Nizhne Tagilsk and Goroblagodatsk, where it is found in shallow See also:drift deposits, containing pebbles of serpentine, which represent the original See also:matrix . The Iset See also:district has acquired importance in See also:recent years . Although the platinum-bearing gravels usually contain a very small proportion of the metal, the See also:average in 1895 being only 11 dwt. to the ton, See also:rich discoveries have occasionally been made in the See also:history of the workings, and nuggets of exceptional See also:size have been unearthed . The largest recorded specimens are one of 310 OZ. from Nizhne Tagilsk, and another of 722 oz. from the Goroblagodatsk district .

In 1831 platinum ore was recognized in the gold-bearing deposits of See also:

Borneo, where it had previously been regarded as worthless, being known to the natives as mas kodok (See also:frog gold) . Although recorded from various parts of the See also:island, its occurrence seems to be definitely known only in Tanah-See also:Laut, in the south-See also:east of Borneo . In See also:Australia platinum ore has been found near Fifield (near Condobelin), New South See also:Wales; whilst in New See also:Zealand it occurs in sands and gravels in the See also:Thames gold-See also:field, the Takaka See also:River and the See also:Gorge River flowing into Awarua See also:Bay . Many localities in See also:North America have yielded platinum, generally in See also:beach sands or in auriferous alluvia, and in some cases the deposits are of commercial importance . The metal is found in See also:Alaska, See also:British See also:Columbia, See also:Oregon (See also:Douglas See also:county) and See also:California (See also:Butte county, Trinity county, Del Norte ccunty) . It has been recorded also from the states of New See also:York and North Carolina . In a nickeliferous sulphide ore worked at See also:Sudbury, in See also:Ontario, platinum has been discovered in the form of an arsenide (Pt As2), which has been called sperrylite by H . L . See also:Wells, who analysed it in 1889, and named it after F . L . Sperry, of Sudbury . It belongs to the See also:pyrites See also:group, and is interesting as being the only known mineral in which platinum occurs in See also:combination except as alloy .

Native platinum seems to be a mineral of rather wide See also:

distribution, but in very sparse quantity . The sands of the See also:Rhine, derived from Alpine rocks, have been found to contain platinum in the proportion of 0.0004% . It has also been found in the sands of the Ivalo River in 'See also:Lapland; it is recorded from Roros in See also:Norway; and it was detected by W . See also:Mallet in some of the gold-sands of the streams in Co . See also:Wicklow, See also:Ireland . The table shows the See also:official amount (in ounces See also:Troy) of platinum produced in Russia for certain years, the actual amounts are much larger: See also:Year . Amount . Year . Amount . 1890 116,640 1904 161,950 1895 141,757 1905 167,950 'goo 163,060 1906 185,492 1901 203,257 1907 172,758 1902 197,024 1908 157,005 1903 192,976 (See also:Rothwell's Mineral See also:Industry, 1908.) Platinum is largely used for the manufacture of chemical apparatus, incandescent lamps, thermo-couples; in the manufacture of sulphuric acid by the contact See also:process, in See also:photography, and in See also:jewelry . The See also:price of See also:tile metal has risen considerably, not so much on account of the restricted supply, but chiefly because the See also:sources of supply have passed into the hands of a few individuals . The following data show the fluctuations in he average price of platinum ingot per once Troy: s. d .

£ s. d . 1874-1898: 1 5 2 to 2 2 0 1899-1905: 3 13 6 „ 4 10 4 1906: 4 15 2 „ 7 19 8 1907: 7 0 0„ 6 18 8 908: 5 2 6 (average) price . Platinum may be extracted from its ore by both wet and dry processes . In the latter method, due to H . Sainte-Claire-Deville and H . J . Debray, the ore is smelted in a furnace constructed of two blocks of lime, and the metallic See also:

button so obtained is Platinum is a greyish-white metal which is exceedingly malleable and ductile; the addition of a small quantity of iridium hardens it and diminishes its ductility very considerably . Its specific gravity is 20.85 to 21.71, and its mean specific heat from o to See also:loo° C. is 0.0323 (J . Violle, Comptes rendus, 1877, 85, p . 543); W . P . White (Amer .

Journ . Sci., 1909, iv . 28, p . 334) gives the See also:

general See also:formula St=o•o3198+3.4Xio st . St being the specific heat at t°C . Its temperature of See also:fusion is in the neighbourhood of 1700 to 1800°C., various intermediate values having been obtained by different investigators (see J . A . Harker, Chem . News, 1905, 91, p . 262; C . Fery and C . Chenevean, Comptes rendus, 1909, 148, p .

401; also C . W . Waidner and G . H . See also:

Burgess, ibid., 1909, 148, p . 1177) . Its latent heat of fusion is 27.18 calories (Violle, loc. cit) . The metal has been obtained in the crystalline See also:condition by See also:distillation in the electric furnace, or by decomposing its fluoride at a red heat (H . See also:Moissan) . Platinum, like palladium, absorbs large quantities of See also:hydrogen and other gases, the occluded See also:gas then becoming more "active"; for this See also:reason platinum is used largely as a catalytic See also:agent . Several forms of platinum, other than the massive form, may be obtained . Spongy platinum is produced when ammonium platinochloride is ignited; platinum See also:black on the reduction of acid solutions of platinum salts; and colloidal platinum by passing an electric arc between two platinum wires under the See also:surface of pure water (G .

Bredig, Zeit. phys . Chem., 1901, 37, pp . 1, 323) . Platinum is practically unoxidizable; it combines directly with See also:

phosphorus, See also:arsenic, See also:antimony, See also:silicon, See also:boron, and See also:fluorine, and with almost all other metals . It is practically unattacked by all acids, dissolving only in aqua regia or in mixtures which generate See also:chlorine . When fused with alkaline hydroxides in the presence of See also:air it forms platinates . It is readily attacked by fused nitrates, and by potassium See also:cyanide and ferrocyanide . All the platinum compounds when heated strongly decompose, and leave a residue of the metal . Of platinum salts, in the true sense of the word, none exist; there is no carbonate, nitrate, sulphate, &c; halide salts, however, are known, but are obtained in an indirect manner . Platinum monoxide, PtO, obtained by See also:heating the corresponding See also:hydrate, is a dark-coloured See also:powder which is easily reduced to the metal (L . See also:Wohler, See also:Bee., 1903, 36, p . 3475) .

The hydrated form, PtO.2H2O, is obtained impure by precipitating the dichloride with See also:

caustic soda, or by adding caustic soda to a boiling solution of potassium platinous chloride, K2PtCI4, the precipitate being rapidly washed and dried in vacuo (L . Wohler, Zeit. anorg . Chem., 1904, 40, p . 423) . It is a black powder; when freshly prepared it is soluble in concentrated acids, but when dried it is insoluble . It is an acidic See also:oxide, the dioxide being both acidic and basic . It behaves as a strong oxidizing and reducing agent . C . Engler and L . Wohler (Zeit. anorg . Chem., 1901, 29, p . 1) have shown that platinum black, containing occluded See also:oxygen, is soluble in dilute hydrochloric acid and also liberates See also:iodine from potassium iodide, and that the ratio between the amount of platinum dissolved and the amount of oxygen occluded agrees with the formation of a comppound corresponding to the formula PtO, _ Platinum dioxide (platinic oxide), PtOr4H2O, is obtained by adding an excess of caustic soda solution to a boiling solution of chlorplatinic acid, the hot solution being diluted and neutralized with acetic acid .

It loses its water of hydration when heated, finally decomposing into platinum and oxygen . When freshly prepared it is soluble in dilute acids . Other hydrated forms of composition, PtO2.3H2O and PtO2.2H2O, have been described (E . Prost, See also:

Bull. See also:soc. chim., 1886, 46, p . 156; H . Topsoe, Ber., 187o, 3, p . 462) . The tetrahydrate may be considered as an acid, H2Pt(OH)s, for salts are known (namely the platinates) corresponding to it, those of the See also:alkali metals being soluble in water, and possessing an alkaline reaction (M . See also:Blondel, See also:Ann. chim. phys., 1905 [viii.], 6, p . 81) . A similar set of chlorine-holding compounds is also known, the chlorine replacing one or more hydroxyl See also:groups and giving rise to complexes of composition, H2[PtCls(OH)], H2[PtCI4(OH)2], Ht[PtC12(OH)4] and H2[PtCI(OH)s] . The platinic salts (derived from PtO2) are yellow or See also:brown solids, which are readily reduced to the metallic condition .

They give with sulphuretted hydrogen a dark brown precipitate, soluble in excess of ammonium sulphide . Potassium iodide gives a brown solution with See also:

gradual formation of a precipitate . They form characteristic precipitates with potassium and ammonium chlorides . The platinous salts are brown or colourless solids which, with sulphuretted hydrogen, give a dark brown precipitate of platinum sulphide, and with potassium iodide a gradual precipitation of platinic iodide, PtI2 . Platinum trioxide, PtO3, is obtained as See also:K20.3PtO3, by electrolysing a solution of platinic hydroxide in potash, this See also:compound with acetic acid giving the oxide as a brown, easily decomposable powder (L . Wohl: r and F . See also:Martin, Bee., 1909, 42, p . 3326) . • Platinum bichloride, PtC12, is obtained by heating chlorplatinic acid to 300-350° C . (J . J . See also:Berzelius), or, mixed with more or less platinic chloride, by passing chlorine over spongy platinum at a temperature of 250 C .

Phoenix-squares

(P . See also:

Schutzenberger, Comptes rendus, 187o, 70, pp . 1134, 1287) . It may also be obtained by the decomposition of the compound HC1•PtCl2.2H2O (see below) at loo' C., this method giving a very pure product (L . F . Nilson, Journ. prak . Chem., 1877 (2), 15, p . 26o) . It is a brown or greyish See also:green coloured solid, which is soluble in hydrochloric acid . It decomposes into its constituent elements when heated . It combines with many chlorides to form characteristic double salts . Platinum bichloride combines with See also:carbon monoxide, yielding compounds of composition, PtC12.CO, PtCl2•zCO, 2PtC12.3CO (P .

Schutzenberger, Ann. chim. phys., 187o (4), 21, p . 350) . Hydrogen platinochloride or chlorplatmous acid, H2PtCl4, is only known in solution, and as such is obtained when platinum bichloride is dissolved in hydrochloric acid, or by decomposing the See also:

barium See also:salt with sulphuric acid, or the silver salt with hydrochloric acid . Its salts, the platinochlorides or chlorplatinites, are obtained by reducing the chlorplatinates or directly from the acid itself . They are mostly soluble in water giving red solutions . They are readily oxidized, and nascent hydrogen reduces them to metallic platinum . Potassium platinochloride or chlorplatinite, K2PtCI4, is prepared by reducing hydrogen platinichloride with See also:sulphur dioxide, or potassium platinichloride with potassium oxalate in the presence of iridium (Klason, Ber., 1904, 37, p . 1360); or by adding potassium chloride to a solution of platinum bichloride in hydrochloric acid . It crystallizes in dark red prisms, is readily soluble in water, but insoluble in See also:alcohol . The solution of the See also:free acid when concentrated in vacuo leaves a residue of HCI.PtCl2.2H20 . When the free acid is reduced by alcohol, or when See also:ethylene is passed into a solution of platinum bichloride in hydrochloric acid, PtCl2•C2H4 is obtained as a brown amorphous See also:mass which decomposes when heated . When the bichloride is heated in a current of carbon monoxide, a sublimate of platinomonocarbonyl dichloride, PtC12CO, dicarbonyl dichloride,PtC12(CO)2, and tiicarbonyl tetrachloride, Pt2C14(CO)3, is obtained .

The first forms See also:

bright yellow needles and the second white acicular crystals . The bichloride also combines with phosgene to form PtC12.2LOCl2 . Platinic chloride, PtCl4, is obtained when chlorplatinic acid is heated in a current of dry hydrochloric acid gas to 165° C . (W . Pullinger, Journ . Chem . Soc., 1892, 61, p . 422) or in a current of dry chlorine at 275° C . (A . See also:Rosenheim and W . Lowenstamm, Zeit. anorg . Chem., 1903, 37, p .

394) . It forms a reddish brown crystalline mass which is very hygroscopic . Numerous hydrates are known . The chloride is characterized by the readiness with which it forms double salts with the metallic chlorides and with the hydrochlorides of most organic bases . Chlorplatinic acid, H2PtCI6.6H20, is obtained by dissolving platinum in aqua regia containing an excess of hydrochloric acid, or by the See also:

action of chlorine (dissolved in hydrochloric acid) on platinum sponge . It crystallizes in needles, which are very deliquescent and dissolve easily in water . It melts in its own water of See also:crystallization at 7o° C., and when heated in vacuo to loo° C. it leaves a residue of composition HCI.PtC14.2H20 . The potassium and ammoniumn salts and the salts it forms with organic bases are characterized by their exceedingly small solubility in water . The aqueous solution of the acid reddens See also:litmus and decomposes the metallic See also:carbonates . Its salts may he prepared by the See also:direct action of the acid on the metallic hydroxides or carbonates, and are usually of an See also:orange or yellow colour and are mostly soluble in water . Potassium chlorplatinate, K2PtC16, is obtained, in the form of a yellow crystal-See also:line precipitate, when a concentrated solution of a potassium saltis added to a solution of chlorplatinic acid . It crystallizes in octahedra which are scarcely soluble in water, and practically insoluble in See also:absolute alcohol .

It decomposes at a red heat into platinum, chlorine and potassium chloride . The corresponding See also:

sodium salt, Na2PtC1s.6H20, is much more soluble in water and in alcohol . The ammonium salt, (NH4)2PtCls, resembles the potassium salt in its solubility in water and in alcohol . Corresponding See also:brome- and iodo- compounds are known . Platinum bifloride and tetrafluoride, PtF2 and PtF4, were obtained simultaneously by H . Moissan (Ann. chim. phys., 1894 (6), 24, p . 282) by the action of fluorine on platinum at 500-600° C . They may be separated by taking See also:advantage of their different solubilities in water . Platinum monosulphide, PtS, is obtained by the direct See also:union of platinum and sulphur; by heating ammonium chlorplatinate with sul phur; or by the action or aulphuretted hydrogen on the chlorplatinites . It is a dark coloured powder which is almost insoluble in aqua regia . It decomposes when heated strongly leaving a residue of metallic platinum, the same reduction taking See also:place at comparatively See also:low temperatures when it is heated in a current of hydrogen . Platinic sulphide, PtS2, is formed when the chlorplatinates are heated with sulphuretted hydrogen to 6o° C .

The precipitate must be rapidly washed and dried in vacuo, since it oxidizes rapidly on exposure to air . It is a black powder, which when heated strongly in air decomposes and leaves a residue of platinum, but if heated in See also:

absence of air leaves a residue of the monosulphide . It is scarcely affected by acids and is little soluble in solutions of the alkaline sulphides . Sulphides of composition Pt2S3 and PtsS6 have been described (R . See also:Schneider, Pogg . Ann., 1869, 138, p . 604; 1873, 148, p . 633; 1873, 149, p . 381) . A salt of composition, Pt(OH)4.H2SO4.See also:H2O, has been prepared by M . Blondel (Ann. chim. phys., 1905, (8), 6, p . 81) by the solution of the hydrate H2Pt(OH)s, i.e .

PtO2.4H20, in dilute sulphuric acid (I:I) at 0° C . On the addition of See also:

cold concentrated sulphuric acid to the solution so obtained, the above salt is precipitated in the form of See also:minute needles, which readily decompose in the presence of water . A platinum sulphate, Pt(SO4)2.2H20, has been obtained by L . Stuchlik (Ber., 1904, 37, p . 2913) by the action of sulphuric acid (s.g . 1.84) on platinum under the See also:influence of an alternating current . A crystalline precipitate is obtained, which is soluble in water and is very hygroscopic . The platinonitrites of composition M2Pt(NO2)4 are mostly obtained by double decomposition from the potassium salt, which is formed by adding a warm aqueous solution of potassium nitrite to one of potassium chlorplatinate . They are mostly colourless or See also:pale yellow solids which are more or less soluble in water (L . F . Nilson, Ber., 1876, 9, p . 1722) .

The corresponding platino-oxalates M2Pt(C204)2 were first obtained by J . W . See also:

Dobereiner (Pogg . Ann., 1833, 104, p . 18o) and their constitution was determined by H . G . Soderbaum (Ber., 1888, 21, p . 567 R; Zeit. anorg . Chem., 1894, 6, p . 45) . The sodium salt, from which the others are obtained by double decomposition, is formed by adding a warm solution of oxalic acid to sodium platinate . On recrystallization from alkaline solutions the salts are obtained in yellow or orange crystals (see M .

Vezes, Bull. soc. chim., 1898 (3), 19, p . 875) . These salts are scarcely soluble in water and decompose explosively when suddenly heated . The free acid is obtained by decomposing the silver salt with hydrochloric acid, the See also:

indigo See also:blue solution so obtained on concentration in vacuo yielding a red crystalline mass, which dissolves in water with an indigo blue colour, changing to yellow on dilution . Platinum cyanide, Pt(CN)2, is formed by the addition of mercuric cyanide to a solution of a chlorplatinite, or by the decomposition of See also:mercury or ammonium platinocyanide by heat . It is an amorphous powder which is insoluble in water, acids or alkalis, but is soluble in a solution of hydrocyanic acid . It See also:burns when heated . The platinocyanides are derived from the acid H2Pt(CN)6, which is formed by the decomposition of the mercury or copper-salt with sulphuretted hydrogen, or of the barium salt with sulphuric acid . It crystallizes from water in See also:cinnabar-red prisms which contain five molecules of water of crystallization; in the anhydrous condition it is of a yellowish green colour . It decomposes carbonates . Its salts, which are characterized by the See also:property of polychroism, may be prepared by the usual methods, or by the solution of metallic platinum in the alkaline cyanides or alkaline See also:earth cyanides under the influence of an alternating current (A . Brochet and J .

See also:

Petit, Ann. chim. phys., 1904 (8), 3, p . 460; M . See also:Berthelot, Comptes rendus, 1904, 138, p . 1130) . Those of the alkali and alkaline earth metals are soluble in water . Many combine with the halogen elements to form complex salts of the type M2Pt(CN)4.C12. x H2O . By the decomposition of the barium salts of this type, addition products of the free acid, of composition H2Pt(CN)4.Cl2.4H2O and H2Pt(CN)s.Br2, have been obtained (C . Blomstrand, Ber., 1869, 2, p . 202) . They are deliquescent solids which are exceedingly soluble in water . Potassium platinocyanide, K2Pt(CN)4.3H20, is obtained by dissolving platinum bichloride in potassium cyanide; by heating potassium ferrocyanide with spongy platinum; or by heating ammonium chlorplatinate with potassium cyanide . It crystallizes in needles which effloresce readily .

The dry salt is exceedingly hygroscopic and is very soluble In water . When boiled with aqua regia it forms the chlorine addition product, K2Pt(CN)4.C12.2H20 . It combines directly with iodine . Barium platinocyanide, BaPt(CN)4.4H20, is prepared by the action of baryta water on the copper salt; by dissolving platinum in barium cyanide under the influence of an alternating current; by the addition of barium cyanide to platinum bichloride; or by the simultaneous action of hydrocyanic and sulphurous acids on a mixture of baryta and chlorplatinic acid (P . Bergsoe, Zeit. anorg . Chem., 1899, 19, p . 318) . It crystallizes in yellow See also:

monoclinic prisms and is soluble in hot water . It is employed for the manufacture of fluorescent screens used for the detection of X-rays . The platinum salts combine with See also:ammonia to form numerous derivatives which can be considered as salts of characteristic bases . The first compound of this type was isolated in 1828 by See also:Magnus, who obtained a green salt by the action of ammonia on platinum bichloride . Two See also:series of these salts are known, one in which the metal corresponds to bivalent platinum, the other in which it corresponds to tetravalent platinum .

The general formulae of the groups in each series are shown below, the method of See also:

classification being that due to See also:Werner . Divalent (platinous) Salts . Tetravalent (platinic) Salts . Hexammine salts[Pt(NH3)e]Xs Tetrammine „ [Pt(NH3)QX2]X2 Triammine „ [Pt(NH3)3X3]X Diammine „ [Pt(NH3)2X41 Monammine „ [Pt(NH3)X3IR In the above table X represents a monovalent acid See also:radical and R a monovalent basic radical . For methods of preparation of salts of these series see P . T . Cleve, Bull. soc. chim . 1867 et seq.; S . M . Jorgensen, Journ. prak . Chem . 1877 et seq .

; C.W . Blomstrand, Ber . 1871 et seq . ; and A . Werner, Zeit. anorg . Chem . 1893 et seq . A very See also:

complete account of the method of classification and the general theory of the metal ammonia compounds is given by A . Werner, Ber . 1907, 40, p . 15 . Platinum also forms a series of complex phosphorus compounds .

At 250° finely divided platinum and phosphorus pentachloride combine to form PtC12.PC13, as dark See also:

claret-coloured crystals . With chlorine this substance gives PtC13•PC14 as a yellow powder, and with water it yields phosphoplatinic acid, PtC12.P(OH)3, which may be obtained as orange-red deliquescent prisms . The atomic See also:weight of platinum was determined by K . Seubert (Ann . 1888, 207, p . 1; Ber . 1888, 21, p . 2179) by analyses of ammonium and potassium platinochlorides; the value 194.86 being obtained .

End of Article: atomic weight 145.0 PLATINUM [symbol Pt (0=16)]
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