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TIN (Lat.- stannum, whence the chemic...

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Originally appearing in Volume V26, Page 997 of the 1911 Encyclopedia Britannica.
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TIN (See also:Lat.- stannum, whence the chemical See also:symbol " Sn "; atomic See also:weight =117.6, 0=16)  , a metallic chemical See also:element . Being a component of See also:bronze, it was used as a See also:metal thousands of years See also:prior to the See also:dawn of See also:history; but it does not follow that prehistoric bronzes were made from metallic See also:tin . When the unalloyed metal was first introduced cannot be ascertained with certainty . The ." tin " of the See also:Bible (Kaavlmpos in the See also:Septuagint) corresponds to the See also:Hebrew bedhil, which is really a See also:copper alloy known as See also:early as 1600 B.C. in See also:Egypt . All we know is that about the 1st See also:century the See also:Greek word Ka?QimEpos designated tin, and that tin was imported from See also:Cornwall into See also:Italy after, if not before, the invasion of See also:Britain by See also:Julius See also:Caesar . From See also:Pliny's writings it appears that the See also:Romans in his See also:time did not realize the distinction between tin and See also:lead: the former was called plumbum See also:album or candidum to distinguish it from plumbum nigrum (lead proper) . The word stannum definitely assumed its See also:present meaning in the 4th century (H . See also:Kopp) . By the early Greek alchemists the metal was named See also:Hermes, but at about the beginning of the 6th century, it was termed Zeusor See also:Jupiter, and the See also:symbol 2( assigned to it; it was also referred to as diabolus metallorum, on See also:account of the brittle See also:alloys which it formed.9'95 Occurrence.-Grains of metallic tin occur intermingled with the See also:gold ores of See also:Siberia, See also:Guiana and See also:Bolivia, and in a few other localities . Of minerals containing this element mention may be made of cassiterite (q.v.) or tinstone, SnO2, tin See also:pyrites, Cu4SnS4+(Fe,Zn)2SnS4; the metal also occurs in some epidotes, and in See also:company with See also:columbium, See also:tantalum and other metals . Of these " tinstone " is of the greatest commercial importance . It occurs in its See also:matrix, either in or closely associated with fissure See also:veins or disseminated through See also:rock masses .

It is also found in the See also:

form of rolled lumps and grains, " stream tin," in alluvial gravels; the latter are secondary deposits, the products of the disintegration of the first-named See also:primary deposits . Throughout the See also:world, primary deposits of tinstone are in or closely connected with See also:granite or See also:acid eruptive rocks of the same type, its See also:mineral associates being See also:tourmaline, fluorspar, See also:topaz, wolfram and arsenical pyrites, and the invariable See also:gangue being See also:quartz: the only exception to this mode of occurrence is to be found in Bolivia, where the tin ore occurs intimately associated .with See also:silver ores, See also:bismuth ores and various sulphides, whilst the gangue includes See also:barytes and certain See also:carbonates . Over five-sixths of the world,'s See also:total See also:production is derived from secondary alluvial deposits, but all the tin obtained in Cornwall (the alluvial deposits having been worked out) and Bolivia is from vein See also:mining, while a small portion of that yielded by See also:Australasia comes from veins and from granitic rocks carrying disseminated tinstone . Production.—During ' the 18th century the world's See also:supply of tin was mainly See also:drawn from the deposits of See also:England, See also:Saxony and Bohemia; in 18ai England produced about 2500 tons, while the supplies of Saxony and Bohemia See also:bad been greatly diminished . The See also:English supply increased, with some oscillations, to between six and seven thousand tons annually in the See also:period 184o-186o, when it suddenly See also:rose to about so,000 tons, and this figure was fairly well sustained until about 189o, rwhpn a period of depression set in; the yield for 1900 was 4336 tons, and for egos about 4200 tons . In the opening decades of the 19th century supplies began to be drawn from See also:Banka; in i82o this See also:island contributed 1200 tons; the production was increased to 12,000 tons in 1900, when a diminution set in, .996o tons being the output during 1905 . See also:Billiton became of See also:note in 1853 with a production of 40 tons, which increased to;6000 in 1goo and has since declined to about 3000 tons in 1905 . The Straits Settlements ranked as an important producer in 187o with 2337 tons; it now supplies the greater See also:part of the world's supply, contributing 46,795 tons in 1900, and over 6o,000 tons in 1905 . Australian deposits were worked in 1872, and in the following See also:year the production was 3000 tons; the maximum outputs were in 1881-1883, averaging Io,000 tons annually; but the supply declined to 2420 tons in 1898 and has since increased to about 5028 tons in 1905 . Bolivia produced Sol tons in 1883, 10,245 in 1900 and 12,500 in 1905 . The world's supply in woo was 72,911 See also:long tons; this increased in 1904 to 97,790 tons, but in 1905, principally owing to a shortage in the supplies from the Straits and Banka, the yield See also:fell to 94,089 tons . Metallurgy.—The operations in the metallurgy of tin may be enumerated as: (1) mining and dressing, (2) smelting, (3) refining .

The first See also:

stage has for its purpose the production of a fairly pure tinstone; the second the See also:conversion of the See also:oxide into metallic tin; and the third preparing a tin pure enough for commercial purposes . Mining and Dressing.—The alluvial deposits are almost invariably worked opencast, those of the See also:Malay See also:Peninsula and See also:Archipelago chiefly by See also:Chinese labour: in a few instances See also:hydraulic mining has been resorted to, and in other cases true underground mining is carried on; but the latter is both exceptional and difficult . The alluvial extracted, which in the Malay Peninsula and Archipelago carries from 5 to 6o lb of tinstone (or " See also:black tin," as it is termed by Cornish miners) to the cubic yard of See also:gravel, is washed in various See also:simple sluicing appliances, by which the lighter See also:clay, See also:sand and stones are removed and tinstone is See also:left behind comparatively pure, containing usually 65 to 75% of metallic tin (chemically pure tinstone contains 78.7 %) . Lode tin, as tinstone derived from primary deposits is often termed, is See also:mined in the See also:ordinary method, the very hard gangue 'in which it occurs necessitating a liberal use of See also:explosives . The vein-stuff is broken small either by See also:hand or in rock-breakers, and stamped to See also:fine See also:powder in See also:stamp See also:mills, which are practically large mechanically-worked pestles and mortars, the stamp proper weighing from Soo to moo lb . The mineral, crushed small enough to pass a See also:sieve with perforations 21a in. in See also:diameter, leaves the stamps in suspension in See also:water, and passes through a See also:series of troughs in which the heavier mineral is collected; this then passes through a series of washing operations, which leaves a mixture consisting chiefly of tinstone and arsenical pyrites, which is calcined and washed again, until finally black tin containing about 6o to 65% of metal is left . The calcination is preferably effected in See also:mechanical roasters, it being especially necessary to agitate the ore continually, otherwise it cakes . The crude tinstuff raised in Cornwall carries on an See also:average a little over 2% of black tin . The Bolivian tin ore is treated by first extracting the silver by amalgamation, &c., and afterwards concentrating the residues; there are, however, considerable difficulties in the way of treating the poorer of these very complex ores, and several chemical processes for extracting their metallic contents have been worked out . Of the impurities of the ore the See also:wolframite (tungstate of See also:iron and See also:manganese) is the most troublesome, because on account of its high specific gravity it cannot be washed away as gangue . To remove it, Oxland fuses the ore with a certain proportion of carbonate of soda, which suffices to convert the See also:tungsten into soluble alkaline tungstate, without producing noteworthy 'quantities of soluble stannate from the oxide of tin; the tungstate is easily removed by treatment with water . 2 .

Smelting.—The dressed ore is smelted with See also:

carbon by one of two See also:main methods, viz. either in the See also:shaft See also:furnace or the reverberatory; the former is the better suited to stream tin, the latter to lode tin, but either ore can be smelted in either way, although reverberatory practice yields a purer metal . Shaft furnace smelting is confined to those parts of the world where See also:charcoal can still be obtained in large quantities at moderate prices . The furnace consists of a shaft, circular (or more rarely rectangular) in See also:plan, into which alternate layers of See also:fuel and ore are charged, an See also:air blast being generally injected near to the bottom of the furnace through one or more tuyeres . This was the See also:primitive See also:process all over the world ; in the See also:East, See also:South See also:America and similar regions it still holds its own . In See also:Europe, Australasia and one large See also:works at See also:Singapore it has been practically replaced by the reverberatory furnace process, first introduced into Cornwall about the year 1700 . In this process the purified ore is mixed with about one-fifth of its See also:weight of a non-caking See also:coal or See also:anthracite smalls, the mixture being moistened to prevent it from being blown off by the See also:draught, and is then fused on the See also:sole of a reverberatory furnace for five or six See also:hours . The slag and metal produced are then run off and the latter is See also:cast into bars; these are in See also:general contaminated with,iron, See also:arsenic, copper and other impurities . 3 . Refining.—All tin, except a small quantity produced by the shaft furnace process from exceptionally pure stream tin ore, requires refining by liquation and " boiling " before it is ready for the See also:market . In the English process the bars are heated cautiously on an inclined See also:hearth, when relatively pure tin runs off, while a See also:skeleton of impure metal remains . The metal run off is further purified by poling, i.e. by stirring it with the See also:branch of a See also:tree—the See also:apple tree being preferred traditionally . This operation is no doubt intended to remove the See also:oxygen diffused throughout the metal as oxide, part of it perhaps chemically by reduction of the oxide to metal, the See also:rest by conveying the finely diffused oxide to the See also:surface and causing it to unite there with the oxide scum .

After this the metal is allowed to rest for a time in the pot at a temperature above its freezing point and is then ladled out into See also:

ingot forms, care being taken at each stage to ladle off the See also:top stratum . The See also:original top stratum is the purest, and each succeeding See also:lower stratum has a greater proportion of impurities; the lowest consists largely of a solid or semi-solid alloy of tin and iron . To test the purity of the metal the tin-smelter heats the bars to a certain temperature just below the fusing point, and then strikes them with a See also:hammer or lets them fall on a See also:stone See also:floor from a given height . If the tin is pure it splits into a See also:mass of granular strings . Tin which has been thus manipulated and proved incidentally to be very pure is sold as See also:grain tin . A lower quality goes by the name of See also:block tin . Of the several commercial varieties Banka tin is the purest; it is indeed almost chemically pure . Next comes English grain tin . For the preparation of chemically pure tin two methods are employed . (I) Commercially pure tin is treated with nitric acid, which converts the tin proper into the insoluble metastannic acid, while the copper, iron, &c., become nitrates; the metastannic acid is washed first with dilute nitric acid, then with water, and is lastly dried and reduced by See also:fusion with black See also:flux or See also:potassium See also:cyanide . (2) A See also:solution of pure stannous chloride in very dilute hydrochloric acid is reduced with an electric current . According to Stolba, beautiful crystals of pure tin can be obtained as follows: A See also:platinum See also:basin, coated over with See also:wax or See also:paraffin outside, except a small circle at the very lowest point, is placed on a See also:plate of amalgamated See also:zinc, lying on the bottom of a See also:beaker, and is filled with a solution of pure stannous chloride .

The beaker also is cautiously filled with acidulated water up to a point beyond the edge of the platinum basin . The whole is then left to itself, when crystals of tin gradually See also:

separate out on the bottom of the basin . Properties.—An ingot of tin is pure See also:white (except for a slight tinge of See also:blue) ; the See also:colour depends, however, upon the temperature at which it is poured—if too See also:low, the surface is dull, if too high, iridescent . It exhibits considerable lustre and is not subject to tarnishing on exposure to normal air . The metal is See also:pretty soft and easily flattened out under the hammer, but almost devoid of tenacity., That it is elastic, with narrow limits, is proved by its clear See also:ring when struck with a hard See also:body in circumstances permitting of See also:free vibration . The specific gravity of cast tin is 7.29, of rolled tin 7.299, and of electrically deposited tin 7.143 to 7.178 . A tin ingot is distinctly crystalline; hence the characteristic crackling See also:noise, or " cry " of tin, which a See also:bar of tin gives out when being See also:bent: This structure can be rendered visible by superficial See also:etching with dilute acid; and as the minuter crystals dissolve more quickly than the larger ones, the surface assumes a frosted See also:appearance (moiree metallique) . The metal is dimorphous: by cooling molten tin at ordinary air temperature tetragonal crystals are obtained, while by cooling at a temperature just below the melting point rhombic forms are produced . When exposed for a sufficient time to very low temperatures (to -39° C. for 14 hours), tin becomes so brittle that it falls into a See also:grey powder, termed the grey modification, under a pestle; it indeed sometimes crumbles into powder spontaneously . At ordinary temperatures tin proves fairly ductile under the hammer, and its ductility seems to increase as the temperature rises up to about See also:loo° C . At some temperature near its fusing point it becomes brittle, and still more brittle from -14° C. downwards . Iron renders the metal hard and brittle; arsenic, See also:antimony and bismuth (up to 0.5%) reduce its tenacity; copper and lead (1 to 2 %) make it harder and stronger but impair its malleability; and stannous oxide reduces its tenacity Tin fuses at about 230° C.; at a red See also:heat it begins to volatilize slowly; at 1600° to 1800° C. it boils .

The hot vapour produced combines with the oxygen of the air into white oxide, SnO2 . Its coefficient of linear expansion between o° and loo° is 0.002717; its specific heat (3.6562; its thermal and See also:

electrical conductivities are 145 to 152 and 114.5 to 140.1 respectively compared to silver as 10oo . See also:Industrial Applications.--Commercially pure tin is used for making such apparatus as evaporating basins, infusion pots, stills, &c . It is also employed for making two varieties of tin-See also:foil--one for the silvering of mirrors (see See also:MIRROR), the other for wrapping up See also:chocolate, See also:toilet See also:soap, See also:tobacco, &c . The mirror foil must contain some copper to prevent it from being too readily amalgamated by the See also:mercury . For making tin-foil the metal is rolled into thin sheets, pieces of which are beaten out with a wooden See also:mallet . As pure tin does not tarnish in the air and is See also:proof against acid liquids, such as See also:vinegar, See also:lime juice, &c., it is utilized for culinary and domestic vessels . But it is expensive, and tin vessels have to be made very heavy to give them sufficient stability of form; hence it is generally employed merely as a protecting coating for utensils made essentially of topper or iron . The tinning of a copper basin is an easy operation . The basin, made scrupulously clean, is heated to beyond the fusing point of tin . Molten tin is then poured in, a little powdered sal-ammoniac added, and the tin spread over the inside with a bunch of See also:tow . The sal-ammoniac removes the last unavoidable film of oxide, leaving a purely metallic surface, to which the tin adheres firmly .

Phoenix-squares

For tinning small See also:

objects of copper or See also:brass (i.e. pins, hooks, &c.) a wet-way process is followed . One part of cream of See also:tartar, two of See also:alum and two of See also:common See also:salt are dissolved in boiling water, and the solution is boiled with granulated metallic tin (or, better, mixed with a little stannous chloride) to produce a tin solution; and into this the articles are put at a boiling heat . In the See also:absence of metallic tin -thereis no visible See also:change; but, as soon as the metal is introduced, an electrolytic See also:action sets in and the articles get coated over with a firmly adhering film of tin . Tinning wrought iron is effected by See also:immersion . The most important form of the operation is making tinned from ordinary See also:sheet iron (making what is called " sheet tin "): This process was mentioned by See also:Agricola ; it was practised in Bohemia in 162o, and in England a century later . The iron plates, having been carefully cleaned with sand and hydrochloric or sulphuric acid, and lastly with water, are plunged into heated See also:tallow to drive away the water without oxidation of the metal . They are next steeped in a See also:bath, first of molten ferruginous, then of pure tin . They are then taken out and kept suspended in hot tallow to enable the surplus tin to run off . The tin of the second bath dissolves iron gradually and becomes See also:fit for the first bath . To tin cast-iron articles they must be decarburetted superficially by ignition within a bath of ferric oxide (powdered See also:haematite or similar material), then cleaned with acid, and tinned by immersion, as explained above . (See TIN-PLATE.) By far the greater part of the tin produced metallurgically is used for making tin alloys (see See also:PEWTER, BRONZE) . Compounds of Tin .

Tin forms two well-marked series of salts, in one of which it is divalent, these salts being derived from stannous oxide, SnO, in the other it is tetravalent, this series being derived from stannic oxide, SnO2 . Stannous Oxide, SnO, is obtained in the hydrated form Sn2O(OH)2 from a solution of stannous chloride by addition of See also:

sodium carbonate; it forms a white precipitate, which can be washed with air-free water and dried at 8o° C. without much change by oxidation ; if it be heated in carbon dioxide the black SnO remains . Precipitated stannous See also:hydrate dissolves readily in See also:caustic potash; if the solution is evaporated quickly it suffers decomposition, with formation of metal and stannate, 2SnO-1-2KOH =KiSnOs+Sn+See also:H2O . If it is evaporated slowly, anhydrous stannous oxide crystallizes out in forms which are combinations of the See also:cube and See also:dodecahedron . Dry stannous oxide, if touched with a glowing body, catches See also:fire and See also:burns to stannic oxide, SnO2 . Stannous oxalate when heated by itself in a See also:tube leaves stannous oxide . Stannic Oxide, SnOi.—This, if the See also:term is taken to include the hydrates, exists in a variety of forms . (1) Tinstone (see above and also CASSITERITE) is proof against all acids . Its disintegration for See also:analytical purposes can be effected by fusion with caustic See also:alkali in silver basins, with the formation of soluble stannate, or by fusion with See also:sulphur and sodium carbonate, with the formation of a soluble thiostannate . (2) A similar oxide (flares jovis) is produced by burning tin in air at high temperatures or exposing any of the hydrates to a strong red heat . Such tin-ash, as it is called, is used for the polishing of See also:optical glasses . See also:Flores stanni is a finely divided mixture of the metal and oxide obtained by fusing the metal in the presence of air for some time .

(3) Metastannic acid (generally written HioSn6Oio, to account for the complicated See also:

composition of metastannates, e.g. the sodium salt HsNa2Sn50ie) is the white See also:compound produced from the metal by means of nitric acid . It is insoluble in water and in nitric acid and apparently so in hydrochloric acid; but if heated with this last for some time it passes into a compound, which, after the acid See also:mother liquor has been decanted off, dissolves in water . The solution when subjected to See also:distillation behaves very much like a See also:physical solution of the oxide in hydrochloric acid, while a solution of orthostannic acid in hydrochloric acid behaves like a solution of SnCl4 in water, i.e. gives off no hydrochloric acid, and no precipitate of hydrated SnO2 . Metastannic acid is distinguished from orthostannic acid by its insolubility in nitric and sulphuric acids . The salts are obtained by the action of alkalies on the acid . (4) Orthostannic acid is obtained as a white precipitate on the addition of sodium carbonate or the exact quantity of precipitated See also:calcium carbonate to a solution of the chloride . This acid, H2SnOs, is readily soluble in acids forming stannic salts, and in caustic potash and soda, with the formation of orthostannates . Of these sodium stannate, Na2SnOs, is produced industrially by See also:heating tin with See also:Chile See also:saltpetre and caustic soda, or by fusing very finely powdered tinstone with caustic soda in iron vessels . A solution of the pure salt yields fine prisms of the composition Na2SnOi+IoH2O, which effloresce in the air . The salt is used as a See also:mordant in See also:dyeing and See also:calico-See also:printing . Alkaline and other stannates when treated with aqueous hydrofluoric acid are converted into fluostannates (e.g . K2SnOs into K2SnFs), which are closely analogous to, and isomorphous with, fluosilicates .

A colloidal or soluble stannic acid is obtained by dialysing a mixture of tin tetrachloride and alkali, or of sodium stannate and hydrochloric acid . On heating it is converted into colloidal metastannic acid . A hydrated tin trioxide, SnO2, was obtained by See also:

Spring by adding See also:barium dioxide to a solution of stannous chloride and hydrochloric acid; the solution is dialysed, and the colloidal solution is evaporated to form a white mass of 2SnOs•H2O . Stannous Chloride, SnCl2, can only be obtained pure by heating pure tin in a current of pure dry hydrochloric acid See also:gas . It is a white solid, fusing at 2 o° C. to an oily liquid which boils at 6o6%, and volatilizing at a red heat in See also:nitrogen, a vacuum or hydrochloric acid, without decomposition . The vapour See also:density below 700° C. corresponds to Sn2Cl4, above 800° C. to nearly SnCl2 . The chloride readily combines with water to form a crystallizable hydrate SnCl2.2H20, known as " tin salt " or " tin crystals." This salt is also formed by dissolving tin in strong hydrochloric acid and allowing it to crystallize, and is industrially prepared by passing sufficiently hydrated hydrochloric acid gas over granulated tin contained in stoneware bottles and evaporating the concentrated solution produced in tin basins over granulated tin . The basin itself is not attacked . The crystals are very soluble in See also:cold water, and if the salt is really pure a small proportion of water forms a clear solution; but on adding much water most of the salt is decomposed, with the formation of a precipitate of oxychloride, 2Sn(OH)Cl•H20 . According to See also:Michel and Kraft, one litre of cold saturated solution of tin crystals weighs 1827 grammes and contains 1333 grammes of SnCl2 . The same oxychioride is produced when the moist crystals, or their solution, are exposed to the air . Hence all tin crystals as kept in the laboratory give with water a turbid solution, which contains stannic in addition to stannous chloride .

The See also:

complete conversion of stannous into stannic chloride may be effected by a See also:great many reagents—for instance, by See also:chlorine (See also:bromine, See also:iodine) readily; by mercuric chloride in the heat, with precipitation of See also:calomel or metallic mercury; by ferric chloride in the heat, with formation of ferrous chloride; by arsenious chloride in strongly hydrochloric solutions, with precipitation of chocolate-See also:brown metallic arsenic . All these reactions are available as tests for " stannosum " or the respective agents . In opposition to stannous chloride, even sulphurous acid (solution) behaves as an oxidizing See also:agent . If the two reagents are mixed a precipitate of yellow stannicsulphide is produced . A See also:strip of metallic zinc when placed in a solution of stannous chloride precipitates the tin in crystals and takes its See also:place in the solution . Stannous chloride is largely used in the laboratory as a reducing agent, in dyeing as a mordant . Stannic Chloride, SnCl4, named by Andreas Libavius in 16os Spiritus argenti viva sublimate from its preparation by distilling tin or its See also:amalgam with corrosive sublimate, and afterwards termed Spiritus fumans Libavii, is obtained by passing dry chlorine over granulated tin contained in a See also:retort; the tetrachloride distils over as a heavy liquid, from which the excess of chlorine is easily removed by shaking with a small quantity of tin filings and re-distilling . It is a colourless fuming liquid of specific gravity 2.269 at o°; it freezes at -33° C., and boils at 113.9° . The chloride unites energetically with water to form crystalline hydrates (e.g . SnCl4.3H5O), easily soluble in water . With one-third its weight of water it forms the so-called "See also:butter of tin." It combines readily with alkaline and other chlorides to form See also:double salts, e.g . M2SnCls, analogous to the chloroplatinates; the salt (NH4)2SnC16 is known industrially as " See also:pink salt " on account of its use as a mordant to produce a pink colour .

The oxymuriate of tin used by dyers is SnCl4•5H20 . The See also:

plain chloride solution is similarly used . It is usually prepared by dissolving the metal in aqua regia . Stannous Fluoride, SnF2, is obtained as small, white See also:monoclinic tables by evaporating a solution of stannous oxide in hydrofluoric acid in a vacuum . Stannic Fluoride, SnF4, is obtained in solution by dissolving hydrated stannic oxide in hydrofluoric acid; it forms a characteristic series of salts, the stannofluorides, M2SnF6, isomorphous with the silico-, titano-, germano- and zirconofluorides . Stannous bromide, SnBr2, is a See also:light yellow substance formed from tin and hydrobromic acid . Stannic bromide, SnBr4, is a white crystalline mass, melting at 33° and boiling at 201 °, obtained by the See also:combination of tin and bromine, preferably in carbon bisulphide solution . Stannous iodide, SnI2, forms yellow red needles, and is obtained from potassium iodide and stannous chloride . Stannic iodide, Snl4, forms red octahedra and is prepared similarly to stannic bromide . Both iodides combine with See also:ammonia . Stannous sulphide, SnS, is obtained as a lead-grey mass by heating tin with sulphur, and as a brown precipitate by adding sulphuretted See also:hydrogen to a stannous solution ; this is soluble in ammonium poly-sulphide, and dries to a black powder . Stannic sulphide, SnS2, is obtained by heating a mixture of tin (or, better, tin amalgam), sulphur and sal-ammoniac in proper proportions in the beautiful form of aurum musivum (See also:mosaic gold)—a solid consisting of See also:golden yellow, metallic lustrous scales, and used chiefly as a yellow "bronze " for See also:plaster-of-See also:Paris statuettes, &c .

The yellow precipitate of stannic sulphide obtained by adding sulphuretted hydrogen to a stannic solution readily dissolves in solutions of the alkaline sulphides to form thiostannates of the See also:

formula M2SnS2; the free acid, H2SnSs, may be obtained as an almost black powder by drying the yellow' precipitate formed when hydrochloric acid is added to a solution of a thiostannate . See also:Analysis.—Tin compounds when heated on charcoal with sodium carbonate or potassium cyanide in the reducing See also:blowpipe See also:flame yield the metal and a scanty ring of white SnO2 . Stannous salt solutions yield a brown precipitate of SnS with sulphuretted hydrogen, which is insoluble in cold dilute acids and in real sulphide of ammonium, (NH4)2S; but the yellow, or the colourless reagent on addition of sulphur, dissolves the precipitate as SnS2 salt . The solution on acidification yields a yellow precipitate of this sulphide . Stannic salt solutions give a yellow precipitate of SnS2 with sulphuretted hydrogen, which is insoluble in cold dilute acids but readily soluble in sulphide of ammonium, and is re-precipitated therefrom as SnS2 on acidification . Only stannous salts (not stannic) give a precipitate of calomel in mercuric chloride solution . A mixture of stannous and stannic chloride, when, added to a sufficient quantity of solution of chloride of gold, gives an intensely See also:purple precipitate of gold purple (purple of See also:Cassius) . The test is very delicate, although the colour is not in all cases a pure purple . Tin is generally quantitatively estimated as the dioxide . The solutions are oxidized, precipitated with ammonia, the precipitate dissolved in hydrochloric acid, and re-thrown down by boiling with sodium sulphate . The precipitate is filtered, washed, dried and ignited .

End of Article: TIN (Lat.- stannum, whence the chemical symbol " Sn "; atomic weight =117.6, 0=16)
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REfining of tin pure tin metal from dry powder scrap contents folowing impurites 1)copper - 3.4% 2)Lead - 4.5 % 3) Nickle - 3.2% 4) iron - 2% 5) alluminium - 2.8% 6) zinc - 1.4% 7) Tin - 27%. I want to refine tin metal from above impurites by chemical method.
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