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METALLOGRAPHY .—The examination of metals and See also:alloys by the aid of the See also:microscope has assumed much importance in comparatively See also:recent years, and it might at first be considered to be a natural development of the use of the microscope in determining the constitution of rocks, a study to which the name petrography has been given . It would appear, however, that it is an See also:extension of the study of the structure of meteoric irons . There can be no question that in the See also:main it was originated by Dr H . C . Sorby, who in 1864 gave the See also:British Association an See also:account of his See also:work . Following the work of Sorby came that of See also:Professor A . See also:Mar!ens of See also:Charlottenburg, presenting many features of originality . F . Osmond has obtained results in connexion with See also:iron and See also:steel which are of the highest See also:interest . A See also:list of the more important papers by these and other workers will be found in the appended bibliography . Preparation of the Specimen.—Experience alone can enable the operator to determine what portion of a See also:mass of See also:metal or alloy will afford a trustworthy See also:sample of the whole . In studying a See also:series of binary alloys it has been found advantageous in certain cases to obtain one See also:section which will show in a See also:general way the variation in structure from one end of the series to the other . This has been effected by pouring the lighter constituent carefully on the See also:surface of the heavier constituent, and allowing solidification to take See also:place . •A section through the culot so obtained will show a gradation in structure from pure metal on one See also:side to pure metal on the other . A thin slice of metal is usually cut by means of a hack-saw driven by mechanism . The thickness of the piece should not be less than 4 in. and in See also:order that it may be firmly held between the fingers it should not be less than 1 in. square . The preliminary stages of polishing are effected by See also:emery See also:paper placed preferably on wooden disks capable of being revolved at a high See also:rate of See also:speed . The finest grade of emery paper that can be obtained is used towards the end of the operation . Before use the finer papers should be rubbed with a hard steel surface to remove any coarse particles . The completion of the operation of polishing is generally effected on wet See also:cloth or See also:parchment covered with a small amount of carefully washed jeweller's See also:rouge . Various See also:mechanical appliances are employed to minimize the labour and See also:time required for the polishing . These usually consist of a series of interchangeable revolving disks, each of which is covered with emery paper, cloth or parchment, according to the particular See also:stage of polishing for which it is required . In the See also:case of brittle alloys and of alloys having a very soft constituent, which during polishing tends to spread over and obliterate the harder constituents, polishing is in many cases altogether avoided by casting the alloy on the surface of See also:glass or See also:mica . In this way, with a little care, a perfect surface is obtained, and it is only necessary to develop the structure by suitable See also:etching . In adopting this method, however, instances have occurred in which the removal of the See also:cast surface has shown a structure differing considerably from the See also:original . Polishing in Bas-See also:Relief.—If the polishing be completed with See also:fine rouge on a See also:sheet of wet parchment, placed upon a comparatively soft bas such as a piece of See also:deal, certain soft constituents of an alloy may often be eroded in such a manner as to leave the hardest portions in relief . For the later stages of polishing H . L . Le Chatelier recommends the use of alumina obtained by the calcination of ammonium See also:alum; and for the final See also:polish of soft metals, See also:chromium See also:oxide . Although in some cases a See also:pattern becomes visible after polishing, yet more frequently a See also:mirror-like surface is produced in which no pattern can be detected, or if there is a pattern it is blurred, as if seen through a See also:veil or mist . This is due to a thin layer of metal which has been dragged, or smeared, uniformly over the whole surface by the See also:friction of the polishing See also:process . Such a surface layer is formed in all cases of polishing, and the See also:peculiar lustre of burnished See also:silver or steel is probably due to this layer . But to the metallographist it is an inconvenience, as it conceals scratches See also:left by imperfect polishing, and also hides the pattern . It is therefore desirable to conduct the polishing so as to make this layer as thin as possible: it is claimed for alumina that it can be so used as to produce a much thinner surface layer than that due to the employment of rouge . The surface layer is very readily removed by appropriate liquid reagents, and, the true surface of the metal having been laid See also:bare, the etching reagent acts differently on the individual substances in the alloy and the pattern can thus be emphasized to any required extent . Osmond divides etching reagents into three classes—acids, See also:halogens and salts . As regards acids, See also:water containing from z to ro% of hydrochromic See also:acid is useful . It is made by mixing to grams of See also:potassium bichromate with ro grams of sulphuric acid in roo grams of water . The use of nitric acid requires much experience . It is frequently employed in the examination of steels, See also:Sir W . C . See also:Roberts-See also:Austen preferred a 1% See also:solution in See also:alcohol, but many workers use concentrated acid, and effect the etching by allowing a stream of water to dilute the film of acid left on the surface of the specimen after dipping it . Of the halogens, See also:iodine is the most useful . A solution in alcohol is applied, so that a single drop covers See also:half a square See also:inch of surface . The specimen is then washed with alcohol, and dried with a piece of fine See also:linen or See also:chamois See also:leather . See also:Tincture of iodine also affords a means of identifying See also:lead in certain alloys by the formation of a yellow iodide of lead, while the vapour of iodine has in certain cases been used to tint the constituents . Thin coloured films may often be produced by the oxidation of the specimen when heated in See also:air . This, as a means of developing the structure, in the case of the See also:copper alloys is specially useful .
Tinted crystals may thus be distinguished from the investing layer caused by the presence of a See also:minute quantity of another constituent
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The See also:temper See also:colours produced by See also:heating iron or steel in air are well known
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See also:Carbide of iron is less oxidizable than the iron with which it is intimately associated, and it assumes a See also: Every micrographer has his own views as should be an achromatic one, as See also:colour effects cause trouble in photographing the See also:objects . For See also:lower See also:powers the Lieberkuhn parabolic illuminator is useful . Certain See also:groups of alloys show better under oblique See also:illumination, which may be effected by the aid of a See also:good condensing See also:lens, the See also:angle of incidence being limited by the distance of the See also:object from the See also:objective in the case of high magnification . As regards objectives, the most useful are the Zeiss 2 mm., 4 mm. and 24 mm.; two other useful objectives for See also:low powers being 35 mm. and 70 mm., both of which are projecting objectives . A projecting See also:eye-piece, prefer-ably of low See also:power, should be employed with all but the two latter objectives . The See also:immersion lens, the Zeiss 2 mm., is used with specially thickened See also:cedar oil, and if the distance from the objective to the See also:plate is 7 feet, magnifications of over 2000 diameters can easily be obtained . As regards sensitized plates, excellent results have been obtained with Lumiere plates sensitive to yellow and See also:green The various brands of " process " plates are very serviceable where the contrasts on the specimen are not See also:great . Some reproductions of photo-micrographs of metals and alloys will be found in the plate accompanying the See also:article ALLOYS . W . C . Roberts-Austen and F . Osmond, " On the Structure of Metals, its Origin and Causes," Phil .
Trans
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See also:Roy
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See also:Soc. clxxxvii
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417—4.32; and See also:Bull. de la Soc. d'encouragement pour l'industrie nationale, 5e eerie, i
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1136 (Aoflt 1896) ; G
.
Charpy, " Micro-
Micrographic Apparatus. scopic Study of Me-
tallic Alloys," Bull
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to the See also:form of an See also:installation to be adopted, and it will therefore I de la sec. d'encouragement pour l'industrie nationale (See also: A practised observer can See also:focus on a plate 1353 and cxcv . 279; F . Osmond, " See also:Crystallography of Iron," Annales of clear glass by the aid of a subsidiary low-power microscope See also:des Mines (See also:January ,9o0) ; Le Chatelier, Technology of Metallolens . If a semi-transparent plate is employed it should be as fine graphs," Metallogr¢phist, vol. iv . No . 1; Contribution a l'etude des as possible . The surface of the table is cut in such a way near H alliages . Societe d'encour¢gement pour l'industrie nationale (1901); See also:Smeaton, " Notes on the Etching of Steel Sections," Iron and Steel that the observer who is seated may conveniently examine the See also:Magazine, vol. ix . No . 3 . (W . C . R.-A.; F . H . NE.) object on the stage of the microscope, the portion B turning METALLURGY, the See also:art of extracting metals from their ores; aside for this purpose . The subsequent focusing is effected by a the See also:term being customarily restricted to commercial as opposed See also:rod, FFF, and gearing attached to the fine See also:adjustment of the to laboratory methods . It is convenient to treat See also:electrical processes of extraction as forming the subjects of See also:Electrochemistry and See also:Electrometallurgy (qq.v.) . The following table enumerates in the order of their importance the metals which,our subject at See also:present is understood to include; the second See also:column gives the chemical characters of the ores utilized, italics indicating those of subordinate importance . The term " oxide " includes carbonate, See also:hydrate, and, when marked with*, silicate . Metal . See also:Character of Ores . Iron Oxides, sulphide . Copper Complex sulphides, also oxides, metal . Silver Sulphide and reguline metal, chloride . See also:Gold Reguline metal . Lead Sulphide and basic carbonate, sulphate, &c . See also:Zinc Sulphide, oxide.* See also:Tin Oxide . Metallographist, vol. i . No . 3; " Metallography applied to Foundry Work," The Iron and Steel Magazine, vol. ix . No . 6, and vol. x . No . 1; J . E . See also:Stead, " Crystalline Structure of Iron and Steel," Journ . Iron and Steel Inst . (1898), i . 145; " See also:Practical Metallography," Prot . See also:Cleveland Inst. of See also:Engineers (Feb . 26, 1900) ; See also:Ewing and Rosenhain, microscope, GA; flap J when raised forms the support of the See also:lamp used for illumination . As an illuminant an arc See also:light has many advantages, as the exposure of the plate used will seldom exceed to seconds . The filament of a Nernst lamp can be used as the source of light; though not so brilliant as the arc it possesses the great See also:advantage of perfect immobility . For the best results, especially with high powers, the source of light must be small, so that its See also:image can be focussed on to the surface of the object; this advantage is possessed by both of these illuminants . Next in value comes the See also:acetylene See also:flame, and an incandescent lamp or a See also:gas lamp with a See also:mantle will give good results, but with much longer exposure . Actual illumination is best effected by a See also:Beck See also:vertical illuminator or a Zeiss See also:prism . It is necessary that the lens used for concentrating the light on the illuminator General Sequence of Operations.—Occasionally, but rarely, Sulphides.—Iron, copper, lead, zinc, See also:mercury, silver and See also:antimony very frequently present themselves in this See also:state of See also:combination, as metallic ores occur as practically pure compact masses, from components of a See also:family of ores which may be divided into two which the accompanying See also:matrix or " See also:gangue " can be detached sections: (L)' such as substantially consist of simple sulphides, as by See also:hand and See also:hammer . In most cases the " ore " (see See also:MINERAL, iron See also:pyrites (FeS2), See also:galena (See also:PbS), zinc See also:blende (ZnS), See also:cinnabar (HgS) ; DEPOSITS; See also:VEINS), as it comes out of the mine or See also:quarry, is and (2) complex sulphides, such as the various kinds of sulphureous simply mixture of ore and in which the latter copper ores (all substantially compounds or mixtures of sulphides a m proper gangue, of copper and iron) ; See also:bournonite, a complex sulphide of lead, See also:anti-not unfrequently predominates . Hence it is generally necessary mony and copper; rothgiltigerz, sulphide of silver, antimony, and to purify the ore before the liberation of the metal is attempted. See also:arsenic; fahlerz, sulphides of arsenic and antimony, combined with Most metallic ores are specifically heavier than the accompanying sulth ide es of and otherrsul ver, i wi, zinone c, another' silver; and mixtures impurities and their See also:purification is generally effected by reducing In treating a sulphureous ore, the first step as a See also:rule is to subject the crude ore to a fine enough See also:powder to detach the metallic it to oxidation by roasting it in a reverberatory or other See also:furnace, from the earthy See also:part, and then washing away the latter by a which leads to the burning away of at least part of the arsenic and current of water, as far as possible (see ORE-DRESSING). part of the See also:sulphur . The effect on the several individual metallic The See also:majority of ores being chemical compounds, the extraction sulphides (supposing only one of these to be present) is as follows: — g L . Those of silver (Ag2S) and mercury (HgS) yield sulphur dioxide of their metals demands chemical treatment . The chemical gas and metal; in the case of silver, sulphate is formed at low See also:tern- operations involved may be classified as follows:— peratures . Metallic mercury, in the circumstances, goes off as a 1 . Fiery Operations.—The ore, generally with some " See also:flux," vapour, which is collected and condensed; silver -remains as a See also:regulus, is exposed to the See also:action of See also:fire . The fire in most cases has a but pure sulphide of silver is hardly ever worked . 2 . Sulphides of iron and zinc yield the oxides Fe20a and ZnO as chemical, in addition to its See also:physical, See also:function . Moreover the final products, some basic sulphate being formed at the earlier stages, furnace (q.v.) is designed so as to facilitate the action of the See also:heat especially in the case of zinc . The oxides can be reduced by See also:carbon. and furnace gases in the desired direction . It is intended either 3 . The sulphides of lead and copper yield, the former a mixture to See also:burn away certain components of the ore—in which case it of oxide and normal sulphate, the latter one of oxide and basic sulphate . Sulphate of lead is See also:stable at a red heat; sulphate of copper must be so regulated as to contain a sufficient excess of unburned breaks up into oxide, sulphur dioxide and See also:oxygen . In practice, oxygen; or it is meant to deoxidize (" reduce ") the ore,when the neither oxidation process is ever pushed to the end; it is stopped See also:draught must be restricted so as to keep the ore constantly as soon as the mixture of roasting-product and unchanged sulphide d up in combustible flame gases (carbon monoxide, contains oxygen and sulphur in the ratio of 02 : S . The See also:access of wrapped is then stopped and the whole heated to a higher temperature, See also:hydrogen, See also:marsh-gas, &c.) . The majority of the chemical when the whole of the sulphur and oxygen is eliminated . This operations of metallurgy fall into this See also:category, and in these method is largely utilized in the smelting of lead from galena and of processes other metal-reducing agents than those naturally copper from copper pyrites . contained in the fire (or blast) are only exceptionally employed . 4 . Sulphide of antimony, when roasted in air, is converted into a See also:kind of alloy of sulphide and oxide; the same holds for iron, only 2 . Amalgamation.—The ore by itself (if it is a reguline one), its oxysulphide is quite readily converted into the pure oxide . Fe2Oa or with certain reagents (if it is not), is worked up with mercury by further roasting . Oxysulphide of antimony, by suitable processes so that the metal is obtained as an See also:amalgam, which can be separ- can be reduced to metal, but these processes are rarely used, because ated mechanically from the dross . The purified amalgam is the same end is far more easily obtained by " precipitation," i.e . withdrawing the sulphur by See also:fusion with metallic iron, forming distilled, when the mercury is recovered as a distillate while the metallic antimony and sulphide of iron . Both products fuse, but metal remains. readily part, because fused antimony is far heavier than fused 3 . Wet Processes.—Strictly speaking, certain amalgamation sulphide of iron . A precisely similar method is used occasionally methods fall under this See also:head; but, in its See also:ordinary See also:acceptance, the for the reduction of lead from galena . Sulphide of lead, when fused term refers to processes in which the metal is extracted either ao egulus (it= LPb) and a " See also:mat " FeS which, ho ever,See also:Ion cooling, from the natural ore, or from the ore after roasting or other decomposes into the ordinary sulphide FeS,.and finely divided iron. preliminary treatment, by an acid or See also:salt solution, and from this What we have been explaining are See also:special cases of a more general solution precipitated—generally in the reguline form—by some metallurgic proposition: Any one of the metals, copper, iron, tin, zinc, lead, silver, antimony, arsenic, in general, is capable of de-suitable reagent. sulphurizing (at least partially) any of the others that follows it in Few methods of metal extraction at once yield a pure product. the series just given, and it does so the more readily and completely What as a rule is obtained is a more or less impure metal, which the greater the number of intervening terms . Hence, supposing requires to be "refined " to become See also:fit for the See also:market. a See also:complete mixture of these metals to be melted down under circum- stances admitting of only a partial sulphuration of the whole, the Chemical Operations.—Amalgamation and wet-way processes copper has the best See also:chance of passing into the " mat," while the have limited applications, being practically confined to copper, gold arsenic is the first to be eliminated as such, or, in the presence of and silver . We therefore here confine ourselves, in the main, to oxidants, as oxide . pyro-chemical operations . Arsenides.—Although arsenides are amongst the commonest The method to be adopted for the extraction of a metal from its impurities of ores generally, ores consisting essentially of arsenides ore is determined chiefly, though not entirely, by the nature of the are comparatively rare . The most important are certain See also:double non-metallic component with which the metal is combined . The arsenides of See also:cobalt and See also:nickel, which in practice are always See also:con-simplest case is that of the reguline ores where there is no non- taminated with the arsenides or other compounds of See also:foreign metals, metallic See also:element . The important case is that of gold. such as iron, See also:manganese, &c . The general mode of working these Oxides, Hydrates, See also:Carbonates and Silicates.—All iron and tin ores ores is as follows . The ore is first roasted by itself, when a part of proper fall under this heading, which, besides, comprises certain ores the arsenic goes off as such and as oxide, while a complex of lower of copper, of lead and of zinc . 1'he first step consists in subjecting arsenides remains . This See also:residue is now subjected to careful oxidisx, the crude ore to a roasting or calcining process, the object of which See also:ing fusion in the presence of some solvent for metallic bases . The is to remove the water and carbon dioxide, and burn away, to some effect is that the several metals are oxidized away and pass into the extent at least, the sulphur, arsenic or organic See also:matter . The residue slag (as silicates) in the following order—manganese, iron, cobalt, consists of an impure oxide of the respective metal, which in all cases nickel; and at any stage the as yet unoxidized residue of arsenide is reduced by treatment with See also:fuel at a high temperature . Should assumes the form of a fused regulus, which sinks down through. the the metal be present as a silicate, See also:lime must be added in the smelting slag as a " speis." (This term has the same meaning in reference to remove the See also:silica and liberate the oxide. to arsenides as " mat " has in regard to sulphides.) By stopping The temperature required for the reduction of zinc lies above the the process at the right moment, we can produce a speis which boiling point of the metal; hence the mixture of ore and reducing contains only cobalt and nickel, and if at this stage also the flux is See also:agent (See also:charcoal is generally used) must be heated in a,See also:retort combined renewed we can further produce a speis which contains only nickel with condensing apparatus . In all the other cases the reduction and a slag which substantially is one of cobalt only . The composiis effected in the fire itself, a See also:tower-shaped blast furnace being pre- tion of the speises generally varies from AsMe 812 to AsMe2, where ferably used . The furnace is charged with alternate layers of fuel " Me " means one atomic See also:weight of metal in toto, so that in general and ore (or rather ore and flux, see below), and the whole kindled 'Me = xFe + yCo + zNi, where x + y + z = I . The siliceous Metal . Character of Ores . Mercury . . Sulphide, reguline metal . Antimony . Sulphide . See also:Bismuth ..... Reguline metal . Nickel and cobalt . Arsenides . See also:Platinum, See also:iridium, &c . . Reguline . from below . The metallic oxide, partly by the See also:direct action of the carbon with which it is in contact, but principally by that of the carbon monoxide produced in the lower strata from the oxygen of the blast and the hot carbon there, is reduced to the metallic state; the metal fuses and runs down, with the slag, to the bottom of the furnace, whence both are withdrawn by opening plug-holes . cobalt is utilized as a blue pigment called " smalt "; the nickel-speis is worked up for metal . See also:Minor Reagents.—Besides the oxidizing and reducing agents present in the fire, and the " fluxes " added for the See also:production of slags, various minor reagents may be noticed . Metallic iron as a desulphurizer has already been referred to . Oxide of lead, PbO (litharge), is largely used as an oxidizing agent . At a red heat, when it melts, it readily attacks all metals, except silver and gold, the general result being the formation of a mixed oxide and of a mixed regulus, a See also:distribution, in other words, of both the lead and the metal acted on between slag and regulus . More important is its action on metallic sulphides, which, in general, results in the formation of three things besides sulphur dioxide, viz. a mixed oxide slag including the excess of litharge, a regulus of lead (which may include bismuth and other more readily reducible metals), and, if the litharge is not sufficient for a complete oxidation, a " mat " comprising the more readily sulphurizable metals . Oxide of lead, being a most powerful solvent for metallic oxides generally, is also largely used for the separation of silver or gold from base metallic oxides . Metallic lead is to metals generally what oxide of lead is to metallic oxides . It accordingly is available as a solvent for taking up small particles of metal diffused throughout a mass of slag, and uniting them into one regulus . This leads us to the process of " cupellation," which serves for the extraction of gold (q.v.; see also See also:ASSAYING) and silver from their alloys with base metals . Fluxes.—All ores are contaminated with more or less gangue, which in general consists of infusible matter, and if left unheeded in the reduction of the metallic part of the ore would retain more or less of the metal disseminated through it, or at best foul the furnace . To avoid this, the ore as it goes into the furnace is mixed with " fluxes " so selected as to convert the gangue into a fusible . " slag," which readily runs down through the fuel with the regulus and separates from the latter . The quality and proportion of flux should, if possible, be so chosen that the formation of the slag sets in only after the metal has been reduced and molten; or else part of the basic oxide of the metal. to be extracted may be dissolved by the slag and its reduction thus be prevented or retarded . Slags are not a necessary evil; if an ore were See also:free from gangue we should add gangue and flux from without to produce a slag, because one of its functions is to form a layer on the regulus which protects it against the further action of the blast or furnace gases . Fluxes may be arranged under the three heads of (I) fluor-spar, (2) basic fluxes and (3) acid fluxes . Fluor-spar fuses up at a red heat with silica, sulphates of calcium and See also:barium, and a few other infusible substances into homogeneous masses . It shows little tendency to dissolve basic oxides, such as lime, &c . One part of fluor-spar liquefies about half a part of silica, four parts of calcium sulphate and one and a half parts of barium sulphate . Upon these facts its extremely wide application in metallurgy is founded . Carbonate of soda (or potash is the most powerful basic flux . It dissolves silica and all silicates into fusible glasses . On the other hand, See also:borax may be taken as a type for the acid fluxes . At a red heat, when it forms a viscid fluid, it readily dissolves all basic oxides into fusible complex borates . Now the gangue of an ore in general consists either of some basic material such as carbonate of lime (or See also:magnesia), ferric oxide, alumina, &c., or of silica (See also:quartz) or some more or less acid silicate, or else of a mixture of the two classes of bodies . So any kind of gangue might be liquefied by means of borax or by means of alkaline carbonate; but neither of the two is used otherwise than for assaying; what the metal-smelter does is to add to a .basic gangue the proportion of silica, and to an acid ore the proportion of lime, or, indirectly, of ferrous or perhaps manganous oxide, which it may need for the formation of a slag of the proper qualities . The slag must possess the proper degree of saturation . In other words, taking SiO2+ nMeO (where MeO means an See also:equivalent of base) as a See also:formula for the potential slag, n must have the proper value . If n is too small, i.e. if the slag is too acid, it may dissolve part of the metal to be recovered; if n is too great, i.e. the slag too basic, it may refuse to dissolve, for instance, the ferrous oxide which is meant to go into it, and this oxide will then be reduced, and its metal (iron in our example) contaminate the regulus . In reference to the problem under discussion, it is See also:worth noting that oxides of lead and copper are more readily reduced to metals than oxide of iron Fe203 is to FeO, the latter more readily to FeO than FeO itself to metal, and FeO more readily to metal than manganous oxide is . Oxide of calcium (lime) is not reducible at all . The order of basicity in the oxides (their readiness to go into the slag) is precisely the See also:reverse . Most slags being, as we have seen, complex silicates, it is a most important problem of scientific metallurgy to determine the relations in this class of bodies between chemical See also:composition on the one hand and fusibility and solvent power for certain oxides (CaO, FeO, Fe2Oi, Al203, SiO2, &c.) on the other . Their general composition may be expressed as n(MO-f-xSiO2)+m[(fe or al)O +xSiO2] (M=Ca, Mg, Fe, K2, &c.; fe =Fe, al=;Al.) The following mode of classifying and naming composition in silicates is metallurgical; scientific chemists designate Class I. as orthosilicates, Class II. as metasilicates, Class III. as sesquisilicates . In the formulae M stands for K2, Ca, Fe, &c., or for al=fAl, fe=;Fe, &c . Name . Formula . Oxygen Ratio. x I . Singulo-silicates ISiOi+IMO tease . Acid . ` 1 i . ISi0ii-IMO i 2 I II . . . Bi-silicates It should be possible to represent each quality of a silicate as a function of x, n/m, and of the nature of the individual bases that make up the MO and (fe or al) 0 respectively . Our actual knowledge falls far See also:short of this possibility . The problem, in fact, is very difficult, the more so as it is complicated by the existence of aluminates, compounds such as Al203 . 3CaO, in which the alumina plays the part of acid, and the occasional existence of compounds of fluorides and silicates in certain slags .
The formation of slags, or, what comes to the same thing, of metallic silicates, was especially studied by See also:Percy, See also: In See also:modern times See also:brass has been much used, chiefly for the See also:sake of its cheapness as compared with bronze . In beauty, durability and delicacy of surface it is very inferior to bronze, and, though of some commercial importal CE, has been of but little use in the production of works of art . To some extent copper was used in an almost pure state during See also:medieval times, especially from the 12th to the 15th See also:century, mainly for objects of ecclesiastical use, such as pyxes, monstrances, reliquaries and croziers, partly on account of its softness under the tool, and also because it was slightly easier to. apply See also:enamel and See also:gilding to pure copper than to bronze (see fig . I) . In the medieval Se |