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atomic weight 40.0 CALCIUM [symbol Ca...

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Originally appearing in Volume V04, Page 972 of the 1911 Encyclopedia Britannica.
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weight 40.0 See also:CALCIUM [See also:symbol Ca (o= x6)]  , a metallic chemical See also:element, so named by See also:Sir See also:Humphry See also:Davy from its occurrence in See also:chalk (Latin calx) . It does not occur in nature in the See also:free See also:state, but in See also:combination it is widely and abundantly diffused . Thus the sulphate constitutes the minerals See also:anhydrite, See also:alabaster, See also:gypsum, and selenite; the carbonate occurs dissolved in most natural See also:waters and as the minerals chalk, See also:marble, See also:calcite, See also:aragonite; also in the See also:double See also:carbonates such as See also:dolomite, See also:bromlite, See also:barytocalcite; the fluoride as fluorspar; the fluophosphate constitutes the See also:mineral See also:apatite; while all the more important mineral silicates contain a proportion of this element . Extraction.—See also:Calcium See also:oxide or See also:lime has been known from a very remote See also:period, and was for a See also:long See also:time considered to be an elementary or undecomposable See also:earth . This view was questioned in the 18th See also:century, and in 18o8 Sir Humphry Davy (Phil . Trans., 1808, p . 303) was able to show that lime was a combination of a See also:metal and See also:oxygen . His attempts at isolating this metal were not completely successful; in fact, metallic calcium remained a laboratory curiosity until the beginning of the 20th century . Davy, inspired by his successful See also:isolation of the metals See also:sodium and See also:potassium by the See also:electrolysis of their hydrates, attempted to decompose a mixture of lime and mercuric oxide by the electric current; an See also:amalgam of calcium was obtained, but the separation of the See also:mercury was so difficult that even Davy himself was not sure as to whether he had obtained pure metallic calcium . Electrolysis of lime or calcium chloride in contact with mercury gave similar results . See also:Bunsen (See also:Ann., 1854, 92, p . 248) was more successful when he electrolysed calcium chloride moistened with hydrochloric See also:acid; and A .

Matthiessen (Jour . Chem . See also:

Soc., 1856, p . 28) obtained the metal by electrolysing a mixture of fused calcium and sodium chlorides . See also:Henri See also:Moissan obtained the metal of 99% purity by electrolysing calcium iodide at a See also:low red See also:heat, using a See also:nickel See also:cathode and a See also:graphite anode; he also showed that a more convenient See also:process consisted in See also:heating the iodide with an excess of sodium, forming an amalgam of the product, and removing the sodium by means of See also:absolute See also:alcohol (which has but little See also:action on calcium), and the mercury by See also:distillation . The electrolytic isolation of calcium has been carefully investigated, and this is the method followed for the commercial See also:production of the metal . In 1902 W . Borchers and L . Stockem (Zeil. See also:fur Eleclrochemie, 1902, p . 8757) obtained the metal of 90 % purity by electrolysing calcium chloride at a temperature of about 780°, using an See also:iron cathode, the anode being the graphite See also:vessel in which the electrolysis was carried out . In the same See also:year, O . See also:Ruff and W .

See also:

Plato (Ber . 1902, 35, p . 3612) employed a mixture of calcium chloride (too parts) and fluorspar (16.5 parts), which was fused in a See also:porcelain crucible and electrolysed with a See also:carbon anode and an iron cathode . Neither of these processes admitted of commercial application, but by a modification of Ruff and Plato's process, W . Ruthenau and C . Suter have made the metal commercially available . These chemists electrolyse either pure calcium chloride, or a mixture of this See also:salt with fluorspar, in a graphite vessel which serves as the anode . The cathode consists of an iron See also:rod which can be gradually raised . On electrolysis a layer of metallic calcium is formed at the See also:lower end of this rod on the See also:surface of the electrolyte; the rod is gradually raised, the thickness of the layer increases, and ultimately a rod of metallic calcium, forming, as it were, a continuation of the iron cathode, is obtained . This is the See also:form in which calcium is put on the See also:market . An See also:idea as to the advance made by this method is recorded in the variation in the See also:price of calcium . At the beginning of 1904 it was quoted at 5s. per See also:gram, £250 per kilogram or £110 per See also:pound; about a year later the price was reduced to 21S. per kilogram, or I 2S. per kilogram in quantities of too kilograms .

These quotations apply to See also:

Germany; in the See also:United See also:Kingdom the price (1905) varied from 27s. to 30S. per kilogram (12s. to 13S. per lb.) . See also:Pro perties.—A freshly prepared surface of the metal closely resembles See also:zinc in See also:appearance, but op exposure to the See also:air it rapidly tarnishes, becoming yellowish and ultimately See also:grey or See also:white in See also:colour owing to the formation of a surface layer of calcium See also:hydrate . A faint See also:smell of See also:acetylene may be perceived during the oxidation in moist air; this is probably due to traces of .calcium See also:carbide . It is rapidly acted on by See also:water, especially if means are taken to remove the layer of calcium hydrate formed on the metal; alcohol acts very slowly . In its chemical properties it closely resembles See also:barium and See also:strontium, and to some degree See also:magnesium; these four elements comprise the so-called metals of the " alkaline earths." It combines directly with most elements, including See also:nitrogen; this can be taken See also:advantage of in forming almost a perfect vacuum, the oxygen combining to form the oxide, CaO, and the nitrogen to form the nitride, Ca3N2 . Several of its See also:physical properties have been determined by K . See also:Arndt (Ber., 1904, 37, p . 4733) . The metal as prepared by electrolysis generally contains traces of See also:aluminium and See also:silica . Its specific gravity is 1.54, and after remelting 1.56; after distillation it is 1.52 . It melts at about 800°, but sublimes at a lower temperature . Compounds.—Calcium hydride, obtained by heating electrolytic calcium in a current of See also:hydrogen, appears in See also:commerce under the name hydrolite .

Water decomposes it to give hydrogen free from See also:

ammonia and acetylene, i gram yielding about 'co See also:cos. of See also:gas (Prats Aymerich, Abst . J . C . S., 1907, ii p . 460) . Calcium forms two oxides —the monoxide, CaO, and the dioxide, CaO, . The monoxide and its hydrate are more familiarly known as lime (q.v.) and slaked-lime . The dioxide was obtained as the hydrate, CaO2.8H2O, by P . See also:Thenard (Ann . Chim . Phys., 1818, 8, p . 213), who precipitated lime-water with hydrogen peroxide .

It is permanent when dry; on heating to 130° C. it loses water and gives the anhydrous dioxide as an unstable, See also:

pale See also:buff-coloured See also:powder, very sparingly soluble in water . It is used as an antiseptic and oxidizing See also:agent . Whereas calcium chloride, bromide, and iodide are deliquescent solids, the fluoride is practically insoluble in water; this is a See also:parallelism to the soluble See also:silver fluoride, and the insoluble chloride, bromide and iodide . Calcium fluoride, CaF2, constitutes the mineral fluor-spar (q.v.), and is prepared artificially as an insoluble white powder by precipitating a See also:solution of calcium chloride with a soluble fluoride . One See also:part dissolves in 26,000 parts of water . Calcium chloride, CaC12, occurs in many natural waters, and as a by-product in the manufacture of carbonic acid (carbon dioxide), and potassium chlorate . Aqueous solutions See also:deposit crystals containing 2, 4 or 6 molecules of water . Anhydrous calcium chloride, prepared by heating the hydrate to 200° (preferably in a current of hydrochloric acid gas, which prevents the formation of any oxychloride), is very hygroscopic, and is used as a desiccating agent . It fuses at 723° . It combines with gaseous ammonia and forms crystalline compounds with certain See also:alcohols . The crystallized salt dissolves very readily in water with a considerable absorption of heat; hence its use in forming " freezing mixtures." A temperature of -55° C. is obtained by mixing io parts of the hexahydrate with 7 parts of See also:snow . A saturated solution of calcium chloride contains 325 parts of CaCl2 to too of water at the boiling point(179.5°) .

Phoenix-squares

Calcium iodide and bromide are white deliquescent solids and closely resemble the chloride . Chloride of lime or " See also:

bleaching powder " is a calcium chlorhypochlorite or an equimolecular mixture of the chloride and hypochlorite (see See also:ALKALI MANUFACTURE and BLEACHING) . Calcium carbide, CaC2, a See also:compound of See also:great See also:industrial importance as a source of acetylene, was first prepared by F . See also:Wohler . It is now manufactured by heating lime and carbon in the electric See also:furnace (see ACETYLENE) . Heated in See also:chlorine or with See also:bromine, it yields carbon and calcium chloride or bromide; at a dull red heat it See also:burns in oxygen, forming calcium carbonate, and it becomes incandescent in See also:sulphur vapour at 500°, forming calcium sulphide and carbon disulphide . Heated in the electric furnace in a current of air, it yields calcium See also:cyanamide (see CYANAMIDE) . Calcium carbonate, CaCO3, is of exceptionally wide See also:distribution in both the mineral and See also:animal kingdoms . It constitutes the bulk of the chalk deposits and See also:limestone rocks; it forms over one-See also:half of the mineral dolomite and the See also:rock magnesium limestone; it occurs also as the dimorphous minerals aragonite (q.v.) and calcite (q.v.) . See also:Tuff (q.v.) and travertine are calcareous deposits found in volcanic districts . Most natural waters contain it dissolved in carbonic acid; this confers " temporary hardness " on the water . The dissipation of the dissolved carbon dioxide results in the formation of " fur " in kettles or boilers, and if the solution is falling, as from the roof of a See also:cave, in the formation of See also:stalactites and stalagmites .

In the animal kingdom it occurs as b4~th calcite and aragonite in the tests of the See also:

foraminifera, echinoderms, See also:brachiopoda, and See also:mollusca; also in the skeletons of See also:sponges and See also:corals . Calcium carbonate is obtained as a white precipitate, almost insoluble in water (I part requiring io,000 of water for solution), by mixing solutions of a carbonate and a calcium salt . Hot or dilute See also:cold solutions deposit See also:minute orthorhombic crystals of aragonite, cold saturated or moderately strong solutions, hexagonal (See also:rhombohedral) crystals of calcite . Aragonite is the least See also:stable form; crystals have been found altered to calcite . Calcium nitride, Ca,N2, is a greyish-yellow powder formed by heating calcium in air or nitrogen; water decomposes it with See also:evolution of ammonia (see H . Moissan, Comp' . Rend., 127, p . 497) . Calcium nitrate, Ca(NO,)2.4H2O, is a highly deliquescent salt, crystallizing in.See also:monoclinic prisms, and occurring in various natural waters, as an efflorescence in limestone caverns, and in the See also:neighbour-See also:hood of decaying nitrogenous organic See also:matter . Hence its synonyms, " See also:wall-See also:saltpetre " and " lime-saltpetre "; from its disintegrating action on See also:mortar, it is sometimes referred to as " saltpetre rot.' The anhydrous nitrate, obtained by heating the crystallized salt, is very phosphorescent, and constitutes " Baldwiq's See also:phosphorus." A bask nitrate, Ca(NO3)2•Ca(OH)2.3H20; is obtained by dissolving calcium hydroxide in a solution of the normal nitrate . Calcium phosphide, Ca3P2, is obtained as a reddish substance by passing phosphorus vapour over strongly heated lime . Water decomposes it with the evolution of spontaneously inflammable hydrogen phosphide; hence its use as a marine See also:signal See also:fire (" See also:Holmes See also:lights "), (see L .

Gattermann and W . Haussknecht, Ber., 189o, 23, p . 1176, and H . Moissan, Compt . Rend., 128, p . 787) . Of the calcium orthophosphates, the normal salt, Ca3(PO4)27 is the most important . It is the See also:

principal inorganic constituent of bones, and hence of the " See also:bone-ash " of commerce (see PHOSPHORUS) ; it occurs with fluorides in the mineral apatite (q.v.) ; and the concretions known as See also:coprolites (q.v.) largely consist of this salt . It also constitutes the minerals ornithite, Caa(PO4)2.2H20, osteolite and sombrerite . The mineral brushite, CaHPO4.2H2O, which is isomorphous with the acid arsenate pharmacolite, CaHAsO4.2H20, is an acid phosphate, and assumes monoclinic forms . The normal salt may be obtained artificially, as a white gelatinous precipitate which shrinks greatly on drying, by mixing solutions of sodium hydrogen phosphate, ammonia, and calcium chloride . Crystals may be obtained by heating di-calcium pyrophosphate, Ca2P2O7, with water under pressure .

It is insoluble in water; slightly soluble in solutions of carbonic acid and See also:

common salt, and readily soluble in concentrated hydrochloric and nitric acid . Of the acid orthophosphates, the mono-calcium salt, CaH4(PO4)2, may be obtained as crystalline scales, containing one See also:molecule of water, by evaporating a solution of the normal salt in hydrochloric or nitric acid . It dissolves readily in water, the solution having an acid reaction . The artificial manure known as " superphosphate of lime " consists of this salt and calcium sulphate, and is obtained by treating ground bones, coprolites . &c., with sulphuric acid . The di-calcium salt, Ca2H2(PO4)2, occurs in a concretionary form in the ureters and See also:cloaca of the See also:sturgeon, and also in See also:guano . It is obtained as rhombic plates by mixing dilute solutions of calcium chloride and sodium phosphate, and passing carbon dioxide into the liquid . Other See also:phosphates are also known . Calcium monosulphide, CaS, a white amorphous powder, sparingly soluble in water, is formed by heating the sulphate with See also:charcoal, or by heating lime in a current of sulphuretted hydrogen . It is particularly noteworthy from the See also:phosphorescence which it exhibits when heated, or after exposure to the See also:sun's rays; hence its synonym " See also:Canton's phosphorus," after See also:John Canton (1718-1772), an See also:English natural philosopher . The sulpliydrate or hydrosulphide, Ca(SH)2, is obtained as colourless, prismatic crystals of the See also:composition Ca(SH)2.6H20, by passing sulphuretted hydrogen into See also:milk of lime . The strong aqueous solution deposits colourless, four-sided prisms of the hydroxy-hydrosulphide, Ca(OH)(SH) .

The disulphide, CaS2, and pentasulphide, CaSSi are formed when milk of lime is boiled with See also:

flowers of sulphur . These sulphides form the basis of See also:Balmain's luminous paint . An oxysulphide, 2CaS•CaO, is sometimes See also:present in " soda-See also:waste," and See also:orange-coloured, acicular crystals of 4CaS•CaSO4.18H2O occasionally See also:settle out on the long See also:standing of oxidized " soda- or alkali-waste " (see ALKALI MANUFACTURE) . Calcium sulphite, CaSO3, a white substance, soluble in water, is prepared by passing sulphur dioxide into milk of lime . This solution with excess of sulphur dioxide yields the " bisulphite of lime " of commerce, which is used in the " chemical " manufacture of See also:wood-pulp for See also:paper making . Calcium sulphate, CaSO4, constitutes the minerals anhydrite (q.v.), and, in the hydrated form, selenite, gypsum (q.v.), alabaster (q.v.), and also the adhesive See also:plaster of See also:Paris (see See also:CEMENT) . It occurs dissolved in most natural waters, which it renders " permanently hard." It is obtained as a white crystalline precipitate, sparingly soluble in water (Too parts of water dissolve 24 of the salt at 15° C.), by mixing solutions of a sulphate and a calcium salt; it is more soluble in solutions of common salt and hydrochloric acid, and especially of sodium thiosulphate . Calcium silicates are exceptionally abundant in the mineral kingdom . Calcium metasilicate, CaSiO3, occurs in nature as mono-clinic crystals known as See also:tabular spar or See also:wollastonite; it may be prepared artificially from solutions of calcium chloride and sodium silicate . H . Le Chatelier (Annales See also:des mines, 1887, p . 345) has obtained artificially the compounds: CaSiO3, Ca2SiO4, Ca3Si2O7, and CasSiOs .

(See also G . Oddo, Chemisches Centralblatt, 1896, 228.) Acid calcium silicates are represented in the mineral kingdom by gyrolite, H2Ca2(SiO3)3•See also:

H2O, a lime zeolite, sometimes regarded as an altered form of See also:apophyllite (q.v.), which is itself an acid calcium silicate containing an alkaline fluoride, by okenite, H2Ca(SiO0)2•H2O, and by xonalite 4CaSiO3•H2O . Calcium silicate is also present in the minerals: See also:olivine, pyroxenes, amphiboles, See also:epidote, felspars, See also:zeolites,to a Bunsen See also:flame, which when viewed through See also:green See also:glass appears to be See also:finch-green; this distinguishes it in the presence of strontium, whose See also:crimson coloration is See also:apt to See also:mask the orange-red calcium flame (when viewed through green glass the strontium flame appears to be a very faint yellow) . In the spectroscope calcium exhibits two intense lines—an orange See also:line (a), (X 6163), a green line (3), (X 4229), and a fainter See also:indigo line . Calcium is not precipitated by sulphuretted hydrogen, but falls as the carbonate when an alkaline carbonate is added to a solution . Sulphuric acid gives a white precipitate of calcium sulphate with strong solutions; ammonium oxalate gives calcium oxalate, practically insoluble in water and dilute acetic acid, but readily soluble in nitric or hydrochloric acid . Calcium is generally estimated by precipitation as oxalate which, after drying, is heated and weighed as carbonate or oxide, according to the degree and duration of the heating .

End of Article: atomic weight 40.0 CALCIUM [symbol Ca (o= x6)]
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