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CARBON (symbol C, atomic weight 12)

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Originally appearing in Volume V05, Page 307 of the 1911 Encyclopedia Britannica.
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CARBON (See also:symbol C, atomic See also:weight 12)  , one of the chemical non-metallic elements . It is found native as the See also:diamond (q.v.), See also:graphite (q.v.), as a constituent of all See also:animal and See also:vegetable tissues and of See also:coal and See also:petroleum . It also enters (as See also:carbonates) into the See also:composition of many minerals, such as See also:chalk, See also:dolomite, 306 See also:calcite, See also:witherite, See also:calamine and spathic See also:iron ore . In See also:combination with See also:oxygen (as See also:carbon dioxide) it is also found to a small extent in the See also:atmosphere . It is a solid substance which occurs in several modifications, differing very much in their See also:physical properties . Amorphous carbon is obtained by the destructive See also:distillation of many carbon compounds, the various kinds differing very greatly as regards physical, characters and purity, according to the substance used for their preparation . The most See also:common varieties met with are lampblack, See also:gas carbon, See also:wood See also:charcoal, animal charcoal and See also:coke . Lampblack is prepared by burning See also:tar, See also:resin, See also:turpentine and other substances See also:rich in carbon, with a limited See also:supply of See also:air; the products of See also:combustion being conducted into condensing See also:chambers in which cloths are suspended, on which the carbon collects . It is further purified by See also:heating in closed vessels, but even then it still contains a certain amount of See also:mineral See also:matter and more or less See also:hydrocarbons . It is used in the manufacture of printer's See also:ink, in the preparation of See also:black paint and in See also:calico See also:printing . Gas carbon is produced by the destructive distillation of coal in the manufacture of See also:illuminating gas (see Gas: Manufacture), being probably formed by the decomposition of gaseous hydrocarbons . It is a very dense See also:form of carbon, and is a See also:good conductor of See also:heat and See also:electricity .

It is used in the manufacture of carbon rods for arc See also:

lights, and for the negative See also:element in the See also:Bunsen See also:battery . Charcoal is a porous form of carbon; several varieties exist . See also:Sugar charcoal is obtained by the carbonization of sugar . It is purified by boiling with acids, to remove any mineral matter, and is then ignited for a See also:long See also:time in a current of See also:chlorine in See also:order to remove the last traces of See also:hydrogen . Animal charcoal (See also:bone black) is prepared by charring bones in iron retorts . It is a very impure form of carbon, containing on the See also:average about 8o%, of See also:calcium phosphate . It possesses a much greater decolorizing and absorbing See also:power than wood charcoal . A variety of animal charcoal is sometimes prepared by calcining fresh See also:blood with See also:potassium carbonate in large cylinders, the See also:mass being purified by boiling out with dilute hydrochloric See also:acid and subsequent reheating . Wood charcoal is a hard and brittle black substance, which retains the See also:external structure of the wood from which it is made . It is prepared (where wood is plentiful) by stacking the wood in heaps, which are covered with See also:earth or with brushwood and See also:turf, and then burning the heap slowly in a limited supply of air . The combustion of the wood is conducted from the See also:top downwards, and from the exterior towards the centre; See also:great care has to be taken that the See also:process is carried out slowly . The disadvantage in this process is that the by-products, such as pyroligneous acid, See also:acetone, wood spirit, &c., are lost; as an alternative method, wood is frequently carbonized in ovens or retorts and the volatile products are condensed and utilized .

Charcoal varies considerably in its properties, depending upon the particular variety of wood from which it is prepared, and also upon the process used in its manufacture . It can be made at a temperature as See also:

low as 300° C., and is then a soft, very friable material possessing a low ignition point . When made at higher temperatures it is much more dense, and its ignition point is considerably higher . Charcoal See also:burns when heated in air, usually without the formation of See also:flame, although a flame is apparent if the temperature be raised . It is characterized by its power of absorbing gases; thus, according to J . See also:Hunter [Phil . Mag., 1863 (4), 25, p . 3631, one See also:volume of charcoal absorbs (at o° C. and 76o mm. pressure) 171.7 res. of See also:ammonia, 86.3 ccs. of nitrous See also:oxide, 67.7 ccs. of carbon monoxide, 21.2 ccs. of carbon dioxide, 17.9 ccs. of oxygen, 15.2 ccs. of See also:nitrogen, and 4.4 ccs. of hydrogen [see also J . See also:Dewar, See also:Ann . Chim . Phys., 1904 (8), 3, p . 51 .

It also has the power of absorbing colouring matters from See also:

solution . Charcoal is used as a See also:fuel and as a reducing See also:agent in metallurgical processes . The element carbon unites directly with hydrogen to form See also:acetylene when an electric arc is passed between carbon poles in an atmosphere of hydrogen (M . See also:Berthelot) ; it also unites directly with See also:fluorine, producing, chiefly, carbon tetrafluoride CF4 . It burns when heated in an atmosphere of oxygen, forming carbon dioxide, and when heated in See also:sulphur vapour it forms carbon bisulphide (q.v.) . When heated with nitrogenous substances, in the presence of carbonated or See also:caustic See also:alkali, it forms cyanides . It combines directly with See also:silicon, at the temperature of the electric See also:furnace, yielding See also:carborundum, SiC; and H . See also:Moissan has also shown that it will combine withmany metals at the temperature of the electric furnace, to form carbides (q.v.) . The specific heat of carbon varies with the temperature the following values having been obtained by H . F . See also:Weber (Jahresberichte, 1874, p . 63): Diamond .

Graphite . Porous wood carbon . t° . Sp . Ht . t° . Sp . Ht. t° . Sp . Ht . -50.5 0.0635 -50.3 0.1138 0-23 0.1653 - to-6 0.0955 -10.7 0.1437 0-99 0'1935 +10.7 0.1128 +Io.8 0.1604 0—223 0.2385 85.5 0.1765 61.3 0.1990 206.1 0.2733 201.6 0.2966 606.7 0.4408 641'9 0'4454 985.0 0'4589 977.0 0.4670 The atomic See also:

weight of carbon has been determined by J . B . A .

See also:

Dumas and by J . S . See also:Stas [Ann . Chico . Phys., 1841 (3), 1, p . 1 ; Jahresb., 1849, 2231 by estimating the amount of carbon dioxide formed on burning graphite or diamond in a current of oxygen, the value obtained being 12.0 (o =16) . Confirmatory See also:evidence has also been obtained by 0 . L . See also:Erdmann and R . F . Marchand (Jour . Prak .

Chem., 1841, 23, p . 159; see also F . W . See also:

Clarke, Jahresb., 1881, p . 7) . Compounds.—Three oxides of carbon are known, namely, carbon suboxide, C302, carbon monoxide, CO, and carbon dioxide, See also:CO2 . Carbon suboxide, C202, is formed by the See also:action of See also:phosphorus pent-oxide on See also:ethyl malonate (0 . Diels and B . See also:Wolf, See also:Bee., 1906, 39, p . 689), See also:CH2(000C2H5)2=2C2H4+2H2O+C3O2 . At See also:ordinary temperatures it is a colourless gas, possessing a penetrating and suffocating See also:smell . It liquefies at 7° C .

It is an exceedingly reactive See also:

compound, combining with See also:water to form malonic acid, with hydrogen chloride to form malonyl chloride, and with ammonia to form malonamide . When kept for some time in sealed tubes it changes to a yellowish liquid, from which a yellow flocculent substance gradually separates, and finally it suddenly solidifies to a dark red mass, which appears to be a polymeric form . Its vapour See also:density agrees with the molecular See also:formula C3O2, and this formula is also confirmed by exploding the gas with oxygen and measuring the amount of carbon dioxide produced (see See also:KETENES) . Carbon monoxide, CO, is found to some extent in volcanic gases . It was first prepared in 1776 by J . M . F . Lassone (Mem . Acad . See also:Paris) by heating See also:zinc oxide with carbon, and was for some time considered to be identical with hydrogen . See also:Cruikshank concluded that it was are. oxide of carbon, a fact which was confirmed by See also:Clement and J . B .

Phoenix-squares

Desormes (Ann . Chico . Phys., 18oi, 38, p . 285) . It may be prepared by passing carbon dioxide over red-hot carbon, or red-hot iron; by heating carbonates (See also:

magnesite, chalk, &c.) with zinc dust or iron; or by heating many metallic oxides with carbon . It may also be prepared by heating formic and oxalic acids (or their salts) with concentrated sulphuric acid (in the See also:case of oxalic acid, an equal volume of carbon dioxide is produced) ; and by heating potassium ferrocyanide with a large excess of concentrated sulphuric acid, K4Fe (C N )s +6H2SO4 +6H2O = 2 K2SO4 +FeSO4 + 3(NH4)2SO4 +6C0 . It is a colourless, odourless gas of specific gravity 0.967 (air = I) . It is one of the most difficultly liquefiable gases, its See also:critical temperature being -139.5° C., and its critical pressure 35'5 atmos . The liquid boils at -190° C., and solidifies at -211 ° C . (L . P . Cailletet, Comptes rendus, 1884, 99, p .

706) . It is only very slightly soluble in water . It burns with a characteristic See also:

pale See also:blue flame to form carbon dioxide . It is very poisonous, uniting with the haemoglobin of the blood to form carbonyl-haemoglobin . It is a powerful reducing agent, especially at high temperatures . It is rapidly absorbed by an ammoniacal or acid (hydrochloric acid) solution of cuprous chloride . It unites directly with chlorine, forming carbonyl chloride or phosgene (see below), and with See also:nickel and iron to form nickel and iron carbonyls (see NICKEL and IRON) . It also combines directly with potassium hydride to form potassium formate (see FoRMIC Am)) . The volume composition of carbon monoxide is established by exploding a mixture of the gas with oxygen, two volumes of the gas combining with one volume of oxygen to form two volumes of carbon dioxide . This fact, coupled with the determination of the vapour density of the gas, establishes the molecular formula CO . Carbon dioxide, CO2, is a gas first distinguished from air by See also:van See also:Helmont (1577—1644), who observed that it was formed in See also:fermentation processes and during combustion, and gave to it the name gas sylvestre . J .

Black (Edin . Phys. and Lit . Essays, 1755) showed that it was a constituent of the carbonated alkalis and called it " fixed air." T . O . See also:

Bergman, in 1774, pointed out its acid See also:character, and A . L . See also:Lavoisier (1781—1788) first proved it to be an oxide of carbon by burning carbon in the oxygen obtained from the decomposition of mercuric oxide . It is a See also:regular constituent of the atmosphere, and is found in many See also:spring See also:waters and in volcanic gases; it also occurs in the uncombined See also:condition at the Grotto del See also:Cane (See also:Naples) and in the See also:Poison Valley (See also:Java) . It is a constituent of the minerals See also:cerussite, See also:malachite, See also:azurite, spathic iron ore, calamine, See also:strontianite, witherite, calcite See also:aragonite, See also:limestone, &c . It may be prepared by burning carbon in excess of air or oxygen, by the See also:direct decomposition of many carbonates by heat, and by the decomposition of carbonates with mineral acids, M2CO2+2HC1=2MC1+See also:H2O+CO2 . It is also formed in ordinary fermentation processes, in the combustion of all carbon compounds (oil, gas, candles, coal, &c.), and in the process of respiration . It is a colourless gas, possessing a faint pungent smell and a slightly acid See also:taste .

It does not See also:

burn, and does not support ordinary combustion, but the alkali metals and See also:magnesium, if strongly heated, will continue to burn in the gas with formation of oxides and liberation of carbon . Its specific gravity is 1.529 (air= I) . It is readily condensed, passing into the liquid condition at o° C. under a pressure of 35 atmospheres . Its critical temperature is 31.35° C., and its critical pressure is 72.9 atmos . The liquid boils at -78.2° C . (I atmo.), and by rapid evaporation can be made to solidify to a See also:snow-See also:white solid which melts at—65° C . (see LIQUID GASES) . Carbon dioxide is moderately soluble in water, its coefficient of solubility at o° C. being 1.7977 (R . Bunsen) . It is still more soluble in See also:alcohol . The solution of the gas in water shows a faintly acid reaction and is supposed to contain carbonic acid, H2CO8 . The gas is rapidly absorbed by solutions of the caustic alkalis, with the See also:production of alkaline carbonates (q.v.), and it combines readily with potassium hydride to form potassium formate .

It unites directly with ammonia gas to form ammonium carbamate, NH2OOONH4 . It may be readily recognized by the white precipitate which it forms when passed through See also:

lime or baryta water . Carbon dioxide dissociates, when strongly heated, into carbon monoxide and oxygen, the reaction being a balanced action; the extent of See also:dissociation for varying temperatures and pressures has been calculated by H . Le Chatelier (Zeit . Phys . Chem., 1888, 2, p . 782; see H . Sainte-Claire Deville, Comptes rendus, 1863, 56, p . 195 et seq.) . The volume composition of carbon dioxide is determined by burning carbon in oxygen, when it is found that the volume of carbon dioxide formed is the same as that of the oxygen required for its production, hence carbon dioxide contains its own volume of oxygen . Carbon dioxide finds See also:industrial application in the preparation of soda by the Solvay process, in the sugar See also:industry, in the manufacture of mineral waters, and in the artificial production of See also:ice . Carbonyl chloride (phosgene), COCl2, was first obtained by See also:John See also:Davy (Phil .

Trans., 1812, 40, p . 220) . It may be prepared by the direct See also:

union of carbon monoxide and chlorine in sunlight (Th . Wilm and G . Wischin, Ann., 1868, 14, p . 150) ; by the action of phosphorus pentoxide on carbon tetrachloride at 200—210° C . (G . Gustayson, Ber., 1872, 5, . 30), 4CC14+P4010 =2CO2+4POCls+ 200012 ; by the oxidation of-See also:chloroform with chromic acid mixture (A . Emmerlingg and B . Lengyel, Ber., 1869, 2, p . 54), 4CHC18+302 = 400012+2H2O+2C12; or most conveniently by heating carbon tetrachloride with fuming sulphuric acid (H .

Erdmann, Ber., 1893, 26, p . 1993), 2S02+CC14=S205C12+0001, . It is a colourless gas, possessing an unpleasant pungent smell . Its vapour density is 3.46 air =1) . It may be condensed to a liquid, which boils at 8° C . It is readily soluble in See also:

benzene, glacial acetic acid, and in many hydrocarbons . Water decomposes it violently, with formation of carbon dioxide and hydrochloric acid . It reacts with alcohol to form chlorcarbonic ester and ultimately diethyl carbonate (see CARBONATEs), and with ammonia it yields See also:urea (q.v.) . It is employed commercially in the production of colouring matters (see See also:BENZOPHENONE), and for various synthetic processes . Carbon oxysulphide, See also:COS, was first prepared by C . Than in 1867 (Ann . Suppl., 5, p .

236) by passing carbon monoxide and sulphur vapour through a See also:

tube at a moderate heat . It is also formed by the action of sulphuretted hydrogen on the isocyanic See also:esters, 2CONC2H6+H2S=COS+CO(NHC2H6)2, by the action of concentrated sulphuric acid on the isothiocyanie esters, RNCS+H20 = COS+RNH2, or of dilute sulphuric acid on the thiocyanates . In the latter reaction various other compounds, such as carbon dioxide, carbon bisulphide and hydrocyanic acid, are produced . They are removed by passing the vapours in See also:succession through concentrated solutions of the caustic alkalis, concentrated sulphuric acid, and triethyl phosphine; the residual gas is then purified by liquefaction (W . Hempel, Zeit. angew . Chemie, 1901, 14, p . 865) . It is also formed when sulphur trioxide reacts with carbon bisulphide at See also:ioo° C., CS2+3SO3 =COS+4SO2, and by the decomposition of ethyl potassium thiocarbonate with hydrochloric acid, CO(OC2H6)SK+ HCI=COS+KCI+C2H5OH . It is a colourless, odourless gas, which burns with a blue flame and is decomposed by heat . Its vapour density is 2.1046 (air =1) . The liquefied gas boils at -47° C. under atmospheric pressure . It is soluble in water; the aqueous solution gradually decomposes on See also:standing, forming carbon dioxide and sulphuretted hydrogen .

It is easily soluble in solutions of the caustic alkalis, provided they are not too concentrated, forming solutions of alkaline carbonates and sulphides, COS+4KHO=K2CO5+ K2S-l- 2H2O .

End of Article: CARBON (symbol C, atomic weight 12)
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