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See also:BORON (See also:symbol B, atomic See also:weight I I)
, one of the non-metallic elements, occurring in nature in the See also:form of boracic (boric) See also:acid, and in various borates such as See also:borax, tincal, boronatrocalcite and See also:boracite
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It was isolated by J
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See also:Gay Lussac and L
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See also:Thenard in 18o8 by See also:heating See also:boron trioxide with See also:potassium, in an See also:iron See also:tube
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It was also isolated at about the same See also:time by See also:Sir H
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See also:Davy, from boracic acid
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It may be obtained as a dark See also: 296) heats three parts of the oxide with one See also:part of See also:magnesium powder . The dark product obtained is washed with See also:water, hydrochloric acid and hydrofluoric acid, and finally calcined again with the oxide or with borax, being protected from See also:air during the operation by a layer of See also:charcoal . Pure amorphous boron is a See also:chestnut-coloured powder of specific gravity 2.45; it sublimes in the electric arc, is totally unaffected by air at See also:ordinary temperatures; and See also:burns on strong ignition with See also:production of the oxide B2O3 and the nitride BN . It combines directly with See also:fluorine at ordinary temperature, and with See also:chlorine, See also:bromine and See also:sulphur on heating . It does not react with the See also:alkali metals, but combines with magnesium at a See also:low red See also:heat to form a boride, and with other metals at more or less elevated temperatures . It reduces many metallic oxides, such as See also:lead monoxide and cupric oxide, and decomposes water at a red heat . Heated with sulphuric acid and with nitric acid it is oxidized to boric acid, whilst on See also:fusion with alkaline See also:carbonates and hydroxides it gives a borate of the alkali See also:metal . Like See also:silicon and See also:carbon, very varying values had been given for its specific heat, until H . F . See also:Weber showed that the specific heat increases rapidly with increasing temperature . By strongly heating a mixture of boron trioxide and See also:aluminium, protected from the air by a layer of charcoal, F . See also:Wohler and H . Sainte-Claire Deville obtained a See also:grey product, from which, on dissolving out the aluminium with sodium hydroxide, they obtained a crystalline product, which they thought to be a modification of boron, but which was shown later to be a mixture of aluminium borides with more or less carbon . Boron dissolves in molten aluminium, and on cooling, transparent, almost colourless crystals are obtained, possessing a lustre, hardness and refractivity near that of the See also:diamond . In 1904 K . A . Ktihne (D.R.P . 147,87.1) described a See also:process in which See also:external heating is not necessary, a mixture of aluminium turnings, sulphur and boric acid being ignited by a hot iron See also:rod, the resulting aluminium suiphide, formed as a by-product, being decomposed by water . Boron hydride has probably never been isolated in the pure See also:condition; on heating boron trioxide with magnesium filings, a magnesium boride Mg3B2 is obtained, and if this be decomposed with dilute hydrochloric acid a very evil-smelling See also:gas, consisting of a mixture of See also:hydrogen and boron hydride, is obtained . This mixture burns with a See also:green See also:flame forming boron trioxide; whilst boron is deposited on passing the gas mixture through a hot tube, or on depressing a See also:cold See also:surface in the gas flame . By cooling it with liquid air Sir W . See also:Ramsay and H . S . See also:Hatfield obtained from it a gas of See also:composition B3H3 . The mixture probably contained also some BH3 (W . Ramsay and H . S . Hatfield, Proc . Chem . See also:Soc., 17, p . 152) . Boron fluoride BF3 was first prepared in 1808 by Gay Lussac and L . Thenard and is best obtained by heating a mixture of the trioxide and fluorspar with concentrated sulphuric acid . It is a colourless pungent gas which is exceedingly soluble in water . It fumes strongly in air, and does not attack See also:glass . It rapidly absorbs the elements of water wherever possible, so that a See also:strip of See also:paper plunged into the gas is rapidly charred .
It does not See also:burn, neither does it support See also:combustion
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A saturated solution of the gas, in water, is a colourless, oily, strongly fuming liquid which after a time decomposes, with separation of metaboric acid, leaving hydrofluoboric acid HF•BF3 in solution
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This acid cannot be isolated in the See also:free condition, but many of its salts are known
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Boron fluoride also combines with See also:ammonia gas, equal volumes of the two gases giving a See also: It is decomposed by water, and with a solution of yellow See also:phosphorus in carbon bisulphide it gives a red powder of composition PBI2, which sublimes in vacuo at 210° C. to red crystals, and when heated in a current of hydrogen loses its iodine and leaves a See also:residue of boron phosphide PB . Boron nitride BN is formed when boron is burned either in air or in See also:nitrogen, but can be obtained more readily by heating to redness in a See also:platinum crucible a mixture of one part of anhydrous borax with two parts of dry ammonium chloride . After fusion, the melt is well washed with dilute hydrochloric acid and then with water, the nitride remaining as a white powder . It can also be prepared by heating borimide B2(NH)3; or by heating boron trioxide with a metallic See also:cyanide . It is insoluble in water and unaffected by most reagents, but when heated in a current of See also:steam or boiled for some time with a See also:caustic alkali, slowly decomposes with See also:evolution of ammonia and the formation of boron trioxide or an alkaline borate; it dissolves slowly in hydrofluoric acid . Borimide B2(NH)3 is obtained on See also:long heating of the See also:compound B2S3.6NH3 in a stream of hydrogen, or ammonia gas at 115–120° C . It is a white solid which decomposes on heating into boron nitride and ammonia . Long-continued heating with water also decomposes it slowly . Boron sulphide B2S3 can be obtained by the direct union of the two elements at a white heat or from the tri-iodide and sulphur at 440° C., but is most conveniently prepared by heating a mixture of the trioxide and carbon in a stream of carbon bisulphide vapour . It forms slightly coloured small crystals possessing a strong disagree-able See also:smell, and is rapidly decomposed by water with the formation of boric acid and sulphuretted hydrogen . A pentasulphide B2S5 is prepared, in an impure condition, by heating a solution of sulphur in carbon bisulphide with boron iodide, and forms a white crystalline powder which decomposes under the See also:influence of water into sulphur, sulphuretted hydrogen and boric acid . Boron trioxide B2O3 is the only known oxide of boron; and may be prepared by heating amorphous boron in See also:oxygen, or better, by strongly igniting boric acid . After fusion the mass solidifies to a transparent vitreous solid which dissolves readily in water to form boric acid (q.v.) ; it is exceedingly hygroscopic and even on See also:standing in moist air becomes opaque through absorption of water and formation of boric acid . Its specific gravity is 1.83 (J . See also:Dumas) . It is not volatile below a white heat, and consequently, if heated with salts of more volatile acids, it expels the acid forming oxide from such salts; for example, if potassium sulphate be heated with boron trioxide, sulphur trioxide is liberated and potassium borate formed . It also possesses the See also:power of combining with most metallic oxidesat high temperatures, forming borates, which in many cases show characteristic See also:colours . Many organic compounds of boron are known; thus, from the See also:action of the trichioride on See also:ethyl See also:alcohol or on methyl alcohol, ethyl borate B(OC2H5)3 and methyl borate B(OCH3)3 are obtained . These are colourless liquids boiling at 119° C. and 72° C. respectively, and both are readily decomposed by water . |
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