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NITRIC ACID (aqua fortis), HNO3

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Originally appearing in Volume V19, Page 712 of the 1911 Encyclopedia Britannica.
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NITRIC See also:

ACID (aqua fortis), HNO3  , an important See also:mineral See also:acid . It is mentioned in the De inventione veritatis ascribed to See also:Geber, wherein it is obtained by calcining a mixture of See also:nitre, See also:alum and See also:blue See also:vitriol . It was again described by See also:Albert le See also:Grand in the 13th See also:century and by Raimon See also:Lull, who prepared it by See also:heating nitre and See also:clay and called it " eau forte." See also:Glauber devised the See also:process in See also:common use to-See also:day, viz. by heating nitre with strong sulphuric acid . Its true nature was not determined until the 18th century, when A . L . See also:Lavoisier (1776) showed that it contained See also:oxygen, whilst in 1785 H . See also:Cavendish determined its constitution and showed that it could be synthesized by passing a stream of electric See also:sparks through moist See also:air . The acid is found to exist to a slight extent in the See also:free See also:condition in some See also:waters, but chiefly occurs in See also:combination with various metals, as nitrates,: principally as nitre or See also:saltpetre, KNO3, and See also:Chile saltpetre, NaNO3• It is formed when a stream of electric sparksis passed through moist air, and in the oxidation of nitrogenous See also:matter in the presence of See also:water . For experimental purposes it is usually obtained by distilling See also:potassium or See also:sodium nitrate with concentrated sulphuric acid . The acid so obtained usually contains more or less water and some dissolved See also:nitrogen peroxide which gives it a yellowish red See also:colour . It may be purified by redistillation over See also:barium and See also:silver nitrates, followed by treatment of the distillate with a stream of ozonized air . The product so obtained is then redistilled under diminished pressure and finally distilled again from a sealed and evacuated apparatus (V .

Veley and See also:

Manley, Phil . Trans., 1898, A . 291, p . 365) . On the large See also:scale it is obtained by distil-See also:ling Chile saltpetre with concentrated sulphuric acid in See also:horizontal See also:cast See also:iron stills, the vapours being condensed in a See also:series of stoneware Woulfe's bottles . In practice the theoretical quantity of acid and Chile saltpetre is not used, but the See also:charge is so regulated that the mixture of acid and neutral sodium sulphate formed in the See also:retort remains liquid at the temperature employed, and consequently can be readily removed . Various modifications have been made in the See also:form of the condensing apparatus, the Guttmann See also:condenser (Jour . See also:Soc . Chem . Ind., 1893, p . 203) being now frequently employed . This consists of a series of See also:vertical earthenware condensing tubes through which compressed air is passed in See also:order to reduce the quantity of nitrogen peroxide to a minimum .

The temperature of the condenser is so regulated as to bring about the condensation of the nitric acid only, which runs out at the bottom of the See also:

pipe, whilst any uncondensed See also:steam, nitrogen peroxide and other impurities pass into a See also:Lunge See also:tower, where they meet a descending stream of water and are condensed, giving rise to an impure acid . F . Valentiner {Eng . Pat . 610 (1892), 19192 (1895)] recommends See also:distillation and condensation of nitric acid in a partial vacuum . For the See also:production of nitric acid from air see NITROGEN . Fuming nitric acid consists of a See also:solution of nitrogen peroxide in concentrated nitric acid and is prepared by distilling dry sodium nitrate with concentrated sulphuric acid . Nitric acid is a colourless strongly fuming liquid, having a specific gravity of 1.50394 (24.2° C.) (V . Veley, Proc . See also:Roy . Soc., 62, p . 223) .

It is exceedingly hygroscopic and corrosive . On distillation, the pure acid begins to See also:

boil at 78.2° C . (W . See also:Ramsay), partial decomposition into water, oxygen and nitrogen peroxide taking See also:place . The acid solidifies when strongly cooled, the solid melting at – 47° C . Concentrated nitric acid forms with water a See also:constant boiling mixture which boils at 120.5° C., contains 68% of acid and possesses a specific gravity of 1414 (15'5° C.) . If a more dilute acid than this be distilled, water passes over in excess and the See also:residue in the retort reaches the above See also:composition and 'boiling point; on distillation of a stronger acid, excess of acid passes into the distillate and the boiling point rises until the values of the constant boiling mixture are reached . On the hydrates of nitric acid see V . Veley, Jour . Chem . Soc., 1903, 83, p . 1015, and F .

Phoenix-squares

W . Kuster, Zeit. anorg . Chem . 1904, 41, p . 1 . On mixing nitric acid with water there is a rise of temperature and a contraction in See also:

volume . The acid is a powerful oxidizing See also:agent . It attacks most metals readily, usually with production of a nitrate or hydrated See also:oxide of the See also:metal and one or other of the oxides of nitrogen, or occasionally with the production of ammonium salts; See also:magnesium, however, liberates See also:hydrogen from the very dilute acid . Its See also:action on metals depends in most cases on the temperature, strength of the acid, and the nature of the products of reaction . Thus in the See also:case of See also:copper, it is found that the diluted acid acts very slowly upon the metal at first, but as the reaction proceeds the capper dissolves more rapidly up to a certain point and then the See also:rate of solution again diminishes . This is possibly due to the accelerating action of the nitrous acid which is produced in the See also:direct action of the copper on the nitric acid and which, when a certain amount has been formed in the See also:system, begins to decompose, thus 3HNO2=HNO3+ 2NO+See also:H2O (V . Veley, Phil .

Trans., 1891, 182, p . 279; G . O . Higley, Amer . Chem . Jour., 1893, 15, p . 71, 1895, 17, p . 18, 1896, 18, p . 587) . Iron when brought into contact with nitric acid under certain conditions, remains passive to the acid . Thus at 550 C. it is passive to an acid of specific gravity 1.42, and at 31° C. to an acid of specific gravity 1.38 . No satisfactory explanation of this passivity has been given (see J .

B . Senderens, See also:

Bull . Soc . Chem., 1896 [3], 15, p . 691; A . Finkelstein, Zeit. phys . Chem., 1901, 39, p . 91; W . J . See also:Muller, ibid . 1904, 48, p . 577) .

Nitric acid is without action on See also:

gold, See also:platinum, See also:iridium and See also:rhodium . The salts of nitric acid, known as nitrates, are mostly readily soluble in water and crystallize well . They are all decomposed when heated to a sufficiently high temperature, with See also:evolution for the most See also:part of oxygen and nitrogen peroxide, leaving a residue of oxide of the metal . They may be recognized by the fact that on the addition of a solution of ferrous sulphate, followed by that of concentrated sulphuric acid (the mixture being kept quite See also:cold), the ferrous sulphate solution becomes of a deep See also:brown colour, owingto the reducing action of the ferrous sulphate on the nitric acid which is liberated by the action of the sulphuric acid on the nitrate . As an alternative method the nitrate may be warmed with some fragments of copper and sulphuric acid which has been diluted with its own volume of water, when characteristic brown vapours will be seen . Nitric acid finds extensive application in the manufacture of sulphuric acid, certain See also:coal-See also:tar colouring matters, See also:explosives, and in the production of various nitrates . In See also:medicine, nitric acid is used externally in a pure See also:state as a See also:caustic to destroy chancres, warts and phagadenic ulcers; and diluted preparations are employed in the treatment of See also:dyspepsia, &c . Poisoning by strong nitric acid produces a widespread gastro-See also:enteritis, burning See also:pain in the See also:oesophagus and See also:abdomen and bloody See also:diarrhoea . There may also be See also:blood in the urine . See also:Death occurs from collapse or from secondary destructive changes in the intestinal See also:canal . Characteristic yellow staining of the skin See also:round the mouth from the formation of xanthoproteic acid serves to distinguish it from poisoning by other acids . The antidotes are mild alkalis, together with the use of See also:opium to relieve pain .

End of Article: NITRIC ACID (aqua fortis), HNO3
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include the uses of nitric acid in the production of TNT.
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