Nitric-acid Sentence Examples

nitric-acid
  • Iridium tetrachloride, IrC1 41 is obtained by dissolving the finely divided metal in aqua regia; by dissolving the hydroxide in hydrochloric acid; and by digesting the hydrated sesquichloride with nitric acid.

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  • It decomposes steam at a red heat, and slowly dissolves in dilute hydrochloric and sulphuric acids, but more readily in nitric acid.

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  • It is somewhat readily oxidized; nitric acid gives carbonic and oxalic acids, and chromic acid, carbonic and acetic acids.

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  • Heated with sulphuric acid and with nitric acid it is oxidized to boric acid, whilst on fusion with alkaline carbonates and hydroxides it gives a borate of the alkali metal.

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  • Brugnatelli, who found in 1798 that if silver be dissolved in nitric acid and the solution added to spirits of wine, a white, highly explosive powder was obtained.

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  • Cadmium nitrate, Cd(N03)2.4H20, is a deliquescent salt, which may be obtained by dissolving either the metal, or its oxide or carbonate in dilute nitric acid.

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  • Molybdenum trioxide, Mo03, is prepared by oxidizing the metal or the sulphide by heating them in air, or with nitric acid.

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  • It is easily soluble in hot nitric acid.

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  • Nitro-phenols are readily obtained by the action of nitric acid on phenol.

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  • Two oxides of germanium are known, the dioxide, GeO2, being obtained by roasting the sulphide and treatment with nitric acid.

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  • The nitric acid is most likely taken up chiefly as nitrate of lime, but probably as nitrate of potash also, and it is significant that the high nitrogen-yielding clover takes up, or at least retains, very little soda.

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  • These are washed with ammonium chloride until the filtrate is colourless, ignited, fused with caustic potash and nitre, the melt dissolved in water and nitric acid added to the solution until the colour of potassium ruthenate disappears.

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  • Glauber showed how to prepare hydrochloric acid, spiritus salis, by heating rock-salt with sulphuric acid, the method in common use to-day; and also nitric acid from saltpetre and arsenic trioxide.

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  • Thus, he interpreted the interaction of benzene and nitric acid as C6H61-HN03 = C 6 H 5 NO 2 +H 2 0, the "residues" of benzene being C 6 H 5 and H, and of nitric acid HO and N02.

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  • The metallic film is tested with 20% nitric acid and with bleaching-powder solution.

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  • Silver chloride goes into solution, and may be precipitated by dilute nitric acid.

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  • The residue from the ammonium sulphide solution is warmed with dilute nitric acid.

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  • The halogens may be estimated by ignition with quicklime, or by heating with nitric acid and silver nitrate in a sealed tube.

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  • On boiling with concentrated nitric acid it yields picric acid.

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  • Nascent hydrogen reduces it to hydroxylamine (q.v.), whilst solutions of hypochlorites oxidize it to nitric acid.

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  • It may also be obtained by distilling nitric acid over phosphorus pentoxide.

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  • It dissolves in water, forming nitric acid.

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  • It is a very stable compound, chlorine, concentrated nitric acid and hydriodic acid having no action upon it.

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  • Dilute nitric acid readily dissolves the metal, with formation of nitrate Pb(N03)2.

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  • It is also obtained by passing chlorine into a suspension of lead oxide or carbonate, or of magnesia and lead sulphate, in water; or by treating the sesquioxide or red oxide with nitric acid.

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  • It oxidizes a manganese salt (free from chlorine) in the presence of nitric acid to a permanganate; this is a very delicate test for manganese.

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  • It dissolves in strong nitric acid with the formation of the nitrate and sulphate, and also in hot concentrated hydrochloric acid.

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  • Lead nitrate, Pb(N03)2, is obtained by dissolving the metal or oxide in aqueous nitric acid; it forms white crystals, difficultly soluble in cold water, readily in hot water and almost insoluble in strong nitric acid.

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  • Aromatic Nitro Compounds.-The aromatic nitro compounds are generally obtained by the direct action of nitric acid.

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  • In one process the purified ore is disintegrated with hot nitric acid to produce nitrates, which are then converted into sulphates by evaporation with sulphuric acid.

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  • It is obtained as fine lemon yellow deliquescent prisms by evaporating a solution of any of the oxides in nitric acid.

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  • It is insoluble in water and in nitric acid and apparently so in hydrochloric acid; but if heated with this last for some time it passes into a compound, which, after the acid mother liquor has been decanted off, dissolves in water.

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  • On oxidation with potassium permanganate it gives homovanillin, vanillin, &c.; with chromic acid in acetic acid solution it is converted into carbon dioxide and acetic acid, whilst nitric acid oxidizes it to oxalic acid.

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  • Pelouze in 1838, who observed that when paper or cotton was immersed in cold concentrated nitric acid the materials, though not altered in physical appearance, became heavier, and after washing and drying were possessed of self-explosive properties.

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  • Bottger of Frankfort and Otto and Knop, all of whom added to our knowledge of the subject, the last-named introducing the use of sulphuric along with nitric acid in the nitration process.

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  • The products of the action of nitric acid on cellulose are not nitro compounds in the sense that picric acid is, but are nitrates or nitric esters.

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  • Strong sulphuric acid in contact with it liberates first nitric acid and later oxides of nitrogen, leaving a charred residue or a brown solution according to the quantity of acid.

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  • They all contain albumen and throw down a precipitate with heat and nitric acid.

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  • When the solution in the strong acid is allowed to stand, some nitric acid is first evolved, and as the temperature rises this is followed by a general decomposition of the substance, though not necessarily an explosive one.

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  • The former is completely decomposed when fused with caustic potash and the latter by a prolonged boiling with nitric acid.

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  • It is oxidized by nitric acid to d-saccharic and mucic acids; and acetic anhydride gives an octa-acetate.

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  • Nitrostyrolene results when styrolene is treated with fuming nitric acid.

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  • Its chief uses are in glass-making to promote fluidity, in metallurgy to oxidize impurities, as a constituent of gunpowder and in pyrotechny; it is also used in the manufacture of nitric acid.

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  • The chief applications of Chile saltpetre are in the nitric acid industry, and in the manufacture of ordinary saltpetre for making gunpowder, ordinary Chile saltpetre being unsuitable by reason of its deliquescent nature, a property, however, not exhibited by the perfectly pure salt.

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  • Its chief applications are as a manure and in the nitric acid industry.

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  • Cold dilute nitric acid dissolves zinc as nitrate, with evolution of nitrous oxide.

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  • It combines directly with the halogens, and dissolves in cold dilute sulphuric acid, in hot strong hydrochloric acid and in aqua regia, but less readily in nitric acid.

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  • It gives the normal sulphate as a yellow, deliquescent, amorphous mass when treated with nitric acid.

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  • Ladenburg, Ber., 1886, 19, p. 783); by heating the esters of nitric acid with alcoholic ammonia at 10o C. (0.

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  • Concentrated nitric acid attacks them violently, producing various oxidation products, but if the amino group be "protected" by being previously acetylated, then nitro derivatives are obtained.

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  • For example, in the less modern methods for manufacturing nitric acid the vapours were conducted directly into double-necked bottles (bombonnes) immersed in water.

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  • Strontium nitrate, Sr(N03)2, is obtained by dissolving the carbonate in dilute nitric acid.

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  • Potassium bichromate oxidizes it to malonic acid; nitric acid oxidizes it to oxalic acid; and hydriodic acid reduces it to succinic acid.

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  • The metal is soluble in solutions of chlorine, bromine, thiosulphates and cyanides; and also in solutions which generate chlorine, such as mixtures of hydrochloric acid with nitric acid, chromic acid, antimonious acid, peroxides and nitrates, and of nitric acid with a chloride.

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  • In the " dry " methods the silver is converted into sulphide or chloride, the gold remaining unaltered; in the " wet " methods the silver is dissolved by nitric acid or boiling sulphuric acid; and in the electrolytic processes advantage is taken of the fact that under certain current densities and other circumstances silver passes from an anode composed of a gold-silver alloy to the cathode more readily than gold.

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  • The sulphur and litharge, or Pfannenschmied, process was used to concentrate the gold in an alloy in order to make it amenable to " quartation," or parting with nitric acid.

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  • Parting by nitric acid is of considerable antiquity, being mentioned by Albertus Magnus (13th cent.), Biringuccio (1540) and Agricola (1556).

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  • It is now rarely practised, although in some refineries both the nitric acid and the sulphuric acid processes are combined, the alloy being first treated with nitric acid.

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  • The operation may be conducted in vessels of glass or platinum, and each pound of granulated metal is treated with a pound and a quarter of nitric acid of specific gravity 1.32.

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  • The silver is quite free from gold, and the gold after boiling with nitric acid has a fineness of over 999.

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  • The normal nitrate, Bi(N03)3.5H20, is obtained in large transparent asymmetric prisms by evaporating a solution of the metal in nitric acid.

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  • It is easily soluble in nitric acid.

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  • The blackish brown sulphide precipitated from bismuth salts by sulphuretted hydrogen is insoluble in ammonium sulphide, but is readily dissolved by nitric acid.

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  • This second group may be divided into a-Barbaloins, obtained from Barbadoes aloes, and reddened in the cold, and Barbaloins, obtained from Socotrine and Zanzibar aloes, reddened by ordinary nitric acid only when warmed, or by fuming acid in the cold.

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  • Tellurous acid, H 2 TeO 3, is obtained when the tetrachloride is decomposed by water, or on dissolving tellurium in nitric acid and pouring the solution into water.

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  • Picric acid can also be obtained from it by first treating acetylene with sulphuric acid, converting the product into phenol by solution in potash and then treating the phenol with fuming nitric acid.

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  • In the massive state it is insoluble in all acids, but when freshly precipitated from solutions it dissolves in fuming nitric acid.

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  • All soluble orthophosphates give with silver nitrate a characteristic yellow precipitate of silver phosphate, Ag 3 PO 4, soluble in ammonia and in nitric acid.

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  • It is insoluble in water; slightly soluble in solutions of carbonic acid and common salt, and readily soluble in concentrated hydrochloric and nitric acid.

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  • Of the acid orthophosphates, the mono-calcium salt, CaH4(P04)2, may be obtained as crystalline scales, containing one molecule of water, by evaporating a solution of the normal salt in hydrochloric or nitric acid.

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  • Ammonium nitrate, NH 4 NO 3, is prepared by neutralizing nitric acid with ammonia, or ammonium carbonate, or by double decomposition between potassium nitrate and ammonium sulphate.

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  • Hot concentrated nitric acid oxidizes it to picric acid and oxalic acid, whilst on treatment with hydrochloric acid and potassium chlorate it yields chloranil (tetrachloroquinone).

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  • In 1780 he proved that the acidity of sour milk is due to what was afterwards called lactic acid; and by boiling milk sugar with nitric acid he obtained mucic acid.

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  • It is completely oxidized to iodic acid when boiled with fuming nitric acid.

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  • The soluble iodides, on the addition of silver nitrate to their nitric acid solution, give a yellow precipitate of silver iodide, which is insoluble in ammonia solution.

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  • It is prepared by oxidizing potassium ferrocyanide with a diluted nitric acid.

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  • Wohler reduced the sesquioxide by zinc, and obtained a shining green powder of specific gravity 6.81, which tarnished in air and dissolved in hydrochloric acid and warm dilute sulphuric acid, but was unacted upon by concentrated nitric acid.

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  • The spectrum of nitrobenzene is also worth comparing with benzene and nitric acid.

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  • Potash fusion converts it into acetic acid; nitric acid oxidizes it to acetic and oxalic acids; chromic acid mixture to acetaldehyde and acetic acid, and potassium permanganate to a0-dioxybutyric acid.

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  • Lacombe in 1904 obtained the pure salts by fractional crystallization of the nitric acid solution with magnesium nitrate in the presence of bismuth nitrate.

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  • Thus he clearly described the preparation of hydrochloric acid by the action of oil of vitriol on common salt, the manifold virtues of sodium sulphate - sal mirabile, Glauber's salt - formed in the process being one of the chief themes of his Miraculum mundi; and he noticed that nitric acid was formed when nitre was substituted for the common salt.

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  • Since the time of Henry Cavendish no one seemed even to have asked the question whether the residue was, in truth, all capable of conversion into nitric acid.

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  • 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 pipe, whilst any uncondensed steam, nitrogen peroxide and other impurities pass into a Lunge tower, where they meet a descending stream of water and are condensed, giving rise to an impure acid.

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  • For the production of nitric acid from air see Nitrogen.

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  • Fuming nitric acid consists of a solution of nitrogen peroxide in concentrated nitric acid and is prepared by distilling dry sodium nitrate with concentrated sulphuric acid.

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  • On mixing nitric acid with water there is a rise of temperature and a contraction in volume.

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  • Iron when brought into contact with nitric acid under certain conditions, remains passive to the acid.

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  • 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 cold), the ferrous sulphate solution becomes of a deep brown colour, owing to the reducing action of the ferrous sulphate on the nitric acid which is liberated by the action of the sulphuric acid on the nitrate.

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  • In medicine, nitric acid is used externally in a pure state as a caustic to destroy chancres, warts and phagadenic ulcers; and diluted preparations are employed in the treatment of dyspepsia, &c. Poisoning by strong nitric acid produces a widespread gastroenteritis, burning pain in the oesophagus and abdomen and bloody diarrhoea.

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  • The nitrate, Al(N03)3, is obtained as deliquescent crystals (with 81120) by evaporating a solution of the hydroxide in nitric acid.

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  • Dilute nitric acid oxidizes it to acetic and oxalic acids, while potassium permanganate oxidizes it to acetone, carbon dioxide and oxalic acid.

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  • Martius yellow, C10H5(N02)20Na H20, the sodium salt of 2.4 dinitro-a-naphthol (for notation see Naphthalene), is prepared by the action of nitric acid on a-naphthol -2.4-disulphonic acid.

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  • Naphthol yellow S., C10H4(ONa) (NO 2) 2 S0 3 Na, prepared by the action of nitric acid on a-naphthol - 2.4.

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  • It burns in air, and also in chlorine and bromine, and is readily oxidized by nitric acid.

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  • Lanthanum nitrate, La(N03)3 6H 2 0, is obtained by dissolving the oxide in nitric acid.

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  • Potassium permanganate oxidizes it to f3-oxyisovaleric acid (CH 3) 2 C(OH) CH2.002H, whilst nitric acid gives, among other products, dinitropropane, (CH3)2C(N02)2.

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  • In a fine state of division it takes fire on heating in air, but is permanent at ordinary temperatures in oxygen or air; it is readily attacked by hydrochloric and sulphuric acids, but scarcely acted on by nitric acid.

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  • C(OH) 000H, whilst concentrated nitric acid converts it into dinitroisopropane.

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  • Thallous nitrate, T1NO 31 is obtained as white, rhombic prisms by crystallizing a solution of the metal, oxide, carbonate, &c., in nitric acid.

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  • The chlorine is not completely precipitated by silver nitrate in nitric acid solution, the ionization apparently not proceeding to all the chlorine atoms. Thallic iodide, T11 3, is interesting on account of its isomorphism with rubidium and caesium tri-iodides, a resemblance which suggests the formula T11 (12) for the salt, in which the metal is obviously monovalent.

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  • In this process phosphates must be absent, and the nitric acid liberated during the reaction should be neutralized as soon as possible.

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  • It yields a nitroso derivative, is nitrated by nitric acid to dilituric acid and brominated by bromine.

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  • With nitric acid in the presence of sulphuric acid it yields a nitro derivative.

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  • The pure metal readily evolves hydrogen when acted upon by sulphuric and hydrochloric acids, and is readily attacked by dilute nitric acid.

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  • Gallium oxide Ga203 is obtained when the nitrate is heated, or by solution of the metal in nitric acid and ignition of the nitrate.

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  • It exists in two crystalline forms. Nitric acid passed into its chloroform solution gives phenyl diazonium nitrate.

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  • Fuming nitric acid gives a paratrinitro substitution derivative which on reduction gives paraleucaniline; the salt of the carbinol formed on oxidizing this substance is the valuable dye rosaniline.

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  • It is very heavy, its density being about 11; it inflames when heated in air and is not attacked by alkalis; it readily dissolves in nitric acid and aqua regia, but with difficulty in hydrochloric acid.

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  • Hydrochloric and sulphuric acids are almost without action on the metal, but it dissolves readily in dilute nitric acid.

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  • Rubidium nitrate, RbNO 3, obtained by the action of nitric acid on the carbonate, crystallizes in needles or prisms and when strongly heated is transformed into a mixture of nitrite and oxide.

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  • Chalcopyrite is decomposed by nitric acid with separation of sulphur and formation of a green solution; ammonia added in excess to this solution changes the green colour to deep blue and precipitates red ferric hydroxide.

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  • For this purpose a filtered solution of bleaching-powder and a very dilute solution of nitric acid may be employed.

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  • By boiling this varnish with dilute nitric acid vapours of acrolein are given off, and the substance gradually becomes a solid non-adhesive mass the same as the ultimate oxidation product of both raw and boiled oil.

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  • In the 1785 paper he proved the correctness of this supposition by showing that when electric sparks are passed through common air there is a shrinkage of volume owing to the nitrogen uniting with the oxygen to form nitric acid.

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  • Further, remarking that little was known of the phlogisticated part of our atmosphere, and thinking it might fairly be doubted "whether there are not in reality many different substances confounded together by us under the name of phlogisticated air," he made an experiment to determine whether the whole of a given portion of nitrogen (phlogisticated air) of the atmosphere could be reduced to nitric acid.

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  • Concentrated nitric acid has also very little action, but with the dilute acid a vigorous action ensues.

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  • Cupric nitrate, Cu(NO 3) 2, is obtained by dissolving the metal or oxide in nitric acid.

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  • Cooh, is obtained by the oxidation of milk, sugar, dulcite, galactose, quercite and most varieties of gum by nitric acid.

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  • Antimony trioxide occurs as the minerals valentinite and senarmontite, and can be artificially prepared by burning antimony in air; by heating the metal in steam to a bright red heat; by oxidizing melted antimony with litharge; by decomposing antimony trichloride with an aqueous solution of sodium carbonate, or by the action of dilute nitric acid on the metal.

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  • When the latter have oxidized ammonia to nitrite, however, the former step in and oxidize it still further to nitric acid.

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  • In ores containing much copper, this metal is largely concentrated in the lead button, making it hard, and necessitating repeated scorifications and, in some cases, a preliminary removal of the copper by solution of the ore in nitric acid.

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  • Nearly all lead ores contain more or less sulphur; and as in the process of solution in nitric acid this is oxidized to sulphuric acid which unites with the lead to form the very insoluble lead sulphate, it is simpler to add sulphuric acid to convert all the lead into sulphate and then evaporate until the nitric acid is expelled.

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  • The ore (0 5 gramme) is digested with a mixture of potassium nitrate and nitric acid.

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  • A saturated solution of potassium chlorate in strong nitric acid is added, and the mass evaporated to dryness.

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  • This method is modified in practice by the character of the ores, carbonates and silicates free from sulphides being decomposed by hydrochloric acid, with the addition of a little nitric acid.

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  • One gramme of the ore is treated in a flask with a mixture of nitric and sulphuric acids and evaporated until all the nitric acid is expelled.

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  • To the filtrate (or, if no silver is present, to the diluted nitric acid solution) io cc. of ammonia are added, and a standard solution of potassium cyanide is run in from a burette until the blue colour has nearly disappeared.

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  • In this process, the residues are boiled with a dilute sulphuric acid to which nitric acid and potassium chlorate are added in order to transform the element into selenic acid, H 2 Se0 4, which is then reduced to selenious acid, H 2 Se0 3, by boiling with hydrochloric acid, and finally to selenium by sulphur dioxide.

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  • Selenium dioxide, Se02, is prepared by burning selenium in oxygen, or by oxidizing selenium with nitric acid and heating the residue.

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  • Silver nitrate in the presence of nitric acid gives with bromides a pale yellow precipitate of silver bromide, AgBr, which is sparingly soluble in ammonia.

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  • For their quantitative determination they are precipitated in nitric acid solution by means of silver nitrate, and the silver bromide well washed, dried and weighed.

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  • Chromic acid oxidizes it to acetic acid and carbon dioxide; potassium permanganate oxidizes it to pyruvic acid; nitric acid to oxalic acid, and a mixture of manganese dioxide and sulphuric acid to acetaldehyde and carbon dioxide.

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  • On oxidation with nitric acid the primary compounds give monoalkyl phosphinic acids, R PO(OH) 2r the secondary yielding dialkyl phosphinic acids, R 2 PO(OH).

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  • Dilute nitric acid oxidizes it first to para-toluic acid and then to terephthalic acid.

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  • As this reaction of its own accord takes place only to a very small extent, an" oxygen carrier "is always introduced in the shape of the vapours of nitric acid or the lower oxides of nitrogen.

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  • The supply of the nitric acid required to make up this loss is obtained in England by "potting" that is, by decomposing solid nitrate of soda by sulphuric acid in a flue between the pyrites burners and the chambers.

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  • The formation of murexide is used as a test for the presence of uric acid, which on evaporation with dilute nitric acid gives alloxantin, and by the addition of ammonia to the residue the purple red colour of murexide becomes apparent.

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  • It dissolves in dilute cold nitric acid with the formation of ferrous and ammonium nitrates, no gases being liberated; when heated or with stronger acid ferric nitrate is formed with evolution of nitrogen oxides.

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  • Pyrite may be prepared artificially by gently heating ferrous sulphide with sulphur, or as brassy octahedra and cubes by slowly heating an intimate mixture of ferric oxide, sulphur and salammoniac. It is insoluble in dilute acids, but dissolves in nitric acid with separation of sulphur.

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  • Ferric sulphate, Fe2(S04)3, is obtained by adding nitric acid to a hot solution of ferrous sulphate containing sulphuric acid, colourless crystals being deposited on evaporating the solution.

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  • Ferric nitrate, Fe(NO3) 3, is obtained by dissolving iron in nitric acid (the cold dilute acid leads to the formation of ferrous and ammonium nitrates) and crystallizing, when cubes of Fe(NO3)3.6H20 or monoclinic crystals of Fe(N03)3.9H20 are obtained.

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  • On reduction it yields hexahydrotoluene; oxidation with dilute nitric acid or chromic acid gives benzoic acid; whilst chromyl chloride and water give benzaldehyde.

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  • Pyrovanadic acid is deposited as a dark brown unstable powder when an acid vanadate is decomposed by nitric acid.

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  • It is easily oxidized by heating with concentrated nitric acid to arsenic acid, and with concentrated sulphuric acid to arsenic trioxide; dilute nitric acid only oxidizes it to arsenious acid.

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  • A blank experiment should always be carried out in testing for small quantities of arsenic, to ensure that the materials used are quite free from traces of arsenic. It is to be noted that the presence of nitric acid interferes with the Marsh test; and also that if the arsenic is present as an arsenic compound it must be reduced to the arsenious condition by the action of sulphurous acid.

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  • It is then allowed to stand twenty-four hours, filtered, washed with dilute ammonia, dried, ignited to constant weight and weighed, the filter paper being incinerated separately after moistening with nitric acid.

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  • The prismatic variety of the oxide can be obtained by crystallization from a saturated boiling solution in potassium hydroxide, or by the crystallization of a solution of silver arsenite in nitric acid.

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  • On oxidation by nitric acid they yield sulphonic acids.

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  • The trichromates are obtained by the addition of nitric acid (of specific gravity about 1.2) to solutions of the bichromates.

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  • It is also obtained when sebacic, stearic and oleic acids are oxidized with nitric acid.

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  • They yield mucic and oxalic acids when treated with nitric acid.

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  • Sulphuric acid converts it into l-arabinose; and nitric acid oxidizes it to oxalic acid (without the intermediate formation of mucic acid as in the case of gum arable).

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  • Linseed does not give the latter reaction; by treatment with boiling nitric acid it yields mucic and oxalic acids.

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  • During this manual operation the dosage program for nitric acid was unintentionally activated for a second time.

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  • It transforms in the air to form gaseous nitric acid and toxic organic nitrates.

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  • Further it will eventually breakdown to produce nitric acid and hence give rise to acid rain which harms the environment.

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  • Reprocessing involves the dissolution of the spent fuel in boiling concentrated nitric acid and subsequent physico-chemical separations of uranium and plutonium.

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  • It is the finer Type I PSC's consisting of nitric acid trihydrate which give the spectacular colorful displays.

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  • In this process the osmiridium is fused with zinc and the excess of zinc evaporated; the residue is then ignited with barium nitrate, extracted with water and boiled with nitric acid.

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  • The double chloride is fused with nitre, the melt extracted with water and the residue fused with lead, the excess of lead being finally removed by solution in nitric acid and aqua regia.

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  • Cobalt nitrate, Co(NO 3) 2.6H 2 0, is obtained in dark-red monoclinic tables by the slow evaporation of a solution of the metal, its hydroxide or carbonate, in nitric acid.

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  • Jowitschitsch (Ann., 1906, 347, p. 2 33) inclines to Scholl's formula; he found that the synthetic silver salt of glyoxime peroxide resembled silver fulminate in yielding hydroxylamine with hydrochloric acid, but differed in being less explosive, and in being soluble in nitric acid.

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  • The synthesis of nitric acid by passing electric sparks through moist air by Cavendish is a famous piece of experimental work, for in the first place it determined the composition of this important substance, and in the second place the minute residue of air which would not combine, although ignored for about a century, was subsequently examined by Lord Rayleigh and Sir William Ramsay, who showed that it consists of a mixture of elementary substances - argon, krypton, neon and xenon (see Argon).

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  • In 1849 he discovered anhydrous nitric acid (nitrogen pentoxide), a substance interesting as the first obtained of the so-called " anhydrides " of the monobasic acids.

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  • The amount of nitric acid varies from place to place; rain-water, collected in the country, has been found to contain an average of o 5 parts in a million, but town rain-water contains more, the greater amounts being present in the more densely populated districts.

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  • Baumann, Ber., 1885, 18, p. 883), and with concentrated nitric acid they yield dinitroparaffins (G.

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  • Fischer, Ann., 1882, 215, p. 283), or from glycerin diacetate and concentrated nitric acid in the cold (E.

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  • Hydrochloric acid and its metallic salts can be recognized by the formation of insoluble silver chloride, on adding silver nitrate to their nitric acid solution, and also by the formation of chromium oxychloride (see above).

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  • By fusing iron with saltpetre and extracting the melt with water, or by adding a solution of ferric nitrate in nitric acid to strong potash, an amethyst or purple-red solution is obtained which contains potassium ferrate.

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  • It is the finer Type I PSC 's consisting of nitric acid trihydrate which give the spectacular colorful displays.

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  • Nitrous oxide is a gas produced by the burning of organic matter, during the production of nitric acid and nylon, and through the use of fertilizer.

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