Ammonium nitrate and nitrite, for instance, intensify the action of a water on lead.
Von Liebig (1823), who heated a mixture of alcohol, nitric acid and mercuric nitrate; the salt is largely manufactured by processes closely resembling the last.
Cadmium oxide, CdO, is a brown powder of specific gravity 6.5, which can be prepared by heating the metal in air or in oxygen; or by ignition of the nitrate or carbonate; by heating the metal to a white heat in a current of oxygen it is obtained as a dark red crystalline sublimate.
Ann., 1826, 8, p. 23), by converting lead molybdate into lead nitrate, obtained the value 95.
The solution on the addition of ammoniacal silver nitrate behaves similarly to that of potassium pentathionate, but differs from it in giving an immediate precipitate of sulphur with ammonia, whereas the solution of the pentathionate only gradually becomes turbid on standing.
Nitrate of soda, Peruvian guano and superphosphate of lime in the form of bones dissolved by sulphuric acid were now added to the list of manures, and the practice of analysing soils became more general.
Much of this is doubtless taken up as nitrate, yet the direct application of nitrate of soda has comparatively little beneficial influence on their growth.
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.
It forms a characteristic explosive silver salt on the addition of ammoniacal silver nitrate to its aqueous solution, and an amorphous precipitate which explodes on warming with ammoniacal cuprous chloride.
But it is found that even when more than sixty times the amount of potassium thiocyanate required by this equation is added, a portion of the ferric nitrate still remains unconverted, doubtless owing to the occurrence of the reverse change Fe (CNS) 3 +3KNOs =Fe(N03) 3+3KCNS.
1 The metals of the alkaline-earths were somewhat neglected; we find Georg Agricola considering gypsum (calcium sulphate) as a compound of lime, while calcium nitrate and chloride became known at about the beginning of the 17th century.
Boyle recognized many reagents which gave precipitates with certain solutions: he detected sulphuric and hydrochloric acids by the white precipitates formed with calcium chloride and silver nitrate respectively; ammonia by the white cloud formed with the vapours of nitric or hydrochloric acids; and copper by the deep blue solution formed by a solution of ammonia.
Certain substances are insoluble in all these reagents, and other methods, such as the fusion with sodium carbonate and potassium nitrate, and subsequent treatment with an acid, must be employed.
In the first group, we have to notice the titration of a cyanide with silver nitrate, when a milkiness shows how far the reaction has gone; the titration of iron with permanganate, when the faint pink colour shows that all the iron is oxidized.
Phosphorus is obtained as a soluble phosphate (which can be examined in the usual way) by lixiviating the product obtained when the substance is ignited with potassium nitrate and carbonate.
The halogens may be estimated by ignition with quicklime, or by heating with nitric acid and silver nitrate in a sealed tube.
10, p. 290); the operation is easier if the lime be mixed with sodium carbonate, or a mixture of sodium carbonate and potassium nitrate be used.
Are included sulphur and ammonium nitrate; monotropy is exhibited by aragonite and calcite.
By treating blue ultramarine with silver nitrate solution, "silverultramarine" is obtained as a yellow powder.
Glucoseoxime on warming with acetic anhydride is simultaneously acetylated and dehydrated, yielding an acetylated gluconitrile, which when warmed with ammoniacal silver nitrate loses hydrocyanic acid and is transformed into an acetyl pentose.
It is also prepared by heating ammonium nitrite (or a mixture of sodium nitrite and ammonium chloride): NH 4 NO 2 =2H20+N21 by heating a mixture of ammonium nitrate and chloride (the chlorine which is simultaneously produced being absorbed by milk of lime or by a solution of sodium hydroxide): 4NH4N03+2NH4C1=5N2 +C1 2 +12H 2 O; by heating ammonium dichromate (or a mixture of ammonium chloride and potassium dichromate): (NH4)2Cr207 = Cr203+4H20+ N2; by passing chlorine into a concentrated solution of ammonia (which should be present in considerable excess): 8NH3+3C12=6NH4C1-F-N2; by the action of hypochlorites or hypobromites on ammonia: 3NaOBr-+2NH 3 =3NaBr+3H 2 OH-N 2; and by the action of manganese dioxide on ammonium nitrate at 180-20o° C. It is also formed by the reduction of nitric and nitrous oxides with hydrogen in the presence of platinized asbestos at a red heat (G.
Nitric acid (up to 50%) is formed in the first tower, and weaker acids in the successive ones; the last tower contains milk of lime which combines with the gases to form calcium nitrite and nitrate (this product, being unsuitable as a manure, is decomposed with the acid, and the evolved gases sent back).
It was found advantageous not to work for acid but for a basic calcium nitrate (normal calcium nitrate being very deliquescent); for this purpose the acid is treated with the requisite amount of milk of lime.
Priestley, who obtained it by reducing nitrogen peroxide with iron, may be prepared by heating ammonium nitrate at 170-260° C., or by reducing a mixture of nitric and sulphuric acid with zinc. It is a colourless gas, which is practically odourless, but possesses a sweetish taste.
In a purer condition it may be obtained by the action of sulphuric acid on a mixture of potassium nitrate and ferrous sulphate, or of hydrochloric acid on a mixture of potassium nitrate and ferric chloride.
Nitrogen peroxide is also prepared by heating lead nitrate and passing the products of decomposition through a tube surrounded by a freezing mixture, when the gas liquefies.
Phys., 1850 , 28, p. 241) by the action of dry chlorine on silver nitrate: 4AgN03+2C12=4AgC1+2N205 +02.
Sodium nitrite, the most commonly used salt of the acid, is generally obtained by heating the nitrate with metallic lead; by heating sodium nitrate with sulphur and sodium hydroxide, the product then being fractionally crystallized;(Read, Holliday & Sons): 3NaNO 3 +S+2NaOH = Na2S04+3NaN02+H20; by oxidizing atmospheric nitrogen in an electric arc, keeping the gases above 300° C., until absorption in alkaline hydroxide solution is effected (German Pat.
The nitrogen-bacteria that concern us here are of two main categories: (I) those that assimilate elementary nitrogen from its solution in sea-water, building it up into combination with carbohydrate as proteid; and (2) those that break down nitrate into nitrite, nitrite into ammonia and ammonia into elementary nitrogen.
The reagents in common use are: Millon's reagent, a solution of mercuric nitrate containing nitrous acid, this gives a violet-red coloration; nitric acid, which gives a yellow colour, turning to gold when treated with ammonia (xanthoproteic reaction); fuming sulphuric acid, which gives violet solutions; and caustic potash and copper sulphate, which, on warming, gives a red to violet coloration (biuret reaction).
It is found that the most accurate and convenient apparatus to use is a platinum bowl filled with a solution of silver nitrate containing about fifteen parts of the salt to one hundred of water.
One method for this purpose is to convert it into a solution of the nitrate U02(N03)2, and from it to precipitate the metal as oxalate by oxalic acid (Peligot).
O, is obtained by heating uranyl nitrate to 250° as a yellow solid, insoluble in water, but soluble in acids with the formation of uranyl salts.
Uranyl nitrate, U02(N03)2.6H20, is the most important uranium salt.
Uranyl nitrate is used in photography, and also in analytical chemistry as a precipitant for phosphoric acid (as uranyl ammonium phosphate, U02 NH4 P04).
Besides wool, leading imports are jute, cotton, flax, timber, petroleum, coal, pitch, wine, cereals, oil-seeds and oil-cake, nitrate of soda and other chemical products, and metals.
They act as reducing agents, silver nitrate in the presence of ammonia being rapidly reduced to the condition of metallic silver.
Dilute nitric acid readily dissolves the metal, with formation of nitrate Pb(N03)2.
The corresponding hydrate, Pb(OH)2, is obtained as a white crystalline precipitate by adding ammonia to a solution of lead nitrate or acetate.
It dissolves in strong nitric acid with the formation of the nitrate and sulphate, and also in hot concentrated hydrochloric acid.
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.
The normal ortho-phosphate, Pb3(P04)2, is a white precipitate obtained by adding sodium phosphate to lead acetate; the acid phosphate, PbHPO 4, is produced by precipitating a boiling solution of lead nitrate with phosphoric acid; the pyrophosphate and meta-phosphate are similar white precipitates.