and HNO3 is made on the spot from NaNO3 and H2SO4. SO2 enters a large leaden chamber, often 100 to 300 feet long, and jets of steam and small portions of HNO3 are also forced in. The "chamber acid" thus formed is very dilute, and must be evaporated first in leaden pans, and finally in glass or platinum retorts, since strong H2SO4, especially if hot, dissolves lead. See Experiment 124. Study Figure 29, and write the reactions. 2 HNO3 breaks up into 2 NO2, H2O, and O. 94. Importance.—Sulphuric acid has been called, next to human food, the most indispensable article known. There is hardly a product of modern civilization in the manufacture of which it is not directly or indirectly used. Nearly a million tons are made yearly in Great Britain alone. It is the basis of all acids, as Na2CO3 is of alkalies. It is the life of chemical industry, and the quantity of it consumed is an index of a people's civilization. Only a few of its uses can be stated here. The two leading ones are the reduction of Ca3(PO4)2 for artificial manures and the sodium carbonate manufacture. Foods depend on the productiveness of soils and on fertilizers, and thus indirectly our daily bread is supplied by means of this acid; and from sodium carbonate glass, soap, saleratus, baking- powders, and most alkalies are made directly or indirectly. H2SO4 is employed in bleaching, dyeing, printing, telegraphy, electroplating, galvanizing iron and wire, cleaning metals, refining Au and Ag, making alum, blacking, vitriols, glucose, mineral waters, ether, indigo, madder, nitroglycerine, gun- cotton, parchment, celluloid, etc., etc.
FUMING SULPHURIC ACID.
95. Nordhausen or Fuming Sulphuric Acid, H2S207 used in dissolving indigo and preparing coal-tar pigments, is made by distilling FeSO4. 4FeSO4 + H2O = H2S207 + 2Fe203 + 2S02. This was the original sulphuric acid. It is also formed when S03 is dissolved in H2SO4. When exposed to the air, S03 escapes with fuming.
CHAPTER XX.
AMMONIUM HYDRATE.
96. Preparation of Bases.—We have seen that many acids are made by acting on a salt of the acid required, with a stronger acid. This is the direct way. The following experiments will show that bases may be prepared in a similar way by acting on salts of the base required with other bases, which we may regard as stronger than the ones to be obtained.
97. Preparation of NH4OH and NH3.
Experiment 57.—Powder 10 g. ammonium chloride, NH4Cl, in a mortar and mix with 10 g. calcium hydrate, Ca(OH)2; recently slaked lime is the best. Cover with water in a flask, and connect with Woulff bottles, as for making HCl (Fig. 22); heat the flask for fifteen minutes or more. The experiment may be tried on a smaller scale with a t.t. if desired.
The reaction is: 2NH4Cl + Ca(OH)2 = CaCl2 + 2NH4OH. NH4OH is broken up into NH3, ammonia gas, and water. NH4OH = NH3 + H2O. These pass over into the first bottle, where the water takes up the NH3, for which it has great affinity. One volume of water at 0° will absorb more than 1000 volumes of NH3. Thus NH4OH may be called a solution of NH3, in H2O. Write the reaction.
Experiment 58.—Powder and mix 2 or 3 g. each of ammonium nitrate, NH4NO3, and Ca(OH)2; put them into a t.t., and heat slowly. Note the odor. 2NH4NO3 + Ca(OH)2 = ?