80. Chlorhydric, Hydrochloric or Muriatic, Acid is a Gas.—As used, it is dissolved, in water, for which it has great affinity. Water will hold, according to temperature, from 400 to 500 times its volume of HCl. Hundreds of thousands of tons of the acid are annually made, mostly in Europe, as a bye-product in Na2CO3 manufacture. The gas is passed into towers through which a spray of water falls; this absorbs it. The yellow color in most commercial HCl indicates impurities, some of which are Fe, S, As, and organic matter. As, S, etc., come from the pyrites used in making H2SO4. Chemically pure (C.P.) acid is freed from these, and is without color. The gas may be dried by passing it through a glass tube holding CaCl2 (Fig. 16) and collecting it over mercury.
The muriatic acid of commerce consists of about two- thirds water by weight. HCl can also be made by direct union of its constituents.81. Uses.—HCl is used to make Cl, and also bleaching- powder. Its use as a reagent in the laboratory is illustrated by the following experiment:— Experiment 49.—Put into a t.t. 2 cc. AgNO3 solution, add 5 cc. H2O, then add slowly HCl so long as a ppt. (precipitate) is formed. This ppt. is AgCl. Now in another t.t. put 2 cc. Cu(NO3)2, solution, add 5 cc. H2O, then a little HCl. No ppt. is formed. Now if a solution of AgNO3 and a solution of Cu(NO3)2 were mixed, and HCl added, it is evident that the silver would be precipitated as chloride of silver, while the copper would remain in solution. If now this be filtered, the silver will remain on the filter paper, while in the filtrate will be the copper. Thus we shall have performed an analysis, or separated one metal from another. Perform it. Note, however, that any soluble chloride, as NaCl, would produce the same result as HCl.
BROMHYDRIC AND IODIHYDRIC ACIDS.
82. NaCl, being the most abundant compound of Cl, is the source of commercial HCl. KCl treated in the same way would give a like product. Theoretically HBr and HI might be made in the same way from NaBr and NaI, but the affinity of H for Br and I is weak, and the acids separate into their elements, when thus prepared.
83. To make HI.
Experiment 50.—Drop into a t.t. three or four crystals of I, and add 10 cc. H2O. Hold in the water the end of a d.t. from which H2S gas is escaping. Observe any deposit, and write the reaction.
FLUORHYDRIC ACID.
84. Preparation and Action.
Experiment 51.—Put 3 or 4 g. powdered CaF2, i.e. fluor spar or fluorite, into a shallow lead tray, e.g. 4x5 cm, and pour over it 4 or 5 cc. H2SO4. A piece of glass large enough to cover this should previously be warmed and covered on one side with a very thin coat of beeswax. To distribute itevenly, warm the other side of the glass over a flame. When cool, scratch a design (Fig. 24) through the wax with a sharp metallic point. Lay the glass, film side down, over the lead tray. Warm this five minutes or more by placing it high over a small flame (Fig. 25) to avoid melting the wax. Do not inhale the fumes. Take away the lamp, and leave the tray and glass where it is not cold, for half an hour or more. Then remove the wax and clean the glass with naphtha or benzine. Look for the etching.
Two things should have occurred: (1) the generation of HF. Write the equation for it. (2) Its etching action on glass. In this last process HF acts on SiO2 of the glass, forming H2O and SiF4. Why cannot HF be kept in glass bottles?