Page:Scientific Papers of Josiah Willard Gibbs.djvu/430

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394
VAPOR-DENSITIES.

below half an atmosphere the experiments both of Naumann and of Troost show a deficiency of density as compared with the formula. For an indefinite diminution of pressure, there can be little doubt that the real density, like the value given by the formula, approaches the theoretical value 2.073. The greatest excess in numbers obtained by experiment is .07; the greatest deficiency is .19, which occurs at 59.7mm; the next in order of magnitude is .11, which occurs more than once. These discrepancies are certainly such as may be accounted for by errors of observation. They do not appear to be greater than we might expect on the hypothesis of the entire correctness of the formula. On the other hand, the agreement is greater than we should expect, if we reject the theory on which the formula was obtained. It is about such as we might expect in a suitable formula of interpolation with three constants, which have been determined by the values of the density for one atmosphere, for half an atmosphere, and for infinitesimal pressures. But we must regard the actual formula, in its application to this single temperature, as having only two constants, of which one is determined so as to make the formula give the theoretical value for infinitesimal pressures, and the other so as to make it agree with the experiments of Cahours at the pressure of one atmosphere.

An entirely different method has been employed by Horstmann[1] to determine the vapor-density of this substance. A current of dried air is forced through the liquid acid, which is heated to promote evaporation, and the mixture of air and vapor is cooled to any desired temperature, with deposition of the excess of acid, by passing upward through a spiral tube in a suitable bath. The acid is then separated from the air, and the quantity of each determined. It is assumed that the air is exactly saturated with vapor on leaving the coil, and that it has the temperature of the bath. If we know the pressure of saturated vapor for that temperature, and assume the validity of Dalton's law, it is easy to calculate the density of the vapor. For the pressure of the air is found by subtracting the pressure of the vapor from the total pressure (the experiments were so conducted that this was the same as the actual pressure of the atmosphere), and the ratio of the weights of the acid and the air obtained by analysis, divided by the ratio of their pressures, will give the ratio of their densities. The pressures of saturated vapor employed by Horstmann are those given by Landolt,[2] and differ greatly from the determinations of Regnault, in some cases being nearly twice as great, a difference noticed but not explained by Landolt, who however gives

  1. Berichte der deutschen chemischen Gesellschaft, Jahrg. iii (1870), S. 78; and Jahrg. xi (1878), S. 1287.
  2. Lieb. Ann., suppl. vi (1868), p. 157.