The Elements of Qualitative Chemical Analysis, vol. 1, parts 1 and 2.: With Special Consideration of the Application of the Laws of Equilibrium and of the Modern Theories of Solution.Stieglitz, Julius
Science
The Elements of Qualitative Chemical Analysis, vol. 1, parts 1 and 2.: With Special Consideration of the Application of the Laws of Equilibrium and of the Modern Theories of Solution.
Stieglitz, Julius
Chemistry, Analytic -- Qualitative
[59] Or, on the basis of the accepted molecular weights, abnormally
high osmotic pressures, abnormally great lowerings of the
freezing-point, raisings of the boiling-point, etc., were obtained.
Van 't Hoff, originally, on account of these discrepancies,
considered this extension of the Avogadro Hypothesis to hold
only for the "majority" of substances in solution, not for all
(Arrhenius, ‹loc. cit.›). It was considered to have ‹universal›
application (for dilute solutions) only after Arrhenius had
explained the exceptions with the aid of his theory of electrolytic
dissociation.
[60] That is, hydrogen chloride, in aqueous solution, depresses the
vapor tension and the freezing-point and elevates the boiling-point
considerably more than an ‹equimolecular› quantity, for instance,
of glucose does, and gives a considerably higher osmotic pressure.
The differences are relatively greater, the more dilute the
solutions used.
[61] A fourth interpretation advanced at one time in opposition to
the theory of ionization is that salts like sodium chloride and
zinc chloride are ‹hydrolyzed› and thereby produce more solute
molecules, ‹e.g.› NaCl + H_{2}O → NaOH + HCl. Aside from the fact
that such hydrolysis of salts, when it does occur (Chapter X.), is
easily detected, and that it can be proved not to occur appreciably
in the case of sodium chloride (‹loc. cit.›), this interpretation
fails utterly to account for the results obtained with ‹acids,
e.g.› HCl, HNO_{3}, H_{2}SO_{4}, and with ‹bases›, ‹e.g.› NaOH,
Ba(OH)_{2}, which in aqueous solutions show an increase in the
number of molecules as great as shown by salts. This explanation is
therefore untenable.
[62] ‹Z. phys. Chem.›, «1», 631, (1887). Previous papers were
published in the transactions of the Royal Academy of Sweden
(Stockholm). For a history of the theory see Ostwald, ‹Z. phys.
Chem.›, «69», p. 1 (1909), and Arrhenius, ‹The Willard Gibbs
Address›, ‹J. Am. Chem. Soc.›, 1911 («Stud.»).
[63] In the case of double salts, such as sodium-ammonium
phosphate, and similar compounds, the dissociation leads to
the formation of more than two products. The molecules of two
or more different products may then be charged positively and,
conversely, there may be two or more different products of
dissociation carrying negative charges. We have, for instance,
Na(NH_{4})HPO_{4} ⇄ Na^{+} + NH_{4}^{+} + H^{+} + PO_{4}^{3−}
and Na(NH_{4})HPO_{4} ⇄ Na^{+} + NH_{4}^{+} + HPO_{4}^{2−}. In
all cases the rule concerning the sum of all the charges, as
expressed in (2), must be fulfilled, the charge on the phosphate
ion, PO_{4}^{3−}, being three times as great as that on a sodium,
ammonium, or hydrogen ion; that on the acid phosphate ion,
HPO_{4}^{2−}, being twice as great.
[64] Ion = the going or the migrating particle.
Public-domain text, read in full here on John Shaqi.
Reviews
Reviews
No reviews yet
Be the first to share your thoughts on this work.
Elsewhere in the archive
Join the Discussion
Join the discussion
Sign in to leave a comment or review.
Sign InorCreate an account