VAPOR PRESSURES OF AQUEOUS SOLUTIONS OF SILVER NITRATE, OF AMMONIUM NITRATE, AND OF LITHIUM NITRATE

1956 ◽  
Vol 34 (2) ◽  
pp. 151-159 ◽  
Author(s):  
A. N. Campbell ◽  
J. B. Fishman ◽  
G. Rutherford ◽  
T. P. Schaefer ◽  
L. Ross

This paper is devoted to the direct determination of the vapor pressures of solutions of the nitrates of silver, of ammonium, and of lithium, at temperatures varying from 30 °C. to 105 °C. and at concentrations varying from 10 to 85 weight % (for lithium nitrate, the limited solubility precluded measurements beyond 65%). From the vapor pressures, the enthalpies of evaporation of water (by a modification of the Clapeyron–Clausius equation), the differential heats of dilution, and the activities of water (as compared with the mole fractions of the solvent) have been calculated. From the results we conclude that the water of hydration of the ammonium and silver ions (if, indeed, these ions are hydrated at all) is very loosely attached, while that of the lithium ion is strongly bound.

1937 ◽  
Vol 9 (6) ◽  
pp. 264-267 ◽  
Author(s):  
K. C. D. Hickman ◽  
J. C. Heckler ◽  
N. D. Embree

1958 ◽  
Vol 36 (10) ◽  
pp. 1325-1331 ◽  
Author(s):  
A. N. Campbell ◽  
E. M. Kartzmark ◽  
A. G. Sherwood

Equivalent conductances, viscosities, and densities were determined for solutions equimolar in two of the three salts lithium nitrate, ammonium nitrate, and silver nitrate. The three possible combinations of two salts were each studied at 25 °C and at 35 °C.The observed conductances and viscosities were compared with those of the single salt solutions at the same total ion concentration. The conductances were lower than the mean of the conductances of the single salt solutions. The viscosities were also lower than the mean viscosities.


1996 ◽  
Vol 50 (10) ◽  
pp. 1307-1313 ◽  
Author(s):  
Paul E. Field ◽  
Roger J. Combs ◽  
Robert B. Knapp

Infrared absorbance measurements through a gas flow cell are made with the closed-loop circulation of vapor/air mixtures equilibrated with the use of temperature-regulated aqueous solutions. Constant reproducible vapor pressures of organic solutes are established with the equilibrated aqueous solutions. The water solvent depresses the vapor pressure of the pure organic solutes of methanol, ethanol, isopropanol, acetone, and methyl ethyl ketone (MEK). Knowledge of the solution liquid mole fractions, the pure component vapor pressures, and the Wilson coefficients permits determination of the solute vapor pressures to within 2% accuracy. Reliable aqueous solution preparation requires only the correct weighings of pure constituent materials before mixing to achieve the targeted solute liquid mole fractions. Absorbances are measured for four of the five solutes over a range of seven concentrations and for MEK over four concentrations. These concentrations show the absorbance region of adherence to Beer's law with an experimental precision of approximately ±2% for the solutes studied. Absorptivities that are calculated from the Beer's law slope are compared to the available infrared absorbance data.


1973 ◽  
Vol 51 (17) ◽  
pp. 3006-3009 ◽  
Author(s):  
A. N. Campbell

The direct determination of the limiting conductance of 1/3In3+ ion is not possible because of hydrolysis. This figure has been obtained by a method which may be open to criticism as 56.3 mhos, at 25°. If anything, this figure is too high.


1959 ◽  
Vol 37 (8) ◽  
pp. 1288-1293 ◽  
Author(s):  
A. N. Campbell ◽  
R. J. Friesen

Equivalent conductances, densities, and viscosities of aqueous solutions of ammonium nitrate, of silver nitrate, and of lithium nitrate were determined at 25 °C and at 35 °C at concentrations ranging from 0.01 N to 1.0 N.Experimental equivalent conductances have been compared with those calculated by the Wishaw–Stokes and Falkenhagen–Leist equations. Suitable choice of one parameter, the distance of closest approach, permits reproduction of the experimental data with an error of less than 0.5%. A study of the deviations of the calculated from the experimental conductances reveals that the distance of closest approach (so-called) varies appreciably with concentration and temperature.


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