THE ELECTROLYTIC CONDUCTANCES OF SODIUM CHLORATE AND OF LITHIUM CHLORATE IN WATER AND IN WATER–DIOXANE

1966 ◽  
Vol 44 (8) ◽  
pp. 925-934 ◽  
Author(s):  
A. N. Campbell ◽  
E. M. Kartzmark ◽  
B. G. Oliver

The conductances, densities, and viscosities of aqueous solutions of sodium chlorate were determined over the complete range of concentration at 25 °C and at 35 °C. An attempt was made to reproduce the results at 25 °C with the viscosity-corrected Falkenhagen–Leist and Wishaw–Stokes equations. The limiting equivalent conductances of sodium chlorate at 25 °C and 35 °C in water were also determined.The conductances, densities, and viscosities of sodium chlorate at 25 °C and 35 °C were determined in a solvent consisting of 64.5% dioxane, 35.5% water. The limiting equivalent conductances of sodium chlorate at 25 °C and 35 °C and of lithium chlorate at 25 °C in this solvent were determined by analyzing the data with the Fuoss–Onsager equation for associated electrolytes.Finally, conductances of sodium chlorate and lithium chlorate at 25 °C were determined in a solvent consisting of 90% dioxane, 10% water.

1962 ◽  
Vol 40 (5) ◽  
pp. 839-844 ◽  
Author(s):  
A. N. Campbell ◽  
E. M. Kartzmark ◽  
G. R. Lakshminarayanan

Equivalent conductances, densities, and viscosities of aqueous solutions of sodium octanoate have been determined at 25° and 35 °C, at concentrations ranging from 0.0002 M to 2.8 M. The limiting equivalent conductances of the octanoate ion have been determined as 23.08 mhos and 29.09 mhos, at 25° and 35 °C respectively.Comparison has been made of our experimental conductances with those calculated, using the equations of Robinson–Stokes, of Falkenhagen–Leist, and of Fuoss.No evidence has been found of micelle formation in solutions of sodium octanoate.


1958 ◽  
Vol 36 (2) ◽  
pp. 330-338 ◽  
Author(s):  
A. N. Campbell ◽  
E. Bock

The limiting equivalent conductances of ammonium chloride, ammonium bromide, and ammonium nitrate as well as the limiting ionic conductances of the ammonium and nitrate ions were determined at 35 °C. with a probable error of 0.05%. The values found were [Formula: see text] 180.97 mhos, [Formula: see text] 182.73 mhos, [Formula: see text] 174.21 mhos, [Formula: see text] 88.73 mhos, and [Formula: see text] 85.48 mhos. These values were obtained by the application of the Shedlovsky method of extrapolation to equivalent conductance data, which had been corrected for the hydrolysis of the ammonium ion.Observed equivalent conductances of aqueous solutions of ammonium nitrate at 35 °C., in the concentration range from 0.0002 N to 10 N, have been compared with those calculated by means of the Wishaw–Stokes and Falkenhagen–Leist equations. The Wishaw–Stokes equation was found to give better agreement with experiment than the Falkenhagen–Leist equation.


2016 ◽  
Vol 55 (39) ◽  
pp. 10436-10444
Author(s):  
Biljana Z. Radiša ◽  
Mićo M. Mitrović ◽  
Branislava M. Misailović ◽  
Andrijana A. Žekić

1960 ◽  
Vol 38 (10) ◽  
pp. 1939-1945 ◽  
Author(s):  
A. N. Campbell ◽  
J.I. Friesen

The equivalent conductances, densities, and viscosities of aqueous solutions of sodium hexanoate have been determined at 25 °C and 35 °C at concentrations ranging from 0.0003 M to saturation.The limiting equivalent conductances of the hexanoate ion have been determined as 27.37 ± 0.04 mhos at 25 °C and 34.69 ± 0.05 mhos at 35 °C.The Robinson–Stokes and the Falkenhagen–Leist equations have been applied to the data. The Robinson–Stokes equation reproduces the data within 0.7 mho up to 0.5 M at 25 °C when å = 13 Å. At 35 °C the data are reproduced within 0.5 mho up to 0.05 M with å = 10 Å. The Falkenhagen–Leist equation reproduces the data at 25 °C within 0.4 mho up to 0.1 M with å = 5.5 Å. An å = 4.0 Å reproduces the 35 °C data within 0.5 mho up to 0.05 M.From the form of the conductance curves and from an estimation of the apparent molecular weight it was concluded that the hexanoate ion does not form ionic micelles.


1965 ◽  
Vol 43 (6) ◽  
pp. 1729-1737 ◽  
Author(s):  
A. N. Campbell ◽  
G. R. Lakshminarayanan

The equivalent conductances of aqueous solutions of sodium decanoate, sodium laurate, and sodium myristate have been determined from the very dilute region up to saturation concentration, at 25° and 35°. The limiting conductances have been obtained from the measurements in the usual way. In addition and for the sake of completeness, the limiting equivalent conductances of sodium formate, sodium acetate, sodium propionate, and sodium butyrate have also been determined at 35°, since they were not known at this temperature.The effect of increasing chain length on mobility is discussed. From a consideration of the experimental and the theoretical values of the slopes of the plots of equivalent conductance against the square root of the concentration, it is concluded that some sort of interaction, possibly a reversible dimerization of anions, occurs, even in the dilute region, and this could account for the lower experimental values of the slope. This phenomenon has been observed with other long chain electrolytes, however, and the hypothesis of dimerization is not the only possible one.The critical micelle concentrations have been determined, and recent concepts of micelle formation are applied to interpret their structure. The surface tensions of the aqueous solutions have been measured at 25° and 50°.


1959 ◽  
Vol 37 (5) ◽  
pp. 889-892 ◽  
Author(s):  
E. Bock ◽  
A. N. Campbell

Measurements have been made of the equivalent conductances of aqueous solutions of potassium iodate, potassium chlorate, and silver nitrate at 35.00 °C at concentrations ranging from 0.8 × 10−4 to 16×10−4 N. From these, the limiting equivalent conductances and association constants A as obtained by the use of the Fuoss–Shedlovsky extrapolation procedure were found to be at 35.0 °C:[Formula: see text]


1964 ◽  
Vol 17 (3) ◽  
pp. 304 ◽  
Author(s):  
RH Stokes ◽  
IA Weeks

The limiting equivalent conductances of several electrolytes have been measured at 25� in aqueous solutions of the synthetic sucrose polymer Ficoll. Though the viscosity of the solutions is several times that of sucrose solutions of the same percentage by weight of solute, the limiting conductances of small ions in them are little different from those in sucrose solutions. It is concluded that the polymer molecules form loose networks to a large extent permeable to small ions.


Sign in / Sign up

Export Citation Format

Share Document