High Temperature Aqueous Electrolyte Concentration Cells and the Ionization of Liquid Water to 200 °C

1973 ◽  
Vol 51 (15) ◽  
pp. 2590-2595 ◽  
Author(s):  
Digby D. MacDonald ◽  
P. Butler ◽  
D. Owen

High temperature aqueous electrolyte concentration cells with and without liquid junction are described. These cells were used to measure the ionization constant of water in 0.1, 0.25,0.5, and]1.0 mol/kg KCl solutions at temperatures to 200 °C. Extrapolation to infinite dilution yielded the following functions for the temperature dependence of log Kw0 and the thermodynamic parameters for ionization: log Kw0 = −4046.16/T + 3.537 − 0.01323T; ΔG0 = 77458.0 − 67.71T + 0.253187T2 J/mol; ΔH0 = 77458.0 − 0.253187T2 J/mol; ΔS0 = 67.71 − 0.5063T J/K mol; ΔCp0 = −0.5063T J/K mol.

1976 ◽  
Vol 54 (22) ◽  
pp. 3553-3558 ◽  
Author(s):  
David William Shoesmith ◽  
Woon Lee

The ionization constant of liquid D2O has been measured over the temperature range 298 to 523 K using an aqueous electrolyte concentration cell. Values for the standard free energy, enthalpy, entropy, and heat capacity of ionization have been calculated. The results are compared to similar results for liquid H2O


1973 ◽  
Vol 51 (16) ◽  
pp. 2747-2749 ◽  
Author(s):  
DiGBY D. Macdonald ◽  
D. Owen

Transport numbers for H+ and Cl− have been measured as a function of concentration and temperature to 200 °C using electrolyte concentratio cells. The infinite dilution transport number for H+ decreases with temperature while that for Cl− increases. This temperature dependence is discussed in terms of thermal destruction of the three dimensional structure of liquid water.


Author(s):  
I. Khidirov ◽  
V. V. Getmanskiy ◽  
A. S. Parpiev ◽  
Sh. A. Makhmudov

This work relates to the field of thermophysical parameters of refractory interstitial alloys. The isochoric heat capacity of cubic titanium carbide TiCx has been calculated within the Debye approximation in the carbon concentration  range x = 0.70–0.97 at room temperature (300 K) and at liquid nitrogen temperature (80 K) through the Debye temperature established on the basis of neutron diffraction analysis data. It has been found out that at room temperature with decrease of carbon concentration the heat capacity significantly increases from 29.40 J/mol·K to 34.20 J/mol·K, and at T = 80 K – from 3.08 J/mol·K to 8.20 J/mol·K. The work analyzes the literature data and gives the results of the evaluation of the high-temperature dependence of the heat capacity СV of the cubic titanium carbide TiC0.97 based on the data of neutron structural analysis. It has been proposed to amend in the Neumann–Kopp formula to describe the high-temperature dependence of the titanium carbide heat capacity. After the amendment, the Neumann–Kopp formula describes the results of well-known experiments on the high-temperature dependence of the heat capacity of the titanium carbide TiCx. The proposed formula takes into account the degree of thermal excitation (a quantized number) that increases in steps with increasing temperature.The results allow us to predict the thermodynamic characteristics of titanium carbide in the temperature range of 300–3000 K and can be useful for materials scientists.


1996 ◽  
Vol 442 ◽  
Author(s):  
J.-M. Spaeth ◽  
S. Greulich-Weber ◽  
M. März ◽  
E. N. Kalabukhova ◽  
S. N. Lukin

AbstractThe electronic structure of nitrogen donors in 6H-, 4H- and 3C-SiC is investigated by measuring the nitrogen hyperfine (hf) interactions with electron nuclear double resonance (ENDOR) and the temperature dependence of the hf split electron paramagnetic resonance (EPR) spectra. Superhyperfine (shf) interactions with many shells of 13C and 29Si were measured in 6H-SiC. The hf and shf interactions are discussed in the framework of effective mass theory. The temperature dependence is explained with the thermal occupation of the lowest valley-orbit split A1 and E states. It is proposed that the EPR spectra of P donors observed previously in neutron transmuted 6H-SiC at low temperature (<10K) and high temperature (>60K) are all due to substitutional P donors on the two quasi-cubic and hexagonal Si sites, whereby at low temperature the E state is occupied and at high temperature the A1 state. The low temperature spectra are thus thought not to be due to P-vacancy pair defects as proposed previously.


1992 ◽  
Vol 105-110 ◽  
pp. 477-484 ◽  
Author(s):  
C.S. Sundar ◽  
A. Bharathi ◽  
Yan Ching Jean ◽  
W.Y. Ching ◽  
X. Lu ◽  
...  

2011 ◽  
Vol 13 (4) ◽  
pp. 873 ◽  
Author(s):  
Aritomo Yamaguchi ◽  
Norihito Hiyoshi ◽  
Osamu Sato ◽  
Masayuki Shirai

1988 ◽  
Vol 21 (4) ◽  
pp. 1174-1176 ◽  
Author(s):  
C. De Rosa ◽  
G. Guerra ◽  
V. Petraccone ◽  
R. Centore ◽  
P. Corradini

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