Temperature Dependence of Thermodynamic Properties of Thallium Chloride and Thallium Bromide

Author(s):  
H. B. Kavanoz

AbstractThermodynamic properties as lattice parameters, thermal expansion, heat capacities

2019 ◽  
Vol 33 (23) ◽  
pp. 1950271 ◽  
Author(s):  
Y. I. Aliyev ◽  
Y. G. Asadov ◽  
A. O. Dashdemirov ◽  
R. D. Aliyeva ◽  
T. G. Naghiyev ◽  
...  

The Ag[Formula: see text]Cu[Formula: see text]Se and Ag[Formula: see text]Cu[Formula: see text]Se compounds have been synthesized and grown as single crystals. High-temperature X-ray diffraction method was used to study polymorphic transformations. It is shown that the Ag[Formula: see text]Cu[Formula: see text]Se crystals of high-temperature FCC modification are decomposed into Ag2Se and AgCuSe when the temperature decreases below T = 488 K and Ag[Formula: see text]Cu[Formula: see text]Se is decomposed into Cu2Se and AgCuSe when the temperature decreases below T = 540 K. Transformations in both compounds are reversible. Crystalline parameters are obtained and the temperature dependence of the lattice parameters for each phase is built.


1993 ◽  
Vol 07 (01n03) ◽  
pp. 895-898
Author(s):  
S. MORI ◽  
T. KANOMATA ◽  
H. YAMAUCHI ◽  
H. YOSHIDA ◽  
T. KANEKO

The temperature dependence of the magnetization ,σ, the pressure effect on the Curie temperature, TC, and the thermal expansion for MnZnSb are measured. The value of dTC/dp is +3.6 K/kbar. Negative exchange strictions are observed for the lattice parameters a and c. The results are discussed using a phenomenological theory based on the molecular field theory.


Author(s):  
Sumit K. Kumar ◽  
Rainer Kurz ◽  
John P. O’Connell

In the design and testing of gas compressors, the correct determination of the thermodynamic properties of the gas. such as enthalpy, entropy and density from pressure, temperature and composition, plays an important role. Due to the wide range of conditions encountered, pressure, specific volume and temperature (p-v-T) equations of state (EOS) and ideal gas heat capacities, along with measured data, are used to determine the isentropic efficiency of a compressor configuration and to model the actual behavior of real gases and compressors. There are many possible model choices. The final selection should depend on the applicability of the EOS to the gas and the temperature dependence of the heat capacities, as well as the particular process of interest along with the range of pressures and temperatures encountered. This paper compares the thermodynamic properties from five commonly used equations in the gas compressor industry: the Redlich-Kwong (RK), Redlich-Kwong-Soave (RKS), Peog-Robinson (PR), Benedict-Webb-Rubin-Starling (BWRS), and Lee-Kesler-Plocker (LKP) models. It also compares them with a high accuracy EOS for methane from Wagner and Setzmann in the common range for gas compressors. The validity of a linear temperature dependence for ideal gas heat capacities is also evaluated. The objective was to determine if the models give significant differences in their predicted efficiencies. It was found that different EOS gave somewhat different enthalpy changes for methane, ethane and nitrogen for real compressions. This appeared to be connected to the different densities given by the models. Interestingly, the isentropic enthalpy changes are quite similar, suggesting that the effect is canceled out when two properties are involved. However, since the efficiency is the ratio of isentropic enthalpy change to actual enthalpy change, the EOS yield different efficiencies. These differences are on the same order as the typical tolerances allowed for prediction and testing of industrial gas compressors (3 to 5%) and comparisons with the highly accurate equation of state for pure methane from Wagner and Setzmann (1991) showed similar differences. Commonly, the ideal gas heat capacity is assumed linear in temperature from 10 to 150°C (50 to 300°F). Comparison of this form with a quadratic expression from the literature and the highly accurate equation of Wagner and Setzmann for methane, showed insignificant differences among the methods for temperatures up to 600°K (1080°R).


Author(s):  
A. Kupsch ◽  
D. C. Meyer ◽  
P. Gille ◽  
P. Paufler

AbstractThe temperature dependence of lattice parameters


The thermodynamic properties of H 2 O ice and D 2 O ice have been analysed in terms of the effective harmonic spectrum of lattice vibrations. In this approximation the vibrations are treated as harmonic, but with frequencies which are both volume and temperature dependent. Analysis of the heat capacity then gives properties of the effective spectrum at 0 °K, and the average temperature dependence of the spectrum at constant volume. It has been shown that the parts of the spectrum associated with translational and librational motion of the molecules are distinct, and their contributions to the thermodynamic properties may be separated. The moments v -2 , v -1 , v , v 2 , v 4 and v 6 together with the geometric mean frequency v g have been derived for the separate parts of the spectrum. The reduced librational moments, ( v n L ) 1/n , are independent of n within the experimental uncertainty. This shows that the spectrum of librational frequencies consists of a fairly sharp and symmetrical band. From the very low temperature data the coefficients of the terms in v 2 , v 4 and v 6 in the low frequency expansion of the translational spectrum have been derived, together with the position and approximate weight of the first peak in the spectrum. The ratios of the moments for H20 and D 2 O show that the intermolecular forces are stronger for D 2 O than for H 2 O. From the thermal expansion data, by analysing the Gruneisen function y( T, V ) = βV/X s C p , values for some of the parameters y( n ) = — (l/ n )dln v n /dln V , which describe the volume dependence of the moments, have been obtained for the separate parts of the spectrum. These are useful in estimating the volume dependence of various crystal properties. The properties of the effective harmonic spectrum and its average total temperature dependence (including thermal expansion effects) are in good agreement with the results of a variety of spectroscopic experiments. The moments derived from the thermodynamic data have been used to calculate the mean square amplitudes of vibration of O, H and D atoms and the results are in good agreement with the results of X-ray and neutron scattering experiments.


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