Calorimetric properties

W. PocfSncckcr. Theoretical Investigations of the Heat Transfer at Quantitative DSC-Measurements and Its Influence on the Determination of the Thermal and Calorimetrical Properties. Thermochim. Acta 1991,187, 309-322. 

Hasl, G. and Pauly, H. 1971. Calorimetric properties of the bound water in protein solutions. Biophysik 7, 283-294 (German). 

The determination of in situ hydrates spawned a wave of research to measure hydrate properties needed for geological research and gas recovery. Several measurements were made of sonic velocity and thermal conductivity of hydrates in sediments (e.g., Stoll and Bryan, 1979 Pearson et al., 1984 Asher, 1987 Waite et al., 2005), while others measured the calorimetric properties (e.g., Rueff, 1985 Handa, 1986a,b,c,d Rueff et al 1988) needed to estimate dissociation energy. Davidson (1983) summarized hydrate properties as being similar to ice, with a few notable exceptions. Chapter 2 presents comparisons of physical property measurements of ice and hydrate. 

Calculation of the free enthalpy of reaction from group contributions, 752 Calorimetric properties, 109 Capacity... 

Liao, H.-J., Okechukwu, P. E., Damodaran, S., and Rao, M. A. 1996. Rheological and calorimetric properties of heated com starch-soybean protein isolate dispersions. J. Texture Stud. 27 403 18. 

Buitink, J., Walters-Vetucci, C., Hoekstra, F.A., and Leprince, O. Calorimetric properties of dehydrating pollen. Plant Physiol, 111, 235, 1996. 

The heat capacity quantifies the amount of thermal energy absorbed by a material upon heating, or released by it upon cooling. The heat capacity can be used to calculate all of the other thermodynamic properties, such as the enthalpy, entropy and Gibbs free energy, as functions of the temperature and pressure. The thermodynamic properties are often called calorimetric properties because they are usually measured by calorimetry [1-6]. 

A. phase transitions, volumetric properties, calorimetric properties, electrical/optical/magnetical properties, mechanical and acoustic properties. 

Finally, we should point out that, while the exceptions to the Third Law noted above may be a headache for scientists who measiue calorimetric properties of materials, they pose no practical problems in most chemical applications. Chemical reactions alone do not change nuclear spin, and in many cases do not alter isotope ratios significantly, so that configurational contributions to the entropy of reactants are normally balanced by those of the products in a reaction. In most cases these effects are thermodynamically minor or insignificant. 

FEL 03b] Feller J.F., Bourmaud A., Following of rheological and calorimetric properties... 

YAM Yamazaki, Y., Tada, T., and Kunugi, S., Effect of aciyhc acid incorporation on the pressure-temperature behavior and the calorimetric properties of poly(Y-isopropyl-aciylamide) in aqueous solutions. Colloid Polym. Sci., 278, 80, 2000. 

Solis, F.J., Weiss-Malik, R. Vernon, B. 2005, Local monomer activation model for phase behavior and calorimetric properties of LCST gel-forming polymers . Macromolecules, vol. 38, no. 10, pp. 4456-4464. 

Calorimetric Properties of Pure Matrices and 3 vol% Polypropylene Nanocomposites... 

Chapter 7 (Calorimetric Properties of Hydrothermal Solutions, V. M. Valyashko (Russia) and M. S. Gruszkiewicz (USA)), indicates the experimentally determined calorimetric quantities of considerable current use, gives a brief description of experimental methods for hydrothermal measurements and contains a summary table with information about the systems studied and the corresponding calorimetric measurements. 

According to the above derivation, molecular potential parameters ate clearly related to different parameters of the cubic equation of state. In contrast to many well-known EOSs such as SRK (Soave, 1972), the functional form of a derived in this work, shows the correct behavior of fluids at high temperatures (Segura et al., 2003). Since, (X function is continues at no anomalous behavior may be seen in predicted calorimetric properties at and near the critical point (Deiters, 1999). In addition, as a result of using a correct temperature dependent form for the covolume good agreement with experimental data at very high pressure has been obtained. 

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