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      Pure and Pseudo-pure Fluid Thermophysical Property Evaluation and the Open-Source Thermophysical Property Library CoolProp

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          Abstract

          Over the last few decades, researchers have developed a number of empirical and theoretical models for the correlation and prediction of the thermophysical properties of pure fluids and mixtures treated as pseudo-pure fluids. In this paper, a survey of all the state-of-the-art formulations of thermophysical properties is presented. The most-accurate thermodynamic properties are obtained from multiparameter Helmholtz-energy-explicit-type formulations. For the transport properties, a wider range of methods has been employed, including the extended corresponding states method. All of the thermophysical property correlations described here have been implemented into CoolProp, an open-source thermophysical property library. This library is written in C++, with wrappers available for the majority of programming languages and platforms of technical interest. As of publication, 110 pure and pseudo-pure fluids are included in the library, as well as properties of 40 incompressible fluids and humid air. The source code for the CoolProp library is included as an electronic annex.

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          Second viscosity and thermal-conductivity virial coefficients of gases: Extension to low reduced temperature

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            Motions of Molecules in Liquids: Viscosity and Diffusivity

            The fluidity of a simple liquid is proportional to its degree of expansion over the volume, V(0), at which its molecules are so crowded as to inhibit self-diffusion and viscous (as distinguished from plastic) flow. The equation of proportionality is 1/eta = B[(V - V(0))/V(0)] where eta is the viscosity and V is the molal volume. Values of B are the same for normal paraffins from C(3)H(8) to C(7)H(16) and then decrease progressively as the paraffin lengths increase. Values for other liquids, C(6)H(6), CCl(4), P(4), CS(2), CHCl(3), and Hg, appear to vary with repulsive forces. liquids can be moderately fluid when expanded by less than 10 percent; this shows the unreality of some theoretical treatments of the liquid state. Diffusivity begins from the temperature at which V equals V(0) and can be correlated for temperature dependence, and for solute-solvent interrelations.
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              Author and article information

              Journal
              Ind Eng Chem Res
              Ind Eng Chem Res
              ie
              iecred
              Industrial & Engineering Chemistry Research
              American Chemical Society
              0888-5885
              1520-5045
              13 January 2014
              12 February 2014
              : 53
              : 6
              : 2498-2508
              Affiliations
              []Energy Systems Research Unit, University of Liège , Liège, Belgium
              []Department of Mechanical Engineering, Technical University of Denmark , Kongens Lyngby, Denmark
              Author notes
              Article
              10.1021/ie4033999
              3944605
              24623957
              91d7c0a9-5408-4d1c-b71b-5a9289a481e2
              Copyright © 2014 American Chemical Society
              History
              : 10 October 2013
              : 13 January 2014
              : 02 January 2014
              Categories
              Article
              Custom metadata
              ie4033999
              ie-2013-033999

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