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In relation to this article, we declare that there is no conflict of interest.
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Received February 24, 2005
Accepted August 12, 2005
articles This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/bync/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
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On the information and methods for calculation of Sanchez-Lacombe and group-contribution lattice-fluid equations of state

1Mathematics Research Group, School of Science, Beijing Jiaotong University, Beijing, 100044, China 2State Key Laboratory of Chemical Resource Engineering, Beijing University of Chemical Technology, Box35, Beijing, 100029, China
leizhg@mail.buct.edu.cn
Korean Journal of Chemical Engineering, January 2006, 23(1), 102-107(6), 10.1007/BF02705699
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Abstract

The algorithms for calculation of densities from Sanchez-Lacombe (S-L) and group-contribution latticefluid (GCLF) equations of state have been put forward, respectively. From the S-L equation of state the relationship between the equation characteristic parameters and critical properties was deduced, and the influence of molecular weight of the polymers on critical properties was investigated. However, for the GCLF equation of state, it was surprising to find that there as many as four roots were found at a saturation temperature and pressure for gases, while still two roots above the critical temperature. For polymers, only two roots could be found. So the formerly accepted consistency between the magnitude of the density and vapor or liquid phase is not applicable yet. A way about how to identify the root and corresponding phase was suggested.

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