## Abstract An analytical technique based on the method of least squares has been developed to fit experimental second virial coefficients to the functional form derived from the LennardβJones (6β12) potential. Both the functional form and the normal equations of the least squares fit are rigorousl
An empirical correlation of second virial coefficients
β Scribed by Constantine Tsonopoulos
- Publisher
- American Institute of Chemical Engineers
- Year
- 1974
- Tongue
- English
- Weight
- 1011 KB
- Volume
- 20
- Category
- Article
- ISSN
- 0001-1541
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β¦ Synopsis
Abstract
A new correlation of second virial coefficients of both polar and nonpolar systems is presented. It uses the PitzerβCurl correlation for nonpolar compounds, but in a modified form. The second virial coefficient of nonhydrogen bonding compounds (ketones, acetaldehyde, acetonitrile, ethers) and weakly hydrogen bonding compounds (phenol) is fitted satisfactorily with only one additional parameter per compound, which is shown to be a strong function of the reduced dipole moment. Two parameters are needed for hydrogen bonding compounds (alcohols, water), but for alcohols, one parameter has been kept constant and the other expressed as a function of the reduced dipole moment. The extension of the correlation to mixtures is satisfactory, direct, and involves only one coefficient per binary.
π SIMILAR VOLUMES
## Abstract One of the most readily available characteristics of a polymer sample is its intrinsic viscosity in a particular solvent. This datum can often be estimated reasonably from a single relative viscosity measurement. A number of theories permit the calculation of the second virial coefficie