Gas-phase densities of the systems: pure water, methane, n-hexane, n-octane, and benzene were measured at temperatures from 523.15 K to 673.15 K and at pressures up to approximately 100 MPa. Second and third virial coefficients were determined for each system, and the cross virial coefficients were
Volumetric properties of supercritical ethanen-n-heptane mixtures: The isothermal compressibility in the critical region
✍ Scribed by P. Ehrlich; P. C. Wu
- Publisher
- American Institute of Chemical Engineers
- Year
- 1973
- Tongue
- English
- Weight
- 570 KB
- Volume
- 19
- Category
- Article
- ISSN
- 0001-1541
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✦ Synopsis
Abstract
The isothermal compressibility (at constant composition x) k~T,x~, was calculated in the neighborhood of the critical locus for seven mixtures containing 3.5 to 19.6 mole % heptane and analyzed in terms of the reduced pressure variable σ = (P – P̂)/P̂ where P̂ is the pressure at which k~T,x~ becomes very large. The data can be represented by the equation k~T,x~ = const. σ^−λ^ along the critical isotherm and one near it and by the locus P̂(T). λ was found to be a strong function of x. The divergence of the isothermal compressibility of the mixtures near the critical locus is in conflict with predictions from classical equations of state but in accordance with modern concepts of the critical region.
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