Although the general conclusions remain unaffected, the following equations should read:
On the thermodynamics of alcohol—hydrocarbon solutions
✍ Scribed by Renon Henri; J.M. Prausnitz
- Publisher
- Elsevier Science
- Year
- 1967
- Tongue
- English
- Weight
- 682 KB
- Volume
- 22
- Category
- Article
- ISSN
- 0009-2509
No coin nor oath required. For personal study only.
✦ Synopsis
This article critically reconsiders a continuous linear association model based on the work of Flory and Scatchard. The model is used to reduce experimental equilibrium data for solutions of alcohols and saturated hydrocarbons;
special attention is given to recent extensive enthalpy data of Van Ness which cover a broad range of composition and temperature. The model gives an excellent representation of the experimental results for solutions concentrated in alcohol. However, for dilute solutions, or for high temperatures, where the degree of association is small, the assumptions used by Flory do not apply and the model fails.
📜 SIMILAR VOLUMES
For alcohol-ahphak hydrocarbon solutions, the athermal assoclakd solut~oon theory of Wlehe and Bagley 1s modlfied by mtroducmg a physical interaction term of the Scatchard-Hfidebrand type expression Good fits between the modlfied theory and experunental data for the excess Gibbs free energy of mlxmg
The modlfied Wiehe-Bagley expresslons for GE, He and VE of alcohol-Inert solvent solutions are apphed to alcohol-active solvent solutions Excellent agreement v&h expernnental data IS obtamed, even for HE and VB curves showing a maxunum and mnumum m the composition plots 'l&c alcohol polymerlzatron e
and A. Turner (Lancashire Tar Distillers Limited, Cadishead, Manchester, U.K.). Nitrogen adsorption data at 77°K and carbon dioxide adsorption at 195\*K on various coal and pitch solvent extract resin fractions is considered. The data is treated so that the monolayer capacity, the micropore volume,