Fluctuation theory of hydrogen bonding in near-critical fluids
β Scribed by Boris A. Veytsman; Ram B. Gupta
- Publisher
- American Institute of Chemical Engineers
- Year
- 1996
- Tongue
- English
- Weight
- 631 KB
- Volume
- 42
- Category
- Article
- ISSN
- 0001-1541
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β¦ Synopsis
Abstract
Recent experiments indicate that the number of hydrogen bonds in solutions increases in the critical region of the solvent. This effect can be explained by the density fluctuations near the critical point. A theory of this unusual effect is developed. The theoretical predictions are compared with the experimental data on hydrogen bonding between perfluoroβtertβbutanol and dimethyl ether in supercritical sulfur hexafluoride. The theory requires no adjustable parameters and is in excellent agreement with the experimental data. Possible applications of this effect for hydrogenβbonding solutions and polymer mixtures are discussed.
π SIMILAR VOLUMES
The possibility of a complete thermodynamic description of the behaviour of dilute solutions on the basis of the Krichevskii function J = (β p/β x) β V,T , which performs well in the near-critical region, is hampered by its weak temperature dependence. A previous determination of the solubility of C
## Hydrogenation of palm oil in near-critical and supercritical propane Palm oil was hydrogenated in a single-phase mixture with propane and hydrogen. This was done in a small (0.5 ml), continuous fixed-bed reactor, using a 1% Pd/C catalyst. Temperature (65-135 o C), H 2 /TG ratio (4-50 mol/mol) a