## Abstract The structure‐retention relationship in reversed phase micro high performance liquid chromatography has been investigated for substituted alkylbenzene derivatives. The correlation between van der Waals volume and retention data was completely linear and any deviation from this relation
Correlations between retention volumes and the interfacial tension of the two phases in liquid—liquid chromatography
✍ Scribed by C. Eon; B. Novosel; G. Guiochon
- Publisher
- Elsevier Science
- Year
- 1973
- Tongue
- English
- Weight
- 832 KB
- Volume
- 83
- Category
- Article
- ISSN
- 1873-3778
No coin nor oath required. For personal study only.
✦ Synopsis
It is shown that the interfacial tension between the mobile and the stationary phases reflects the partition properties of the two phases, and this can be taken as a criteria of choice of the systems used in liquid-liquid chromatography. A semi-theoretical treatment shows that the Gibbs free energy of partition of the solute between the two phases is quasi-proportional to the surface tension, pro-'vided that the solubility of each phase in the other is small. Such behaviour is observed with organic solvent-water systems for solvents that give a surface tension greater than 20-25 dynes/cm. As mixtures of mobile phases behave in the same way, the retention times in programmed gradient analysis can be predicted.
📜 SIMILAR VOLUMES
The rule of intersection point between retention of homologues and column temperature in reversed-phase liquid chromatography is reported, based on the thermodynamic theory, with the basic equation of the retention in reversed-phase liquid chromatography, proposed by Vigh and others. We have derived