Sorption of Cyclohexylamine by Montmorillonites
- 1 January 1970
- journal article
- research article
- Published by Wiley in Israel Journal of Chemistry
- Vol. 8 (6), 935-945
- https://doi.org/10.1002/ijch.197000119
Abstract
Infrared spectra indicate that protonation of cyclohexylamine sorbed by montmorillonite depends upon the interlayer cations and the origin of the lattice charge. No protonation occurs with Cs and very little with Na, but with all the other interlayer cations studied cyclohexylammonium ions are formed. Protonation occurs more readily if the lattice charge originates in the octahedral layer. Various associations are inferred between interlayer hydroxides, hydrated cations, ionic and molecular cyclohexylamine and water. The sorption of cyclohexylamine is compared with that of aniline and the validity of the concept “surface acidity” is questioned.This publication has 4 references indexed in Scilit:
- Effect of Acidity in Montmorillonite Interlayers on the Sorption of Aniline DerivativesClays and Clay Minerals, 1969
- Reactivity of Montmorillonite Surfaces with Weak Organic BasesSoil Science Society of America Journal, 1968
- Sorption of Aniline by MontmorilloniteIsrael Journal of Chemistry, 1968
- Infrared Absorption Spectrometry in Clay StudiesClays and Clay Minerals, 1967