| Literature DB >> 24206836 |
Vincenzo Leone1, Pasquale Iovino, Stefano Salvestrini, Sante Capasso.
Abstract
Sorption isotherms from water solutions for toluene, cyclohexane, o-xylene, benzyl alcohol, phenol and cyclohexanol onto a humic acid-zeolite adduct were determined at 4, 14, 24 and 34 °C and utilized to calculate the isosteric enthalpy (ΔadsHi) and isosteric entropy (ΔadsSi) of the process. For hydrocarbon compounds, toluene, cyclohexane and o-xylene, both ΔadsHi and ΔadsSi were negative, the process was exothermic. In contrast, for hydroxyl compounds, benzyl alcohol, phenol and cyclohexanol, ΔadsHi and ΔadsSi were positive, the increase in entropy possibly reflecting the release of water molecules during sorption. The results suggest that sorption/desorption of either class of compounds could be controlled by operating on the temperature.Entities:
Keywords: Humic acids-zeolitic tuff adduct; Isosteric enthalpy; Non-ionic organic pollutants; Sorption
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Year: 2013 PMID: 24206836 DOI: 10.1016/j.chemosphere.2013.08.019
Source DB: PubMed Journal: Chemosphere ISSN: 0045-6535 Impact factor: 7.086