کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
6309736 | 1618876 | 2014 | 6 صفحه PDF | دانلود رایگان |
- We studied sorption of organic compounds onto a humic acids-zeolitic tuff adduct.
- Sorption of hydrocarbon compounds was exothermic.
- Sorption of hydroxyl compounds was endothermic.
- Entropy increment during sorption may be related to release of solvating water.
- Sorption/desorption could be controlled by operating on the temperature.
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 (ÎadsHi) and isosteric entropy (ÎadsSi) of the process. For hydrocarbon compounds, toluene, cyclohexane and o-xylene, both ÎadsHi and ÎadsSi were negative, the process was exothermic. In contrast, for hydroxyl compounds, benzyl alcohol, phenol and cyclohexanol, ÎadsHi and ÎadsSi 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.
Journal: Chemosphere - Volume 95, January 2014, Pages 75-80