Reducing the particle size of the adsorbents is an efficient way of manipulating the adsorption/desorption characteristics of the adsorbate. Therefore, we tested the effect of micronisation of two natural clinoptilolite specimens on the ammonium (NH4+) adsorption/desorption. One g of adsorbent equilibrated with 20 mL solution containing 0-600 mg NH4+ L-1 at constant ionic strength. The adsorbate was extracted by molar KCl solution. Sorption kinetic was studied at 50, 300 and 600 mg L-1 concentrations for 5, 10, 20, 30 min; 1, 2, 4, 8, 16, and 24 h. The sorption data well confirmed both Freundlich and Langmuir sorption models. The Langmuir adsorption capacities (16667 mg kg-1) of both zeolites were similar but the sorption maximum of Gordes zeolite with 250-500 µm was smaller (14286 mg kg-1). The particle size dependency was apparent for Gordes zeolite. The desorption ratio was dependent on initial NH4+ concentration, particle size, and zeolite type. In general, there was an increase in desorption ratio up to 300-400 mg L-1 initial ammonium concentrations. Results of the kinetic study indicated that the adsorption data better fitted the pseudo second-order kinetic model than the Elovich model. Zeolite having well-structured porous nature can be used in larger particle size to scavenge NH4+ from the polluted water sources, but initial sorption rate can be improved by particle size reduction. The sorption data indicated that the zeolites may be used for NH4+ removal from the polluted water sources or improving the sorption capacity of coarse soils to alleviate ammonium leaching problem.
Süleyman Demire Üniversitesi BAP Koordinasyon Birimi
4526-YL2-15
The funding for this study provided by Süleyman Demirel University Research Foundation with project number 4526-YL2-15 is gratefully appreciated.
4526-YL2-15
Primary Language | English |
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Subjects | Agricultural, Veterinary and Food Sciences |
Journal Section | Original Papers |
Authors | |
Project Number | 4526-YL2-15 |
Publication Date | December 23, 2019 |
Submission Date | November 26, 2019 |
Acceptance Date | December 18, 2019 |
Published in Issue | Year 2019 Volume: 3 Issue: 2 |