Please use this identifier to cite or link to this item: https://doi.org/10.1016/j.cej.2011.12.054
Title: Removal of arsenite from aqueous solution by a zirconia nanoparticle
Authors: Zheng, Y.-M. 
Yu, L.
Wu, D.
Paul Chen, J. 
Keywords: Adsorption
Arsenite
Isotherm
Kinetics
Mechanism
Nanoparticle
Issue Date: 15-Apr-2012
Source: Zheng, Y.-M., Yu, L., Wu, D., Paul Chen, J. (2012-04-15). Removal of arsenite from aqueous solution by a zirconia nanoparticle. Chemical Engineering Journal 188 : 15-22. ScholarBank@NUS Repository. https://doi.org/10.1016/j.cej.2011.12.054
Abstract: This study evaluated the effectiveness of a readily prepared zirconia nanoparticle in removing arsenite (As(III)) from aqueous solution. It was demonstrated, without pre-oxidation of arsenite, the sorbent was highly effective for As(III) removal with a maximum adsorption capacity of 1.85. mmol-As/g. The sorbent had a high adsorption capacity toward As(III) at pH 5-10, and the optimal pH was around 8. The kinetics studies showed that most of the arsenite uptake occurred rapidly in the first 10. h, and the adsorption equilibrium was obtained within 48. h. The pseudo-second order model described the kinetics data well, and intraparticle diffusion model implied that two rate-limiting steps were involved in the sorption process. The adsorption isotherm data were well described by the Langmuir model. The adsorption was independent on ionic strength, implying As(III) may form inner-sphere complexes on the sorbent. The presence of humic acid or typical anions (e.g., fluoride, silicate, phosphate, and sulfate) did not greatly pose negative effects on the As(III) adsorption. However, the uptake of As(III) was hindered by the existence of bicarbonate. FTIR and XPS spectroscopic analyses suggested that hydroxyl and sulfate groups were involved in the As(III) uptake. Finally, an adsorption mechanism was proposed for better understanding on the adsorption of As(III). © 2011 Elsevier B.V..
Source Title: Chemical Engineering Journal
URI: http://scholarbank.nus.edu.sg/handle/10635/59186
ISSN: 13858947
DOI: 10.1016/j.cej.2011.12.054
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