TY - JOUR
T1 - Removal of Arsenite from Water by Ce-Al-Fe Trimetal Oxide Adsorbent
T2 - Kinetics, Isotherms, and Thermodynamics
AU - Sun, Cuizhen
AU - Qiu, Jinwei
AU - Zhang, Zhibin
AU - Marhaba, Taha F.
AU - Zhang, Yanhao
N1 - Publisher Copyright:
© 2016 Cuizhen Sun et al.
PY - 2016
Y1 - 2016
N2 - Ce-Al-Fe trimetal oxide adsorbent was prepared. The morphology characteristics of the new adsorbent were analysed by the transmission electron microscope (SEM) method. The SEM results implied its ability in the adsorption of As (III). To verify the analyses, bench-scale experiments were performed for the removal of As (III) from water. In the experiments of adsorption, As (III) adsorption capacity of the trimetal oxide adsorbent was presented significantly higher than activated aluminium oxide and activated carbon. As (III) adsorption kinetics resembled pseudo-second-order adsorption mode. When initial As (III) concentration was 3, 8, and 10 mg·L-1, the maximum adsorption capacity achieved was 1.48, 3.73, and 5.12 mg·g-1, respectively. In addition, the experimental adsorption data were described well by the Freundlich adsorption isotherm model at 20, 30, and 40°C. The enthalpy change (Δ S), the standard free energy (Δ G), and entropy change (Δ H) indicated that the nature of As (III) adsorption was exothermic and spontaneous with increasing randomness on the interface of solid and liquid. And the adsorption mechanism can be interpreted as chemisorption with As (III) multilayer coverage formation on the adsorbent surface.
AB - Ce-Al-Fe trimetal oxide adsorbent was prepared. The morphology characteristics of the new adsorbent were analysed by the transmission electron microscope (SEM) method. The SEM results implied its ability in the adsorption of As (III). To verify the analyses, bench-scale experiments were performed for the removal of As (III) from water. In the experiments of adsorption, As (III) adsorption capacity of the trimetal oxide adsorbent was presented significantly higher than activated aluminium oxide and activated carbon. As (III) adsorption kinetics resembled pseudo-second-order adsorption mode. When initial As (III) concentration was 3, 8, and 10 mg·L-1, the maximum adsorption capacity achieved was 1.48, 3.73, and 5.12 mg·g-1, respectively. In addition, the experimental adsorption data were described well by the Freundlich adsorption isotherm model at 20, 30, and 40°C. The enthalpy change (Δ S), the standard free energy (Δ G), and entropy change (Δ H) indicated that the nature of As (III) adsorption was exothermic and spontaneous with increasing randomness on the interface of solid and liquid. And the adsorption mechanism can be interpreted as chemisorption with As (III) multilayer coverage formation on the adsorbent surface.
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U2 - 10.1155/2016/8617219
DO - 10.1155/2016/8617219
M3 - Article
AN - SCOPUS:84979760212
SN - 2090-9063
VL - 2016
JO - Journal of Chemistry
JF - Journal of Chemistry
M1 - 8617219
ER -