TY - JOUR
T1 - Removal of Sb(V) from complex wastewater of Sb(V) and aniline aerofloat using Fe3O4–CeO2 absorbent enhanced by H2O2
T2 - efficiency and mechanism
AU - Wang, Xiaohui
AU - Deng, Renjian
AU - Wang, Chuang
AU - Long, Pei
AU - Hou, Baolin
AU - Chen, Weimin
AU - Chen, Fan
AU - Ren, Bozhi
AU - Hursthouse, Andrew
PY - 2024/8/31
Y1 - 2024/8/31
N2 - Effective elimination of heavy metals from complex wastewater is of great significance for industrial wastewater treatment. Herein, bimetallic adsorbent Fe3O4–CeO2 was prepared, and H2O2 was added to enhance Sb(V) adsorption by Fe3O4–CeO2 in complex wastewater of Sb(V) and aniline aerofloat (AAF) for the first time. Fe3O4–CeO2 showed good adsorption performance and could be rapidly separated by external magnetic field. After five adsorption/desorption cycles, Fe3O4–CeO2 still maintained good stability. The maximum adsorption capacities of Fe3O4–CeO2 in single Sb(V), AAF + Sb(V), and H2O2+AAF + Sb(V) systems were 77.33, 70.14, and 80.59 mg/g, respectively. Coexisting AAF inhibited Sb(V) adsorption. Conversely, additional H2O2 promoted Sb(V) removal in AAF + Sb(V) binary system, and made the adsorption capacity of Fe3O4–CeO2 increase by 14.90%. H2O2 could not only accelerate the reaction rate, but also reduce the optimal amount of adsorbent from 2.0 g/L to 1.2 g/L. Meanwhile, coexisting anions had little effect on Sb(V) removal by Fe3O4–CeO2+H2O2 process. The adsorption behaviors of Sb(V) in three systems were better depicted by pseudo-second-order kinetics, implying that the chemisorption was dominant. The complexation of AAF with Sb(V) hindered the adsorption of Sb(V) by Fe3O4–CeO2. The complex Sb(V) was oxidized and decomposed into free state by hydroxyl radicals produced in Fe3O4–CeO2+H2O2 process. Then the free Sb(V) was adsorbed by Fe3O4–CeO2 mostly through outer-sphere complexation. This work provides a new tactic for the treatment of heavy metal-organics complex wastewater.
AB - Effective elimination of heavy metals from complex wastewater is of great significance for industrial wastewater treatment. Herein, bimetallic adsorbent Fe3O4–CeO2 was prepared, and H2O2 was added to enhance Sb(V) adsorption by Fe3O4–CeO2 in complex wastewater of Sb(V) and aniline aerofloat (AAF) for the first time. Fe3O4–CeO2 showed good adsorption performance and could be rapidly separated by external magnetic field. After five adsorption/desorption cycles, Fe3O4–CeO2 still maintained good stability. The maximum adsorption capacities of Fe3O4–CeO2 in single Sb(V), AAF + Sb(V), and H2O2+AAF + Sb(V) systems were 77.33, 70.14, and 80.59 mg/g, respectively. Coexisting AAF inhibited Sb(V) adsorption. Conversely, additional H2O2 promoted Sb(V) removal in AAF + Sb(V) binary system, and made the adsorption capacity of Fe3O4–CeO2 increase by 14.90%. H2O2 could not only accelerate the reaction rate, but also reduce the optimal amount of adsorbent from 2.0 g/L to 1.2 g/L. Meanwhile, coexisting anions had little effect on Sb(V) removal by Fe3O4–CeO2+H2O2 process. The adsorption behaviors of Sb(V) in three systems were better depicted by pseudo-second-order kinetics, implying that the chemisorption was dominant. The complexation of AAF with Sb(V) hindered the adsorption of Sb(V) by Fe3O4–CeO2. The complex Sb(V) was oxidized and decomposed into free state by hydroxyl radicals produced in Fe3O4–CeO2+H2O2 process. Then the free Sb(V) was adsorbed by Fe3O4–CeO2 mostly through outer-sphere complexation. This work provides a new tactic for the treatment of heavy metal-organics complex wastewater.
KW - enhanced adsorption
KW - Sb(V)
KW - aniline aerofloat
KW - H2O2 oxidation
KW - complex wastewater
U2 - 10.1016/j.jenvman.2024.121610
DO - 10.1016/j.jenvman.2024.121610
M3 - Article
SN - 0301-4797
VL - 365
JO - Journal of Environmental Management
JF - Journal of Environmental Management
M1 - 121610
ER -