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    Recyclable high-affinity arsenate sorbents based on porous Fe2O3/La2O2CO3 composites derived from Fe-La-C frameworks
    Huo, JB (Huo, Jiang-Bo); Gupta, K (Gupta, Kiran); Lu, CY (Lu, Changyong); Hansen, HCB (Hansen, Hans Chr. Bruun); Fu, ML* (Fu, Ming-Lai)

    Efficient removal of aqueous arsenic is still a great challenge in particular for producing clean drinking water and for waste water treatment. To this end, a novel magnetic porous Fe-La composite, comprising La2O2CO3 and Fe2O3, was fabricated via a self-sacrificing template method based on bimetallic (Fe, La)-MOFs calcined at 550 °C. Batch adsorption results demonstrated that Fe-LaXY (X and Y represent the feeding mole ratio of Fe and La precursors) exhibited a maximum adsorption capacity of As(V) (241, 251 and 410 mg g-1 for Fe-La51, Fe-La21 and Fe-La11, respectively), and they also showed satisfactory adsorption kinetics, which can be ascribed to a strong coordination between La and arsenate species. Coexisting sorbates including carbonate, silicate, sulfate, and humic acid had a slight influence on adsorption performance of arsenate, while phosphate isostructural to arsenate gave severe interference. More importantly, the Fe-La11 could be easily separated from water due to its magnetism (7.0 emu g-1), and it also exhibited excellent recyclability (above 80% of removal efficiency at the fifth cycle) as well as stability in terms of release of Fe and La ions (< 0.5 mg L-1 at pH 4.0–10.0). Based on results from X-ray photoelectron spectroscopy (XPS), Powder X-ray diffraction (PXRD) and Raman spectroscopy, it is demonstrated that ligand exchange of surface hydroxyl groups and the formation of inner-sphere surface complexes are main responsible for the As(V) removal mechanism. Combining the magnetic properties, the absorption properties and the recyclability make Fe-LaXY derived from bimetallic MOFs promising sorbents for arsenate removal.

    Key words:Magnetic; Fe-La composite; Bimetallic MOFs; Adsorbent; Arsenic

    Volume:585

    Page:

    Journal:COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS

    https://doi.org/10.1016/j.colsurfa.2019.124018

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