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Removal of tetracycline from water by Fe-Mn binary oxide.

Abstract

Significant concerns have been raised over the presence of antibiotics including tetracyclines in aquatic environments. A series of Fe-Mn binary oxide with different Fe:Mn molar ratios was synthesized by a simultaneous oxidation and coprecipitation process for TC removal. Results showed that Fe-Mn binary oxide had higher removal efficiency than that of hydrous iron oxide and hydrous manganese oxide, and that the oxide with a Fe:Mn molar ratio of 5:1 was the best in removal than other molar ratios. The tetracycline removal was highly pH dependent. The removal of tetracycline decreased with the increase of initial concentration, but the absolute removal quantity was more at high concentration. The presence of cations and anions such as Ca2+, Mg2+, CO3(2-) and SO4(2-) had no significant effect on the tetracycline removal in our experimental conditions, while SiO3(2-) and PO4(3-) had hindered the adsorption of tetracycline. The mechanism investigation found that tetracycline removal was mainly achieved by the replacement of surface hydroxyl groups by the tetracycline species and formation of surface complexes at the water/oxide interface. This primary study suggests that Fe-Mn binary oxide with a proper Fe:Mn molar ratio will be a very promising material for the removal of tetracycline from aqueous solutions.

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  • Authors

    Liu H, Yang Y, Kang J, Fan M, Qu J

    Institution

    State Key Laboratory of Environmental Aquatic Chemistry, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085, China. hjliu@rcees.ac.cn

    Source

    Journal of environmental sciences (China) 24:2 2012 pg 242-7

    MeSH

    Chromatography, High Pressure Liquid
    Ferric Compounds
    Hydrogen-Ion Concentration
    Ions
    Iron
    Manganese Compounds
    Organic Chemicals
    Oxides
    Spectroscopy, Fourier Transform Infrared
    Tetracycline
    Water Purification

    Pub Type(s)

    Evaluation Studies
    Journal Article
    Research Support, Non-U.S. Gov't

    Language

    eng

    PubMed ID

    22655383