TY - JOUR
T1 - Sorption of trivalent cerium by a mixture of microbial cells and manganese oxides
T2 - Effect of microbial cells on the oxidation of trivalent cerium
AU - Ohnuki, Toshihiko
AU - Jiang, Mingyu
AU - Sakamoto, Fuminori
AU - Kozai, Naofumi
AU - Yamasaki, Shinya
AU - Yu, Qianqian
AU - Tanaka, Kazuya
AU - Utsunomiya, Satoshi
AU - Xia, Xiaobin
AU - Yang, Ke
AU - He, Jianhua
N1 - Funding Information:
This work was performed with the approval of Photon Factory, KEK (Proposal Nos. 2007G522, 2007G663 and 2009G676) and Shanghai Synchrotron Radiation Facility for alternative use after Fukushima Daiichi Power Plant Accident. Part of the present study was supported by a Grant-in-Aid of the Ministry of Education, Culture, Sports, Science and Technology to T.O. We thank associate editor, Alfonso Mucci and anonymous reviewers for their valuable comments that helped to improve the manuscript.
Publisher Copyright:
© 2015 Elsevier Ltd.
PY - 2015/8/5
Y1 - 2015/8/5
N2 - Sorption of Ce by mixtures of synthetic Mn oxides and microbial cells of Pseudomonas fluorescens was investigated to elucidate the role of microorganisms on Ce(III) oxidative migration in the environment. The mixtures, upon which Ce was sorbed following exposure to solutions containing 1.0×10-4 or 1.0×10-5molL-1Ce(III), were analyzed by scanning electron microscopy energy dispersive X-ray spectroscopy (SEM-EDS) and micro-X-ray fluorescence (micro-XRF) at synchrotron facilities. A Ce LIII-edge micro XANES spectra analysis was also performed to determine the oxidation states of Ce adsorbed to the Mn oxides and microbial cells in the mixtures. The distribution ratios (Kd) of Ce between the individual solids and solution increased with increasing pH of the solution, and was nearly the same in mixtures containing varying amounts of microbial cells. SEM-EDS and micro-XRF analyses showed that Ce was sorbed by both MnO2 and microbial cells (1.7×10-1 or 3.3×10-1gL-1). In addition, nano-particles containing Ce and P developed on the surface of the microbial cells. XANES analysis showed that lower fractions of Ce(III) were oxidized to Ce(IV) in the mixtures containing greater amounts of microbial cells. Micro-XANES analysis revealed that Ce was present as Ce(III) on the microbial cells and as Ce(IV) on Mn oxides. These results strongly suggest that the association of Ce(III) with the microbial cell surface and the formation of Ce phosphate nano-particles are responsible for suppressing the oxidation of Ce(III) to Ce(IV) in the mixtures.
AB - Sorption of Ce by mixtures of synthetic Mn oxides and microbial cells of Pseudomonas fluorescens was investigated to elucidate the role of microorganisms on Ce(III) oxidative migration in the environment. The mixtures, upon which Ce was sorbed following exposure to solutions containing 1.0×10-4 or 1.0×10-5molL-1Ce(III), were analyzed by scanning electron microscopy energy dispersive X-ray spectroscopy (SEM-EDS) and micro-X-ray fluorescence (micro-XRF) at synchrotron facilities. A Ce LIII-edge micro XANES spectra analysis was also performed to determine the oxidation states of Ce adsorbed to the Mn oxides and microbial cells in the mixtures. The distribution ratios (Kd) of Ce between the individual solids and solution increased with increasing pH of the solution, and was nearly the same in mixtures containing varying amounts of microbial cells. SEM-EDS and micro-XRF analyses showed that Ce was sorbed by both MnO2 and microbial cells (1.7×10-1 or 3.3×10-1gL-1). In addition, nano-particles containing Ce and P developed on the surface of the microbial cells. XANES analysis showed that lower fractions of Ce(III) were oxidized to Ce(IV) in the mixtures containing greater amounts of microbial cells. Micro-XANES analysis revealed that Ce was present as Ce(III) on the microbial cells and as Ce(IV) on Mn oxides. These results strongly suggest that the association of Ce(III) with the microbial cell surface and the formation of Ce phosphate nano-particles are responsible for suppressing the oxidation of Ce(III) to Ce(IV) in the mixtures.
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U2 - 10.1016/j.gca.2015.04.043
DO - 10.1016/j.gca.2015.04.043
M3 - Article
AN - SCOPUS:84929340254
SN - 0016-7037
VL - 163
SP - 1
EP - 13
JO - Geochimica et Cosmochimica Acta
JF - Geochimica et Cosmochimica Acta
ER -