Interactions of rare earth elements with bacteria and organic ligands

被引:46
作者
Ozaki, T [1 ]
Suzuki, Y
Nankawa, T
Yoshida, T
Ohnuki, T
Kimura, T
Francis, AJ
机构
[1] Japan Atom Energy Res Inst, Adv Sci Res Ctr, Tokai, Ibaraki 3191195, Japan
[2] Nagoya Univ, Dept Mat Phys & Energy Engn, Nagoya, Aichi 4648603, Japan
[3] Japan Atom Energy Res Inst, Dept Mat Sci, Tokai, Ibaraki 3191195, Japan
[4] Brookhaven Natl Lab, Dept Environm Sci, Upton, NY 11973 USA
关键词
rare earth elements; bacteria; organic ligands; coordination environment; biodegradation;
D O I
10.1016/j.jallcom.2005.04.142
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
We investigated the interactions of rare earth elements (REEs) Eu(III) and/or Ce(III, IV) with the common soil bacterium Pseudomonas fluorescens and organic ligands, such as malic acid, citric acid, a siderophore (DFO), cellulose, chitin, and chitosan. Malic acid formed complexes with Eu(111), but degradation of malic acid was observed when the ratio of malic acid to Eu(IH) was higher than 100. Citric acid formed a stoichiometric complex with Eu(III) that was not degraded by R fluorescens. Adsorption of Eu(III) from the DFO complex occurred as a free ion dissociated from DFO and not as the Eu(III)-DFO complex. Cerium(III) was oxidized to Ce(IV) during complexation with DFO to form the Ce(IV)-DFO complex. Time-resolved laser-induced fluorescence spectroscopy (TRLFS) analysis showed that cellulose, chitin, and chitosan, respectively, formed a weak complex, an inner-spherical complex, and an outer-spherical complex with Eu(III). This method also demonstrated that the coordination environment of Eu(III) adsorbed on P fluorescens possessed similar characteristics to that of chitin, and revealed that adsorption of Eu(III) on P. fluorescens was through a multidentate and predominantly inner-spherical coordination. (c) 2005 Elsevier B.V. All rights reserved.
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页码:1334 / 1338
页数:5
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