Photocatalyzed deposition and concentration of soluble uranium(VI) from TiO2 suspensions

被引:68
作者
Chen, J
Ollis, DF
Rulkens, WH
Bruning, H
机构
[1] Wageningen Univ Agr, Dept Environm Technol, NL-6700 EV Wageningen, Netherlands
[2] N Carolina State Univ, Dept Chem Engn, Raleigh, NC 27695 USA
关键词
uranium; TiO(2) suspensions; photocatalytic decomposition;
D O I
10.1016/S0927-7757(98)00506-8
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
A reversible, photocatalytic reductive deposition of uranium on TiO(2) or Pt/TiO(2) occurs in deaerated U(VI)/EDTA solutions, accompanied by CO(2) released from the oxidation of EDTA. A maximum of 50-60% uranium(VI) is deposited and an ultimate CO(2) release equivalent to a single decarboxylation of EDTA was reached under our experiment conditions no matter how long the illumination time. In aerated solutions, no uranium deposited, but a large CO(2) release still occurred, presumably from EDTA mineralization. Nearly 100% of the deposited, reduced products from uranium(VI) on TiO(2). Pt/TiO(2) can be reoxidized and desorbed to regenerate dissolved uranium(VI) simply by solution exposure to air after illumination. The reductive deposition process can be repeated, indicating a potential cycle process. Modification of TiO(2) with platinum has only a slight influence on this reductive deposition of uranium on TiO(2). (C) 1999 Elsevier Science B.V. All rights reserved.
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页码:339 / 349
页数:11
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