Uranyl-citrate speciation in acidic aqueous solutions -: an XAS study between 25 and 200 °C

被引:37
作者
Bailey, EH
Mosselmans, JFW
Schofield, PF
机构
[1] Univ Nottingham, Sch Biosci, Nottingham NG7 2RD, England
[2] CCLRC, Daresbury Lab, Warrington WA4 4AD, Cheshire, England
[3] Nat Hist Museum, Dept Mineral, London SW7 5BD, England
关键词
uranium; citrate; structure; stability; high temperature; XAS;
D O I
10.1016/j.chemgeo.2004.10.011
中图分类号
P3 [地球物理学]; P59 [地球化学];
学科分类号
0708 ; 070902 ;
摘要
Speciation of uranium(VI) in citrate (2-hydroxypropane-1,2,3-tricarboxylic acid) solutions between 25 and 200 degrees C, at pH values between 0.8 and 3.7 and at citrate[U ratios between 0.5 and 50 has been investigated using U L-III-edge X-ray absorption spectroscopy (XAS). At 25 degrees C and Cit/U > 2, we observed a decrease in U-O-eq bond distance as pH was increased, accompanied by an increase in the number of coordinating O atoms around the uranyl ion. This indicates a speciation change due to polymerisation of the monomer [UO2(Cit)](-), present around pH 1, to form the dimer [(UO2)(2)(Cit)(2)](2-) at pH 1.8 and above. The dimer [(UO2)(2)(Cit)(2)](2-) is bridged via the alcohol groups of the citrate ligand. At Cit/U <= 2, hydrolysis species appear to dominate at room temperature. Upon heating, no speciation changes were observed, however evidence from U-O-eq bond distances and coordination numbers strongly suggests that uranyl-citrate species are present in solution up to 200 degrees C. Above 200 degrees C, decomposition of the citrate ligand was observed. The existence of the uranyl-citrate species in the temperature range 25-200 degrees C demonstrates the importance of including citrate and other organic ligands in models of uranium transport. (c) 2004 Elsevier B.V. All rights reserved.
引用
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页码:1 / 16
页数:16
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