X-ray absorption spectroscopic study of trivalent and tetravalent actinides in solution at varying pH values

B. Brendebach, N. Banik, C. Marquardt, J. Rothe, M. Denecke, H. Geckeis
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引用次数: 51

Abstract

Abstract We perform X-ray absorption spectroscopy (XAS) investigations to monitor the stabilization of redox sensitive trivalent and tetravalent actinide ions in solution at acidic conditions in a pH range from 0 to 3 after treatment with holding reductants, hydroxylamine hydrochloride (NH2OHHCl) and Rongalite (sodium hydroxymethanesulfinate, CH3NaO3S). X-ray absorption near edge structure (XANES) measurements clearly demonstrate the stability of the actinide species for several hours under the given experimental conditions. Hence, structural parameters can be accurately derived by extended X-ray absorption fine structure (EXAFS) investigations. The coordination structure of oxygen atoms belonging to water ligands surrounding the actinide ions does not change with increasing pH value (approximately 11 O atoms at 2.42 Å in the case of U(IV) at pH 1, 9 O atoms at 2.52 Å for Np(III) at pH 1.5, and 10 O atoms at 2.49 Å for Pu(III) up to pH 3), indicating that hydrolysis reactions are suppressed under the given chemical conditions.
不同pH值溶液中三价和四价锕系元素的x射线吸收光谱研究
摘要采用x射线吸收光谱(XAS)研究了在pH范围为0 ~ 3的酸性条件下,盐酸羟胺(NH2OHHCl)和熔铝酸盐(羟甲磺酸钠,CH3NaO3S)处理后,氧化还原敏感的三价和四价锕系离子在酸性条件下的稳定性。在给定的实验条件下,x射线吸收近边结构(XANES)测量清楚地证明了锕系元素在几个小时内的稳定性。因此,通过扩展x射线吸收精细结构(EXAFS)研究可以准确地推导出结构参数。锕系离子周围属于水配体的氧原子的配位结构不随pH值的增加而改变(pH值为1时,U(IV)的配位结构约为11个O原子在2.42 Å, pH值为1.5时,Np(III)的配位结构约为9个O原子在2.52 Å, pH值为3时,Pu(III)的配位结构约为10个O原子在2.49 Å),表明在给定的化学条件下水解反应受到抑制。
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