Controls on the Fate and Speciation of Np(V) During Iron (Oxyhydr)oxide Crystallization

详细信息    查看全文

• 作者：Pieter Bots ; Samuel Shaw ; Gareth T.W. Law ; Timothy A. Marshall ; J. Frederick W. Mosselmans ; Katherine Morris
• 刊名：Environmental Science & Technology
• 出版年：2016
• 出版时间：April 5, 2016
• 年：2016
• 卷：50
• 期：7
• 页码：3382-3390
• 全文大小：398K
• ISSN：1520-5851

文摘

The speciation and fate of neptunium as Np(V)O₂⁺ during the crystallization of ferrihydrite to hematite and goethite was explored in a range of systems. Adsorption of NpO₂⁺ to iron(III) (oxyhydr)oxide phases was reversible and, for ferrihydrite, occurred through the formation of mononuclear bidentate surface complexes. By contrast, chemical extractions and X-ray absorption spectroscopy (XAS) analyses showed the incorporation of Np(V) into the structure of hematite during its crystallization from ferrihydrite (pH 10.5). This occurred through direct replacement of octahedrally coordinated Fe(III) by Np(V) in neptunate-like coordination. Subsequent analyses on mixed goethite and hematite crystallization products (pH 9.5 and 11) showed that Np(V) was incorporated during crystallization. Conversely, there was limited evidence for Np(V) incorporation during goethite crystallization at the extreme pH of 13.3. This is likely due to the formation of a Np(V) hydroxide precipitate preventing incorporation into the goethite particles. Overall these data highlight the complex behavior of Np(V) during the crystallization of iron(III) (oxyhydr)oxides, and demonstrate clear evidence for neptunium incorporation into environmentally important mineral phases. This extends our knowledge of the range of geochemical conditions under which there is potential for long-term immobilization of radiotoxic Np in natural and engineered environments.