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Plutonium and Americium Alpha Radiolysis of Nitric Acid Solutions
Author(s) -
Gregory P. Horne,
Colin Gregson,
Howard E. Sims,
Robin M. Orr,
Robin J. Taylor,
Simon M. Pimblott
Publication year - 2017
Publication title -
the journal of physical chemistry b
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.864
H-Index - 392
eISSN - 1520-6106
pISSN - 1520-5207
DOI - 10.1021/acs.jpcb.6b12061
Subject(s) - americium , plutonium , radiolysis , nitric acid , radiochemistry , alpha (finance) , chemistry , nuclear chemistry , inorganic chemistry , radical , medicine , biochemistry , construct validity , nursing , patient satisfaction
The yield of HNO 2 , as a function of absorbed dose and HNO 3 concentration, from the α-radiolysis of aerated HNO 3 solutions containing plutonium or americium has been investigated. There are significant differences in the yields measured from solutions of the two different radionuclides. For 0.1 mol dm -3 HNO 3 solutions, the radiolytic yield of HNO 2 produced by americium α-decay is below the detection limit, whereas for plutonium α-decay the yield is considerably greater than that found previously for γ-radiolysis. The differences between the solutions of the two radionuclides are a consequence of redox reactions involving plutonium and the products of aqueous HNO 3 radiolysis, in particular H 2 O 2 and HNO 2 and its precursors. This radiation chemical behavior is HNO 3 concentration dependent with the differences between plutonium and americium α-radiolysis decreasing with increasing HNO 3 concentration. This change may be interpreted as a combination of α-radiolysis direct effects and acidity influencing the plutonium oxidation state distribution, which in turn affects the radiation chemistry of the system.

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