Heptavalent state of neptunium and plutonium

Autor: V. P. Shilov, A.D. Gel'man, F.A. Zakharova, N. N. Krot, M.P. Mefodiyeva, Yu.A. Komkov, V.I. Spitsyn, I.V. Smirnova
Rok vydání: 1969
Předmět:
Zdroj: Journal of Inorganic and Nuclear Chemistry. 31:2733-2745
ISSN: 0022-1902
DOI: 10.1016/0022-1902(69)80187-9
Popis: In alkaline media Np(VI) is oxidised to heptavalent state by O 3 , oxygen compounds of hexa- and octavalent Xe, persulphate, periodate, hypochlorite, and hypobromite ions, bismuthates and, electrolytically, on platinum anode. The redox potential of the pair Np(VII)/Np(VI) in 1 M alkaline solutions is in the range of 0·40-0·76 V. To obtain Pu(VII) in diluted alkaline solutions O 3 and S 2 O 8 = ions can be used. In strong alkali Pu(VI) is also oxidized by hypochlorite, hypohromite and perxenate ions. The redox potential of the pair Pu(VII)/Pu(VI) in 1 M KOH is in the range of 0·76-1·24 V. Absorption spectra of alkaline solutions of Np(VII) and Pu(VII) are independent of the way they were taken and are practically unaffected by changing concentration of OH − ions over a broad range. The colour of solutions of Pu(VII) and Np(VII) in the visible part of the spectrum is in a satisfactory agreement with the Lambert-Beer law. Np(VII) and Pu(VII) can be converted in alkaline solutions to hexavalent state by means of numerous reducers. The stoichiometric evidence obtained for a number of reduction reactions confirms the monoelectronic metal transfer from hepta to hexavalent form. Compounds [Co(NH 3 ) 6 ].NpO 5 .3H 2 O, [Pt(NH 3 ) 5 Cl]NpO 5 .H 2 O, Ba 3 (NpO 5 ) 2 . n H 2 O, S 3 (NpO 5 ) 2 . n H 2 O and Ba 3 (PuO 5 ) 2 . n H 2 O. have been obtained in a solid state. Some of their properties have been studied. It has been found that Np(VII) and Pu(VII) exist in alkaline media as NpO 5 3− and PuO 5 3− anions. The latter are an anionic form of amphoteric hydroxides MeO 2 (OH) 3 .NpO 2 (OH) 3 . n H 2 O has been obtained in a solid state. Some peculiar properties of heptavalent state of Np and Pu are discussed.
Databáze: OpenAIRE