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Hydrolysis of Uranium(VI) at Variable Temperatures (10−85 °C)

P. ZanonatoContribution from the Dipartimento di Chimica Inorganica Metallorganica ed Analitica, Università di Padova, via Loredan 4, 35131, Padova, Italy; Istituto di Chimica Inorganica e delle Superfici del C.N.R. of Padova, Corso Stati Uniti 4, 35127, Padova, Italy; Chemistry Division, Argonne National Laboratory, Argonne, Illinois 60439; and Glenn T. Seaborg Center, Lawrence Berkeley National Laboratory, Berkeley, California 94720Plinio Dí BernardoContribution from the Dipartimento di Chimica Inorganica Metallorganica ed Analitica, Università di Padova, via Loredan 4, 35131, Padova, Italy; Istituto di Chimica Inorganica e delle Superfici del C.N.R. of Padova, Corso Stati Uniti 4, 35127, Padova, Italy; Chemistry Division, Argonne National Laboratory, Argonne, Illinois 60439; and Glenn T. Seaborg Center, Lawrence Berkeley National Laboratory, Berkeley, California 94720Arturo BismondoContribution from the Dipartimento di Chimica Inorganica Metallorganica ed Analitica, Università di Padova, via Loredan 4, 35131, Padova, Italy; Istituto di Chimica Inorganica e delle Superfici del C.N.R. of Padova, Corso Stati Uniti 4, 35127, Padova, Italy; Chemistry Division, Argonne National Laboratory, Argonne, Illinois 60439; and Glenn T. Seaborg Center, Lawrence Berkeley National Laboratory, Berkeley, California 94720Guokui LiuContribution from the Dipartimento di Chimica Inorganica Metallorganica ed Analitica, Università di Padova, via Loredan 4, 35131, Padova, Italy; Istituto di Chimica Inorganica e delle Superfici del C.N.R. of Padova, Corso Stati Uniti 4, 35127, Padova, Italy; Chemistry Division, Argonne National Laboratory, Argonne, Illinois 60439; and Glenn T. Seaborg Center, Lawrence Berkeley National Laboratory, Berkeley, California 94720Xueyuan ChenContribution from the Dipartimento di Chimica Inorganica Metallorganica ed Analitica, Università di Padova, via Loredan 4, 35131, Padova, Italy; Istituto di Chimica Inorganica e delle Superfici del C.N.R. of Padova, Corso Stati Uniti 4, 35127, Padova, Italy; Chemistry Division, Argonne National Laboratory, Argonne, Illinois 60439; and Glenn T. Seaborg Center, Lawrence Berkeley National Laboratory, Berkeley, California 94720Linfeng RaoContribution from the Dipartimento di Chimica Inorganica Metallorganica ed Analitica, Università di Padova, via Loredan 4, 35131, Padova, Italy; Istituto di Chimica Inorganica e delle Superfici del C.N.R. of Padova, Corso Stati Uniti 4, 35127, Padova, Italy; Chemistry Division, Argonne National Laboratory, Argonne, Illinois 60439; and Glenn T. Seaborg Center, Lawrence Berkeley National Laboratory, Berkeley, California 94720
2004en
ABI

Аннотация

The hydrolysis of uranium(VI) in tetraethylammonium perchlorate (0.10 mol dm(-3) at 25 degrees C) was studied at variable temperatures (10-85 degrees C). The hydrolysis constants (*beta(n,m)) and enthalpy of hydrolysis (Delta H(n,m)) for the reaction mUO(2)(2+) + nH(2)O = (UO(2))(m)(OH)(n)((2m-n))+) + nH(+) were determined by titration potentiometry and calorimetry. The hydrolysis constants, *beta(1,1), *beta(2,2), and *beta(5,3), increased by 2-5 orders of magnitude as the temperature was increased from 10 to 85 degrees C. The enthalpies of hydrolysis, Delta H(2,2) and Delta H(5,3), also varied: Delta H(2,2) became more endothermic while Delta H(5,3) became less endothermic as the temperature was increased. The heat capacities of hydrolysis, Delta C(p(2,2)) and Delta C(p(5,3)), were calculated to be (152 +/- 43) J K(-1) mol(-1) and -(229 +/- 34) J K(-1) mol(-1), respectively. UV/Vis absorption spectra supported the trend that hydrolysis of U(VI) was enhanced at elevated temperatures. Time-resolved laser-induced fluorescence spectroscopy provided additional information on the hydrolyzed species at different temperatures. Approximation approaches to predict the effect of temperature were tested with the data from this study.

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