Physicochemical properties of uranium in lower oxidation states

2006 ◽  
Vol 48 (6) ◽  
pp. 535-551 ◽  
Author(s):  
S. A. Kulyukhin ◽  
N. B. Mikheev ◽  
A. N. Kamenskaya ◽  
N. A. Konovalova ◽  
I. A. Rumer
Processes ◽  
2021 ◽  
Vol 9 (6) ◽  
pp. 1073
Author(s):  
Claudia Campillo-Cora ◽  
Laura Rodríguez-González ◽  
Manuel Arias-Estévez ◽  
David Fernández-Calviño ◽  
Diego Soto-Gómez

Chromium is an element that possess several oxidation states and can easily pass from one to another, so its behavior in soils is very complex. For this reason, determining its fate in the environment can be difficult. In this research work we tried to determine which factors affect the chromium fractionation in natural soils, conditioning chromium mobility. We paid special attention to the parent material. For this purpose, extraction experiments were carried out on spiked soils incubated for 50–60 days, using H2O, CaCl2 and diethylenetriaminepentaacetic acid (DTPA). The most efficient extraction rate in all soils was achieved using water, followed by CaCl2 and DTPA. We obtained models with an adjusted R2 of 0.8097, 0.8471 and 0.7509 for the H2O Cr, CaCl2 Cr and DTPA Cr respectively. All models were influenced by the amount of chromium added and the parent material: amphibolite and granite influenced the amount of H2O Cr extracted, and schist affected the other two fractions (CaCl2 and DTPA). Soil texture also played an important role in the chromium extraction, as well as the amounts of exchangeable aluminum and magnesium, and the bioavailable phosphorus. We concluded that it is possible to make relatively accurate predictions of the behavior of the different Cr fractions studied, so that optimized remediation strategies for chromium-contaminated soils can be designed on the basis of a physicochemical soil characterization.


1964 ◽  
Vol 17 (11) ◽  
pp. 1191 ◽  
Author(s):  
JC Sheldon

The evidence for, and the factors determining, the formation of metal-to-metal (m-m) bonds in transition metal oxides, sulphides, halides, and related complexes are discussed. It is proposed that when metals of high preferred valence state are constrained to low formal oxidation states, m-m bonds will form to allow the metal to exercise a higher valency. It is assumed that (n-l)d orbitals are used for such bonds and predictions of the feasibility of m-m bonding are possible by the comparison of the size of such orbitals with the expected inter-metal distances in polymeric metal oxides and halides. It is concluded that binary oxides and halides (excepting fluorides) of the lower oxidation states of Zr, Hf, Nb, Ta, Mo, W, and Re and of a few neighbouring elements will display m-m bonds.


2005 ◽  
Vol 47 (5) ◽  
pp. 423-439 ◽  
Author(s):  
N. B. Mikheev ◽  
S. A. Kulyukhin ◽  
A. N. Kamenskaya ◽  
N. A. Konovalova ◽  
I. A. Rumer

Author(s):  
K. I. Slovetskaya ◽  
Yu. S. Khodakov ◽  
A. M. Rubinshtein ◽  
Kh. M. Minachev

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