4.7 Article

Co-transport of uranyl carbonate and silica colloids in saturated quartz sand under different hydrochemical conditions

期刊

SCIENCE OF THE TOTAL ENVIRONMENT
卷 765, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.scitotenv.2020.142716

关键词

Uranyl carbonate; Silica colloids; Co-transport; Pollution; Uranium species

资金

  1. National Natural Science Foundation of China [11675072]
  2. Hunan Provincial Innovation Foundation for Postgraduate [CX20190719]

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The study investigated the co-transport mechanisms of UC and cSiO(2) in a saturated porous medium with different ionic strength, pH, and UC concentration. It revealed factors influencing the transport efficiency, such as the deposition of cSiO(2) on quartz sand at low UC concentrations.
Uranyl carbonate (UC) and silica colloids (cSiO(2)) are widely distributed in carbonate-rich subsurface environments associated with uranium pollution. Mobile colloids such as cSiO(2) can affect uranium's transport efficiency in the groundwater environment. Therefore, elucidating the mechanism of UC and cSiO(2) co-transport in a saturated porous medium with different ionic strength (IS), pH, and UC concentration is essential for the prevention and control of groundwater radioactive pollution. At low UC concentrations (<2.1 x 10(-5) M), cSiO(2) is more prone to be deposited on the surfaces of quartz sand (QS) than UC, resulting in cSiO(2) preventing UC transport. Compared to pH 7 and 9, at pH 5 the adsorption of uranium [in the form of 81.5% UO2CO3(aq), 8.6% UO22+, and 5.2% UO2OH+] on cSiO(2) renders cSiO(2) more prone to aggregate, causing smaller amounts of cSiO(2) (86.6%) and UC (55.8%) to be recovered. Mechanisms responsible for the evolution of the pH and zeta potential in effluents have been proposed. Chemical reactions (ligand-exchange reactions and deprotonation) that occur in the QS column between UC and cSiO(2)/QS cause the pH of the suspension to varying, which in turn causes changes in the zeta potential and particle size of cSiO(2). Eventually, the recovery rates of cSiO(2) and UC are changed, depending upon the colloid particle size. Changes in ionic strength can seriously affect the stability of cSiO(2) particles, and that effect is more significant when UC is present. Moreover, colloidal filtration theory, a non-equilibrium two-site model, and the Derjaguin-Landau-Verwey-Overbeek theory successfully describe the individual-transport and co-transport of cSiO(2) and UC in the column. This study provides a strong basis for investigating UC pollution control in porous media. (C) 2020 Elsevier B.V. All rights reserved.

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