Co-transport of U(VI) and akaganeite colloids in water-saturated porous media: Role of U(VI) concentration, pH and ionic strength

被引:47
|
作者
Ge, Mengtuan [1 ]
Wang, Dengjun [2 ,3 ]
Yang, Junwei [1 ]
Jin, Qiang [1 ]
Chen, Zongyuan [1 ,4 ]
Wu, Wangsuo [1 ,4 ]
Guo, Zhijun [1 ,4 ]
机构
[1] Lanzhou Univ, Sch Nucl Sci & Technol, Radiochem Lab, Lanzhou 730000, Gansu, Peoples R China
[2] CNR, 919 Kerr Res Dr, Ada, OK 74820 USA
[3] US EPA, 919 Kerr Res Dr, Ada, OK 74820 USA
[4] Lanzhou Univ, Minist Educ, Key Lab Special Funct Mat & Struct Design, Lanzhou 730000, Gansu, Peoples R China
基金
中国国家自然科学基金;
关键词
U(VI); Akaganeite colloid; Co-transport; Concentration effect; Modelling; REACTIVE TRANSPORT; FACILITATED TRANSPORT; URANIUM; NANOPARTICLES; SAND; REMEDIATION; DESORPTION; PHOSPHATE; MAGNETITE; SEDIMENTS;
D O I
10.1016/j.watres.2018.10.004
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Remediating uranium contamination becomes a worldwide interest because of increasing uranium release from mining activities. Due to ubiquitous presence of pyrite and the application of iron-based technology, colloidal iron oxy-hydroxides such as akaganeite colloid (AKC) extensively exist in uranium polluted water at uranium tailing sites. In this context, we studied individual and co-transport of U(VI) and AKC in water-saturated sand columns at 50 mg/L AKC and environmentally relevant U(VI) concentrations (5.0 x 10(-7) similar to 5.0 x 10(-5) M). It was found that, in addition to the impact of pH and ionic strength, whether AKC facilitated U(VI) transport depended on U(VI) concentration as well. The presence of AKC facilitated U(VI) transport at relatively low U(VI) concentration (5.0 x 10(-7) similar to 5.0 x 10(-6) M), which was due to the strong adsorption of U(VI) on AKC and faster transport of AKC than that U(VI) as observed in their individual transport experiments. At relatively high U(VI) concentrations (5.0 x 10-5 M), however, AKC impeded U(VI) transport because U(VI) of high concentration decreased AKC colloidal stability and increased AKC aggregation and attachment. Thus, U(VI) and AKC co-transport was even blocked completely at relatively high pH and ionic strength. The mechanisms behind the co-transport of U(VI) and AKC were also confirmed by assessing the evolutions of aqueous pH and AKC zeta potential and particle size distribution in the column effluents. A two-site non-equilibrium model and a two-site kinetic attachment/detachment model well-described the breakthrough curves of U(VI) and AKC, respectively. Knowledge generated from this study provides a thorough understanding of uranium transport in the absence/presence of AKC, and brings new insights into the influence of contaminant concentration on co-transport in the presence of colloids. (C) 2018 Elsevier Ltd. All rights reserved.
引用
收藏
页码:350 / 361
页数:12
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