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Comparison of Adsorption Behaviors of Kaolin from Column and Batch Tests: Concept of Dual Porosity

吸附 延迟因子 吸附 多孔性 化学 相(物质) 色谱法 传质 穿透曲线 热力学 栏(排版) 混合(物理) 分析化学(期刊) 柱色谱法 有机化学 数学 连接(主束) 物理 几何学 量子力学
作者
Guan-Nian Chen,Yuchao Li,Xinru Zuo,Han Ke,Yunmin Chen
出处
期刊:Journal of Environmental Engineering [American Society of Civil Engineers]
卷期号:146 (9) 被引量:13
标识
DOI:10.1061/(asce)ee.1943-7870.0001792
摘要

Batch equilibrium tests with various soil-liquid ratios (S/L=1∶2.5, 1∶5, 1∶10, and 1∶20) and column tests with a flow interruption and rest period were performed to evaluate the adsorption behavior of kaolin. Identical isotherms were obtained from the batch equilibrium tests, illustrating that the S/L ratio has minimal impacts on adsorption behavior if complete mixing is ensured. In the column tests, a long non-Fickian tailing was observed in the breakthrough curve, and a decrease in the concentration of the liquid phase was observed in the closed system during the flow interruption and rest period although the column achieved local equilibrium. These results demonstrated that sorption equilibrium in the soil columns was not reached even when a stable exit concentration was achieved. The dual porosity (DP) concept was used to interpret the test results. Insufficient adsorption in the immobile phase is the major cause of the relatively low adsorbed concentration in short-term column tests, and a higher ratio of mobile phase voids compared to that of mobile phase adsorption capacity leads to a lower apparent retardation factor. The long-term transfer between the two phases is another key point that should be accounted for in the data analysis and modeling of column tests. Differences in immobile phase adsorption levels between tests under laboratory conditions and those under in situ conditions lead to discrepancies, which may confound the apparent retardation factor.
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