首页> 外文期刊>Journal of Geochemical Exploration: Journal of the Association of Exploration Geochemists >Mobility of arsenic in aquifer sediments at Datong Basin, northern China: Effect of bicarbonate and phosphate
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Mobility of arsenic in aquifer sediments at Datong Basin, northern China: Effect of bicarbonate and phosphate

机译:中国北方大同盆地含水层沉积物中砷的迁移:碳酸氢盐和磷酸盐的影响

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Effects of phosphate and bicarbonate concentration on mobilization of arsenic in aquifer sediments have not been extensively studied in flow-through experiments, where the dynamic-release behavior of elements can be monitored. In this work, these effects were investigated both through batch and column experiments, using a high-arsenic sediment sample from the Datong Basin, northern China. A solution of 1.0 mM Ca(NO3)2 was first applied to a water-saturated column packed with the sediment; this was followed by leaching with either 0.10 mM Na2HPO4 or 8.2 mM NaHCO3 solutions. When the sediment was initially leached with 1.0 mM Ca(NO3)2 solution, a rapid spike of As, Fe, Mn, and major cations was observed in the first 20 column pore volumes, reflecting the initial equilibration of the sediment to the influent Ca(NO3)2 in response to cation exchange (for cations) and sorption equilibrium (for Mn, Fe, As).After the Ca(NO3)2 solution was replaced with either the Na2HPO4 or NaHCO3 solution, a rapid increase in As concentration in the effluent was observed, consistent with the batch test results. Induced desorption of As from oxyhydroxide sorbents by Na2HPO4 suggests that phosphate competition was the major factor responsible for the observed increase of As, as indicated by a coinciding increase of K~+ replaced in the exchange process. In the column leached with 8.2 mM NaHCO3, high concentrations of sodium result in greater clay dispersion, and the transport of Fe/Mn oxyhydroxides with adsorbed arsenic may account for the enhanced arsenic concentration in the effluent, as suggested by the concurrently observed increase in Fe and Mn concentrations in the effluent.
机译:流通性实验尚未广泛研究磷酸盐和碳酸氢盐浓度对含水层沉积物中砷迁移的影响,在该实验中可以监测元素的动态释放行为。在这项工作中,使用来自中国北方大同盆地的高砷沉积物样品,通过分批和柱实验对这些影响进行了研究。首先将1.0 mM Ca(NO3)2溶液加到装有沉淀物的水饱和柱中;然后用0.10 mM Na2HPO4或8.2 mM NaHCO3溶液浸提。当最初用1.0 mM Ca(NO3)2溶液浸出沉积物时,在前20个柱孔体积中观察到As,Fe,Mn和主要阳离子的快速增加,反映了沉积物与流入的Ca的初始平衡。 (NO3)2响应阳离子交换(对于阳离子)和吸附平衡(对于Mn,Fe,As).Ca(NO3)2溶液替换为Na2HPO4或NaHCO3溶液后,As中的As浓度迅速增加观察到废水,与批量测试结果一致。 Na2HPO4引起的氢氧化物吸附剂对As的脱附表明,磷酸盐的竞争是观察到的As增加的主要因素,交换过程中K +的同时增加表明了这一点。同时观察到的Fe含量升高表明,在用8.2 mM NaHCO3浸提的色谱柱中,高浓度的钠会导致粘土的分散性增加,Fe / Mn羟基氧化物与吸附的砷的迁移可能会导致废水中砷浓度的升高。和废水中的锰浓度。

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