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Enhanced recovery of water due to ammonia nitrogen contamination caused by mining processes

机译:由于采矿过程引起的氨氮污染,提高了水的回收率

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摘要

During in situ mining processes, high concentrations of ammonium sulfate solution are directly injected into the mountain to replace the rare earth. However, the residual ammonia nitrogen (AN) in the vadose zone from this injected solution is a serious pollutant of groundwater and soil. Unfortunately, in situ leaching methods using clean water are not effective at removing the AN. In this work, we developed a novel leaching method and examined its efficiency, as well as studied the mechanisms behind the adsorption and desorption of AN. It was found that the majority of the ammonium adsorbed in the soil was in soluble and exchangeable forms. The saturated adsorption capacity under mining conditions was 810 mg kg(-1), where only 36 % of the adsorbed AN was able to be leached out by water. However, the amount of AN leached out increased to 85 % when a KCl solution was used as the leaching agent at an optimized concentration of 2.8 mM. Furthermore, this improved leaching agent worked well at a wide range of solution pHs. Therefore, this method is an efficient means by which to remediate AN contamination after mining processes of RE ores.
机译:在现场开采过程中,将高浓度的硫酸铵溶液直接注入山中以替代稀土。但是,这种注入溶液在渗流带中残留的氨氮(AN)是地下水和土壤的严重污染物。不幸的是,使用净水的原位浸出方法不能有效去除AN。在这项工作中,我们开发了一种新颖的浸出方法并检查了其效率,并研究了AN吸附和解吸的机理。已经发现,土壤中吸附的大多数铵都是可溶和可交换的形式。采矿条件下的饱和吸附容量为810 mg kg(-1),其中只有36%的被吸附的AN能够被水浸出。但是,当使用KCl溶液作为最佳浓度2.8 mM的浸出剂时,AN的浸出量增加到85%。此外,这种改进的浸出剂在很宽的溶液pH值下都能很好地发挥作用。因此,该方法是在稀土矿开采过程之后补救AN污染的有效手段。

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