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Dissolved Inorganic Contaminants in a Floodplain Soil: Comparison of In Situ Soil Solutions and Laboratory Methods

机译:洪泛区土壤中溶解的无机污染物:原位土壤溶液和实验室方法的比较

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The applicability of laboratory tests for the prediction of soil solution composition and concentrations of inorganic contaminants is still under debate. Therefore, we carried out two batch-leaching tests differing in their liquid/solid ratios and column experiments (saturated flow, two flow velocities, four flow interruptions ranging from 4 h to 21 days) with a contaminated humic horizon (total contents: As, 196 mg kg~(-1); Cd, 4 mg kg~(-1); Cr, 202 mg kg~(-1); Cu, 227 mg kg~(-1); Ni, 64 mg kg~(-1); Pb, 308 mg kg~(-1); Zn, 1,176 mg kg~(-1)) from a Mollic Fluvisol near the rivers Elbe and Saale (Germany) and compared the aqueous contaminant concentrations with those of soil solutions obtained in situ with ceramic suction cups on a monthly basis between 2002 and 2006. Contaminant release in the field slightly depended on the water regime, pH, and redox potential and was characterized by partially high concentrations (e.g., As, 47 μg 1~(-1); Cd, 136 μg 1~(-1); Ni, 328 μg 1~(-1); Zn, 8.68 mg 1~(-1)), which exceeded the German inspection values. Metal concentrations obtained in batch-leaching tests partially fitted to those determined in the soil solution and to those from the column experiments even irrespective of the varying liquid/solid ratios. The column experiments yielded realistic concentrations of Cr, Cu, Ni, and Pb and their ranges. Furthermore, they provided an insight into release kinetics and release processes as well as into potential contaminant release due to enforced reducing conditions. As column experiments allow a larger temporal sampling resolution and enable quickly to manipulate experimental conditions, they are a useful complement of soil solution monitoring.
机译:实验室测试在预测土壤溶液组成和无机污染物浓度方面的适用性仍存在争议。因此,我们进行了两个批次/浸出试验,它们的液/固比不同,并且进行了柱实验(饱和流速,两种流速,四种流速中断时间从4小时到21天不等),并且腐殖质层受到污染(总含量:As, 196 mg kg〜(-1); Cd,4 mg kg〜(-1); Cr 202 mg kg〜(-1); Cu,227 mg kg〜(-1); Ni 64 mg kg〜(- 1);从易北河和萨勒河(德国)附近的Moluic氟维松醇中提取铅,308 mg kg〜(-1);锌1,176 mg kg〜(-1),并将含水污染物浓度与所获得的土壤溶液中的污染物浓度进行比较在2002年至2006年期间,每月使用陶瓷吸盘进行原位处理。在田间,污染物的释放在一定程度上取决于水的状况,pH和氧化还原电位,其特征在于部分高浓度(例如,As,47μg1〜(- 1); Cd,136μg1〜(-1); Ni,328μg1〜(-1); Zn,8.68 mg 1〜(-1)),超过了德国的检测标准。分批浸出测试中获得的金属浓度与土壤溶液中测定的金属浓度以及通过柱实验获得的金属浓度均部分拟合,甚至与液/固比的变化无关。柱实验得出了Cr,Cu,Ni和Pb及其范围的实际浓度。此外,他们提供了对释放动力学和释放过程以及由于强制还原条件导致的潜在污染物释放的见解。由于色谱柱实验可以提供更大的时间采样分辨率并可以快速操作实验条件,因此它们是土壤溶液监测的有用补充。

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