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Evaluation of contaminant transport parameters for hexavalent chromium migration through saturated soil media

机译:评价六价铬在饱和土壤介质中迁移的污染物迁移参数

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Hexavalent chromium (Cr6+) is released in the lithospheric environment through leachate pollution in chrome tanning industries. Transportation of Cr6+ containing plume through soil needs to be assessed by estimation of some mechanistic parameters such as diffusion coefficient (D), distribution coefficient (K-d) and retardation factor (R). An investigation was undertaken with three soil samples, S1, S2 and B, to examine their potential use as liner material for controlling Cr6+ pollution in soil environment. Batch adsorption kinetic test was carried out to estimate the K-d and R values of soil samples S1 and S2. A numerical solution technique was adopted for prediction of such transport parameters in simulated field condition using the finite difference method (FDM). The efficacy of the present numerical solution technique (FDM) is compared with subsequent column experiment data with Soil-B along with the analytical solution. It was observed that the experimental value of "D = 3.04 x 10(-8) m(2)/s for Soil-B'' by using the applied technique closely fitted to that value evaluated by the analytical method (r(2) = 0.98). The values of 'K-d' for Soils S1 and S2 were found to be 0.008 and 0.021 mL/g, respectively, using batch adsorption. The values of 'R' of the soil samples S1 and S2 were obtained as 1.037 and 1.053, respectively. All the above results were obtained in correspondence to the initial hexavalent chromium concentration level of 7.5 mg/L in the simulated leachate sample.
机译:六价铬(Cr6 +)通过铬鞣行业中的渗滤液污染而在岩石圈环境中释放。含Cr6 +的烟羽在土壤中的运输需要通过估算一些力学参数来评估,例如扩散系数(D),分布系数(K-d)和阻滞系数(R)。对三个土壤样品S1,S2和B进行了调查,以检验它们作为控制土壤环境中Cr6 +污染的衬垫材料的潜在用途。进行了批量吸附动力学试验,以估算土壤样品S1和S2的K-d和R值。采用了数值求解技术,通过有限差分法(FDM)预测了模拟田间条件下的此类输运参数。将本数值解技术(FDM)的功效与随后使用Soil-B以及分析溶液进行的柱实验数据进行了比较。观察到,通过使用与分析方法所评估的值非常接近的应用技术,“ D = B的D = 3.04 x 10(-8)m(2)/ s的实验值”(r(2) = 0.98)。使用分批吸附法发现土壤S1和S2的'Kd'值分别为0.008和0.021 mL / g,土壤样品S1和S2的'R'值分别为1.037和以上所有结果均与模拟渗滤液样品中的初始六价铬浓度水平7.5 mg / L相对应。

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