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Competitive sorption-desorption kinetics of arsenate and phosphate in soils

机译:砷和磷酸盐在土壤中的竞争性吸附-解吸动力学

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摘要

The competition between arsenate (AsO4-3) and phosphate (PO4-3) on mineral surfaces has the potential of increasing arsenic mobility and bioavailability in the soil and water environment. In this study, kinetics of competitive sorption of AsO4-3 and PO4-3 in three soils was investigated in batch systems by simultaneously introducing the ligands at different molar ratios. Adsorption was carried out at different retention times, and release was investigated using successive dilutions after adsorption. Nonlinear sorption isotherms of AsO4-3 and PO4-3 were observed for all soils. Rates and amounts of AsO4-3 adsorption were significantly reduced when PO4-3 concentrations in the soil solution increased. In addition, the relative sorption preference of AsO4-3 and PO4-3 did not exhibit changes with reaction time. Desorption and sequential extractions results indicated that a significant amount of AsO4-3 was irreversibly retained by all soils. Kinetic retention data of AsO4-3 and PO4-3 were successfully described using a mechanistic multireaction model that accounted for competitive retention. This study indicates that competition of AsO4-3 and PO4-3 for adsorption sites should be considered in models predicting arsenic release from soils receiving high phosphorus inputs.
机译:矿物表面上砷酸盐(AsO4-3)与磷酸盐(PO4-3)之间的竞争具有增加土壤和水环境中砷迁移率和生物利用度的潜力。在这项研究中,通过同时引入不同摩尔比的配体,研究了三种土壤中AsO4-3和PO4-3竞争性吸附的动力学。在不同的保留时间进行吸附,并使用吸附后的连续稀释液研究释放情况。在所有土壤中均观察到了AsO4-3和PO4-3的非线性吸附等温线。当土壤溶液中PO4-3浓度增加时,AsO4-3的吸附速率和吸附量显着降低。另外,AsO4-3和PO4-3的相对吸附偏好不随反应时间而变化。解吸和顺序萃取结果表明,所有土壤中都不可逆地保留了大量AsO4-3。 AsO4-3和PO4-3的动力学保留数据已使用解释竞争保留的机制多元反应模型成功进行了描述。这项研究表明,在预测砷从高磷输入土壤中释放的模型中,应考虑AsO4-3和PO4-3对吸附位的竞争。

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