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模拟土壤中Ni(II)和Zn(II)的竞争吸附与迁移:比较两种多组分方法。

Modeling the competitive sorption and transport of Ni(II) and Zn(II) in soils: Comparing two multicomponent approaches.

作者信息

Padilla Joshua T, Selim H Magdi, Gaston Lewis A

机构信息

USDA Agricultural Research Service, Coastal Plain Soil, Water & Plant Research Center, 2611 W. Lucas St., Florence, SC 29501, USA.

School of Plant, Environmental and Soil Sciences, Louisiana State University, Baton Rouge, LA 70803, USA.

出版信息

J Contam Hydrol. 2023 Jan;252:104108. doi: 10.1016/j.jconhyd.2022.104108. Epub 2022 Nov 15.

Abstract

The mobility of contaminants in soil is controlled by sorption reactions which can be affected by the presence of other solutes that compete for sorption sites. The ability to model such effects is necessary for evaluating the environmental risk of a given contaminant. In this study, the competitive sorption and transport of nickel (Ni) and zinc (Zn) in Olivier and Windsor soils was investigated using batch equilibration and miscible displacement experiments. During batch experiments, the sorption of Ni and Zn was mutually reduced in multicomponent systems, indicating that the metal cations compete for sorption sites. When applied concurrently, the retardation of both ions decreased and peak effluent concentrations increased relative to single ion experiments, demonstrating that competition increased the mobility of both ions during miscible displacement experiments. A novel Freundlich-type multicomponent isotherm (CDI) and its kinetic analog (CDIT) were developed and compared to the commonly used SRS isotherm and SRS-based kinetic approach (SRST) in describing the experimental data. The CDI provided a superior description of the competitive batch data, especially at low surface coverage, and may therefore be more applicable to multicomponent sorption than the SRS. The Olivier and Windsor transport data were best described by the CDIT and SRST, respectively, however, both models generally described the data well. Since both approaches gave comparable descriptions of the transport data while the CDI outperformed the SRS in describing the batch data, the CDI/CDIT may be more generally applicable to multicomponent systems and warrants further study.

摘要

土壤中污染物的迁移性受吸附反应控制,而吸附反应可能会受到其他竞争吸附位点的溶质的影响。对这种影响进行建模的能力对于评估特定污染物的环境风险而言是必要的。在本研究中,利用批次平衡和混溶置换实验,研究了镍(Ni)和锌(Zn)在奥利维尔土壤和温莎土壤中的竞争吸附与迁移情况。在批次实验期间,多组分体系中Ni和Zn的吸附相互减少,这表明金属阳离子竞争吸附位点。当同时施加时,相对于单离子实验,两种离子的阻滞作用降低,流出物峰值浓度增加,这表明在混溶置换实验中竞争作用增加了两种离子的迁移性。开发了一种新型的弗罗因德利希型多组分等温线(CDI)及其动力学类似物(CDIT),并将其与常用的SRS等温线和基于SRS的动力学方法(SRST)进行比较,以描述实验数据。CDI对竞争性批次数据的描述更佳,尤其是在低表面覆盖率时,因此与SRS相比,可能更适用于多组分吸附。奥利维尔土壤和温莎土壤的迁移数据分别用CDIT和SRST描述效果最佳,不过,两种模型总体上对数据的描述都很好。由于两种方法对迁移数据的描述相当,而CDI在描述批次数据方面优于SRS,因此CDI/CDIT可能更普遍适用于多组分体系,值得进一步研究。

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