薄膜中的扩散梯度
土壤水分
环境化学
沉积物
解吸
化学
土壤科学
分析物
环境科学
有机质
吸附
地质学
色谱法
古生物学
有机化学
作者
Huaji Liu,Li Na,Jian Shen,Hamidreza Arandiyan,Yuan Wang,Xinze Wang
出处
期刊:Chemosphere
[Elsevier BV]
日期:2023-12-28
卷期号:350: 141061-141061
被引量:4
标识
DOI:10.1016/j.chemosphere.2023.141061
摘要
The diffusive gradients in thin films (DGT) technique serves as a passive sampling method, inducing analyte transport and concentration. Its application is widespread in assessing labile components of metals, organic matter, and nutrients across various environmental media such as water, sediments, and saturated soils. The DGT devices effectively reduce the porewater concentration through irreversible binding of solutes, consequently promoting the release of labile species from the soil/sediment solid phase. However, the precise quantification of simultaneous adsorption and desorption of labile species using DGT devices alone remains a challenge. To address this challenge, the DGT-Induced Fluxes in Soils and Sediments (DIFS) model was developed. This model simulates analyte kinetics in solid phases, solutions, and binding resins by incorporating factors such as soil properties, resupply parameters, and kinetic principles. While the DIFS model has been iteratively improved to increase its accuracy in portraying kinetic behavior in soil/sediment, researchers’ incomplete comprehension of it still results in unrealistic fitting outcomes and an oversight of the profound implications posed by kinetic parameters during implementation. This review provides a comprehensive overview of the optimization and utilization of DIFS models, encompassing fundamental concepts behind DGT devices and DIFS models, the kinetic interpretation of DIFS parameters, and instances where the model has been applied to study soils and sediments. It also highlights preexisting limitations of the DIFS model and offers suggestions for more precise modeling in real-world environments.
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