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模拟表面活性剂、硬度和天然有机物对银纳米颗粒在饱和多孔介质中沉积和迁移的影响。

Modeling the effects of surfactant, hardness, and natural organic matter on deposition and mobility of silver nanoparticles in saturated porous media.

机构信息

Department of Civil and Environmental Engineering, University of South Carolina, Columbia, 300 Main Street, SC, 29208, USA.

Department of Civil and Environmental Engineering, Korea Army Academy at Young-Cheon, 495 Hogook-ro, Kokyungmeon, Young-Cheon, Gyeongbuk, 38900, South Korea.

出版信息

Water Res. 2016 Oct 15;103:38-47. doi: 10.1016/j.watres.2016.07.022. Epub 2016 Jul 12.

DOI:10.1016/j.watres.2016.07.022
PMID:27429353
Abstract

This study aims to provide insights into the mechanisms governing the deposition and retention of silver nanoparticles (AgNPs) in saturated porous media. Column experiments were conducted with quartz sand under saturated conditions to investigate the deposition kinetics of AgNPs, their mobility at different groundwater hardnesses (10-400 mg/L as CaCO3), and humic acid (HA, 0-50 mg/L as dissolved organic carbon [DOC]). An anionic surfactant, sodium dodecyl sulfate (SDS), was used as a dispersing agent to prepare a SDS-AgNPs suspension. The deposition kinetics of AgNPs were highly sensitive to the surfactant concentration, ionic strength, and cation type in solution. The breakthrough curves (BTCs) of SDS-AgNPs suggested that the transport and retention were influenced by groundwater hardness and HA. At low water hardness and high HA, high mobility of SDS-AgNPs was observed in saturated conditions. However, the retention of SDS-AgNPs increased substantially in very hard water with a low concentration of HA, because of a decreased primary energy barrier and the straining effect during the course of transport experiments. A modified clean-bed filtration theory and a two-site kinetic attachment model showed good fits with the BTCs of SDS-AgNPs. The fitted model parameters (katt and kstr) could be used successfully to describe that the retention behaviors were dominated by electrostatic and electrosteric repulsion, based on extended Derjaguin-Landau-Vaerwey-Overbeek calculations.

摘要

本研究旨在深入了解控制银纳米颗粒(AgNPs)在饱和多孔介质中沉积和保留的机制。通过在饱和条件下使用石英砂进行柱实验,研究了 AgNPs 的沉积动力学、在不同地下水硬度(10-400mg/L 以碳酸钙计)和腐殖酸(HA,0-50mg/L 以溶解有机碳 [DOC] 计)下的迁移率。阴离子表面活性剂十二烷基硫酸钠(SDS)被用作分散剂来制备 SDS-AgNPs 悬浮液。AgNPs 的沉积动力学对表面活性剂浓度、溶液中的离子强度和阳离子类型高度敏感。SDS-AgNPs 的穿透曲线(BTC)表明,地下水硬度和 HA 影响运输和保留。在低水硬度和高 HA 条件下,SDS-AgNPs 在饱和条件下表现出高迁移率。然而,在 HA 浓度低、水硬度非常高的情况下,SDS-AgNPs 的保留量大大增加,因为在运输实验过程中,初级能量势垒降低和筛分效应。改进的清洁床过滤理论和双位点动力学附着模型与 SDS-AgNPs 的 BTC 拟合良好。拟合模型参数(katt 和 kstr)可成功用于描述基于扩展的德加古因-朗道-范韦尔韦克计算,保留行为主要由静电和电动排斥控制。

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