纳米反应器
环境修复
地下水修复
零价铁
化学
地下水
污染
化学工程
降级(电信)
腐蚀
自愈水凝胶
环境化学
吸附
水处理
人体净化
纳米技术
多孔性
地下水污染
纳米颗粒
催化作用
氯化溶剂
可渗透反应墙
纳米尺度
作者
Kaijian Sang,Zhenjie Li,Xu Tao,Chaohuang Chen,Min Chen,Haichun Gao,Jiang Xu,Jie Hou,Kun Yang,Daohui Lin
标识
DOI:10.1021/acs.est.5c16925
摘要
The remediation of dense nonaqueous phase liquids (DNAPLs) in groundwater presents a persistent challenge, as conventional technologies suffer from side reactions with bulk water rather than chlorinated solvents within DNAPL source zones. By engineering DNAPL-responsive poly( N -isopropylacrylamide) (PNIPAM) hydrogels with precisely controlled hydrophobic domains, we fabricated nanoscale zerovalent iron (nZVI) reactors (nZVI @ PNIPAM) via in situ reduction of incorporated Fe 3+ ions. The hydrogel encapsulation enabled nZVI to remain well-dispersed, spontaneously penetrated porous media, and significantly suppressed side reactions with water. Crucially, the nanoreactors leveraged the selective interaction between DNAPLs and PNIPAM’s hydrophobic functional groups as a trigger, exposing encapsulated reactive nZVI exclusively at contamination interfaces through a rapid conformational transition and dehydration of PNIPAM. This interfacial interaction yields unprecedented efficiency, achieving 4.4–12.3-fold higher electron utilization for degradation of seven typical chlorinated solvents than conventional nZVI while suppressing water corrosion over 600-fold. Field-relevant evaluations demonstrated consistent performance across broad hydrochemical conditions (pH 6–9, 0–1000 mg L –1 KCl, 0–200 mg L –1 natural organic matter), with over 90% DNAPL removal in real contaminated groundwater. Our mechanistic discovery of pollutant-responsive activation represents a significant advance over current diffusion-limited approaches, potentially revolutionizing targeted in situ groundwater remediation strategies.
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