反应性(心理学)
电子转移
化学
零价铁
硫黄
环境修复
无氧运动
环境化学
细胞外
生物物理学
生物
生物化学
生态学
污染
生理学
有机化学
医学
替代医学
病理
吸附
作者
Xia Feng,Wenhua Dong,C.P. Chen,Yi Liu,Zhiyu Pan,Yiman Gao,Xiaohong Hu,Du Chen,Daohui Lin,Lizhong Zhu,Jiang Xu
出处
期刊:Small
[Wiley]
日期:2025-03-13
卷期号:21 (16): e2500203-e2500203
被引量:5
标识
DOI:10.1002/smll.202500203
摘要
Abstract Lattice sulfur‐impregnated nanoscale zerovalent iron (S‐nFe 0 ) has been recognized as a promising groundwater remediation agent. However, little information is available on its reactivity with ubiquitous extracellular antibiotic resistance genes (eARGs) in anaerobic groundwater, and how S content and speciation affect their interactions. Here, the efficient anaerobic degradation of eARGs by S‐nFe 0 (6 log within 5 min), resulting in completely inhibited transformation is showed. The removal rate of eARGs by S‐nFe 0 (0.26 mg m −2 min −1 ) is correlated well with the S‐induced hydrophobicity and electron transfer ability of materials, and this reactivity improvement (up to 22‐fold) compared to nFe 0 largely depended on the S content and speciation. Multiple measurements are applied to verify the degradation of eARGs and their interactions with materials, where Fe−O−P coordination, hydrophobic interaction, and electron transfer play critical roles. The application potential of S‐nFe 0 is strongly supported by their long‐term reactivity and stability in real groundwater and universal reactivity with multiple eARGs. These findings elucidate the mechanistic role of lattice S in the degradation of eARGs by S‐nFe 0 , unveil binding sites and interactions between eARGs and S‐nFe 0 , and will advance understanding toward better design of S‐nFe° for eARGs‐contaminated groundwater remediation.
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