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铁(氢)氧化物光驱动四环素转化的研究进展:自生成过氧化氢的主导作用。

Insights into sunlight-driven transformation of tetracycline by iron (hydr)oxides: The dominating role of self-generated hydrogen peroxide.

机构信息

Central Iron and Steel Research Institute Group, Beijing 100081, China.

College of Quality and Technical Supervision, Hebei University, Baoding 071002, China.

出版信息

Water Res. 2024 Jul 1;258:121800. doi: 10.1016/j.watres.2024.121800. Epub 2024 May 19.

Abstract

Iron (hydr)oxides are abundant in surface environment, and actively participate in the transformation of organic pollutants due to their large specific surface areas and redox activity. This work investigated the transformation of tetracycline (TC) in the presence of three common iron (hydr)oxides, hematite (Hem), goethite (Goe), and ferrihydrite (Fh), under simulated sunlight irradiation. These iron (hydr)oxides exhibited photoactivity and facilitated the transformation of TC with the initial phototransformation rates decreasing in the order of: Hem > Fh > Goe. The linear correlation between TC removal efficiency and the yield of HO• suggests that HO• dominated TC transformation. The HO• was produced by UV-induced decomposition of self-generated HO and surface Fe-triggered photo-Fenton reaction. The experimental results indicate that the generation of HO• was controlled by HO, while surface Fe was in excess. Sunlight-driven HO production in the presence of the highly crystalline Hem and Goe occurred through a one-step two-electron reduction pathway, while the process was contributed by both O-induced Fe oxidation and direct reduction of O by electrons on the conduction band in the presence of the poorly crystalline Fh. These findings demonstrate that sunlight may significantly accelerate the degradation of organic pollutants in the presence of iron (hydr)oxides.

摘要

铁(氢)氧化物在地表环境中广泛存在,由于其较大的比表面积和氧化还原活性,它们积极参与有机污染物的转化。本工作研究了在模拟阳光照射下,三种常见的铁(氢)氧化物(赤铁矿(Hem)、针铁矿(Goe)和水铁矿(Fh))存在下,四环素(TC)的转化。这些铁(氢)氧化物表现出光活性,促进了 TC 的转化,初始光转化速率按以下顺序降低:Hem > Fh > Goe。TC 去除效率与 HO•生成率之间的线性相关性表明 HO•主导了 TC 的转化。HO•是由自生成的 HO 的 UV 诱导分解和表面 Fe 引发的光芬顿反应产生的。实验结果表明,HO•的生成受 HO 控制,而表面 Fe 过剩。在高结晶 Hem 和 Goe 的存在下,阳光驱动的 HO 生成是通过一步两电子还原途径发生的,而在低结晶 Fh 的存在下,该过程是由 O 诱导的 Fe 氧化和电子在导带中直接还原 O 共同贡献的。这些发现表明,阳光可能会显著加速铁(氢)氧化物存在下有机污染物的降解。

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