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在黑暗中用钨酸铋高效活化过硫酸盐以降解有机污染物。

Efficient activation of persulfate with bismuth tungstate in dark for degradation of organic pollutants.

作者信息

Ye Zilong, Peng Renfu, Liu Wenwen, Li Ronghuan, Zou Qi

机构信息

College of Physical Science and Engineering Technology, Yichun University, Yichun, 336000, China.

College of Physical Science and Engineering Technology, Yichun University, Yichun, 336000, China.

出版信息

Environ Res. 2025 May 15;273:121258. doi: 10.1016/j.envres.2025.121258. Epub 2025 Feb 27.

Abstract

Bismuth tungstate (BiWO, BWO) is usually utilized as a photocatalyst for the degradation of various organic pollutants. However, its catalytic potential without light irradiation in persulfate (PS) based advanced oxidation processes (AOPs) has been overlooked, despite its significant redox capacity. Herein, the flower-like orthorhombic BWO was synthesized using a simple hydrothermal method, followed by an evaluation of its catalytic activity in dark through the removal of aqueous organic dye rhodamine B and antibiotic levofloxacin in PS based AOPs. The results indicate that the BWO/PS system exhibits remarkable efficacy in removing both pollutants compared to the counterparts, demonstrating the effective activation of PS with BWO. Additionally, N-de-ethylation and conjugated ring destruction processes during rhodamine B removal were confirmed by liquid chromatography-mass spectrometry, further substantiating the occurrence of degradation reactions. Furthermore, the electrochemical and radical identification experiments were conducted to elucidate the mechanism underlying PS activation with BWO for pollutant degradation. The results suggest that the electron transfer between BWO and PS induces PS activation, leading to the generation of singlet oxygen and superoxide radical. Therein, singlet oxygen acts as the dominate active species while superoxide radical plays a supportive role in pollutant degradation. Moreover, cyclic experiments reveal the moderate phase and structural stability of BWO in terms of activating PS and the BWO/PS system still can remove rhodamine B exceeding 80% in actual waters. The work provides a new candidate for PS activation and highlights the applicability of conventional bismuth compounds in PS based AOPs system for wastewater treatment without additional energy input.

摘要

钨酸铋(BiWO₄,BWO)通常用作光催化剂来降解各种有机污染物。然而,尽管其具有显著的氧化还原能力,但其在基于过硫酸盐(PS)的高级氧化过程(AOPs)中无光照射时的催化潜力却被忽视了。在此,采用简单的水热法合成了花状正交晶系BWO,然后通过在基于PS的AOPs中去除水性有机染料罗丹明B和抗生素左氧氟沙星来评估其在黑暗中的催化活性。结果表明,与其他体系相比,BWO/PS体系在去除这两种污染物方面表现出显著的效果,证明了BWO对PS的有效活化。此外,液相色谱 - 质谱法证实了罗丹明B去除过程中的N - 去乙基化和共轭环破坏过程,进一步证实了降解反应的发生。此外,进行了电化学和自由基鉴定实验,以阐明BWO活化PS降解污染物的潜在机制。结果表明,BWO与PS之间的电子转移诱导了PS的活化,导致单线态氧和超氧自由基的产生。其中,单线态氧是主要的活性物种,而超氧自由基在污染物降解中起辅助作用。此外,循环实验揭示了BWO在活化PS方面具有适度的相和结构稳定性,并且BWO/PS体系在实际水体中仍能去除超过80%的罗丹明B。这项工作为PS活化提供了一种新的候选材料,并突出了传统铋化合物在基于PS的AOPs系统中用于废水处理而无需额外能量输入的适用性。

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