Regulation of friction pair to promote conversion of mechanical energy to chemical energy on Bi2WO6 and realization of enhanced tribocatalytic activity to degrade different pollutants

降级(电信) 罗丹明B 污染物 激进的 光催化 羟基自由基 聚合物 化学工程 催化作用 罗丹明 材料科学 电子顺磁共振 化学 化学稳定性 光化学 有机化学 计算机科学 电信 物理 核磁共振 量子力学 工程类 荧光
作者
Meixuan Wu,Yaning Zhang,Yuyan Yi,Baocheng Zhou,Pengfei Sun,Xiaoping Dong
出处
期刊:Journal of Hazardous Materials [Elsevier BV]
卷期号:459: 132147-132147 被引量:19
标识
DOI:10.1016/j.jhazmat.2023.132147
摘要

Recently, friction-induced tribocatalysis has received tremendous attention through converting mechanical energy to chemical energy. However, its efficiency is much lower than those of photocatalysis and piezocatalysis, and its environmental application is limited in dye degradation. Herein, we developed a facile approach to improve the tribocatalytic activity of Bi2WO6 via adding trace polymer powders to form friction pairs with Bi2WO6. Among various polymers, PTFE was demonstrated to be the best counterpart of Bi2WO6. Subsequently, the PTFE dosage, stirring rate, magnetic bar size and number, and stirring mode were further optimized. The PTFE-promoted Bi2WO6 tribocatalysis was verified to possess excellent performance not only for removing different dyes, but also for degrading chlorophenols that are typical persistent organic pollutants. Multiple uses of the recycled catalysts indicated its good stability and prominent tribocatalytic durability. EPR measurements suggested the generation of hydroxyl radical and superoxide radical, which were determined to be continuously generated within 12 h at the rates of 0.88 μM h−1 and 85 μM h−1, respectively. Subsequently, a possible mechanism was proposed to explain the enhanced performance of the PTFE-promoted Bi2WO6 tribocatalysis. Finally, on basis of the detected intermediates, the degradation pathways of Rhodamine B and 2,4-Dichlorophenol during tribocatalysis were suggested.
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