MXenes公司
催化作用
钝化
化学
成核
化学工程
双酚A
碳纤维
激进的
氧化还原
降级(电信)
反应性(心理学)
无机化学
材料科学
图层(电子)
有机化学
复合数
复合材料
替代医学
环氧树脂
病理
工程类
电信
医学
计算机科学
作者
Sisheng Guo,Yuqi Zheng,Xinyue Zhang,Xinying Lei,Hao Sun,Tao Wen
标识
DOI:10.1016/j.apcata.2023.119543
摘要
MXenes materials are burgeoning candidates for advanced water purification. However, the self-restacking and surface passivation of MXenes severely hamper the utilization of their electronic properties and surface reactivity. Herein, we employed the strategy of carbon nanoplating stabilization of MXenes for not only effectively stabilizing the structure of MXenes but also providing nucleation growth of MnO2. The MXene@C@MnO2-activated PMS system was able to degrade ~ 100% of bisphenol A (BPA) (20 mg/L) within 4 min with the turnover frequency (TOF) of 8.14 min-1. Specifically, the generation of superoxide radicals by activation of peroxymonosulfate (PMS) through reversible redox cycling between Mn(IV) and Mn(III) cations was regarded as the crucial driver of BPA removal. The scale-up experiment in actual water bodies achieved more than 90% BPA removal at 1200-bed volumes with stable catalytic properties during 20 h continuous operation. This work offers a potential macroscopic MXene-based nanohybrids for advanced oxidation processes.
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