单线态氧
催化作用
化学
纳米团簇
镍
光化学
双酚A
协同催化
活性氧
氧气
无机化学
石墨氮化碳
光催化
有机化学
生物化学
环氧树脂
作者
Junjie You,Junyi Li,Heng Zhang,Meng-Fan Luo,Bo Xing,Yi Ren,Yang Liu,Zhaokun Xiong,Chuan-Shu He,Bo Lai
标识
DOI:10.1016/j.jhazmat.2022.130440
摘要
In this work, a g-C3N4 supported NiCx nanoclusters catalyst (NiCx-CN) was developed, and its performance in activating peroxymonosulfate (PMS) was evaluated. Mechanism investigation stated that although singlet oxygen (1O2) was formed in the catalytic process, its contribution to BPA elimination was weeny. Interestingly, through the experiment with dimethyl sulfoxide as the probe, it was considered that the high-valent nickel-oxo species (Ni&+=O), generated after the interaction of NiCx-CN and PMS, was the dominating reactive oxygen species (ROS). Theoretical calculations (DFT) implied that NiCx-CN might lose electrons to generate high-valent Ni, which was consistent with the detection of Ni3+ on the surface of the used NiCx-CN. Besides, the prepared NiCx-CN showed advantages in resisting the interference of inorganic anions. Meanwhile, three BPA degradation routes had been proposed based on the transformation intermediates. This study will establish a new protocol for PMS activation using heterogeneous Ni-based catalysts to efficiently degrade organic pollutants via a nonradical mechanism.
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