化学
碳纳米管
吸附
激进的
酚类
苯酚
高碘酸盐
光化学
有机化学
纳米技术
材料科学
作者
Jiali Peng,Peng Zhou,Hongyu Zhou,Bingkun Huang,Minglu Sun,Chuan-Shu He,Heng Zhang,Zhimin Ao,Wen Liu,Bo Lai
标识
DOI:10.1021/acs.est.2c08266
摘要
, Hammett constants and logarithm of the octanol-water partition coefficient). The adsorption of phenols on CNT surfaces and their electronic properties are critical factors affecting the oxidation process. Besides, in the CNTs/PI system, phenol adsorbed the CNT surfaces was oxidized by the CNTs-PI* complexes, and products were mainly generated via the coupling reaction of phenoxyl radical. Most of the products adsorbed and accumulated on the CNT surfaces realized phenol removal from the bulk solution. Such a unique non-mineralization removal process achieved an extremely high apparent electron utilization efficiency of 378%. The activity evaluation and theoretical calculations of CNT derivatives confirmed that the carbonyl/ketonic functional groups and double-vacancy defects of the CNTs were the primary active sites, where high-oxidation-potential CNTs-PI* were formed. Further, the PI species could achieve a stoichiometric decomposition into iodate, a safe sink of iodine species, without the generation of typical iodinated byproducts. Our discovery provides new mechanistic insight into CNTs-driven PI activation for the green future of environmental remediation.
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