碳化
化学
吸附
降级(电信)
催化作用
污染物
碳纤维
双酚A
杂原子
化学工程
多孔性
苯酚
光化学
有机化学
材料科学
工程类
复合数
电信
复合材料
环氧树脂
计算机科学
戒指(化学)
作者
Hang Zhang,Xiaorong Gan,Shuo Chen,Hongtao Yu,Xie Quan
标识
DOI:10.1016/j.seppur.2022.121048
摘要
Peroxymonosulfate (PMS) activation is regarded as a powerful method for the degradation of organic pollutants. Carbon materials have attracted much attention for PMS activation toward efficient nonradical oxidation process. The catalytic activity of most nanocarbon materials is usually attributed to heteroatom doping, while the contribution of intrinsic defects has been explored little. Herein, self-template method was used to synthesize porous carbon with rich intrinsic defects. The results showed that the intrinsic defects enhanced adsorption and activation of PMS. FT-IR and DFT results revealed the adsorption of PMS on the vacancy defect resulted in the elongation of the peroxy bonds, producing a higher potential of surface-bound oxidative complexes (3DPC-X-PMS*). Electron transfer from pollutants to PMS* was achieved and phenol was degraded with a kinetic constant of 1.45 min−1, higher than most reported carbon-based materials. Other pollutants including bisphenol A, sulfamethoxazole and 4-chlorophenol also can be degraded efficiently. Furthermore, it can keep original catalytic activity in complicated water matrix. The work provides a strategy to develop efficient carbon materials and contributes to the better understanding of the role of intrinsic defects for PMS activation in the degradation of organic pollutants.
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