生物炭
化学
锰
氧化还原
催化作用
降级(电信)
电子转移
核化学
兴奋剂
无机化学
光化学
材料科学
有机化学
电信
光电子学
计算机科学
热解
作者
Zhifeng Liu,Miao He,Lin Tang,Binbin Shao,Qinghua Liang,Ting Wu,Yuan Pan,Xiansheng Zhang,Songhao Luo,Qingyun He,Lin Ge
标识
DOI:10.1016/j.jcis.2022.12.008
摘要
Mn and N co-doped biochar (Mn-N-TS) was prepared as an effective catalyst to activate peroxymonosulfate (PMS) for ciprofloxacin (CIP) degradation. As opposed to Mn-TS and N-TS, Mn-N-TS had more active sites containing N and Mn, as well as a greater specific surface area (923.733 m2 g-1). The Mn-N-TS exhibited excellent PMS activation ability. In the Mn-N-TS/PMS system, the CIP removal efficiency was 91.9% in 120 min. Mn and N co-doping could accelerate electron transfer between CIP and PMS molecules. Simultaneously, defect sites, graphitic N, pyridinic N, C═O groups, and Mn(II)/Mn(III)/Mn(IV) redox cycles acted as active sites to activate PMS and generate free radicals (OH, SO4- and 1O2). Furthermore, the Mn-N-TS/PMS system could effectively degrade CIP in a wide pH range, background substances, and actual water. Finally, a probable mechanism of PMS activation by Mn-N-TS was proposed. In conclusion, this work gave a novel direction for the rational design of Mn and N co-doped biochar.
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