生物炭
化学
降级(电信)
催化作用
亚甲蓝
动力学
核化学
反应速率常数
光催化
有机化学
热解
计算机科学
量子力学
物理
电信
作者
Yuanping Li,Yuqing Liu,Yihuan Liu,Yaoning Chen,Yaoning Chen,Li Chen,Haoqin Yan,Yanrong Chen,Yanrong Chen,Fangting Xu,Meiling Li,Linshenzhang Li
标识
DOI:10.1016/j.jwpe.2022.102864
摘要
In this study, sludge biochar (SBC) was prepared by pyrolysis method, MnO2 and MnO2@SBCs with different MnO2/SBC mass ratios (3%, 5%, 10% and 20%) were synthesized by co-precipitation method. The catalytic performance was examined by activating peroxymonosulfate (PMS) for methylene blue (MB) degradation. MB can be completely removed within 30 min when the mass ratio of MnO2/SBC is greater than 5% and the degradation kinetics of MB is more in line with the pseudo-first-order kinetic model in the MnO2@SBC/PMS system. Besides, the pseudo-first-order kinetic constants (k) in MnO2@SBC/PMS are significantly higher than that in SBC/PMS and MnO2/PMS, and the largest degradation rate of MB is in 5% MnO2@SBC/PMS system. MnO2@SBC exhibited excellent PMS activation ability in a wide range of pH (5–9) with complete degradation of MB in 30 min. Furthermore, MnO2@SBC has good stability after five usages still activating PMS for complete degradation of MB in 180 min. The quenching experiments and EPR spectrum indicated that both SO4−, OH and 1O2 were the main reactive oxygen species. Finally, the probable MB degradation pathway was proposed in the MnO2/PMS system. This study provides a reliable insight into sludge resource utilization, sludge biochar modification and its catalytic performance improvement.
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