生物炭
双酚A
化学
催化作用
降级(电信)
分解
纳米颗粒
热解
可重用性
表面改性
化学工程
氮气
羟基自由基
光化学
激进的
有机化学
物理化学
程序设计语言
环氧树脂
工程类
软件
电信
计算机科学
作者
Zhilin Zhang,Heng Ding,Yan Li,Jian Yu,Lei Ding,Yanli Kong,Jiangya Ma
标识
DOI:10.1016/j.seppur.2021.120136
摘要
Nitrogen-doped biochar encapsulating Fe/Mn nanoparticles (Fe/[email protected]800) was synthesized as a cost-effective catalyst for activating peroxymonosulfate (PMS) towards the degradation of bisphenol-A (BPA). Superior catalytic performance of Fe/[email protected]800 was observed as BPA was completely degraded within 20 min and with a reaction rate 75.88-fold higher than that of pristine biochar. This observation ascribed to redox cycles between Fe and Mn with multivalent states and nitrogen functionalization in Fe/[email protected]800, accelerating the electronic migration in the activation of PMS. Further investigation indicated radical pathways, especially SO4− and OH serve a predominant role in the oxidative decomposition of BPA. Also, O2− and non-radical (1O2) assumed an indispensable role in this process. Environmental factors had little effect on the synergistic process of radical and non-radical. The potential BPA degradation pathway was inferred by Density Functional Theory (DFT) calculation and intermediates analysis. In terms of excellent separability, reusability, stability, and universality, Fe/[email protected]800 exhibited promising application prospects.
科研通智能强力驱动
Strongly Powered by AbleSci AI