生物炭
纳米复合材料
催化作用
降级(电信)
化学工程
铜
X射线光电子能谱
热解
环境修复
材料科学
化学
猝灭(荧光)
纳米技术
冶金
污染
有机化学
荧光
生物
物理
工程类
电信
量子力学
计算机科学
生态学
作者
Yue Wang,Lele Qiao,Xueyi Zhang,Zhenglong Liu,Tielong Li,Haitao Wang
标识
DOI:10.1016/j.seppur.2023.125077
摘要
Biochar-based nanocomposites are recognized as promising catalysts for peroxymonosulfate (PMS) activation due to their cost-effectiveness, large surface area, and desirable activity. However, their conventional preparation involves laborious and energy-consuming high-temperature pyrolysis. In this study, we introduce an efficient approach to synthesize FeCu@BC nanocomposites using iron and copper chlorides with green tea via a mechanochemical method. Characterization results show that copper incorporation enhances the defect degree of biochar, increasing oxygen vacancies in FeCu@BC. Remarkably, FeCu@BC exhibits an outstanding efficiency of 92.24% in degrading TC, achieving more than 85% TC removal even under challenging conditions with varying pH levels and competing ions, making it a promising catalyst for practical applications. Through detailed investigations, we identify O2− and 1O2 as the primary active species responsible for TC degradation, supported by quenching and EPR tests. Furthermore, copper doping significantly improves electron transfer between FeCu@BC and PMS, promoting PMS activation during degradation. XPS analysis provides insights into the transformation of doped copper species, acting as potential active sites that facilitate PMS decomposition to generate O2− and 1O2. With significant advantages in cost-effectiveness and avoidance of energy-intensive pyrolysis, the mechanochemically synthesized FeCu@BC nanocomposites hold great promise for wide application in efficient wastewater treatment and environmental remediation.
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