Activation of peroxymonosulfate by magnetic Fe3S4/biochar composites for the efficient degradation of 2,4,6-trichlorophenol: Synergistic effect and mechanism

生物炭 催化作用 X射线光电子能谱 化学 电子顺磁共振 介电谱 降级(电信) 碳纤维 电化学 化学工程 光化学 材料科学 热解 有机化学 复合材料 复合数 物理化学 物理 工程类 电信 核磁共振 计算机科学 电极
作者
Hui Li,Siyang Li,Lide Jin,Lu Zhen,Minghui Xiang,Chen Wang,Wenbing Wang,Jin Zhang,Chunyang Li,Haijiao Xie
出处
期刊:Journal of environmental chemical engineering [Elsevier BV]
卷期号:10 (1): 107085-107085 被引量:49
标识
DOI:10.1016/j.jece.2021.107085
摘要

The synergistic catalytic degradation of metal carbon-based composites is a feasible strategy to improve the efficiency of advanced oxidation processes (AOPs) by means of green chemistry. In this work, Fe3S4 nanoparticles were anchored on the surface of peanut shell biochar to prepare magnetic Fe3S4/biochar (Fe3S4/BC) composites, which were applied to activate peroxymonosulfate (PMS) to degrade 2,4,6-trichlorophenol (2,4,6-TCP). The addition of biochar not only reduced the aggregation of Fe3S4 nanoparticles, but also accelerated the electron transfer rate, and the constructed C-O-Fe bridges accelerated the regeneration of Fe(Ⅱ), which made Fe3S4/BC have better catalytic performance than pure Fe3S4 even though the use of metal sulfides was reduced. Fe on the surface of Fe3S4/BC was the catalytic reaction center. The dominant role of sulfate radical (SO4·-) and hydroxyl radical (HO·) on the degradation of 2,4,6-TCP was verified by electron paramagnetic resonance (EPR) and free radical quenching experiments. The mechanism of C-O-Fe bridges was verified by density functional theory (DFT) calculation. The mechanism of PMS activation by Fe3S4/BC was elucidated by electrochemical impedance spectroscopy (EIS) and X-ray photoelectron spectroscopy (XPS). Based on the detection results of intermediate products, the possible degradation pathways to 2,4,6-TCP were proposed. This work provides new insights into the synergistic catalytic mechanism of metal carbon-based sulfides and promotes the development of environmentally friendly and efficient metal carbon-based catalysts.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
刚刚
Akim应助科研通管家采纳,获得10
刚刚
JamesPei应助科研通管家采纳,获得10
刚刚
英俊的铭应助科研通管家采纳,获得10
刚刚
刚刚
汉堡包应助科研通管家采纳,获得10
刚刚
李爱国应助科研通管家采纳,获得10
刚刚
yingji发布了新的文献求助10
刚刚
酷波er应助科研通管家采纳,获得10
刚刚
传奇3应助科研通管家采纳,获得20
1秒前
一杯芝士应助科研通管家采纳,获得10
1秒前
1秒前
1秒前
2秒前
yjh1515790968发布了新的文献求助10
2秒前
3秒前
斯文败类应助开朗颜演采纳,获得10
3秒前
摆烂女硕发布了新的文献求助10
3秒前
peng发布了新的文献求助10
4秒前
chen完成签到,获得积分10
5秒前
小糖完成签到,获得积分10
5秒前
NicotineZen完成签到,获得积分10
6秒前
Alessnndre发布了新的文献求助10
6秒前
Gueyao完成签到,获得积分10
6秒前
斯文败类应助擅作主张采纳,获得10
7秒前
万能图书馆应助SS是采纳,获得10
7秒前
Bill发布了新的文献求助10
7秒前
chen发布了新的文献求助10
7秒前
顾矜应助细心觅风采纳,获得10
8秒前
8秒前
xulei完成签到,获得积分10
8秒前
8秒前
研友_LX7zK8完成签到,获得积分10
9秒前
9秒前
SS是完成签到,获得积分10
10秒前
12秒前
Yang完成签到,获得积分10
12秒前
科研通AI6.2应助yingji采纳,获得10
13秒前
焜少完成签到,获得积分10
13秒前
残夏完成签到,获得积分10
13秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Geist der Kunst und Kultur 1000
Social Psychology in the Real World 800
Resistance Spot Welding Dataset for Automobile Body-in-White Quality Analysis 748
悉尼大学博士学位论文,题目:Modelling and testing of one-sided stitched laminated composites. 作者:Kristopher P. Plain 700
Machine Learning for Asset Management and Pricing 600
Numerical analysis of the coupled atmosphere-ocean models (CAO II). II 600
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7412066
求助须知:如何正确求助?哪些是违规求助? 9015961
关于积分的说明 19204265
捐赠科研通 7043942
什么是DOI,文献DOI怎么找? 3233560
关于科研通互助平台的介绍 2395786
邀请新用户注册赠送积分活动 2215582