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
爱德华发布了新的文献求助10
1秒前
1秒前
大方亦瑶完成签到,获得积分10
1秒前
NaNa发布了新的文献求助10
2秒前
龛龛完成签到,获得积分10
2秒前
LiuChao发布了新的文献求助10
2秒前
大力的大白菜真实的钥匙完成签到,获得积分10
3秒前
3秒前
4秒前
4秒前
听忆发布了新的文献求助10
4秒前
dididi发布了新的文献求助10
4秒前
不安凡白完成签到,获得积分10
5秒前
Ava应助周小福采纳,获得10
5秒前
5秒前
5秒前
宗铁强完成签到,获得积分10
5秒前
稳重海豚完成签到,获得积分10
6秒前
xue完成签到,获得积分10
6秒前
6秒前
molihuakai应助77采纳,获得10
6秒前
mingjing发布了新的文献求助10
6秒前
牛的不low的完成签到,获得积分10
7秒前
7秒前
7秒前
刘柑橘完成签到,获得积分10
7秒前
失眠的紫霜完成签到,获得积分10
7秒前
CodeCraft应助可爱半山采纳,获得10
8秒前
8秒前
xue发布了新的文献求助10
9秒前
NexusExplorer应助科研工作者采纳,获得10
9秒前
9秒前
丹霞应助明亮凡儿采纳,获得10
10秒前
Doric完成签到,获得积分20
10秒前
英姑应助大方亦瑶采纳,获得10
11秒前
岳小完成签到,获得积分10
11秒前
11秒前
11秒前
时尚的电脑完成签到,获得积分10
11秒前
学术蝗虫完成签到,获得积分10
12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
The Cambridge History of China: Volume 4, Sui and T'ang China, 589–906 AD, Part Two 1500
Cowries - A Guide to the Gastropod Family Cypraeidae 1200
Quality by Design - An Indispensable Approach to Accelerate Biopharmaceutical Product Development 800
Pulse width control of a 3-phase inverter with non sinusoidal phase voltages 777
Signals, Systems, and Signal Processing 610
Research Methods for Applied Linguistics: A Practical Guide 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 物理 内科学 复合材料 催化作用 物理化学 光电子学 电极 细胞生物学 基因 无机化学
热门帖子
关注 科研通微信公众号,转发送积分 6400713
求助须知:如何正确求助?哪些是违规求助? 8217528
关于积分的说明 17414225
捐赠科研通 5453742
什么是DOI,文献DOI怎么找? 2882258
邀请新用户注册赠送积分活动 1858825
关于科研通互助平台的介绍 1700576