Novel heterogeneous Fenton catalysts for promoting carbon iron electron transfer by one-step hydrothermal synthesization

被引:5
作者
Cheng, Liulong [1 ]
Lu, Zhuoye [1 ]
Liu, Junjun [1 ]
Liu, Jingyi [1 ]
Zhao, Yu [1 ]
Ni, Zhuobiao [1 ]
Lin, Qingqi [1 ]
Zhu, Runliang [2 ,3 ]
Chen, Xiaojuan [4 ]
Lin, Weikun [1 ]
Qiu, Rongliang [1 ,5 ]
Zhu, Yanping [1 ]
机构
[1] South China Agr Univ, Coll Nat Resources & Environm, Guangdong Lab Lingnan Modern Agr, Guangdong Prov Key Lab Agr & Rural Pollut Abatemen, Guangzhou 510642, Peoples R China
[2] Chinese Acad Sci, Guangzhou Inst Geochem, CAS Key Lab Mineral & Metallogeny, Guangdong Prov Key Lab Mineral Phys & Mat, Guangzhou 510640, Peoples R China
[3] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[4] Foshan Univ, Foshan 528225, Peoples R China
[5] Sun Yat Sen Univ, China Sch Environm Sci & Engn, Guangzhou 510006, Peoples R China
基金
中国国家自然科学基金;
关键词
Hydrothermal carbon; Humboldtine; Electron transfer; Fe(III)/Fe(II) redox cycle; As(III) removal; SITU ATR-FTIR; ACTIVATED CARBON; ADSORPTION; PERSULFATE; CARBONIZATION; DEGRADATION; REMOVAL; BIOMASS; WATER; FERRIHYDRITE;
D O I
10.1016/j.jcis.2023.11.150
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Carbon materials play a crucial role in promoting the Fe(III)/Fe(II) redox cycle in heterogeneous Fenton reactions. However, the electron transfer efficiency between carbon and iron is typically low. In this study, we prepared a novel heterogeneous Fenton catalyst, humboldtine/hydrothermal carbon (Hum/HTC), using a onestep hydrothermal method and achieved about 100 % reduction in Fe(III) during synthesis. Moreover, the HTC continuously provided electrons to promote Fe(II) regeneration during the Fenton reaction. Electron paramagnetic resonance (EPR) and quenching experiments showed that Hum/HTC completely oxidized As(III) to As(V) via free radical and non-free radical pathways. Attenuated total reflectance Fourier-transform infrared (ATR-FTIR) and two-dimensional correlation spectroscopy (2D-COS) analyses revealed that monodentate mononuclear (MM) and bidentate binuclear (BB) structures were the dominant bonding methods for As(V) immobilization. 40 %Hum/HTC exhibited a maximum As(III) adsorption capacity of 167 mg/g, which was higher than that of most reported adsorbents. This study provides a novel strategy for the efficient reduction of Fe (III) during catalyst synthesis and demonstrates that HTC can continuously accelerate Fe(II) regeneration in heterogeneous Fenton reactions.
引用
收藏
页码:597 / 608
页数:12
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