Evaluation of the stability of polyacrylonitrile-based carbon fiber electrode for hydrogen peroxide production and phenol mineralization during electro-peroxone process

被引:36
作者
Xia, Guangsen [1 ,2 ]
Wang, Huijiao [2 ]
Zhan, Juhong [2 ]
Yin, Xiaomeng [1 ]
Wu, Xiaocui [1 ]
Yu, Gang [2 ]
Wang, Yujue [2 ]
Wu, Mingbo [1 ]
机构
[1] China Univ Petr East China, Coll Chem Engn, Coll New Energy, State Key Lab Heavy Oil Proc, Qingdao 266580, Peoples R China
[2] Tsinghua Univ, Beijing Key Lab Emerging Organ Contaminants Contr, State Key Joint Lab Environm Simulat & Pollut Con, Sch Environm, Beijing 100084, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
Carbon; Electro-peroxone; Hydrogen peroxide; Oxygen reduction reaction; Ozone; OXYGEN REDUCTION; ACTIVATED CARBON; CONVENTIONAL OZONATION; OPERATIONAL PARAMETERS; WATER-TREATMENT; H2O2; PRODUCTION; AQUEOUS-MEDIUM; NITROGEN; DEGRADATION; EFFICIENT;
D O I
10.1016/j.cej.2020.125291
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
This study evaluated the stability of polyacrylonitrile-based carbon fiber cathode for hydrogen peroxide (H2O2) production and phenol mineralization during multiple cycles of electro-peroxone (E-peroxone) process. Results show that the oxidation of bulk carbon fiber by electro-generated H2O2 and bubbled ozone (O-3) is negligible during the E-peroxone process. Nevertheless, the carbon fiber surface was oxidized to some extent as the cathode was repeatedly used in the multi-cycle E-peroxone process. Due to the oxidation by H2O2 and O-3, nitrogen-containing groups on the carbon fiber surface were converted from pyridinic-N to pyridonic-N during the E-peroxone process. These changes resulted in an increase in the activity of the cathode for oxygen reduction reaction (ORR), but a decrease in the selectivity of the cathode for two-electron ORR to H2O2. After the carbon fiber cathode was used for 30 cycles of the E-peroxone treatment of phenol solutions, the cathodic potentials for ORR shifted positively by similar to 450 mV, which is beneficial to reduce the energy consumption of electrochemical H2O2 production. Nevertheless, the apparent current efficiency (ACE) for H2O2 production decreased from similar to 91.5% for the virgin cathode to similar to 48.2% for the used cathode. Despite the decrease in the ACE for H2O2 production, sufficient amounts of H2O2 could still be produced during the E-peroxone process with the used cathode. Therefore, complete phenol mineralization was maintained during all 30 cycles of the E-peroxone treatment of phenol solutions. These results suggest that the polyacrylonitrile-based carbon fiber is a promising cathode material for long-term E-peroxone operations.
引用
收藏
页数:10
相关论文
共 60 条
[1]   Electrochemical anodic oxidation of nitrogen doped carbon nanowall films: X-ray photoelectron and Micro-Raman spectroscopy study [J].
Achour, A. ;
Vizireanu, S. ;
Dinescu, G. ;
Le Brizoual, L. ;
Djouadi, M. -A. ;
Boujtita, M. .
APPLIED SURFACE SCIENCE, 2013, 273 :49-57
[2]   DETERMINATION OF OZONE IN WATER BY THE INDIGO METHOD [J].
BADER, H ;
HOIGNE, J .
WATER RESEARCH, 1981, 15 (04) :449-456
[3]   Electro-peroxone treatment of Orange II dye wastewater [J].
Bakheet, Belal ;
Yuan, Shi ;
Li, Zhaoxin ;
Wang, Huijiao ;
Zuo, Jiane ;
Komarneni, Sridhar ;
Wang, Yujue .
WATER RESEARCH, 2013, 47 (16) :6234-6243
[4]   Modular Advanced Oxidation Process Enabled by Cathodic Hydrogen Peroxide Production [J].
Barazesh, James M. ;
Hennebel, Tom ;
Jasper, Justin T. ;
Sedlak, David L. .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2015, 49 (12) :7391-7399
[5]   Electrochemically assisted decomposition of ozone for degradation and mineralization of Diuron [J].
Bavasso, Irene ;
Montanaro, Daniele ;
Di Palma, Luca ;
Petrucci, Elisabetta .
ELECTROCHIMICA ACTA, 2020, 331
[6]   Enhancing the performance of electro-peroxone by incorporation of UV irradiation and BDD anodes [J].
Bensalah, Nasr ;
Bedoui, Ahmed .
ENVIRONMENTAL TECHNOLOGY, 2017, 38 (23) :2979-2987
[7]   Electro-Fenton Process and Related Electrochemical Technologies Based on Fenton's Reaction Chemistry [J].
Brillas, Enric ;
Sires, Ignasi ;
Oturan, Mehmet A. .
CHEMICAL REVIEWS, 2009, 109 (12) :6570-6631
[8]   Active sites of nitrogen-doped carbon materials for oxygen reduction reaction clarified using model catalysts [J].
Guo, Donghui ;
Shibuya, Riku ;
Akiba, Chisato ;
Saji, Shunsuke ;
Kondo, Takahiro ;
Nakamura, Junji .
SCIENCE, 2016, 351 (6271) :361-365
[9]   Comparison of emerging contaminant abatement by conventional ozonation, catalytic ozonation, O3/H2O2 and electro-peroxone processes [J].
Guo, Yang ;
Zhao, Erzhuo ;
Wang, Jun ;
Zhang, Xiaoyuan ;
Huang, Haiou ;
Yu, Gang ;
Wang, Yujue .
JOURNAL OF HAZARDOUS MATERIALS, 2020, 389
[10]   Electro-peroxone degradation of diethyl phthalate: Cathode selection, operational parameters, and degradation mechanisms [J].
Hou, Meifang ;
Chu, Yaofei ;
Li, Xiang ;
Wang, Huijiao ;
Yao, Weikun ;
Yu, Gang ;
Murayama, Seiichi ;
Wang, Yujue .
JOURNAL OF HAZARDOUS MATERIALS, 2016, 319 :61-68