DICP OpenIR
Oxidative degradation of azo dye by hydrogen peroxide electrogenerated in situ on anthraquinonemonosulphonate/polypyrrole composite cathode with heterogeneous CuO/gamma-Al2O3 catalyst
Zhang, Guoquan1; Wang, Shuai1; Zhao, Sha1; Fu, Lei2; Chen, Guohua3; Yang, Fenglin1
KeywordAnthraquinone Copper Oxide Eaops Heterogeneous Hydroxyl Radical
Source PublicationAPPLIED CATALYSIS B-ENVIRONMENTAL
2011-08-11
DOI10.1016/j.apcatb.2011.05.042
Volume106Issue:3-4Pages:370-378
Indexed BySCI
SubtypeArticle
WOS HeadingsScience & Technology ; Physical Sciences ; Technology
WOS SubjectChemistry, Physical ; Engineering, Environmental ; Engineering, Chemical
WOS Research AreaChemistry ; Engineering
WOS Keyword2-CHLOROPHENOL EMPLOYING GOETHITE ; PHOTOELECTRO-FENTON DEGRADATION ; DOPED DIAMOND ANODES ; ELECTRO-FENTON ; ELECTROCHEMICAL OXIDATION ; AQUEOUS-MEDIUM ; HYDROXYL RADICALS ; WATER ; ACID ; DECOMPOSITION
AbstractHeterogeneous electrocatalytic wet H2O2 oxidation technique for the removal of azo dye amaranth from aqueous solution was studied in the presence of solid CuO/gamma-Al2O3 catalyst and anthraquinonemonosulphonate/polypyrrole (AQS/PPy) composite cathode able to electrogenerate H2O2 in situ. The spherical CuO/gamma-Al2O3 catalysts with various CuO loadings and calcined at different temperatures were characterized by BET, ESEM-EDS, XRD and XPS. Several parameters affecting H2O2 electrogeneration and dye degradation such as solution pH, cathode potential (E-ca), oxygen flow rate (V-O2), CuO loading, reaction temperature as well as catalyst calcination temperature were investigated. Experimental results revealed that the optimal condition for H2O2 electrogeneration on the AQS/PPy composite modified cathode is V-O2 = 0.4 ml min(-1), E-ca = 0.4V and pH 4.3. On this occasion, ca. 90% chroma decay and 60% TOC removal of dye were achieved with 450 degrees C-calcined 5.78 wt%-CuO/gamma-Al2O3 catalyst and 70 degrees C reaction temperature. Dye degradation follows the second-order kinetics. Leaching tests showed that the leaching copper amount during the oxidation is only 4.0-7.0% per run and the role of heterogeneous activity is dominant. The catalytic activity of CuO/gamma-Al2O3 catalyst could be recovered after multiple runs by a re-calcination step. Furthermore, the stability of the AQS/PPy composite after consecutive operation was also investigated by chronoamperometric and EIS techniques. (C) 2011 Elsevier B.V. All rights reserved.
Language英语
WOS IDWOS:000294092400012
Citation statistics
Cited Times:41[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttp://cas-ir.dicp.ac.cn/handle/321008/142445
Collection中国科学院大连化学物理研究所
Affiliation1.Dalian Univ Technol, Minist Educ, Key Lab Ind Ecol & Environm Engn, Sch Environm Sci & Technol, Dalian 116024, Peoples R China
2.Chinese Acad Sci, Dalian Inst Chem Phys, Fuel Cell Syst & Engn Lab, Dalian 116023, Peoples R China
3.Hong Kong Univ Sci & Technol, Dept Chem Engn, Kowloon, Hong Kong, Peoples R China
Recommended Citation
GB/T 7714
Zhang, Guoquan,Wang, Shuai,Zhao, Sha,et al. Oxidative degradation of azo dye by hydrogen peroxide electrogenerated in situ on anthraquinonemonosulphonate/polypyrrole composite cathode with heterogeneous CuO/gamma-Al2O3 catalyst[J]. APPLIED CATALYSIS B-ENVIRONMENTAL,2011,106(3-4):370-378.
APA Zhang, Guoquan,Wang, Shuai,Zhao, Sha,Fu, Lei,Chen, Guohua,&Yang, Fenglin.(2011).Oxidative degradation of azo dye by hydrogen peroxide electrogenerated in situ on anthraquinonemonosulphonate/polypyrrole composite cathode with heterogeneous CuO/gamma-Al2O3 catalyst.APPLIED CATALYSIS B-ENVIRONMENTAL,106(3-4),370-378.
MLA Zhang, Guoquan,et al."Oxidative degradation of azo dye by hydrogen peroxide electrogenerated in situ on anthraquinonemonosulphonate/polypyrrole composite cathode with heterogeneous CuO/gamma-Al2O3 catalyst".APPLIED CATALYSIS B-ENVIRONMENTAL 106.3-4(2011):370-378.
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