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The Application of an Activated Carbon Supported Cu-Ce/Ac Oxide Anode on the Electrocatalytic Degradation of Phenol
The Cu-AC (AC: activated carbon) and Cu/Ce-AC composite materials were synthesized using a one-pot sol-gel method. The surface microstructure and composition of the resulting samples were characterized by Brunauer–Emmett–Teller (BET) specific surface area analysis, scanning electronmicroscopy/energy...
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Published in: | International journal of electrochemical science 2017-10, Vol.12 (10), p.9640-9651 |
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container_title | International journal of electrochemical science |
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creator | Qu, Jun-e Zhou, Shu Wang, Hairen Cao, Zhiyong Liu, Hongfang |
description | The Cu-AC (AC: activated carbon) and Cu/Ce-AC composite materials were synthesized using a one-pot sol-gel method. The surface microstructure and composition of the resulting samples were characterized by Brunauer–Emmett–Teller (BET) specific surface area analysis, scanning electronmicroscopy/energy dispersive x-ray(SEM/EDX), and XPS(X-ray photoelectron spectroscopy) compared to pure AC. Finally, the electrochemical catalytic activity of the prepared materials for the oxidative degradation of phenol were contrastively studied. It was found that the Cu/Ce-AC catalyst had larger surface area, greater pHPZC value (pH value at the point of zero charge), stronger ability to chemisorb active oxygen, and more possible forms of higher oxides generated from chemisorbed hydroxyl radicals, than AC and Cu/AC. These factors synthetically resulted in its more prominence electro catalytic activity for phenol degradation compared to AC and Cu/AC. The 50min continuous electrochemical degradation for phenol by using Cu/Ce-AC achieved over 97% COD and 80% TOC removals at initiate phenol concentration =504mg/L, temperature = 25°C, pH = 3.0 and j = 80 A·m-2. The considerable electro catalytic performance of Cu-Ce/AC material makes it a promising anode for electrochemical treatment of organic pollutants in aqueous solution. |
doi_str_mv | 10.20964/2017.10.09 |
format | article |
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The surface microstructure and composition of the resulting samples were characterized by Brunauer–Emmett–Teller (BET) specific surface area analysis, scanning electronmicroscopy/energy dispersive x-ray(SEM/EDX), and XPS(X-ray photoelectron spectroscopy) compared to pure AC. Finally, the electrochemical catalytic activity of the prepared materials for the oxidative degradation of phenol were contrastively studied. It was found that the Cu/Ce-AC catalyst had larger surface area, greater pHPZC value (pH value at the point of zero charge), stronger ability to chemisorb active oxygen, and more possible forms of higher oxides generated from chemisorbed hydroxyl radicals, than AC and Cu/AC. These factors synthetically resulted in its more prominence electro catalytic activity for phenol degradation compared to AC and Cu/AC. The 50min continuous electrochemical degradation for phenol by using Cu/Ce-AC achieved over 97% COD and 80% TOC removals at initiate phenol concentration =504mg/L, temperature = 25°C, pH = 3.0 and j = 80 A·m-2. The considerable electro catalytic performance of Cu-Ce/AC material makes it a promising anode for electrochemical treatment of organic pollutants in aqueous solution.</description><identifier>ISSN: 1452-3981</identifier><identifier>EISSN: 1452-3981</identifier><identifier>DOI: 10.20964/2017.10.09</identifier><language>eng</language><publisher>Elsevier B.V</publisher><subject>Cu-Ce/Ac anode ; electrochemical degradation ; phenol ; sol-gel method</subject><ispartof>International journal of electrochemical science, 2017-10, Vol.12 (10), p.9640-9651</ispartof><rights>2017 The Authors. 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The surface microstructure and composition of the resulting samples were characterized by Brunauer–Emmett–Teller (BET) specific surface area analysis, scanning electronmicroscopy/energy dispersive x-ray(SEM/EDX), and XPS(X-ray photoelectron spectroscopy) compared to pure AC. Finally, the electrochemical catalytic activity of the prepared materials for the oxidative degradation of phenol were contrastively studied. It was found that the Cu/Ce-AC catalyst had larger surface area, greater pHPZC value (pH value at the point of zero charge), stronger ability to chemisorb active oxygen, and more possible forms of higher oxides generated from chemisorbed hydroxyl radicals, than AC and Cu/AC. These factors synthetically resulted in its more prominence electro catalytic activity for phenol degradation compared to AC and Cu/AC. The 50min continuous electrochemical degradation for phenol by using Cu/Ce-AC achieved over 97% COD and 80% TOC removals at initiate phenol concentration =504mg/L, temperature = 25°C, pH = 3.0 and j = 80 A·m-2. The considerable electro catalytic performance of Cu-Ce/AC material makes it a promising anode for electrochemical treatment of organic pollutants in aqueous solution.</description><subject>Cu-Ce/Ac anode</subject><subject>electrochemical degradation</subject><subject>phenol</subject><subject>sol-gel method</subject><issn>1452-3981</issn><issn>1452-3981</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNptUMlOwzAQtRBIVKUnfsB3lNZb4vgYhbJIlYpEOUeu41CjEEeOW9G_Z9IixIE5zPrmaeYhdEvJnBGViQUjVM6hIuoCTahIWcJVTi__5NdoNgwfBEwoLqScoGGzs7jo-9YZHZ3vsG-w7nBhojvoaGtc6rCF9uu-7304NfZJaReFwesvV8Nu58EDIgLRsrUmBg9Uuj1GZ_C9fQ-6_mV-2dnOtzfoqtHtYGc_cYreHpab8ilZrR-fy2KVGE6zmGwZsVJRKonRjU2ZkSzPpFBKUalFqmUGc8IbJcBrwjIyjg1IkedcGM6n6O7Ma4IfhmCbqg_uU4djRUl1kqwaJRsrogCdntEWTjo4G6rBONsZW7sAX1W1d__ufQMm0m24</recordid><startdate>201710</startdate><enddate>201710</enddate><creator>Qu, Jun-e</creator><creator>Zhou, Shu</creator><creator>Wang, Hairen</creator><creator>Cao, Zhiyong</creator><creator>Liu, Hongfang</creator><general>Elsevier B.V</general><scope>6I.</scope><scope>AAFTH</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>201710</creationdate><title>The Application of an Activated Carbon Supported Cu-Ce/Ac Oxide Anode on the Electrocatalytic Degradation of Phenol</title><author>Qu, Jun-e ; Zhou, Shu ; Wang, Hairen ; Cao, Zhiyong ; Liu, Hongfang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c316t-b20e791170cafe52c72867499917a45a760e703f94703a02608674c0968834c33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Cu-Ce/Ac anode</topic><topic>electrochemical degradation</topic><topic>phenol</topic><topic>sol-gel method</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Qu, Jun-e</creatorcontrib><creatorcontrib>Zhou, Shu</creatorcontrib><creatorcontrib>Wang, Hairen</creatorcontrib><creatorcontrib>Cao, Zhiyong</creatorcontrib><creatorcontrib>Liu, Hongfang</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>CrossRef</collection><jtitle>International journal of electrochemical science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Qu, Jun-e</au><au>Zhou, Shu</au><au>Wang, Hairen</au><au>Cao, Zhiyong</au><au>Liu, Hongfang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Application of an Activated Carbon Supported Cu-Ce/Ac Oxide Anode on the Electrocatalytic Degradation of Phenol</atitle><jtitle>International journal of electrochemical science</jtitle><date>2017-10</date><risdate>2017</risdate><volume>12</volume><issue>10</issue><spage>9640</spage><epage>9651</epage><pages>9640-9651</pages><issn>1452-3981</issn><eissn>1452-3981</eissn><abstract>The Cu-AC (AC: activated carbon) and Cu/Ce-AC composite materials were synthesized using a one-pot sol-gel method. The surface microstructure and composition of the resulting samples were characterized by Brunauer–Emmett–Teller (BET) specific surface area analysis, scanning electronmicroscopy/energy dispersive x-ray(SEM/EDX), and XPS(X-ray photoelectron spectroscopy) compared to pure AC. Finally, the electrochemical catalytic activity of the prepared materials for the oxidative degradation of phenol were contrastively studied. It was found that the Cu/Ce-AC catalyst had larger surface area, greater pHPZC value (pH value at the point of zero charge), stronger ability to chemisorb active oxygen, and more possible forms of higher oxides generated from chemisorbed hydroxyl radicals, than AC and Cu/AC. These factors synthetically resulted in its more prominence electro catalytic activity for phenol degradation compared to AC and Cu/AC. The 50min continuous electrochemical degradation for phenol by using Cu/Ce-AC achieved over 97% COD and 80% TOC removals at initiate phenol concentration =504mg/L, temperature = 25°C, pH = 3.0 and j = 80 A·m-2. The considerable electro catalytic performance of Cu-Ce/AC material makes it a promising anode for electrochemical treatment of organic pollutants in aqueous solution.</abstract><pub>Elsevier B.V</pub><doi>10.20964/2017.10.09</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Cu-Ce/Ac anode electrochemical degradation phenol sol-gel method |
title | The Application of an Activated Carbon Supported Cu-Ce/Ac Oxide Anode on the Electrocatalytic Degradation of Phenol |
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