Hak-Hyeon Kim, Hongshin Lee, N. Park, Byeong-Dae Lee, Changha Lee
{"title":"碳酸氢盐存在下铜催化类芬顿反应对苯酚的增强氧化","authors":"Hak-Hyeon Kim, Hongshin Lee, N. Park, Byeong-Dae Lee, Changha Lee","doi":"10.26802/JAOTS.2017.0038","DOIUrl":null,"url":null,"abstract":"In this study, the copper-catalyzed Fenton-like reaction in the presence of bicarbonate (i.e., the Cu(II)/HCO3−/H2O2 system) was examined for the phenol degradation. The rate of phenol degradation by the copper-catalyzed Fenton-like reaction ([Cu(II)]0 = 0.1 mM, [H2O2]0 = 10 mM, pH = 10) was accelerated by 17-fold in the presence of 50 mM HCO3−. The rate of phenol degradation by the Cu(II)/HCO3−/H2O2 system increased with increasing doses of Cu(II) and HCO3−, but showed an optimal value for the H2O2 dose and pH at 5 mM and 10, respectively. The Cu(II)/HCO3−/H2O2 system was selective in degrading phenolic compounds; benzoic acid was resistant to degradation. Cu(III) species (likely complexed forms with carbonate) are believed to be the reactive oxidants responsible for the phenol degradation by the Cu(II)/HCO3−/H2O2 system. Meanwhile, aerating CO2 gas successfully accelerated the phenol degradation by the copper-catalyzed Fenton-like reaction, implying that CO2 aeration can be a practical option to supply bicarbonate when implementing the Cu(II)/HCO3−/H2O2 system.","PeriodicalId":14870,"journal":{"name":"Journal of Advanced Oxidation Technologies","volume":"166 1","pages":"54-66"},"PeriodicalIF":0.0000,"publicationDate":"2018-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"3","resultStr":"{\"title\":\"Enhanced Oxidation of Phenol by Copper-catalyzed Fenton-like Reaction in the Presence of Bicarbonate\",\"authors\":\"Hak-Hyeon Kim, Hongshin Lee, N. Park, Byeong-Dae Lee, Changha Lee\",\"doi\":\"10.26802/JAOTS.2017.0038\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"In this study, the copper-catalyzed Fenton-like reaction in the presence of bicarbonate (i.e., the Cu(II)/HCO3−/H2O2 system) was examined for the phenol degradation. The rate of phenol degradation by the copper-catalyzed Fenton-like reaction ([Cu(II)]0 = 0.1 mM, [H2O2]0 = 10 mM, pH = 10) was accelerated by 17-fold in the presence of 50 mM HCO3−. The rate of phenol degradation by the Cu(II)/HCO3−/H2O2 system increased with increasing doses of Cu(II) and HCO3−, but showed an optimal value for the H2O2 dose and pH at 5 mM and 10, respectively. The Cu(II)/HCO3−/H2O2 system was selective in degrading phenolic compounds; benzoic acid was resistant to degradation. Cu(III) species (likely complexed forms with carbonate) are believed to be the reactive oxidants responsible for the phenol degradation by the Cu(II)/HCO3−/H2O2 system. Meanwhile, aerating CO2 gas successfully accelerated the phenol degradation by the copper-catalyzed Fenton-like reaction, implying that CO2 aeration can be a practical option to supply bicarbonate when implementing the Cu(II)/HCO3−/H2O2 system.\",\"PeriodicalId\":14870,\"journal\":{\"name\":\"Journal of Advanced Oxidation Technologies\",\"volume\":\"166 1\",\"pages\":\"54-66\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2018-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"3\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Advanced Oxidation Technologies\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.26802/JAOTS.2017.0038\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q\",\"JCRName\":\"Chemistry\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Advanced Oxidation Technologies","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.26802/JAOTS.2017.0038","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q","JCRName":"Chemistry","Score":null,"Total":0}
引用次数: 3
摘要
在本研究中,研究了在碳酸氢盐存在下(即Cu(II)/HCO3−/H2O2体系)铜催化的类fenton反应对苯酚的降解。在50 mM HCO3−的存在下,铜催化的类fenton反应([Cu(II)]0 = 0.1 mM, [H2O2]0 = 10 mM, pH = 10)对苯酚的降解速度提高了17倍。Cu(II)/HCO3−/H2O2体系对苯酚的降解速率随Cu(II)和HCO3−浓度的增加而增加,但在H2O2浓度和pH分别为5 mM和10 mM时达到最佳值。Cu(II)/HCO3−/H2O2体系对酚类化合物有选择性降解;苯甲酸不易降解。Cu(III)物种(可能与碳酸盐络合形式)被认为是Cu(II)/HCO3−/H2O2系统降解苯酚的活性氧化剂。同时,通过铜催化的类fenton反应,曝气CO2气体成功地加速了苯酚的降解,这意味着在实施Cu(II)/HCO3−/H2O2体系时,CO2曝气可以作为一种实用的选择来供应碳酸氢盐。
Enhanced Oxidation of Phenol by Copper-catalyzed Fenton-like Reaction in the Presence of Bicarbonate
In this study, the copper-catalyzed Fenton-like reaction in the presence of bicarbonate (i.e., the Cu(II)/HCO3−/H2O2 system) was examined for the phenol degradation. The rate of phenol degradation by the copper-catalyzed Fenton-like reaction ([Cu(II)]0 = 0.1 mM, [H2O2]0 = 10 mM, pH = 10) was accelerated by 17-fold in the presence of 50 mM HCO3−. The rate of phenol degradation by the Cu(II)/HCO3−/H2O2 system increased with increasing doses of Cu(II) and HCO3−, but showed an optimal value for the H2O2 dose and pH at 5 mM and 10, respectively. The Cu(II)/HCO3−/H2O2 system was selective in degrading phenolic compounds; benzoic acid was resistant to degradation. Cu(III) species (likely complexed forms with carbonate) are believed to be the reactive oxidants responsible for the phenol degradation by the Cu(II)/HCO3−/H2O2 system. Meanwhile, aerating CO2 gas successfully accelerated the phenol degradation by the copper-catalyzed Fenton-like reaction, implying that CO2 aeration can be a practical option to supply bicarbonate when implementing the Cu(II)/HCO3−/H2O2 system.
期刊介绍:
The Journal of advanced oxidation technologies (AOTs) has been providing an international forum that accepts papers describing basic research and practical applications of these technologies. The Journal has been publishing articles in the form of critical reviews and research papers focused on the science and engineering of AOTs for water, air and soil treatment. Due to the enormous progress in the applications of various chemical and bio-oxidation and reduction processes, the scope of the Journal is now expanded to include submission in these areas so that high quality submission from industry would also be considered for publication. Specifically, the Journal is soliciting submission in the following areas (alphabetical order): -Advanced Oxidation Nanotechnologies -Bio-Oxidation and Reduction Processes -Catalytic Oxidation -Chemical Oxidation and Reduction Processes -Electrochemical Oxidation -Electrohydraulic Discharge, Cavitation & Sonolysis -Electron Beam & Gamma Irradiation -New Photocatalytic Materials and processes -Non-Thermal Plasma -Ozone-based AOTs -Photochemical Degradation Processes -Sub- and Supercritical Water Oxidation -TiO2 Photocatalytic Redox Processes -UV- and Solar Light-based AOTs -Water-Energy (and Food) Nexus of AOTs