{"title":"Fenton试剂氧化氯化苯酚的研究","authors":"F. Potter, J. A. Roth","doi":"10.1089/HWM.1993.10.151","DOIUrl":null,"url":null,"abstract":"ABSTRACT Oxidation of chlorinated phenols using Fenton's reagent (hydrogen peroxide and ferrous iron catalyst) both oxidize and dechlorinate phenol species. The kinetics of the Fenton's oxidation of the three monochlorophenol isomers and five of the six dichlorophenol isomers were examined under batch and semibatch conditions. Concentrations of the organic species, oxidant utilization and caustic demand required to maintain a pH of 3.5 were monitored. The in-situ chloride concentration were monitored in selected tests as well. Ultimate oxidation to CO2, H2O, and HCl was not obtained under the test conditions, but the extent of oxidation to final products can be estimated from the measured parameters. A mechanism is hypothesized to explain the observed behavior of the oxidation processes. Test results show that the monochlorinated phenols oxidize about as rapidly as phenol itself. The dechlorinated phenols demonstrate a wide range of oxidation rates under the same test conditions. Mineralization was slight...","PeriodicalId":386820,"journal":{"name":"Hazardous waste and hazardous materials","volume":"23 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"1900-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"75","resultStr":"{\"title\":\"Oxidation of Chlorinated Phenols Using Fenton's Reagent\",\"authors\":\"F. Potter, J. A. Roth\",\"doi\":\"10.1089/HWM.1993.10.151\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"ABSTRACT Oxidation of chlorinated phenols using Fenton's reagent (hydrogen peroxide and ferrous iron catalyst) both oxidize and dechlorinate phenol species. The kinetics of the Fenton's oxidation of the three monochlorophenol isomers and five of the six dichlorophenol isomers were examined under batch and semibatch conditions. Concentrations of the organic species, oxidant utilization and caustic demand required to maintain a pH of 3.5 were monitored. The in-situ chloride concentration were monitored in selected tests as well. Ultimate oxidation to CO2, H2O, and HCl was not obtained under the test conditions, but the extent of oxidation to final products can be estimated from the measured parameters. A mechanism is hypothesized to explain the observed behavior of the oxidation processes. Test results show that the monochlorinated phenols oxidize about as rapidly as phenol itself. The dechlorinated phenols demonstrate a wide range of oxidation rates under the same test conditions. Mineralization was slight...\",\"PeriodicalId\":386820,\"journal\":{\"name\":\"Hazardous waste and hazardous materials\",\"volume\":\"23 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1900-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"75\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Hazardous waste and hazardous materials\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1089/HWM.1993.10.151\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Hazardous waste and hazardous materials","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1089/HWM.1993.10.151","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Oxidation of Chlorinated Phenols Using Fenton's Reagent
ABSTRACT Oxidation of chlorinated phenols using Fenton's reagent (hydrogen peroxide and ferrous iron catalyst) both oxidize and dechlorinate phenol species. The kinetics of the Fenton's oxidation of the three monochlorophenol isomers and five of the six dichlorophenol isomers were examined under batch and semibatch conditions. Concentrations of the organic species, oxidant utilization and caustic demand required to maintain a pH of 3.5 were monitored. The in-situ chloride concentration were monitored in selected tests as well. Ultimate oxidation to CO2, H2O, and HCl was not obtained under the test conditions, but the extent of oxidation to final products can be estimated from the measured parameters. A mechanism is hypothesized to explain the observed behavior of the oxidation processes. Test results show that the monochlorinated phenols oxidize about as rapidly as phenol itself. The dechlorinated phenols demonstrate a wide range of oxidation rates under the same test conditions. Mineralization was slight...