{"title":"光触媒, オゾンあるいは過酸化水素によるCN^-イオン含有水溶液の分解","authors":"佐貫 須美子, 拓史 山本, 正輝 持舘","doi":"10.2473/SHIGENTOSOZAI.122.489","DOIUrl":null,"url":null,"abstract":"Decomposition reactions of aqueous CN- ions by TiO2 photocatalyst, ozone and/or hydrogen peroxide were investigated. The principal findings obtained are as follows:1) The presence of dissolved oxygen was necessary to decompose aqueous CN- ions photocatalytically. CN- was oxidized to CNO- with TiO2 catalyst, and then to CO32- and NO3-. Oxidation reaction of CNO- to CO32- and NO3- was far slower compared to that of CN- to CNO-. Photocatalytic oxidation reaction of CNO- at pHs 7 and 10 proceeded distinctly faster compared to that at pH 12. 2) Although ozone oxidation of CN- took the same paths as photocatalytic reactions, but it was faster than that of photocatalytic routes. Combined use of photocatalyst and ozone for the decomposition of CN- was more efficient.3) Decomposition product of CN- with hydrogen peroxide was found as CNO- and N2. Joint use of hydrogen peroxide and photocatalyst promoted reaction of CN- to N2.","PeriodicalId":21719,"journal":{"name":"Shigen-to-sozai","volume":"38 1","pages":"489-496"},"PeriodicalIF":0.0000,"publicationDate":"2006-11-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Shigen-to-sozai","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2473/SHIGENTOSOZAI.122.489","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Decomposition reactions of aqueous CN- ions by TiO2 photocatalyst, ozone and/or hydrogen peroxide were investigated. The principal findings obtained are as follows:1) The presence of dissolved oxygen was necessary to decompose aqueous CN- ions photocatalytically. CN- was oxidized to CNO- with TiO2 catalyst, and then to CO32- and NO3-. Oxidation reaction of CNO- to CO32- and NO3- was far slower compared to that of CN- to CNO-. Photocatalytic oxidation reaction of CNO- at pHs 7 and 10 proceeded distinctly faster compared to that at pH 12. 2) Although ozone oxidation of CN- took the same paths as photocatalytic reactions, but it was faster than that of photocatalytic routes. Combined use of photocatalyst and ozone for the decomposition of CN- was more efficient.3) Decomposition product of CN- with hydrogen peroxide was found as CNO- and N2. Joint use of hydrogen peroxide and photocatalyst promoted reaction of CN- to N2.