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作 者:王君[1] 潘志军[1] 张朝红[2] 张向东[1] 温福宇[1] 孙伟[1] 张邯玉[1]
机构地区:[1]辽宁大学化学系,沈阳110036 [2]辽宁大学环境科学系,沈阳110036
出 处:《无机化学学报》2005年第10期1566-1570,共5页Chinese Journal of Inorganic Chemistry
基 金:国家自然科学基金资助项目(No.20371023)
摘 要:The mixed crystal nanometer TiO2 sonocatalyst was prepared by ultrasonic irradiation in hydrogen peroxide solution. The sonocatalytic activities were validated through the degradation of acid red B solution by ultrasonic irradiation in the presence of the title TiO2 catalyst. The results show that the sonocatalytic activity of the title TiO2 catalyst is obviously higher than that of original rutile and anatase nanometer TiO2 catalysts. The degradation ratio of acid red B in the presence of the title TiO2 catalyst surpasses 75%, while the degradation ratios are only 54.62% and 35.24% for rutile and anatase nanometer TiO2 catalysts, respectively.The mixed crystal nanometer TiO2 sonocatalyst was prepared by ultrasonic irradiation in hydrogen peroxide solution. The sonocatalytic activities were validated through the degradation of acid red B solution by ultrasonic irradiation in the presence of the title TiO2 catalyst. The results show that the sonocatalytic activity of the title TiO2 catalyst is obviously higher than that of original rutile and anatase nanometer TiO2 catalysts. The degradation ratio of acid red B in the presence of the title TiO2 catalyst surpasses 75%, while the degradation ratios are only 54.62% and 35.24% for rutile and anatase nanometer TiO2 catalysts, respectively.
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