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机构地区:[1]云南师范大学化学化工学院,云南昆明650500
出 处:《工业催化》2015年第12期986-990,共5页Industrial Catalysis
基 金:国家自然科学基金(20663007)资助项目
摘 要:在[Bmim]PF6离子液体介质中微波辅助制备稀土元素Ce掺杂改性的TiO_2光催化剂TiO_2-Ce,以甲基橙溶液和苯酚溶液为模拟污染物,在紫外光照和微波辐射-紫外光照降解条件下考察TiO_2-Ce催化剂的光催化活性。利用荧光技术以对苯二甲酸作为荧光探针检测TiO_2-Ce催化剂表面产生的羟基自由基,并对光催化降解反应进行动力学分析,以了解光催化降解反应机理。结果表明,通过优化反应条件制得的TiO_2-Ce催化剂具有较高光催化降解活性和热稳定性,在紫外光照和微波辐射-紫外光照条件下降解60 min后,甲基橙降解率分别为98.6%和99.3%,苯酚降解率分别为96.6%和97.2%。荧光光谱分析表明,TiO_2-Ce在微波辐射-紫外光照条件下产生的羟基自由基比紫外光照多,因而微波辐射-紫外光照具有强化TiO_2-Ce降解模拟污染物作用的效果。反应动力学数据表明,TiO_2-Ce光催化降解甲基橙溶液反应呈一级反应动力学规律,其表观速率常数k最大值为0.056 2 min-1。Using room temperature ionic liquid [ Bmim] PF6 as the reaction medium,cerium doped TiO2 photoeatalyst TiOz-Ce was prepared by microwave drying method and sol-gel method. The activity of TiO2-Ce photocatalyst for photocatalytic degradation of methyl orange and phenol solutions as simulated pollutants was respectively investigated under ultraviolet irradiation(UV) and microwave irradiation with ultraviolet irradiation (MW-UV). With terephthalie acid as the fluorescence probe, the influence of ~ OH on the surface of TiO2-Ce on its photocatalytic activity was investigated by the fluorescence technology. In order to understand the reaction mechanism, the photocatalytic degradation kinetics was experimentally determined. The results showed that TiO2-Ce catalysts prepared under the optimum condition had higher photocatalytic activity and heat stability. The degradation rates of methyl orange and phenol solution reached 98.6%, 99.3%, 96. 6%, and 97. 2%, respectively, under the condition of UV and MW-UV irradiation for 60 rain. The results of fluorescence spectra characterization indicated that the UV irradiation combining with MW technology could effectively improve the catalytic efficiency of TiO2-Ce catalyst due to more amount of hydroxyl radicals produced under MW-UV irradiation than that under UV irradiation. The reaction kinetics data showed that the photocatalytic degradation of methyl orange on TiO2-Ce catalyst fitted the first order kinetics model, and the maximum of apparent rate constant k was 0.056 2 rain-
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