摘要
以苯酚的光催化降解为模型反应,研究了锐钛矿相和金红石相二氧化钛纳米晶(7~40nm)的光催化活性.与市售的氧化钛相比,两种晶相的纳米氧化钛均有很高的光催化活性,锐钛矿相氧化钛对苯酚的深度矿化有更高的选择性.TiO2吸附的水及羟基会降低氧化钛的光催化活性.由于粒径减小使氧化钛的吸收带边界蓝移,粒径小的氧化钛有更高的催化活性,粒径<15nm时,显示出量子尺寸效应.
In the present study, particulate suspensions of nanosized(particle size less than 10nm)anatase and rutile TiO2 under UV irradiation in a loop photoreactor catalyzed the oxidation of a typical organic contaxninant: phenol. Both nanosized anatase and rutile TiO2 have a much higher photocatalytic activity than bulk TiO2 (particle size more than 100nm), however, anatase shows a higher selectivity for complete mineralization: the concentration of p-quinone as intermediate of this photocatalytic reaction is at lower level than those of rutile. Species adsorbed by titanium dioxide such as H2O and OH play a significant role in the photodegradation of phenol as well as particle size. With the decrement of paxticle size especially less than 15nm, the photocatalytic activity of TiO2 increases dynamicajly.
出处
《无机材料学报》
SCIE
EI
CAS
CSCD
北大核心
2000年第3期556-560,共5页
Journal of Inorganic Materials
基金
上海市科委新材料研究中心资助!98JC14021