个人信息Personal Information
教授
博士生导师
硕士生导师
性别:男
毕业院校:中国科学院兰州化学物理研究所
学位:博士
所在单位:环境学院
办公地点:环境楼 B415
联系方式:Tel: 0411-84706658
电子邮箱:xyli@dlut.edu.cn
Photocatalytic degradation of gaseous toluene with multiphase TixZr1-xO2 synthesized via co-precipitation route
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论文类型:期刊论文
发表时间:2015-01-15
发表刊物:JOURNAL OF COLLOID AND INTERFACE SCIENCE
收录刊物:SCIE、EI、PubMed
卷号:438
页面范围:1-6
ISSN号:0021-9797
关键字:Multiphase TixZr1-xO2; Photocatalysis; Toluene degradation; In situ Fourier transform infrared (FTIR)
摘要:In the present work, the multiphase TixZr1-xO2 particles containing cubic-phase ZrO2 were fabricated via co-precipitation route. The mole ratios of Ti and Zr elements were controlled by three levels: Ti/Zr = 7/3 (maximum), Ti/Zr = 5/5 (medium), and Ti/Zr = 3/7 (minimum). The materials prepared were characterized by using X-ray diffraction (XRD), field emission scanning electron microscope (FE-SEM), energy-dispersive X-ray (EDX), X-ray photoelectron spectroscopy (XPS), UV-vis diffuse reflectance spectra (DRS) and photoluminescence (PL) spectra. For the maximum usage of solar power with fabricated catalysts, elimination of gaseous toluene was chosen as a model to evaluate the performances under visible light. The results indicated that the degradation efficiency of toluene was about 80% after 6 h reaction using Ti0.3Zr0.2O2 as the photocatalyst. On the other hand, the multiphase TixZr1-xO2 (x = 0.7 or 0.5) photocatalysts showed significant enhancement in the activity, compared with the commercial TiO2 (Degussa P25). The enhanced performances of TixZr1-xO2 might be attributed to the lower charge recombination rate of photoinduced electron-hole pairs. In addition, some intermediates (the benzaldehyde and benzoic acid) and final product (CO2) adsorbed on the surface of the particles were also detected by using in situ Fourier transform infrared (FTIR) spectroscopy. (C) 2014 Elsevier Inc. All rights reserved.