A comparative study of different diatomite-supported TiO2 composites and their photocatalytic performance for dye degradation

被引:22
作者
Zhang, Guangxin [1 ]
Wang, Bin [1 ]
Sun, Zhiming [1 ]
Zheng, Shuilin [1 ]
Liu, Shushu [1 ]
机构
[1] China Univ Min & Technol Beijing, Sch Chem & Environm Engn, Beijing 100083, Peoples R China
关键词
Support; Diatomite; TiO2; Dye; Photocatalysis; METHYLENE-BLUE; RHODAMINE-B; DOPED TIO2; REMOVAL; ADSORPTION; SURFACE; PARAMETERS; CATALYST; TOLUENE; DESIGN;
D O I
10.1080/19443994.2015.1085449
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Three kinds of diatomites as catalyst carriers were adopted to prepare supported TiO2 catalysts by a typical hydrolysis-deposition method. The prepared composites were characterized by X-ray diffraction, Fourier transform infrared spectroscopy, N-2 adsorption-desorption, scanning electron microscopy transmission electron microscopy, UV-vis diffuser reflectance, and chemical oxygen demand. The photocatalytic properties of composites were determined using rhodamine B, methyl orange, and methylene blue as target pollutants under UV light irradiation. A comparative study on the photocatalytic properties of composite catalysts was carried out. It is indicated that the catalytic performance of TiO2/diatomite is significantly influenced by the physicochemical properties of diatomite supports. Compared with pure TiO2, the TiO2/diatomite composites exhibited smaller crystalline size of TiO2 and better dispersibility, which induced higher specific surface area and better photo-degradation efficiency. The highest activity of the photocatalyst should be attributed to the acid-activated support, which provided more active sites for the degradation reaction. Besides, the durabilities of catalysts were also investigated. The experimental results indicated that the prepared composite is a promising material for the wastewater treatment for its good photocatalytic property and reusability.
引用
收藏
页码:17512 / 17522
页数:11
相关论文
共 47 条
[1]   Removal of rhodamine B by ozone-based advanced oxidation process [J].
Bai Cuiping ;
Xiong Xianfeng ;
Gong Wenqi ;
Feng Dexin ;
Xian Mo ;
Ge Zhongxue ;
Xu Nian .
DESALINATION, 2011, 278 (1-3) :84-90
[2]   Adsorption behavior of copper and cyanide ions at TiO2-solution interface [J].
Barakat, MA .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 2005, 291 (02) :345-352
[3]   The influence of selected parameters on the photocatalytic degradation of azo-dyes in the presence of TiO2 aqueous suspension [J].
Baran, Wojciech ;
Adamek, Ewa ;
Makowski, Andrzej .
CHEMICAL ENGINEERING JOURNAL, 2008, 145 (02) :242-248
[4]   Visible-light-activated Ce-Si co-doped TiO2 photocatalyst [J].
Chen, Qifeng ;
Jiang, Dong ;
Shi, Weimei ;
Wu, Dong ;
Xu, Yao .
APPLIED SURFACE SCIENCE, 2009, 255 (18) :7918-7924
[5]   Solar photocatalytic decolourization of Crystal violet using supported TiO2: effect of some parameters and comparative efficiency [J].
Djellabi, R. ;
Ghorab, M. F. .
DESALINATION AND WATER TREATMENT, 2015, 53 (13) :3649-3655
[6]   Photocatalytic degradation of toluene over doped and coupled (Ti,M)O2 (M = Sn or Zr) nanocrystalline oxides: Influence of the heteroatom distribution on deactivation [J].
Fresno, Fernando ;
Hernandez-Alonso, Maria D. ;
Tudela, David ;
Coronado, Juan M. ;
Soria, Javier .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2008, 84 (3-4) :598-606
[7]   Visible-light-induced degradation of rhodamine B by nanosized Bi2WO6 [J].
Fu, HB ;
Pan, CS ;
Yao, WQ ;
Zhu, YF .
JOURNAL OF PHYSICAL CHEMISTRY B, 2005, 109 (47) :22432-22439
[8]  
Fujishima A., 2000, J PHOTOCH PHOTOBIO C, V1, P1, DOI [10.1016/S1389-5567(00)00002-2, DOI 10.1016/S1389-5567(00)00002-2]
[9]   ENVIRONMENTAL APPLICATIONS OF SEMICONDUCTOR PHOTOCATALYSIS [J].
HOFFMANN, MR ;
MARTIN, ST ;
CHOI, WY ;
BAHNEMANN, DW .
CHEMICAL REVIEWS, 1995, 95 (01) :69-96
[10]   Photocatalytic discolorization of methyl orange solution by Pt modified TiO2 loaded on natural zeolite [J].
Huang, Miaoliang ;
Xu, Chunfang ;
Wu, Zibao ;
Huang, Yunfang ;
Lin, Jianming ;
Wu, Jihuai .
DYES AND PIGMENTS, 2008, 77 (02) :327-334