Fabrication of TiO2/MoS2@zeolite photocatalyst and its photocatalytic activity for degradation of methyl orange under visible light

被引:139
作者
Zhang, Weiping [1 ]
Xiao, Xinyan [1 ]
Zheng, Lili [1 ]
Wan, Caixia [1 ]
机构
[1] S China Univ Technol, Sch Chem & Chem Engn, Guangzhou 510640, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
TiO2; MoS2; Zeolite; Visible-light; Photocatalysis; IN-SITU SYNTHESIS; HYDROTHERMAL SYNTHESIS; ASSISTED SYNTHESIS; MOS2; NANOSHEETS; POROUS MOS2; COMPOSITES; GRAPHENE; NANOCOMPOSITE; NANOPARTICLES; DECOMPOSITION;
D O I
10.1016/j.apsusc.2015.08.054
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
TiO2/MOS2@zeolite composite photocatalysts with visible-light activity were fabricated via a simple ultrasonic-hydrothermal synthesis method, using TiCl4 as Ti source, MoS2 as a direct sensitizer, glycerol water solution with certain dispersion agent as hydrolytic agent, and zeolite as carrier. The structure, morphology, composition, optical properties, and specific surface area of the as-prepared photocatalysts were characterized by using XRD, FTIR, SEM-EDS, TEM, XPS, UV-vis, PL and BET analyzer, respectively. And the photocatalytic degradation of methyl orange (MO) in aqueous suspension has been employed to evaluate the photocatalytic activity and degradation kinetics of as-prepared photocatalysts with xenon lamp as irradiation source. The results indicate that: (1) TiO2/MoS2@zeolite composite photocatalysts exhibit enhanced photocatalytic activities for methyl orange (MO) degradation compared to Degussa P25; (2) photocatalytic degradation of MO obeys Langmuir-Hinshelwood kinetic model (pseudo-first order reaction), and its degradation rate constant (k(app)) (2.304 h(-1)) is higher than that of Degussa P25 (0.768 h(-1)); (3) the heterostructure consisted of zeolite, MoS2 and TiO2 nanostructure could provide synergistic effect for degradation of MO due to the efficient electron transfer process and better absorption property of TiO2/MoS2@zeolite composite photocatalyst. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:468 / 478
页数:11
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