Enhanced photocatalytic hydrogen production in a UV-irradiated fluidized bed reactor

被引:38
|
作者
Reilly, Kevin [1 ]
Fang, Baizeng [1 ]
Taghipour, Fariborz [1 ]
Wilkinson, David P. [1 ]
机构
[1] Univ British Columbia, Dept Chem & Biol Engn, 2360 East Mall, Vancouver, BC V6T 1Z3, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Hydrogen; Water splitting; Photocatalysis; Fluidized bed; Energy conversion; WATER PHOTOELECTROLYSIS; TIO2; PEROXIDE; PHOTOREACTOR; DEGRADATION; TRICHLOROETHYLENE; PERFORMANCE; ABSORPTION; PHOTOLYSIS; MECHANISM;
D O I
10.1016/j.jcat.2017.07.003
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
UV-irradiated fluidized bed reactor system and Pt-loaded TiO2 spheres were developed for photocatalytic water splitting. This novel approach was explored as a means to minimize the parasitic back reaction, mass transport and radiation distribution effects that limit the performance and scalability of immobilized-film and suspended slurry photocatalysts typically employed for photocatalytic hydrogen production. By fluidizing Pt-loaded TiO2 spheres in a 2.2 M Na2CO3 solution, steady hydrogen production rates up to 211 mu mol/h with an apparent quantum efficiency of 1.33% were achieved upon UV-irradiation. This demonstrates a marked 44% increase in the apparent quantum efficiency when compared to the performance of a traditional Pt-loaded TiO2 suspended slurry photocatalyst in the same reactor. It is hypothesized that this enhanced performance is primarily due to improved separation of the evolved H-2 and O-2 from the Pt-loaded photocatalyst particles, thus reducing the parasitic back reaction. (C) 2017 Elsevier Inc. All rights reserved.
引用
收藏
页码:63 / 73
页数:11
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