Photocatalytic hydrogen production in a solar pilot plant using a Au/TiO2 photo catalyst

被引:54
|
作者
Arzate Salgado, Sandra Yazmin [1 ]
Ramirez Zamora, Rosa Maria [1 ]
Zanella, Rodolfo [2 ]
Peral, Jose [3 ]
Malato, Sixto [4 ]
Maldonado, Manuel I. [4 ]
机构
[1] Univ Nacl Autonoma Mexico, Inst Ingn Coordinac Ingn Ambiental, Mexico City 04510, DF, Mexico
[2] Univ Nacl Autonoma Mexico, Ctr Ciencias Aplicadas & Desarrollo Tecnol, AP 70-186, Mexico City 04510, DF, Mexico
[3] Univ Autonoma Barcelona, Dept Quim, Edifici Cn, Bellaterra 08193, Cerdanyola Del, Spain
[4] Plataforma Solar Almeria CIEMAT, Carretera Senes,Km 4, Tabernas 04200, Almeria, Spain
关键词
Compound parabolic collector (CPC); Solar hydrogen; Wastewater as sacrificial agent; DEPOSITION-PRECIPITATION; TIO2; WATER; GENERATION; OXIDATION; NAOH;
D O I
10.1016/j.ijhydene.2016.05.039
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
The purpose of the present work was to study the efficiency of an Au/TiO2 photocatalyst for the simultaneous hydrogen production and organic pollutant removal from aqueous solutions, under direct solar irradiation, and at pilot-plant scale. Several sacrificial agents (pollutants) like alcohols, organic acids, and the organic content of municipal and industrial wastewaters at acid pH were tested. Also, the effect of salt concentration and ionic strength was checked. The experiments were performed in a Compound Parabolic Collector (CPC) at the Plataforma Solar de Almeria (PSA). The Au/TiO2 catalyst showed a remarkable activity towards hydrogen production. Indeed, 6500 mu mol H-2.L-1 were generated after 5 h, with an accumulated radiation energy of 100 kJ.L-1, and a catalyst concentration of 0.2 g.L-1. The dissolved organic carbon (DOC) concentration showed a positive influence towards the hydrogen production, while the ionic strength showed a clear negative effect. The highest rate of photocatalytic hydrogen production was attained using formic acid as sacrificial agent. (C) 2016 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:11933 / 11940
页数:8
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