Photocatalytic H2 production from ethanol(aq) solutions: The effect of intermediate products

被引:26
|
作者
Sola, A. C. [1 ,2 ,3 ]
Homs, N. [1 ,2 ,3 ]
Ramirez de la Piscina, P. [1 ,2 ]
机构
[1] Univ Barcelona, Dept Quim Inorgan & Organ, Seccio Quim Inorgan, mar, C Marti & Franques 1-11, E-08028 Barcelona, Spain
[2] Univ Barcelona, Inst Nanociencia & Nanotecnol, C Marti & Franques 1-11, E-08028 Barcelona, Spain
[3] Catalonia Inst Energy Res IREC, Jardins Dones Negre 1, Barcelona 08930, Spain
关键词
Ethanol photoreforming; Acetaldehyde photoreforming; Acetic acid photoreforming; 2,3 butanediol photoreforming; H-2 production rate; Renewable H-2; HYDROGEN-PRODUCTION; IN-SITU; PT/TIO2; TIO2; ACETALDEHYDE; DEGRADATION; CATALYSTS; WATER; FTIR; CO;
D O I
10.1016/j.ijhydene.2016.05.268
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 production of H-2 via the photocatalytic transformation of aqueous solutions of ethanol, over Pt/anatase was studied in a semi-batch reactor. High H-2/COx ratios were obtained indicating that the photoreforming of ethanol only occurred in a small proportion of the ethanol. The main products detected in the liquid phase after the photocatalytic conversion of ethanol solutions were acetaldehyde, acetic acid and 2,3-butanediol, with acetaldehyde being the most abundant. The photoreaction of acetaldehyde(4, acetic acid((aq)) or 2,3-butanediol((aq)) resulted in lower amounts of H-2 compared with that of ethanol((aq)). The main reaction pathway for the photocatalytic transformation of acetaldehyde((aq)) is via the formation of acetic acid and H-2. Then, CO2 and CH4 are formed from the decomposition of acetic acid((aq)). The decrease in the H-2 production rate during the photocatalytic reforming of ethanol solutions is related to the presence of the intermediate products formed in the liquid phase that are not removed from the reaction medium. Carboxylate species and metallic Pt were present on the surface of the post-reaction catalyst. (C) 2016 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:19629 / 19636
页数:8
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