High purity hydrogen production via aqueous phase reforming of xylose over small Pt nanoparticles on a γ-Al2O3 support

被引:19
|
作者
Kim, Yoondo [1 ,2 ]
Kim, Minkyeong [1 ]
Jeong, Hyangsoo [1 ]
Kim, Yongmin [1 ]
Choi, Sun Hee [1 ]
Ham, Hyung Chul [3 ]
Lee, Seung Woo [4 ]
Kim, Jin Young [1 ]
Song, Kwang Ho [2 ,5 ]
Yoon, Chang Won [1 ,6 ]
Jo, Young Suk [1 ]
Sohn, Hyuntae [1 ]
机构
[1] Korea Inst Sci & Technol KIST, Ctr Hydrogen & Fuel Cell Res, Seoul 02792, South Korea
[2] Korea Univ, Green Sch, Seoul 02841, South Korea
[3] Inha Univ, Dept Chem Engn, Incheon 22212, South Korea
[4] Georgia Inst Technol, GW Woodruff Sch Mech Engn, Atlanta, GA 30332 USA
[5] Korea Univ, Dept Chem & Biol Engn, Seoul 02841, South Korea
[6] Kyung Hee Univ, KHU KIST Dept Converging Sci & Technol, Seoul 02447, South Korea
基金
新加坡国家研究基金会;
关键词
Hydrogen; Xylose; Biomass; APR; Aqueous phase reforming; Platinum; SUPERCRITICAL WATER GASIFICATION; OXYGENATED HYDROCARBONS; RENEWABLE HYDROGEN; METAL DISPERSION; ETHYLENE-GLYCOL; SOL-GEL; BIOMASS; CATALYSTS; CONVERSION; OXIDATION;
D O I
10.1016/j.ijhydene.2020.03.014
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
In this study, aqueous phase reforming (APR) of xylose was conducted over highly dispersed Pt nanoparticles supported on a gamma-Al2O3 support (Pt-SNP). Formation of small Pt nanoparticles was confirmed by X-ray diffraction and transmission electron microscopy, which revealed that most of the particles ranged between 0.8 and 1.6 nm in size and the average particle size was 1.3 nm. Temperature-programmed reduction analysis indicated that these small Pt nanoparticles were highly reducible under the reducing environment compared to the commercial Pt/gamma-Al2O3 catalysts (Pt-commercial). The catalytic activities of both Pt-SNP and Pt-commercial catalysts were examined in a semi-batch autoclave reactor system for the APR of xylose. It was found that Pt-SNP showed higher carbon to gas conversion with high hydrogen selectivity than Pt-commercial. This was likely due to the increased density of edge sites in the Pt-SNP catalyst that facilitated the cleavage of the C-C bonds rather than the C-O bonds, leading to greater hydrogen production. Furthermore, the Pt-SNP catalyst showed better carbon deposit resistance as compared to Pt-commercial. The amount of carbon deposition on the Pt-SNP catalyst surface and the organic carbon species dissolved in the post-reaction xylose solution were significantly lower compared to that of Pt-commercial. Finally, high purity hydrogen production was achieved using a continuous fixed-bed hybrid reactor including an aqueous phase reformer and a home-made Pd/Ta dense metallic composite membrane. A stable hydrogen gas production (99.999%) was obtained over the Pt-SNP catalyst, which demonstrated the success of a potentially commercial APR reactor system that continuously converted the aqueous xylose solution to hydrogen with high purity. (C) 2020 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:13848 / 13861
页数:14
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