Production of high-purity H2 through sorption- enhanced water gas shift over a combination of two intermediate-temperature CO2 sorbents

被引:11
作者
Xu, Huawu [1 ]
Hu, Yuanwu [1 ]
Cheng, Zhenmin [1 ]
Zhou, Zhiming [1 ]
机构
[1] East China Univ Sci & Technol, Sch Chem Engn, Shanghai 200237, Peoples R China
基金
中国国家自然科学基金;
关键词
Sorption-enhanced water gas shift; Hydrotalcite-based sorbents; MgO-based sorbents; High-purity hydrogen; HYDROGEN-PRODUCTION; CARBON-DIOXIDE; FOSSIL-FUELS; HYDROTALCITE; ADSORPTION; CAPTURE; CATALYSTS; AL; PERFORMANCE; MORPHOLOGY;
D O I
10.1016/j.ijhydene.2023.02.108
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
Sorption-enhanced water gas shift (SEWGS) that integrates the WGS reaction and in situ CO2 removal in one reactor is a promising technology for producing high-purity hydrogen. In this study, a series of Mg-Al hydrotalcite-based CO2 sorbents were prepared, characterized, and evaluated at low CO2 pressure (0.01 bar). It shows that the layered double oxide prepared at pH = 10 (abbr. LDO_10) has a higher CO2 adsorption uptake at 30-400 & DEG;C than other LDO_x, owing to its large surface area. After doping with M2CO3 (M = Li, Na, K, or Cs), the resulting M-LDO_10 sorbents exhibit different CO2 uptake, with Li-LDO_10 the lowest and K-LDO_10 the highest. It is considered that the high total basicity contributed to the high CO2 uptake of K-LDO_10. A single-layered reactor (physically mixed Cu/Ce0.6Zr0.4O2 (catalyst) and K-LDO_10) can realize a stable production of high-purity H2 in 10 SEWGS cycles, but the duration time is rather short (& LE;1 min). By combining our previously developed MgO-based sorbent (AMS-Mg95Ca5) with K-LDO_10 in a four-layered configuration, i.e., three (Cu/Ce0.6 Zr0.4O2|AMS-Mg95Ca5) layers followed by one (Cu/Ce0.6Zr0.4O2 + K-LDO_10) layer, high-purity H2 (>99.9%) without CO contamination is stably produced with extended duration time (22-31 min) in 10 SEWGS cycles (300 & DEG;C, 12 bar, and H2O/CO molar ratio of 1.5). & COPY; 2023 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:25185 / 25196
页数:12
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