Numerical study of hydrogen production via sorption-enhanced steam methane reforming in a fluidized bed reactor at relatively low temperature

被引:25
|
作者
Chen, Yumin [1 ]
Zhao, Yongchun [1 ]
Zheng, Chuguang [1 ]
Zhang, Junying [1 ]
机构
[1] Huazhong Univ Sci & Technol, State Key Lab Coal Combust, Wuhan 430074, Hubei Province, Peoples R China
基金
美国国家科学基金会;
关键词
Hydrogen production; Mathematical modeling; Fluidization; Reaction engineering; Kinetics; Adsorption; PROCESS PERFORMANCE; 2-FLUID MODEL; CO2; CAPTURE; VALIDATION; SIMULATION; KINETICS; SORBENT; ADSORPTION; VELOCITY; LI2ZRO3;
D O I
10.1016/j.ces.2013.01.024
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Production of hydrogen by sorption enhanced methane steam reforming (SE-SMR) process at a relatively low temperature in a two-dimensional cylindrical bubbling fluidized bed reactor was studied using an Eulerian-Eulerian approach. The study aims to investigate the influence of operating pressure, superficial velocity, catalyst-to-adsorbent ratio (C/A, weight) and sorption kinetics on the SE-SMR process. A H-2 concentration of >87% on a dry basis can be obtained at 500 degrees C and 0.1 MPa using hydrotalcite-like compounds (HTC) as CO2-acceptor. A relatively low catalyst-to-adsorbent ratio (similar to 0.5) is preferable for reducing operating cost and enhancing hydrogen production. Higher operating pressure is favorable for the utilization of sorbent, but unfavorable for the conversion of methane. Simulations prove that sorbents with slow kinetics can only serve as CO2 acceptor, but cannot enhance the methane steam reforming (SMR) process effectively. Another interesting observation is that the way the superficial velocity affects the CO2 capture efficiency is determined by the sorption kinetics. For HTC, it is the bigger bubble size rather than the reduction of gas residence time that mainly accounts for the decrease of the CO2 capture efficiency under higher velocities investigated. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:67 / 80
页数:14
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