Sorption-enhanced steam-methane reforming: CaO-CaCO3 Capture technology

被引:7
|
作者
Cobden, P. D. [1 ]
Elzinga, G. D. [1 ]
Booneveld, S. [1 ]
Dijkstra, J. W. [1 ]
Jansen, D. [1 ]
van den Brink, R. W. [1 ]
机构
[1] Energy Res Ctr Netherlands, NL-1755 ZG Petten, Netherlands
来源
关键词
Pre-combustion decarbonisation; CaO; CaCO3; CO2; sorbent; Cyclic capacity; Temperature swing;
D O I
10.1016/j.egypro.2009.01.097
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
Calcium oxide (CaO) has been investigated in the context of CO2 capture. In its application for the sorption-enhanced steammethane reforming process (SE-SMR), CO2 is captured in a sorption mode through the formation of CaCO3, at which stage, the conversion of CH4 to H-2 is also enhanced. Subsequently, the CO2 is released in a separate desorption mode where the CaCO3 is calcined to CaO. In a combined system modeling and experimental approach a sweet-spot in operational conditions has been determined in terms of adsorption-reaction and desorption temperature and pressure. Additionally the required performance in terms of cyclic capacity has been determined in relation to system efficiency. Long term cyclic capacity under sweet-spot conditions has been demonstrated in a lab-scale experiment in excess of 200 loading cycles, with stabilization of cyclic capacity occurred after 100 cycles, and above the required minimum of 15% of the thermodynamic capacity. Increasing the adsorption temperature above 600 degrees C reactivated the CaO-CaCO3 sorbent system. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:733 / 739
页数:7
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