Continuous CO2 Capture in Dual Fluidized Beds Using Silica Supported Amine

被引:26
|
作者
Zhao, Wenying [1 ]
Zhang, Zhi [1 ]
Li, Zhenshan [1 ]
Cai, Ningsheng [1 ]
机构
[1] Tsinghua Univ, Dept Thermal Engn, Beijing Municipal Key Lab Utilizat & Reduct CO2, Key Lab Thermal Sci & Power Engn,Minist Educ, Beijing 100084, Peoples R China
来源
GHGT-11 | 2013年 / 37卷
关键词
CO2; capture; dual fluidized beds; supported amine; water vapour; mechanisms; FIRED POWER-PLANT; CARBON-DIOXIDE; REACTION-KINETICS; REMOVAL; ABSORPTION; SORBENTS;
D O I
10.1016/j.egypro.2013.05.088
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
In this study, a supported amine sorbent was prepared by impregnating silica particles (150 similar to 300 um) with methanol solution of polyethylenimine (PEI with the molecular weight of 600 g . mol(-1)) to immobilize amine into the pores of the silica support. The optimal CO2 capacity of the PEI-based sorbent was as high as 2.0 mmol . g(-1). During the adsorption and desorption of 10 times, the CO2 capacity of the PEI-based sorbents kept stable, indicating PEI-based sorbents had excellent thermal stability. Dual bubbling fluidized bed reactors were constructed to demonstrate the process feasibility of continuous CO2 capture from flue gases with supported amine sorbent. Long-term stable operation and continuous solids circulation between the two reactors was achieved, and the CO2 in the flue gases was continuously captured by the supported amine sorbent. Experimental results indicated that similar to 84.4% CO2 capture efficiency could be achieved in the absence of water. The low regeneration temperature, high adsorption temperature and the short sorbent residence time in absorber were considered to be the limiting factors affecting the working capacity of sorbents. Water vapour could promote the adsorption process and increase the CO2 capture efficiency to approximately 90.6 similar to 97%. The effect of water vapour on reaction mechanism between CO2 and various amine groups was discussed. (C) 2013 The Authors. Published by Elsevier Ltd.
引用
收藏
页码:89 / 98
页数:10
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