Multistage Fluidized Bed Reactor Performance Characterization for Adsorption of Carbon Dioxide

被引:28
作者
Roy, Sudeshna [1 ]
Mohanty, C. R. [1 ]
Meikap, B. C. [1 ,2 ]
机构
[1] Indian Inst Technol, Dept Chem Engn, Kharagpur 721302, W Bengal, India
[2] Univ Kwazulu Natal UKZN, Sch Chem Engn, ZA-4041 Durban, South Africa
关键词
CAO-BASED SORBENT; CO2; CAPTURE; EFFICIENCY; METHANE; COALS; CYCLE; GAS;
D O I
10.1021/ie901133r
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Carbon dioxide and its different compounds are generated as primary greenhouse gases from the flue gases of coal-fired thermal power plants, boilers, and other stationary combustion processes. This greenhouse gas causes global warming after being emitted to the environment. To deal with this problem, a new dry scrubbing process was tested in this study. A three-stage countercurrent fluidized bed adsorber was developed, designed, and fabricated. It was used as a removal apparatus and operated in a continuous regime for the two-phase system. The height of each stage was 0.30 m, and the inner diameter was 0.10 m. The paper presents the removal Of CO2 from gas mixtures by chemical sorption on porous granular calcium oxide particles in the reactor at ambient temperature. The advantages of a multistage fluidized bed reactor for high mass transfer and high gas-solid contact can enhance the removal of the gas when using a dry method. The effects of the operating parameters such as sorbent, superficial gas velocity, and the Weir height on CO2 removal efficiency in the multistage fluidized bed were investigated. The results indicate that the removal efficiency of the carbon dioxide was around 71% at a high solid flow rate corresponding to lower gas velocity at room temperature. In comparison with wet scrubbers, this dry process appears to have lower cost, less complicated configuration, and simpler disposal of used sorbent. The results in this study assume importance from the perspective of use of a multistage fluidized bed adsorber for control of gaseous pollutants at high temperature.
引用
收藏
页码:10718 / 10727
页数:10
相关论文
共 18 条
[1]   The maximum capture efficiency of CO2 using a carbonation/calcination cycle of CaO/CaCO3 [J].
Abanades, JC .
CHEMICAL ENGINEERING JOURNAL, 2002, 90 (03) :303-306
[2]   Reactivity of highly cycled particles of CaO in a carbonation/calcination loop [J].
Grasa, Gemma S. ;
Abanades, J. Carlos ;
Alonso, Monica ;
Gonzalez, Belen .
CHEMICAL ENGINEERING JOURNAL, 2008, 137 (03) :561-567
[3]   Improved immobilized carbon dioxide capture sorbents [J].
Gray, ML ;
Soong, Y ;
Champagne, KJ ;
Pennline, H ;
Baltrus, JP ;
Stevens, RW ;
Khatri, R ;
Chuang, SSC ;
Filburn, T .
FUEL PROCESSING TECHNOLOGY, 2005, 86 (14-15) :1449-1455
[4]   Meso-porous Ni/Mg/Al catalysts for methane reforming with CO2 [J].
Hou, ZY ;
Yashima, T .
APPLIED CATALYSIS A-GENERAL, 2004, 261 (02) :205-209
[5]   High-pressure methane and carbon dioxide adsorption on dry and moisture-equilibrated Pennsylvanian coals [J].
Krooss, BM ;
van Bergen, F ;
Gensterblum, Y ;
Siemons, N ;
Pagnier, HJM ;
David, P .
INTERNATIONAL JOURNAL OF COAL GEOLOGY, 2002, 51 (02) :69-92
[6]   Modified CaO-based sorbent looping cycle for CO2 mitigation [J].
Li, Yingjie ;
Zhao, Changsui ;
Chen, Huichao ;
Liang, Cai ;
Duan, Lunbo ;
Zhou, Wu .
FUEL, 2009, 88 (04) :697-704
[7]   Ca-based sorbent looping combustion for CO2 capture in pilot-scale dual fluidized beds [J].
Lu, Dennis Y. ;
Hughes, Robin W. ;
Anthony, Edward J. .
FUEL PROCESSING TECHNOLOGY, 2008, 89 (12) :1386-1395
[8]   Sequential SO2/CO2 capture enhanced by steam reactivation of a CaO-based sorbent [J].
Manovic, Vasilije ;
Anthony, Edward J. .
FUEL, 2008, 87 (8-9) :1564-1573
[9]   Flue gas and pure CO2 sorption properties of coal:: A comparative study [J].
Mazumder, S. ;
van Hemert, P. ;
Busch, A. ;
Wolf, K-H. A. A. ;
Tejera-Cuesta, P. .
INTERNATIONAL JOURNAL OF COAL GEOLOGY, 2006, 67 (04) :267-279
[10]   Hydrodynamics of a multistage countercurrent fluidized bed reactor with downcomer for lime-dolomite mixed particle system [J].
Mohanty, C. R. ;
Adapala, Sivaji ;
Meikap, B. C. .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 2008, 47 (18) :6917-6924