On steam hydration of CaO-based sorbent cycled for CO2 capture

被引:67
作者
Blamey, John [1 ]
Manovic, Vasilije [2 ,3 ]
Anthony, Edward J. [2 ,3 ]
Dugwell, Denis R. [1 ]
Fennell, Paul S. [1 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Dept Chem Engn, London SW7 2AZ, England
[2] Cranfield Univ, Ctr Combust, Cranfield MK43 0AL, Beds, England
[3] Cranfield Univ, CCS, Cranfield MK43 0AL, Beds, England
基金
英国工程与自然科学研究理事会;
关键词
Calcium looping; Hydration; Fluidised bed; Carbon capture; LOOPING CYCLE; REACTIVATION; ENHANCEMENT; CARBONATION; MECHANISM; CAPACITY;
D O I
10.1016/j.fuel.2015.02.026
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
The reversible reaction of CaO with CO2 can be used for post- and pre-combustion capture of CO2; however, the reactivity of CaO particles is found to reduce upon repeated use. Hydration has been shown to be an effective method of increasing the reactivity of (or reactivating) CaO to CO2 for CO2 capture. Here, a lab-scale fluidised bed reactor was used to investigate reactivation of sorbent using steam at two different hydration temperatures of 473 and 673 K. Prior to hydration, the sorbent was cycled at three different calcination temperatures of 1123, 1173 and 1223 K; the carbonation temperature was kept constant at 973 K. Following hydration, the sorbent was either carbonated directly or carbonated indirectly via a CaO intermediate. The hydration extent was found to decrease with increasing calcination temperature before hydration and with increasing hydration temperature. The carbonation extent following hydration was found to increase linearly with hydration extent - depending on the method of carbonation - with direct carbonation resulting in higher conversions. Mass loss from the fluidised bed was found to be higher for lower hydration temperatures and increased calcination temperatures before cycling. The hydration behaviour of sorbent was subsequently investigated using a TGA at three different steam hydration temperatures of 483, 578 and 678 K. Material for the TGA tests was prepared using the lab-scale fluidised bed reactor, with a calcination temperature of 1173 K and a carbonation temperature of 973 K. In this case, the number of cycles was varied from 0 to 13, in order to provide a wider range of sorbent properties. Data from the TGA were used to project subsequent carbonation conversions and relative increases in carrying capacity across hydration. The TGA hydration tests emphasise the importance of hydration temperature and prior cycling conditions and length on the increase in carrying capacity following hydration. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:269 / 277
页数:9
相关论文
共 25 条
[1]   Demonstration of steady state CO2 capture in a 1.7 MWth calcium looping pilot [J].
Arias, B. ;
Diego, M. E. ;
Abanades, J. C. ;
Lorenzo, M. ;
Diaz, L. ;
Martinez, D. ;
Alvarez, J. ;
Sanchez-Biezma, A. .
INTERNATIONAL JOURNAL OF GREENHOUSE GAS CONTROL, 2013, 18 :237-245
[2]   Effect of sorbent hydration on the average activity of CaO in a Ca-looping system [J].
Arias, B. ;
Grasa, G. S. ;
Abanades, J. C. .
CHEMICAL ENGINEERING JOURNAL, 2010, 163 (03) :324-330
[3]   The calcium looping cycle for large-scale CO2 capture [J].
Blamey, J. ;
Anthony, E. J. ;
Wang, J. ;
Fennell, P. S. .
PROGRESS IN ENERGY AND COMBUSTION SCIENCE, 2010, 36 (02) :260-279
[4]   Reactivation of CaO-Based Sorbents for CO2 Capture: Mechanism for the Carbonation of Ca(OH)2 [J].
Blamey, John ;
Lu, Dennis Y. ;
Fennell, Paul S. ;
Anthony, E. J. .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 2011, 50 (17) :10329-10334
[5]   Mechanism of Particle Breakage during Reactivation of CaO-Based Sorbents for CO2 Capture [J].
Blamey, John ;
Paterson, Nigel P. M. ;
Dugwell, Denis R. ;
Fennell, Paul S. .
ENERGY & FUELS, 2010, 24 (08) :4605-4616
[6]   REACTIVATION OF PARTIALLY-SULFATED LIMESTONE PARTICLES FROM A CFB COMBUSTOR BY HYDRATION [J].
COUTURIER, MF ;
MARQUIS, DL ;
STEWARD, FR ;
VOLMERANGE, Y .
CANADIAN JOURNAL OF CHEMICAL ENGINEERING, 1994, 72 (01) :91-97
[7]   Regeneration of sintered limestone sorbents for the sequestration of CO2 from combustion and other systems [J].
Fennell, P. S. ;
Davidson, J. F. ;
Dennis, J. S. ;
Hayhurst, A. N. .
JOURNAL OF THE ENERGY INSTITUTE, 2007, 80 (02) :116-119
[8]   CO2 capture capacity of CaO in long series of carbonation/calcination cycles [J].
Grasa, Gemma S. ;
Abanades, J. Carlos .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 2006, 45 (26) :8846-8851
[9]   Improved long-term conversion of limestone-derived sorbents for in situ capture of CO2 in a fluidized bed combustor [J].
Hughes, RW ;
Lu, D ;
Anthony, EJ ;
Wu, YH .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 2004, 43 (18) :5529-5539
[10]   Developing an innovative method, HyPr-RING, to produce hydrogen from hydrocarbons [J].
Lin, SY ;
Suzuki, Y ;
Hatano, H ;
Harada, M .
ENERGY CONVERSION AND MANAGEMENT, 2002, 43 (9-12) :1283-1290