CO2 Carrying Behavior of Calcium Aluminate Pellets under High-Temperature/High-CO2 Concentration Calcination Conditions

被引:78
|
作者
Manovic, Vasilije [1 ]
Anthony, Edward J. [1 ]
机构
[1] Nat Resources Canada, CanmetENERGY, Ottawa, ON K1A 1M1, Canada
关键词
CAO-BASED SORBENT; FLUIDIZED-BED; LOOPING COMBUSTION; CAPTURE CAPACITY; COAL PRODUCTION; SURFACE-AREA; LIMESTONES; CYCLES; RECARBONATION; REACTIVATION;
D O I
10.1021/ie901795e
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Sintering and a resulting loss of activity during calcination/carbonation can introduce substantial economic penalties for a CO2 looping cycle using CaO-based sorbents. In a real system, sorbent regeneration must be done at a high temperature to produce an almost pure CO2 stream, and this will increase both sintering and loss of sorbent activity. The influence of severe calcination conditions on the CO2 carrying behavior of calcium aluminate pellets is investigated here. Up to 30 calcination/carbonation cycles were performed using a thermogravimetric analyzer apparatus. The maximum temperature during the calcination stage in pure CO2 was 950 °C, using different heating/cooling rates between two carbonation stages (700 °C, 20% CO2). For comparison, cycles were also done using N 2 during the calcination stages. In addition, the original Cadomin limestone, used for pelletization, was also examined in its original form and the results obtained were compared with those for the aluminate pellets. As expected, high temperature during calcination strongly reduced CO2 carrying capacities of both sorbents. However, aluminate pellets showed better resistance to these severe conditions. The conversion profiles obtained are significantly different to those obtained under milder conditions, with significant increased activity during the slower, diffusion-controlled, carbonation stage. Moreover, scanning electron microscopy analysis of samples after prolonged carbonation showed that pore filling occurred at the sorbent particle surfaces preventing diffusion of CO2 toward the particle interior. © 2010 American Chemical Society.
引用
收藏
页码:6916 / 6922
页数:7
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