An investigation of the kinetics of CO2 uptake by a synthetic calcium based sorbent

被引:81
作者
Liu, Wen [1 ]
Dennis, John S. [1 ]
Sultan, D. Saquib [1 ]
Redfern, Simon A. T. [2 ]
Scott, StuartA. [3 ]
机构
[1] Univ Cambridge, Dept Chem Engn & Biotechnol, Cambridge CB2 3RA, England
[2] Univ Cambridge, Dept Earth Sci, Cambridge CB2 3EQ, England
[3] Univ Cambridge, Dept Engn, Cambridge CB2 1PZ, England
基金
英国工程与自然科学研究理事会;
关键词
Absorption; Calcium looping; Diffusion; Kinetics; Simulation; Sorbent; GAS-SOLID REACTIONS; COMBUSTION GASES; FLUIDIZED-BED; GRAIN MODELS; CAPTURE; CARBONATION; CALCINATION; TECHNOLOGY; CYCLES; PORE;
D O I
10.1016/j.ces.2011.11.036
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
This study examines the kinetics of carbonation by CO2 at temperatures of ca. 750 degrees C of a synthetic sorbent composed of 15 wt% mayenite (Ca12Al14O33) and CaO, designated HA-85-850, and draws comparisons with the carbonation of a calcined limestone. In-situ XRD has verified the inertness of mayenite, which neither interacts with the active CaO nor does it significantly alter the CaO carbonation-calcination equilibrium. An overlapping grain model was developed to predict the rate and extent of carbonation of HA-85-850 and limestone. In the model, the initial microstructure of the sorbent was defined by a discretised grain size distribution, assuming spherical grains. The initial input to the model - the size distribution of grains - was a fitted parameter, which was in good agreement with measurements made with mercury porosimetry and by the analysis of SEM images of sectioned particles. It was found that the randomly overlapping spherical grain assumption offered great simplicity to the model, despite its approximation to the actual porous structure within a particle. The model was able to predict the performance of the materials well and, particularly, was able to account for changes in rate and extent of reaction as the structure evolved after various numbers of cycles of calcination and carbonation. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:644 / 658
页数:15
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