Sequestration of Flue Gas CO2 by Direct Gas–Solid Carbonation of Air Pollution Control System Residues
journal contributionposted on 18.12.2012 by Sicong Tian, Jianguo Jiang
Any type of content formally published in an academic journal, usually following a peer-review process.
Direct gas–solid carbonation reactions of residues from an air pollution control system (APCr) were conducted using different combinations of simulated flue gas to study the impact on CO2 sequestration. X-ray diffraction analysis of APCr determined the existence of CaClOH, whose maximum theoretical CO2 sequestration potential of 58.13 g CO2/kg APCr was calculated by the reference intensity ratio method. The reaction mechanism obeyed a model of a fast kinetics-controlled process followed by a slow product layer diffusion-controlled process. Temperature is the key factor in direct gas–solid carbonation and had a notable influence on both the carbonation conversion and the CO2 sequestration rate. The optimal CO2 sequestrating temperature of 395 °C was easily obtained for APCr using a continuous heating experiment. CO2 content in the flue gas had a definite influence on the CO2 sequestration rate of the kinetics-controlled process, but almost no influence on the final carbonation conversion. Typical concentrations of SO2 in the flue gas could not only accelerate the carbonation reaction rate of the product layer diffusion-controlled process, but also could improve the final carbonation conversion. Maximum carbonation conversions of between 68.6% and 77.1% were achieved in a typical flue gas. Features of rapid CO2 sequestration rate, strong impurities resistance, and high capture conversion for direct gas–solid carbonation were proved in this study, which presents a theoretical foundation for the applied use of this encouraging technology on carbon capture and storage.