分解
分压
动力学
化学
化学分解过程
热重分析
大气压力
等温过程
动能
热力学
分析化学(期刊)
活化能
热分解
化学分解
反应速率常数
传质
物理化学
色谱法
有机化学
物理
量子力学
氧气
海洋学
地质学
作者
Wenfei Yue,Wenli Song,Chuigang Fan,Songgeng Li
标识
DOI:10.1016/j.ces.2023.118646
摘要
Calcium looping often suffers from sintering during CaCO3 decomposition process, and CaCO3 decomposition in vacuum is a potential solution. Kinetic analysis of CaCO3 decomposition in vacuum is seldom, and most of the kinetics in the literature is obtained from thermogravimetric analyzer in atmospheric pressure. In addition, the reported kinetic data seems scattered, and varies depending on the analyzer employed. This study is focused on the intrinsic kinetics of isothermal CaCO3 decomposition in a vacuum fixed bed from 700 °C to 850 °C. Besides conventional internal/external mass transfer elimination via reducing size/increasing gas velocity, the effect of CO2 partial pressure is specially discussed under vacuum condition. It is found that, this influence could be eliminated only when the relative difference between equilibrium pressure and maximum CO2 partial pressure (Peq -P*CO2)/Peq was higher than 0.98. Tests at atmospheric pressure were also conducted with the same particle size and gas volumetric feeding rate for comparison. The intrinsic reaction rate constants of CaCO3 decomposition in vacuum are 1.05 × 10-3 s−1– 4.76 × 10-3 s−1 between 700 °C and 850 °C, and the activation energy of this reaction is 92.58 kJ/mol.
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