Transition mechanism of the reaction interface of the thermal decomposition of calcite

被引:6
|
作者
Li, Zhi [1 ]
Zhao, Zhen [2 ]
Wang, Qi [1 ]
Wang, Guocheng [1 ]
机构
[1] Univ Sci & Technol Liaoning, Sch Mat & Met, Anshan 114051, Peoples R China
[2] Anshan Normal Univ, Sch Chem & Life Sci, Anshan 114007, Peoples R China
基金
美国国家科学基金会;
关键词
(CaO)(m)-(CO2)(n)Interface; Density functional theory; Association energy; Gibbs free energy; GENERALIZED GRADIENT APPROXIMATION; SIMULTANEOUS TG/DSC MEASUREMENTS; AB-INITIO CALCULATIONS; THERMOGRAVIMETRIC DATA; GROWTH STRATEGIES; FUNCTIONAL THEORY; KINETIC-ANALYSIS; PART I; CARBONATE; CLUSTERS;
D O I
10.1016/j.jcrysgro.2018.04.005
中图分类号
O7 [晶体学];
学科分类号
0702 ; 070205 ; 0703 ; 080501 ;
摘要
Even the reaction layer (excited state CaCO3) is so thin that it is difficult to detect, it is significantly restrict the orientation of the solid product (excited state CaO) of the thermal decomposition of calcite. Quantum chemical calculation with GGA-PW91 functional reveals that the ground-state (CaCO3)(m) clusters are more stable than the hybrid objects (CaCO3)(m)-(CaO)(n) clusters. The lowest-energy (CaCO3)(m) clusters are more Kinetically stable than that of (CaCO3)(m-n)(CaO)(n) clusters and then than that of (CaO)(n) clusters except (CaCO3)(CaO)(3) clusters from the HOMO-LUMO gaps. (CaCO3)(2) clusters should co-exist at room temperature and they prefer to decompose with the temperature increasing. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:13 / 17
页数:5
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