The transformation of amorphous calcium carbonate to calcite and classical nucleation theory

被引:25
作者
Freeman, C. L. [1 ]
Harding, J. H. [1 ]
机构
[1] Univ Sheffield, Dept Mat Sci & Engn, Mappin St, Sheffield S1 3JD, S Yorkshire, England
基金
英国工程与自然科学研究理事会;
关键词
A1; Interfaces; A1 Computer simulation; A1 Supersaturated solutions; A2 Growth from solutions; B1; Minerals; B1 Calcium compounds; NONCLASSICAL NUCLEATION; CRYSTAL NUCLEATION; INSIGHTS; CRYSTALLIZATION; KINETICS; GROWTH; WATER;
D O I
10.1016/j.jcrysgro.2022.126978
中图分类号
O7 [晶体学];
学科分类号
0702 ; 070205 ; 0703 ; 080501 ;
摘要
The interfaces of calcite with water, dehydrated and hydrated amorphous calcium carbonate are studied with molecular dynamics simulations. The interfacial energies demonstrate that the calcite interface is most stable when in contact with water or low concentration solutions rather than amorphous calcium carbonate. These values are used to test the interplay between supersaturation and the interfacial energy for calcite. They demonstrate that a dissolution-reprecipitation process should always be energetically preferred to a solid state transformation of amorphous calcium carbonate to calcite.
引用
收藏
页数:6
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