Water as the Key to Proto-Aragonite Amorphous CaCO3

被引:86
作者
Farhadi-Khouzani, Masoud [1 ]
Chevrier, Daniel M. [2 ,3 ]
Zhang, Peng [2 ,3 ]
Hedin, Niklas [4 ]
Gebauer, Denis [1 ]
机构
[1] Univ Konstanz, Dept Chem, Phys Chem, Univ Str 10,Box 714, D-78457 Constance, Germany
[2] Dalhousie Univ, Dept Chem, Halifax, NS, Canada
[3] Dalhousie Univ, Sch Biomed Engn, Halifax, NS, Canada
[4] Stockholm Univ, Dept Mat & Environm Chem, S-10691 Stockholm, Sweden
基金
加拿大自然科学与工程研究理事会; 瑞典研究理事会;
关键词
amorphous calcium carbonate; biomineralization; NMR spectroscopy; polyamorphism; water; CALCIUM-CARBONATE; NONCLASSICAL NUCLEATION; BIOMINERALIZATION; POLYAMORPHISM; NANOPARTICLES; CLUSTERS; GROWTH; PHASE;
D O I
10.1002/anie.201603176
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Temperature and pH value can affect the short-range order of proto-structured and additive-free amorphous calcium carbonates (ACCs). Whereas a distinct change occurs in proto-vaterite (pv) ACC above 45 degrees C at pH 9.80, proto-calcite (pc) ACC (pH 8.75) is unaffected within the investigated range of temperatures (7-65 degrees C). IR and NMR spectroscopic studies together with EXAFS analysis showed that the temperature-induced change is related to the formation of proto-aragonite (pa) ACC. The data strongly suggest that the binding of water molecules induces dipole moments across the carbonate ions in pa-ACC as in aragonite, where the dipole moments are due to the symmetry of the crystal structure. Altogether, a (pseudo-)phase diagram of the CaCO3 polyamorphism in which water plays a key role can be formulated based on variables of state, such as the temperature, and solution parameters, such as the pH value.
引用
收藏
页码:8117 / 8120
页数:4
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