Glass transition temperatures and crystallization kinetics of a synthetic, anhydrous, amorphous calcium-magnesium carbonate

被引:5
|
作者
Hess, Kai-Uwe [1 ]
Schawe, Juergen E. K. [2 ,3 ]
Wilding, Martin [4 ]
Purgstaller, Bettina [5 ]
Goetschl, Katja E. [5 ]
Sturm, Sebastian [6 ]
Mueller-Caspary, Knut [6 ]
Sturm, Elena V. [1 ]
Schmahl, Wolfgang [1 ]
Griesshaber, Erika [1 ]
Bissbort, Thilo [1 ]
Weidendorfer, Daniel [1 ]
Dietzel, Martin [5 ]
Dingwell, Donald B. [1 ]
机构
[1] Ludwig Maximilians Univ Munchen, Earth & Environm Sci, Theresienstra, 41 III, D-80333 Munich, Germany
[2] Mettler Toledo GmbH, Nanikon, Switzerland
[3] Swiss Fed Inst Technol, Dept Mat, Lab Met Phys & Technol, CH-8093 Zurich, Switzerland
[4] UK Catalysis Hub, Res Complex, Harwell, Berks, England
[5] Graz Univ Technol, Inst Appl Geosciences, A-8010 Graz, Austria
[6] Ludwig Maximilians Univ Munchen, Fak Chem & Pharmazie, Physikal Chem, D-81377 Munich, Germany
来源
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY A-MATHEMATICAL PHYSICAL AND ENGINEERING SCIENCES | 2023年 / 381卷 / 2258期
关键词
amorphous calcium-magnesium carbonate; glass transition temperature; lyophilization; crystallization dynamics; scanning; transmission electron microscopy; fast; scanning differential scanning calorimetry; TRANSFORMATION; CURVES;
D O I
10.1098/rsta.2022.0356
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
We report the first calorimetric observations of glass transition temperatures and crystallization rates of anhydrous, amorphous calcium-magnesium carbonate using fast scanning differential scanning calorimetry. Hydrous amorphous Ca0.95Mg0.05CO3<middle dot>0.5H(2)O (ACMC) solid was precipitated from a MgCl2-NaHCO3 buffered solution, separated from the supernatant, and freeze-dried. An aliquot of the freeze-dried samples was additionally dried at 250 degrees C for up to 6 h in a furnace and in a high-purity N-2 atmosphere to produce anhydrous ACMC. The glass transition temperature of the anhydrous Ca0.95Mg0.05CO3 was determined by applying different heating rates (1000-6000 K s(-1)) and correcting for thermal lag to be 376 degrees C and the relaxational heat capacity was determined to be Cp = 0.16 J/(g K). Additionally, the heating rate dependence of the temperature that is associated with the corrected crystallization peaks is used to determine the activation energy of crystallization to be 275 kJ mol(-1). A high-resolution transmission electron microscopy study on the hydrous and anhydrous samples provided further constraints on their compositional and structural states. This article is part of the theme issue 'Exploring the length scales, timescales and chemistry of challenging materials (Part 1)'.
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页数:13
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