石膏(CaSO4·2H2O)在热脱水过程中的结构演化

IF 0.9 4区 地球科学 Q4 MINERALOGY
A. Kyono, R. Ikeda, S. Takagi, Wataru Nishiyasu
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引用次数: 0

摘要

本文在30 ~ 200℃的温度范围内对石膏进行了原位高温同步X射线衍射反应研究,研究了石膏经过半水合反应到可溶硬石膏的连续结构变化。热重分析曲线和差热分析曲线显示脱水分两个阶段进行。三角形空间群p31 - 1 - 21的β -半水合物在90℃以上的反应峰逐渐变陡,而石膏的反应峰在160℃时减弱,不能明显观察到。石膏中的氧化钙8十二面体和硫酸钙4四面体随温度的升高膨胀很小。石膏中水氧(Ow)原子的占位参数保持在1.0左右,在实验误差范围内。当水分子从石膏中失去时,它立即转化为β -半水合物,而不保持其结构。石膏的体积热膨胀系数为1.31 × 10−4 K−1。在130 ~ 140℃温度下,β -半水合物中Ow的位占率从0.8持续下降到约0.5,形成具有六方空间基p622的可溶硬石膏。因此,β -半水脱水可以用化学式caso4·x h2o(0.5≤x≤0.8)来表示。在90 ~ 140℃范围内,β -半水合物的体积热膨胀系数为1.54 × 10−4 K−1。140℃以上β -半水合物与可溶硬石膏共存;β -半水化合物含量随温度升高而降低。在β -半水合物中,水分子不断地从CaO - 9四面体中释放出来,从而导致其收缩。因此,结构变化为较小的ca8十二面体触发其转化为可溶硬石膏而不会破坏其一维线性链。随着进一步加热,β -半水合物在170℃时完全转变为可溶硬石膏。在170 ~ 200℃范围内测定的可溶硬石膏的体积热膨胀系数为1.69 × 10−5 K−1,比石膏和β -半水石膏的体积热膨胀系数小一个数量级。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Structural evolution of gypsum (CaSO4·2H2O) during thermal dehydration
Herein, an in situ high – temperature synchrotron X – ray di ff raction study of gypsum is performed in the temperature range of 30 – 200 °C to investigate the continuous structural change from gypsum to soluble anhydrite through hemihydrate. Thermogravimetric and di ff erential thermal analysis curves reveal that dehydration occurs in two stages. The di ff raction peaks of β – hemihydrate with the trigonal space group P 3 1 21 gradually become sharper above 90 °C, whereas those of gypsum become less intense and cannot be distinctly observed at 160 °C. The CaO 8 dodecahedra and SO 4 tetrahedra in gypsum expand negligibly with temperature. The site occupancy parameter of the water oxygen (Ow) atom in gypsum remains at approximately 1.0, within the experimental error. When water molecules are lost from gypsum, it immediately transforms into β – hemihydrate, without maintaining its structure. The volumetric thermal expansion coe ffi cient of gypsum is 1.31 × 10 − 4 K − 1 . The site occupancy of Ow in β – hemihydrate continuously decreases from 0.8 and reaches approximately 0.5 at temperatures of 130 – 140 °C, where soluble anhydrite with a hexagonal space group P 6 2 22 begins to form. Therefore, β – hemihydrate dehydration can be translated by the chemical formula CaSO 4 · x H 2 O (0.5 ≤ x ≤ 0.8). The volumetric thermal expansion coe ffi cient of β – hemihydrate, determined at temperatures between 90 and 140 °C is 1.54 × 10 − 4 K − 1 . β – Hemihydrate coexists with soluble anhydrite above 140 °C; however, the amount of β – hemihydrate decreases with temperature. In β – hemihydrate, water molecules are continuously released from the CaO 9 tetradecahedra, thereby resulting in its contraction. Consequently, the structural change to a smaller CaO 8 dodecahedron triggers its transformation into soluble anhydrite without the collapse of its one – dimensional linear chains. With further heating, β – hemihydrate completely transforms into soluble anhydrite at 170 °C. The volumetric thermal expansion coe ffi cient of soluble anhydrite determined in the temperature range of 170 – 200 °C is 1.69 × 10 − 5 K − 1 , which is an order of magnitude smaller than the values of gypsum and β – hemihydrate.
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来源期刊
CiteScore
1.80
自引率
14.30%
发文量
5
审稿时长
>12 weeks
期刊介绍: The Journal of Mineralogical and Petrological Sciences (JMPS) publishes original articles, reviews and letters in the fields of mineralogy, petrology, economic geology, geochemistry, planetary materials science, and related scientific fields. As an international journal, we aim to provide worldwide diffusion for the results of research in Japan, as well as to serve as a medium with high impact factor for the global scientific communication Given the remarkable rate at which publications have been expanding to include several fields, including planetary and earth sciences, materials science, and instrumental analysis technology, the journal aims to encourage and develop a variety of such new interdisciplinary scientific fields, to encourage the wide scope of such new fields to bloom in the future, and to contribute to the rapidly growing international scientific community. To cope with this emerging scientific environment, in April 2000 the journal''s two parent societies, MSJ* (The Mineralogical Society of Japan) and JAMPEG* (The Japanese Association of Mineralogists, Petrologists and Economic Geologists), combined their respective journals (the Mineralogical Journal and the Journal of Mineralogy, Petrology and Economic Geology). The result of this merger was the Journal of Mineralogical and Petrological Sciences, which has a greatly expanded and enriched scope compared to its predecessors.
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