In situ X-ray Scattering of the Crystallisation of Basic Magnesium Chlorides using a Laboratory Instrument

IF 6.1 Q1 CHEMISTRY, MULTIDISCIPLINARY
Katie S. Pickering, Dr. Steven Huband, Dr. Kirill L. Shafran, Prof. Richard I. Walton
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引用次数: 0

Abstract

We demonstrate a method for in situ monitoring of the crystallisation of basic magnesium chlorides using a laboratory-based SAXS (small angle X-ray scattering)/ WAXS (wide angle X-ray scattering) instrument. By simultaneous acquisition of SAXS/WAXS, time-resolved particle size and phase evolution information was obtained from room temperature to 120 °C. The WAXS data were analysed using two-phase Rietveld refinements, to produce crystallisation curves. From Avrami-type kinetic analysis two competing mechanistic processes were proposed for the formation of Mg3Cl(OH)5 ⋅ 4 H2O with a nucleation-type mechanism extending further into the reaction with increased temperature. When comparing SAXS and WAXS, an offset between the consumption of MgO and the reduction of the sphere contribution to the SAXS scattering is observed. This is rationalised by the formation of an amorphous Mg(OH)2 layer on the MgO particle surface. Although laboratory-based SAXS/WAXS instruments have limitations compared to synchrotron-based sources, we have demonstrated how they can provide new insights into the formation of materials.

Abstract Image

使用实验室仪器对碱性氯化镁结晶的原位X射线散射
我们展示了一种使用基于实验室的SAXS(小角x射线散射)/ WAXS(广角x射线散射)仪器原位监测碱性氯化镁结晶的方法。通过同时采集SAXS/ WAXS,在室温至120℃范围内获得了时间分辨粒度和相演化信息。WAXS数据采用两相Rietveld细化法进行分析,得到结晶曲线。通过avrami型动力学分析,提出了两种相互竞争的mg3cl (OH) 5·4h2o生成机理,随着反应温度的升高,形成核型机理进一步延伸。当比较SAXS和WAXS时,观察到MgO的消耗和球对SAXS散射贡献的减少之间的抵消。在MgO颗粒表面形成无定形的Mg(OH) 2层是合理的。尽管基于实验室的SAXS/ WAXS仪器与基于同步加速器的源相比有局限性,但我们已经展示了它们如何为材料的形成提供新的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.30
自引率
0.00%
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