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Kinetics study on the dehydroxylation and phase transformation of Mg3Si2O5(OH)(4)

机译:Mg3Si2O5(OH)(4)的脱羟基化和相转化的动力学研究

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Determination of the decomposition mechanism and phase transformation of lizardite [Mg3Si2O5(OH)(4)] within laterite was carried out using thermal analysis kinetics during the heat-treatment process. Non-isothermal kinetic heating experiments at temperatures ranging from room temperature to 1273 K showed two characteristic peaks at approximately 898 K and 1094 K, corresponding to dehydroxylation and a phase transformation, respectively. Generalized master plots were used as a straightforward approach for determining the kinetic models. The Avrami-Erofeev reaction model was found to provide the best fit to the dehydroxylation process, and diffusion patterns with an apparent activation energy of 219 kJ mol(-1) are discussed. The results indicated that dehydroxylation was controlled by a constant nucleation rate and two-dimensional diffusion. In addition, the crystalline transformation of lizardite presented a reaction process-dependent evolution of the apparent activation energy, which decreased rapidly with increasing extent of the conversion. Based on the analyses, the phase transformation of lizardite may belong to reactions complicated by diffusion. (C) 2017 Elsevier B.V. All rights reserved.
机译:在热处理过程中使用热分析动力学在红外测定尿酸盐[Mg3Si2O5(OH)]的分解机制和相变的测定。在室温至1273k的温度下的非等温动力学加热实验在约898k和1094k的情况下,分别对应于脱羟基化和相变的两个特征峰。广义母图被用作确定动力学模型的直接方法。发现Avrami-erofeev反应模型提供最适合脱羟基化过程,讨论具有219kJ摩尔(-1)的表观活化能的扩散图案。结果表明,通过恒定的成核速率和二维扩散来控制脱羟基化。此外,蜥蜴的结晶转化呈现了表观活化能量的反应过程依赖性演化,随着转化程度的增加而迅速降低。基于分析,蜥蜴的相变可能属于扩散复杂的反应。 (c)2017年Elsevier B.V.保留所有权利。

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