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基于多速率模型的氧化镁水化机理

Mechanism of Magnesium Oxide Hydration Based on the Multi-Rate Model.

作者信息

Xing Zhibo, Bai Limei, Ma Yuxin, Wang Dong, Li Meng

机构信息

College of Mining Engineering, North China University of Science and Technology, Tangshan 063210, China.

出版信息

Materials (Basel). 2018 Sep 27;11(10):1835. doi: 10.3390/ma11101835.

Abstract

The hydration of different active MgO under an unforced and ultrasonic condition was conducted in this paper to investigate the chemical kinetics model of the apparent reaction and discuss the mechanism combined with the product morphology. The dynamics fitting result shows that both the first-order and multi-rate model describe the hydration process under ultrasound well, while only the multi-rate model was right for the hydration process under an unforced condition. It indicated that the rate order of hydration was different in the hydration process under an unforced condition. The XRD and SEM show that the MgO hydration was a process of dissolution and crystallization. Part of the magnesium ions produced by dissolution of MgO did not diffuse into the solution in time, and adhered to the magnesium oxide surface and grew in situ instead. As a result, the difference in the hydration rate of the remaining MgO particles becomes wider and not in the same order (order of magnitude). The ultrasonic cavitation could prevent the in-situ growth of Mg(OH)₂ crystal nuclei on the surface of MgO. It not only greatly improved the hydration rate of MgO and produced monodisperse Mg(OH)₂ particles, but also made the first-order kinetics model fit the hydration process of MgO well.

摘要

本文研究了不同活性氧化镁在无外力和超声条件下的水化过程,以探究表观反应的化学动力学模型,并结合产物形态探讨其机理。动力学拟合结果表明,一级模型和多速率模型均能很好地描述超声作用下的水化过程,而在无外力条件下的水化过程中,只有多速率模型适用。这表明在无外力条件下的水化过程中,水化反应级数不同。XRD和SEM表明,氧化镁水化是一个溶解和结晶的过程。氧化镁溶解产生的部分镁离子没有及时扩散到溶液中,而是附着在氧化镁表面并原位生长。结果,剩余氧化镁颗粒的水化速率差异变得更大,且不在同一量级。超声空化可以阻止氢氧化镁晶核在氧化镁表面的原位生长。它不仅大大提高了氧化镁的水化速率,生成了单分散的氢氧化镁颗粒,还使一级动力学模型很好地拟合了氧化镁的水化过程。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c9aa/6212817/8ce6d6b434b1/materials-11-01835-g001.jpg

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