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Dynamic Diffraction Studies on the Crystallization, Phase Transformation, and Activation Energies in Anodized Titania Nanotubes

机译:阳极氧化二氧化钛纳米管中结晶,相变性和活化能量的动态衍射研究

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摘要

The influence of calcination time on the phase transformation and crystallization kinetics of anodized titania nanotube arrays was studied using in-situ isothermal and non-isothermal synchrotron radiation diffraction from room temperature to 900 °C. Anatase first crystallized at 400 °C, while rutile crystallized at 550 °C. Isothermal heating of the anodized titania nanotubes by an increase in the calcination time at 400, 450, 500, 550, 600, and 650 °C resulted in a slight reduction in anatase abundance, but an increase in the abundance of rutile because of an anatase-to-rutile transformation. The Avrami equation was used to model the titania crystallization mechanism and the Arrhenius equation was used to estimate the activation energies of the titania phase transformation. Activation energies of 22 (10) kJ/mol for the titanium-to-anatase transformation, and 207 (17) kJ/mol for the anatase-to-rutile transformation were estimated.
机译:研究了使用原位等温和非等温同步辐射衍射从室温至900℃的原位等温和非等温同步阵列的相变和结晶动力学对阳极氧化二氧化钛纳米管阵列的相变和结晶动力学的影响。锐钛酶首先在400℃下结晶,而金红石在550℃结晶。阳极氧化二氧化钛纳米管的等温加热通过煅烧时间在400,450,500,550,600和650℃下增加导致锐钛矿丰度略微降低,但由于锐钛矿,金红石丰富的增加-to-rutile转型。 AVRAMI等式用于模拟二氧化钛结晶机制,并且Arhenius方程用于估计二氧化钛相变的激活能量。估计用于钛 - 锐钛矿转化的22(10)kJ / mol的活化能量,以及207(17)kJ / mol用于锐钛矿对金红石转化。

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