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Crystallization kinetics study of In-doped and (In-Cr) co-doped TiO2 nanopowders using in-situ high-temperature synchrotron radiation diffraction

机译:使用原位高温同步辐射衍射掺杂和(IN-CR)共掺杂TiO2纳米粉粉的结晶动力学研究

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The influence of TiO2 nanopowder doping with 4 wt% indium and 2 wt% each of indium and chromium on phase transformation was studied. Samples were heated from ambient temperature to 950 degrees C in sealed quartz capillaries, and in-situ synchrotron radiation diffraction measurements were obtained. Capillary sealing yielded an increase in capillary gas pressure to 0.42 MPa at 950 degrees C in proportion to absolute temperature by Gay-Lussac's Law. The initial synthesized samples were amorphous, and crystalline anatase appeared at 200 degrees C. Crystalline rutile appeared at 850 degrees C for the nanomaterials that were doped with In and In and Cr. A change in sealed-capillary oxygen partial pressure yielded a decrease and an increase in crystallization temperature, respectively, for the amorphous-to-anatase and anatase-to-rutile transformations. Crystalline titania (anatase and rutile) formed from the amorphous titania by 800 degrees C and 900 degrees C, for materials doped with In and In-Cr, respectively. The anatase concentration that was dominant in the In-doped materials up to 950 degrees C and the higher rutile concentration for the In-Cr doped materials from 900 to 950 degrees C results from the defect structure that was induced by doping. Cr-ions in the Ti sub-lattice retarded the transformation of anatase to rutile when compared with the retarding effect of mixed In/Cr ions. The transformation results because of the relatively smaller radius of Cr-ions when compared with the In-ions. The differences in phase-transformation kinetics for In, In-Cr and for undoped nanopowders in the literature agree with the calculated transformation activation energies. (C) 2019 Production and hosting by Elsevier B.V. on behalf of King Saud University.
机译:研究了TiO2纳米粉末用4wt%铟和2wt%的铟和2wt%的影响,研究了相变同相变铟和铬。在密封的石英毛细管中从环境温度加热到950℃的样品,获得原位同步辐射衍射测量。毛细管密封含量在950摄氏度下毛细管气体压力增加至0.42MPa,与Gay-Lussac的法律的绝对温度成比例。初始合成样品是无定形的,并且在200摄氏度为200℃下出现结晶锐钛矿。结晶金红石以850℃出现在掺杂进入和中的纳米材料和Cr。密封毛细管氧分压的变化分别降低,结晶温度升高,用于无定形 - 锐钛矿和锐钛矿对金红石转化。用800℃和900℃的无定形二氧化钛形成的结晶二氧化钛(锐钛矿和金红石)分别用于掺杂在-CR中的材料。在掺杂物质中优化的锐钛矿浓度高达950℃,并且IN-CR掺杂物质的浓度高出900至950℃的浓度,由掺杂诱导的缺陷结构产生。与混合在/ Cr离子的延迟效果相比,Ti子晶格中的Cr-离子延迟了锐钛矿对金红石的转化。与离子相比,转化结果是因为与离子相比相对较小的Cr-离子。在文献中,In-Cr中的相变动力学的差异与文献中的未掺杂纳米孔的差异与计算的转化激活能量一致。 (c)2019年Elsevier B.V的生产和托管。代表沙特大学国王。

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