Effect of temperature on the preparation of yttrium oxide in microwave field

被引:16
作者
Chen, Kaihua [1 ,2 ]
Peng, Jinhui [1 ,2 ]
Srinivasakannan, C. [3 ]
Yin, Shaohua [1 ,2 ]
Guo, Shenghui [1 ,2 ]
Zhang, Libo [1 ,2 ]
机构
[1] Kunming Univ Sci & Technol, State Key Lab Complex Nonferrous Met Resources Cl, Kunming 650093, Yunnan, Peoples R China
[2] Kunming Univ Sci & Technol, Fac Met & Energy Engn, Kunming 650093, Yunnan, Peoples R China
[3] Khalifa Univ Sci & Technol, Petr Inst, Chem Engn Dept, Abu Dhabi, U Arab Emirates
基金
中国国家自然科学基金;
关键词
Yttrium oxalate; Microwave-assisted calcination; Decomposition; Yttria; SELECTIVE CATALYTIC-REDUCTION; THERMAL BARRIER COATINGS; NITRIC-OXIDE; DECOMPOSITION; METHANE; OXALATE;
D O I
10.1016/j.jallcom.2018.01.258
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
High-purity yttrium oxide (Y2O3) powder is successfully prepared by microwave-assisted calcination of yttrium oxalate. The decomposition process of yttrium oxalate was analyzed by TG-DSC indicate formation of Y2O3 undergoes three stages. The X-ray diffraction (XRD) analysis indicates that there is no peak of yttrium oxalate hydrate (Y-2(C2O4)(3)center dot 10H(2)O) after microwave-assisted calcination at 600 degrees C for 2 h, with the formation of cubic crystalline Y2O3 structure. Fourier transformed infrared spectroscopy (FT-IR) analysis show similar results with emergence of Y2O3 after calcination at 600 degrees C for 2 h. The precursor had a median particle size diameter 30.719 mu m, while that of all the calcined powders at different temperatures significantly decreased to about 4 mu m. Scanning electron microscopy (SEM) observations demonstrate the morphologies of the precursor and product, and the calcined Y2O3 preserved the amorphous character of the precursor, with rod-like shape. All the TG-DSC, XRD, FT-IR and SEM were utilized to understand the molecular changes in the process of microwave-assisted calcination of Y-2(C2O4)(3) to Y2O3. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:13 / 19
页数:7
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