煅烧
微晶
傅里叶变换红外光谱
材料科学
透射电子显微镜
热重分析
粒径
打赌理论
扫描电子显微镜
分析化学(期刊)
纳米颗粒
比表面积
矿物学
核化学
化学工程
纳米技术
化学
吸附
冶金
复合材料
色谱法
催化作用
有机化学
工程类
标识
DOI:10.1111/j.1551-2916.2009.03555.x
摘要
Alumina nanoparticles were synthesized following hydrothermal process at 170°C for 6 h, using glucose and other water‐based precursor materials. The uncalcined and calcined (550°–1200°C) particles were characterized by differential thermal analysis, thermogravimetry, Fourier transform infrared spectroscopy (FTIR), X‐ray diffraction (XRD), and multipoint Brunauer–Emmett–Teller (BET) surface area. The microstructures of the calcined (at 550°C) particles were examined by field‐emission scanning electron microscopy (FESEM) and transmission electron microscopy (TEM). XRD and FTIR studies revealed that gamma‐alumina (γ‐Al 2 O 3 ) persisted up to 1000°C followed by the appearance of alpha‐alumina (α‐Al 2 O 3 ) at 1200°C. BET surface area analysis confirmed that the specific surface area of γ‐Al 2 O 3 was higher compared with α‐Al 2 O 3 . Because of particle agglomeration, the crystallite sizes obtained by the BET method showed larger values than those determined by the XRD method for the samples calcined at 550°–1200°C. For 550°C‐treated sample, FESEM micrograph showed the aggregated particles of size 20–80 nm, while TEM image of the same sample revealed a particle size of 5–10 nm.
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