以黄钠铁矶渣制取的硫酸亚铁溶液为原料,经过净化后采用沉淀法制备α-Fe2O3微粉。通过热重/差热分析、X射线衍射分析、扫描电镜和光谱分析等测试手段,对α-Fe2O3微粉进行表征。研究结果表明:前驱体FeCO3在600800℃热处理2h的产物是α-Fe2O3,晶核生长活化能为12.4kJ/mol,颗粒均匀呈球形,粒径小于100nm,杂质含量低纯度高;在沉淀过程中加入分散剂和表面活性剂,抑制了前驱体FeCO3颗粒的长大和团聚,制备的α-Fe2O3粒径小,粒径分布范围窄。
α-Fe2O3 powder were prepared by precipitation method using FeSO4 purified from sodium jarosite’s slag as starting materials, and were characterized by X-ray diffraction, TCrDTA analysis and SEM photograph. The results show that uniform and spherical α-Fe2O3 nanoparticles with high purity are obtained by FeCO3 precursors calcinated for 2 h at 600-800℃, the growth activation energy of grains is 12.4 kJ/mol. The presence of dispersive agents and surfactants in process of precipitation can control the growth and aggregation of FeCO3 grains, so that the synthesized α-Fe2O3 powders have a size smaller than 100 nm and a narrow size distribution range, and a high purity.