磁性Fe3O4纳米颗粒制备方案的比较

Ruoyu Hong , Jianhua Li , Jian Wang , Hongzhong Li
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引用次数: 49

摘要

采用NH3·H2O水溶液和NaOH水溶液共沉淀法制备磁性Fe3O4纳米颗粒。采用SEM、TEM、HRTEM、FT-IR、XRD、VSM等仪器对磁性纳米颗粒的性质进行了表征。结果表明,在水中用NH3·H2O合成的Fe3O4纳米粒子磁性最强,但反应时间最长。在水中使用NaOH的工艺最简单,反应时间最短,但颗粒特性不如其他两种方法。共沉淀法制备的Fe3O4磁性纳米颗粒平均粒径最小,但颗粒聚集严重。用饱和油酸钠将磁性Fe3O4纳米粒子包被油酸,并测量表面修饰后纳米粒子的极性。用NH3·H2O而非NaOH制备的Fe3O4纳米颗粒可以成功且彻底地包覆。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparison of schemes for preparing magnetic Fe3O4 nanoparticles

Magnetic Fe3O4 nanoparticles were prepared by means of coprecipitation using NH3·H2O in water and in alcohol, and using NaOH in water. A series of instruments such as SEM, TEM, HRTEM, FT-IR, XRD and VSM were used to characterize the properties of the magnetic nanoparticles. The results indicated that the magnetism of Fe3O4 nanoparticles synthesized using NH3·H2O in water was the highest, although the reaction time was the longest. The process using NaOH in water was the simplest and the reaction time was the shortest, but the particle characteristics were inferior to those of the other two methods. The mean size of magnetic Fe3O4 nanoparticles prepared by coprecipitation in alcohol was the smallest among the three, but the nanoparticles aggregated severely. The magnetic Fe3O4 nanoparticles were coated with oleic acid using saturated sodium oleate, and the polarity of the surface-modified nanoparticles was measured. Fe3O4 nanoparticles prepared using NH3·H2O, not NaOH, could be coated successfully and thoroughly.

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