Issues Affecting the Synthetic Scalability of Ternary Metal Ferrite Nanoparticles

Lauren Morrow, A. Barron
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引用次数: 5

Abstract

Ternary Mn-Zn ferrite (MnxZn1-xFe2O4) nanoparticles (NPs) have been prepared by the thermal decomposition of an oleate complex, sodium dodecylbenzenesulfonate (SDBS) mediated hydrazine decomposition of the chloride salts, and triethylene glycol (TREG) mediated thermal decomposition of the metal acetylacetonates. Only the first method was found to facilitate the synthesis of uniform, isolable NPs with the correct Mn : Zn ratio (0.7 : 0.3) as characterized by small angle X-ray scattering (SAXS), transmission electron microscopy (TEM), and inductively coupled plasma-optical emission spectroscopy (ICP-OES). Scaling allowed for retention of the composition and size; however, attempts to prepare Zn-rich ferrites did not result in NP formation. Thermogravimetric analysis (TGA) indicated that the incomplete decomposition of the metal-oleate complexes prior to NP nucleation for Zn-rich compositions is the cause.
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影响三元金属铁氧体纳米颗粒合成可扩展性的问题
通过油酸配合物的热分解、十二烷基苯磺酸钠(SDBS)介导的氯盐肼分解和三甘醇(TREG)介导的金属乙酰丙酮酸盐的热分解制备了锰锌铁氧体纳米颗粒(MnxZn1-xFe2O4)。通过小角x射线散射(SAXS)、透射电子显微镜(TEM)和电感耦合等离子体光学发射光谱(ICP-OES)表征,发现只有第一种方法可以合成均匀、可分离的纳米粒子,且Mn: Zn比为0.7:0.3。缩放允许保留成分和大小;然而,试图制备富锌铁氧体并没有导致NP的形成。热重分析(TGA)表明,富锌成分在NP成核之前金属油酸配合物的不完全分解是其原因。
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