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Thermal transformation of trinuclear Fe(III) acetato complex intercalated montmorillonite

机译:三核醋酸铁络合物插层蒙脱石的热转变

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Fe(III) pillared montmorillonite was prepared using trinuclear acetato complex of Fe(III) as the pillaring agent and the resulted material was characterised by different analytical techniques. Basal spacing of the material is found to be l8 A even after calcination at 500deg.C indicating the formation of stable pillars. Thermal analysis indicate that the complex decomposes slowly from the silicate layer at higher temperature to form metal oxyhydroxide pillars. Sample calcined at 500deg.C shows the highest surface area of 284 m~2/g. Mbssbauer analysis was carried to identify the exact phase of Fe(III) formed during thermal treatment. From the Mossbauer spectra recorded at 298 and 77 K, it is observed that the species formed from the decomposition of the acetyl group of the complex is γ-FeOOH even at 500deg.C; whereas, the pure complex decomposed directly to ∝-Fe_2O_3 at 300deg.C. This confirmed the role played by the silicate 1ayer in directing the phase formation of Fe(III) during the heat treatment.
机译:以Fe(III)的三核醋酸盐配合物为柱撑剂,制备了Fe(III)柱撑蒙脱土,并通过不同的分析技术对其进行了表征。即使在500℃下煅烧后,该材料的基础间距仍为18A,表明形成了稳定的支柱。热分析表明,该配合物在较高温度下从硅酸盐层缓慢分解,形成金属羟基氧化物柱。 500℃下煅烧的样品的最大表面积为284m 2 / g。进行Mbssbauer分析以鉴定热处理过程中形成的Fe(III)的确切相。从在298和77 K下记录的莫斯鲍尔光谱,观察到即使在500℃下,由配合物的乙酰基分解所形成的物种也为γ-FeOOH。而纯配合物在300℃下直接分解为∝-Fe_2O_3。这证实了硅酸盐1ayer在指导热处理过程中指导Fe(III)相形成中的作用。

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