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Synthesis of Pure Magnetite Nanoparticles Using Microwave Hydrothermal and Sonication

机译:微波水热和超声合成纯磁铁矿纳米粒子

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Relatively pure Fe3O4 nanoparticles was synthesized by microwave hydrothermal (MWH) and sonication-assisted co-precipitation.The precipitating agent was 0.5 % hexamine in 10 % ammonia solution.This was added to 100 mL of 0.01 M HC1 containing stoichiometric amount of stable salt of Fe~(3+) and Fe~(2+) ions.The formaldehyde produced from hydrolysis of hexamine prevents partial oxidation of Fe~(2+) during the precipitation process.For stabilization of colloidal suspension a small amount of a bifunctional fatty acid was used to coat the Fe3O4 nanoparticles and make them hydrophobic.The extraction of Fe3O4 nanoparticles from aqueous phase into chloroform gave a stable magnetite suspension which was attracted by a magnet.The product was analyzed by XRD,LLS,EDX and quantities chemical analysis of iron content in magnetite.The average diameter of nanoparticles was found to be about 6.2 nm.The order of main factors according to their effectiveness on the yield of product was determined using a factorial design and ANOVA.
机译:通过微波水热(MWH)和超声辅助共沉淀法合成相对纯的Fe3O4纳米颗粒,将沉淀剂为0.5%的六胺在10%的氨溶液中,然后将其添加到100 mL的0.01 M HCl中,该溶液中含有化学计量的稳定的HCl盐。 Fe〜(3+)和Fe〜(2+)离子。六胺水解产生的甲醛可防止沉淀过程中Fe〜(2+)的部分氧化。为稳定胶体悬浮液,应添加少量双功能脂肪酸用Fe3O4纳米粒子包覆并使其疏水化。将Fe3O4纳米粒子从水相中萃取到氯仿中得到稳定的磁铁矿悬浮液,并被磁铁吸引。用XRD,LLS,EDX和铁的化学分析对产物进行分析。纳米粒子的平均直径约为6.2 nm,主要因素的排序取决于它们对产物收率的有效性。析因设计和方差分析。

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