以三齿希夫碱配体为前驱体的硝酸铜(II)配合物固相热分解制备纳米氧化铜

Niaz Monadi, S. Saeednia, P. Iranmanesh, M. H. Ardakani, S. Sinaei
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引用次数: 4

摘要

本文报道了以三齿希夫碱配体(1)为前驱体的硝酸水铜(II)配合物的固态热分解合成和表征氧化铜纳米颗粒。通过声化学和溶剂热法制备了铜配合物,并用扫描电镜(SEM)、x射线粉末衍射(XRD)和红外光谱(ft - ir)对其进行了表征。采用热重分析(TGA)研究了化合物(1)的热稳定性。研究了初始试剂的用量和反应时间对纳米结构化合物(1)的大小和形貌的影响。在500℃的空气气氛下,简单地合成了CuO纳米颗粒。用声化学法和溶剂热法分别制备了直径约200 nm和30 nm的CuO纳米颗粒。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Preparation and Characterization of Copper Oxide Nanoparticles Through Solid State Thermal Decomposition of an Aqua Nitrato Copper(II) Complex with a Tridentate Schiff-base Ligand as a New Precursor
In this study the synthesis and characterization of copper oxide nanoparticles via solid state thermal decomposition of a recently synthesized aqua nitrato copper(II) complex with a tridentate Schiff-base ligand (1) as a new precursor are reported. The copper complexes were obtained by sonochemical and solvothermal process and characterized by Scanning Electron Microscopy (SEM), X-ray powder Diffraction (XRD) and FT-IR spectroscopy. The thermal stability of compound (1) was studied by Thermogravimetric Analysis (TGA). The amount of initial reagents and the role of reaction time on size and morphology of nanostructure compound (1) were studied. CuO nanoparticles were simply synthesized at 500 oC under air atmosphere. The diameter of CuO nanoparticles was estimated to be about 200 and 30 nm from copper complex precursor obtained by sonochemical and solvothermal methods respectively.
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