In this study, copper oxide (CuO) nanostructures were successfully prepared by adding EG (ethylene glycol) and PEG (4000, 8000) (polyethylene glycol) via an in-situ chemical precipitation method. EG and PEG (4000, 8000) were effective for changing the particular size of CuO and we examined the effects of drying type such as freeze drying, muffle and horizontal furnace on the size of CuO nanostructure. The structure, morphology and elemental analysis of CuO nanostructure were analyzed by field-emission scanning electron microscopy (FE-SEM), X-ray diffraction (XRD) and energy dispersive X-ray spectroscopy (EDS). Also, the CuO nanostructures showed excellent electrical conductivity by the changing of PEG’s molecular weight and drying processes.
In this study, tin oxide (SnO2) nanoparticles were synthesized by hydrothermal method in the presence of hydrazine and ammonia by adding surfactant for 12 h in a Teflon autoclave at 100• C reaction temperature. Tin(II) chloride hydrate as an inorganic precursor, hexadecyl trimethyl ammonium bromide (CTAB), and tetrapropyl ammonium bromide (TPAB) as cationic, and sodium dodecyl sulfonate (SDS) as anionic surfactants were used. The results showed that the size and shape of nanoparticles depended on the surfactant types. The nanoparticles sizes between 17.5 and 19.7 nm were obtained by changing types of surfactants. Synthesized tin oxide nanoparticles were characterized by field emission scanning electron microscopy, transmission electron microscopy, X-ray diffraction, and the Fourier transform infrared spectroscopy.
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