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Effect of ultrasound power and calcination temperature on the sonochemical synthesis of copper oxide nanoparticles for textile dyes treatment
Author(s) -
Saravanan Sundaram,
Sivasankar Thirugnanasambandam
Publication year - 2016
Publication title -
environmental progress and sustainable energy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.495
H-Index - 66
eISSN - 1944-7450
pISSN - 1944-7442
DOI - 10.1002/ep.12271
Subject(s) - calcination , nanoparticle , materials science , scanning electron microscope , copper oxide , polyethylene glycol , chemical engineering , copper , nuclear chemistry , particle size , sonochemistry , inorganic chemistry , nanotechnology , chemistry , organic chemistry , catalysis , metallurgy , composite material , engineering
Copper oxide (CuO) nanoparticles were synthesized by sonochemical technique using copper nitrate trihydrate and ammonium carbonate as precursors in the presence of polyethylene glycol (PEG). The reagents aqueous solution are exposed to ultrasound at different ultrasound power of 44, 66, 88, 110, and 132 W. The precipitated product was calcined at the temperatures of 400°C, 500°C, 600°C, and 700°C. The size, structure, and morphology of calcined CuO nanoparticles were characterized by X‐ray diffraction (XRD), scanning electron microscope (SEM), and energy‐dispersive X‐ray spectroscopy (EDAX). From the XRD observation, it is evident that the high purity CuO nanoparticles ranging from approximately 14 to approximately 54 nm were obtained. Additionally, SEM and EDAX investigation revealed that its structure and particle size are strongly dependent on the calcination temperature than ultrasound power. Most of the CuO nanoparticles formed were spherical in shape. Further, the application of the synthesized CuO nanoparticles toward the treatment of textile organic dyes such as Reactive Black 5 and Basic Blue 3 showed the synthesized CuO was highly effective in degradation of the environmental pollutants. © 2015 American Institute of Chemical Engineers Environ Prog, 35: 669–679, 2016