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Science and Technology Development Journal
Article . 2011 . Peer-reviewed
License: CC BY
Data sources: Crossref
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GREEN SYNTHESIS OF COPPER OXIDE NANOPARTICLES

Authors: Thao Huu Vo; Hanh Ngoc Nguyen;

GREEN SYNTHESIS OF COPPER OXIDE NANOPARTICLES

Abstract

Nanoparticles of metal and metallic oxides have become a very active research area in the field of material chemistry. The surface effect is mainly responsible for deviation of the properties of nano-materials from that of the bulk. Nanosize copper oxide was synthesized by hydrolysis of copper salts in basic medium using biodegradable non-ionic polymer polyethylene glycol (PEG) as surface active agent The X-ray powder diffraction patterns (XRD) present typical peaks of copper oxides formed. The transmission electron microscopy (TEM) and scanning electron microscopy (SEM) images determined the shape and the nanosizes of the particles of about 10-30nm. The results exhibited the role of intermediate nanosize copper hydroxide species on the formation of copper oxide nanoparticles. The influence of synthesis temperature, reaction time, calcination temperature, etc. was studied.

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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
1
Average
Average
Average
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