The synthesis of copper nanoparticles was studied by wet chemical methods using copper sulfate pentahydrate (CuSO4·5H2O) and nitrogen ligands allylamine (AAm) and polyallylamine (PAAm) as stabilizers. The results suggest that the use of these ligands leads to the exclusive formation of metallic copper nanoparticles (Cu-NPs). The use of partially crosslinked polyallylamine (PAAmc) leads to nanoparticles (NPs) with low yields and high coating content, while linear PAAm leads to NPs with high yields and low coating content. The chemical composition of the particles was determined by XRD and average particle diameters were determined by the Debye-Scherrer equation. TGA analysis provided evidence of the content and thermal stability of the coating on the nanoparticles and PAAm. The morphology, particle size distribution, and presence of PAAm coating were observed through TEM. The use of AAm in the synthesis of NPs could be a good alternative to reduce costs. By using TGA, TEM, and DSC techniques, it was determined that synthesized NPs with AAm presented a coating with similar characteristics to NPs with PAAm, suggesting that AAm underwent polymerization during the synthesis.
The synthesis of copper nanoparticles (Cu NPs) stable to chemical oxidation has attracted much attention due to their novel application possibilities. The physicochemical properties of Cu NPs define their utilization in diverse fields, including biological applications, solar cells, high conductivity inks for printed electronics, and other specific applications. In this study we present the synthesis of oxide-free Cu NPs by wet chemistry routes and their chemical oxidation during the storage exposed to ambient conditions. The Cu NPs synthesized in PAAm and AAm/glycerol presence exhibit no oxidation during synthesis and atmospheric conditions storage for 60 and 37 months, respectively. The obtained results compared with those coming from oxidation of partially passivated commercial Cu NPs at 99.8% purity, are presented. The role of the Cu NPs coating is critical to avoid oxidation, and it can be an important feature to achieve good dispersion in different polymers. The Cu NPs oxidation was studied by XRD, TGA, TEM, FTIR, and HR-TEM.
Copper nanoparticles (Cu-NPs) with sizes lower than 31 nm were prepared by wet chemical reduction using copper sulfate solution, hydrazine, and mixture of allylamine (AAm) and polyallylamine (PAAm) as stabilizing agents. The use of AAm/PAAm mixture leads to the formation of Cu and CuO nanoparticles. The resulting nanostructures were characterized by XRD, TGA, and TEM. The average particle diameters were determined by the Debye-Scherrer equation. Analysis by TGA, TEM, GS-MS, and1HNMR reveals that synthesized NPs with AAm presented a coating with similar characteristics to NPs with PAAm, suggesting that AAm underwent polymerization during the synthesis. The synthesis of NPs using AAm could be a good alternative to reduce production costs.
A nylon 6 nanocomposite with copper nanoparticles processed by ultrasound-assisted extrusion was prepared at concentrations between 0.01 and 0.50 wt.%, and its thermal and mechanical properties were determined. The presence of the crystalline phase α (α1 and α2) in the polymer matrix was confirmed by X-ray diffraction, and the presence of the α2 phase showed a greater increase than the α1 phase as a function of the copper nanoparticle concentration. This process was attributed to secondary crystallization. Furthermore, it was determined that the chemical composition of the nanoparticles is a blend of metallic copper and cupric oxide. The formation of copper nanowires was observed by scanning electron microscopy, and the concentration of 0.10% exhibited the best dispersion in comparison with the other concentrations. The melting temperature of the nanocomposites underwent a slight decrease in comparison with the nylon 6, while thermal stability, crystallization temperature, and crystallinity were increased in relation to the pure polymer. This behavior is attributed to an efficient dispersion of the nanoparticles and to their functionality as crystal nucleation sites. For the 0.10% concentration nanocomposite, higher mechanical properties were obtained; tensile strength increased by 8.9%, and the tensile modulus increased by 25.4%; as a consequence, elongation at break was 62% less than that of the polymer matrix.
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