In this study, graphene colloids were prepared using the electric spark discharge method (ESDM) with graphite rods (99.9% purity) in deionized water (DW) at a normal temperature and pressure. Five different types of graphene colloids were prepared using an electrical discharge machine (EDM) with five different pulse cycle switching times (Ton:Toff ) = 10:10, 30:30, 50:50, 70:70, and 90:90 μs. According to the Ultraviolet-visible spectra (UV-Vis) and Zetasizer analysis, the results showed that the 10:10 μs parameter was the most suitable for the preparation of graphene colloids. UV-Vis was also used to detect the concentration of the graphene colloids; a comparison with a graphene oxide (GO) confirmed that this method could be used to calculate the discharge time needed to produce graphene colloids with different concentrations in the ESDM process.
This study used an electrical discharge machine (EDM) to perform an electrical spark discharge method (ESDM), which is a new approach for reducing graphene oxide (GO) at normal temperature and pressure, without using chemical substances. A silver (Ag) electrode generates high temperature and high energy during gap discharge. Ag atoms and Ag nanoparticles (AgNP) are suspended in GO, and ionization generates charged Ag+ ions in the Ag plasma with a strong reducing property, thereby carrying O away from GO. A large flake-like structure of GO was simultaneously pyrolyzed to a small flake-like structure of reduced graphene oxide (rGO). When Ag was used as an electrode, GO was reduced to rGO and the exfoliated AgNP surface was coated with rGO, thus forming an rGOAg complex. Consequently, suspensibility and dispersion were enhanced.
Electrical discharge machine was used to prepare platinum nanocolloid by electric spark discharge method (ESDM) at room temperature. Preparation of platinum nanocolloid needed only traditional electrical discharge machine, platinum wire (99.5%) and magnet mixer. Then verify whether platinum nanoparticles be could successfully prepared under different preparation and their suspension stability. The optical properties and zeta potential were measured by UV-vis and Zetasizer, and their characteristic peaks (surface plasmon resonant), while suspension stability was analysed. The results of transmission electron microscope showed size, shape and dispersibility of platinum nanoparticles with a size of mostly <10 nm. X-ray diffraction was used to measure crystal lattice structure and component of platinum nanoparticles. In this work, platinum nanocolloid in conditions of normal and centrifuge were analysed. Zeta potential of normal colloid was decreased from −29.5 to −18.8 mV after precipitation, while zeta potential of the centrifuged colloid still maintained at −40 mV, confirming the good suspension stability of platinum nanocolloid prepared by ESDM after centrifugation.
In this study, submerged arc discharge method (SADM) was used to prepare graphene-nanosilver composites (graphene impregnated with nanosilver) and verified whether it can be prepared under different methods. The optical properties, zeta potentials, and particle sizes of the composites were analyzed through ultraviolet-visible spectroscopy and Zetasizer. The suspensibility of composites were much better than that of noncomposites. Then, we compared the components of composites and noncomposites through transmission electron microscopy. The results confirmed that even when fabricated from similar materials, the composites and noncomposites yielded by SADM featured significantly different properties.
Through the use of an electric discharge machine, this study performed the electrical spark discharge method in deionised water under normal temperature and pressure for Cu nanocolloid (CuNC) preparation. The CuNCs had a zeta potential of 12.3 mV, indicating poor suspension stability. The suspension stability was effectively increased (zeta potential 32.5 mV) through the addition of polyvinyl alcohol (PVA) to form PVA-containing CuNCs PVA/CuNCs. Next, the following pulse-width modulation (Ton:Toff) parameters were tested to determine the optimal setting for PVA/CuNC preparation: 10:10, 30:30, 50:50, 70:70 and 90:90 µs. The optimal preparation parameter was then determined according to the absorbance, zeta potential and size distribution results. Finally, the surface properties and crystal structure of the PVA/CuNCs were characterised through transmission electron microscopy (TEM) and X-ray diffraction (XRD). When the Ton:Toff was set to 30:30 µs, preparation efficiency was optimal, as was suspension stability, as indicated by the absorbance value (0.534), zeta potential (32.5 mV) and size distribution (85.47 nm). Transmission electron microscopy revealed that Cu nanoparticles that were more dispersed in the PVA/CuNCs had a diameter smaller than 10 nm and a crystal line width of 0.2028 nm. X-ray diffraction showed that the PVA/CuNCs contained intact Cu crystal structures.
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