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The optimal parameters are found for preparing nanofluid in our submerged arc nanoparticle synthesis system (SANSS) using a copper electrode. A suspended copper oxide nanofluid is thus produced at the current of 8.5–10 A, voltage of 220 V, pulse duration of 12 μs, and dielectric liquid temperature of 2°C. The CuO nanoparticle are characterized by transmission electron microscopy (TEM), field emission scanning electron microscope (FESEM), X-ray diffraction (XRD), electron diffraction pattern (SAD) and electron spectroscopy for chemical analysis (ESCA). The equality volume spherical diameter of the obtained copper oxide particle is 49.1 nm, regular shape and narrow size distribution.

Tungsten oxide nanoparticles are prepared by evaporating and oxidizing the tungsten boat in helium and oxygen atmosphere and then quenched to the liquid nitrogen temperature. The as-prepared tungsten oxide nanoparticles are porous-free with uniform size. The morphology and particle size distribution of the as-prepared and after sinter treatments tungsten oxide nanoparticles are revealed by TEM and AFM. The long-range order of these nanoparticles can be examined by X-ray diffraction technique. The as-prepared nanoparticles exhibit a mixture structure of monoclinic and hexagonal crystals. Preliminary X-ray diffraction results indicate that the hexagonal structure is transformed to monoclinic structure after annealing to above 600°C. In order to better distinguish the structural properties of the tungsten oxide (WO3− x) nanoparticles before and after annealing, the X-ray absorption spectrum technique is utilized; thus, the detailed local atomic arrangement of oxygen and/or tungsten can be determined. According to the XAS result, the shape of the W L3-edge undergoes no considerable changes. This infers that structural transformation of tungsten oxide nanoparticle may be caused by the migration of oxygen after sintering. From the O K-edge of absorption spectrum, it suggests that a mixture phase structure is obtained when sintered below 300°C. And this result indicates that heat treatment to approximately 600°C produces a stable structure of a monoclinic crystal of WO3.

This article reports the gas-sensing capability of nanocrystalline (NC) transition metal-coated piezoelectric quartz crystal (PQC). NC transition metal particles of Pd and Ag with particles size of 10–15 nm, while Pt and Au are 20–25 nm are used. The NC particles deposited on the quartz substrate adsorbs gaseous pollutants, thereby increasing the weight of the quartz substrate and decreasing its vibration frequency. We have found that transition metals, Pd, Pt, Au, and Ag in particular, show good sensitivity for NH3-detection; the maximum frequency change occurs at 150°C for Pd and Pt and at 100°C for Au and Ag. The NC Pd- and NC Pt-coated PQC also show good sensitivity for CO2-detection at 150°C. Likewise, the NC Au-coated PQC shows very good sensitivity for NO2-detection but at a higher temperature (180°C). The frequency change as a function of the pollutant gas concentration (Δ f-curve) follows the Langmuir adsorption isotherm (unimolecular adsorption) except in the case of NC Pd-coated PQC under NH3 and NC Au-coated PQC under NO2. The Δ f-curve for the NC Pd-coated PQC is convex with respect to the NH3 concentration axis. The Δ f-curve for the NC Au-coated PQC is convex in the low NO2 concentration region, and concave in the high NO2 concentration region. Both curves indicate multi-molecular adsorption, Type III and Type V adsorption, respectively. Therefore, the good sensitivity and stability of these gas sensors can be attributed to physical adsorption of the pollutant gases as a result of van der Waals attraction.