Synthesis of Thermally Spherical CuO Nanoparticles

Copper oxide (CuO) nanoparticles were successfully synthesized by a thermal method. The CuO nanoparticles were further characterized by thermogravimetric analysis (TGA), differential thermal analysis (DTA), X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive X-ray spectrometry (EDS), and high resolution transmission electron microscopy (HRTEM), respectively. The specific surface area (SSABET) of CuO nanoparticles was determined by nitrogen adsorption. The SSABET was found to be 99.67 m2/g (dBET of 9.5 nm). The average diameter of the spherical CuO nanoparticles was approximately 6–9 nm

The Monitoring of H2S and SO2 Noxious Gases from Industrial Environment with Sensors Based on Flame-Spray-Made SNO2 Nanoparticles

The noxious gas sensors were developed successfully using flame-spray-made SnO2 nanoparticles as the sensing materials. The functionalized nanoparticle properties were further analyzed by XRD, BET and TEM analyses. The SnO2 nanoparticles (SSABET: 141.6 m2/g) were investigated revealing non-agglomerated spheroidal, hexagonal, rectangle (3 - 10 nm), and rod-like (3 - 5 nm in width and 5 - 20 nm in length) morphologies. The sensing films were prepared by spin coating onto the Al2O3 substrates interdigitated with Au electrodes. The sensing films were significantly developed in order to detect with H2S (0.5 - 10 ppm) and SO2 (20 - 500 ppm) at the operating temperature ranging from 200 - 350°C. After sensing test, the cross-section of sensing film was analyzed by SEM analyses. It was found that SnO2 sensing film showed higher sensitive to H2S gas with very fast response at lower concentrations (3 s, to 10 ppm). The cross sensitivities of the sensor towards different concentrations of H2S, CO, H2, and C2H2 were measured at 300°C. The sensor evidently shows much less response to CO, H2, and C2H2 than to H2S indicating higher selectivity for H2S of the SnO2 sensor at the lower concentration (10 ppm). In addition, the SnO2 sensor was the most suitable candidate for the efficient detection of H2S noxious gas

Highly Efficient Visible-Light-Induced Photocatalytic Activity of Fe-Doped TiO2 Nanoparticles

Bare TiO2 and nominal 5.0 at% Fe-doped TiO2 nanoparticles were synthesized by the modified sol-gel method. The samples were physically characterized in order to obtain the correlation between structure and photocatalytic properties by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), Brunauer, Emmett and Teller (BET), and UV-vis diffuse reflectance spectrophotometry (UV-vis DRS). XRD results indicated that phase structures of bare TiO2 and Fe-doped TiO2 nanoparticles were the mixture of anatase and rutile phases. The content of rutile phase in 5.0 at% Fe-doped TiO2 nanoparticles decreased . TEM images revealed that the shape of bare and 5.0 at% Fe-doped TiO2 was almost spherical and the average particle size was in the range of 10-30 nm. Specific surface areas of the samples were found as 75 and 134 m2/g for bare TiO2 and nominal 5.0 at% Fe-doped TiO2, respectively. The results from UV-vis reflectance spectra clearly indicated the shift of absorption band edge towards visible region upon doping TiO2 with iron. Photocatalytic activity of bare TiO2 and 5.0 at% Fe-doped TiO2 nanoparticles was examined by studying the mineralization of oxalic acid under visible light irradiation and the results clearly showed that Fe-doped TiO2 sample exhibited higher activity than bare TiO2

Effects of Niobium-Loading on Sulfur Dioxide Gas-Sensing Characteristics of Hydrothermally Prepared Tungsten Oxide Thick Film

Nb-loaded hexagonal WO3 nanorods with 0–1.0 wt% loading levels were successfully synthesized by a simple hydrothermal and impregnation process and characterized for SO2 sensing. Nb-loaded WO3 sensing films were produced by spin coating on alumina substrate with interdigitated gold electrodes and annealed at 450°C for 3 h in air. Structural characterization by X-ray diffraction, high-resolution transmission electron microscopy, and Brunauer-Emmett-Teller analysis showed that spherical, oval, and rod-like Nb nanoparticles with 5–15 nm mean diameter were uniformly dispersed on hexagonal WO3 nanorods with 50–250 nm diameter and 100 nm–5 µm length. It was found that the optimal Nb loading level of 0.5 wt% provides substantial enhancement of SO2 response but the response became deteriorated at lower and higher loading levels. The 0.50 wt% Nb-loaded WO3 nanorod sensing film exhibits the best SO2 sensing performances with a high sensor response of ~10 and a short response time of ~6 seconds to 500 ppm of SO2 at a relatively low optimal operating temperature of 250°C. Therefore, Nb loading is an effective mean to improve the SO2 gas-sensing performances of hydrothermally prepared WO3 nanorods

Photocatalytic Degradation of Phenol Using Nb-Loaded ZnO Nanoparticles

Niobium-doped Zinc Oxide nanoparticles (Nb-doped ZnO NPs) in the range of 20 and 40 nm were synthesized by Flame Spray Pyrolysis (FSP) technique. The crystalline phase, morphology and size of the nanoparticles were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM) and UV-vis spectroscopy. The specific surface area of the nanoparticles was measured by nitrogen adsorption (BET analysis). The pure ZnO and Nb-doped ZnO NPs were found to have the clear spherical, hexagonal and rod-like morphologies. To the best of our knowledge, the application of Nb-doped ZnO NPs as a photocatalyst has not been reported yet. In this study, the photocatalytic activities of pure ZnO and Nb-doped ZnO NPs were determined by studying the mineralization of phenol under UV light illumination. The results indicated that all Nb-doped ZnO NPs have better photocatalytic activity than the pure ZnO nanoparticles. It was found that, 0.50 mol% Nb-doped ZnO NPs exhibited the fastest response to the degradation of phenol

Photocatalytic Degradation of Phenol over Highly Visible-Light Active BiOI/TiO2 Nanocomposite Photocatalyst

BiOI/TiO2 nanocomposites were successfully prepared by the two-step method, co-precipitation/solvothermal method. The amount of BiOI in the composites were varied as 0, 5.0, 7.5, 10.0 and 12.5 mol%. XRD results exhibited sharp and narrow diffraction peaks of both BiOI and TiO2 in all composite samples. Morphologies of as-prepared samples consisted of spherical shapes of TiO2 and nanosheets of BiOI. Difuse Reflectance UV-visible (DR-UV-vis) spectra of composites drastically shifted into the visible range and the reduced band gap energies were observed. The composits obviously showed an enhanced phenol degradation of ca. 6 times higher than that of pure BiOI, pure TiO2 and Degussa P25. The maximum photocatalytic activity of ca. 68% was found for 10.0 mol% BiOI/TiO2 nanocomposite because of its increased visible-light-harvesting ability and its efficient electron-hole separation efficiency as observed from DR-UV-vis and PL spectra results

Synthesis and Characterization of the Novel BiVO4/CeO2 Nanocomposites

Novel BiVO4/CeO2 nanocomposites were synthesized by the hydrothermal method combined with the homogeneous precipitation method. The mole ratios of BiVO4:CeO2 were 0.4:0.6, 0.5:0.5, and 0.6:0.4. The obtained BiVO4/CeO2 nanocomposites were characterized by X-ray diffraction (XRD) for phase composition and crystallinity. Particle sizes, morphology and elemental composition of BiVO4/CeO2 composites were examined by scanning electron microscopy (SEM), transmission electron microscopy (TEM), and energy dispersive X-ray spectroscopy (EDS). The Brunauer, Emmett and Teller (BET) adsorption-desorption of nitrogen gas for specific surface area determination at the temperature of liquid nitrogen was performed on all samples. UV-vis diffuse reflectance spectra (UV-vis DRS) were used to identify the absorption range and band gap energy of the composite catalysts. The results indicated that BiVO4/CeO2 samples retained monoclinic scheelite and fluorite structures. The morphologies of nanocomposite samples consisted of rod-like, plate-like and spheroidal shapes. Specific surface area (SSABET) of the novel synthesized catalysts drastically increased from 38 - 150 m2/g whereas an average BET-equivalent particle diameter (dBET) significantly decreased from 30 - 12 nm, upon increasing the amount of CeO2 in the BiVO4/CeO2 composite. The absorption spectra of all nanocomposite samples were shifted to the visible region, suggesting the potential application of this novel composite as an active visible-light driven photocatalyst

Facile Horner-Emmons Synthesis of Defect-Free Poly(9,9-dialkylfluorenyl-2,7-vinylene)

ABSTRACT: This paper describes a simple new strategy for preparing poly(9,9-dialkylfluorenyl-2,7-vinylenes) (PFVs) having high molecular weights and no detectable saturated defects along the conjugated backbone. The new route utilizes a modified Horner-Emmons method by coupling suitably designed comonomers to form the targeted conjugated polymers. The newly prepared PFVs were directly compared to PFVs prepared via a previously established Gilch polymerization route. The structure and optical properties of all PFVs were characterized by gel permeation chromatography (GPC), NMR spectroscopy, UV-vis, fluorescence, and photoluminescence spectroscopy. The findings indicate that the modified Horner-Emmons route gave PFVs with lower molecular weights but substantially higher yields and fewer defects than those prepared by using the Gilch route

Photocatalytic Mineralization of Organic Acids over Visible-Light-Driven Au/BiVO 4

Au/BiVO4 visible-light-driven photocatalysts were synthesized by coprecipitation method in the presence of sodium dodecyl benzene sulfonate (SDBS) as a dispersant. Physical characterization of the obtained materials was carried out by X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDX), UV-Vis diffuse reflectance spectroscopy (DRS) and Brunauer, and Emmett and Teller (BET) specific surface area measurement. Photocatalytic performances of the as-prepared Au/BiVO4 have also been evaluated via mineralizations of oxalic acid and malonic acid under visible light irradiation. XRD and SEM results indicated that Au/BiVO4 photocatalysts were of almost spherical particles with scheelite-monoclinic phase. Photocatalytic results showed that all Au/BiVO4 samples exhibited higher oxalic acid mineralization rate than that of pure BiVO4, probably due to a decrease of BiVO4 band gap energy and the presence of surface plasmon absorption upon loading BiVO4 with Au as evidenced from UV-Vis DRS results. The nominal Au loading amount of 0.25 mol% provided the highest pseudo-first-order rate constant of 0.0487 min−1 and 0.0082 min−1 for degradations of oxalic acid (C2) and malonic acid (C3), respectively. By considering structures of the two acids, lower pseudo-first-order rate constantly obtained in the case of malonic acid degradation was likely due to an increased complexity of the degradation mechanism of the longer chain acid