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    Preparation, characterization and photocatalytic properties of rubber-TiO2-rGO composite sheets for dye decomposition in wastewater
    (2017-01-01)
    Tejangkura, Worapol
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    In this work, rubber-TiO<inf>2</inf>-rGO (RT-rGO) composite sheets were successfully prepared by a simple latex mixing-casting method using TiO<inf>2</inf> and natural rubber latex with different amounts of rGO loading. The prepared RT-rGO sheet samples were characterized by XRD, FT-IR, Raman, SEM and EDS techniques. The photocatalytic properties of the prepared RT-rGO sheets as catalyst were evaluated using methylene blue (MB) dye solution under UV light irradiation. The result indicated that all the composite sheets loaded with rGO had better photocatalytic activities than the sheet without rGO loading. RT-rGO6.2% sheet showed the highest removal efficiency of 93.3% which has the rate constant (kapp) as 98.2 times higher than the unloaded sheet. Furthermore, the efficiency of the RT-rGO sheet upon the repeated usage was also studied. The result indicated that the sheet could be easily used, recovered and reused many times with no need for the cleaning in between successive uses. Thus, the RT-rGO sheet appears to be an attractive-material for the wastewater treatment or the water purification industry.
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    Removal of methylene blue dye using metal-free g-C3N4 photocatalyst over natural sunlight irradiation
    This work presented the high activity of metal-free g-C<inf>3</inf>N<inf>4</inf> photocatalyst for methylene blue (MB) removing over natural sunlight irradiation. These g-C<inf>3</inf>N<inf>4</inf> photocatalysts materials were synthesized by a conventional thermal condensation method using melamine as a precursor under treated at the various annealing temperatures (450 °C, 500 °C, 550 °C, 600 °C and 650 °C). All assynthesized samples were characterized and confirmed by a several techniques, such as, X-ray diffraction (XRD), Fourier transformed infrared spectroscopy (FTIR), UV-vis diffuse reflectance spectrometer (DRS), scanning electron microscope (SEM), energy dispersive X-ray spectroscopy (EDS), and Brunauer-Emmett-Teller (BET) specific surface area. XRD and FTIR results confirmed that the as-synthesized g-C<inf>3</inf>N<inf>4</inf> samples were completely synthesized at annealing temperature of 500 °C. SEM images showed the morphologies of the g-C<inf>3</inf>N<inf>4</inf> samples had more flake-like structures upon the increasing of annealing temperatures. WhileDRS results indicated that the absorption edges of as-synthesized g-C<inf>3</inf>N<inf>4</inf> samples were shifted to visible-light region, except the sample as-synthesized at 650 °C (g-C<inf>3</inf>N<inf>4</inf>-650 °C). Moreover, the photocatalytic properties of metalfree g-C<inf>3</inf>N<inf>4</inf> photocatalyst materials were evaluated by degrading of MB dye solution under natural sunlight irradiation for 100 min. The results revealed that the highest photocatalytic activity was exhibited by the sample synthesized at 600 °C, which the apparent rate constant (kapp.) was 0.0291min<sup>-1</sup>. The orders of activities as:g-C<inf>3</inf>N<inf>4</inf>-600°C > g-C<inf>3</inf>N<inf>4</inf>-650 °C > g-C<inf>3</inf>N<inf>4</inf>-550 °C > g-C<inf>3</inf>N<inf>4</inf>-500°C > g-C<inf>3</inf>N<inf>4</inf>-450°C. Hence, the metal-free g-C<inf>3</inf>N<inf>4</inf> photocatalyst appears to be an attractivematerial for water or wastewater purification applications over activated by sunlight irradiation.
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    Effect of synthesized Ag nanoparticles by using the different amounts of polyvinylpyrrolidone for Ag-natural rubber hybrid sheets and their antibacterial properties
    (2017-01-01)
    Prasanseang, Warot
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    Ag-natural rubber (Ag-NR) hybrid sheets were successfully prepared with a very simple and low cost method. In this method, silver nanoparticles (AgNPs) were firstly synthesized by a rapid and green microwave-assisted using polyvinylpyrroridone (PVP) media. The effect of PVP weight ratios towards the size of AgNPs was also investigated. Then, Ag-NR hybrid sheet samples were prepared by latex mixing-casting method using concentrated natural rubber (NR) latex with the synthesized AgNPs colloids. The characteristic absorption, particles sizes and shapes of the obtained AgNPs were examined through UV-vis, TEM and SAED. Also, the prepared Ag-NR sheet samples were characterized using XRD, FT-IR, SEM and EDS techniques. It was found that the particles sizes of all the synthesized AgNPs had spherical-like shape, and the mean sizes were increased from 29.7 to 90.4 nm upon increasing PVP contents. EDS results showed the AgNPs were well-dispersed and impregnated into the rubber matrix. Moreover, the antibacterial properties of the prepared Ag-NR sheets were tested by agar disk-diffusion method with Gram-positive and Gramnegative bacteria as Staphylococcus aureus (S. aureus) and Escherichia coli (E. coli), respectively. The results showed that the hybrid sheets exhibited excellent antibacterial properties against these bacteria, in which the zones of inhibition were also dependent on the synthesized AgNPs by utilizing the different amounts of PVP.
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    Synthesis of nanocrystalline cobalt ferrite by the sonochemical method in highly basic aqueous solution
    (2017-01-01)
    Pasupong, Patchara
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    This study reported the preparation of nanocrystalline CoFe2O4 in single step by the sonochemical method in highly basic aqueous solution without requiring of high temperature calcination process. To prepare nanocrystalline CoFe2O4, the mixed solution of the required molar ratio of cobalt nitrate hexahydrate (Co(NO<inf>3</inf>).6H2O) and ferric nitrate nonahydrate (Fe(NO<inf>3</inf>).9H2O) was precipitated in high concentration of sodium hydroxide medium solution (NaOH) under high intensity ultrasonic irradiation (20 kHz, 150 W/cm2). The effect of NaOH concentration (5, 10, 15 and 20 M) on phase formation, microstructure and magnetic property of CoFe2O4 was investigated. X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR) and thermogravimetric analysis (TGA) results showed that the as-prepared powders were single phase CoFe2O4 with cubic spinel structure. Transmission electron microscopy (TEM) and scanning electron microscopy (SEM) study showed that nanocrystalline CoFe2O4 had monosized distorted spherical morphology and an agglomeration of the nanocrystalline CoFe2O4 into nanoparticles was observed when increasing the NaOH concentration. The nanocrystalline CoFe2O4 exhibited superparamagnetic property and the saturation magnetization (Ms) obtained from vibrating sample magnetometry (VSM) was found to correlate with the crystallite size and varied from 39-45 emu/g.
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    Preparation and photocatalytic activities of tio2-rgo nanocomposite catalysts for mb dye degradation over sunlight irradiation
    (2018-01-01) ; ;
    Tejangkura, Worapol
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    Prasanseang, Warot
    This research aims to investigate photocatalytic activities of titanium dioxide (TiO<inf>2</inf>) incorporated with reduced graphene oxide (rGO) nanocomposite catalysts. These TiO<inf>2</inf>-rGO photocatalysts were easily prepared through a direct-mixing of TiO<inf>2</inf> powder suspended in acidic solution under the different amounts of rGO loading (0.25, 0.50, 0.75 and 1.00 wt%). Then, the obtained TiO<inf>2</inf>-rGO samples were characterized by a several techniques. The results demonstrated that the crystalline phases of all samples are corresponding to pristine TiO<inf>2</inf>, whereas the characteristic peaks of rGO in the TiO<inf>2</inf>-rGO nanocomposites could be observed and also confirmed by Raman spectroscopy. TEM results showed that the TiO<inf>2</inf> nanoparticles were well-combined with rGO nanosheets. Moreover, the photocatalytic activities of all TiO<inf>2</inf>-rGO photocatalyst samples were evaluated by photodegrading of methylene blue (MB) dye solution under natural sunlight irradiation. The results revealed that all TiO<inf>2</inf>-rGO nanocatalysts exhibited much higher activity than those of the bare TiO<inf>2</inf>. The improved photocatalytic activity can be attributed to the presence of rGO nanosheets, leading to the decrease of electron (e<sup>-</sup>)-hole (h<sup>+</sup>) recombination of TiO<inf>2</inf> catalyst, increasing charge transfer rate of electrons and surface-adsorbed amount of MB molecules which enhances the photocatalytic activity.
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    Investigation of the influences of reaction temperature and time on the chemical reduction of graphene oxide by conventional method using Vitamin C as a reducing agent
    (2017-01-01) ; ;
    Kongtaweelert, Samart
    The aim of this work is to investigate the synthesis of reduced graphene oxide (rGO) aqueous suspension by a conventional heating method using vitamin C as a reducing agent. The influences of reaction temperatures (70, 90 and 100 °C) and heating times (30, 45 and 60 min) on the chemical reduction of graphene oxide (GO) were studied. Then, the obtained rGO samples were characterized by FT-IR, Raman, UV-Vis, XRD and TEM techniques. The FT-IR and Raman results showed that the reduction degree of GO to rGO was increased with the rising of the reaction temperature and time. Moreover, the UV-Vis spectra demonstrated that the absorption band at around 230 nm (π-π*) of pristine GO had shift to the longer wavelength upon the chemical reduction, indicating that GO is reduced to rGO. The optimal condition of the chemical reduction of GO to achievable rGO was the temperature of 90 °C with the 45 min of heating time. This condition yielded the rGO black aqueous suspension with the high quality and stability. Thus, this method of synthesis has an advantage of the rGO dispersion which led to many potential applications.