Byong Chol Bai

Improved photodegradation properties and kinetic models of a solar-light-responsive photocatalyst when incorporated into electrospun hydrogel fibers.

The capacity of a photocatalyst system to degrade water pollutants was optimized using solar-light-sensitive TiO(2) and the swelling behavior of a hydrogel. TiO(2) synthesized via a sol-gel process was modified by multielement doping to change its solar-light-responsive properties. A hydrogel was used for the rapid absorption of both anionic and cationic water pollutants. TiO(2) particles were immobilized in/on hydrogel fibers by an electrospinning method for the easy recovery of TiO(2), and the ability of the hydrogel/TiO(2) composite to degrade dye molecules was studied. The TiO(2) particles were observed to have maintained their original anatase-type crystallinity in/on the electrospun hydrogel fibers. The dye degradation capacity of the hydrogel/TiO(2) composite was investigated using both anionic and cationic dyes under sunlight. Two mechanisms were suggested by which the hydrogel/TiO(2) composite can remove dye particles from the water: (1) the absorption of dyes by the hydrogel and (2) the degradation of the dye by the TiO(2) in the hydrogel. Both of these mechanisms were investigated in this study. We found that the dye was effectively absorbed by the hydrogel fibers as demonstrated by the swelling behavior of the hydrogel and the nano-size effects. The dye was then introduced to the TiO(2) particles for degradation.

Influence of oxyfluorination on activated carbon nanofibers for CO 2 storage

The oxyfluorination effects of activated carbon nanofibers (OFACFs) were investigated for CO2 storage. Electrospun CFs were prepared from a polyacrylonitrile/N,N-dimethylformamide solution via electrospinning and heat treatment. The electrospun CFs were chemically activated in order to generate the pore structure, and then oxyfluorination was used to modify the surface. The samples were labeled CF (electrospun CF), ACF (activated CF), OFACF-1 (O2:F2 = 7:3), OFACF-2 (O2:F2 = 5:5) and OFACF-3 (O2:F2 = 3:7). The functional group of OFACFs was investigated using X-ray photoelectron spectroscopy analysis. The C-F bonds formed on surface of ACFs. The intensities of the C-O peaks increased after oxyfluorination and increased the oxygen content in the reaction gas. The specific surface area, pore volume and pore size of OFACFs were calculated by the Brunauer–Emmett–Teller and density functional theory equation. Through the N2 adsorption isotherm, the specific surface area and pore volume slightly decreased as a result of oxyfluorination treatment. Neverthe less, the CO2 adsorption efficiency of oxyfluorinated ACF improved around 16 wt% due to the semi-ionic interaction effect of surface modificated oxygen functional groups and CO 2 molecules.

The hydrogen storage capacity of metal-containing polyacrylonitrile-based electrospun carbon nanofibers

Polyacrylonitrile-based carbon nanofibers (CNFs) containing Ti and Mn were prepared by electrospinning. The effect of metal content on the hydrogen storage capacity of the nanofibers was evaluated. The nanofibers containing Ti and Mn exhibited maximum hydrogen adsorption capacities of 1.6 and 1.1 wt%, respectively, at 303 K and 9 MPa. Toward the development of an improved hydrogen storage system, the optimum conditions for the production of metalized CNFs were investigated by characterizing the specific surface areas, pore volumes, sizes, and shapes of the fibers. According to the results of Brunauer-EmmettTeller analysis, the activation of the CNFs using potassium hydroxide resulted in a large pore volume and specific surface area in the samples. This is attributable to the optimized pore structure of the metal-containing polyacrylonitrile-based electrospun CNFs, which may provide better sites for hydrogen adsorption than do current adsorbates.

Pore structure control of activated carbon fiber for CO gas sensor electrode

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