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Byung-Joo Kim

Publications and source records attributed to Byung-Joo Kim.

7 recordsLinked to original sources

A study on pore-opening behaviors of graphite nanofibers by a chemical activation process.

In this work, porous graphite nanofibers (GNFs) were prepared by a KOH activation method in order to manufacture porous carbon nanofibers. The process was conducted in the activation temperature range of 900-1100 degrees C, and the KOH:GNFs ratio was fixed at 3.5:1. The textural properties of the porous carbons were analyzed using N2 adsorption isotherms at 77 K. The BET, D-R, and BJH equations were used to observe the specific surface areas and the micro- and mesopore structures, respectively. From the results, it was found that the textural properties, including the specific surface area and the pore volumes, were proportionally enhanced with increasing activation temperatures. However, the activation mechanisms showed quite significant differences between the samples activated at low and high temperatures.

Journal Article↗

Adsorption behavior of propylamine on activated carbon fiber surfaces as induced by oxygen functional complexes.

In this study, the surfaces of activated carbon fibers (ACFs) were modified by nitric acid to introduce surface oxygen complexes and to observe the influence of those complexes on the propylamine adsorption of the ACFs. It was found that the oxygen complexes including carboxylic and phenolic groups were predominantly increased, resulting in the increase of total surface acidity. However, the specific surface areas and the total pore volumes of the modified ACFs were decreased by 5-8% due to the increased blocking (or demolition) of micropores in the presence of newly introduced complexes. Despite the decrease of textural properties, it was found that the amount of propylamine adsorbed by the modified ACFs was increased by approximately 17%. From the XPS results, it was observed that propylamine reacted with strong or weak acidic groups, such as COOH or OH, on the ACF surfaces, resulting in the formation of pyrrolic-, pyridonic-, or pyridine-like structures.

Adsorption↗

Oxidation behaviors of metallic copper particles in NO reduction mechanism of copper/activated carbons.

The reduction of nitric oxide (NO) over Cu/ACFs, prepared by copper electroplating, has been studied. It is found that copper content on the ACFs increases with increasing plating time (up to 45 wt%), while the textural properties including specific surface areas and total pore volumes decrease. As an experimental result, the NO reduction efficiency is increased in all of the Cu/ACFs, and it is confirmed that NO is converted into nitrogen and oxygen on the Cu/ACF surfaces (at 500 degrees C). Especially, the Cu metals on the ACF surfaces scavenge oxygen by oxidizing themselves into Cu2O and finally CuO as a reductant. It is indicated that copper metals on the Cu/ACFs play a major role in the NO removal in this system.

Carbon↗

NOX4 as an oxygen sensor to regulate TASK-1 activity.

When oxygen sensing cells are excited by hypoxia, background K+ currents are inhibited. TASK-1, which is commonly expressed in oxygen sensing cells and makes a background K+ current, is inactivated by hypoxia. Thus TASK-1 is a candidate molecule responsible for hypoxic excitation. However, TASK-1 per se cannot sense oxygen and may require a regulatory protein that can. In the present study, we propose that the NADPH oxidase NOX4 functions as an oxygen-sensing partner and that it modulates the oxygen sensitivity of TASK-1. Confocal imaging revealed the co-localization of TASK-1 and NOX4 in the plasma membrane. In HEK293 cells expressing NOX4 endogenously, the activity of expressed TASK-1 was moderately inhibited by hypoxia, and this oxygen response was significantly augmented by NOX4. Moreover, the oxygen sensitivity of TASK-1 was abolished by NOX4 siRNA and NADPH oxidase inhibitors. These results suggest a novel function for NOX4 in the oxygen-dependent regulation of TASK-1 activity.

Biosensing Techniques↗

Ammonia removal of activated carbon fibers produced by oxyfluorination.

In this study, activated carbon fibers (ACFs) were produced by an oxyfluorination treatment to enhance the capacity of ammonia gas removal. The introduction of polar groups, such as CF, CO, and COOH, on the ACFs was confirmed by a XPS analysis, and N2/77 K adsorption isotherm characteristics including specific surface area and total and micropore volumes were studied by the BET and t-plot methods. The ammonia-removal efficiency was confirmed by a gas-detecting tube technique. As a result, the specific surface area and micropore volume of ACFs were slightly destroyed as the surface treatment time was increased. However, the oxyfluorinated ACFs led to an increase of fluorine and oxygen-containing polar functional groups in ACF surfaces, resulting in an increase in the ammonia-removal efficiency of the ACFs produced.

Adsorption↗

A study on NO removal of activated carbon fibers with deposited silver nanoparticles.

In this study, activated carbon fibers (ACFs), onto which silver (Ag) nanoparticles have been introduced by an electroplating technique, were used to remove NO. Surface properties of the ACFs were determined by X-ray diffraction and scanning electron microscopy. N2 adsorption isotherms at 77 K were investigated by BET and t-plot methods to characterize the specific surface areas and pore volumes, and NO removal efficiency was confirmed by a gas chromatographic technique. As for the experimental results, Ag content on the ACFs increased with plating time. However, adsorption properties such as the BET specific surface area and the total pore volume were somewhat decreased in the presence of Ag nanoparticles. NO removal efficiency of all Ag-ACFs was higher than that of untreated ACFs and increased with Ag content. However, a decrease in the extent of NO removal was shown in the excessively plated ACFs, which might be associated with the blocking of the micropores in the carbon; therefore, an optimal Ag content needs to exist in the presence of initially well-developed micropores to lead to an increase in the efficient NO removal ability of the ACF.

Carbon↗

Influence of oxygen plasma treatment on hydrogen chloride removal of activated carbon fibers.

The oxygen plasma treatment of activated carbon fibers (ACFs) was carried out to introduce oxygen-containing groups onto carbon surfaces. Surface properties of the ACFs were determined by X-ray photoelectron spectroscopy (XPS) and scanning electron microscopy (SEM). N2/77 K adsorption isotherms were investigated by BET and D-R plot methods to characterize specific surface area, pore volume, and pore size distribution. The efficiency of hydrochloride removal was confirmed by two kinds of methods; one is detecting tubes (range: 1-40 ppm), and the other is a gas chromatography technique. As experimental results, the hydrochloride removal efficiency of the ACFs was increased with the number of plasma treatment times up to around 300%, resulting from newly formed oxygen-containing functional groups (especially phenolic and carboxylic) on carbon surfaces, in the decreased specific surface areas or pore volumes. These results indicate that the plasma treatment leads to the increase of hydrochloride removal due to the improvement of surface functional groups containing oxygen on the carbon surfaces.

Journal Article↗