• Applied Chemistry for Engineering
• /
• v.34 no.3
• /
• pp.313-317
• /
• 2023

In this study, the physicochemical characterization and adsorption performance of air pollutants (VOCs, SO₂, and CO₂) were evaluated for the recycling of zeolite used in the ion exchange process. The surface characteristics of the zeolite used were confirmed through Scanning Electron Microscopy (SEM) and X-Ray Diffraction (XRD) analysis, and the composition and specific surface area were measured through X-Ray Fluorescence (XRF) and Brunauer-Emmett-Teller (BET). There was no change in the surface properties of the used zeolite, but the content of potassium and calcium increased and the specific surface area decreased. The toluene, sulfur oxides, and carbon dioxide adsorption performance of the used zeolite was evaluated, and it was confirmed that the performance was improved compared to the fresh zeolite. In particular, for toluene and sulfur oxides, the adsorption amount increased by 2.6 times and 2.3 times, respectively, which might be due to the enhancement of the polymerization reaction and the increase of the base point, according to the composition of the used zeolite.

• Journal of the Korean institute of surface engineering
• /
• v.49 no.5
• /
• pp.416-422
• /
• 2016

We have investigated the effects of applied potential, deposition time and electrolyte types on shapes and physical properties of Cu dendrites by potentiostatic electrodeposition. Finer shape of dendrites was observed at less cathodic potential by 100mV than at the limiting current, due to 'effective overpotential'. The shape of copper dendrite is related to the deposition time, too. The dendrite depositing for 10 min showed the finest shape. The finer dendrite has the less apparent density and the larger specific surface area. Dendrite from chloride solution has the lowest density and the largest surface area among three plating solutions, sulfate, chloride and pyrophosphate.

• Transactions of the Korean hydrogen and new energy society
• /
• v.33 no.3
• /
• pp.202-208
• /
• 2022

Pt-Ni nanocatalysts were loaded on carbon black by spontaneous reduction reaction of platinum (II) acetylacetonate and nickel (II) acetylacetonate, and they were characterized by transmission electron microscopy (TEM), thermogravimetric analyzer (TGA), energy dispersive x-ray analyzer (EDS), BET surface area and fuel cell test station. The distribution of the Pt and Ni nanoparticles was observed by TEM, and the loading weight of Pt-Ni nanocatalysts on the carbon black was measured by TGA. The elemental ratio of Pt and Ni was estimated by EDS. It was found that the loading weight of Pt-Ni nanoparticles was 5.54 wt%, and the elemental ratio of Pt and Ni was 0.48:0.35. Specific surface area was measured by BET analysis instrument and I-V characteristics were estimated.

• Journal of Forest and Environmental Science
• /
• v.23 no.1
• /
• pp.51-55
• /
• 2007

The effect of ratio between chemical activating agent and raw material in the preparation of activated carbons from wood has been studied. Pinus koraiensis wood and zinc chloride ($ZnCl_2$) were used for materials in this study. Mixtures of wood and zinc chloride were heated under nitrogen flow in the temperature ranging from room-temperature to $600^{\circ}C$ for 1 hr using thermogravimetric technique. During heat treatment, activated carbons with various pore size and specific surface properties were obtained. The maximum BET surface area and total pore volume were $1468m^2/g$ and 1.74 cc/g, respectively, at the mixture ratio of 1 (wood powder) to 5 ($ZnCl_2$). It can be concluded that the differences in the properties of the activated carbons were related significantly with the ratio of chemical activating regent.

• Applied Chemistry for Engineering
• /
• v.29 no.3
• /
• pp.318-324
• /
• 2018

In this study, PAN (polyacrylonitrile) based activated carbon fibers were prepared by water vapor activation method which is a physical activation method. Activation was performed with temperature and time as parameters. When the activation temperature reached 700, 750 and $800^{\circ}C$, the activation was carried out under the condition of a water vapor flow rate of 200 ml/min. In order to analyze the pore structure of activated carbon fibers, the specific surface area ($S_{BET}$) was measured by the adsorption/desorption isotherm of nitrogen gas and AFM analysis was performed for the surface analysis. Tensile tests were also conducted to investigate the effect of the pore structure on mechanical properties of fibers. As a result, the $S_{BET}$ of fibers after the activation showed a value of $448{\sim}902m^2/g$, the tensile strength decreased 58.16~84.92% and the tensile modulus decreased to 69.81~83.89%.

• Bulletin of the Korean Chemical Society
• /
• v.33 no.5
• /
• pp.1523-1526
• /
• 2012

In this work, we prepared activated multi-walled carbon nanotubes/polyacrylonitrile (A-MWCNTs/C) composites by film casting and activation method. Electrochemical properties of the composites were investigated in terms of serving as MWCNTs-based electrode materials for electric double layer capacitors (EDLCs). As a result, the A-MWCNTs/C composites had much higher BET specific surface area, and pore volume, and lower volume ratio of micropores than those of pristine MWCNTs/PAN ones. Furthermore, some functional groups were added on the surface of the A-MWCNTs/C composites. The specific capacitance of the A-MWCNTs/C composites was more than 4.5 times that of the pristine ones at 0.1 V discharging voltage owing to the changes of the structure and surface characteristics of the MWCNTs by activation process.

• Korean Journal of Materials Research
• /
• v.12 no.8
• /
• pp.641-649
• /
• 2002

The redox properties of a homogeneously-precipitated $TiO_2$ rutile powder with a BET surface area of ~$200 m^2$/g, consisting of an acicular primary particle, were characterized using photocatalytic reaction in aqueous 4-chlorophenol, Cu-EDTA and Pb-EDTA solutions under ultraviolet irradiation, compared to those of commercial P-25 X$200 m_2$ powder with a spherical primary particle as well as home-made anatase $TiO_2$ powder with ~$200 m^2$/g BET surface area. Here, the anatase powder also includes mainly the primary particles very similar to the acicular shapes of the rutile $TiO_2$ powder. The rutile powder showed the fastest decomposition rate and the largest amount in the photoredor, compared with the anatase or P-25 powder, while the anatase powder unexpectedly showed the slowest rate and the smallest amount in the same experiments regardless of almost the same surface area. From results, the excellent photoredox abilities of this rutile powder appears to be due to specific powder preparation method, like a homogeneous precipitation leading to direct crystallization from the solution, regardless of their crystalline structures even when having the similar particle shape and surface area.

• 한국신재생에너지학회:학술대회논문집
• /
• 2010.06a
• /
• pp.132.2-132.2
• /
• 2010

Mesoporous tinoxide ($SnO_2$) as anode materials for Li-ion battery were prepared by hydrothermal method and templating method using SBA-15 as template. And electrochemical properties of $SnO_2$ electrode were investigated with cyclic voltammogram (CV). The morphology and structures of $SnO_2$ were characterized by transmission electron microscopy (TEM) and X-ray diffractometer (XRD), respectively. The specific surface area was defined by $N_2$ adsorption with BET(Brunauer-Emmett-Teller) method. As a result, the surface area of mesoporous $SnO_2$ which was made from templating method is higher than the case of using hydrothermal method. In addition, in anodic performance, mesoporous $SnO_2$ which is prepared by templating method showed higher charge-discharge capasity compared to hydrothermal method and exhibited excellent stability over the entire cycle number. It was indicated that electrochemical performances of mesoporous $SnO_2$mainly affected to the structural features, such as specific surface area and porosity.

• Journal of the Korean Wood Science and Technology
• /
• v.23 no.1
• /
• pp.54-60
• /
• 1995

This paper reports on the changes of equilibrium moisture contents and specific surface areas of Poplar wood(Populus euramericana) for various steam explosion treatments. Equilibrium moisture contents(EMC) and specific surfaces of steam exploded woods were measured under the moisture adsorption course at 25$^{\circ}C$, and compared with those of other materials and wood meals. The EMCs of steam exploded wood meal were 1~5% less in comparison with that of wood meal. In the case of delignified steam exploded wood meal and delignified wood meal, the same tendency was appeared too. But absolute values of EMCs for delignified wood meals were larger than those of the wood meal. For the changes of EMC by the steam exploded conditions, the EMC decreased with the increase of the steam explosion pressure. On the other hand, specific surface areas were calculated from BET plots based on amounts of monomolecular vapor adsorption of various wood meals. Specific surface areas of the wood meal and delignified wood meal were 90~145, 34~90($m^2/g$) respectively, and which were greater in comparison with those of steam exploded wood meals and delignified steam exploded wood meals. From these results, it is considered that the amount of water vapor adsorption was decreased by the increase of the crystallinity, effect of heat treatment, and coating by melted lignin in during the steam explosion.

• Proceedings of the Korean Institute of Electrical and Electronic Material Engineers Conference
• /
• 2004.11a
• /
• pp.683-686
• /
• 2004

In recent years, the supercapacitor and hybrid capacitor have related with substitutional energy source focused of many scientists because of their usage in power sources for electric vehicles, computers and other electric devices. The storage energy of electrical charge is based on electrostatic interactions in the electric double layer at the electrode/electrolyte interface, resulting in high rate capability and long cycle performance compared with batteries based on Faradaic electrode reactions. So we have been considered to carbon nanofibers as the ideal material for supercapacitors due to their high utilization of specific surface area, good conductivity, chemical stability and other advantages. In this work, we aimed to find out that the capacitance have increased because of electrochemical capacitance to provide by carbon nanofibers. Also carbon nanofibers based on chemical method and water treatment have been resulted larger capacitances and also exhibit better electrochemical behaviors about 15% than before of nontreated state. And also optical observations with treated and nontrteated carbon nanofibers discussed by the TEM, SEM, EDX, BET works and specific surface area analyzer. Their results also focused on the surface area of electrode and electrical capacitance was also improved by the effect of surface treatments.