• Journal of Korean Society of Water and Wastewater
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• v.27 no.3
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• pp.363-371
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• 2013

In this study, effect of activated carbon size on flux and fouling of membrane was investigated on activated carbon and membrane hybrid system. The activated carbon was prepared with crushing and screening. The activated carbon was named by A100, B100, A200, B200, A325 and B325 due to size of activated carbon. The permeability for A100, B100, A200 and B200 showed no significant difference. However, the permeability for A325 and B325 was decreased rapidly and was lowed due to increase the concentration of NOM. Main resistance for A100, B100, A200 and B200 was identified as irreversible fouling. However main resistance for A325 and B325 was identified as reversible fouling. The smaller activated carbon adsorbs NOM faster than bigger particles, which can show high permeability at early stage of the operation and then showed faster decrease of permeability at end of the operation.

• Carbon letters
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• v.20
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• pp.1-9
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• 2016

Activated carbon was synthesized from coconut shells. The Brunauer, Emmett and Teller surface area of the synthesized activated carbon was found to be 1640 m²/g with a pore volume of 1.032 cm³/g. The average pore diameter of the activated carbon was found to be 2.52 nm. By applying the size-strain plot method to the X-ray diffraction data, the crystallite size and the crystal strain was determined to be 42.46 nm and 0.000489897, respectively, which indicate a perfect crystallite structure. The field emission scanning electron microscopy image showed the presence of well-developed pores on the surface of the activated carbon. The presence of important functional groups was shown by the Fourier transform infrared spectroscopy spectrum. The adsorption of methyl orange onto the activated carbon reached 100% after 12 min. Kinetic analysis indicated that the adsorption of methyl orange solution by the activated carbon followed a pseudo-second-order kinetic mechanism (R² > 0.995). Therefore, the results show that the produced activated carbon can be used as a proper adsorbent for dye containing effluents.

• Textile Coloration and Finishing
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• v.27 no.1
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• pp.50-61
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• 2015

The merits of activated carbon for removal of organic compounds have been well known in the various industrial fields. Fixing methods with activated carbon in the non-woven fabric have the advantages of fast adsorption and ease of handling when compared with bonding and coating methods. In this study, we have examined deodorization of non-woven fabrics fixed with activated carbon. We have been tested the deodorization of various kinds activated carbon and non-woven fabric structures. The effective mixing ratio of activated carbon was 5% on the weight of fabrics, which are closely related to the fabric structure. The activated carbon with higher mesh size show the better deodorization effect.

• Carbon letters
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• v.9 no.2
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• pp.137-144
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• 2008

The commercial activated carbons are typically prepared by activation from coconut shell char or coal char containing lots of inorganic impurities. They also have pore structure and pore size distribution depending on nanostructure of precursor materials. In this study, two types of commercial activated carbons were applied for EDLC electrode by removing impurities with acid treatments, and controlling pore size distribution and contents of functional group with heat treatment. The effect of the surface functional groups on electrochemical performance of the activated carbon electrodes was investigated. The initial gravimetric and volumetric capacitance of coconut based activated carbon electrode which was acid treated by $HNO_3$ and then heat treated at $800^{\circ}C$ were 90 F/g and 42 F/cc respectively showing 94% of charge-discharge efficiency. Such a good electrochemical performance can be possibly applied to the medium capacitance of EDLC.

• Journal of Korean Society of Water and Wastewater
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• v.20 no.5
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• pp.719-726
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• 2006

Adsorption isotherms and kinetics for taste and odor (T&O) compounds and natural organic matters (NOMs) were performed to evaluate the impacts of activated carbon particle size on coagulation and adsorption. Adsorption capacities for iodine, T&O compounds, and NOM of all the activated carbons under #325 mesh were more excellent than those of virgin activated carbons. Small activated carbon particles were more rapidly adsorbed low molecular weight T&O compounds in the water, while those were slowly adsorbed high molecular weight NOM. When the activated carbon and alum were added simultaneously, the adsorption capacity for organics was better than alum was added alone.

• Applied Chemistry for Engineering
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• v.9 no.5
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• pp.615-618
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• 1998

The zeolite crystals were synthesized by hydrogel process into the pore of activated carbon. The effect of activated carbon in the course of the crystallization of zeolite was investigated. The phenomena of impregnation of zeolite crystals into the pore of the activated carbon were also examined. The results show that in case of the addition of 5% of activated carbon to the aluminosilicate gel including the mole composition of zeolite A, zeolite A was purely synthesized without the existence of other type of zeolite. However, in case of the addition of 20% of activated carbon, zeolite X was purely synthesized. In the pore mouth and internal of activated carbon, zeolite crystals having the size under $1{\mu}m$ was observed. From the results of the pore size and particle size distributions, it was confirmed that the synthetic sample was the composite material impregnated by the zeolite crystals into the pore of activated carbon, not the simple mixture of zeolite and activated carbon.

• Carbon letters
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• v.11 no.3
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• pp.201-205
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• 2010

Activated carbons are well known as adsorbents for gases and vapors. Micro porous carbons are used for the sorption/separation of light gases, whereas, carbon with bigger pore size are applied for removal of large molecules. Therefore, the control of pore size of activated carbon plays a vital role for their use in specific applications. In the present work, steam activation parameters have been varied to control pore size of the resulting activated carbon. It was found that flow rate of steam has profound effect on both surface characteristic and surface morphology. The flow rate of steam was optimized to retain monolith structure as well as higher surface area.

• Journal of the Korean Ceramic Society
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• v.36 no.6
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• pp.577-582
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• 1999

Activated carbon fibers were prepared from stabilized PAN fibers by chemical activation using hydroxide. The variations in specific surface area amount of iodine adsorption micro-structure and pore size distribution in the activated carbon fibers after the activation process were discussed. In the chemical activation using potassium hydroxide specific surface area of about 2545m2/g and amount of iodine adsorption of 2049 mg/g were obtained at the condition of KOH/fiber ratio of 1 and 800$^{\circ}C$ Nitrogen adsorption isotherms for PAN based activated carbon fibers showed the type I in the Brunauer-Deming-Deming-Teller classification indicating the micro-pores consisting the activated fibers.

• Carbon letters
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• v.8 no.1
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• pp.30-36
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• 2007

Oxidized PAN (OXI-PAN) fibers were used for the precursors of activated carbon fiber in study. How drying temperature affected the properties of carbon fibers on activating process of carbon fibers was investigated. The specific surface areas of activated carbon fibers have been determined on a series of chemically activated carbons with KOH and NaOH. The experimental data showed variations in specific surface area, iodine and silver adsorptions by the activated carbon fibers. The amount of iodine adsorption increases with increasing specific surface areas in both activation methods. This was because the ionic radius of iodine was smaller than the interior micropore size of activated carbon fibers. Silver adsorbed well in NaOH activated carbon fibers rather than KOH activated carbon fibers in this study.

• Carbon letters
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• v.5 no.2
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• pp.51-54
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• 2004

Isotropic pitch-based carbon fiber was isothermally activated in $CO_2$ atmosphere. Structural parameters of the isotropic carbon fibers and activated carbon fibers (ACFs) were evaluated by X-ray diffraction (XRD). The $d_{002}$ and La of the carbon fibers were measured to be 4.04 ${\AA}$ and 23.6 ${\AA}$ and those of ACFs were 4.29 ${\AA}$ and 22.7 ${\AA}$, respectively, representing less ordered through activation process. The pores in the ACFs were characterized by BET, and they showed super-high specific surface area of maximum value 3,495 $m^2/g$ from average pore size of 8.3 ${\AA}$ at 59% burn-off. It was recognized that 8-9 ${\AA}$ was optimum range of pore size for efficient creation of high specific surface area. The average size of the pores formed at higher temperature ($1100^{\circ}C$) was larger than that of the pores formed at lower temperature ($900^{\circ}C$).