• Analytical Science and Technology
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• v.13 no.5
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• pp.573-583
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• 2000

Activated carbon fibers (ACFs) were prepared from various precursors of plantic, synthetic, and mixed fabrics of viscous rayon and cotton. Their adsorption performances of phenol and methylene blue in aqueous phase were evaluated through their adsorption isotherms, adsorption rates and breakthrough curves. The two adsorbates showed type I adsorption isotherm on ACFs. Adsorption rates to ACFs were 100 fold faster than to GAC. The effective diffusion coefficients of the adsorbates in ACFs were twenty fold greater than in GAC. The ACFs removed completely ten organic pollutants from a prepared water specimens through the 2nd column of a natural filtration method where 50 L of the water samples were treated.

• Analytical Science and Technology
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• v.13 no.1
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• pp.89-95
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• 2000

Three grades of activated carbon fibers (ACFs) were prepared from various precursors of plantic, synthetic, and mixed fabrics of viscose rayon and cotton. The ACFs an exhibited type I isotherms on the adsorption of nitrogen or argon. Micropore analysis revealed that the ACFs have uniform micropore size distribution in which their peak diameters were in the range of $5.6{\pm}0.3{\AA}$. The BET surface area of ACFs up to $1600m^2g^{-1}$ was proportional to the adsorption capacity of iodine. The BET values of the ACFs prepared were proportional to the burn-off degree of the products.

• Applied Chemistry for Engineering
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• v.26 no.5
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• pp.598-603
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• 2015

In this study, electrochemical properties of pitch-based activated carbon fibers (ACFs) were investigated by different heat-treatment temperature of the pitch-based ACFs in order to improve the specific capacitance of electric double-layer capacitor (EDLC). The ACFs were prepared by different heat-treatment temperatures of 1050 and $1450^{\circ}C$, after activation with 4 M KOH at $800^{\circ}C$ using stabilized pitch fiber. The specific surface area of prepared ACFs increased from $828m^2/g$ to $987m^2/g$, also the micropore and mesopore volumes of prepared ACFs were increased. These results because pore was produced by desorbing oxygen and hydrogen elements within the ACFs, and pore size was increased by contraction ACFs by heat-treatment process. Because of the porous properties, the specific capacitance was increased from 73 F/g to 119 F/g using cyclic voltammetry with 1 M $H_2SO_4$ at scan rates of 5 mV/s.

• Korean Chemical Engineering Research
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• v.57 no.3
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• pp.425-431
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• 2019

As rechargeable metal-air batteries will be ideal energy storage devices in the future, an active cathode electrocatalyst is required with bi-functionality on both oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) during discharge and charge, respectively. Here, a class of perovskite cathode catalyst with a micro-tubular structure has been developed by controlling bi-functionality from different Ru and Ni dopant ratios. A micro-tubular structure is achieved by the activated carbon fiber (ACF) templating method, which provides uniform size and shape. At the perovskite formula of $LaCrO_3$, the dual dopant system is successfully synthesized with a perfect incorporation into the single perovskite structure. The chemical oxidation states for each Ni and Ru also confirm the partial substitution to B-site of Cr without any changes in the major perovskite structure. From the electrochemical measurements, the micro-tubular feature reveals much more efficient catalytic activity on ORR and OER, comparing to the grain catalyst with same perovskite composition. By changing the Ru and Ni ratio, the $LaCr_{0.8}Ru_{0.1}Ni_{0.1}O_3$ micro-tubular catalyst exhibits great bi-functionality, especially on ORR, with low metal loading, which is comparable to the commercial catalyst of Pt and Ir. This advanced catalytic property on the micro-tubular structure and Ru/Ni synergy effect at the perovskite material may provide a new direction for the next-generation cathode catalyst in metal-air battery system.