• 한국수처리학회지
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• 제26권6호
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• pp.125-132
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• 2018

We studied a simple approach for synthesis of mesoporous Y(M-Y) from commercial zeolite Y precursors by treating of NaOH with $CH_3(CH_2)_{15}N(Br)(CH_3)_3$ as template. The physicochemical properties of the mesoporous zeolites Y were then analyzed using XRD, nitrogen full-isotherms at 77 K, SEM and TEM. The nitrogen adsorption-desorption analysis showed that surface area and pore diameter of synthesized mesoporous zeolite Y(M-Y) were $1072m^2/g$ and ~3.3 nm, respectively. And M-Y was applied for the removal of $Mn^{2+}$ and $Fe^{2+}$ from aqueous solution. This material, which introduces mesoporosity with zeolite Y character, displayed a superior adsorption capacity than commercial zeolite Y when used as an adsorbent for the removal of $Mn^{2+}$ and $Fe^{2+}$.

• Carbon letters
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• 제3권2호
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• pp.93-98
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• 2002

Short pitch fibers were prepared from petroleum based isotropic precursor pitch by melt-blown technology. The pitch fibers were stabilized in oxidizing condition, followed by steam activations at various conditions. The fiber surface and pore structures of the activated carbon fibers (ACFs) were respectively characterized by using SEM and applying BET theory from nitrogen adsorption at 77 K. The weight loss of the oxidized fiber was proportional to activation temperature and activation time, independently. The adsorption isotherms of the nitrogen on the ACFs were constructed and analyzed to be as Type I consisting of micropores mainly. The specific surface area of the ACFs proportionally increased with the weight loss at a given activation temperature. The specific surface area was ranged 850~1900 $m^2/g$ with pores of narrow distribution in sizes. The average pore size was ranged 5.8~14.1 ${\AA}$ with the larger value from the more severe activation condition.

• Fibers and Polymers
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• 제5권1호
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• pp.52-58
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• 2004

Previous investigation results revealed that after the Low Temperature Plasma (LTP) treatment, the hydrophilicity of wool fiber was improved significantly. Such improvement enhances the wool dyeing and finishing processes which might be due to the changes of the wool surface to a more reactive one. In this paper, wool fibers were treated with LTP with different gases, namely, oxygen, nitrogen and gas mixture (25 % hydrogen/75 % nitrogen). Investigations showed that chemical composition of wool fiber surface varied differently with the different plasma gas used. The surface chemical composition of the different LTP-treated wool fibers was evaluated with different characterization methods, namely FTIR-ATR, XPS and saturated adsorption value. The experimental results were thoroughly discussed.

• Bulletin of the Korean Chemical Society
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• 제31권11호
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• pp.3217-3220
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• 2010

The electronic structures and bonding configuration of histidine on Ge(100) have been investigated with various sample treatments using core-level photoemission spectroscopy (CLPES). Interpretation of the Ge 3d, C 1s, N 1s, and O 1s core level spectra being included in these systems revealed that both the imino nitrogen in the imidazole ring and the carboxyl group in the glycine moiety concurrently participate in the adsorption of histidine on a Ge(100) surface at 380 K. Moreover, we could clearly confirm that the imino nitrogen with a free lone pair in the imidazole group adsorbs on Ge(100) more strongly than the carboxyl group in the glycine moiety by examining systems annealed at various temperatures.

• 한국환경과학회지
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• 제17권5호
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• pp.493-500
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• 2008

This paper describes the adsorption/desorpton efficiency of a modified activated carbon by irradiated microwave to treat toluene. By employing microwave energy, the regeneration time was considerably shortened compared with conventional thermal heating regeneration. New adsorbent called ACB (Activated Carbon-Bentonite) was prepared from powder activated carbon with mixing bentonite as a binder. Specific surface area, average pore size and total pore volume of ACB were calculated from the nitrogen adsorption/desorption isotherm. The surface of ACB was characterized with scanning electron microscope(SEM). The results showed that the specific surface area, total pore volume, average pore size of ABC was not influenced by regenerating cycle with microwave irradiation. Toluene was adsorbed onto ACB which desorbed by MW irradiation. Absorption capacity of ACB was 0.117 $g_{toluene}/g_{ACB}$. Desorption efficiency of toluene increased as higher microwave output was applied.

• 한국세라믹학회지
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• 제36권6호
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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.

• Korean Chemical Engineering Research
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• 제47권4호
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• pp.495-500
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• 2009

고정층 반응기에서 활성탄 흡착제를 사용하여 질소 기류에서 벤젠 증기의 파과곡선을 측정하였다. 흡착실험은 흡착온도 $25{\sim}50^{\circ}C$, 질소 가스의 유량 $80{\sim}150cm^3/min$, 흡착제의 공급량 3~5 g, 그리고 벤젠 증기의 농도는 포화조의 온도를 $25{\sim}40^{\circ}C$로 변화시켜 행하였으며, 파과곡선의 비선형해석으로부터 비활성화 모델의 흡착속도상수와 비활성속도상수를 구하고 비활성화 모델과 흡착 등온 모델과의 상관관계를 고찰하였다.

• Carbon letters
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• 제10권3호
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• pp.221-224
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• 2009

In this work, the $CO_2$ adsorption behaviors of amine functionalized activated carbons (ACs) were investigated. The surface of ACs was modified with urea, melamine, diethylenetriamine (DETA), pentaethylenehexamine (PEHA), polyethylenimine (PEI), and 3-aminopropyl-triethoxysilane (ATPS). The various surface properties of amine functionalized ACs were characterized by Boehm's method, nitrogen full isotherms, XPS, and TGA analyses. The active ingredients impregnated on the ACs show significant influence on the adsorption for $CO_2$ and its volumes adsorbed on amine functionalized ACs are larger than that on the pristine ACs, which is due to the grafted amine groups of the AC surfaces.

• Carbon letters
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• 제6권3호
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• pp.141-147
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• 2005

The carbon sample "O", phosphoric acid-activated carbon "OP", zinc chloride-activated carbon "OZ", and two steam activated carbons "OS" and "OS2" with different burn-off of 25% and 58% respectively, were prepared from olive stones. The textural properties were determined from the results of nitrogen adsorption at 77 K and by analyzing these results through the application of different adsorption models. The chemistry of the carbon surfaces was determined from the base neutralization capacities, acid neutralization capacity and surface pH. The sorption of $Pb^{2+}$ ions on to the carbons prepared was followed under dynamic and equilibrium conditions. The differences between the values of the textural parameters were attributed to the inapplicability of some adsorption models and to the heterogeneity of the microporous carbons. The sorption of $Pb^{2+}$ ions is favored on carbon and activated carbons. However, chemically activated carbons are more effective compared with steam-activated ones. The sorption of $Pb^{2+}$ ions were related to the chemistry of the surface rather than to the textural properties.

• Carbon letters
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• 제8권1호
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• pp.17-24
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• 2007

Microporous carbons with narrow pore size distribution have been successfully synthesized by using hydrolyzed and calcined silica as templates and phenol formaldehyde (pf) resin as carbon precursor. Phenol formaldehyde-silica micro composites were prepared by solution route. Subsesequently, silica templates were removed by HF leaching. Resulting carbons were steam activated. The porous carbons were characterized by nitrogen adsorption-desorption isotherm, SEM, FTIR analysis, iodine adsorption, thermogravimetry analysis, etc. Adsorption isotherms show that the porous carbon prepared from calcined silica as templates are microporous with 88% pores of size <2 nm porosity and are of type I isotherm, while porous carbon prepared by using hydrolyzed silica are microporous with 89% microporosity, shows hysteresis loop at high relative pressure indicating the presence of some mesoporosity in samples. The microporosity in porous carbon materials has a bearing on the nature of silica templates used for pore formation.