• Journal of Korean Society of Environmental Engineers
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• v.22 no.12
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• pp.2141-2148
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• 2000

This study is to investigate changes of pore structure with different burn-off degree of steam activated carbons manufactured from domestic anthracite. The activated carbons were characterized by adsorption of nitrogen at 77 K. Steam activation substantially enhanced the porosity of the activated carbons. Burn-off increased linearly according to increasing activation time, and total pore volume and BET surface area increased with burn-off. Activation at $800^{\circ}C$ increased more micropore volume than that at $950^{\circ}C$. Activated carbons manufactured at high temperature had less microporosity than that at lower temperature, but had more developed macroporosity. The steam activation produced an enlargement of pore below $100{\AA}$ diameter in the activated carbons. Furthermore, the porosity in the $6{\sim}40{\AA}$ pore diameters range increased considerably with the degree of burn-off.

• Applied Chemistry for Engineering
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• v.2 no.2
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• pp.147-154
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• 1991

Thermogravimetric measurements have been carried out to investigate the stabilization and carbonization of copolymer of acrylonitrile(95 wt %) and methyl acrylate(5 wt %) at various heating rates. The cyclization and dehydrogenation during the stabilization were important factors to determine pore development in the carbonization process. The pore and the specific surface area during the carbonization began to develope at the temperature higher than $400^{\circ}C$.

• Journal of Korean Society of Environmental Engineers
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• v.22 no.7
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• pp.1319-1330
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• 2000

Activated carbons prepared by chemical activation of organic waste sludges with $ZnCl_2$ and $K_2S$ have been studied in terms of their pore development and adsorptivity. Pore development of the carbons prepared from organic waste sludges was characterized by the nitrogen adsorption at 77K. The $ZnCl_2$-activated carbon produced by chemical activation with zinc chloride exhibited type I isotherm characteristics according to the BDDT classification, suggesting the presence of micropores formed by activation process. The isotherms of the commercial powdered activated carbon and $K_2S$-activated carbon reveal a hysteresis similar to that of type IV in BDDT classification, indicating the formation of mesopores. This result implies that the major pores of $K_2S$-activated carbon are composed of meso and micropores, and a macropores are minor. The adsorptive capacities of metal on the $K_2S$-activated carbon prepared from organic waste sludges were found to be superior to those on a commercial granular activated carbon. The Langmuir and Freundlich isotherms yield a fairly good fit to the adsorption data, indicating a monolayer adsorption of metals onto $K_2S$-activated carbon. The adsorptive capacity of the $K_2S$-activated carbon was superior to $ZnCl_2$-activated carbon for $PO_4$-P, and vice versa for $NO_3$-N. From the results of the studies reported here, it can be concluded that activated carbons with adsorptivity superior to commercial granular activated carbons can be produced from organic waste sludge using a two-step carbonization/activation procedure with zinc chloride or potassium sulfide as the activating agents.

• Applied Chemistry for Engineering
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• v.5 no.3
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• pp.385-394
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• 1994

Numerical solutions were obtained to the model equations for various of the parameters characterizing the pore structure, effective internal diffusion, and the chemical reaction constant. The conversion was decreased with the cause of pore closure at the surface of reacting particles, reduction of porosity, surface area of reaction and effective diffusion coefficient in the solid with the progress of reaction. Total conversion was strongly dependent on the local conversion at surface. According to the decreasing of impregnated concentration of the copper oxide and the increase of the flue gases concentration, total conversion was increased. The conversion was affected by gas flow rate and pore size distribution in the reacting solid.

• Journal of the Korean Ceramic Society
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• v.38 no.1
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• pp.1-8
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• 2001

선택적 가스분리를 위한 분자체탄소(Molecular Sieve Carbon: MSC)로서의 활용을 위해 제조된 활성탄소섬유의 흡착능과 분자체 특성이 다양한 분자크기를 갖는 가스 흡착실험을 통해 조사되었다. 각 활성화 조건별 세공크기분포와 세공발달 전개과정을 유추함으로서, 세공크기분포의 조절이 가능하게 되었으며 활성탄소섬유의 분자체 탄소로서 활용을 용이하게 할 수 있었다. 800, 85$0^{\circ}C$의 온도로 수증기에 의해 활성화한 활성탄소섬유의 경우 burn-off가 각각 50, 40% 정도를 가진 활성탄소섬유가 비교적 작은 분자크기(0.3~0.4nm)의 흡착질에 대한 분자체 특성을 나타냈다. 또한, 다양한 분자크기의 흡착질을 포함하는 혼합가스의 유속과 흡착온도의 조절로서 원하는 흡착질의 선택적 분리를 위해 활성탄소섬유가 갖는 분자체 특성 향상을 보였다.

• Korean Chemical Engineering Research
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• v.49 no.5
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• pp.521-529
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• 2011

Methanol-to-olefin (MTO) reaction was studied over MWW zeolite with independently developed two pores (circular and straight) and MFI zeolite with intercrossed sinusoidal and straight pores in order to investigate the effect of pore structure on their catalytic behavior. MWW and MFI zeolites with similar acidity exhibited commonly high conversion and slow deactivation in the MTO reaction, but their product selectivities were considerably different: linear hydrocarbons of $C_3-C_9$ were mainly produced on MWW, while the yield of $C_2{^=}$ and aromatics were high on MFI. Polyaroamatic hydrocarbons (PAHs) were accumulated on MWW, but a small amount of benzene and aromatics on MFI. The impregnation of phosphorous on MWW caused significant decreases in the catalytic activity and toluene adsorption, but the decreases were relatively small on MFI. Although the straight pores of MWW were inactive in the MTO reaction due to the accumulation of PAHs, its circular pores which suppressed the formation of PAHs sustained catalytic activity for the production of linear hydrocarbons. Therefore, the impregnation of phosphorous on the circular pores of MWW caused a significant decrease in catalytic activity. The phosphorous impregnation on the cross sections of MFI altered the product selectivity due to the neutralization of strong acid sites, but catalytic deactivation was negligible. The difference of MWW and MFI zeolites in the MTO reaction was explained by their difference in pore structure.

• Journal of Korean Society of Environmental Engineers
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• v.29 no.5
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• pp.515-520
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• 2007

Recently, the treat of sludge is usually progressed by ocean disposal. But it will be totally banned by content of its heavy metal according to London Dumping Convention, gradually. The stable way of treat of sewage sludge should be examined urgently. To solve the problem, recently, there are efficient and environment-oriented method. One of them is to produce absorbent through the activation. This study produces absorbent through steam activation. As basic experiment, optimum activation condition for preparation of good absorbent is researched through study of the fellowing variables : steam flow rate, activated temperature, activation time. As the result of this with standard on iodine adsorptivity, it is chosen, that steam flow rate "30 mL/hr", activation temperature $"500^{\circ}C"$, activation time "60 minutes". At the time, iodine adsorptivity and yield shown that 228.4 mg/g, 77.23%. And also, by using nitrogen adsorption, SEM and EDS are confirmed that pore development, specific surface area, mean pore size, chemical component and content. Pore developed by steam activation is also confirmed that it is micropore.

• Proceedings of the Korean Environmental Sciences Society Conference
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• 2006.11a
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• pp.525-528
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• 2006

감귤박을 원료로 하여 활성화제인 KOH를 사용한 약품활성화공정을 수행하여 감귤박-활성탄을 제조하고, 흡착능 및 세공분포 등을 분석한 결과 요오드 흡착능이 KS 규격 중 1급(활성탄 1,100 mg/g 이상)보다 높은 값으로 나타나 양질의 활성탄을 제조할 수 있음을 보였다. 또한 약품활성화법을 사용함으로써 탄화공정에서 제조된 탄화시료보다 월등히 높은 비표면적과 미세세공의 발달이 이루어져 KOH를 이용한 약품활성화법이 활성탄의 제조공정으로서 활용할 수 있음을 확인할 수 있었다.

• Clean Technology
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• v.15 no.4
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• pp.265-272
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• 2009

In this study the experiments on the static adsorption of benzene were carried out using activated carbon made from sewage sludge. The experiment was performed at 303.15 K, 318.15 K and 333.15 K under the pressure up to 7.999kPa. Isothermal adsorption curves were obtained using Langmuir isotherm, Freundlich isotherm and Toth isotherm for comparison. Based on fitting the adsorption quantity of Benzene (q), the isothermal adsorption curves obtained from Langmuir isotherm and Toth isotherm showed the higher accuracy. Although there was little difference in accuracy between result from Langmuir isotherm and that from Toth isotherm, the adsorption quantity of Benzene (q) was expressed in terms of Langmuir isotherm because less parameters were required for Langmuir isotherm than for Toth isotherm. Moreover SEM images of the activated carbon from sewage sludge and the commercial activated carbon were taken to observe the pore size development. The results showed that the perforation development of the commercial activated carbon (DARCO A.C., SPG-100 A.C.) was better than that of activated carbon from sewage sludge. Adsorption quantity of benzene on commercial activated carbon was confirmed to be higher than that on activated carbon from sewage sludge. However the maximum adsorption quantity of benzene on activated carbon from sewage sludge was close to that on SGP-100 A.C. at 303.15K. Therefore, we may conclude that it is feasible to commercialize the process to manufacturing activated carbon from sewage sludge.

• Applied Chemistry for Engineering
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• v.4 no.1
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• pp.113-124
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• 1993

Thermogravimetric analysis of copolymer of acrylonitrile(95%) and methyl acrylate(5%) have been carried out to investigate the activation under $H_2O$(30%) -$N_2$atmosphere at various heating rates. The kinetic equation [$f=1-\exp(-a{\Delta}T)^b$] which was derived on the basis of the nonisothermal activation process of carbon fiber in the $H_2O$(30%)-$N_2$system showed good agreement with experimetal results. The pore volume upon conversion was in good agreement with the model of theoretical pore volume. The pore structures of the activated carbon fiber were influenced by the heating rate, activation temperature and internal-external conversions.