• Carbon letters
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• 제15권4호
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• pp.295-298
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• 2014

In this work, nanoporous carbons (NPCs) were prepared by the self-assembly of polymeric carbon precursors and block copolymer template in the presence of tetraethyl orthosilicate and colloidal silica. The NPCs' pore structures and total pore volumes were analyzed by reference to $N_2$/77 K adsorption isotherms. The porosity and elemental mercury adsorption of NPCs were increased by activation with carbon dioxide. It could be resulted that elemental mercury adsorption ability of NPCs depended on their specific surface area and micropore fraction.

• 한국지하수토양환경학회:학술대회논문집
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• 한국지하수토양환경학회 2003년도 총회 및 춘계학술발표회
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• pp.418-421
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• 2003

Surfactant enhanced in-situ soil flushing was peformed to remediate the soil and groundwater at an oil contaminated site, and the effluent solution was treated by the chemical treatment process including DAF(Dissolved Air Flotation). A section from the contaminated site(4.5m$\times$4.5m$\times$6.0m) was selected for the research, which was composed of heterogeneous sandy and silt-sandy soils with average Hydraulic conductivity of 2.0$\times$10$^{-4}$ cm/sec. Two percent of sorbitan monooleate(POE 20) and 0.07% of iso-prophyl alcohol were mixed for the surfactant solution and 3 pore volumes of surfactant solution were injected to remove oil from the contaminant section. Four injection wells and two extraction wells were built in the section to flush surfactant solution. Water samples taken from extraction wells and the storage tank were analyzed by GC(gas-chromatography) for TPH concentration with different time. Five pore volumes of solution were extracted while TPH concentration in soil and groundwater at the section were below the Waste Water Discharge Limit(WWDL). Total 18.5kg of oil (TPH) was removed from the section. The concentration of heavy metals in the effluent solution also increased with the increase of TPH concentration, suggesting that the surfactant enhanced in-situ flushing be available to remove not only oil but heavy metals from contaminated sites. Results suggest that in-situ soil flushing and chemical treatment process including DAF could be a successful process to remediate contaminated sites distributed in Korea.

• 한국세라믹학회지
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• 제14권4호
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• pp.236-241
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• 1977

Three kinds of specimen, consisting of the graded pyrophyllite particles alone, a substituent of 8 percent fire clay for the finer portion ($F_2$) of it, and 0.8 percent inorganic binder-added composite were prepared under the following conditions respectively; moisture content=4.5~5.0%, forming pressure=250kg/$\textrm{cm}^2$ and sintering temperature=1, 000~1, 30$0^{\circ}C$. The various properties such as modulus of rupture, apparent porosity, bulk specific gravity, pore size and pore distributiion were measured in order to collaborate with sintering phenomena. The results obtained are as follows: (1) Apparent porosity isgradually decreased with rising the sintering temperature to 1, 25$0^{\circ}C$. (2) The binder-added specimen showed the lowest value in porosity. (3) The optimum sintering temperature of specimens was considered to be 1, 25$0^{\circ}C$. (4) The wider differences between pore volumes of specimens could be obtained by method of mercurypenetration porosimeter than by the conventional method for porosity.

• Bulletin of the Korean Chemical Society
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• 제33권11호
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• pp.3749-3754
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• 2012

Nanoporous carbons with a high specific surface area were prepared directly from thermoplastic acrylic resin as carbon precursor and MgO powder as template by carbonization over the temperature range, $500-1000^{\circ}C$. The effect of the carbonization temperature on the pore structure and $CO_2$ adsorption capacity of the obtained porous carbon was examined. The textural properties and morphology of the porous carbon materials were analyzed by $N_2/-196^{\circ}C$ and $CO_2/0^{\circ}C$ adsorption/desorption isotherms, SEM and TEM. The $CO_2$ adsorption capacity of the prepared porous carbon was measured at $25^{\circ}C$ and 1 bar and 30 bar. The specific surface area increased from 237 to $1251m^2/g$, and the total pore volumes increased from 0.242 to $0.763cm^3/g$ with increasing the carbonization temperature. The carbonization temperature acts mainly by generating large narrow micropores and mesopores with an average pore size dependent on the level of carbonization of the MgO-templated nanoporous carbons. The results showed that the MgO-templated nanoporous carbons at $900^{\circ}C$ exhibited the best $CO_2$ adsorption value of 194 mg/g at 1 bar.

• Steel and Composite Structures
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• 제50권1호
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• pp.15-24
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• 2024

This research presents dynamical reaction investigation of pore-dependent and nano-thickness beams having functional gradation (FG) constituents exposed to a movable particle. The nano-thickness beam formulation has been appointed with the benefits of refined high orders beam paradigm and nonlocal strain gradient theory (NSGT) comprising two scale moduli entitled nonlocality and strains gradient modulus. The graded pore-dependent constituents have been designed through pore factor based power-law relations comprising pore volumes pursuant to even or uneven pore scattering. Therewith, variable scale modulus has been thought-out until process a more accurate designing of scale effects on graded nano-thickness beams. The motion equations have been appointed to be solved via Ritz method with the benefits of Chebyshev polynomials in cosine form. Also, Laplace transform techniques help Ritz-Chebyshev method to obtain the dynamical response in time domain. All factors such as particle speed, pores and variable scale modulus affect the dynamical response.

• 한국토양비료학회지
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• 제13권2호
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• pp.57-63
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• 1980

시판(市販)되고 있는 광재규산질비료를 사별(篩別)하여 10목이하(目以下) 20-35목(目) 및 100목이상(目以上)의 3개입자군(個粒子群)으로 분리(分離)하고 그들을 토양(土壤)에 처리했을 때 토양용액(土壤溶液)의 규산함량변화(珪酸含量變化), 토양(土壤)에서의 이동성(移動性) 등을 조사(調査)한바 다음과 같은 결과(結果)를 얻었다. 1. 규산질비료(珪酸質肥料) 20mg을 증류수50ml로 침출(浸出) 했을 때 용액(溶液)의 규산농도(珪酸濃度)는 10목이하(目以下), 20-35목(目), 100목이상(目以上) 입자(粒子)에 처하여 각각 0.3, 1.0, 3.2ppm 이었으며 1N-Na-acetate용액(溶液)으로 침출(浸出)했을 때의 농도(濃度)는 각각 24.5, 126.2, 225.5ppm 이었다. 2. 규산질비료(珪酸質肥料) 20mg을 첨가(添加)한 상양(上壤)20g을 증류수 50ml로 침출(浸出)했을 때 10목이하(目以下), 20-35목(目), 100목이상(目以上) 입자(粒子)의 규산질비료(珪酸質肥料)를 처리한 토양용액중(土壤溶液中)의 규산농도(珪酸濃度)는 규산(珪酸)을 첨가(添加)하지 않았을 때 보다 각각 0.25, 0.97, 3.28ppm 증가하였다. 3. 토양용액(土壤溶液)의 pH는 규산질비료(珪酸質肥料)의 첨가(添加) 여부와 관계(關係)없이 담수일수(湛水日數)와 함께 2~4주(週)까지는 상승(上昇)하고 그 후(後) 6~10주(週)까지 하강(下降)하였다. 이때 수용액중(水溶液中)의 규산농도(珪酸濃度)는 pH와 역상관(逆相關)을 냐타내었으나 담수(湛水) 6~10주이후(週以後)에는 pH와 관계(關係)없이 수용액중(水溶液中)의 규산농도(珪酸濃度)는 증가하였다. 4. 토양투하수(土壤透下水)의 분액별(分液別) 규산농도(珪酸濃度)는 규산질비료(珪酸質肥料)를 첨가(添加)하지 않았을 경우 투과수(透過水)의 양(量)이 0.88 pore volume에 달(達)했을 때 최고치(最高値)를 나타내었으며 20-35목(目), 100목이상(目以上)의 규산질비료(珪酸質肥料)를 첨가(添加)하였을 때에는 각 각 0.94, 1.03pore volume에서 최고농도(最高濃度)를 나타내었다. 5. 1.5pore volume의 증류수를 투하(透下)시킨 후(後) 토양(土壤) column의 부위별(部位別) 규산함량(珪酸含量)을 분석(分析)한 바 수용성(水溶性) 규산(珪酸) 함량(含量)은 6~9cm이하에서는 깊이에 관계없이 일정(一定)하나 그 위 부위(部位)에서는 위로 갈수록 낮은 함량(含量)을 나타내었다. 그러나 1N-Na-acetate 가용규산(可溶珪酸)은 이동(移動)되지 않고 규산(珪酸) 처리부위에 집적(集積)되어 있었다.

• 한국세라믹학회지
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• 제25권3호
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• pp.217-224
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• 1988

Alkoxide 법으로 합성한 알루미나의 동공 구조를 BET 법으로 구한 흡 탈착 등온선의 hysteresis loop와 동공 분포로부터 고찰하였다. 알루미나는 aluminum isopropoxide를 화학량의 물로 가수분해하여 제조하였고, 가수분해 온도는 3$^{\circ}C$와 8$0^{\circ}C$에서 수행하였다. 이어 20$0^{\circ}C$부터 50$0^{\circ}C$까지 단계적으로 승온시키며 일정시간 열처리하였다. 3$^{\circ}C$ 가수분해 시료의 동공부피는 열처리 온도에 비례하여 증가하였으며, 동공크기는 쌍입분포(twin peaked pore size distribution)형으로 나타났다. 그러나 8$0^{\circ}C$ 가수분해 시료는 열처리에 의하여 동공부피가 감소하고, 동공크기는 단입분포(single peaked pore size distribution)로 나타났다. 이러한 관찰 결과로부터 전자의 동공형태는 slit형, 후자는 ink-bottle형을 하고 있는 것으로 추정되었다. 이와 같이 가수분해 온도는 동공 형태를 결정하는 중요한 인자일 뿐만 아니라, 층상 알루미나의 구조수 일탈 거동을 결정하는데 중요하다. 열처리 효과는 단지 최종 제품의 동공 분포를 결정하는데 영향을 주고 있는 것으로 해석되었다.

• 분석과학
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• 제28권1호
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• pp.40-46
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• 2015

하이드로촤는 음식물폐기물과 같이 수분을 함유하고 있는 바이오매스의의 열수가압탄화반응을 통해 얻어질 수 있다. 열수가압탄화반응의 고체 생성물인 하이드로촤는 다양한 오염물질의 흡착제로서 훌륭한 잠재가능성을 가지고 있다. 흡착제의 표면적과 기공의 부피는 흡착능을 결정하는 매우 중요한 요소 중 하나로 알려져 있다. 이를 측정하기 위해서 고가의 장비 구비 및 숙련된 전문가를 필요로 하며 장비를 갖추지 못한 경우 샘플 측정료 등의 부담이 따르기 때문에 어느 곳에서나 사용하기가 힘들다. 본 연구에서는 요오드와 메틸렌블루 흡착을 통한 적정법을 이용하여 표면적 및 기공 부피를 측정하였으며 BET 분석 결과와 관련성을 평가하였다. 적정법을 통하여 계산된 표면적 및 기공 부피와 실제 수치는 정확하게 일치하지는 않지만 그 경향은 유사하다. 그 결과로 흡착제로서의 활용을 위한 하이드로촤의 최적 조건은 반응온도 $230^{\circ}C$, 반응시간 4 시간으로 결정하였다. 표면적 및 기공 부피의 계산은 아이오딘과 메틸렌블루의 흡착값의 조합을 이용하여 가능하고, 이 적정법을 이용하는 표면적 측정방법은 간단하고 빠르게 최적조건을 결정할 수 있다.

• 한국토양비료학회지
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• 제43권3호
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• pp.275-282
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• 2010

The laboratory column experiments were used to transport of metal elements by infiltration-related dispersion and/or diffusion in mine tailing of the Guryong gold mine. The mine tailing shows the neutral pH (for a pore water) and contains quartz, chlorite, pyrite and calcite. Both a non-reactive solute ($Cl^-$ of 100 mg $L^{-1}$) and a reactive solute (1N HCl), were injected continuously through columns. The breakthrough curve in the non-reactive experiment reached at a maximum under 1.5 pore volumes (PV). The longitudinal dispersion (0.607 cm) and hydrodynamic dispersion coefficient ($1.96{\times}10^{-7}cm^{2}sec^{-1}$) were calculated by the slope. In the reactive experiment, the plateau curve was appeared in the pH values of 5.3, 4.5 and 1.7. The releases of metal elements such as Fe, Mn, Al, Cu, Zn, Pb, and Cd were observed to be related to the pH buffering. High concentrations of Mn, Cd and Zn were observed at the first pH plateau (4 PV and pH 5.3), whereas Fe, Cu, Al and Pb were released as the pH decreased to 4.0 or less. The resulting order of metals mobility, based on the effluent water, is Mn=Cd>Zn>Cu>Fe>Al>Pb.

• 환경위생공학
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• 제20권4호통권58호
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• pp.45-50
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• 2005

Titania gel formations were prepared by sol-gel method using titanium(IV) chloride $(TiCl_4)$, and its characteristics were analyzed by varying the $epoxide/TiCl_4$ ratio and the amount of water In the end, titania $(TiO_2)$ aerogel were prepared using supercritical drying process. VOCs such as benzene, toluene, and m-xylene (BTX) were oxidized using prepared titania aerogel and commercially available $TiO_2$, and its performance was compared. The surface area, pore volume, and average pore diameter of 1,2-epoxybutane are significantly smaller than the propylene oxide. And the titania aerogels with 6 moi of epoxides have high surface areas, pore volumes, and average pore diameters. As a result of photo-oxidation, conversion of benzene was reached about $70\%$, and other reactants were reached about $60\%$ similarly. The conversion of BTX was increased as inlet concentration decreased. The reactivity of titania calcined at $600^{\circ}C$ was greater than $400^{\circ}C$ and $800^{\circ}C$. Water is required as a reactants for the oxidation of VOCs, and the continuous consumption of hydroxyl radicals required replenishments to maintain catalyst activity. The activity ratio increased with increasing reaction time when enough amount of water was present in the reactor.