• Korean Chemical Engineering Research
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• 제54권6호
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• pp.838-846
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• 2016

산업체에서 많이 사용되는 연소공정은 배가스 성분의 회수나 제거를 필요로 한다. 최근에는 배가스로부터 이산화탄소를 회수하기 위해 제올라이트 13X를 사용하는 MBA(이동상흡착) 공정이 개발되었다. 본 연구에서는 제올라이트 13X에 대한 이산화탄소, 질소, 이산화황 및 수증기의 흡착 실험을 수행하여 흡착평형 및 고체입자 안으로의 흡착속도를 조사하였다. 여러 실험온도에서의 흡착데이터를 Langmuir, Toth, Freundlich 등온흡착식에 적용하여 각 흡착등온식의 파라미터를 구했고, 이론식에 의한 예측값과 실험데이터가 잘 일치함을 확인하였다. 이산화황과 수증기가 불순물로 존재할 경우에 주성분인 이산화탄소의 흡착량을 측정하였다. 이성분 흡착 데이터는 순수 성분에 대해 얻어진 파라미터를 extended Langmuir 등온흡착식에 적용하여 예측한 결과와 잘 일치하였다. 다만, $H_2O$ 불순물이 대략 ${\sim}10^{-5}H_2O\;mol/g$ zeolite 13X 이하 존재할 때에는 $CO_2$ 흡착량이 순수 $CO_2$의 흡착보다 오히려 소량 증가하는 현상이 관찰되었다. 실험으로 측정한 흡착속도를 구형 입자 확산모델에 적용하여 이산화탄소, 이산화황, 질소, 수분의 확산계수와 활성화에너지를 구했다. 미량의 불순물이 흡착되어있을 때는 이산화탄소나 이산화황의 확산계수가 줄어들었다. 본 연구에서 얻어진 파라미터 값들은 실제 흡착공정의 설계에 유용할 것이다.

• 한국신재생에너지학회:학술대회논문집
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• 한국신재생에너지학회 2009년도 추계학술대회 논문집
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• pp.159-159
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• 2009

In this work, nitrogen and oxygen functionalities was introduced to the graphite nanofibers (GNFs) and their effect on electrocatalytic performance of the GNF supports for direct methanol fuel cells (DMFCs) was invesigated. The nitrogen and oxygen groups were introduced through the urea treatments and acid treatment, respectively. And, PtRu catalysts deposited on modified GNFs were prepared by a chemical reduction method. The catalysts were characterized by means of elemental analysis, nitrogen adsorption, and X-ray photoelectron spetroscopy (XPS). The structure and morphological characteristics of the catalysts were characterized by X-ray diffraction (XRD) and transmission electron microscopy (TEM). As a result, the Pt-Ru nanoparticles were impregnated on GNFs with good formation in 3-5 nm. And, the cyclic voltammograms for methanol oxidation revealed that the methanol oxidation peak varied depending on changes of surface functional groups. It was thus considered that the PtRu deposition was related to the reduction of PtRu and surface characteristics of the carbon supports. The changes of surface functional groups were related to PtRu reduction, significantly affect the methanol oxidation activity of anode electrocatalysts in DMFCs.

• 한국대기환경학회지
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• 제27권2호
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• pp.191-200
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• 2011

A way to adsorptively remove indoor carbon dioxide at relatively lower concentration under ambient temperature was studied. A small lab-scale carbon dioxide adsorption and desorption reactors were prepared, and 5A and 13X zeolites were packed in this reactors to investigate their adsorption and desorption characteristics. The inflow carbon dioxide concentration was controlled to 5,000 ppm, relatively higher concentration found in indoor spaces with air quality problems, by diluting carbon dioxide with nitrogen gas. The flow rate was varied as 1~5 L/min, and the carbon dioxide concentration after this reactor was constantly monitored to examine the adsorption characteristics. It was found that 5A adsorbed more carbon dioxide than 13X. A lab-scale carbon dioxide desorption reactor was also prepared to investigate the desorption characteristics of zeolites, which is essential for the regeneration of used zeolites. The desorption temperature was varied as $25{\sim}200^{\circ}C$, and the desorption pressure was varied as 0.1~1.0 bar. Carbon dioxide desorbed better at higher temperature, and lower pressure. 5A could be regenerated more than three times by thermal desorption at $180^{\circ}C$. It is required to modify zeolites for higher adsorption and better regeneration performances.

• 환경위생공학
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• 제15권1호
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• pp.25-33
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• 2000

1%, 2%, 10%, 및 20%의 가교도를 갖는 클로로메틸화된 1,4-divinyl benzene에 1-aza-15-crown-5 거대고리 ligand를 치환반응으로 결합시키고, 이들 수지로부터 흡착에 미치는 pH, 시간, 수지의 가교도 그리고 용매의 유전상수 크기에 따른 흡착특성을 조사하였다. 금속이온들은 pH 4 이상에서 우라늄과 칼슘 이온들은 루테튬 이온보다 큰 흡착률을 보였으며, 금속이온들의 흡착 평형시간은 약 2 시간이었다. 한편, ethanol 매질에서의 흡착선택성은 $UO_2^{2+}>Ca^{2}>Lu^{3+}$ 이었고, 흡착력은 1%, 2%, 10%, 20%의 가교도 순 이었으며, 용매의 유전상수(물 : 78.54, 메탄올 : 32.63, 에탄올 : 24.30) 크기에 반비례하였다. 컬럼에서 1%의 가교도를 가진 수지와 금속이온들을 흡착시킨 후 용리액으로 pH2.5 $HNO_3$을 사용하여 각각 분리할 수 있었다.

• 한국세라믹학회지
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• 제33권4호
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• pp.432-440
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• 1996

본 연구는 졸-겔법을 이용하여 알칼리 조건인 pH 10에서 제조한 ZrO2의 하소온도에 따른 분말특성과 코발트 흡착량에 미치는 하소온도의 영향에 대하여 검토하였다. 졸-겔법을 이용하여 ZrO2 분말을 제조하고, 600, 800, 1000, 1200, 140$0^{\circ}C$로 하소한 후, X-선 회절법, SEM, BET 방법, Fourier transform 적외선(FT-IR), 열중량 및 열시차분석법(TG-DTA)등을 이용하여 특성을 분석하였다. 알칼리조건인 pH 10에서 제조한 ZrO2는 하소온도가 $600^{\circ}C$일때 고온수에서 코발트 흡착량이 가장 우수하였으며, 이때 $600^{\circ}C$로 하소한 ZrO2의 비표면적은 24.03m2/g이였으며 25$0^{\circ}C$의 고온수에서 코발트 흡착량은 0.16m-eq/g이였다.

• Carbon letters
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• 제6권4호
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• pp.227-233
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• 2005

Carbonization products C1, C2, C3, C4 and C5 were prepared by the carbonization of date pit in limited air, at 500, 600, 700, 800 and $1000^{\circ}C$, respectively. C1-V-600, C3-V-600, C1-V-1000 and C3-V-1000 were prepared by thermal treatment of C1 and C3 under vacuum at 600 and $1000^{\circ}C$. The textural properties were determined from nitrogen adsorption at 77 K and from carbon dioxide adsorption at 298 K. The surface pH, the FTIR spectra and the acid and base neutralization capacities of some carbons were investigated. The amounts of surface oxygen were determined by out-gassing the carbon-oxygen groups on the surface as $CO_2$ and CO. The adsorption of water vapor at 308 K on C1, C2, C3 and C4 was measured and the decomposition of $H_2O_2$ at 308 K was also investigated on C1, C2, C3, C4 and C5. The surface area and the total pore volume decreased with the rise of the carbonization temperature from 500 to $1000^{\circ}C$. The adsorption of water vapor is independent on the textural properties, while it is related to the amount of acidic carbon-oxygen groups on the surface. The catalytic activity of $H_2O_2$ decomposition does not depend on the textural properties, but directly related to the amount of basic carbon-oxygen complexes out-gassed as CO, at high temperatures.

• 공업화학
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• 제20권6호
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• pp.658-662
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• 2009

본 연구에서는 탄소나노튜브를 KOH를 이용하여 활성화 한 후 이를 아민으로 표면처리한 탄소나노튜브의 이산화탄소 흡착거동에 관하여 고찰하였다. 아민 처리한 탄소나노튜브의 물리화학적 특성은 X-ray photoelectron spectroscopy (XPS), $N_2$ adsorption isotherm, thermogravimetric analysis (TGA), 그리고 temperature programmed desorption (TPD)을 이용하여 분석하였다. 실험 결과, 활성화된 탄소나노튜브 표면의 아미노 관능기는 산성가스인 이산화탄소를 선택적으로 흡착하기 위한 염기성 자리로서 작용하였다. 상온에서의 이산화탄소 흡착량은 미처리된 탄소나노튜브가 가장 크게 나타났으나 온도가 증가할수록 급격한 감소를 나타내었으며 PEHA 처리한 경우 완만한 흡착거동을 보였다. 이는 탄소표면의 아미노 관능기와 이산화탄소 사이의 상호작용 때문이라 판단된다.

• Korean Chemical Engineering Research
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• 제56권6호
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• pp.784-791
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• 2018

다양한 합성조건에서 UiO-66 입자를 합성하여 수소정제용 이산화탄소 흡착량에 대한 연구를 수행하였다. 이를 위하여 통계학적 실험계획법을 이용하여 실험계획을 세우고 도출된 결과를 이용하여 분석하였다. 합성시간, 온도 및 아세트산의 용량이 증가할 수록 UiO-66입자의 결정도가 증가하였다. 특히 아세트산의 용량이 입자의 결정도를 결정하는데 중요한 인자로 확인되었다. 질소흡착법으로 측정한 입자의 비표면적의 경우도 유사한 경향을 보였다. 실험계획법 중 일반요인분석을 이용하여 주요 인자에 대한 주효과도 및 교호작용을 분석하였다. 또한 비선형 회귀법을 이용하여 이산화탄소 흡착량을 예측하였고, 모든 범위에서 대하여 흡착성능을 표면도와 등고선도를 통해 제시하였다.

• 한국지하수토양환경학회지:지하수토양환경
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• 제15권3호
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• pp.44-51
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• 2010

Contamination of groundwater from point and non-point sources is one of major problems of water resource manangement in Jeju island. This study characterized groundwater and soil contamination in Hallim area which is one of the areas of significantly contaminated soil and groundwater in Jeju Island. The amount of loaded contaminant (ALC) of Jeju area was estimated as 13,212 ton N/yr and 3,210 ton P/yr, The ALC of Hallim area was amounted to 2,895 ton N/yr and 1,102 ton P/yr, which accounted for 21.9% and 34.3% of the Jeju's ALC, respectively. The soil pH values (5.6-5.9) were not much different in land use areas. By contrat, average cation exchange capacity (CEC) of 14.1 $cmol^+/kg$ was high comparing to the nationwide range of 7.7-10.9 $cmol^+/kg$. Further, Sodium adsorption ratios (SARs) of horse ranch, pasture, and cultivating land for livestock were as high as 0.19, 0.17, and 0.16 respectively, comparing to the other landuse areas. Nitrate nitrogen at 22.2% of total groundwater wells exceeded 10 mg/L (the criteria of nitrate nitrogen for drinking water), averaginged 6.62 mg/L with maximum 28.95 mg/L. Groundwater types belonged to Mg-$HCO_3$, Na-$HCO_3$, Ca-$HCO_3$, and Na-Cl, among which Mg-$HCO_3$ type occupied more than 70% of the total samples, indicating the presence of anthropogenic sources. The concentration of nitrate nitrogen was negatively related to altitude and well depth, and positively related to the concentration of Ca, Mg, and $SO_4$ which might originate from chemical fertilizer. The ratio of nitrogen isotopes was estimated as an average of 8.10$^{\circ}/_{\circ\circ}$, and the maximum value of 17.9$^{\circ}/_{\circ\circ}$. According to the nitrogen isotope ratio, the most important nitrogen source was assessed as chemical fertilizer (52.6%) followed by sewage (26.3%) and livestock manures (21.1%).

• 한국토양비료학회지
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• 제48권2호
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• pp.73-80
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• 2015

Arsenic which is found in several different chemical forms and oxidation states and causes acute and chronic adverse health effects is a toxic trace element widely distributed in soils and aquifers from both geologic and anthropogenic sources. Arsenic which has a mysterious ability to change color, behavior, reactivity, and toxicity has diverse chemical behavior in the natural environment. Arsenic which has stronger ability to readily change oxidation state than nitrogen and phosphorus due to a consequence of the electronic configuration of its valence orbitals with partially filled states capable of both electron donation and acceptance although the electronegativity of arsenic is greater than that of nitrogen and similar to that of phosphorus. Arsenate (V) is the thermodynamically stable form of As under aerobic condition and interacts strongly with solid matrix. However, it has been known that adsorption and oxidation reactions of arsenite (III) which is more soluble and mobile than As(V) in soils are two important factors affecting the fate and transport of arsenic in the environment. That is, the movement of As in soils and aquifers is highly dependent on the adsorption-desorption reactions in the solid phase. This article, however, focuses primarily on understanding the fate and speciation of As in soils and what fate arsenic will have after it is incorporated into soils.