• 공업화학
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• 제4권4호
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• pp.746-752
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• 1993

PCB와 HA 사이의 착화합 정도에 대한 양적인 측정을 위해 투석막을 이용한 평형실험이 여러 가지 변수에 대해 먼저 수행되었다. 활성탄에 대한 PCB의 흡착특성 파악을 위해서 HA가 용해된 물과 용해되지 않은 물을 이용하여 PCB에 대한 흡착평형 및 속도실험을 행하였다. 실험결과 HA에 대한 PCB의 착화합 정도는 PH, $Ca^{2+}$농도, 이온세기 및 HA의 농도에 큰 영향을 받는 것을 확인하였다. PCB의 활성탄에 대한 흡착능력은 HA가물에 존재할 때 크게 감소하였으며 흡착특성은 HA, PCB와 HA에 착화합된 PCB 등의 물질이 서로 경쟁적으로 활성탄에 흡착하게 되는 복잡한 특성을 보일 것으로 판단되었다.

• 한국추진공학회:학술대회논문집
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• 한국추진공학회 2007년도 제28회 춘계학술대회논문집
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• pp.143-147
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• 2007

케로신과 디젤은 단일 구성물이 아닌 여러 가지 탄화수소 연료로 이루어진 혼합연료이며 화학반응 메커니즘에 대한 모델링이 매우 어려운 실정이다. 본 연구에서는 Dagaut가 개발한 298 화학종, 2352 화학반응 단계를 이용하였으며 완전혼합반응기 연소모델을 적용하여 농후 연소 비평형 화학 반응을 계산하였다. 또한 Frenklach의 soot 모델을 적용하여 soot 생성 연구를 수행하였으며 Dagaut의 화학반응 모델에 Appel이 제안한 화학 반응 단계를 추가하여 케로신과 디젤 연료에 대한 soot 모사를 가능하게 하였으며 수정된 모델은 간단한 soot 반응 메커니즘을 사용하였음에도 불구하고 soot 생성 예측이 가능하였다.

• 대한화학회지
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• 제30권4호
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• pp.359-368
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• 1986

Crown ether (DC18C6, DC24C8)과 HDEHP로 알칼리 금속 이온을 용매 추출할 때의 추출평형을 연구하였다. 추출평형상수는 DC18C6계에서 $Na^+순으로 증가하였으며 DC24C8계에서는 $Rb^+순으로 증가하였다. 유기용매상으로 추출되는 추출종은 $M_1(crown ether)_1\;(HDEHP)_1$이며 추출평형상수의 크기는 crown ether의 유기용매상과 수용액상에서의 분배비와 crown ether-알칼리금속 착물의 안정도 상수에 의해서 결정된다.

• 공업화학
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• 제4권4호
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• pp.672-682
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• 1993

sodium amide에 의한 methylpropyl ketone과 ethyl acetate의 반응으로 2, 4-heptadione(이하 24HTD)을 합성하고, 클로로포름 용매하에 Cu(II)의 용매추출 실험으로부터 추출평형 및 추출속도 특성을 고찰하였다. 흡광도와 Cu(II)의 농도변화 측정으로부터 24HTD의 분배계수와 해리정수, 24HTD와 Cu 착화합물의 안정도 상수, 분배계수 및 총괄추출 평형정수 등을 구하고 추출기구를 구명하였다. 24HTD에 의한 Cu(II)의 추출 화학종은 1:2의 형태인 $CuR_2$였으며, 24HTD-클로로포름에 의한 Cu(II)의 총괄 초기 추출속도는 $R_0=k[\bar{HR}]([Cu^{2+}]/[H^+])^{0.5}$로 표시되었다.

• 한국대기환경학회지
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• 제24권2호
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• pp.238-248
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• 2008

This study investigated mercury emission at various combustion conditions and analyzed mercury species in flue gas from coal combustion at a laboratory scale furnace in coal. The results of this study can be used to predict and to assess mercury emission at coal boilers and power plants. The coal used in the plants generally contains about $0.02{\sim}0.28\;mg$ of mercury per kg. Bituminous and anthracite coal used for the experiment contained 0.049 and 0.297 mg/kg of mercury, respectively. Mercury emissions during coal combustion at temperatures range of $600^{\circ}C$ to $1,400^{\circ}C$ was measured and analysed using Ontario Hydro method; the speciation changes were also observed in mercury emissions. The results showed higher fraction of elemental mercury than that of oxidised mercury at most temperatures tested in this experiment. The fraction of elemental mercury was lower in combustion of anthracite coal than in bituminous combustion. As expected, equilibrium calculations and real power plants data showed good similarity. The distribution of particle size in flue gas had the higher peak in size above $2.5\;{\mu}m$. However the peak of mercury enrichment in dust was at $0.3\;{\mu}m$, which could be easily emitted into atmosphere without filtration in combustion system. When the CEA(Chemical equilibrium and Application) code was used for combustion equilibrium calculation, Cl was found to be the important component effecting mercury oxidation, especially at the lower temperatures under $900^{\circ}C$.

• 한국결정성장학회:학술대회논문집
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• 한국결정성장학회 1996년도 The 9th KACG Technical Annual Meeting and the 3rd Korea-Japan EMGS (Electronic Materials Growth Symposium)
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• pp.5-18
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• 1996

The solid state cesium ion source os alumino-silicate based zeolite which contains cerium. The material is an ionic conductor. Cesiums are stably stored in the material and one can extract the cesiums by applying electric field across the electrolyte. Cesium ion bombardment has the unique property of producing high negative ion yield. This ion source is used as the primary source for the production of a negative ion without any gas discharge or the need for a carrier gas. The deposition of materials as an ionic species in the energy range of 1.0 to 300eV is recently recognized as a very promising new thin film technique. This energetic non-thermal equilibrium deposition process produces films by “Kinetic Bonding / Energetic Condensation" mechansim not governed by the common place thermo-mechanical reaction. Under these highly non-equilibrium conditions meta-stable materials are realized and the negative ion is considered to be an optimum paeticle or tool for the purpose. This process differs fundamentally from the conventional ion beam assisted deposition (IBAD) technique such that the ion beam energy transfer to the deposition process is directly coupled the process. Since cesium ion beam sputter deposition process is forming materials with high kinetic energy of metal ion beams, the process provider following unique advantages:(1) to synthesize non thermal-equilibrium materials, (2) to form materials at lower processing temperature than used for conventional chemical of physical vapor deposition, (3) to deposit very uniform, dense, and good adhesive films (4) to make higher doposition rate, (5) to control the ion flux and ion energy independently. Solid state cesium ion beam sputter deposition system has been developed. This source is capable of producing variety of metal ion beams such as C, Si, W, Ta, Mo, Al, Au, Ag, Cr etc. Using this deposition system, several researches have been performed. (1) To produce superior quality amorphous diamond films (2) to produce carbon nitirde hard coatings(Carbon nitride is a new material whose hardness is comparable to the diamond and also has a very high thermal stability.) (3) to produce cesiated amorphous diamond thin film coated Si surface exhibiting negative electron affinity characteristics. In this presentation, the principles of solid state cesium ion beam sputter deposition and several applications of negative metal ion source will be introduced.

• Carbon letters
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• 제7권3호
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• pp.171-179
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• 2006

A carbonaceous sorbent was prepared from rice husk via sulphuric acid treatment. After preparation and washing, the wet carbon with moisture content 85% was used in its wet status in this study due to its higher reactivity towards Cr(VI) than the dry carbon. The interaction of Cr(VI) and the carbon was studied and two processes were investigated in terms of kinetics and equilibrium namely Cr(VI) removal and chromium sorption. Cr(VI) removal and chromium sorption were studied at various initial pH (1.6-7), for initial Cr(VI) concentration (100 mg/l). At equilibrium, maximum Cr(VI) removal occurred at low initial pH (1.6-2) where, Cr(III) was the only available chromium species in solution. Cr(VI) removal, at such low pH, was related to the reduction to Cr(III). Maximum chromium sorption (60.5 mg/g) occurred at initial pH 2.8 and a rise in the final pH was recorded for all initial pH studied. For the kinetic experiments, approximate equilibrium was reached in 60-100 hr. Cr(VI) removal data, at initial pH 1.6-2.4, fit well pseudo first order model but did not fit pseudo second order model. At initial pH 2.6-7, Cr(VI) removal data did not fit, anymore, pseudo first order model, but fit well pseudo second order model instead. The change in the order of Cr(VI) removal process takes place in the pH range 2.4-2.6 under the experimental conditions. Other two models were tested for the kinetics of chromium sorption with the data fitting well pseudo second order model in the whole range of pH. An increase in cation exchange capacity, sorbent acidity and base neutralization capacity was recorded for the carbon sorbent after the interaction with acidified Cr(VI) indicating the oxidation processes on the carbon surface accompanying Cr(VI) reduction.

• 한국물환경학회지
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• 제30권2호
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• pp.175-183
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• 2014

The influence of temperature on the treatment efficiency of chlorinated organic substances contained in groundwater by permeable reactive barrier which is composed of $Fe^{\circ}$ has been investigated by constructing the Pourbaix diagrams for Fe-$H_2O$ system at different temperatures based on thermodynamic estimation. In aerobic condition, the equilibrium potentials for $Fe^{\circ}/Fe^{2+}$ and $Fe^{2+}/Fe^{3+}$ were observed to increase, therefore, the dechlorination reaction for organic pollutants by $Fe^{\circ}$ was considered to decline with temperature due to the diminished oxidation of reactive barrier. The result for the variations of the ionization fraction of $Fe^{2+}$ and $Fe^{3+}$ ion in the pH range of 0 ~ 2.5 obtained by employing Visual MINTEQ program showed that the ionization fraction of $Fe^{2+}$ increased with pH, however, that of $Fe^{3+}$ decreased symmetrically and the extent of the variation of ionization fraction for both ions was raised as temperature rises. The equilibrium pH for $Fe^{3+}/Fe(OH)_3$ was examined to decrease with temperature so that the treatment efficiency of chlorinated organic substance was expected to decrease with temperature due to the enhanced formation of passivating film in aerobic condition. The change of the reactivity of a specific chemical species with temperature was defined quantitatively based on the area of its stable region in Pourbaix diagram and depending on this the reactivity of $Fe^{3+}$ was shown to decrease with temperature, however, that of $Fe(OH)_3$ was decreased monotonously as temperature is raised for $Fe^{3+}/Fe(OH)_3$ equilibrium system. In anaerobic condition, the equilibrium potential for $Fe^{\circ}/Fe^{2+}$ was observed to rise and the equilibrium pH for $Fe^{2+}/Fe(OH)_2$ were examined to decrease as temperature increases, therefore, similar to that for aerobic condition the efficiency of the dechlorination reaction for organic substances was considered to be diminished when temperature rises because of the reduced oxidation of $Fe^{\circ}$ and increased formation of $Fe(OH)_2$ passivating film.

• Journal of the Korean Wood Science and Technology
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• 제45권5호
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• pp.629-639
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• 2017

현재 합천 해인사에 보관되어 있는 고려속장경(일명 팔만대장경)은 역사적 가치나 규모면에 있어서 세계적인 문화재이나 아직도 어떤 수종으로 만들어졌는지 모르고 있다. 중요한 문화재이기 때문에 손상없이 비파괴적으로 수종을 추정하는 방법이 필요하다. 밀도를 알게 되면 수종을 추정하기 쉽다. 유전율식 목재수분계의 원리를 역으로 이용하면 함수율을 알고 있는 목재의 전건밀도를 얻을 수 있다는데 착안하여 연구를 수행하였다. 국내산 100여 개 수종, 122개 재감의 전건밀도를 치수법과 유전율식 목재수분계 추정법으로 구하여 두 계수의 상관관계와 회귀식을 찾았으며 문헌자료를 이용하여 회귀식의 유의성을 검정하였다. 치수법으로 측정한 전건밀도와 유전율식 목재수분계로 추정한 전건밀도는 매우 높은 상관관계를 나타냈다. 이 관계식을 이용하면 팔만대장경판의 전건밀도를 추정할 수 있으며 나아가 수종을 예측할 수 있을 것이다.

• 한국추진공학회:학술대회논문집
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• 한국추진공학회 2017년도 제48회 춘계학술대회논문집
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• pp.1135-1139
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• 2017

화염 내 화학종의 공간적 분포는 화염의 구조 및 연소 특성을 이해하는데 중요한 지표가 되며, 그 계측을 위해 발광분광법 (Optical emission spectroscopy)은 간단하고 비침투적인 진단 방식으로 인해 널리 활용되고 있다. 본 연구에서는 측정 line-of-sight 방향의 공간 분해 계측 목적으로 개발된 발광분광기를 이용한 로켓 플룸 내 화학종 (OH radical) 분포 계측의 가능성을 제시하였다. 발광분광기의 측정 신호로부터 바닥 상태의 화학종 농도를 예측하기 위해 화염 내 열적 여기와 화학적 여기 기작을 고려하였으며, 열적으로 여기된 종에 대해서 열적 평형 상태를 가정하였다. 또한 발광분광기의 공간 분해 성능 및 공간에 따른 수광 특성을 보정하기 위한 방법론을 제시하였다.