• Proceedings of the Korean Society of Soil and Groundwater Environment Conference
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• 2002.04a
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• pp.49-53
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• 2002

워싱턴주 벤쿠버시 Bonneville 전력소 전주 보관 지역내 PCP와 creosote 오염토양 2g 당 0.020g heme에 0.108g $H_2O$$_2$을 혼합한 산화방법과 0.035g hemoglobin에 0.324g $H_2O$$_2$을 혼합한 산화방법을 비교ㆍ조사하였다. 오염토양에 $^{14}$ C-PCP을 첨가한 다음에 $^{14}$ C의 물질수지를 조사한 결과, 24시간동안 반응 후 $^{14}$ $CO_2$는 heme 과 hemoglobin반응에서는 각각 3.50g와 3.88% 생산되었다. $^{14}$ C 물질수지 분포는 heme 촉매 산화반응에서 용매 상에 43.01% 토양 상에는 46.03%이고, hemoglobin 촉매 산화반응에서는 용매 상에 39.21%와 토양 상에 51.25%로 비슷한 분포를 보였다. 실험실 규모 pan 실험에서 초기 PCP농도 273$\pm$20 mg/kg과 TPH 6379$\pm$45 mg/kg인 오염토양에서 hemoglobin 촉매 산화 반응이 초기반응을 제외하고 7일 이후 반응에서 heme 촉매 산화반응보다 빠르게 분해되었고, 35일 반응 이후 PCP는 10 mg/kg 이하의 값을 나타내었고, TPH도 유사한 결과를 보여 주었다. 그러므로 건조 hemoglobin과 과산화수소에 의한 PCP 오염토양 복원기술은 분해율이 높고 경제성을 가지고 있으므로 기존의 복원공정을 대안으로 제시될 수 있다.

• Resources Recycling
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• v.9 no.4
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• pp.37-43
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• 2000

Leaching of $LiCoO_2$ as a cathodic active materials for recovering Li and Co from spent lithium ion battery was investigated in terms of reaction variables. At the optimum condition determined in the previous work, Li and Co in a $H_2SO_4$ and $HNO_3$ solution were dissolved 70~80% and 40%, respectively. Li and Co were leached over 95% with the addition of a reductant such as $Na_2S_2O_3$ or $H_2O_2$. This behavior is probably due to the reduction of $Co^{3+}$ to $Co^{2+}$. Leaching of $LiCoCo_2$ powder obtained by calcination of an electrode materials from spent batteries was also carried out. Leaching efficiency of Li and Co were over 99% at the optimum condition with $H_2O_2$ addition of 1.7 vol.%. It seems to be due to the activation of $LiCoO_2$ by repeated charging and discharging or an imperfect crystal structure by deintercalation of Li.

• Journal of environmental and Sanitary engineering
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• v.13 no.1
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• pp.1-8
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• 1998

Musty-odorous compound (Geosmin, 2-Methylisobrneol) 수용액 중에 초음파 (200kHz, $6.0W/cm^{2}$)를 조사시켜 조사시간에 따른 농도 및 취기의 변화를 고찰했다. 초음파 조사에 의해 이 물질들은 빠르게 분해되었고 분해 형태는 농도에 대한 유사1차 반응을 나타내었다. 공기 포화 분위기에서 이들의 초기 분해속도는 각각 2.5 $10^{-3}{\;}Msec^{-1}$(2-MIB), 3.2 $10^{-3}{\;}Msec^{-1}$ (Geosmin)로 나타났다. 초음파 조사 시 포화가스 (Envelope gas)의 영향은 아르곤(Ar) 산소($O_{2}$) 공기(Air) 질소($N_{2}$) 순서로 순수한 아르곤(Ar) 분위기에서 musty-odorous compound 류의 분해가 가장 빠르게 진행되었고 그 분해생성물로 CO, $CO_{2}$ 그리고 HCOOH, $CH_{3}COOH$ 등의 저급 유기산류가 검출되었다. 또한 이들의 분해반응은 물의 초음파분해에 따라 생성된 hydroxylradical에 의한 radical반응, cavitation bubble내에서의 고온고압에 의한 열분해 및 직접연소반응으로 진행됨을 알 수 있었다.

• Journal of the Korean Vacuum Society
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• v.15 no.5
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• pp.506-511
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• 2006

ZnO nanorods were prepared by the hydrothermal reaction of a solution containing $Zn(NO_3)_2{\cdot}6H_2O$, NaOH, cyclohexylamine, ethanol and water, and their $NO_2$ and CO sensing behaviors were investigated. By the control of water concentration in solution, the morphology and agglomeration of ZnO nanorods could be manipulated, which is associated with the variation of $[OH^-]$ resulted from an interaction between water and cyclohexylamine. Sea-urchin-like and well-dispersed ZnO nanorods were prepared at low and high water content, respectively. Well-dispersed ZnO nanorods showed 1.8 fold change in resistance at 1 ppm $NO_2$ while there was no significant change in resistance at 50 ppm CO. This selective detection of $NO_2$ in the presence of CO can be used in automated car ventilation systems.

• The Journal of Engineering Research
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• v.6 no.1
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• pp.97-109
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• 2004

The synthesis and crystal structure of amorphous calcium carbonate obtained from gas-liquid reaction of CaO-$C_2 H_5 OH$-$CO_2$ system according to change of added amount of calcium oxide by blowing $CO_2$ gas and reaction time using ethanol and ethylene glycol were investigated by electric conductivity, X-ray diffraction, and scanning electron microscope. The powdery or gelatinous phases were prepared by passing $CO_2$ gas at a flow rate of 1$\ell$/min into the suspensions containing 10~40g of CaO in mixing solutions 900ml of $C_2 H_5 OH$- and 100ml of ethylene glycol. By rapid filtration and drying the both phases at $60^{\circ}C$ under reduced pressure, the phases converted to the spherical vaterite and amorphous phase. The stable phase of amorphous calcium carbonate(ACC) was formed in the region pH 7-9 but the formation regions of amorphous phase were remarkably affected by pH in the mother liquor. It seems that a part of ACC changed into chain calcite as an intermediate products. The initial reactants prior to the formation of precipitated calcium carbonate is ACC. And ACC is unstable in the aqueous solution and crystallizes finally to calcite by the through-solution reaction. Especially ACC was produced or gelatinous phase which precipitated from the reaction of CaO-$C_2 H_5 OH$-$CO_2$ system.

• Economic and Environmental Geology
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• v.42 no.5
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• pp.403-412
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• 2009

The objective of this study is to investigate the geochemical change of feldspar minerals by supercritical $CO_2$, which exists at $CO_2$ sequestration sites. High pressurized cell system (100 bar and $50^{\circ}C$) was designed to create supercritical $CO_2$ in the cell and the surface change and the dissolution of plagioclase and orthoclase were observed when the mineral surface reacted with supercritical $CO_2$ and water (or without water) for 30 days. The polished slab surface of feldspar was contacted with supercritical $CO_2$ and an artificial brine water (pH 8) in the experiments. The experiments for the reaction of feldspar with only supercritical $CO_2$ (without brine water) were also conducted. Results from the first experiment showed that the average roughness value of the plagioclase surface was 0.118 nm before the reaction, but it considerably increased to 2.493 nm after 30 days. For the orthoclase, the average roughness increased from 0.246 nm to 1.916 nm, suggesting that the dissolution of feldspar occurs in active when the feldspars contact with supercritical $CO_2$ and brine water at $CO_2$ sequestration site. The dissolution of $Ca^{2+}$ and $Na^+$ from the plagioclase occurred and a certain part of them precipitated inside of the high pressurized cell as the form of amorphous silicate mineral. For the orthoclase, $Al^{3+}$, $K^+$, and $Si^{+4}$ were dissolved in order and the kaolinite was precipitated. In the experiments without water, the change of the average roughness value and the dissolution of feldspar scarcely occurred, suggesting that the geochemical reaction of feldspars contacted with supercritical $CO_2$ at the environment without the brine water is not active.

• Proceedings of the Korean Institute of Surface Engineering Conference
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• 2002.05a
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• pp.2-2
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• 2002

Quartz Crystal Microbalance(QCM)은 표면에 묻은 물질의 미량의 무게변화도 간단히 측정 할 수 있어 반웅기 내에서 일어나는 현상올 in-situ로 즉시 알 수 있는 장점을 가진 장치이 다. 이 장치를 이용하면 초엄계 이산화탄소 내에서 용해도를 알 수 있고, 대상물질이 녹아냐 가는 속도를 측정하면 확산계수를 구할 수 있다. 그리고, 초음파 혼을 반응용기 내에 설치하 고, 초음파 효과를 알아보았다. 먼저 static system에서 초음파 효과를 알아보았다. Cu(acac)2를 대상으로, 밀폐된 용기에서 수행한 실험에서, 액체와 초임계 이산화탄소 내에서 용해속도를 QCM으로 구할 수 있었다. 용해속도로부터 Cu(acac)2의 확산계수를 측정할 수 있었다. 액체 내에선 $10^{-4}{\;}cm2/sec$, 초임계상태에서 $10^{-2}{\;}cm2/sec$의 값을 갖는 것으로 나타 났다. 그리고, 초음파를 사용할 경우 이 확산계수값이 4-5배정도 증가하는 것으로 냐타났다. 이어서 dynamic system에서 반응을 알아보았다. Cyanex를 함유한 C02를 반응용기에 흘리 면서 QCM표면에 묻은 Co이온의 용해속도를 측정하였다. 초음파는 용해도에 아무 역활을 안하는 것으로 나타났다. 주어진 조건에서 13 microgram/gram-cyanex의 용해도를 갖는 것 으로 나타났다.

• Transactions of the Korean Society of Mechanical Engineers B
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• v.36 no.2
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• pp.225-232
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• 2012

A chemical reactor network (CRN) was developed for a lean premixed gas turbine combustor to predict the emission of pollutants such as NOx and CO. In this study, the predictions of NOx and CO emissions from lean premixed methane-air combustion in the gas turbine were carried out using CHEMKIN and a GRI 3.0 methane-air combustion mechanism, which includes the four NO formation mechanisms for various load conditions. The calculated results were compared with experimental data obtained from a modified test combustor to validate the model. The contributions of the four NO pathways were investigated for various load conditions. The effects of nonuniformity of the mass flux and of the equivalence ratio of the injector on the NOx formation were investigated, and a method of reducing the pollutant formation was suggested for the development of a sub-10 ppm gas turbine combustor.

• Proceedings of the Korean Vacuum Society Conference
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• 2014.02a
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• pp.261.1-261.1
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• 2014

지구상에 존재하는 모든 생물에 의해 배출되는 이산화탄소는 온실가스로써 산업혁명 이후 급격한 농도 증가로 인해 지구 온난화 등의 다양한 환경문제를 초래하고 있다. 지구 온난화의 가시화로 인한 각종 기후 협약 및 탄소배출권 등에 규제로 온실가스 감축의무부과가 확실해져 탈 석유기반 사회로 전환을 위한 이산화탄소를 처리하는 다양한 연구가 각국에서 활발히 진행 중이다. 본 연구에서 마이크로웨이브 플라즈마 토치를 이산화탄소 분해에 이용하게 되었고 그 목적은 이산화탄소가스를 마이크로웨이브로 가열하여 순수한 이산화탄소 플라즈마 토치를 발생함으로서 지구 온난화의 주범인 이산화탄소를 생산적으로 이용하기 위한 것으로 전자파를 발진하는 마그네트론으로는 3kW, 2.45GHz의 주파수를 사용한다. 마이크로웨이브 플라즈마 토치를 이용한 이산화탄소의 분해 시 생성되는 물질을 확인하기 위하여 이산화탄소의 열역학적 평형을 계산하였으며 또한 이산화탄소의 분해 반응의 준 평형상태에서의 속도상수를 이용하여 각 분해반응생성물들의 밀도비율을 계산하였고, 이를 일반화시켜 도시하였다. 위 과정을 통해 고온의 이산화탄소 토치는 탄화수소 연료를 1기압에서 개질할 수 있음을 알 수 있다. 예를 들어 메탄개질은 $CO_2+CH_4{\rightarrow}2CO+2H_2$의 반응식이 된다. 이때 엔탈피와 엔트로피 변화는 각 각 ${\Delta}H=247kJ/mole$과 ${\Delta}S=257J/mole/deg.$이며 이 반응에 대한 gibbs 자유에너지는 $G={\Delta}H-T{\Delta}S$로서 개질 자발반응이 일어나는 온도는 $T={\Delta}H/{\Delta}S=961K$가 된다. 그리고 탄화수소 개질에 참여하는 산소와 CO 라디칼의 밀도가 대단히 높다. 따라서 메탄개질은 이산화탄소 토치를 통하여 1기압에서 쉽게 이루어진다.

• Korean Chemical Engineering Research
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• v.40 no.6
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• pp.746-751
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• 2002

Fluidized bed combustion is a coal combustion technology that can reduce both SOx and NOx emission; SOx is removed by limestone that is fed into the combustion chamber and the NOx is reduced by low temperature combustion in a fluidized bed combustor and air stepping, but $N_2O$ generation is quite high. $N_2O$ is not only a greenhouse gas but also an agent of ozone destruction in the stratosphere. The calcium oxide(CaO) is known to be a catalyst of $N_2O$ decomposition. This study of $N_2O$ decomposition reaction in fixed bed reactor packed over CaO bed has been conducted. Effects of parameters such as concentration of inlet $N_2O$ gas, reaction temperature, CaO bed height and effect of $CO_2$, NO, $O_2$ gas on the decomposition reaction have been investigated. As a result of the experiment, it has been shown that $N_2O$ decomposition reaction increased with the increasing fixed bed temperature. While conversion of the reaction was decreased with increasing $CO_2$ concentration. Also, under the present of NO, the conversion of $N_2O$ decomposition is decreased. From the result of kinetic study gained the heterogeneous reaction rate on $N_2O$ decomposition. In the case of $N_2O$ decomposition over CaO, heterogeneous reaction rate is. $\frac{d[N_2O]}{dt}=\frac{3.86{\times}10^9{\exp}(-15841/R)K_{N_2O}[N_2O]}{(1+K_{N_2O}[N_2O]+K_{CO_2}[CO_2])}$. In this study, it is found that the calcium oxide is a good catalyst of $N_2O$ decomposition.