• Journal of the Korean Applied Science and Technology
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• v.33 no.2
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• pp.232-238
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• 2016

In this study, a liquid carbonation method was applied for producing precipitate calcium carbonate by liquid-liquid reaction. Also a shuttle mechanism of wet chemical absorption using MEA was utilized. The high concentration $CO_2$(A) and exhaust gas(B) was used for collecting carbon dioxide in the 30% MEA aqueous solution, and $CO_2$ was fixed with rate of 0.35 mg of $CO_2$ per mg of sludge through the liquid carbonation process. It was found from SEM data that calcium carbonate was mainly made up with spherical vaerite with the mixing of a small quantity of calcite.

• Journal of Energy Engineering
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• v.10 no.1
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• pp.49-54
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• 2001

최근 자동차용 청정 연료로서의 이용 가능성으로 주목받는 디메틸에테르를 액상 혼합 반응기에서 직접 합성 가스로부터 합성하였다. 메탄올 함성촉매와 감마알루미나의 혼성촉매를 사용한 결과, $H_2$/CO=1일 때, 메탄올 함성 촉매와 탈수촉매의 비가 8:2인 경우, 가장 높은 메탄옥 환산 생산량을 보였다. 또한 공간속도의 변화에 따른 디메틸에테르, 메탄올, 이산화탄소, 메탄 등 각 생성물에 대한 선택도의 변화는 거의 없이 일정하였다. 메탄옥 합성 반응 촉매만을 사용한 경우, 생성물 중 각 성분의 선택도는 반응가스의 공간속도에 따라 달라졌는데, 반응가스의 공간속도가 작아지면 생성물 중 디메틸에테르의 선택도는 변화가 없었으나, 이산화탄소의 발생량이 많고 메탄올의 생성이 적어졌다. 동일한 반응 조건에서 액상 반응과 시강 반응을 비교한 결과, DME 수율이 액상의 경우가 더 높았다.

• Journal of the Korean Applied Science and Technology
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• v.32 no.1
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• pp.116-126
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• 2015

The present study utilized a shuttle mechanism of wet chemical absorption using MEA. In addition, industrial by-products containing a large amount of inorganic alkali substances were utilized for wet carbonization process. Chemical pretreatment of industrial by-products extracted calcium ions. ICP result of calcium ion was obtained up to 17,900 ppm(17.9%) by acidic substance. And also, In this work, 94% of recovery rate was obtained using wet MEA absorption process from $CO_2$ flow at the ambient condition. Through the liquid carbonation process, a sludge was fixed with rate of 0.175 mg of $CO_2$ per mg of sludge. It was found from XRD results that the structure of final product was composed of a calcite structure which is general structure of $CaCO_3$.

• Applied Chemistry for Engineering
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• v.7 no.1
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• pp.67-74
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• 1996

The binary phase equilibrium experiments of carbon dioxide/1,2,3,4 ${\alpha}$-tetrahydro-1-naphthol(${\alpha}$-tetralol) system were conducted to get phase equilibrium and mixture density data at 313.2K, 343.2K and 373.2K and within pressure ranges of 6.0 MPa to 35.0MPa. The phase equilibrium apparatus was type that circulated the vapor and liquid phase, the expended volume measuring system was adopted to microsampling technique for the analysis. The phase equilibrium and mixture density data were obtained for carbon dioxide/${\alpha}$-tetralol system from liquid and vapor phase. The mole fraction of carbon dioxide in liquid phase decreases and the mole fraction of ${\alpha}$-tetralol in vapor phase increases at constant pressure according to increment of temperature, and both the densities of the vapor and liquid phase approach to the mixture critical density as the pressure increases at any temperature. For she thermodynamic analysis, the experimental data were correlated with Peng-Robinson equation in cubic equation of state and compared to theoretical values of carbon dioxide/${\alpha}$-tetralol system. The AAD result was in the range of 1.08%~8.93% in the case of K(1), and was in the range of 45.71%~72.34% in the case of K(2).

• Applied Chemistry for Engineering
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• v.18 no.3
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• pp.239-244
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• 2007

For the simultaneous methane recovery and $CO_2$-stripping, we have been developed dual vent auto circulation bubble lift column reactor, and evaluate optimum conditions for monoethanolamine (MEA) solutions as a $CO_2$ absorbent. At the 5 wt% MEA solution, we investigated the pH change during $CO_2$-stripping and absorption reaction, $CO_2$-stripping rate with reaction time, methane recovery efficiency for various inflow rates of air, $CO_2$-stripping rate for flow liquid over flow height, and $CO_2$-stripping dependency on the temperature of absolvent solutions. The suggested optimum conditions for $CO_2$ recovery with MEA in the dual vent auto circulation bubble lift column reactor were 40 mm over flow liquid height, 1.5 L/min of air inflow rate, and $25^{\circ}C$ of absorbent solution temperature.

• Bulletin of Food Technology
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• v.24 no.3
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• pp.415-427
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• 2011

지난 수십 년간 발표된 연구결과와 특허 수를 감안하면 식품에 적용된 고압 이산화탄소(high pressure carbon dioxide, HPCD) 기술은 특이한 과학적 관심을 받아 왔다. 하지만 주로 액상식품에 대한 HPCD의 미생물 억제 효과만 증명되어 왔을 뿐 고체식품에 대한 활용 연구는 그다지 많지 않은 편이다. 이에 본고에서는 고체식품에 적용된 HPCD 관련 연구사례를 전반적으로 조사하였으며 또한 미래 전망 등에 대해 살펴봄으로써 연구자들의 연구 방향을 제시하고자 하였다.

• Clean Technology
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• v.18 no.3
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• pp.229-249
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• 2012

At present, global warming and depletion of fossil fuels have been one of the big issues which should be solved for sustainable development in the future. CCS (carbon capture and sequestration) technology as the post $CO_2$ reduction technology has been considered as a promising solution for global warming due to increased carbon emission. However, the environmental and ecological effects of CCS have drawn concerns. There are needs for noble post reduction technology. More recently, CCU (carbon capture and utilization) Technology, which emphasizes transforming carbon dioxide into value-added chemicals rather than storing it, has been attracted attentions in terms of preventing global warming and recycling the renewable carbon source. In this paper, various technologies developed for carbon dioxide conversion both in gas and liquid phase have been reviewed. For the thermochemical catalysis in gas phase, the development of the catalytic system which can be performed at mild condition and the separation and purification technology with low energy supply is required. For the photochemical conversion in liquid phase, efficient photosensitizers and photocatalysts should be developed, and the photoelectrochemical systems which can utilize solar and electric energy simultaneously are also in development for more efficient carbon dioxide conversion. The energy needed in CCU must be renewable or unutilized one. CCU will be a key connection technology between renewable energy and bio industry development.

• Journal of the Korea Academia-Industrial cooperation Society
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• v.22 no.2
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• pp.644-650
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• 2021

This study characterized the reforming of methane with carbon dioxide, which is a major cause of global warming. The methane decomposition reaction with carbon dioxide was carried out using transition metal catalysts. The reactivity of tin was lower than that of a transition metal, such as nickel and iron. Most of the decomposition reaction occurred in the solid state. The melting point of tin is 505.03 K. Tin reacts in a liquid phase at the reaction temperature and has the advantage of separating carbon produced by the decomposition of methane from the liquid tin catalyst. Therefore, deactivation due to the deposition of carbon in the liquid tin can be prevented. Methane decomposition with carbon dioxide produced carbon monoxide and hydrogen. Ni was used to promote the catalyst performance and enhance the activity of the catalyst and lifetime. In this study, catalysts were synthesized using the excess wet impregnation method. The effect of the reaction temperature, space velocity was measured to calculate the activity of catalysts, such as the activation energy and regeneration of catalysts. The carbon-deposited tin catalyst regeneration temperature was 1023 K. The reactivity was improved using a nickel co-catalyst and a water supply.

• Proceedings of the KAIS Fall Conference
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• 2011.05a
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• pp.310-313
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• 2011

본 논문에서는 지구온난화의 주요원인 중의 하나인 이산화탄소를 포집하기 위한 새로운 흡수제를 연구하였다. 액상 흡수법에서 가장 중요한 핵심 기술요소는 성능과 경제성면에서 우수한 흡수제를 개발하는 것이다. 흡수평형장치인 VLE(Vapor-Liquid Equilibrium)장치를 사용하여 신규흡수제의 이산화탄소 흡수능을 평가하고 특성을 알아봄으로써 신 흡수제를 개발하고자 하였다. 기존 아민흡수제인 MEA(monoethanolamine), DEA(diethanolamine)와 비교한 결과 아미노산염 흡수제의 경우 MEA (1.108), DEA (1.105)의 이산화탄소 흡수능보다 0.15～0.2 (mol $CO_2$/mol absorbent) 더 높은 흡수능과 2.5～3배 더 빠른 겉보기 속도를 나타내는 것을 확인하였다. 본 연구를 통하여 개발된 아미노산염 흡수제가 경제적인 이산화탄소 포집공정을 구현할 수 있는 가능성을 확인하였다.

• Journal of Hydrogen and New Energy
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• v.26 no.6
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• pp.581-589
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• 2015

In this study, the viscosity of a liquid carbon dioxide ($LCO_2$) that can potentially be used in a wet feed coal gasifier was evaluated. A pressurized capillary viscometer was employed to obtain the viscosity data of $LCO_2$ using two different methods. During the first method, the measurements were conducted under quasi-steady and high pressure flow conditions where two-phase flow was greatly minimized. The viscosity of $LCO_2$ was determined using turbulent friction relationship. At the second flow condition where unsteady flow is induced, the viscosity of $LCO_2$ was measured using the half-time pressure decay data and was further compared with values calculated by the first method.