• Nuclear Engineering and Technology
• /
• 제48권4호
• /
• pp.893-905
• /
• 2016

Numerous advanced reactor concepts have been proposed to replace light water reactors ever since their establishment as the dominant technology for nuclear energy production. While most designs seek to improve cost competitiveness and safety, the implausibility of doing so with affordable materials or existing nuclear fuel infrastructure reduces the possibility of near-term deployment, especially in developing countries. The organic nuclear concept, first explored in the 1950s, offers an attractive alternative to advanced reactor designs being considered. The advent of high temperature fluids, along with advances in hydrocracking and reforming technologies driven by the oil and gas industries, make the organic concept even more viable today. We present a simple, cost-effective, and safe small modular nuclear reactor for offshore underwater deployment. The core is moderated by graphite, zirconium hydride, and organic fluid while cooled by the organic fluid. The organic coolant enables operation near atmospheric pressure and use of plain carbon steel for the reactor tank and primary coolant piping system. The core is designed to mitigate the coolant degradation seen in early organic reactors. Overall, the design provides a power density of 40 kW/L, while reducing the reactor hull size by 40% compared with a pressurized water reactor while significantly reducing capital plant costs.

• Bulletin of the Korean Chemical Society
• /
• 제35권12호
• /
• pp.3576-3582
• /
• 2014

Zeolite-templated carbons (ZTCs), which have high specific surface area, were prepared by a conventional templating method using microporous zeolite-Y for catalyst supports in direct methanol fuel cells. The ZTCs were synthesized at different temperatures to investigate the characteristics of the surface produced and their electrochemical properties. Thereafter, Pt-Ru was deposited at different carbonization temperatures by a chemical reduction method. The crystalline and structural features were investigated using X-ray diffraction and scanning electron microscopy. The textural properties of the ZTCs were investigated by analyzing $N_2$/77 K adsorption isotherms using the Brunauer-Emmett-Teller equation, while the micro- and meso-pore size distributions were analyzed using the Barrett-Joyner-Halenda and Harvarth-Kawazoe methods, respectively. The surface morphology was characterized using transmission electron microscopy and inductively coupled plasma-mass spectrometry. The electrochemical properties of the Pt-Ru/ZTCs catalysts were also analyzed by cyclic voltammetry measurements. From the results, the ZTCs carbonized at $900^{\circ}C$ show the highest specific surface areas. In addition, ZTC900-PR led to uniform dispersion of Pt-Ru on the ZTCs, which enhanced the electro-catalytic activity of the Pt-Ru catalysts. The particle size of ZTC900-PR catalyst is about 3.4 nm, also peak current density from the CV plot is $12.5mA/cm^2$. Therefore, electro-catalytic activity of the ZTC900-PR catalyst is higher than those of ZTC1000-PR catalyst.

• 한국신재생에너지학회:학술대회논문집
• /
• 한국신재생에너지학회 2010년도 춘계학술대회 초록집
• /
• pp.139-139
• /
• 2010

LSM is widely used as a cathode material in SOFC, because of its high electrochemical activity, good stability and compatibility with YSZ electrolyte at high temperature. However, LSM in traditional cathode materials will not generate a satisfactory performance at intermediate temperature. In order to reduce the polarization resistance of cell with the operating temperature of SOFC system, the cathode material of LSCF is one of the most suitable electrode materials because of its high mixed ionic and electronic conductivity. In this report, cathode material, $La_{0.6}Sr_{0.4}Co_{0.2}Fe_{0.8}O_3$ powder for intermediate temperature SOFC was synthesized by Pechini method using the starting materials such as nitrate of La, Sr, Co and Fe including ethylene glycol, etc. As a result, the synthesized powder that calcined above $700^{\circ}C$ exhibits successfully perovskite structure, indicating phase-pure of LSCF. Moreover, the particle size, surface area, crystal structure and morphology of the synthesized oxide powders were characterized by SEM, XRD, and BET, etc. In order to evaluate the electrochemical performance for the synthesized powder, slury mixture using the synthesized cathode material was coated by screen-printing process on the anode-supported electrolyte which was prepared by a tape casting method and co-sintering. Finally, electrochemical studies of the SOFC unit cell, including measurements such as power density and impedance, were performed.

• 한국자동차공학회논문집
• /
• 제22권5호
• /
• pp.116-125
• /
• 2014

Pyrolysis oil (PO), derived from biomass through fast pyrolysis process have the potential to displace significant amounts of petroleum fuels. The PO derived from wood has been regarded as an alternative fuel to be used in diesel engines. However, the use of PO in a diesel engine is very limited due to its poor properties like low energy density, low cetane number, high acidity and high viscosity of PO. Therefore, one of the easiest way to adopt PO to diesel engine without modifications is blended with other fuels that have high centane number. However, PO that has high amount of polar chemicals is immiscible with non polar hydrocarbons of diesel or biodiesel. Thus, to stabilize a homogeneous phase of diesel/biodiesel-PO blends, a proper surfactant should be used. Nevertheless, PO which was produced from different biomass type have varied characteristics and this complicates the selection of a suitable additive for a specific PO-diesel emulsion. In this regard, a more simple approach such as the use of a co-solvent like ethanol or butanol to induce a more stable phase of the PO-diesel mixture could be a promising alternative. In this study, a diesel engine operated with diesel/biodiesel-PO-butanol blends was experimentally investigated. Performance and gaseous & particle emission characteristics of a diesel engine were examined under the engine loads of IMEP 0.2 ~ 0.8MPa.

• 한국재료학회지
• /
• 제28권11호
• /
• pp.640-645
• /
• 2018

The design of non-precious electrocatalysts with low-cost, good stability, and an improved oxygen reduction reaction(ORR) to replace the platinium-based electrocatalyst is significant for application of fuel cells and metal-air batteries with high energy density. In this study, we synthesize iron-carbide($Fe_3C$) embedded nitrogen(N) doped carbon nanofiber(CNF) as electrocatalysts for ORRs using electrospinning, precursor deposition, and carbonization. To optimize electrochemical performance, we study the three stages according to different amounts of iron precursor. Among them, $Fe_3C$-embedded N doped CNF-1 exhibits the most improved electrochemical performance with a high onset potential of -0.18 V, a high $E_{1/2}$ of -0.29 V, and a nearly four-electron pathway (n = 3.77). In addition, $Fe_3C$-embedded N doped CNF-1 displays exellent long-term stabillity with the lowest ${\Delta}E_{1/2}=8mV$ compared to the other electrocatalysts. The improved electrochemical properties are attributed to synergestic effect of N-doping and well-dispersed iron carbide embedded in CNF. Consequently, $Fe_3C$-embedded N doped CNF is a promising candidate for non-precious electrocatalysts for high-performance ORRs.

• 한국분무공학회지
• /
• 제27권2호
• /
• pp.84-93
• /
• 2022

To implement carbon-neutrality in transportation sectors until 2050, hydrogen is considered a promising fuel for internal combustion engines because hydrogen does not contain carbon itself. Although hydrogen does not emit CO₂ emission from its combustion process, the low energy density in a volume unit hinders the adoption of hydrogen. Therefore, the understanding of hydrogen jet behavior and measurement of equivalence ratio must be conducted to completely implement the high-pressure hydrogen direct injection. The main objective of this research is feasibility test of hydrogen local equivalence ratio measurement by laser-induced breakdown spectroscopy (LIBs). To visualize the macroscopic structure of hydrogen jet, high-speed schlieren imaging was conducted. Moreover, LIBs has been adopted to validate the feasibility of hydrogen local equivalence ratio measurement. The hydrogen injection pressure was varied from 4 MPa to 8 MPa and injected in a constant volume chamber where the ambient pressure was 0.5 MPa. The increased injection pressure extends the vertical penetration of hydrogen jet. Due to the higher momentum supply when the injection pressure is high, the hydrogen has easily diffused in all directions. As the laser trigger timing has delayed, the low hydrogen atomic emission was detected due to the longer mixture formation time. Based on equivalence ratio measurement results, LIBs could be applied as a methodology for hydrogen local equivalence ratio measurement.

• 대한환경공학회지
• /
• 제36권11호
• /
• pp.758-763
• /
• 2014

토양 내에서 유기성 오염물질은 혐기성 미생물에 의해 분해되지만 전자수용체의 부족으로 상당량이 토양에 잔류하게 된다. 토양미생물연료전지(soil microbial fuel cells, SMFC)는 전극을 통해 전자 소비를 증진시켜 유기물 분해를 촉진시키고 동시에 전력도 생산하기 때문에, 다양한 유기성 오염원으로 오염된 토양을 환경 친화적으로 복원시킬 수 있는 기술로서 많은 관심을 받고 있다. 본 연구에서는 전극간 거리와 전극 크기가 SMFC의 전기적 성능에 미치는 영향을 연구하였다. 유기물이 풍부한 토양과 인공폐수 혼합물을 이용하여 SMFC를 단일반응조로 구성하였다. SMFC에서 발생된 전력량은 전극간 거리가 멀어지거나 전극 크기가 작아질수록 내부저항이 증가하여 감소하였다. 전극 크기는 $64cm^2$로 고정하고 전극간 거리는 4~9 cm로 변화를 주었을 때, 전극간 거리가 4 cm 조건에서 최대전압 326 mV, 최대전력밀도 $19.5mW/m^2$가 얻어졌고 거리가 멀어질수록 전압발생량은 19~32% 감소하고 최대전력밀도는 56~69% 감소하는 것으로 나타났다. 전극 크기 변화 실험에서는 전극간 거리를 4 cm로 고정하고 전극 크기를 $16{\sim}64cm^2$로 변화를 주었다. 두 전극 크기가 $64cm^2$ 조건에서 최대전압 291 mV, 최대전력밀도 $0.34mW/m^3$로 측정되었으며 산화전극 크기가 작아지면, 최대전압은 19~29% 감소하였고, 환원전극의 경우는 3~12% 감소하였다. 최대전력밀도는 산화전극이 작아지면, 49~68% 감소하였고, 환원전극이 작아지는 경우에는 29~47% 감소하였다. SMFC는 인공폐수와 토양 혼합물질을 반응기 내부물질로 사용하기 때문에, 전자 및 이온전달속도가 느려 환원전극 크기에 비해 산화전극 크기에 더 많은 영향을 받는 것으로 판단된다.

• 마이크로전자및패키징학회지
• /
• 제14권1호
• /
• pp.49-53
• /
• 2007

직접 메탄올 연료전지는 간단한 구조와 디자인 그리고 높은 에너지 밀도와 에너지 변환 효율등의 장점으로 인하여 휴대용 장치들의 전력원으로 사용된다. 본 논문에서는 직접 메탄올 연료전지의 연료 농도를 감지하기 위한 얇은 나피온 막과 Pt 촉매전극의 합성으로 만들어진 메탄을 센서를 제작하였다. 제작된 메탄을 센서를 사용하여 메탄올 농도와 촉매전극(Pt)의 두께 변화에 따른 전류-전압 특성을 분석하였다. Pt 촉매전극 10nm, 전압이 1V 이고 메탄올 농도 1, 2, 3M일 때 전류 값이 각각 $1.30{\times}10^{-6}A,\;1.96{\times}10^{-6}A,\;2.80{\times}10^{-6} A$ 이었다. 메탄올 농도를 2M로 고정하고 촉매전극의 두께를 5, 10, 15nm로 변화시켰을 때 전류 값은 각각 $3.06{\times}10^{-6}A,\;1.96{\times}10^{-6}A,\;1.00{\times}10^{-6}A$ 이었다. 촉매전극이 얇을수록 전류가 증가하고 전기화학반응이 더 활발히 일어나는 것으로 사료된다.

• 한국가스학회지
• /
• 제27권3호
• /
• pp.1-10
• /
• 2023

산업혁명의 발달로 인해 급격하게 증가된 온실가스 배출량을 저감하기 위해 배기 배출물 규제가 계속해서 강화되고 있다. 이를 만족시키기 위해선 친환경 연료의 사용은 필수적이다. 미래의 친환경 연료로서 수소가 주목받고 있지만, 물질적 특성으로 인해 취급과 보관에 큰 어려움을 겪고 있어, 이에 대안으로 암모니아가 제안되었다. 암모니아는 수소 대비 상온 조건에서 쉽게 액화가 가능하며, 에너지밀도가 높다. 이에 엔진의 연료로서 암모니아의 적용성을 검토하기 위해 직접분사식 암모니아 전소 엔진에서 연소제어인자의 변경에 따른 실험을 진행하였다. 본 실험은 점화시기(Spark Timing)와 공기과잉률(Excess Air Ratio) 두 개의 변수를 변경하여 실험을 진행하였다.엔진 속도 1,500 RPM 및 중부하 이상(제동 토크 200 Nm)의 조건에서 암모니아 전소를 하였을 때, 연소 안정성과 질소산화물, 미연 암모니아 등의 배기 배출물의 경향을 관찰하였다. 연소제어인자의 최적화를 통해 암모니아만을 연료로 사용한 경우에도 안정적인 연소가 가능한 조건을 찾을 수 있었고, 향후 운전영역 확장을 위한 전략을 적용할 계획이다.

• 대한기계학회논문집B
• /
• 제38권6호
• /
• pp.501-511
• /
• 2014

바이오매스 원료로부터 급속열분해 반응을 통하여 생산되는 바이오 오일은 화석연료를 대체할 수 있는 잠재력을 가지고 있다. 하지만, 바이오 오일은 에너지 밀도와 세탄가가 낮고 점성도가 높은 연료의 한계성이 있으므로 디젤엔진에 적용하기에는 제한적이다. 따라서, 안정적인 연소를 얻기 위해서는 바이오 오일을 세탄가가 높은 연료와 유화하거나 혼합하여 사용하여야 한다. 하지만 바이오 오일과 화석연료는 극성이 달라서 서로 혼합되지 않으며 가장 손쉽게 혼합되는 연료는 알코올계 연료이다. 본 연구에서는 바이오 오일의 연료특성을 향상시키기 위하여 에탄올 연료와 혼합하였으며, 연료의 자발화 특성을 향상시키기 위하여 세탄가 향상제인 PEG 400, 2-EHN 도 첨가하였다. 또한 최대 15%의 바이오 오일이 혼합된 혼합연료를 디젤엔진에서 안정적으로 연소시키기 위하여 고압축비 피스톤도 적용하였다.