• 한국화재소방학회논문지
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• 제16권3호
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• pp.77-83
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• 2002

질소, 아르곤, 이산화탄소와 같은 불활성가스 및 이들의 혼합물을 소화약제로 하여 n-Heptane을 연료로한 cup-burner test 장치에서 불꽃소화농도와 연소시 배가스의 조성을 측정하였다. 이성분 불활성가스계 혼합소화약제의 소화농도는 혼합물의 구성비를 이용한 모델에 의해 잘 예측됨을 알 수 있었다. 불활성 가스계 혼합 소화약제에 의한 소화작용에 있어서 혼합가스의 평균비중이 클수록 소화 성능이 우수하였다. 또한 밀폐된 공간의 구조가 소화에 영향을 미칠 수 있음을 확인하였다. 연소시 배가스 중 이산화탄소 조성은 사용하는 소화약제의 양이 증가할수록 감소하였다. 일산화질소 발생은 소화약제의 질소 함량과는 상관이 없으며 공기유량을 크게 하여 불꽃을 크게 했을 때 검출되었다.

• 한국수소및신에너지학회논문집
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• 제27권6호
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• pp.727-736
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• 2016

Numerical simulations of n-heptane spray characteristics in a constant volume combustion chamber under diesel engine like conditions with increasing ambient gas density ($14.8-142kg/m^3$) and ambient temperature (800-1000 K) respectively were performed to understand the non-vaporizing and vaporizing spray behavior. The effect of fuel temperature (ranging 273-313 K) on spray characteristics was also simulated. In this simulation, spray modeling was implemented into ANSYS FORTE where the initial spray conditions at the nozzle exit and droplet breakups were determined through nozzle flow model and Kelvin-Helmholtz/Rayleigh-Taylor (KH-RT) model. Simulation results were compared with experimentally obtained spray tip penetration result to examine the accuracy. In case of non-vaporizing condition, simulation results show that with an increment of the magnitude of ambient gas density and pressure, the vapor penetration length, liquid penetration length and droplet mass decreases. On the other hand vapor penetration, liquid penetration and droplet mass increases with the increase of ambient temperature at the vaporizing condition. In case of lower injection pressure, vapor tip penetration and droplet mass are increased with a reduction in fuel temperature under the low ambient temperature and pressure.

• 한국대기환경학회지
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• 제9권2호
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• pp.140-146
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• 1993

CoMo, NiMo/ZSM-5 catalysts were prepared at Si/Al ratios of 100, 200 and characterized by TGA, XRD and SEM. Simultaneous hydrocracking of n-heptane and hydrodesulfurization of DBT were studied over these catalysts at the ranges of temparatures between 400$^\circ$C and 500$^\circ$C, pressure of 30 $\times 10^5$ Pa and contact time of 0.02g cat. hr/ml feed in a fixed bed flow reactor. It was shown that the hydrocracking activity of n-heptane increased in the order of NM 100, CM 100, NM 200 and CM 200 catalysts. It was also shown that the Hydrodesulfurization activity of DBT increased in the order of CM 200, NM 200, CM 100 and NM 100 catalysts and these results were thought to be that the increase of acidity of catalysts might increase hydrocracking activity of these catalysts but deactive those simultaneously. In this study it was shown that CM 100 and NM 200 were active catalysts in simultaneous hydrodesulfurization of DBT and hydrocracking of n-heptane reactions.

• 한국자동차공학회논문집
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• 제10권1호
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• pp.76-83
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• 2002

Mathematically and chemically simplified reaction scheme for n(heptane that simulates autoignitions of the end gases in spark ignition engines has been developed and studied computationally. The five(equation model is described, to predict the essential features of hydrocarbon oxidation. This scheme has been calibrated against autoignition delay times measured in rapid compression machines. The rate constants, activation temperatures, Ta, Arrhenius pre-exponential constants, A, and heats of reaction for stoichiometric nheptane/air has all been optimized. Comparisons between computed and experimental autoignition delay times have validated the present simplified reaction scheme. The influences of heat loss and concentration of chain carrier at the beginning of compression upon autoignition delay times have been computationally investigated.

• 한국연소학회지
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• 제17권2호
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• pp.9-16
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• 2012

Iso-octane, n-heptane and their blends were tested in a constant volume combustion chamber to measure laminar flame speeds. The experimental apparatus was automatically controlled to enhance the accuracy and data acquisition speed. A large database of laminar flame speeds at elevated temperatures and pressures was established. From this database, laminar flame speeds of iso-octane, n-heptane and their blends were investigated and analysed to derive new correlation to predict laminar flame speeds at any blending ratio. The new flame speed model was successfully applied to these fuels with limited range of errors.

• 한국가스학회지
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• 제3권3호
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• pp.34-38
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• 1999

초산의 회합성을 설명할 수 있는 모델식을 비교 제안하기 위해 298.15K와 318.15K의 실험치 자료를 화학적 이론이 고려된 전개식과 일반적인 기액 평형식에 Margules, Wilson, NRTL식을 각각 적용하여 계산한 값들을 서로 비교하였다. 회합성이 고려된 모델식을 적용하여 계산한 값이 실험치와 잘 일치하였다.

• 대한안전경영과학회지
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• 제4권3호
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• pp.35-43
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• 2002

For the unconfined vapor cloud explosion accident by the continuous release of gas-liquid flow of various saturated liquids in a vessel at ground level, overpressures were estimated and analyzed with various release conditions and materials by TNT equivalency model with vapor dispersion. We found that at same release conditions, overpressure showed n-heptane > xylene > n-hexane > toluene > n-heptane > benzene, respectively and that overpressure was increased with increasing the hole diameter and the storage pressure, but it was increased with decreasing the wind speed, the interested distance, and the vessel thickness.

• Korean Chemical Engineering Research
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• 제43권2호
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• pp.259-265
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• 2005

Water+n-methylformamide(NMF), benzene+NMF 그리고 toluene+NMF의 353.15 K 이성분계 등온 기-액상평형을 headspace gas chromatography(HSGC)로 측정하였고, NMF+benzene+n-heptane과 NMF+toluene+n-heptane 삼성분계에 대한 298.15 K 액-액상평형을 tie-line 측정법으로 결정하였다. 이성분계 기-액상평형 데이터는 공비점이 없었으며, $g^E$ 모델식(Margules, van Laar, Wilson, NRTL, UNIQUAC)에 비교적 작은 편차로 잘 상관되었다. 삼성분계 tie-line 데이터는 NRTL식과 UNIQUAC식을 이용하여 상관과 추산을 병행하였으며, Hirata-Fujita식과 Maior-Swenson식을 이용하여 정확도를 검증하였다.

• 한국화재소방학회:학술대회논문집
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• 한국화재소방학회 2010년도 추계학술발표회 자료집
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• pp.246-250
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• 2010

• 한국식품위생안전성학회지
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• 제12권2호
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• pp.132-140
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• 1997

Additives in plastics are capable of migrating from the packaging materials into the foodstuffs, thereby presenting a source of contamination and a potential health risk to the consumer. The migration from packaging materials into foodstuffs is first of all regulated by examining the amounts of global and specific migrated components. Besides, there is worldwide still a need for practical methods for measuring and monitoring migration from polymers, especially for the testing of migration into fatty foodstuffs. Therefore, these studies were undertaken to investigate the safety status of domestic plastic packaging materials with respect to migration. Another objective of this study was to examine the applicability of ethanol as an alternative fatty food simulant substituting for olive oil and n-heptane. The evaporation residues for various dometic plastic samples determined as described in Korean food laws were in the level from 4.3 to 14.5 mg/$\ell$, which were much lower than the limit value of 150 mg/$\ell$. The global migration values into 95 % ethanol showed to be comparable to those into n-heptane, while the olive oil migration values were comparably higher than those into ethanol or n-heptane and moreover they were not reproducible. The kinetic migration begavior of additives in polyolefin samples into 95% ethanol showed a Fickian diffusion process. The results of these studies on global migration and kinetic testings demonstrate that the ethanol could be successfully substitute for the olive oil and n-heptane as an alternative fatty food simulant, at least in contact with polyoefins.