PURPOSES : This study analyzed the amount of fuel consumption and atmospheric emissions by type of asphalt concrete mixtures. METHODS : Asphalt concrete mixture was produced directly at the plant, fuel consumption was measured compared to daily production, and atmospheric emissions emitted during the production process were measured. Hot and warm asphalt mixtures were produced, and analyses were conducted according to weather conditions and production volume. RESULTS : The fuel use per ton was confirmed to reduce energy by approximately 23.5% in WMA compared to HMA due to differences in the production temperature during the production of asphalt mixtures. Additionally, HMA production yielded 1.6 times higher atmospheric emissions for CO2 and 3.8 times higher for NOx than that for WMA, indicating that CO2 and NOx emissions tended to increase as fuel consumption increased. CONCLUSIONS : When producing asphalt mixtures, the production temperature, production volume, atmospheric conditions, and site conditions have a significant impact on fuel usage and atmospheric emissions.

청정 연료인 수소를 생산하기 위해 현재 가장 널리 사용되는 기술인 증기 개질이다. 이 방법으로 생산된 수소는 일산화탄소와 같은 불순물을 함유하고 있어, 이를 연료전지와 같은 응용분야에 사용하기 위해서는 적절한 정제 과정을 반드 시 거쳐야 한다. 최근 효과적인 정제 방법으로 분리막 기술이 각광받고 있다. 본 연구에서는 수소와 일산화탄소 혼합가스에서 수소 분리 및 회수를 위해 바이오가스 고질화용(biogas upgrading) 상용 폴리설폰(polysulfone) 고분자막의 활용 가능성에 대 해서 평가하였다. 먼저, 사용한 상용막의 물리화학적 특성에 대해서 평가하였고, H2/CO를 이용하여 stage-cut, 운전압력과 같 은 다양한 조건에서의 상용막 모듈의 성능 평가를 진행하였다. 마지막으로, 평가 결과를 바탕으로 공정설계를 위한 시뮬레이 션을 진행하였다. 본 연구에서의 상용 분리막 공정의 최대 H2 투과도와 H2/CO 분리계수는 각각 361 GPU와 20.6을 기록하였 다. 또한, CO 제거 효율은 최대 94%를 나타내었으며, 생산 수소 농도는 최대 99.1%를 달성하였다.

The characteristics of pollutant emission for non-premixed flames with LCG 8000 and LCG 6000 represented as low calorific gases were investigated by numerical simulation. Commercial software (ANSYS 16.2 - FLUENT) is used to predict 2-D pollutant emission with GRI 3.0 detailed reaction mechanism. In addition, the addition of hydrogen to LCG 6000 was also considered. As result, the flame length and temperature of LHVGs were decreased with decreasing calorific value at the same condition. In addition, NO concentration was decreased as temperature decreased. However, CO concentration for LCG 8000 predicted to be slightly higher than that for methane due to the high propane concentration. In the case of LCG 6000 with added hydrogen, the flame length was the shortest and NO concentration was the highest due to the highest flame temperature, but CO concentration decreased rapidly due to the addition of the carbon-free fuel.

To test a flameproof enclosure for the safety certificate, a reference pressure of explosion needs to be determined. However, the explosion pressure may be changed according to relative humidity of explosive gases. Therefore, the guideline on relative humidity should be recommended for measuring the explosion pressure for accurate and reproducible testings. This study examined the relationship of explosion pressure with relative humidity of hydrogen (31 vol %)-air and acetylene (14 vol %)-air mixture gases. The explosion pressures were measured by increasing the relative humidity of the gases by 10 % from dry state to 80 % in a cylindrical explosion enclosure of 2.3 L. on ambient temperature and atmospheric pressure (1 atm). The maximum explosive pressures were remained almost constant until the relative humidity reached 10 % for the hydrogen-air mixture and 20 % for the acetylene-air mixture. However, the maximum explosive pressures linearly decreased as the relative humidity increased. Based on the results of the study, it would be recommended to use 10 % relative humidity for the hydrogen-air mixture and 20 % for the acetylene-air mixture as the critical value in testing a flameproof enclosure.

In this study, the combustion characteristics of low calorific gas (LCG) fuels are investigated by numerical simulation. PREMIXED code is used to predict the flame structure and NO emission with two mechanisms, which are GRI 3.0 and USC II chemical reaction mechanisms for CH4 and LCG 8000 and LCG 6000, respectively. Also, elementary reactions related with production and destruction for OH radical are studied because OH radical is dominant for burning velocity and NO emission. As results, the production and the destruction of OH radical for CH4 and LCG 8000 using GRI 3.0 are dominated by reactions of No. 4, No. 2 and No. 3 and by No. 5, No. 3 and No. 7, respectively. For LCG 6000 using USC II, reactions of No. 3, No. 4 and No. 11 and of No. 7, No. 8 and No. 12 dominates to the production and the destruction, respectively. In addition, NO emissions for LCG gas fuel are generated by thermal NO because the flame temperatures are over 1800 K.

We investigate the reduction of SnO2 and the generation of syngas(H2, CO) using methane(CH4) and hydrogen(H2) or a mixed gas of methane and hydrogen as a reducing gas. When methane is used as a reducing gas, carbon is formed by the decomposition of methane on the reduced Sn surface, and the amount of generated carbon increases as the amount and time of the supply of methane increases. However, when hydrogen is used as a reducing gas, carbon is not generated. High purity Sn of 99.8 % and a high recovery rate of Sn of 93 % are obtained under all conditions. The effects of reducing gas species and the gas mixing ratio on the purity and recovery of Sn are not significantly different, but hydrogen is somewhat more effective in increasing the purity and recovery rate of Sn than methane. When 1 mole of methane and 1 mole of hydrogen are mixed, a product gas with an H2/CO value of 2, which is known to be most useful as syngas, is obtained.

기체분리막을 이용한 바이오가스 및 천연가스 등의 CH4 고질화 공정은 타 공정에 비해 경제적이라는 장점이 있지만 필수적으로 CH4 손실이 발생하는 단점이 있다. 이는 CO2에 의한 가소화현상으로 CH4의 투과도가 증가하기 때문이다. 이러한 현상을 개선하고자 CO2 가소화에 대한 영향이 적은 Cellulose계열의 고분자를 이용하여 고선택도 멤브레인을 제막하였으며, 이를 이용하여 CH4 고질화를 위한 연구를 하였다. CO2, CH4, N2, O2 등 단일가스를 이용하여 CA기반의 8종의 고선택도 중공사막에 선택도와 투과도를 측정하였다. CO2/CH4 혼합가스 분리 테스트를 수행하였다.

The autoignition characteristics of n-heptane/n-butanol were investigated both experimentally and numerically. The effects of oxygen concentration and exhaust gas recirculation rate on the autoignition characteristics were evaluated. A rapid compression machine was employed to measure ignition delay times of blended fuels. A numerical study on the ignition delay time was performed using the CHEMKIN-PRO software to calculate ignition delay time and predict the chemical species in the combustion process. The results revealed that the ignition delay time increased with decreasing oxygen concentration due to the thermal load effect of nitrogen. The oxidation reaction of n-heptane in a low temperature regime was limited with decreasing oxygen concentration. The ignition delay time sharply decreased with exhaust gas recirculation because of the intermediate species in the exhaust gas. Exhaust gas recirculation reduced first ignition delay dramatically. However, the time interval between the first and main ignition increased with increased exhaust gas recirculation.