• Proceedings of the Korea Society for Energy Engineering kosee Conference
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• 2006.05a
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• pp.412-419
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• 2006

An Experimental study was conducted on $CO_{2}$ recycle combustion heating system using pure oxygen instead of conventional air as an oxidant, which is thereby producing a flue gas of mostly $CO_{2}$ and water vapor($H_{2}O$ and water vapor($H_{2}O$) and resulting in higher $CO_{2}$ concentration. The advantages of the system are not only the ability to control high temperatures characteristic of oxygen combustion with recycling $CO_{2}$ but also the possibility to reduce NOx emission in the flue gas. A small scale industrial reheating furnace simulator and specially designed variable flame burner were used to characterize the $CO_{2}$ recycle oxy-fuel combustion, such as the variations of furnace pressure, temperature and composition in the flue gas during recycle. It was found that $CO_{2}$ concentration in the flue gas was about 80% without $CO_{2}$recycle. The furnace temperature and pressure and pressure were decreased due to recycle and the NOx emission was also reduced to maintain under 100ppm.

• Proceedings of the Korea Water Resources Association Conference
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• 2011.05a
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• pp.318-318
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• 2011

자연수를 가압(4~5기압)하면서 물과 공기의 비를 4:1~3:1로 혼합하면 수체 내 초미세기포(Diameter $3{\sim}10{\mu}m$)가 발생하는데 이를 산소용해수라 하며 수질정화시설 또는 양식장 등에 널리 사용되고 있다. 산소용해수의 특징은 기포의 비표면적이 넓고 10시간 이상 포화 농도를 유지하여 수체에 잔류하는 시간이 길기 때문에, 일반 산기석을 활용한 포기나 순산소 용해 등의 타 방법과 구별된다. 산소용해수의 산소전달효율은 기존 방법과 큰 차이를 보이기 때문에 실제 적용시에는 대상수를 이용하여 산소전달계수($K_{L}a$)를 사전에 산정할 필요가 있다. 본 연구에서는 한국건설기술 연구원의 안동 수자원 환경실험센터 내 실외형 콘크리트 사각반응수조에 산소용해장치 및 확산장치를 결합한 일체형 시스템을 적용시켜 2010년 9월~2011년 1월의 5개월간 결과를 분석, 본 장치의 $K_{L}a$를 산정 후 수질정화의 활용 면에서 검토하였다. $K_{L}a$의 산정에는 다양한 방법이 이용되나 용존 산소 농도의 제어에 한계가 있는 실외 대형실험장에 적합한 Lewis and Whitman의 Two-film 이론에 근거한 정상포기법을 적용하였다. 체적 $80m^3$의 수조 내에서 현장 유지용수를 대상으로 실험한 결과 산소전달계수는 $0.324\pm0.050$/min, 포화농도는 8.64 mg $O_2$/L, 도달시간은 11 /min이 산정되었으며, 이는 기존 산기석 포기의 산소전달계수 범위인 $0.105\pm0.019$ /min보다 약 3.1배 높은 결과를 보였다. 또한, 확산장치의 수류 순환 방향 및 정도를 검토하기 위하여 실험수조에서 1m단위로 격자를 구성한 후 초음파 유속계로 실측한 결과 0.0~2.5 m/s 의 평면적 유속범위를 도출하였다. 그리고 전체 순환을 고려했을 때 용존산소는 약 8시간 후 8.64 mg $O_2$/L 값에 도달하여 안정화 되었으며, 강한 수류순환과 산소용해수에 의해 하상에 존재하는 퇴적물들의 이송 및 산화촉진을 유도하였다. 이를 근거로 실험수조의 체적과 기준 가동시간인 8시간을 적용시켰을 때, 실험구 수질은 대조구와 비교하여 COD, T-N, T-P가 모두 25~35% 개선되었다. 이 결과는 여과공정 없이 단순 순환만을 고려한 물리적 수질정화 방법의 단독 활용 가능성을 나타내며, 기존 연구에서 나타난 SOD (Sediment oxygen demand) 저감 능력을 감안할 때 향후 폐쇄성 수역의 수질관리에도 효율적으로 활용할 수 있음을 시사한다.

• Journal of the Korea Academia-Industrial cooperation Society
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• v.17 no.1
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• pp.21-27
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• 2016

Global warming due to greenhouse gas emissions is considered as a major problem worldwide, and many countries are making great efforts to reduce carbon dioxide emissions. Many technologies in post-combustion, pre-combustion and oxy-fuel combustion $CO_2$ capture have been developed. Among them, a hybrid pre-combustion $CO_2$ capture system of a water gas shift (WGS) reactor and a membrane gas separation unit was investigated. The 2 stage WGS reactor integrated high temperature shift (HTS) with a low temperature shift (LTS) was used to obtain a higher CO conversion rate. A Pd/Cu dense metal membrane was used to separate $H_2$ from $CO_2$ selectively. The performance of the hybrid system in terms of CO conversion and $H_2$ separation was evaluated using a 65% CO, 30 % $H_2$ and 5% $CO_2$ gas mixture for applications to pre-combustion $CO_2$ capture. The experiments were carried out over the range of WGS temperatures ($200-400^{\circ}C$), WGS pressures (0-20bar), Steam/Carbon (S/C) ratios (2.5-5) in a feed gas flow rate of 1 L/min. A very high CO conversion rate of 99.5% was achieved with the HTS-LTS 2 stage water gas shift reactor, and 83% $CO_2$ was concentrated in the retentate using the Pd/Cu membrane.

• Journal of Korean Society of Environmental Engineers
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• v.29 no.1
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• pp.23-30
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• 2007

The ultimate objective of this study is to develop oxygen-enriched combustion techniques applicable to the system of practical industrial boiler. To this end the combustion characteristics of lab-scale LNG combustor were investigated as a first step using the method of numerical simulation by analyzing the flame characteristics and pollutant emission behaviour as a function of oxygen enrichment level. Several useful conclusions could be drawn based on this study. First of all, the increase of oxygen enrichment level instead of air caused long and thin flame called laminar flame feature. This was in good agreement with experimental results appeared in open literature and explained by the effect of the decrease of turbulent mixing due to the decrease of absolute amount of oxidizer flow rate by the absence of the nitrogen species. Further, as expected, oxygen enrichment increased the flame temperatures to a significant level together with concentrations of $CO_2$ and $H_2O$ species because of the elimination of the heat sink and dilution effects by the presence of $N_2$ inert gas. However, the increased flame temperature with $O_2$ enriched air showed the high possibility of the generation of thermal $NO_x$ if nitrogen species were present. In order to remedy the problem caused by the oxygen-enriched combustion, the appropriate amount of recirculation $CO_2$ gas was desirable to enhance the turbulent mixing and thereby flame stability and further optimum determination of operational conditions were necessary. For example, the adjustment of burner with swirl angle of $30\sim45^{\circ}$ increased the combustion efficiency of LNG fuel and simultaneously dropped the $NO_x$ formation.

• Clean Technology
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• v.25 no.3
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• pp.245-255
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• 2019

Pressurized oxy-fuel combustion is a promising technology for $CO_2$ capture with a benefit of improving power plant efficiency compared with atmospheric oxy-fuel combustion. Prior to $CO_2$ compression in this process, a flue gas condenser (FGC) is used to remove $H_2O$ while recovering the latent heat. At the same time, the FGC has a potential for high-efficiency removal of $SO_x$ and $NO_x$ by exploiting their good solubility in water. In this study, experiments were carried out in a lab-scale, direct contact FGC under different pressures varying between 1 and 20 bar to evaluate the removal efficiency of $SO_2$ and $NO_x$ for individual gases and their mixture. In the tests for individual gases, 20% and 76% of $NO_x$ was removed at 1 bar and 10 bar, respectively. Even higher removal efficiencies were achieved for $SO_2$, and also these were maintained for longer as the pressure increased. In the tests for $SO_2$ and $NO_x$ mixture, the removal efficiency of $NO_x$ increased from 13% at 1 bar to 56% at 20 bar because of higher solubility at elevated pressures. $SO_2$ in the mixture was initially dissolved almost completely and then increased by 1,219 ppm at 1 bar and by 165 ppm at 20 bar. Overall, the removal efficiency of $SO_2$ and $NO_x$ was increased at elevated pressures, but it was lower in the mixture compared with individual gases at identical conditions because of a lower pH and associated chemical reactions in water.