• Title/Summary/Keyword: Flue-gas

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Low-Temperature Combustion of Ethanol over Supported Platinum Catalysts (백금 담지 촉매상에서 에탄올의 저온연소)

  • Kim, Moon Hyeon
    • Journal of Environmental Science International
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    • v.26 no.1
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    • pp.67-78
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    • 2017
  • Combustion of ethanol (EtOH) at low temperatures has been studied using titania- and silica-supported platinum nanocrystallites with different sizes in a wide range of 1~25 nm, to see if EtOH can be used as a clean, alternative fuel, i.e., one that does not emit sulfur oxides, fine particulates and nitrogen oxides, and if the combustion flue gas can be used for directly heating the interior of greenhouses. The results of $H_2-N_2O$ titration on the supported Pt catalysts with no calcination indicate a metal dispersion of $0.97{\pm}0.1$, corresponding to ca. 1.2 nm, while the calcination of 0.65% $Pt/SiO_2$ at 600 and $900^{\circ}C$ gives the respective sizes of 13.7 and 24.6 nm when using X-ray diffraction technique, as expected. A comparison of EtOH combustion using $Pt/TiO_2$ and $Pt/SiO_2$ catalysts with the same metal content, dispersion and nanoparticle size discloses that the former is better at all temperatures up to $200^{\circ}C$, suggesting that some acid sites can play a role for the combustion. There is a noticeable difference in the combustion characteristics of EtOH at $80{\sim}200^{\circ}C$ between samples of 0.65% $Pt/SiO_2$ consisting of different metal particle sizes; the catalyst with larger platinum nanoparticles shows higher intrinsic activity. Besides the formation of $CO_2$, low-temperature combustion of EtOH can lead to many other pathways that generate undesired byproducts, such as formaldehyde, acetaldehyde, acetic acid, diethyl ether, and ethylene, depending strongly on the catalyst and reaction conditions. A 0.65% $Pt/SiO_2$ catalyst with a Pt crystallite size of 24.6 nm shows stable performances in EtOH combustion at $120^{\circ}C$ even for 12 h, regardless of the space velocity allowed.

The effect of moisture on SCR reaction of NMO (Natural Manganese Ore) (천연망간광석 SCR 반응에서 수분의 영향)

  • Kim, Sungsu;Hong, Sungchang
    • Applied Chemistry for Engineering
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    • v.18 no.4
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    • pp.350-355
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    • 2007
  • The effect of moisture in flue gas on SCR reaction of NMO (Natural Manganese Ore) was studied. The experiments were performed over NMO with NO, $NH_3$ at independent condition or simultaneous condition. $NH_3$ can be oxidized at low temperature by the lattice oxygen in NMO catalyst. The concentration of NO and $NO_2$ by $NH_3$ oxidation with moisture is higher above $300^{\circ}C$ than that without moisture. Moisture would competitively adsorb with NO and $NH_3$ on NMO catalyst. It caused poor NOx conversion to compete against $H_2O$. Besides the NOx conversion efficiency was reduced at below $250^{\circ}C$ because of the dipped $H_2O$ competitively adsorbed $NH_3$. The reactivity of NMO varied with the calcination temperature and the optimum calcination temperature was $400^{\circ}C$ regardless $H_2O$.

Absorptive Separation of Sulfur Dioxide using Flat Membrane Contactor (평판형 분리막 접촉기를 이용한 이산화황 흡수 분리)

  • Lee Yong-Taek;Lee Young-Jin;Song In-Ho;Jeon Hyun-Soo;Ahn Hyo-Seong;Lee Hyung-Keun
    • Membrane Journal
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    • v.16 no.3
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    • pp.196-203
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    • 2006
  • A flue gas emission known to cause an acid rain, containing sulfur dioxide, is tightly controlled by a regulation. The membrane contactor could be one of the alternatives which might be useful technologies for better performance of desulfurization. The fundamental sulfur dioxide separation data were obtained by a flat membrane contactor so that they could be utilized for the full scale membrane contactor. The separation of sulfur dioxide was measured in terms of the concentration of NaOH absorbent, the concentration of sulfur dioxide, the feed flow rate and different membrane materials. As the concentration of absorbent increased, the removal efficiency increased. By increasing the concentration of sulfur dioxide, the removal efficiency decreased. As the feed flow rate increased, it was observed that the removal efficiency decreased. Finally, the effect of the membrane material on separation was found to be negligible.

Development of a Hot Water Boiler System with a Rice Hull Furnace (왕겨 연소기(燃燒機)를 이용(利用)한 온수(溫水)보일러 시스템 개발(開發) (I) -실험적(實驗的) 연구(硏究)-)

  • Lee, Y.K.;Park, S.J.;Baek, P.K.;Noh, S.H.
    • Journal of Biosystems Engineering
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    • v.12 no.4
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    • pp.31-43
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    • 1987
  • This study was performed to develop a hot water boiler system with small scale automatic rice hull furnace for the multi-purpose use in the farm. For the experiment a prototype hot water boiler system with rice hull furnace was fabricated, which was equipped with automatic hull feeder, igniter and ash removal device. Optimum operational conditions of the prototype: system were analyzed. The results arc summarized as follows. 1. The temperature measured right above the burning surface should be higher than $500^{\circ}C$ combustion. 2. The top zone of the combustion chamber was the most suitable location of the thermocouple to pick up the control temperature for the automatic operation of the rice hull furnace. 3. The content of carbon monoxide in the flue gas was increased with the filling height of burning material but it was less than 0.3 percent in volume in this experiment. When the filling height was expressed as the ratio of rice hull feed rate to the volume of the combustion chamber above the burning surface, the optimum ratio was about $150kg/m^3-h$. 4. The combustion efficiency of the prototype was higher than 95 percent when the feed rate was 1.1 to 2.3 kg/h and moisture content of rice hull was 22.4 percent (w.b.) or less. 5. It was estimated that the optimum operational conditions of the system were 1.3 to 2.0 kg/h in feed rate, 70 to 100 percent in excess air and 500 to $510^{\circ}C$ in control temperature. 6. The efficiency of coil heal exchanger increased with a decrease in feed rate of rice hull. When the rice hull feed rates were 1.1, 1.7 and 2.3 kg/h, the efficiencies of coil heat exchanger were about 34, 30 and 25 percent and heat transfer rates were 5.7, 7.6 and 8.8 MJ/h, respectively. When the flat plate heat exchanger was used in addition to the coil heat exchanger, the efficiency of the heat exchanger system increased to 48 percent.

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A Study on a Process for Conversion of Carbon Dioxide through Saline Water Electrolysis (염수 전기분해와 연계한 이산화탄소의 전환 공정 연구)

  • Lee, Dong Woog;Lee, Ji Hyun;Lee, Junghyun;Kwak, No-Sang;Lee, Sujin;Shim, Jae-Goo
    • Korean Chemical Engineering Research
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    • v.55 no.1
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    • pp.86-92
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    • 2017
  • A process, which converts carbon dioxide contained in the flue gas of coal-fired power plants to sodium bicarbonate, was studied experimentally and numerically. In this process, the carbon dioxide reacts with sodium hydroxide which is produced through saline water electrolysis. A bench scale reactor system was prepared for experiments of this process and numerical process modeling was performed for the bench scale reactor system. Comparing the process modeling results with the experimental data, responsibility of the process modeling was confirmed. Using this model, commercial scale process was simulated. Mass and energy balance of this process were calculated. Temperature profile in the reactor and carbon dioxide removal rate were obtained.

Combustion Characteristics of Waste Sewage Sludge using Oxy-fuel Circulating Fluidized Bed (슬러지 순산소 유동층 연소특성)

  • Jang, Ha-Na;Sung, Jin-Ho;Choi, Hang Seok;Seo, Yong-Chil
    • Korean Chemical Engineering Research
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    • v.55 no.6
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    • pp.846-853
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    • 2017
  • Cold bed and $30kW_{th}$ pilot bed tests using circulating fluidized bed (CFB) were conducted to apply oxy-fuel technology for waste sludge combustion as a carbon capture and storage technology. In cold bed test, the minimum fluidization velocity ($u_{mf}$) and superficial velocity for fast fluidization was determined as 0.120 m/s and 2.5 m/s, respectively. In the pilot test, air and oxy-fuel combustion experiments for waste sludge were conducted using CFB unit. The flue-gas temperature in 21~25% oxy-fuel combustion was higher than that of air and up to 30% oxy-fuel combustion. In addition, the concentration of carbon dioxide was more than 80% with the oxygen injection range from 21% to 25% in oxy-fuel CFB waste sludge combustion.

Effects of Sulfuric Acid Concentration and Alloying Elements on the Corrosion Resistance of Cu-bearing low Alloy Steels

  • Kim, Ki Tae;Kim, Young Sik
    • Corrosion Science and Technology
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    • v.17 no.4
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    • pp.154-165
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    • 2018
  • During the process of sulfur dioxide removal, flue gas desulfurization equipment provides a serious internal corrosion environment in creating sulfuric acid dew point corrosion. Therefore, the utilities must use the excellent corrosion resistance of steel desulfurization facilities in the atmosphere. Until now, the trend in developing anti-sulfuric acid steels was essentially the addition of Cu, in order to improve the corrosion resistance. The experimental alloy used in this study is Fe-0.03C-1.0Mn-0.3Si-0.15Ni-0.31Cu alloys to which Ru, Zn and Ta were added. In order to investigate the effect of $H_2SO_4$ concentration and the alloying elements, chemical and electrochemical corrosion tests were performed. In a low concentration of $H_2SO_4$ solution, the major factor affecting the corrosion rate of low alloy steels was the exchange current density for $H^+/H_2$ reaction, while in a high concentration of $H_2SO_4$ solution, the major factors were the thin and dense passive film and resulting passivation behavior. The alloying elements reducing the exchange current density in low concentration of $H_2SO_4$, and the alloying elements decreasing the passive current density in high concentration of $H_2SO_4$, together play an important role in determining the corrosion rate of Cu-bearing low alloy steels in a wide range of $H_2SO_4$ solution.

Estimation of Washing Duration of Desulfurized Absorber in a Heavy Oil Power Plant (중유화력발전소 탈황 흡수탑 세정시기예측)

  • Jang, Yeong Gi;Yoo, Hoseon
    • Plant Journal
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    • v.12 no.1
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    • pp.24-28
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    • 2016
  • In desulfurization facilities of oil-fired power plant, gypsum scale is attached in the absorber inner surface as the operating time increases. For this reason, the maximum possible load of the power generation is set down, resulting in further generation stop. Cleaning of absorber for scale removal can be determined at the time of setting down of the maximum possible load. In this study, 6 weeks before the maximum possible load of the power generation was down set, at the same time and desulfurization facilities outlet $SO_2$ concentration value was more than 130ppm, absorber differential pressure exceeded $380mmH_2O$, it was confirmed to be the time that has elapsed 44 weeks after the previous absorber cleaning. Cleaning time of the absorber was predicted to be a time which has elapsed 50 weeks from the previous cleaning time.

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Reaction Characteristics of Elemental and Oxidized Mercury with Fly Ash Components (비산재 성분과 원소 및 산화수은의 반응특성)

  • Lee, Sang-Sup;Kim, Kwang-Yul;Oh, Kwang-Joong;Jeon, Jun-Min;Kang, Dong-Chang
    • Clean Technology
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    • v.19 no.4
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    • pp.453-458
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    • 2013
  • Fly ash has capacity to oxidize or adsorb mercury in a flue gas. Mercury oxidation and adsorption efficiencies of fly ash vary depending on the properties of fly ash. This study was designed to understand reaction characteristics of mercury with fly ash components. The fly ash components were tested to determine their oxidation and adsorption capabilities for elemental mercury and oxidized mercury. A sample was synthesized with fly ash components and tested. The test results were compared with those of the fly ash sample obtained from a coal-fired power plant. $Fe_2O_3$, CuO and carbon black showed higher oxidation or adsorption efficiency for elemental mercury while CaO, MgO, CuO and carbon black showed higher adsorption efficiency for mercury chloride. In addition, the synthesized sample showed comparable mercury oxidation and adsorption efficiencies to the fly ash sample.

Removal of Carbon Monoxide from Anthracite Flue Gas by Catalytic Oxidation (I) (촉매반응에 의한 연탄 연소가스로부터 일산화탄소의 제거 (제1보))

  • Chung Ki Ho;Lee, Won Kook
    • Journal of the Korean Chemical Society
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    • v.20 no.5
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    • pp.431-437
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    • 1976
  • On the condition of adequate air supply, complete removal of carbon monoxide,occurred above $650^{\circ}C$. Using catalysts, the oxidation of carbon monoxide occurred at lower temperatures; on both $MnO_2 \;and\;30%\;MnO_2-70%\;CuO\;at\;250{\circ}C,\;on\;CuO\;at\;450{\circ}C,\;on\;50%\;MnO_2-50%\;CuO\;at\;200{\circ}C,\;and\;on\;70%\;MnO_2-30%\;CuO\;at\;180{\circ}C$. Manganese dioxide (p-type) showed higher activity than cupric oxide (n-type) and a catalyst consisting of 60% $MnO_2-40%$ CuO had the highest activity of all the $MnO_2$-CuO mixture. Over the range of transitional temperature, carbon monoxide removal efficiency decreased linearly with increasing inlet carbon monoxide concentration while temperature was fixed. Residence time of gases in the catalytic reactor, in the range of 0.9 to 1.8 seconds, gave no effect on carbon monoxide conversion.

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