• Title/Summary/Keyword: packed bed

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A Study on Degradation of Nitrogen Compounds by Biofilm Reactor Packed with Porous Media (다공성 담체를 이용한 생물막 반응조의 질소화합물 분해에 관한 연구)

  • Cho, Hae-Mi;Kim, So-Yeon;Yoon, Ji-Hyun;Han, Gee-Bong
    • Journal of Korean Society on Water Environment
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    • v.23 no.5
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    • pp.776-780
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    • 2007
  • A biofilm reactor packed with porous media was investigated for nitrogen removal of synthetic wastewater. The effect of different loading rates on the nitrification was sustained to be steady state with stable efficiency of 50~60% in the range of $0.0083{\sim}0.017gNH_4-N/gMLVSS{\cdot}day$ of F/MN ratio and $1{\sim}2kgNH_4-N/m^3{\cdot}day$ of media volumetric loading rate. However, nitrification efficiency was rapidly decreased to 25~30% as F/MN ratio and media volumetric loading rate were increased to the range of $0.025{\sim}0.034gNH_4-N/gMLVSS{\cdot}day$ and $3{\sim}4kgNH_4-N/m^3{\cdot}day$, respectively. Also the consumption rate of alkalinity was higher under 8 hours of HRT than unter 6 hours of HRT. Accordingly the influent loading rate variation by detention time with influent flow influenced more on the nitrification efficiency than the influent loading rate variation by the influent concentration did. The temperature effect on the nitrification showed 25% higher in summer than in winter as the results reported by other researchers who reported that the nitrification efficiency in biofilm showed 20% increase from 55% to 75% when the temperature was raised from $20^{\circ}C$ to $25^{\circ}C$. Denitrification with sulfur-media showed 90% removal efficiency under steady-state with no effect from the increase of influent concentration and empty bed contact time (EBCT) change such as EBCT was decreased from 8.4 hr to 4.3 hr and $NO_3-N$ loading rate was changed within the range of $0.1{\sim}0.4kgNO^3-N/m^3{\cdot}day$. Accordingly Denitrification with sulfur-media is feasible for post denitrification at the concentration less than $80mgNO^3-N/L$.

Computational Simulation of Hydrocarbon Adsorption in a Packed Column (탄화수소 흡착 컬럼의 전산모사 특성)

  • Yoo, Kyung-Seun;Lee, Su-Jung;Kim, Ji-Eun
    • Journal of the Korea Academia-Industrial cooperation Society
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    • v.21 no.3
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    • pp.10-16
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    • 2020
  • Computational simulations of adsorption columns were carried out to investigate the removal characteristics of VOCs from a laundry shop. n-Decane was selected as the representative component among the VOCs emitted, and the activity of the adsorbents, such as activated carbon, was evaluated using commercial CFD code. The mathematical framework was composed of continuity and Navier-stokes equations, and the simulation was performed using the Matlab program. The adsorption isotherms of LDF, Freundlich, and Langmuir were evaluated, and the adsorption amount of the adsorption isotherms with the adsorption parameter was compared. The simulation was carried out using a particle porosity, dispersion coefficient, particle density, bed diameter, and bed length of 0.79, 42.4 ㎠/min, 485 g/L, 2.0 cm, and 2.5 cm, respectively. The effect of the gas velocity, dispersion coefficient, and voidage on the adsorption amount was compared in the Langmuir adsorption isotherm. The simulation was carried out in the velocity range of 50 to 200 cm/min, dispersion coefficient range of 100 to 400 ㎠/min, and particle porosity range of 0.66 to 0.79. The simulation results of activated carbon with benzene coincided with the Langmuir isotherm. Three types of adsorption isotherm were compared under similar conditions, and the simulation results showed the efficient adsorption condition for hydrocarbons.

Removal of Odorants by Selective Adsorption from Natural Gas for Protection of Steam Reforming Catalyst in Fuel Cell from Sulfur Poisoning (연료전지용 개질기 촉매의 피독방지를 위한 천연가스 중의 황성분 부취제의 선택적 흡착제거)

  • Oh, Sang-Seung;Kim, Geon-Joong
    • Applied Chemistry for Engineering
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    • v.18 no.4
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    • pp.337-343
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    • 2007
  • The reforming catalyst and the electrodes in fuel cells can be poisoned by the organic sulfur compound which is added as an odorant for checking out the leakage of natural gas, and that makes a big problem of system degradation. In this study, various adsorbents, such as silica, ${\gamma}$-alumina, activated carbon, HZSM-5, Ultra-stable Y zeolite (USY), and beta zeolite (BEA), were utilized to remove tetra-hydrothiophene (THT) and tert-butylmercaptan (TBM), and to confirm the performance in the adsorption of those odorants by using a continuous adsorptive bed. The effects of Si/Al ratio of zeolites, adsorption temperature and the type of balance gas (methane or He) on the adsorption performance in the packed bed have been investigated. In addition, the competitive adsorption between TBM and THT on the adsorbents was also estimated. The result shows that H-type BEA zeolite exhibited the highest adsorption capacity for TBM and THT odorant, and the higher amount of THT was removed adsorptively on the same adsorbent than TBM. The physical and chemical adsorption of those compounds on acid sites of zeolite were confirmed by temperature programmed desorption (TPD) and infrared spectrum (IR) analyses.

Experimental Study of Steam Reforming Assisted by Catalytic Combustion in Concentric Annular Reactor (촉매연소를 이용한 동심 원관형 반응기 내의 수증기 개질 반응에 관한 실험적 연구)

  • Ghang, Tae-Gyu;Yu, Sang-Seok;Kim, Yong-Mo;Ahn, Kook-Young
    • Transactions of the Korean Society of Mechanical Engineers B
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    • v.34 no.4
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    • pp.375-381
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    • 2010
  • In this paper, the heat-transfer characteristics of steam reforming in an annular reactor are presented. Heat is supplied by the catalytic combustion of syn-gas. The thermal behaviors of exothermic and endothermic reactions in a directly coupled concentric-tube packed-bed reactor were investigated experimentally. The gas mixture supplied for catalytic combustion consisted of the off-gas emitted from MCFC anode. Methane in steam at a suitable S/C (steam-to-carbon) ratio was used in the reforming reactions. On the basis of the experimental results, a simple simulation was performed to predict the temperature profile required in the reforming side of the reactor to achieve optimum hydrogen yield. The results of this study may be utilized as reference data in future studies for further development of coupled reactors.

Research on Heat and Mass Transfer Coefficient in the Packing Layer With a Solar Desiccant Heating/Cooling System (태양열 데시컨트 냉난방시스템 중 충진층에 있어서의 열 물질전달에 관한 연구)

  • Yohana, Eflita;Choi, Kwang-Hwan;Kim, Bu-Ahn;Kim, Dong-Gyu;Paek, Ki-Dong;Kim, Ji-Won
    • Journal of the Korean Solar Energy Society
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    • v.26 no.3
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    • pp.17-24
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    • 2006
  • 최근에 에너지절약 차원에서 종래의 공조방식을 대신할 새로운 냉난방시스템 개발이 요구되고 있는데, 본 논문에서는 태양열 집열기를 이용하는 데시컨트 시스템 중 제습역할을 실질적으로 담당하는 제습기의 충진층 부분에서의 열 및 물질전달에 관한 일련의 해석 결과를 발표하고 있다. 제습과정에서 액체흡수제는 충진층에서 열 뿐만 아니라 물질전달을 수반하게 되는데, 이 결과 건물에 냉방 및 난방효과를 가져다 준다. 따라서 이 충진층의 최적 설계가시스템의 효율을 극대화하기 위해서는 무엇보다도 중요한데, 이를 위해서는 충진층에서의 열 및 물질전달 양상을 규명하여야 한다. 따라서 금번 실험에서는 공기와 액체흡수제와의 접촉면적을 넓히기 위해서 충진재로써 3cm(직경) ${\times}$ 3cm(높이)인 시판중인 플라스틱 재질을 사용하고, 실질적으로 40cm(너비)${\sim}$40cm(깊이)${\times}$40cm(높이)의 충진층을 직접 제작하여 실험을 행하였다. 그 결과, 공기측 열 및 물질전달 계수는 공기 온도와 밀접한 관계를 갖고 있으며, 또한 물질전달계수는 열전달계수와 같은 경향을 보이고 있음을 알 수 있었다.

Decomposition of Ethylene using a Hybrid Catalyst-packed Bed Plasma Reactor System (플라즈마 충진 촉매 시스템을 이용한 에틸렌 저감 연구)

  • Lee, Sang Baek;Jo, Jin-Oh;Jang, Dong Lyong;Mok, Young Sun
    • Journal of Korean Society for Atmospheric Environment
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    • v.30 no.6
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    • pp.577-585
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    • 2014
  • A series of experiments using atmospheric-pressure non-thermal plasma coupled with transition metal catalysts were performed to remove ethylene from agricultural storage facilities. The non-thermal plasma was created by dielectric barrier discharge, which was in direct contact with the catalyst pellets. The transition metals such as Ag and $V_2O_5$ were supported on ${\gamma}-Al_2O_3$. The effect of catalyst type, specific input energy (SIE) and oxygen content on the removal of ethylene was examined to understand the behavior of the hybrid plasma-catalytic reactor system. With the other parameters kept constant, the plasma-catalytic activity for the removal of ethylene was in order of $V_2O_5/{\gamma}-Al_2O_3$ > $Ag/{\gamma}-Al_2O_3$ > ${\gamma}-Al_2O_3$ from high to low. Interestingly, the rate of plasma-catalytic ozone generation was in order of $V_2O_5/{\gamma}-Al_2O_3$ > ${\gamma}-Al_2O_3$ > $Ag/{\gamma}-Al_2O_3$, implying that the catalyst activation mechanisms by plasma are different for different catalysts. The results obtained by varying the oxygen content indicated that nitrogen-derived reactive species dominated the removal of ethylene under oxygen-lean condition, while ozone and oxygen atoms were mainly involved in the removal under oxygen-rich condition. When the plasma was coupled with $V_2O_5/{\gamma}-Al_2O_3$, nearly complete removal of ethylene was achieved at oxygen contents higher than 5% by volume (inlet ethylene: 250 ppm; gas flow rate: $1.0Lmin^{-1}$; SIE: ${\sim}355JL^{-1}$).

The Effect of Sulfur/Limestone Ratio on the Efficiency of Sulfur-Utilizing Denitrification (황/석회석 충전비가 황-이용 탈질효율에 미치는 영향)

  • Shin, Hyung-Soon;Lee, Il-Su;Hwang, Yong-Yoo;Bae, Jae-Ho
    • Journal of Korean Society of Water and Wastewater
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    • v.14 no.3
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    • pp.271-280
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    • 2000
  • This study was conducted to determine the applicable loading rate and to evaluate the possibility of using limestones as an alkalinity source for the removal of ${NO_3}^{-}-N$ remaining after denitrification/nitrification process with the down-flow sulfur packed bed reactor(SPBR). The pretreated sewage was fed to SPBR. Three SPBRs were filled with elemental sulfur particles and limestones and the volumetric ratios of sulfur to limestone were 0%, 12.5% and 25% for R-0%, R-12.5% and R-25%, respectively. The applicable loading rate was evaluated increasing flow rate with influent ${NO_3}^{-}-N$ concentration of 20 mg/L. For R-0% with external alkalinity supply, denitrification efficiency was greater than 96% up to loading rate of $354.8g\;{NO_3}^{-}-N/m^3{\cdot}day$, and corresponding EBCT was 1.4hr. For R-12.5% and R-25%, where alkalinity was supplied by the limestone filled in the reactor, denitrification efficiency was greater than 94% up to loading rate of $283.8g\;{NO_3}^{-}-N/m^3{\cdot}day$, and corresponding EBCT was 1.7hr. The slightly better performance of R-12.5 compared to R-25 suggests that the volumetric sulfur to limestone ratio of 12.5% was enough for the supply of alkalinity required for sulfur-utilizing denitrification. DO was appeared not showing inhibitory effect on sulfur-utilizing denitrification. The clogging of SPBR caused by the produced gas can effectively be eliminated by regular introduction of treated water in up-flow mode.

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Effects of Mixing Condition and Filtration Velocity on Turbidity Removal in a Contact Roughing Filter (접촉여과방식 거친여과지에서 혼화조건과 여과속도가 고탁도 제거에 미치는 영향)

  • Park, Noh-Back;Park, Sang-Min;Hong, Jin-Ah;Jun, Hang-Bae
    • Journal of Korean Society of Water and Wastewater
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    • v.21 no.3
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    • pp.359-366
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    • 2007
  • Slow sand filtrations have been widely used for water treatment in small communities, however their capacity is often limited by high turbidity in the raw water. For this reason, several pre-treatment facilities were required for a slow sand filter. Turbidity removal from the highly turbid raw water was investigated in roughing filters as a pre-treatment process. The roughing filters followed by rapid mixing tank were operated in the form of a contact filtration. In several jar tests, the predetermined optimum aluminium sulfate (alum) doses for turbid water of 30 and 120NTU were 30 and 50mg/L, respectively. At the optimum alum dose, physically optimum parameters including G value of $220sec^{-1}$ and rapid mixing time of 3 minutes were applied to the contact filtration system. Without addition of alum, the filtrate turbidity from the roughing filters, packed respectively with different media such as sand, porous diatomite ball and gravel, was in the range of 5~30NTU at filtration velocities of 30 and 50m/day. However, the application of a contact filtration to roughing filters showed stably lower filtrate turbidity below 1.0NTU at filtration velocity of 30 m/day. Although the filtration velocity increased to 50m/day, filtrate turbidity was still below 1.0NTU in both single and double layer roughing filters. At influent turbidity of 120NTU, the filtrate turbidity was over 5 NTU in the triple layer roughing filter, which shortened the filter run time. The flocs larger than $10{\mu}m$, formed in the rapid mixing tank, were almost captured through the roughing filter bed, while the almost flocs smaller than $10{\mu}m$ remained in filtrate.

Biodiesel Production from Soybean Oil in Continuous Reactors (연속흐름반응기에서 바이오디젤 제조 특성 연구)

  • Kim, Deog-Keun;Lee, Jin-Suk;Park, Ji-Yeon;Park, Soon-Chul
    • 한국신재생에너지학회:학술대회논문집
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    • 2007.06a
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    • pp.589-593
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    • 2007
  • 재생 가능한 자원인 동식물성 기름을 원료로 제조되는 수송용 연료 바이오디젤은 낮은 대기오염물질 배출과 $CO_2$ Neutral 특성으로 환경친화적인 연료로 인정을 받으며 전세계적으로 그 생산량이 급격히 증가하고 있다. 대부분의 상용화 공정은 염기촉매를 이용한 전이에스테르화 반응에 근거하고 있으며 높은 생산성을 위해 연속 공정을 채택하고 있다. 원료유 중의 유리지방산(free fatty acid, FFA)은 염기 촉매와 반응하여 지방산염(Soap)과 수분을 생성하며 반응촉매의 투입양을 증가시카고 반응 후에 글리세롤과 지방산 메틸에스테르와의 분리를 어렵게 만든다. 높은 수율과 후속공정의 부하를 줄이기 위해서는 식물성 원료유 중의 FFA는 고체 산촉매 하에서 메탄올과 에스테르화 반응시켜 전환 제거되어야 한다. 본 연구에서는 고체산 촉매인 Amberlyst-15을 충전한 4단 PBR(Packed Bed Reactor, 충전율 60%(v/v))에서 반응시간과 반응온도에 따른 대두원유의 전처리 효율을 조사하였으며 최적 전처리 조건을 도출하였다. 최적 전처리 조건에서 대두원유는 초기 산가 1.6에서 0.4-0.6으로 연속 전처리할 수 있었다. 본 연구에서는 연속 흐름 반응기인 PFR(Plug Flow Reactor)와 4단 CSTR(Continuous Stirred Tank Reactor)에서 균질계 촉매인 KOH 존재하에 대두유와 메탄올과의 전이에스테르화 반응 특성을 조사하였으며 각 연속 반응시스템에서 최적 운전 조건을 도출하였다. PFR 반응기에서 반응온도, 반응시간, 반응물 흐름방향, static mixer(SM) 개수에 따른 반응특성을 조사한 결과, PFR에서의 최적 반응조건은 하향류 흐름 방향과 3개의 SM를 설치한 조건에서 반응시간 5.8분, 반응온도 90$^{\cdot}C$, 메탄올:오일 몰비 9:1, KOH 농도 0.8%로 도출되었다. CSTR 반응기에서는 반응온도와 체류시간에 따른 반응특성을 조사하였으며 최적반응 조건으로 반응온도 80$^{\cdot}C$, 메탄올/오일 몰비 9:1, KOH 농도 0.8%, 체류시간 18.4분, 교반속도 250rpm로 조사되었다.

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A Study on Preparation and Reactivity of Zinc Titanate Sorbents for H2S Removal (아연-티타늄 복합산화물 탈황제의 제조 및 반응특성 연구)

  • Kim, Ki-Seok;Park, No-Kuk;Lee, Tae-Jin
    • Applied Chemistry for Engineering
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    • v.8 no.1
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    • pp.122-131
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    • 1997
  • Zinc titanate sorbents for $H_2S$ removal were prepared and their reactivities were studied for high temperature desulfurization of coal gas. Sulfidation of zinc titanates by $H_2S$ sorption was conducted in a packed-bed tubular flow reactor at the temperature range of $550{\sim}750^{\circ}C$, and the results reveal that $650^{\circ}C$ was the optimal sulfidation temperature with respect to desulfurization efficiency and zinc loss. The structural change of sorbent particle was investigated by SEM analysis for the forbents sulfided at $650^{\circ}C$ and subsequently regenerated at $750^{\circ}C$. The stability of desulfurization capability as well as the mechanical stability of the zinc titanates was studied by means of the successive cycles of sulfidation-regeneration of sorbents, and the sorbent samples taken after the 10th cycle were characterized using BET, XRD, and SEM/EDX analyses. Zinc titanate sorbents exhibited nearly constant desulfurization capability in the successive cycle operation.

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