• 제목/요약/키워드: ethylene removal

검색결과 99건 처리시간 0.025초

입상형태와 합성담체에 고정화된 혐기성 암모늄 산화균의 연속배양 특성 평가 (Evaluation of continuous cultivation of anaerobic ammonium oxidation bacteria immobilized on synthetic media and granular form)

  • 김지영;윤원상;정진영;최대희
    • 상하수도학회지
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    • 제35권2호
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    • pp.135-142
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    • 2021
  • The activity of anaerobic ammonium oxidation (ANAMMOX) immobilized in synthetic media (Poly Ethylene Glycol, PEG) and granular form was evaluated comparatively to investigate the effect of influent nitrogen concentration and exposure of oxygen. In ANAMMOX granule reactor, when concentration of influent total nitrogen increased to 500mg/L, removal efficiency of ammonium, nitrite and nitrate were shown to 90.5±6.5, 96.6±4.9, and 93.2±6.1%, respectively. In the case of the PEG gel, it showed lower nitrogen removal performance, resulting in that the removal efficiency of ammonium, nitrite and nitrate were shown to 83.3±13.0, 96.4±6.1, and 90.3±7.5%, respectively. In second step, when exposed to oxygen, the nitrogen removal performance in the ANAMMOX granule reactor also remained stable, but the activity of PEG gel ANAMMOX was found to be inhibited. Consequently, the PEG gel ANAMMOX was a higher sensitivity than that of granular ANAMMOX with two variables applied in this study.

폴리(에틸렌 나프탈레이트)의 축중합 반응에서 물질 전달 현상 (Mass Transfer Phenomena in Polycondensation Reaction of Poly(ethylene naphthalate))

  • 이성진;정성일
    • 폴리머
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    • 제28권2호
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    • pp.121-127
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    • 2004
  • 폴리(에틸렌 나프탈레이트)의 축중합 반응은 가역반응이므로 부반응 물질인 에틸렌 글라이콜의 신속한 제거가 높은 분자량의 제품을 얻는데 매우 중요하다. 본 연구에서는 폴리(에틸렌 나프탈레이트)올리고머로 박막을 제조하여 실제 반응기와 동일한 조건 하에서 (28$0^{\circ}C$, <0.1mmHg) 반응시켜 이 때 일어나는 물질 전달 현상을 관찰하고자 하였다. 여러 가치 두께의 박막을 제조하여 반응 실험한 결과 두께가 0.025cm 이하의 영역에서는 박막에서의 물질 전달 저항이 크지 않아 총괄 반응 속도에 영향을 미치지 않음을 관찰하였다. 물질 전달 모델 및 확산 모델을 사용하여 반응 결과를 예측한 결과 두 모델 모두 실험 결과를 잘 예측하였으나 확산 모델의 경우 중합도가 낮은 영역에서 물질 전달 모델에 비해 반응이 더 빨리 진행되는 경향을 보였다. 두 모델을 이용하여 물질 전달 관련 계수를 예측한 결과 폴리(에틸렌 나프탈레이트)에서의 확산 계수는 4.7${\times}$$10^{-6}$$\textrm{cm}^2$/sec, 물질 전달 계수는 1.4${\times}$$10^{-4}$cm/sce로 폴리(에틸렌 테레프탈레이트) 경우보다 작은 값을 보였다.

Polyester 감량 폐수 중에 존재하는 Ethylene Glycol의 처리(II) -반응속도론- (Treatment of Ethylene Glycol in Polyester Weight Loss Wastewater(II) - Reaction Kinetics-)

  • Han, Myung-Ho;Kim, Jeong-Mog;Huh, Man-Woo
    • 한국염색가공학회지
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    • 제8권6호
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    • pp.27-32
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    • 1996
  • This research is to investigate the reaction kinetics by air-lift bioreactor using calcium hydroxide, the neutralization agent and immobilization media, for removing ethylene glycol remained after chemical pretreatment. It was found that the optimum hydraulic retention time was obtained as 24.2hours at the optimum F/M ratio of 1.32kg-$TCOD_{Mn}$/day.kg-MLVSS, and then, infiuent $TCOD_{Mn}$ and MLVSS concentration were 3,290mg/l and 2,472mg/l, respectively. During the steady state, the kinetics constants such as maximum specific substrate removal rate, half saturation velocity coefficient, yield coefficient and endogenous respiration coefficient were estimated in the base of $TCOD_{Mn}$ as substrate concentration. And they were 1.47day$^{-1}$, 3.95mg/l, 0.391 and 0.092day$^{-1}$, respectively. And also, the oxgen use coefficients for cell synthesis, a', and energy of maintenance, b', were obtained as 0.4kg-O$_{2}$/kg-$TCOD_{Mn}$ and 0.056day$^{-1}$, at the steady state by the experimental result of oxygen uptake rate.

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안정적인 SOFC 운전을 위한 디젤 개질기 내 미반응 저탄화수소 제거법 (Methodology for removing unreacted low-hydrocarbons in diesel reformate for stable operation of solid oxide fuel cells)

  • 윤상호;배중면;이상호
    • 한국신재생에너지학회:학술대회논문집
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    • 한국신재생에너지학회 2009년도 춘계학술대회 논문집
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    • pp.773-776
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    • 2009
  • In this paper, new concept of the diesel fuel processing is introduced for the stable operation of solid oxide fuel cells (SOFCs). Heavier hydrocarbons than $CH_4$, such as ethylene, ethane, propane, and etc., induce the carbon deposition on anode of SOFCs. In the reformate of heavy hydrocarbons (diesel, gasoline, kerosene, and JP-8), concentration of ethylene is usually higher than low hydrocarbons such as ethane, propane, and butane. So, removal of low hydrocarbons (over C1-hydrocarbons), especially ethylene, at the reformate gases is important for stable operation of SOFCs. New methodology as named "post-reformer" is introduced for removing the low hydrocarbons at the reformate gas stream. Catalyst of the NECS-PR4 is selected for post-reforming catalyst because the catalyst of NECS-PR4 shows the high selectivity for removing low hydrocarbons and achieving the high reforming efficiency. The diesel reformer and post-reformer are continuously operated for about 200 hours as integrated mode. The reforming performance is not degraded and low hydrocarbons in the diesel reformate are completely removed.

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비열 플라즈마에 의한 NO의 산화에 탄화수소 첨가제가 미치는 영향 (Effect of Hydrocarbons on the Promotion of NO-$NO_2$ Conversion in NonThermal Plasma DeNOx Treatment)

  • 신현호;윤웅섭
    • 한국연소학회:학술대회논문집
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    • 한국연소학회 2000년도 제21회 KOSCO SYMPOSIUM 논문집
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    • pp.33-46
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    • 2000
  • In the present study, a systematic chemical kinetic calculations were made to investigate the augmentation of NO-$NO_2$ conversion due to the addition of various hydrocarbons (methane, ethylene, ethane, propene, propane) in the nonthermal plasma treatment. It is included in the present conclusion that the reaction between hydrocarbon and oxygen radicals induced by electron collision, is believed to be a primarily process for triggering the overall NO oxidation and the eventual NOx reduction. Upon the completion of the initiating step, various radicals (OH, $NO_2$ etc.) successively produced by hydrocarbon decomposition form the primary path of NO-$NO_2$ conversion. When the initiating step is not activated, hydrocarbon consumption rate appeared to be very low, thereby the targeted level of NO conversion can only be achieved by the addition of more input energy. Present study showed ethylene and propene to have higher affinity with 0 radical under all conditions, thereby both of these hydrocarbons show very fast and efficient NO-$NO_2$ oxidation. It was also shown that propene is superior to ethylene in the aspect of NOx removal.

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비열 플라즈마에 의한 NO의 산화에 탄화수소 첨가제가 미치는 영향 (Effect of Hydrocarbons on the Promotion of $NO-NO_{2}$ Conversion in NonThermal Plasma DeNOx Treatment)

  • 신현호;윤웅섭
    • 한국연소학회:학술대회논문집
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    • 한국연소학회 2000년도 제20회 KOSCO SYMPOSIUM 논문집
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    • pp.178-188
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    • 2000
  • In the present study, a systematic chemical kinetic calculations were made to investigate the augmentation of $NO-NO_{2}$ conversion due to the addition of various hydrocarbons (methane, ethylene, ethane, propene, propane) in the nonthermal plasma treatment. It is included in the present conclusion that the reaction between hydrocarbon and oxygen radicals induced by electron collision, is believed to be a primarily process for triggering the overall NO oxidation and the eventual NOx reduction. Upon the completion of the initiating step, various radicals (OH, $HO_{2}$ etc.) successively produced by hydrocarbon decomposition form the primary path of $NO-NO_{2}$ conversion. When the initiating step is not activated, hydrocarbon consumption rate appeared to be very low, thereby the targeted level of NO conversion can only be achieved by the addition of more input energy. Present study showed ethylene and propene to have higher affinity with 0 radical under all conditions, thereby both of these hydrocarbons show very fast and efficient $NO-NO_{2}$ oxidation. It was also shown that propene is superior to ethylene in the aspect of NOx removal.

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비열 플라즈마에 의한 NO의 산화에서의 탄화수소 첨가 효과와 그 반응역학에 대한 수치적 연구 (Numerical Study of the Effects of Hydrocarbon Addition and Corresponding Chemical Kinetics on the Promotion of NO Oxidation in Nonthermal Plasma DeNOx Treatment)

  • 신현호;윤웅섭
    • 한국연소학회지
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    • 제5권2호
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    • pp.37-50
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    • 2000
  • In the present study, a systematic chemical kinetic calculations were made to investigate the augmentation of $NO-NO_2$ conversion due to the addition of various hydrocarbons (methane, ethylene, ethane, propylene, propane) in the nonthermal plasma treatment. It is included in the present conclusion that the reaction between hydrocarbon and oxygen radicals induced by electron collision, is believed to be a primarily process for triggering the overall NO oxidation and the eventual NOx reduction. Upon the completion of the initiating step, various radicals (OH, $HO_2$ etc.) successively are produced by hydrocarbon decomposition form the primary path of $NO-NO_2$ conversion. When the initiating step is not activated, hydrocarbon consumption rate appeared to be very low, thereby the targeted level of NO conversion can only be achieved by the addition of more input energy. Present study showed ethylene and propylene to have higher affinity with O radical under all conditions, thereby both of these hydrocarbons show very fast and efficient $NO-NO_2$ oxidation. It was also shown that propylene is superior to ethylene in the aspect of NOx removal.

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Polymer-supported Zinc Tetrahalide Catalysts for the Coupling Reactions of CO2 and Epoxides

  • Lee, Bo-Ra;Ko, Nan-Hee;Ahn, Byoung-Sung;Cheong, Min-Serk;Kim, Hoon-Sik;Lee, Je-Seung
    • Bulletin of the Korean Chemical Society
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    • 제28권11호
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    • pp.2025-2028
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    • 2007
  • Homogeneous zinc tetrahalide complexes, highly active catalysts for the coupling reactions of alkylene oxide and CO2 produce alkylene carbonates, were heterogenized due to their tendency to decompose produced alkylene carbonates during the distillation process. Heterogenization of homogeneous zinc tetrahalide complexes was achieved by polymerizing 1-alkyl-3-vinylimidazolium zinc tetrahalides. These polymerized zinc tetrahalide catalysts displayed similar activities to their corresponding monomeric analogues for the coupling reactions of carbon dioxide with ethylene oxide (EO) or propylene oxide (PO) to produce ethylene carbonate (EC) or propylene carbonate (PC). TGA studies showed that the polymer-supported zinc tetrahalide catalysts are thermally stable up to 320 oC. The catalyst recycle test showed that the supported catalysts could be reused over six times. After removal of the polymer-supported catalyst through a simple filtration, EC was able to be isolated without decomposition.

Polyester감량폐수 중에 존재하는 Ethylene Glycol의 처리(I) - 반응 특성 - (Treatment of Ethylene Glycol in Polyester Weight Loss Wastewater(I) - Reaction Characteristics -)

  • Kim, Jeong-Mog;Huh, Man-Woo;Han, Myung-Ho
    • 한국염색가공학회지
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    • 제8권5호
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    • pp.84-89
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    • 1996
  • This study carried out batch and continuous experiments using calcium hydroxide as neutralization agent and immobilization media for removing the ethylene glycol in the pretreated polyester weight loss wastewater. The $TCOD_{Mn}$ concentration in the treated wastewater using culture of iramobilization and suspension for the synthetic wastewater were found as 650mg/l and 1,250mg/l after 48hours, respectively. SVI(Sludge Volume Index) and $TCOD_{Mn}$ concentration were 74 and 73mg/l at optimum F/M ratio, 1.32kg-TCO $D_{Mn}$ /day. kg-MLVSS. The $TCOD_{Mn}$ concentration and removal efficiency were 213mg/l and 93.5% by continuous experiments in the air-lift bioreactor, respectively. The $TCOD_{Mn}$ concentration was 82mg/l, and also the MLVSS concentration was 2,550mg/l, when the volumetric loading rate was 3.04kg-$TCOD_{Mn}/m^{2}$ day for real polyester weight loss wastewater.

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RO/NF막 공정을 이용한 BTEX 물질의 제어 특성 평가 (Removal Mechanisms of BTEX Compounds by RO/NF Membrane Processes)

  • 장혜원;박찬혁;홍승관;윤여민;정진영;정윤철
    • 한국물환경학회지
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    • 제22권5호
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    • pp.926-932
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    • 2006
  • A series of bench-scale membrane filtration experiments were performed to systematically investigate the removal mechanisms of reverse osmosis (RO) and nanofiltration (NF) membranes for BTEX (benzene, toluene, ethylene, xylene), trichloroethylene (TCE) and tetrachloroethylene (PCE). The molecular weight of these organic compounds ranged from 78 to 166 dalton. The rejection of organic compounds by RO/NF membranes varied significantly from 59.6 to 99.2% depending on solute and membrane types. Specifically, experimental results demonstrated that the removal efficiency of RO/NF membranes increased as solute molecular characteristics such as W/L (molecular width/length) ${\times}$ $M_W$ (molecular weight) and octanol-water partition coefficient increased. This observation suggested that the rejection of small organic compounds by RO/NF membranes was determined by the combined effect of physical (molecular size and shape) and chemical (hydrophobicity) properties.