• 제목/요약/키워드: selective catalytic oxidation

검색결과 91건 처리시간 0.032초

$La_xCe_{1-x}Co_yCu_{1-y}O_{3-{\alpha}}$ Perovskite촉매의 선택적 CO 산화반응에 관한 연구 (Study on the Selective CO Oxidation Using $La_xCe_{1-x}Co_yCu_{1-y}O_{3-{\alpha}}$ Perovskite Catalysts)

  • 강대규;이영일;손정민
    • 한국수소및신에너지학회논문집
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    • 제18권1호
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    • pp.32-39
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    • 2007
  • CO oxidation and selective CO oxidation of $La_xCe_{1-x}Co_yCu_{1-y}O_{3-{\alpha}}$ perovskite(x=1, 0.9, 0.7. 0.5; y=1, 0.9, 0.7, 0.5) were investigated. For CO oxidation, catalytic activities were studied according to different preparation conditions such as pH and calcination temperature. The influence of the change of the $O_2$ concentration for selective CO oxidation was studied, too. The substitution of Ce for La improved the catalytic activity for CO oxidation and selective CO oxidation and best activity was observed for $La_{0.7}Ce_{0.3}CoO_3$ prepared at pH 11 and calcined at $600^{\circ}C$. The temperature of 90% CO conversion for CO oxidation using $La_{0.7}Ce_{0.3}CoO_3$ was $230^{\circ}C$. In contrast to the enhancement effect by Ce substitution, the partial substitution of Cu for Co in $LaCo_yCu_{1-y}O_{3-{\alpha}}$ decreased catalytic activities for CO oxidation reaction compared to that using $LaCoO_3$. For selective CO oxidation, the best CO conversion was 66% at $230^{\circ}C$ for $La_{0.7}Ce_{0.3}CoO_3$. The CO conversion of $La_{0.7}Ce_{0.3}CoO_3$ was greatly increased from 66% to 91% as increasing $O_2$ concentration from 1% to 2%.

Ce/TiO2 촉매를 이용한 암모니아의 선택적 산화반응 특성 연구 (Characterization Studies for the Selective Catalytic Oxidation of Ammonia Utilizing Ce/TiO2 Catalyst)

  • 이현희;김기왕;홍성창
    • 공업화학
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    • 제24권5호
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    • pp.494-498
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    • 2013
  • 본 연구에서는, 다양한 오염원에서 발생되는 암모니아를 제어하기 위해 $Ce/TiO_2$ 촉매를 이용한 암모니아의 선택적 촉매 산화반응에 관한 연구가 수행되었다. Ce 함량이 10 wt%가 될 때까지는 Ce 함량이 증가할수록 촉매 성능이 증진됨이 관찰되었다. 그러나 그 이상의 함량에서는 오히려 촉매활성이 감소하였다. 따라서 본 연구에 의한 최적 $Ce/TiO_2$ 촉매는 실제 현장에 적용될 수 있을 것으로 판단된다.

PARTIAL OXIDATION OF PROPANE ON NAFION SUPPORTED CATALYTIC MEMBRANE

  • F. Frusteri;C. Espro;F. Arena;F. Arena;E. Passalacqua;A.Patti;A. Parmaliana
    • 한국막학회:학술대회논문집
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    • 한국막학회 1999년도 The 7th Summer Workshop of the Membrane Society of Korea
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    • pp.55-58
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    • 1999
  • Nafion supported catalytic membranes were found to be active, stable and selective in th partial oxidation of propane to oxygenates with H2O2 under mild condition. Addition of Fe2+ in liquid phase enhances the reaction rate. Reaction proceeds according to a radical mechanism based on th electrophilic activation of propane on superacid sites and subsequent reaction of the activated paraffin with OH radicals. The use of a catalytic membrane, which allow separation of the intermediate products from the liquid phase containing the oxidant, was found to be effective to perform selective partial oxidation of propane with high yields to oxygenated products.

$La_{0.5}Ce_{0.5}Co_{1-x}Cu_xO_{3-{\alpha}}$ Perovskite촉매의 선택적 CO 산화반응 및 특성 분석에 관한 연구 (Study on Catalytic Activity of the Selective CO Oxidation and Characterization Using $La_{0.5}Ce_{0.5}Co_{1-x}Cu_xO_{3-{\alpha}}$ Perovskite Catalysts)

  • 손정민
    • 한국수소및신에너지학회논문집
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    • 제18권2호
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    • pp.116-123
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    • 2007
  • [ $La_{0.5}Ce_{0.5}Co_{1-x}Cu_xO_{3-{\alpha}}$ ](X=0, 0.1, 0.3, 0.5) perovskites were prepared by coprecipitation method at pH 7 or pH 11 and its catalytic activity of selective CO oxidation was investigated. The characteristics of these catalysts were analyzed by $N_2$ adsorption, X-ray diffraction(XRD), SEM, $O_2$-temperature programmed desorption(TPD). The pH value at a preparation step made effect on particle morphology. The smaller particle was obtained with a condition of pH 7. The better catalytic activity was observed using catalysts prepared at pH 7 than pH 11. The maximum CO conversion of 98% was observed over $La_{0.5}Ce_{0.5}Co_{0.7}Cu_{0.3}O_{3-{\alpha}}$ at $320^{\circ}C$. Below $200^{\circ}C$, the most active catalyst was $La_{0.5}Ce_{0.5}Co_{0.9}Cu_{0.1}O_{3-{\alpha}}$, of which conversion was 92% at $200^{\circ}C$. By the substitution of Cu, the evolution of ${\alpha}$-oxygen was remarkably enhanced regardless of pH value at preparation step according to $O_2$-TPD. Among the different ${\alpha}$-oxygen species, the oxygen species evolved between $400^{\circ}C$ and $500^{\circ}C$, gave the better catalytic performance for selective CO oxidation including $La_{0.5}Ce_{0.5}CoO_3$ in which Cu was absent.

MW급 석탄연소 배가스에서 탈질촉매시스템을 이용한 원소수은 산화 실증사례 (A Review of Pilot Plant Studies on Elemental Mercury Oxidation Using Catalytic DeNOxing Systems in MW-Scale Coal Combustion Flue Gases)

  • 김문현;응웬 티 프엉 타오
    • 청정기술
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    • 제27권3호
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    • pp.207-216
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    • 2021
  • 석탄화력발전소로부터 배출되는 질소산화물(NO + NO2 = NOx)은 NH3를 환원제로 사용하여 선택적으로 환원시키는 SCR(selective catalytic reduction) 탈질촉매시스템에서 효과적으로 제거될 수 있다. 이 SCR 촉매공정에서 원소수은을 산화시켜 후속공정에서 제거하기 위하여 수많은 산화촉매들이 제안되었으나 MW급 석탄연소시설이나 상업운전 중인 석탄발전소 탈질시스템에서 원소수은 산화성능을 실증한 사례들은 매우 드물다. 실배가스에서 수행한 실증연구들을 심층적으로 조사·분석한 바는 기존 SCR 탈질촉매뿐 아니라 수은산화능을 향상시킨 신촉매의 원소수은 산화활성은 석탄연소, 실배가스 등의 특성에 따라 매우 복잡한 양상을 띤다는 점이다. 그럼에도 불구하고 석탄연소시설에 사용하는 원료탄, 탈질시스템과 실증조건이 원소수은 산화능에 가장 큰 영향을 미치는 핵심 요소이다. 특히, 원료탄에 함유된 할로겐 함량은 탈질촉매공정의 중요성을 넘어서는 것으로 보여진다. 석탄에 존재하는 대표적인 할로겐 성분은 Cl, Br과 F이고 이들 중에서 Cl이 지배적이며 다른 할로겐계처럼 염으로 존재하지만 석탄연소 과정에서 미량의 Cl2와 함께 HCl로 전환된다. 이러한 HCl은 원소수은 산화에 있어서 강력한 산화제로 작용하지만 석탄마다 Cl 함량이 다르기 때문에 HCl 농도 또한 강하게 의존한다.

Selective Production of Aromatic Aldehydes from Heavy Fraction of Bio-oil via Catalytic Oxidation

  • Li, Yan;Chang, Jie;Ouyang, Yong;Zheng, Xianwei
    • Bulletin of the Korean Chemical Society
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    • 제35권6호
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    • pp.1654-1658
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    • 2014
  • High value-added aromatic aldehydes (e.g. vanillin and syringaldehyde) were produced from heavy fraction of bio-oil (HFBO) via catalytic oxidation. The concept is based on the use of metalloporphyin as catalyst and hydrogen peroxide ($H_2O_2$) as oxidant under alkaline condition. The biomimetic catalyst cobalt(II)-sulfonated tetraphenylporphyrin ($Co(TPPS_4)$) was prepared and characterized. It exhibited relative high activity in the catalytic oxidation of HFBO. 4.57 wt % vanillin and 1.58 wt % syringaldehyde were obtained from catalytic oxidation of HFBO, compared to 2.6 wt % vanillin and 0.86 wt % syringaldehyde without $Co(TPPS_4)$. Moreover, a possible mechanism of HFBO oxidation using $Co(TPPS_4)/H_2O_2$ was proposed by the research of model compounds. The results showed that this is a promising and environmentally friendly method for production of aromatic aldehydes from HFBO under $Co(TPPS_4)/H_2O_2$ system.

Selective Oxidation of Cyclohexane at Low Temperature by Fe-Pd Bicatalytic Systems: $FeCl_2$-Pd/alumina System and Pd/$Fe_2O_3$ System

  • 전기원;Lingaiah Nakka;김상범;이규완
    • Bulletin of the Korean Chemical Society
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    • 제18권12호
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    • pp.1269-1273
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    • 1997
  • The system which employs iron, palladium, molecular oxygen and hydrogen as a model mono-oxygenase, has been investigated to develop a new method for selective cyclohexane oxidation uner mild conditions. This system provides much higher yield and selectivity for the formation of cyclohexanol and cyclohexanone compared to that of the existing industrial method. When the catalytic system, FeCl2-Pd/alumina, was employed, the oxidation system required acetone as a solvent to be efficient and acidifying the solvent by a little addition of acetic acid or HCl made the system more efficient. The Pd catalyst was recyclable without a significant deactivation but the recycling of ferrous chloride showed the decrease in the activity. On the other hand, the heterogeneous catalytic system, Pd/Fe2O3 could be recovered easily and reused after drying treatment.

Overview of the Effect of Catalyst Formulation and Exhaust Gas Compositions on Soot Oxidation In DPF

  • Choi Byung Chul;FOSTER D.E.
    • Journal of Mechanical Science and Technology
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    • 제20권1호
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    • pp.1-12
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    • 2006
  • This work reviews the effects of catalyst formulation and exhaust gas composition on soot oxidation in CDPF (Catalytic Diesel Particulate Filter). DOC's (Diesel Oxidation Catalysts) have been loaded with Pt catalyst (Pt/$Al_{2}O_3$) for reduction of HC and CO. Recent CDPF's are coated with the Pt catalyst as well as additives like Mo, V, Ce, Co, Fe, La, Au, or Zr for the promotion of soot oxidation. Alkali (K, Na, Cs, Li) doping of metal catalyst tends to increase the activity of the catalysts in soot combustion. Effects of coexistence components are very important in the catalytic reaction of the soot. The soot oxidation rate of a few catalysts are improved by water vapor and NOx in the ambient. There are only a few reports available on the mechanism of the PM (particulate matter) oxidation on the catalysts. The mechanism of PM oxidation in the catalytic systems that meet new emission regulations of diesel engines has yet to be investigated. Future research will focus on catalysts that can not only oxidize PM at low temperature, but also reduce NOx, continuously self-cleaning diesel particulate filters, and selective catalysts for NOx reduction.

전이금속을 함침한 γ-Al2O3 촉매의 Toluene 분해 (Decomposition of Toluene by γ-Al2O3 Catalysts Impregnated with Transition Metal)

  • 최성우;이철규
    • 한국환경과학회지
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    • 제22권8호
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    • pp.945-951
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    • 2013
  • Alumina-supported catalysts containing different transition metals such as Cu, Cr, Mn, Zn, Co, W were investigated for their activity in the selective oxidation of toluene. Catalytic oxidation of toluene was investigated at atmospheric pressure in a fixed bed flow reactor system over transition metals with $Al_2O_3$ catalyst. The result showed the order of catalytic activities for the complete oxidation of toluene was Mn > Cu> Cr> Co> W> Zn for 5wt.% transition $metals/Al_2O_3$. $Mn/Al_2O_3$ catalysts containing different amount of Mn were characterized by X-ray diffraction spectroscopy for decision of loading amount of metal to alumina. 5 wt.%$Mn/Al_2O_3$ catalyst exhibits the highest catalytic activity, over which the toluene conversion was up to 90% at a temperature of $289^{\circ}C$.

바나듐계 촉매상에서 암모니아를 이용한 질소산화물의 환원반응속도에 수분이 미치는 영향에 관한 연구 (Effect of Water on the Kinetics of Nitric Oxides Reduction by Ammonia over V-based Catalyst)

  • 김영득;정수진;김우승
    • 한국자동차공학회논문집
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    • 제20권6호
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    • pp.73-82
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    • 2012
  • The main and side reactions of the three selective catalytic reduction (SCR) reactions with ammonia over a vanadium-based catalyst have been investigated using synthetic gas mixtures in the temperature range of $170{\sim}590^{\circ}C$. The three SCR reactions are standard SCR with pure NO, fast SCR with an equimolar mixture of NO and $NO_2$, and $NO_2$ SCR with pure $NO_2$. Vanadium based catalyst has no significant activity in NO oxidation to $NO_2$, while it has high activity for $NO_2$ decomposition at high temperatures. The selective catalytic oxidation of ammonia and the formation of nitrous oxide compete with the SCR reactions at the high temperatures. Water strongly inhibits the selective catalytic oxidation of ammonia and the formation of nitrous oxide, thus increasing the selectivity of the SCR reactions. However, the presence of water inhibits the SCR activity, most pronounced at low temperatures. In this study, the experimental results are analyzed by means of a dynamic one-dimensional isothermal heterogeneous plug-flow reactor (PFR) model according to the Eley-Rideal mechanism.