• Title/Summary/Keyword: 산화환원촉매

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The Selective Catalytic Oxidation of Ammonia: Effect of Physicochemical Properties on Pt/TiO2 (Pt/TiO2 촉매의 물리화학적 특성이 NH3-SCO 반응활성에 미치는 영향)

  • Shin, Jung Hun;Kim, Dong Ho;Hong, Sung Chang
    • Applied Chemistry for Engineering
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    • v.28 no.3
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    • pp.279-285
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    • 2017
  • In this study, the study of the selective catalytic oxidation (SCO) for controlling the $NH_3$ at $200{\sim}350^{\circ}C$ range was investigated. Physicochemical properties of the catalysts were determined using XRD and XPS analysis. In the case of catalytic activity according to thermal treatment condition, the reduction catalyst showed better activity than that of using the calcination catalyst. It was confirmed that the valence state of reduction catalyst was mainly $Pt^{2+}$ and $Pt^0$ as analyzed by XPS. Also, when comparing the reaction activities of $Pt/TiO_2$ catalysts according to the reduction temperature, the $NH_3$ conversion of the catalyst reduced at $700^{\circ}C$ showed the most excellent activity. However, the best activity of $NH_3$ conversion to $N_2$ was obtained for the catalyst reduced at $600^{\circ}C$.

Size and Shape Effect of Metal Oxides on Hydrocarbon Selective Catalytic Reduction of Nitrogen Oxides (금속 산화물 촉매의 크기와 형태에 따른 질소산화물의 탄화수소 선택적 촉매환원 특성)

  • Ihm, Tae-Heon;Jo, Jin-Oh;Hyun, Young Jin;Mok, Young Sun
    • Journal of the Korean Institute of Gas
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    • v.19 no.5
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    • pp.20-28
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    • 2015
  • This work investigated the size and shape effect of ${\gamma}$-alumina-supported metal oxides on the hydrocarbon selective catalytic reduction of nitrogen oxides. Several metal oxides including Ag, Cu and Ru were used as the catalysts, and n-heptane as the reducing agent. For the Ag/${\gamma}$-alumina catalyst, the $NO_x$ reduction efficiency in the range of $250{\sim}400^{\circ}C$ increased as the size of Ag decreased (20 nm>50 nm>80 nm). The shape effect of metal oxides on the $NO_x$ reduction was examined with spherical- and wire-shape nanoparticles. Under identical condition, higher catalytic activity for $NO_x$ reduction was observed with Ag and Cu wires than with the spheres, while spherical- and wire-shape Ru exhibited similar $NO_x$ reduction efficiency to each other. Among the metal oxides examined, the best catalytic activity for $NO_x$ reduction was obtained with Ag wire, showing almost complete $NO_x$ removal at a temperature of $300^{\circ}C$. For Cu and Ru catalysts, considerable amount of NO was oxidized to $NO_2$, rather than reduced to $N_2$, leading to lower $NO_x$ reduction efficiency.

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

  • Kim, Moon Hyeon;Nguyen, Thi Phuong Thao
    • Clean Technology
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    • v.27 no.3
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    • pp.207-216
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    • 2021
  • Major anthropogenic emissions of elemental mercury (Hg0) occur from coal-fired power plants, and the emissions can be controlled successfully using NH3-SCR (selective catalytic reduction) systems with catalysts. Although the catalysts can easily convert the gaseous mercury into Hg2+ species, the reactions are greatly dependent on the flue gas constituents and SCR conditions. Numerous deNOxing catalysts have been proposed for considerable reduction in power plant mercury emissions; however, there are few studies to date of elemental mercury oxidation using SCR processes with MW- and full-scale coal-fired boilers. In these flue gas streams, the chemistry of the mercury oxidation is very complicated. Coal types, deNOxing catalytic systems, and operating conditions are critical in determining the extent of the oxidation. Of these parameters, halogen element levels in coals may become a key vehicle for obtaining better Hg0 oxidation efficiency. Such halogens are Cl, Br, and F and the former one is predominant in coals. The chlorine exists in the form of salts and is transformed to gaseous HCl with a trace amount of Cl2 during the course of coal combustion. The HCl acts as a very powerful promoter for high catalytic Hg0 oxidation; however, this can be strongly dependent on the type of coal because of a wide variation in the chlorine contents of coal.

Oxidation of Methane and Reduction of Ammonia using Mn Catalysts (망간 촉매를 이용한 메탄과 암모니아의 산화 및 환원)

  • Jang, Hyun-Tae;Lee, Ji-Yun;Kim, Hyeon-Jeong;Wagle, Roshan;Kim, Sun-Woo
    • Proceedings of the KAIS Fall Conference
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    • 2009.05a
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    • pp.902-905
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    • 2009
  • 축사 또는 쓰레기장에서 에서 발생되는 있는 물질인 암모니아, 아민, 메탄, 탄화수소류 등에 대한 처리를 위한 촉매 개발을 수행하였다. 암모니아를 금속산화물형태의 촉매를 사용하여 산화하였을 경우 $N_2$, NO, $NO_2$, $N_2O$가 일정 비율로 생성되게 된다. 이때의 NO, $NO_2$는 악취는 발생하지 않으나 유독성 가스이므로 이에 대한 선택성이 낮은 촉매를 선별하고 온도에 따른 활성능을 시험하여 최적의 촉매조성을 도출하였다. 다양한 산화가를 지닌 망간을 대상으로 각종 조촉매의 혼합에 따른 실험을 수행하여 최적 조성을 도출 하였다. 촉매 선별작업에서는 충전층을 사용하고, 선별된 촉매에 대하여 모노리스에 코팅하여 사용할 수 있는 모노리스형태의 반응기를 장착하여 모노리스 형태 촉매의 반응성 및 피독특성을 실험하였다.

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Transformation of Pentachlorophenol by Oxidoreductive Catalysts (산화환원 촉매에 의한 Pentachlorophenol의 Transformation)

  • Park, Jong-Woo;Lee, Yun-Ki;Kim, Jang-Eok
    • Applied Biological Chemistry
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    • v.42 no.4
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    • pp.330-335
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    • 1999
  • Pentachlorophenol(PCP), which is very persistent in soil and water environment, was tried to detoxify with oxidoreductive catalysts(peroxidase, laccase, tyrosinase and birnessite). To find out detoxification of PCP, the transformation of PCP through oxidative coupling was investigated in the presence of various oxidoreductive catalysts. PCP incubated with peroxidase was significantly transformed, however, in case of tyrosinase, the transformation was negligible. Using peroxidase, the optimal reaction condition was pH 5.6 and $16^{\circ}C$. The transformation of PCP was very fast in initiation step until 30 min but, that was not observed after 180 min. The transformation of PCP was increased by increasing peroacidase amount. When the effect of humic monomer was investigated as co-substrate on the transformation of PCP, the transformation of PCP was mostly decreased in the incubation with peroxidase, laccase, and birnessite. The transformation of PCP, however, was slightly increased by the incubation with tyrosinase in the presence of humic monomers as co-substrate, except catechol. On the basis of the results obtained, it may be suggested that PCP is able to be effectively detoxified through oxidative coupling mediated with oxidoreductive catalysts.

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Carbon nanofiber and metal oxide composites for photovoltaic cells

  • O, Dong-Hyeon;Gu, Bon-Yul;Bae, Ju-Won;An, Hyo-Jin
    • Proceedings of the Korean Vacuum Society Conference
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    • 2016.02a
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    • pp.412-412
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    • 2016
  • 염료감응 태양전지(dye-sensitized solar cells, DSSCs)는 식물의 광합성원리와 매우 유사한 작동원리를 갖고 있는 전지이며, 간단한 구조, 저렴한 제조단가, 친환경성 등의 등의 장점으로 인하여 많은 관심을 모으고 있다. 이러한 염료감응 태양전지는 빛을 받아들인 염료분자가 전자-홀 쌍을 생성하며 전자는 반도체 산화물을 통해 이동되고 전해질의 산화환원 과정을 통해 염료 분자가 다시 환원되는 순환메커니즘을 따르고 있다. 일반적으로 염료감응 태양전지는 밴드 갭 에너지가 큰 반도체 산화물을 포함하는 작업전극, 산화환원 반응을 통해 전자를 염료로 보내는 전해질, 환원 촉매역할을 하는 상대전극으로 구성되어 있다. 특히, 상대전극으로는 우수한 촉매특성과 높은 전도성을 갖는 백금이 가장 많이 이용되고 있지만 가격이 비싸고 요오드에 취약하기 때문에 상용화에 큰 장애물이다. 따라서, 백금을 대체하기 위해 저가의 탄소나 고분자에 대한 연구가 활발히 진행되고 있고, 그 중 탄소나노섬유(carbon nanofiber, CNFs)는 높은 표면적과 뛰어난 화학적 안정성으로 촉매효율을 증대시킬 수 있어 촉매물질로서 관심이 높아지고 있다. 본 연구에서는 상대전극에 탄소나노섬유기반 복합체를 합성하였고, 성공적으로 저가격 및 고성능의 염료감응 태양전지를 제작하였다. 이때, 지지체인 탄소나노섬유는 전기방사법을 통해 합성하였으며, 수열합성법을 이용하여 금속산화물을 담지하였다. 이렇게 제작된 탄소나노섬유-Fe2O3 복합체는 scanning electron microscopy, transmission electron microscopy, X-ray diffraction, 그리고 X-ray photoelectron spectroscopy 통해 구조적, 화학적 특성을 평가하였으며 전기화학적 특성 및 광전변환 효율을 분석하기 위해 cyclic voltammetry, electrochemical impedance spectroscopy, 그리고 solar simulator를 사용하였다. 본 학회에서 위와 관련된 더 자세한 사항에 대해 논의할 것이다.

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Steam Reforming of Ethylene Glycol over Ni/Al2O3 Catalysts: Effect of the Preparation Method and Reduction Temperature (Ni/Al2O3 촉매를 사용한 에틸렌글리콜의 수증기 개질 반응: 촉매 제조 방법과 환원온도의 영향)

  • Choi, Dong Hyuck;Park, Jung Eun;Park, Eun Duck
    • Korean Chemical Engineering Research
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    • v.53 no.3
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    • pp.372-381
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    • 2015
  • The effect of preparation method on the catalytic activities of the $Ni/Al_2O_3$ catalysts on steam reforming of ethylene glycol was investigated. The catalysts were prepared with various preparation methods such as an incipient wetness impregnation, wet impregnation, and coprecipitation method. In the case of coprecipitation method, various precipitants such as KOH, $K_2CO_3$, and $NH_4OH$ were compared. The prepared catalysts were characterized by using $N_2$ physisorption, inductively coupled plasma-atomic emission spectroscopy, X-ray diffraction, temperatureprogrammed reduction, pulsed $H_2$ chemisorption, temperature-programmed oxidation, scanning electron microscopy, and thermogravimetric analysis. Among the catalysts reduced at 773 K, the $Ni/Al_2O_3$ catalyst prepared by a coprecipitation with KOH or $K_2CO_3$ as precipitants showed the best catalytic performance. The preparation method affected the particle size of Ni, reducibility of nickel oxides, catalytic performance (activity and stability), and types of coke formed during the reaction. The $Ni/Al_2O_3$ catalyst prepared by a coprecipitation with KOH showed the increasing catalytic activity with an increase in the reduction temperature from 773 to 1173 K because of an increase in the reduction degree of Ni oxide species even though the particle size of Ni increased with increasing reduction temperature.

Resazurin Redox Reaction Mechanism Using Silver Nanoparticles Synthesized with Monosaccharides and Disaccharides (단당류와 이당류를 환원제로 합성한 은 나노입자의 Resazurin 산화환원반응 메커니즘)

  • Park, Young Joo;Chang, Ji Woong
    • Applied Chemistry for Engineering
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    • v.31 no.3
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    • pp.299-304
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    • 2020
  • Nanoparticles play an important role as a catalyst in many chemical syntheses. Colloidal nanoparticles were usually synthesized with reducing, capping, and shape directing agents which induce surface poisoning of catalysts. A new green synthesis for silver nanoparticles was developed by utilizing less additives which could be a hazardous waste. A crystallization technique was employed to reduce the amount of reducing and capping agents during synthesis resulting in less surface poisoning of the nanoparticle. The synthesized Ag nanoparticles using monosaccharides and disaccharides as reducing agents could be used as a catalyst for the redox reaction of resazurin and the mechanism of the reaction using Ag nanoparticles was studied.

Effect of Oxidation-reduction Pretreatment for the Hydrogenation of Caster Oil over Ni/SiO2 Catalyst (산화-환원 전처리에 따른 Ni/SiO2 촉매의 캐스터오일 수소화)

  • Choi, Yi Sun;Kim, Soo Young;Koh, Hyoung Lim
    • Applied Chemistry for Engineering
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    • v.28 no.3
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    • pp.326-331
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    • 2017
  • Castor oil can be used as a useful raw material for chemical industries such as intermediates of surfactants through hydrogenation reaction. In this study, effects of the preparation method and pretreatment condition on the nickel catalyst for the hydrogenation of castor oil were investigated. The nickel catalyst was supported on the silica carrier by the precipitation method with different Ni contents, solution pH values, and precipitants. Repeated pretreatments of oxidation and reduction cycles were then carried out. The activity of the nickel catalyst was measured by comparing the iodine value of the castor oil. The dispersion of nickel on the catalyst was analyzed by X-ray diffraction (XRD), $N_2$ adsorption-desorption, and transmission electron microscopy (TEM). The activity of nickel catalyst was also compared by CO oxidation experiments. The redispersion of nickel occurred on the silica by repeated oxidation and reduction cycles, and this effect contributed to promoting the castor oil hydrogenation activity.

Regeneration of Spent Nickel Catalyst for Hydrogenation (수소화 반응용 니켈 폐촉매의 재생)

  • 전종기;박영권;김주식
    • Resources Recycling
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    • v.13 no.3
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    • pp.27-36
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    • 2004
  • Nickel oxide was recovered through roasting of a spent catalyst for hydrogenation reaction. Nickel on Kieselguhr catalysts were prepared by a precipitation method after a treatment of the recovered-nickel oxide with an acid. Effects of roasting temperature of the spent catalyst on recovery of nickel oxide was investigated. Most of nickel oxide could be recovered through roasting of the spent catalyst at $1000^{\circ}C$. In regeneration of catalysts by the precipitation method after the treatment of nickel oxide with an acid, the effect of promoter, precipitation condition and reduction condition on catalytic performance in vegetable oil hydrogenation were investigated. The addition of CaO or $Ce_2$$O_3$ resulted in an increase of catalytic activity.