• 제목/요약/키워드: Bimetallic

검색결과 124건 처리시간 0.024초

티타니아에 담지된 귀금속촉매의 H2O-H2 전처리에 따른 휘발성유기화합물 산화에 미치는 영향 (A Effect of H2O-H2 Pretreatment on VOCs Oxidation over Noble Catalysts on Titania)

  • 김문찬;고선환
    • 공업화학
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    • 제18권6호
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    • pp.552-556
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    • 2007
  • 연구에서는 $TiO_2$ 담체에 귀금속(Pd, Ru, Ir)을 담지시켜 촉매를 제조하였다. 금속분산의 향상을 위해 $H_2O-H_2$ 전처리 기술이 이용되었고, 반응물로서 xylene, toluene 그리고 MEK를 사용하였다. 단일금속과 합금금속의 촉매들은 함침법에 의해 준비하였고, XRD, XPS 분석을 통하여 특성 분석하였다. Pd-Ru, Pd-Ir 촉매는 다양한 활성점을 나타내었고, 그것은 Pd의 metal 영역를 강화시켰다. 합금금속으로 이루어진 촉매가 단일 금속으로 이루어진 촉매에 비해 VOCs 전환율이 더 높았다. $H_2O-H_2$ 전처리 기술은 Pd 입자를 고르게 분산시켰다. 이는 촉매의 효율을 증진시키는 효과를 보여주었다. 본 연구에서 Pd에 소량의 Ru, Ir 첨가는 VOCs의 산화반응을 증진시켰고, $TiO_2$ 담체상에서 $H_2O-H_2$ 전처리는 VOCs의 제거효율을 증진시켰다.

X-ray crystal structure of two-dimensional bimetallic host clathrate with 2-aminoethanol, [Cd{NH2CH2CH2OH}2Ni(CN)4]·3C6H5NH2·H2O

  • Kim, Chong-Hyeak;Moon, Hyoung-Sil;Lee, Sueg-Geun
    • 분석과학
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    • 제21권6호
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    • pp.562-568
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    • 2008
  • A novel two-dimensional cadmium(II)-nickel(II) bimetallic host clathrate, $[Cd{NH_2CH_2CH_2OH}_2Ni(CN)_4]{\cdot}3C_6H_5NH_2{\cdot}H_2O$, 1, has been synthesized and structurally characterized by X-ray single crystallographic method. The clathrate 1 crystallizes in the monoclinic system, space group $P2_1/c$ with a = 14.370(3), b = 7.728(1), c = 28.172(4) ${\AA}$, ${\beta}=97.58(1)^{\circ}$, V = 3101.1(9) ${\AA}^3$, Z = 4. The host framework of the clathrate 1 is built of the cyanide bridges between octahedral Cd(II) atom and square planar Ni(II) atom. The octahedral Cd atoms ligated by two 2-aminoethanol molecules and four cyanide ligands bridged with square planar Ni atoms. The Ni atoms bridges to four Cd atoms via cyanides is made up of puckered quadrangles of composition $\{CdNi(CN)_2\}_2$, all edges are shared. This cyanide bridges form an infinite two-dimensional host networks stacking along b axis. 2-Aminoethanol ligands bond to Cd atom through N atom as a monodentate ligand in the axial position and four cyanides take an equatorial plane with all in trans-configurations. The aniline guest molecules and water molecules are located in between the host layer sheets, respectively.

분자동역학을 이용한 전이금속 나노구조체의 특성연구

  • 윤기훈;조민우
    • EDISON SW 활용 경진대회 논문집
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    • 제3회(2014년)
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    • pp.359-370
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    • 2014
  • 두 가지 서로 다른 원소를 포함한 나노 크기의 금속클러스터가 여러 화학반응의 효과적인 촉매로 각광받고 있다. 그래서 본 연구에서는 분자동역학을 이용하여 48개로 구성된 Au-Pd 나노 금속 클러스터의 다양한 구조와 상전이 현상을 살펴보고자 한다.

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Poly(ethylenimine)-Stabilized Hollow Gold-Silver Bimetallic Nanoparticles: Fabrication and Catalytic Application

  • Shin, Kuan-Soo;Kim, Ji-Hoon;Kim, In-Hyun;Kim, Kwan
    • Bulletin of the Korean Chemical Society
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    • 제33권3호
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    • pp.906-910
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    • 2012
  • Hollow gold-silver bimetallic nanoparticles (AuAg-HNPs) have been synthesized and their optical and structural properties were characterized. Initially Ag nanoparticles (Ag-NPs) were prepared using poly(ethylenimine) (PEI) as a reducing and a stabilizing agent simultaneously. AuAg-HNPs could then be synthesized via galvanic replacement reaction in a PEI aqueous solution by reacting sacrificial Ag template with a precursor compound of Au, i.e., $HAuCl_4$. Due to the presence of abundant amine functional groups in PEI, which could act as the dissolving ligand for AgCl, the precipitation problem of $Ag^+$ in the presence of Cl from $HAuCl_4$ salt was avoided. On this basis, the relatively high concentrations of $HAuCl_4$ and PEI-stabilized Ag nanoparticles could be used for the fabrication of AuAg-HNPs. Because of their increased surface areas and reduced densities, the AuAg-HNPs were expected and confirmed to outperform their solid counterparts in applications such as catalysis for the reduction of 4-nitrophenol in the presence of $NaBH_4$.

Enhanced Electrocatalytic Activity of Low Ni Content Nano Structured NiPd Electrocatalysts Prepared by Electrodeposition Method for Borohydride Oxidation

  • Zolfaghari, Mahdieh;Arab, Ali;Asghari, Alireza
    • Journal of Electrochemical Science and Technology
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    • 제11권3호
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    • pp.238-247
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    • 2020
  • Some nano structured bimetallic NiPd electrocatalysts were electrodeposited on glassy carbon electrodes using a double potential step chronoamperometry. The morphology of the electrodeposited samples was investigated by field emission-scanning electron microscopy, while their compositions were evaluated using energy dispersive X-ray spectroscopy. It was observed that the electrodeposited samples contained a low Ni content, in the range of 0.80 - 7.10%. The electrodeposited samples were employed as the anode electro-catalysts for the oxidation of sodium borohydride in NaOH solution (1.0 M) using cyclic voltammetry, chronoamperometry, rotating disk electrode, and impedance spectroscopy. The number of exchanged electrons, charge transfer resistances, apparent rate constants, and double layer capacitances were calculated for the oxidation of borohydride on the prepared catalysts. According to the results obtained, the NiPd-2 sample with the lowest Ni content (0.80%), presented the highest catalytic activity for borohydride oxidation compared with the other NiPd samples as well as the pure Pd sample. The anodic peak current density was obtained to be about 1.3 times higher on the NiPd-2 sample compared with that for the Pd sample.

수소연료에서 알루미나 담지 백금 촉매상에서의 일산화탄소 선택적 산화 반응 (Preferential Oxidation of CO over Alumina Supported Pt Catalysts in Hydrogen-rich Fuels)

  • 최진순;서동진
    • 한국수소및신에너지학회논문집
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    • 제17권3호
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    • pp.241-247
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    • 2006
  • The catalytic performances for CO preferential oxidation in hydrogen-rich fuels were investigated by varying the types of alumina supports, additives excluding platinum, and synthetic methods of impregnation and sol-gel synthesis. The reactions were conducted in the range of $25{\sim}300^{\circ}C$ over Pt, Co, and/or Na impregnated catalysts supported on commercial gamma-alumina, pseudoboehmite, or sol-gel derived xerogels. Catalytic activities were enhanced by cobalt addition due to strong Pt-Co interactions in the bimetallic phase. Additional sodium promoted not only the formation of the Pt-Co bimetallic interphase but also oxygen adsorption capability, giving rise to increase in the CO oxidation rate at lower temperatures. Moreover, chemical interaction between Pt and Co was considerably enhanced by sol-gel synthesis.

이금속성 형태 몰리브덴 촉매를 이용한 질소화합물의 반응속도 연구 (A Study on the Reaction Kinetics of Nitrogen Compounds over Bimetallic Molybdenum Catalysts)

  • 안범수
    • 한국응용과학기술학회지
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    • 제22권4호
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    • pp.349-354
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    • 2005
  • It is interesting to discover the reaction kinetics of the newly developed molybdenum containing catalysts. The dissociation/adsorption of nitrogen on molybdenum surface is known to be structure sensitive, which is similar to that of nitrogen on iron surface. The rates over molybdenum nitride catalysts are increased with the increase of total pressure. This tendency is the same as that for iron catalyst, but is quite different from that for ruthenium catalyst. The activation energies of the molybdenum nitride catalysts are almost on the same level, although the activity is changed by the addition of the second component. The reaction rate is expressed as a function of the concentration of reactants and products. The surface nature of $CO_3Mo_3N$ is drastically changed by the addition of alkali, changing the main adsorbed species from $NH_2$ to NH on the surface. The strength of $NH_x$ adsorption is found to be changed by alkali dopping.

Pt-Rh 이원금속 촉매의 구조와 반응성에 관한 연구 (A Study on Structure and Reactivity of Pt-Rh Bimetallic Catalysts)

  • 김영길;신기환;이재의
    • 공업화학
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    • 제7권4호
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    • pp.661-669
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    • 1996
  • NaY 제올라이트에 Pt/Rh비를 달리하여 이온교환법으로 제조한 Pt-Rh촉매의 특성을$^{129}Xe$-NMR과 EXAFS 방법으로 특성조사를 하였다. $^{129}Xe$-NMR과 EXAFS 자료는 PtRh 이원금속 클러스터의 표면으로 Rh 원자들이 모이는 것으로 나타났다. 모사 자동차 배기가스를 사용하여 희박, 과농 및 양론조건에서 CO, HC 및 $NO_x$ 전환율을 측정하였으며, Pt-Rh/NaY(Pt/Rh=1) 이원금속 촉매가 다른 촉매들보다 세가지 오염물질에 대한 반응활성이 높게 나타남을 알 수 있었다.

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