• 제목/요약/키워드: Catalytic support

검색결과 263건 처리시간 0.032초

깁사이트를 원료로 한 고온촉매용 담체의 제조 II, 비정질 알루미나의 담체 전구체로서의 특성 (Preparation of High-Temperature catalytic Support from Gibbsite II. Properties of Amophous Alumina as Precursor of Catalyst Support)

  • 김성연;김연식
    • 한국세라믹학회지
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    • 제33권1호
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    • pp.92-100
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    • 1996
  • Amorphous alumina(AA) the precursor of ${\gamma}$-alumina for catalyst support was made in the newly designed ball filled heating column. Some properties of AA as precursor were investigated. In observation of microstruc-ture and pore structure of AA and its derivatives scanning electronic microscope(SEM) and transmission electronic microscope(TEM) were used. It was found that the width of one particle in AA was 45~60$\AA$ and the average distance among the particles ranged 9~12 $\AA$ which suggested a micropore structure. When AA was reacted with water the shape of the surface was found to be altered and acicular bioehmite was formed inside AA which contributed inproved formability. Pore distribution was evaluated for the three samples of AA ground and granulated lump and La2O3 coated alumina. Acid sites were quantitatively determined by ammonia TPD method and the effect of impurity of Na on acid sites was discussed. Water adsorption capacity was evaluated in terms of a desiccant.

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수소-알코올연료전지를 위한 금속-산화물 나노구조제어 (Control of Metal-Oxide Nanostructures for $H_{2}-Alcohol$ Fuel Cells)

  • 박경원;송유정;한상범;이종민
    • 한국신재생에너지학회:학술대회논문집
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    • 한국신재생에너지학회 2007년도 춘계학술대회
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    • pp.141-145
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    • 2007
  • Due to their excellent catalytic activity with respect to methanol oxidation on platinum at low temperature, platinum nanosized catalysts have been a topic of great interest for use in direct methanol fuel cells (DMFCs). Since pure platinum is readily poisoned by CO, a by-product of methanol electrooxidation, and is extremely expensive, a number of efforts to design and characterize Pt-based alloy nanosized catalysts or Pt nanophase-support composites have been attempted in order to reduce or relieve the CO poisoning effect. In this review paper, we summarize these efforts based upon our recent research results. The Pt-based nanocatalysts were designed by chemical synthesis and thin-film technology, and were characterized by a variety of analyses. According to bifunctional mechanism, it was concluded that good alloy formation with $2^{nd}$ metal (e.g., Ru) as well as the metallic state and optimum portion of Ru element in the anode catalyst contribute to an enhanced catalytic activity for methanol electrooxidation. In addition, we found that the modified electronic properties of platinum in Pt alloy electrodes as well as the surface and bulk structure of Pt alloys with a proper composition could be attributed to a higher catalytic activity for methanol electooxdation. Proton conducting contribution of nanosized electrocatalysts should also be considered to be excellent in methanol electrooxidation (Spillover effect). Finally, we confirmed the ensemble effect, which combined all above effects, in Pt-based nanocatalsyts especially, such as PtRuRhNi and $PtRuWO_{3}$, contribute to an enhanced catalytic activity.

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Catalytic Effects and Characteristics of Ni-based Catalysts Supported on TiO2-SiO2 Xerogel

  • Jeong, Jong-Woo;Park, Jong-Hui;Choi, Sung-Woo;Lee, Kyung-Hee;Lee, Chang-Seop
    • Bulletin of the Korean Chemical Society
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    • 제28권12호
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    • pp.2288-2292
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    • 2007
  • The catalytic activities of nickel-based catalysts were estimated for oxidizing acetaldehyde of VOCs exhausted from industrial facilities. The catalysts were prepared by sol-gel methods of SiO2 and SiO2-TiO2 as a xerogel followed by impregnating Al2O3 powder with the nickel nitrate precursor. The crystalline structure and catalytic properties for the catalysts were investigated by use of BET surface area, X-ray diffraction (XRD), Xray photoelectron spectroscopy (XPS) and temperature programmed reduction (TPR) techniques. These results show that nickel oxide is transformed to NiAl2O4 spinel structure at the calcination temperature of 400 °C in response to the steps with after- and co-impregnation of Al2O3 powder in sol-gel process. The NiAl2O4 could suppress the oxidation reaction of acetaldehyde by catalysts. The NiO is better dispersed on SiO2-TiO2/Al2O3 support than SiO2/Al2O3 and SiO2-TiO2-Al2O3 supports. From the testing results of catalytic activities for oxidation of acetaldehyde, Catalysts showed a big difference in conversion efficiencies with the way of the preparation of catalysts and the loading weight of nickel. The catalyst of 8 wt.% Ni/TiO2-SiO2/Al2O3 showed the best conversion efficiency on acetaldehyde oxidation with 100% conversion efficiency at 350 °C.

Catalytic Activity of Au/$TiO_2$ and Pt/$TiO_2$ Nanocatalysts Synthesized by Arc Plasma Deposition

  • Jung, Chan-Ho;Kim, Sang-Hoon;Reddy, A.S.;Ha, H.;Park, Jeong-Y.
    • 한국진공학회:학술대회논문집
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    • 한국진공학회 2012년도 제42회 동계 정기 학술대회 초록집
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    • pp.245-245
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    • 2012
  • Syntheses of oxide supported metal catalysts by wet-chemical routes have been well known for their use in heterogeneous catalysis. However, uniform deposition of metal nanoparticles with controlled size and shape on the support with high reproducibility is still a challenge for catalyst preparation. Among various synthesis methods, arc plasma deposition (APD) of metal nanoparticles or thin films on oxide supports has received great interest recently, due to its high reproducibility and large-scale production, and used for their application in catalysis. In this work, Au and Pt nanoparticles with size of 1-2 nm have been deposited on titania powder by APD. The size of metal nanoparticles was controlled by number of shots of metal deposition and APD conditions. These catalytic materials were characterized by x-ray diffraction (XRD), inductively coupled plasma (ICP-AES), CO-chemisorption and transmission electron microscopy (TEM). Catalytic activity of the materials was measured by CO oxidation using oxygen, as a model reaction, in a micro-flow reactor at atmospheric pressure. We found that Au/$TiO_2$ is reactive, showing 100% conversion at $110^{\circ}C$, while Pt/$TiO_2$ shows 100% conversion at $200^{\circ}C$. High activity of metal nanoparticles suggests that APD can be used for large scale synthesis of active nanocatalysts. We will discuss the effect of the structure and metal-oxide interactions of the catalysts on catalytic activity.

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H2O2 촉매 전환에 의해 생성된 건식산화제를 이용한 NO 산화에 관한 연구 (A study on the NO oxidation using dry oxidant produced by the catalytic conversion of H2O2)

  • 장정희;한기보
    • 한국응용과학기술학회지
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    • 제33권1호
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    • pp.100-109
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    • 2016
  • 본 연구에서는 촉매 상 $H_2O_2$ 전환에 의해 건식산화제가 생성되었으며, 이를 이용한 NO 산화 공정에 대한 연구를 진행하였다. 건식산화제를 생성하기 위한 $H_2O_2$ 촉매 전환에 관한 실험을 수행한 결과, Mn계 촉매의 성능이 가장 우수하였으며, 이를 통해 생성된 건식산화제를 NO 산화공정에 주입하여 다양한 운전조건에서 NO 산화특성을 조사하였다. 그 결과, $H_2O_2$ 주입량, 산화반응온도, 그리고 공간속도가 NO 산화율에 크게 영향을 미치는 것을 확인하였다. 그리고, 산화반응온도와 $H_2O_2$ 주입량이 증가할수록 NO 산화효율이 증가하였으며, 공간속도가 증가할수록 NO 산화효율이 감소하였다.

촉진적 원조를 통한 수원국과의 개발협력에 관한 연구 (International Cooperation Development with Recipient Countries by Catalytic Aid)

  • 이호건
    • 무역학회지
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    • 제41권1호
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    • pp.117-138
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    • 2016
  • ODA란 개발도상국 빈곤층을 대상으로 인간의 기본권을 지키려는 국제사회의 노력과 행동이다. UN은 현재 2030년까지의 개발목표로 SDGs를 설정하였다. SDGs에서는 기존 ODA의 한계를 극복하기 위하여 개념을 확장하고 공공부문과 민간부문이 협력하여 다양한 재원을 조달함으로서 ODA와 그 범위를 넘어서는 개발원조까지 포괄하고 있으며, 이에 적합한 개념이 촉진적 원조이다. 촉진적 원조에 의한 개발협력은 인도주의적 원조 보다는 경제 인프라 및 생산시설 등 경제 발전의 기반을 구축하여 수원국의 지속가능한 개발을 지원하는 사업이다. 본 연구에서는, 한국의 경험과 현재의 역량을 토대로 KSP를 연계하여 민관협력사업 발굴, 집중지원 대상국의 선정 및 원조배분 원칙의 명확화, 사업 특성에 맞는 유·무상 원조의 유연한 적용, SPC 설립에 의한 CSV의 실현 및 이를 종합적으로 이끌어 갈 PCSD 체제의 구축을 제안하였다.

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Synthesis, Characterization and Application of Poly(4-vinylpyridine)-Supported Brønsted Acid as Reusable Catalyst for Acetylation Reaction

  • Borah, Kalyan Jyoti;Dutta, Papia;Borah, Ruli
    • Bulletin of the Korean Chemical Society
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    • 제32권1호
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    • pp.225-228
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    • 2011
  • Poly(4-vinylpyridine)-supported $Br{\phi}nsted$ acids (P4VP-HX) were prepared by wet impregnation technique. These supported acids were found as efficient heterogeneous green catalysts for acetylation of alcohol, amine and phenol with different catalytic activities. The wide application of P4VP-HX as reusable solid acid catalyst in organic reactions is possible because of its simple preparation and handling, stability, simple work up procedure.

Lead Tolerance of Noble Metal Catalysts for CO Oxidation

  • Chang, Tu-Won;Sohn, Youn-Soo
    • Bulletin of the Korean Chemical Society
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    • 제7권1호
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    • pp.12-15
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    • 1986
  • Lead tolerance of $Pt/Al_2O_3$ catalysts was evaluated for CO oxidation depending on the properties of the alumina supports and base metals added as promoter. Among the four different alumina supports, the support with a large macropore volume (0.45 cc/g) and 5% Ce has shown the best resistence to lead poisoning. Most of the base metals added to the Pt-catalysts were found to be ineffective for improving lead resistence, but boron has shown an excellent lead tolerence, although it decreases the initial catalytic activity.

Photocatalytic Degradation of Methylene Blue in Presence of Graphene Oxide/TiO2 Nanocomposites

  • Kim, Sung Phil;Choi, Hyun Chul
    • Bulletin of the Korean Chemical Society
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    • 제35권9호
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    • pp.2660-2664
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    • 2014
  • A simple method of depositing titanium dioxide ($TiO_2$) nanoparticles onto graphene oxide (GO) as a catalytic support was devised for photocatalytic degradation of methylene blue (MB). Thiol groups were utilized as linkers to secure the $TiO_2$ nanoparticles. The resultant GO-supported $TiO_2$ (GO-$TiO_2$) sample was characterized by transmission electron microscopy (TEM), near-edge X-ray absorption fine structure (NEXAFS), and X-ray photoelectron spectroscopy (XPS) measurements, revealing that the anatase $TiO_2$ nanoparticles had effectively anchored to the GO surface. In the photodegradation of MB, GO-$TiO_2$ exhibited remarkably enhanced photocatalytic efficiency compared with thiolated GO and pure $TiO_2$ nanoparticles. Moreover, after five-cycle photodegradation experiment, no obvious deactivation was observed. The overall results showed that thiolated GO provides a good support substrate and, thereby, enhances the photodegradation effectiveness of the composite photocatalyst.