• 제목/요약/키워드: Platinum (Pt) Catalysts

검색결과 97건 처리시간 0.022초

n-Octadecane 으로부터 항공유 제조를 위한 Pt-Mg/mesoporous aluminosilicate 촉매 연구 (A Study of Pt-Mg/Mesoporous Aluminosilicate Catalysts for Synthesis of Jet-fuel from n-Octadecane)

  • 정은아;김철웅;전종기
    • Korean Chemical Engineering Research
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    • 제54권5호
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    • pp.712-718
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    • 2016
  • Y 제올라이트로부터 합성한 메조 포러스 물질을 지지체로 사용한 백금 촉매를 n-octadecane의 수첨업그레이딩 반응을 통한 항공유 제조에 적용 하였다. Y 제올라이트를 골격 구성물질로 사용하여 메조 포러스 알루미노실리케이트($MMZ_{HY}$)를 합성 하였다. $Pt/MMZ_{HY}$ 촉매상에서 Mg 첨가가 n-octadecane의 수첨업그레이딩 반응에 미치는 영향을 고찰 하였다. 촉매의 특성은 X 선 회절, 질소 흡착, 승온환원, 암모니아승온탈착 및 흡착 피리딘 적외선 분광법으로 수행 하였다. 본 연구에서 Mg가 2 wt% 첨가된 $Pt/MMZ_{HY}$ 촉매가 가장 높은 항공유 수율을 보였는데, 이는 Mg의 첨가에 의해 Pt금속의 분산도와 환원도가 증가할 뿐만 아니라, 산점의 양과 세기가 증가하기 때문이다. 또한 $PtMg/MMZ_{HY}$ 촉매 상에서 이소 파라핀에 대한 선택도가 80 % 이상임을 확인하였다.

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.

디젤엔진 배기가스조건하에서의 Pt 및 Ag 담지 알루미나 촉매의 열적 노화 특성과 SOx 피독 특성에 관한 연구 (A Study on the Thermal Aging and SOx Poisoning Characteristics on Alumina Supported Silver Catalyst under Diesel Engine Emission Condition)

  • 신병선
    • 한국대기환경학회지
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    • 제16권2호
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    • pp.199-208
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    • 2000
  • In this study we investigated on the possibility of platinum and silver catalysts as de-NOx catalyst for activity test of supported metal oxide catalysts. the study was performed with the change of amount of metal and support types. The catalyst was prepared the activity of alumina supported silver catalyst produced by dry and wet impregnation method respectively and the resistance of sulfur for optimum supported silver catalyst,. As a result the activity of alumina supported platinum catalyst was showed at low temperature region but the case of silver catalyst activated at high temperature region. So we finally chose alumina supported silver catalyst as de-NOx target catalyst because alumina supported catalyst showed higher activity than alumina supported platinum catalyst.

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Nano-structured Carbon Support for Pt/C Anode Catalyst in Direct Methanol Fuel Cell

  • Choi Jae-Sik;Kwon Heock-Hoi;Chung Won Seob;Lee Ho-In
    • 한국분말재료학회지
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    • 제12권2호
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    • pp.117-121
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    • 2005
  • Platinum catalysts for the DMFC (Direct Methanol Fuel Cell) were impregnated on several carbon supports and their catalytic activities were evaluated with cyclic voltammograms of methanol electro-oxidation. To increase the activities of the Pt/C catalyst, carbon supports with high electric conductivity such as mesoporous carbon, carbon nanofiber, and carbon nanotube were employed. The Pt/e-CNF (etched carbon nanofiber) catalyst showed higher maximum current density of $70 mA cm^{-2}$ and lower on-set voltage of 0.54 V vs. NHE than the Pt/Vulcan XC-72 in methanol oxidation. Although the carbon named by CNT (carbon nanotube) series turned out to have larger BET surface area than the carbon named by CNF (carbon nanofiber) series, the Pt catalysts supported on the CNT series were less active than those on the CNF series due to their lower electric conductivity and lower availability of pores for Pt loading. Considering that the BET surface area and electric conductivity of the e-CNF were similar to those of the Vulcan XC-72, smaller Pt particle size of the Pt/e-CNF catalyst and stronger metal-support interaction were believed to be the main reason for its higher catalytic activity.

프로판 펄스 주입에 의한 백금주석촉매의 탈수소반응 특성 연구 (Study of the Dehydrogenation Characteristics of Pt-Sn Catalysts by Propane Pulse Injection)

  • 고형림;정재원;최이선
    • Korean Chemical Engineering Research
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    • 제57권4호
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    • pp.575-583
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    • 2019
  • 반응물의 펄스주입에 의한 촉매반응결과는 코크가 많은 반응의 경우 초기반응특성을 연구하는데 유용하다. 프로판의 펄스주입으로 알루미나에 담지된 백금주석촉매의 탈수소 반응 특성을 연구하였다. 프로판 주입전 촉매의 환원을 $550^{\circ}C$에서 한 경우, 환원시간이 1시간인 경우 프로필렌의 수율이 최대가 되었다. PtSn (4.5)촉매를 사용하고, 프로판 펄스 주입에 의해 짧은 접촉시간을 모사한 경우 코크의 양이 매우 적었음을 Raman분석으로 알 수 있었다. 백금의 분산도를 다르게 하기위하여 PtSn (4.5)촉매를 수소로 $900^{\circ}C$에서 신터링 후 공기-재분산시의 온도를 다르게 처리한 후, 프로판 펄스 주입한 결과 공기처리 온도가 $600^{\circ}C$ 일 때 프로판의 전환율과 수율은 가장 높았다. 공기-재분산의 온도가 낮을수록 선택도는 높았다. 백금촉매에 주석함량이 증가함에 따라 프로판 전환율은 낮아졌지만, 프로필렌으로의 선택도는 높아져서, 수율은 증가하였다. 이로부터 주석을 첨가한 백금촉매는 코크의 영향이 적은 반응초기부터 백금촉매보다 활성이 낮다는 것을 알 수 있다. 프로판 펄스주입에 의한 탈수소반응은 COx의 생성에 의해 연속주입에 의한 결과보다 높은 전환율을 보이고, 코크의 양이 매우 적은 특징을 보이고 있다. COx의 생성에 의한 선택도 하락은 환원온도와 시간을 증가시키면 줄일 수 있다.

Low temperature preparation of Pt alloy electrocatalysts for DMFC

  • 송민우;이경섭;김영순;신형식
    • 한국신재생에너지학회:학술대회논문집
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    • 한국신재생에너지학회 2009년도 추계학술대회 논문집
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    • pp.171-171
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    • 2009
  • The electrodes are usually made of a porous mixture of carbon-supported platinum and ionomers. $SnO_2$ particles provide as supports that have been used for DMFCs, and it have high catalytic activities toward methanol oxidation. The main advantage of $SnO_2$ supported electrodes is that it has strong chemical interactions with metallic components. The high activity to a synergistic bifunctional mechanism in which Pt provides the adsorption sites for CO, while oxygen adsorbs dissociative on $SnO_2$. The reaction between the adsorbed species occurs at the Pt/$SnO_2$ boundary. The morphological observations were characterized by FESEM and transmission electron microscopy (TEM). $SnO_2$ particles crystallinity was analyzed by the X-ray diffraction (XRD). The surface bonded state of the $SnO_2$ particles and electrode materials were observed by the X-ray photoelectron spectroscopy (XPS). The electric properties of the Pt/$SnO_2$ catalyst for methanol oxidation have been investigated by the cyclic voltametry (CV) in 0.1M $H_2SO_4$ and 0.1M MeOH aqueous solution. The peak current density of methanol oxidation was increased as the $SnO_2$ content in the anode catalysts increased. Pt/$SnO_2$ catalysts improve the removal of CO ads species formed on the platinum surface during methanol electro-oxidation.

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귀금속촉매하에서 암모니아의 전환반응 (Ammonia Conversion in the Presence of Precious Metal Catalysts)

  • 장현태;박윤국;고용식
    • Korean Chemical Engineering Research
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    • 제46권4호
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    • pp.806-812
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    • 2008
  • 귀금속촉매 존재하에서 암모니아 전환반응은 배가스내의 암모니아를 처리하는데 중요한 기술이다. 과잉용액 함침법을 이용하여 $Pt-Rh/Al_2O_3$, $Pt-Rh/TiO_2$, $Pt-Rh/ZrO_2$, $Pt-Pd/Al_2O_3$, $Pd-Rh/Al_2O_3$, $Pd-Rh/TiO_2$, $Pd-Rh/ZrO_2$, $Pt-Pd-Rh/Al_2O_3$, $Pd/Ga-Al_2O_3$, $Rh/Ga-Al_2O_3$, 그리고 $Ru/Ga-Al_2O_3$의 촉매를 제조하였다. 제조된 촉매는 1/4"의 반응기에 $10,000{\sim}50,000hr^{-1}$의 공간속도 조건하에서 촉매활성능 실험을 수행하였다. 암모니아의 초기농도는 2,000 ppm (나머지는 공기)으로 유지하였다. $T_{50}$는 암모니아 전환율이 50%일 때를 나타내는 온도를, $T_{90}$은 90%의 전환율일 때의 온도를 나타낸다. 알루미나를 담지체로 사용했을때의 $T_{50}$$T_{90}$은 다른 담체를 사용했을때의 $T_{50}$$T_{90}$보다 훨씬 낮았다. Pd-Rh촉매의 경우 $Al_2O_3$를 담체로 사용하였을 때 $ZrO_2$$TiO_2$보다 저온 활성이 우수하게 나타났다. 황산화물의 피독실험 결과 본 연구에서는 최종적으로 $Pt-Rh/Al_2O_3$ 촉매가 다른 촉매에 비하여 우수함을 보였다. 실험결과 Pt-Rh가 암모니아 전환공정에서 유용한 촉매라는 사실을 알 수 있다.

고분자 전해질 연료전지용 촉매 소재 개발을 위한 원자층증착법 연구 동향 (Recent Research Progress on the Atomic Layer Deposition of Noble Metal Catalysts for Polymer Electrolyte Membrane Fuel Cell)

  • 한정환
    • 한국분말재료학회지
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    • 제27권1호
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    • pp.63-71
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    • 2020
  • It is necessary to fabricate uniformly dispersed nanoscale catalyst materials with high activity and long-term stability for polymer electrolyte membrane fuel cells with excellent electrochemical characteristics of the oxygen reduction reaction and hydrogen oxidation reaction. Platinum is known as the best noble metal catalyst for polymer electrolyte membrane fuel cells because of its excellent catalytic activity. However, given that Pt is expensive, considerable efforts have been made to reduce the amount of Pt loading for both anode and cathode catalysts. Meanwhile, the atomic layer deposition (ALD) method shows excellent uniformity and precise particle size controllability over the three-dimensional structure. The research progress on noble metal ALD, such as Pt, Ru, Pd, and various metal alloys, is presented in this review. ALD technology enables the development of polymer electrolyte membrane fuel cells with excellent reactivity and durability.

촉매습식산화에 의한 Ethylene Glycol의 분해 (Decomposition of Ethylene Glycol by Catalytic Wet Air Oxidation)

  • 안상준;최장승;이동근
    • 한국염색가공학회지
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    • 제13권4호
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    • pp.264-271
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    • 2001
  • Catalytic wet oxidation of ethylene glycol as refractory compound was studied in a batch slurry reactor using lwt% $Pt/A1_2O_3$, lwt% $Pt/TiO_2,\;Mn/CeO_2$(1:1) and 5wt% $Mn/Al_2O_3$. Experiments were conducted to investigate theeffects of temperature, initial ethylene glycol concentration, catalyst dosage and PH on the ethylene glycol decomposition. When compared with the uncatalyzed reaction, the use of catalysts could increase the rate of ethylene glycol decomposition. The lwt% $Pt/A1_2O_3$ catalyst was preferable to the other catalysts for the destructive oxidation of ethylene glycol. The reaction rate was first order with respect to initial concentration of ethylene glycol. In acidic condition the removal efficiency of ethylene glycol was good, but there was a significant leaching of platinum. Small amount of acetic acid, oxalic acid, masonic acid and formic acid as intermediates were detected during catalytic wet air oxidation of ethylene glycol.

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Electrocatalytic Oxidation of HCOOH on an Electrodeposited AuPt Electrode: its Possible Application in Fuel Cells

  • Uhm, Sung-Hyun;Jeon, Hong-Rae;Lee, Jae-Young
    • Journal of Electrochemical Science and Technology
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    • 제1권1호
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    • pp.10-18
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    • 2010
  • Controlled electrodeposition of dendritic nano-structured gold-platinum (AuPt) alloy onto an electrochemically pretreated carbon paper substrate was conducted in an attempt to improve catalyst utilization and to secure an electronic percolation network toward formic acid (FA) fuel cell application. The AuPt catalysts were obtained by potentiostatic deposition. AuPt catalysts synthesized as bimetallic alloys with 60% Au content exhibited the highest catalytic activity towards formic acid electro-oxidation. The origin of this high activity and the role of Au were evaluated, in particular, by XPS analysis. Polarization and stability measurements with 1 mg $cm^{-2}$ AuPt catalyst (only 0.4 mg $cm^{-2}$ Pt) showed 52 mW $cm^{-2}$ and sustainable performance using 3M formic acid and dry air at $40^{\circ}C$.