• 제목/요약/키워드: Catalyst:

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고분자 연료전지용 MEA 연속 코팅공정 개발 (Continuous Coating Process Development for PEFC Membrane Electrode Assembly)

  • 박석희;윤영기;김창수;이원용
    • 한국신재생에너지학회:학술대회논문집
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    • 한국신재생에너지학회 2006년도 춘계학술대회
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    • pp.110-112
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    • 2006
  • Membrane electrode assembly (MEA) for polymer electrolyte fuel cell (PEFC) are commonly prepared in the research laboratory by spraying, screen-printing and brushing catalyst slurry onto membrane or other support material like carbon paper or polyimide film in a batch style. These hand applications of the catalyst slurry are painstaking process with respect to precision of catalyst loading and reproducibility. It has been generally mentioned that the adoption of continuous process is very helpful to develop the reliable product. In the present work, we report the results of using continuous type coater with doctor-blade to coat catalyst slurry for preparing the MEA catalyst layers In a faster and highly reproducible fashion. We show that while expectedly faster than batch style, the machine coater requires the use of slurry of appropriate composition and a properly selected transfer decal material in order to achieve superior MEA plat lnw loading reproducibility. To make highly viscous catalyst slurry that is imperative for using coater, we use 40wt.% Nafion solution and minimize the content of organic solvent. And the choice of proper high surface area catalyst is important in the viewpoint of making well-dispersed slurry. After catalyst coating onto the support material, we transferred the catalyst layer to both sides of Nafion membrane by hot-pressing In this case, the degree of transfer was Influenced by hot-pressing condition including temperature, pressure, and time. To compare the transferring ability, we compared so many films and detaching papers. And among the support, polyethylene terephthalate(PET) film shows the prominent result.

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유도가열 시스템을 이용한 Ni계 촉매의 톨루엔 산화 반응 특성 연구 (A Study on Toluene Oxidation Reaction Characteristics of Ni-Based Catalyst in Induction Heating System)

  • 이예환;김성철;김성수
    • 공업화학
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    • 제32권6호
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    • pp.627-631
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    • 2021
  • 휘발성유기화합물을 제거하기 위한 기존 촉매 시스템의 문제를 해결하고자 유도가열 촉매 시스템에 대한 연구를 수행하였다. 본 연구에서는 3종류의 Ni계 상용촉매를 적용하였으며, 촉매 부피, 조성, 열처리 분위기, 코일 내 위치를 포함한 유도가열 반응 특성을 조사하였다. 촉매의 조성 및 부피는 유도가열 시스템에 의한 발열 및 톨루엔 산화 성능에 영향을 미쳤다. 특히 철이 첨가된 촉매는 99% 이상의 Ni로 구성된 촉매에 비해 높은 발열을 나타내었으나 낮은 톨루엔 산화 성능을 나타내었다. 또한 Ni계 촉매의 열처리에 있어 공기 분위기는 촉매의 성능을 급격히 저하시킨다. 유도가열 시스템에서 촉매는 코일 내 중심에 위치하는 것이 최적 조건으로 나타났다. 연구를 통해 도출한 최적의 조건에서 촉매를 7회 반복 실험하였으며, 유사한 성능을 확인하였다.

Eco-AZ91 MgH2의 반응열 제어에 미치는 촉매 분산 효과 (Effects of Catalyst Dispersion for Reaction Energy Control on Eco-AZ91 MgH2)

  • 이수선;석송;홍태환
    • 한국수소및신에너지학회논문집
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    • 제34권6호
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    • pp.631-640
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    • 2023
  • This study selected Eco-AZ91 MgH2, which shows high enthalpy as a material for this purpose, as the basic material, and analyzed the change in characteristics by synthesizing TiNi as a catalyst to control the thermodynamic behavior of MgH2. In addition, the catalyst dispersion technology using graphene oxide (GO) was studied to improve the high-temperature aggregation phenomenon of Ni catalyst and to secure a source technology that can properly disperse the catalyst. XRD, SEM, and BET analysis were conducted to analyze the metallurgical properties of the material, and TGA and DSC analysis were conducted to analyze the dehydrogenation temperature and calorific value, and the correlation between MgH2, TiNi catalyst, and GO reforming catalyst was analyzed. As a result, the MgH2-5 wt% TiNi at GO composite could lower the dehydrogenation temperature to 478-492 K due to the reduction of the catalyst aggregation phenomenon and the increase in the reaction specific surface area, and an experimental result for the catalyst dispersion technology by GO could be ensured.

Co-P-B/FeCrAlloy 촉매를 이용한 NaBH4 가수분해 반응 (NaBH4 Hydrolysis Reaction Using Co-P-B Catalyst Supported on FeCrAlloy)

  • 황병찬;조아라;신석재;최대기;남석우;박권필
    • Korean Chemical Engineering Research
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    • 제51권1호
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    • pp.35-41
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    • 2013
  • Co-P-B/FeCrAlloy 촉매의 $NaBH_4$ 가수분해 특성과 내구성에 대해 연구하였다. 5 wt% $NaBH_4$ 농도에서 활성화 에너지가 25.2 kJ/mol로 귀금속 촉매와 비슷했고, $NaBH_4$ 농도가 증가할수록 활성화 에너지가 증가하였다. 20 wt% 이상의 $NaBH_4$ 농도에서 겔 형성이 수소발생과 촉매 내구성에 많은 영향을 줬다. $NaBH_4$ 농도가 높을 때 반응온도가 높을수록 겔 형성이 안 되므로 촉매 손실률이 낮았다. 수소발생과 촉매 내구성을 모두 고려했을 때 담지체를 $1,000^{\circ}C$에서 열처리하고, 초음파 진동없이 촉매를 담지하고, 촉매 담지 후 소성한 촉매가 우수하였다. 25 wt% $NaBH_4$에서는 촉매를 3회 이상 재사용하기 위해서는 $60^{\circ}C$ 이상의 온도에서 반응시켜야 함을 보였다.

이핵 CGC의 구조적인 특성과 에틸렌/1-헥센의 공중합 거동과의 관계 (Relation of Structural Features of Dinuclear Constrained Geometry Catalysts with Copolymerization Properties of Ethylene and 1-Hexene)

  • 까오환투이미;웽티레녕;웬티레탄;노석균
    • 폴리머
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    • 제35권6호
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    • pp.505-512
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    • 2011
  • Para-xylene의 기본 구조로 연결된 4개의 이핵 CGC를 활용하여 에틸렌과 1-헥센의 공중합특성을 조사하여 중합촉매의 구조적인 특징이 중합에 미치는 영향을 조사하였다. 4가지의 이핵 constrained geometry catalyst(CGC) 중에서 3가지는 모두 para-xylene 다리로 연결되어 있으나 벤젠고리 부분에 각각 다른 치환체가 결합된 것으로서 치환체는 수소(Catalyst 1), isopropyl(Catalyst 2), n-hexyl(Cataylst 3)이고, n-octyl(Catalyst 4)인 화합물이었다. 이핵 메탈로센 4가지와 Dow 촉매를 사용하여 에틸렌과 1-헥센을 공중합시켜 다른 치환체를 가진 다리리간드의 구조적인 특성변화가 촉매의 중합특성과 이로부터 생성되는 공중합체의 특성에 미치는 영향을 조사하였다. 실험 결과 다리리간드의 특성에 따라 분명한 경향성과 차이점이 발견되었다. 중합활성은 치환체의 크기가 가장 작은 수소에서 가장 높았으며, isopropyl에서 가장 낮았으며 그 차이는 최대 3배 이상이었다. 반면 분자량은 치환체가 isopropyl인 촉매에서 생성된 공중합체가 가장 컸고, n-hexyl과 1-octyl 치환체 화합물에서 가장 작은 분자량의 공중합체가 생성되었으며 그 차이는 6배에 달하였다. 이핵 CGC의 공중합 특성은 치환체가 긴 알킬기인 n-hexyl 및 1-octyl 화합물이 가장 우수하여 동일한 조건에서 1-헥센을 가장 많이 함유하여 40% 이상의 1-헥센을 포함하는 에틸렌 공중합체를 제조할 수 있었다. 이러한 연구 결과는 촉매구조 변화에 의한 고분자 미세구조 조절이라는 고분자 합성의 가장 어려운 부분이 xylene 다리를 가진 이핵 CGC의 치환체를 조절함으로써 가능함을 보여주는 결과이다.

단일추진제 분해촉매의 연소성능 시험 및 시제품 개발

  • 이균호;유명종;김수겸;최준민
    • 항공우주기술
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    • 제4권1호
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    • pp.49-56
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    • 2005
  • 인공위성 및 발사체의 자세제어용으로 사용되는 단일추진제 추력기용 하이드라진 분해 촉매에 대한 연소성능을 실제 연소시험을 통하여 검증하였다. 촉매연소성능을 확인하기 위한 촉매 시험장치를 (주)한화와 공동으로 설계/제작하였으며, 이를 통하여 하이드라진 분해촉매의 연소지연시간, 촉매활성도, 촉매안정도를 측정함으로써 촉매 연소특성을 평가하였다. 또한 현재 진행 중인 국산화 촉매 시제품의 개발현황에 대해 소개하였다.

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Dissolved Oxygen Removal in a Column Packed with Catalyst

  • Lee, Han-Soo;Hongsuk Chung;Cho, Young-Hyun;Ahn, Do-Hee;Kim, Eun-Kee
    • Nuclear Engineering and Technology
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    • 제28권5호
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    • pp.482-487
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    • 1996
  • The dissolved oxygen removal by H$_2$-O$_2$ reaction in column packed with various catalysts wes examined. The catalysts employed were the prepared polymeric catalyst platinum on activated carbon, and Lewatit OC-1045 which is available commercially. The column experiments with the prepared polymeric catalyst showed the dissolved oxygen reduced to 35 ppb which is below the limit in feed water of power plants. This implies the likely application of the prepared catalyst for practical use. The activated carbon required the pre-treatment for the removal of dissolved oxygen, since the surface of activated carbon contains much oxygen adsorbed initially. The Lewatit catalyst exposed the best performance, however, the aged one showed the gradual loss of catalytic activity due to degradation of resin catalyst.

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VOCs 연소를 위한 자동차 폐촉매의 전처리 효과 (Pretreatment Effect of Waste Automotive Catalysts for VOCs Combustion)

  • 문정선
    • 한국대기환경학회지
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    • 제16권2호
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    • pp.191-198
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    • 2000
  • For a characterization of the pretreated waste automotive catalyst the following analysis techniques were applied : EA(Elemental Analysis) BET(Brunaure-Emmett-Teller) and ICP-AES(Inductively Coupled Plasma-Atomic Emission Spectrometry). The combustion activity of waste automotive catalyst was investigated for methanol acetaldehyde and toluene as model VOCs in a fixed bed reactor. carbon deposit amount was decreased with increasing catalyst showed a good catalytic activity for VOCs combustion at 40$0^{\circ}C$. Catalytic activity for methanol acetaldehyde and toluence combustion was very excellent and decreased with mileage. The catalytic activity of a waste automotive catalyst for methanol combustion increased after acid treatment. The acid effect of catalytic activity was summarized as follows: HNO3>HCI>H2SO4>CH3COOH. The waste automotive catalyst regenerated by the pretreatment method might have a excellent catalytic activity for VOCs combustion.

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저온형 연료전지용 산소의 고활성 환원 촉매 제조 (Preperation of catalyst having high activity on oxygen reduction)

  • 김영우;김형진;이주성
    • 한국에너지공학회:학술대회논문집
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    • 한국에너지공학회 1992년도 학술발표회 초록집
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    • pp.39-40
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    • 1992
  • This paper dealt with the manufacturing of binary alloy catalyst and showed simple electrochemical method for determing catalytic activity of oxygen reduction in acid or alkaline electrolyte. The catalyst was prepared by impregnating transition metal salts on platinum or silver particles adsorbed before on carbon paper substrate. The electrochemical characteristics of the catalysts was investigated with carbon paper electrode or PTFE-boned porous electrode and then cathodic current densities and tafel slopes were compared. As a result, of all binary catalysts utilized in this work, Pt-Fe, Pt-Mo showed better oxygen reduction activity than pure platinum catalyst in acid electrolyte and Ag-Fe, Ag-Pt, and Ag-Ni-Bi-Ti catalyst did than pure silver catalyst in alkaline electrolyte. The current density of Pt-Fe electrode in acid electrolyte was one and half times higher than that of Pt electrode(~500mA/$\textrm{cm}^2$ at 0.7VvsNHE).

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Oxidation of Ethylbenzene Using Nickel Oxide Supported Metal Organic Framework Catalyst

  • Peng, Mei Mei;Jeon, Ung Jin;Ganesh, Mani;Aziz, Abidov;Vinodh, Rajangam;Palanichamy, Muthiahpillai;Jang, Hyun Tae
    • Bulletin of the Korean Chemical Society
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    • 제35권11호
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    • pp.3213-3218
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    • 2014
  • A metal organic framework-supported Nickel nanoparticle (Ni-MOF-5) was successfully synthesized using a simple impregnation method. The obtained solid acid catalyst was characterized by Powder X-ray diffraction (XRD), scanning electron microscopy (SEM), nitrogen adsorption-desorption and thermogravimetric analysis (TGA). The catalyst was highly crystalline with good thermodynamic stability (up to $400^{\circ}C$) and high surface area ($699m^2g^{-1}$). The catalyst was studied for the oxidation of ethyl benzene, and the results were monitored via gas chromatography (GC) and found that the Ni-MOF-5 catalyst was highly effective for ethyl benzene oxidation. The conversion of ethyl benzene and the selectivity for acetophenone were 55.3% and 90.2%, respectively.