• 한국대기환경학회지
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• 제18권3호
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• pp.205-212
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• 2002

The catalytic combustion of benzene, toluene and xylene over Pt-based catalyst was investigated in a fixed bed flow reactor system with atmospheric pressure to recycle the waste industrial catalyst for the processes of removing volatile organic compounds. According to the pretreatment condition, the properties of the waste Pt-based catalyst were characterized by XRD (X-ray diffraction) and BET (Brunauer-Emmett-Toller). In the carte of air pretreatment, 20$0^{\circ}C$ was found to be optimal, and increasing pretreatment temperature resulted in the reduction of the catalytic activity. When Pt-based catalyst pretreated at 20$0^{\circ}C$ by alto was retreated by hydrogen, the catalytic activity increased by increasing treatment temperature. In the case of HNO$_3$aqueous solution pretreatment, the catalytic activity decreased by increasing the concentration of HNO$_3$aqueous solution. The catalytic activity was seen to observe the following sequence : benzene > toluene > xylene.

• 한국분말재료학회지
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• 제19권1호
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• pp.6-12
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• 2012

Electricity is generated by the combined reactions of hydrogen oxidation and oxygen reduction which occur on the Pt/C catalyst surface. There have been lots of researches to make high performance catalysts which can reduce Pt utilization. However, most of catalysts are synthesized by wet-processes and a significant amount of chemicals are emitted during Pt/C synthesis. In this study, Pt/C catalyst was produced by arc plasma deposition process in which Pt nano-particles are directly deposited on carbon black surfaces. During the process, islands of Pt nano-particles were produced and they were very fine and well-distributed on carbon black surface. Compared with a commercialized Pt/C catalyst (Johnson & Matthey), finer particle size, narrower size distribution, and uniform distribution of APD Pt/C resulted in higher electrochemical active surface area even at the less Pt content.

• 분석과학
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• 제19권5호
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• pp.422-432
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• 2006

VOC는 대기오염의 주원인으로서 인식되어왔다. 촉매산화는 저온에서 높은 효율을 나타내기 때문에 VOCs 제거를 위한 가장 중요한 처리기술중 하나이다. 이 연구에서는 ${\gamma}-Al_2O_3$ 담체에 Pt, Pt-Ru 그리고 Pt-Ir을 담시지켜 촉매를 제조하였다. 반응물로서 Xylene, toluene 그리고 MEK를 사용하였다. 단일 또는 두 가지 이상의 촉매들은 함침법에 의해 준비하였고, XRD, XPS, TEM, BET 분석을 통하여 특성화하였다. 그 결과 Pt-Ru, Pt-Ir 촉매는 Pt 촉매에 비해 더 높은 전환율을 나타내었다. ${\gamma}-Al_2O_3$ 담체상에서 Pt-Ir 촉매가 가장 높은 전환율을 보인다. VOCs산화에서, Pt-Ru, Pt-Ir 촉매는 다양한 활성점을 나타내었고 그것은 Pt의 metal 영역를 강화시켰다. 따라서 두 가지 금속으로 이루어진 촉매가 단일 금속으로 이루어진 촉매에 비해 VOCs 전환율이 더 높았다. 이 연구에서 Pt에 소량의 Ru, Ir 첨가는 VOCs의 산화반응을 증진시켰다.

• Korean Chemical Engineering Research
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• 제60권3호
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• pp.459-467
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• 2022

Pt, PtSn 촉매를 제조한 후, 재분산 연구를 위해 수소분위기에서 소결시킨 후 여러 온도에서 산소처리를 적용하여 백금주석입자의 재분산 정도를 확인하고, 프로판 탈수소 반응실험으로 촉매의 활성을 측정하여 촉매의 물리적, 화학적 상태 변화와 활성의 관계를 이해하고자 하였다. 재분산 처리에 따른 촉매 활성 금속의 상태 및 촉매 입자 간 상호작용 등을 보기 위해 X-선 회절분석(XRD), CO-화학흡착(CO-pulse chemisorption), 수소 승온환원(H₂-TPR) 분석을 실시하였다. 산소 재분산 처리 조건에 따라 백금의 분산도 및 입자 크기, 촉매의 결정상 및 환원 거동이 달라지는 것을 확인하였다. 촉매를 재분산 처리하였을 시 500 ℃에서 산소 처리한 촉매가 가장 높은 전환율과 활성회복률을 보였다. 500 ℃로 산소 처리한 촉매가 백금의 분산도도 비교적 높게 나타나고, 평균 입자 크기가 작아지는 것을 XRD와 CO-화학흡착 결과로부터 확인하여 백금주석입자가 재분산되는 것을 알 수 있었다. 이러한 산소처리에 의한 재분산으로 인해 촉매활성이 회복된다는 것을 알 수 있었고, 백금보다 백금주석 촉매의 활성회복률이 더 높았다.

• 한국대기환경학회지
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• 제16권5호
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• pp.529-537
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• 2000

Several Pt-based oxidation catalysts with different loading were prepared with various metal precursor solutions and characterized with H$_2$ chemisorption and TEM for Pt particle size. V was added to Pt-based catalyst for inhibiting SO$_2$oxidation reaction, as result, Pt-V/Ti-Si catalyst prepared by ERMS(Free Reduced Metal in Solution) method showed high enough activity and better inhibition on SO$_2$oxidation than Pt only catalyst. Optimum Pt particle size for diesel oxidation reaction turned out to be the size of around 20 nm. A prototype catalyst was prepared for light=duty diesel passenger car, and teated for the emission reduction performance with Korean regulation test mode(CVS-75 mode) on chassis dynamometer. The catalyst shows the performance reduction of 75~94% for CO, 53~67% for HC and 10~31% for PM. In the case of heavy-duty diesel catalyst, the domestic formal regulation teat mode D-13 was adopted for both Na engine and Turbo engine. The conversions of CO and THC are high enough(86% and 41%) while the reductions of NOx and PM are relatively low(3~11%).

• 한국전기전자재료학회논문지
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• 제36권2호
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• pp.164-169
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• 2023

Nano Pt particles were dispersed on carbon-based supports by a polyol process for a catalyst application in a polymer electrolyte fuel cell. We tried to optimize the effect of pH on the electrostatic forces between the support and the Pt colloids. We investigated the relationship among the surface charges on the carbon support, the solution pH, and the concentration of a glycolate, and the Pt particle size. The produced catalyst with nano Pt particles on the support was evaluated by the long-term cyclic voltammetry (CV) performance test and compared with the results from a commercial catalyst. Our experimental results reveal that the pH-control can modify the particle size distribution and the dispersion of the nano Pt particles. This resulted in a cost-effective method for the synthesis of highly Pt loaded Pt/C catalysts for fuel cells better than a commercial catalyst system.

• 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).

• 청정기술
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• 제25권4호
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• pp.296-301
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• 2019

본 연구는 습윤함침법으로 제조하여 400 ℃에서 소성한 Pt/TiO₂ 촉매를 이용하여 NO 피독에 의한 CO 산화반응특성에 대하여 확인하였다. Pt/TiO₂ 촉매의 NO 피독영향을 확인하기 위하여 CO + O₂ 반응 중 NO를 주입하면서 반응활성의 변화를 관찰하였으며, 200 ℃ 이하에서 CO 전환율이 급격하게 저하되는 것을 확인하였다. 또한125 ℃ 이하에서 CO 전환율을 나타내지 않았다. 125 ℃에서 NO의 주입을 차단하더라도 초기 CO 전환율의 회복이 확인되지 않았다. 이에 따라 NO 주입에 따른 다양한 분석을 수행하였다. 먼저, TPD 분석 결과, 촉매에 NO의 선흡착은 CO 흡착을 방해하였으며 흡착된 CO에서 CO₂로의 전환탈착을 억제하는 것을 확인하였다. 다음으로, NO가 선흡착될 경우, 촉매의 산소전달능력을 감소함을 H₂-TPR 분석을 통하여 확인하였다. 또한 FT-IR 분석을 통하여, 촉매의 redox cycle (Pt²⁺→Pt⁰→Pt²⁺)을 방해하는 것을 확인하였다. 따라서 Pt/TiO₂ 촉매에서 NO의 존재는 CO 산화반응에서의 피독 인자으로 작용을 하였으며, NO 피독을 방지하기 위해서는 촉매의 산소전달능력의 증진이 필요하다고 판단되어진다.

• 전기화학회지
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• 제17권3호
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• pp.201-208
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• 2014

본 연구에서는 산화그래핀과 카본블랙의 혼합담체를 이용하여 내구성이 향상된 백금촉매를 폴리올법으로 제조하였다. 삼전극 순환전압전류법을 이용한 전기화학성능 측정결과 적절한 비율로 조절된 혼합담지체에 백금을 담지시켰을 경우 초기 성능 감소없이 장기내구성이 향상되는 것으로 나타났다. 또한 회전원판전극을 이용하여 산소환원반응을 수행한 결과 혼합담체에 담지된 백금촉매가 카본블랙 단일담체에 담지된 백금촉매보다 우수한 고유활성값을 나타내었다.

• 한국재료학회지
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• 제25권4호
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• pp.191-195
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• 2015

To improve its textural properties as a support for platinum catalyst, carbon aerogel was chemically activated with KOH as a chemical agent. Carbon-supported platinum catalyst was subsequently prepared using the prepared carbon supports(carbon aerogel(CA), activated carbon aerogel(ACA), and commercial activated carbon(AC)) by an incipient wetness impregnation. The prepared carbon-supported platinum catalysts were applied to decalin dehydrogenation for hydrogen production. Both initial hydrogen evolution rate and total hydrogen evolution amount were increased in the order of Pt/CA < Pt/AC < Pt/ACA. This means that the chemical activation process served to improve the catalytic activity of carbon-supported platinum catalyst in this reaction. The high surface area and the well-developed mesoporous structure of activated carbon aerogel obtained from the activation process facilitated the high dispersion of platinum in the Pt/ACA catalyst. Therefore, it is concluded that the enhanced catalytic activity of Pt/ACA catalyst in decalin dehydrogenation was due to the high platinum surface area that originated from the high dispersion of platinum.