• 한국신재생에너지학회:학술대회논문집
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• 2010.11a
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• pp.198.1-198.1
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• 2010

고분자전해질 연료전지(PEMFC)의 핵심부품인 스택의 MEA는 전극과 멤브레인 전해질, GDL(Gas Diffusion Layer)로 구성되며, 전극은 Anoth극과 Cathod극으로 나뉘어 각각의 전극 특성에 적합한 전극촉매를 적용하게 된다. Anoth극과 Cathod극은 탄소 지지체 위에 원하는 사양의 희유금속이 도포되어 존재하는데 이들 희유금속은 그 희귀성으로 인해 사용 후 반드시 재사용되어야 한다. 사용된 전극에서의 희유금속 회수는 산침출, 불순물제거, 추출, 탈거 공정으로 이루어지며, 산침출 시 산화제로 사용된 NaOCl로 인한 침출용액 내의 Na+ 이온의 증가는 불순물제거 공정에 의해 반드시 제거되어야 한다. 따라서 본 연구에서는 CCG 방식으로 전극촉매를 GDL에 코팅한 MEA로부터 백금족 희유금속을 회수 시 MEA에 포함되어 있는 소량의 불순물을 제거하고자 한다.

• 한국신재생에너지학회:학술대회논문집
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• 2011.05a
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• pp.94.1-94.1
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• 2011

In this work, ordered mesoporous carbons (OMCs) were prepared by the conventional templating method using mesoporous silica (SBA-15) for Pt-Ru catalyst supports in fuel cells. The influence of surface modification on carbon supports on the electrochemical activities of Pt-Ru/OMCs was investigated with different pH. The neutral-treated OMCs (N-OMCs), base-treated OMCs (B-OMCs), and acid-treated OMCs (A-OMCs) were prepared by treating OMCs with 2 M $C_6H_6$, 2 M KOH, and 2 M $H_3PO_4$, respectively. The surface characteristic of the carbon supports were determined X-ray photoelectron spectroscopy (XPS). The electrochemical activities of the Pt-Ru catalysts had been enhanced when the OMCs supports were treated by basic or neutral agents, while the electrochemical activities had been decayed for the A-OMCs supported Pt-Ru.

• Proceedings of the KIEE Conference
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• 1997.07d
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• pp.1358-1360
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• 1997

In this paper, the performance of Pt/$WO_3$ and Pt-$WO_3$ electrodes was studied for the direct methanol fuel cell. The characteristics of Pt/$WO_3$ electrode which was prepared by using electrodeposition method was tested with half-cell experiment. The characteristics of Pt-$WO_3$/C electrode which was Prepared by using freeze-drying method was tested with a single cell experiment. The performance of DMFC single cell which was prepared by Pt-$WO_3/C$ and Pt/C showed a current density of $32mA/cm^2$ at $110^{\circ}C$ & 0.3V(0.5mg Pt/$cm^2$).

• 한국신재생에너지학회:학술대회논문집
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• 2010.06a
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• pp.231-231
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• 2010

아직까지 국내에서 사용하는 대부분의 에너지는 화석연료에 의존하고 있다. 지하자원에서 나오는 석탄, 석유와 같은 화석연료는 다른 에너지원에 비해 운송이 간편하고 쉽게 이용할 수 있는 장점이 있지만, 환경오염의 문제성과 오일가상승, 자원의양 및 저장장소가 한정되어 있다는 단점을 가지고 있다. 이에 따라 수소와 같은 대체에너지를 이용하여 환경오염을 예방하고 무한히 사용할 수 있는 에너지원을 개발하기 위한 대체 방안들이 연구되고 있다. 폐기물 가스화시 발생되는 합성가스(CO, $CO_2$, $CH_4$, $H_2$) 내 일차로 생성된 일산화탄소는 수증기와 반응함으로써 이산화탄소로 전환이 가능하다. 잔류 메탄은 이산화탄소를 이용하여 개질함으로써 합성가스내 수소농도를 높일 수 있다. 전환된 잔류가스(CO, $CO_2$, $H_2$)내 일산화탄소는 산소를 이용하여 이산화탄소로 산화시킬 수 있으며, 산화된 이산화탄소는 흡착제를 이용하여 제거가 가능하다. 본 연구에서는 실제 가스화시 발생되는 합성가스를 이용하기 위하여, RPF가스화시 발생되는 합성가스를 직접 포집하여 실험을 진행하였다. 합성가스내 소량의 메탄은 니켈촉매를 이용하여 수소로 전화시켰으며, 잔류하는 일산화탄소는 백금촉매, 이산화탄소는 탄산나트륨 흡착제를 이용하여 연속적으로 제거함으로써 순수한 수소를 제공하였다.

• Journal of Hydrogen and New Energy
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• v.17 no.3
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• pp.301-308
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• 2006

The present work explores the effect of carbon-supported platinum catalyst on the HI decomposition using gas adsorption analyzer, thermogravimetry, X-ray diffractometry, scanning electron microscopy, and gas chromatography. For this purpose, three types of activated carbon (C), Pt/C-1 wt.%, and Pt/C-5 wt.% were prepared. The HI gas conversion is crucially influenced by the amount of Pt on the carbon support. The more the amount of Pt was, the higher results in the HI gas conversion. For three types of catalysts, HI conversion increased with increasing the decomposition temperature but with decreasing the space velocity. The increase of HI conversion with temperature was more pronounced in activated carbon than that in Pt/C. From EDX result, it was found that the activated carbon comprised higher amount of iodine than the Pt/C after the decomposition reaction. This implies that the HI conversion is closely related to the amount of Iodine.

• Korean Chemical Engineering Research
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• v.54 no.2
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• pp.262-267
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• 2016

In this study, we present an excellent approach for easily and uniformly immobilizing Pt, Au and bimetallic PtAu nanoparticles (NPs) on a multi-walled carbon nanotube (MWNT)-coated layer through dry plasma reduction. The NPs are stably and uniformly immobilized on the surface of MWNTs and the nanohybrid materials are applied to counter electrode (CE) of dye-sensitized solar cells (DSCs). The electrochemical properties of CEs are examined through cyclic voltammogram, electrochemical impedance spectroscopy, and Tafel measurements. As a result, both electrochemical catalytic activity and electrical conductivity are highest for PtAu/MWNT electrode. The DSC employing PtAu/MWNT CE exhibits power conversion efficiency of 7.9%. The efficiency is better than those of devices with MWNT (2.6%), AuNP/MWNT (2.7%) and PtNP/MWNT (7.5%) CEs.

• Resources Recycling
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• v.28 no.2
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• pp.46-53
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• 2019

In this study, the extraction and reduction behavior of platinum group metals in a non-aqueous solvent based on ionic liquids was investigated in order to confirm a new extraction technology of platinum group metals. Platinum was selectively extracted using an ionic liquid $[C_4mim]PF_6$ from a mixed solution of $PdCl_2$, $PtCl_4$ and $RhCl_3$ dissolved with concentration ratio of 10:1:0.5 M. After stripping of the metals by 1 M $HNO_3$ solution, the platinum was preferentially reduced by aqueous electrolysis on gold electrode at -0.8 V (vs. Pt-QRE). The residual palladium and rhodium were transferred to ionic liquid of $[C_4mim]Cl$. The metallic palladium and rhodium could be sequentially reduced on gold and STS304 as working electrodes by non-aqueous electrolysis, respectively.

• Journal of Hydrogen and New Energy
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• v.17 no.3
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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.

• Korean Chemical Engineering Research
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• v.50 no.3
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• pp.435-441
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• 2012

The direct conversion of cellulose into polyols in $H_2$ was examined over Pt catalysts supported on various zeolites, viz., mordenite, Y, ferrierite, and ${\beta}$. For comparison, Pt catalysts supported on ${\gamma}-Al_2O_3$, $SiO_2-Al_2O_3$, and $SiO_2$ were also tested. The physical properties of the catalysts were probed with $N_2$ physisorption. The surface acidity was measured with temperature programmed desorption of ammonia ($NH_3$-TPD). The Pt content was quantified with inductively coupled plasma-atomic emission spectroscopy (ICP-AES). The Pt dispersion was determined with CO chemisorptions and transmission electron microscopy (TEM). The conversion of cellulose appeared to be mainly dependent on the reaction temperature and reaction time because it depends on the concentration of $H^+$ ions reversibly formed in hot water. Pt/H-mordenite (20) showed the highest yield to polyols among the tested catalysts. Pt/H-zeolite was superior to Pt/Na-zeolite for this reaction. The polyol yield was dependent on the surface acid density and the external surface area.

• 한국신재생에너지학회:학술대회논문집
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• 2009.06a
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• pp.365-368
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• 2009

메탄올 연료전지에서 기존의 탄소 지지체의 전기화학적인 특성과 유사한 새로운 지지체 물질을 개발하기위해서 $TiO_2$ 산화물을 선정하였고 이것의 전도성을 향상에 관한 연구를 하였다. 새로운 지지체인 Degussa $TiO_2$를 이용하여 고온에서 열처리하는 방법으로써 얻을 수 있었다. 이러한 지지체위에 백금 촉매를 담지하는 합성 실험은 간단한 방법인 sodium borohydride 방법으로써 수행하였고 구조적인 결과를 확인하기 위하여 XRD 분석으로써 확인하였다. 결과로부터 $TiO_2$에서 TiN으로 구조적인 변화를 알 수 있었고 상변화 과정이 높은 에너지와 소스로 인해 바뀐다는 것을 알 수 있었다. 이러한 지지체 촉매 전극의 전기적인 활성을 알아보기 위하여 CVs와 안전성을 확인하기 위하여 CA에서 분석하였다. 기존 탄소 지지체 촉매 전극과 황산과 메탄올 용액하에서 CVs와 CA를 비교하였을 때, 티타늄 질화물 지지체가 CVs에서 유사한 산화, 환원 활성을 나타내었고 CA에서 높은 전류에서 안정성을 보여주었다. 이러한 결과로부터 TiN 지지체는 탄소 지지체와 비교하였을 때 연료전지의 지지체로써의 가능성을 확인 할 수 있었다.