• Bulletin of the Korean Chemical Society
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• 제28권12호
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• pp.2139-2152
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• 2007

Ruthenium complex-catalyzed reactions often require highly qualified tuning of reaction conditions with substrates to attain high yield and selectivity of the products. In this review, our strategies for achieving characteristic ruthenium complex-catalyzed co-oligomerization of different alkenes are disclosed: 1) The codimerization of 2-norbornenes with acrylic compounds by new ruthenium catalyst systems of RuCl3(tpy)/Zn [tpy = 2,2':6',2''-terpyridine] or [RuCl2(η6-C6H6)]2/Zn in alcohols, 2) A novel synthesis of 2-alkylidenetetrahydrofurans from dihydrofurans and acrylates by zerovalent ruthenium catalysts, such as Ru(η4-cod)(η6-cot) [cod = 1,5-cyclooctadiene, cot = 1,3,5-cyclooctatriene] and Ru(η6-cot)(η2-dmfm)2 [dmfm = dimethyl fumarate], 3) Regio- and stereoselective synthesis of enamides by Ru(η6-cot)(η2-dmfm)2-catalyzed codimerization of N-vinylamides with alkenes, and 4) Unusual head-to-head dimerization of styrenes and linear codimerization of styrenes with ethylene by Ru(η6-cot)(η2-dmfm)2 catalyst in the presence of primary alcohols.

• KSBB Journal
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• 제17권4호
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• pp.321-325
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• 2002

광학활성 에폭사이드는 다양한 반응성으로 인하여 고부가 가치 광학활성 의약품 및 농약 합성용 중간체로 널리 이용되고 있다. 광학활성 에폭사이드는 에폭사이드 가수분해효소 (epoxide hydrolase, EH)를 이용하여 저가의 라세믹 기질에 대한 입체선택적 가수분해 반응을 통해 제조할 수 있으며, EH는 유도과정 없이 발현되고 보조인자가 필요 없으며 비교적 효소 안정성도 높아 상업적으로 유용한 효소이다 EH에 대한생화학 및 분자생물학 관련 최근 연구 결과를 바탕으로 촉매활성 증대 및 기질 선택성을 변경시킨 tailer-made형 EH 생촉매 개발이 가능할 것이며, 실규모의 비대칭 광학분할 생물공정 시스템 개발을 통해 EH에 의한 동력학적 가수분해반응을 이용한 광학활성 에폭사이드 생산기술의 상업화가 가능할 것으로 기대된다.

• Bulletin of the Korean Chemical Society
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• 제31권1호
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• pp.133-139
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• 2010

Photoelectrocatalytic decolorization of methlene blue (MB) in the presence of two types of carbon nanotube/titania and yttrium-treated carbon nanotube/titania electrodes in aqueous solutions were studied under visible light. The prepared composite electrodes were characterized by X-ray diffraction, transmission and scanning electron microscopy, energy dispersive X-ray analysis, and photoelectrocatalytic activity. The photoelectrocatalytic performances of the supported catalysts were evaluated for the decolorization of MB solution under visible light irradiation. The results showed that yttrium incorporation enhanced the decolorization rate of MB. It was found that the photoelectrocatalytic degradation of a MB solution could be attributed to the combined effects caused by the photo-degradation of titania, the electron assistance of carbon nanotube network, the enhancement of yttrium and a function of the applied potential. The repeatability of photocatalytic activity was also tested. The presence of yttrium enhanced the hydrophillicity of yttrium-carbon nanotubes/titania electrode because more OH groups can be adsorbed on the surface.

• Macromolecular Research
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• 제15권2호
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• pp.160-166
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• 2007

Novel multiblock copolymers, based on segmented sulfonated hydrophilic-hydrophobic blocks, were synthesized and investigated for their application as proton exchange membranes. A series of segmented sulfonated poly(arylene ether sulfone)-b-polyimide multiblock copolymers, with various block lengths, were synthesized via the coupling reaction between the terminal amine moieties on the hydrophilic blocks and naphthalene anhydride functionalized hydrophobic blocks. Successful imidization reactions required a mixed solvent system, comprised of NMP and m-cresol, in the presence of catalysts. Proton conductivity measurements revealed that the proton conductivity improved with increasing hydrophilic and hydrophobic block lengths. The morphological structure of the multiblock copolymers was investigated using tapping mode atomic force microscopy (TM-AFM). The AFM images of the copolymers demonstrated well-defined nanophase separated morphologies, with the changes in the block length having a pronounced effect on the phase separated morphologies of the system. The self diffusion coefficient of water, as measured by $^1H$ NMR, provided a better understanding of the transport process. Thus, the block copolymers showed higher values than Nafion, and comparable proton conductivities in liquid water, as well as under partially hydrated conditions at $80^{\circ}C$. The new materials are strong candidates for use in PEM systems.

• 한국전기화학회:학술대회논문집
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• 한국전기화학회 2003년도 연료전지심포지움 2003논문집
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• pp.189-192
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• 2003

In this work, we have prepared platinum catalyst by various methods, investigated fuel cell performance and compared performance with commercially available $20\%$ Pt supported on carbon (Pt/C) catalyst. We have found that Pt/C prepared by reduction of chloroplatinic acid in mixed solvent (water+ethylene glycol) gives better performance compared to that produced by reduction of aqueous chloroplatinic acid, which can be attributed to smaller catalyst particle size and lower agglomeration in the mixed solvent. We have also prepared a novel platinum electrocatalyst by depositing platinum on Nafion coated carbon powder and it shows great promise. The performance of electrode prepared using $20\%Pt$ onn Nafion coated carbon mixed with Pt/C was found to be higher than the performance of electrodes using commercially available $20\%$ Pt/C, up to a current density of about $1100mA/cm^2$. The cell voltages obtained were respectively 621 and 603mV, at a current density of: $1000mA/cm^2$, in a single cell using $0.25mgPt/cm^2$ and Nafion 10035 membrane at $80^{\circ}C$ using hydrogen/oxygen reactants at 1 atm pressure.

• 대한방사성의약품학회지
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• 제2권1호
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• pp.17-21
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• 2016

Alkali metal fluoride sources (MFs) such as potassium fluoride (KF) have been widely used as a fluoride source in the nucleophilic displacement reaction. However, they have low solubility and nucleophilicity in most of the organic solvents. Bulky fluoride sources such as tetrabutylammonium fluoride (TBAF) were substituted for MFs to improve these properties. However, hygroscopic property of TBAF makes it less convenient for handling as well as its strong basic property can make the side-reaction occur. Recently, novel fluoride sources have been developed to solve these problems. In this paper, we would like to introduce coordinated fluoride sources as a new fluoride sources such as tetrabutylammonium tetra(t-butyl alcohol)-coordinated fluoride, crown ether metal complex fluoride, and various bulky alcohols coordinated fluoride complexes. In particular, bulky alcohol coordinated fluoride source could generated by the controlled hydrogen-bonded of fluoride with alcohols and these fluoride sources have better stability and reactivity with showing low hygroscopic property. The study of these fluoride sources will help to understand the characteristic of [$^{18}F$]fluoride for increasing the radiochemical yield in the [$^{18}F$]radiofluorination.

• Journal of Photoscience
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• 제6권3호
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• pp.91-96
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• 1999

Zeolites and microporouos materials continue to attract attention as novel hosts for photochemical reactions. Zeolities are attractive because of their ability to selectivity exchange and incorporate species within the void spaces and interconnecting channels, providing a spatial arrangement of molecules. Our research has primarily focused on intrazeolitic electron transfer from excited Ru(bpy)32+ in supercages of zeolite Y to a series of bipyridinium ions. In the Ru(bpy)32+ viologen-zeolite Y samples, the slowing of the back electron transfer from the bipyridinium radical cation to Ru(bpy)32+ allows for charge propagation via self exchange between diquat molecules. This provides an opportunity for permanent charge separation. When the migrating charge on the diquat radical within the zeolite reaches the surface, it can be transferred to a neutral viologen (PVS) in solution, resulting in permanent charge separation. The advantage of long-lived charge separation can be exploited for useful chemistry if suitable catablysts can be assembled on the zeolities. We have studied Ru(bpy)2 as water oxdiation catalysts. We have demonstrated that synthesis of RuO2 fibers on a zeolite via thermal decomposition of Ru3(CO)12 leads to the most active water decomposition catalyst reported to date. Because of the extensive interest of photochemical water reduction to H2, much is known about catalytic systems usin gone electron catalyst, and even more importantly, that no reaction of viologen occurred with H2 over this catalyst. The present challenge is to incorporate all these elements of the system into an architecture and we are examining zeolite membranes for this purpose.

• 한국수소및신에너지학회논문집
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• 제32권6호
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• pp.464-469
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• 2021

A reforming catalyst for hydrogen production from ammonia is being studied. Non-novel metal based Ni catalysts for use in ammonia reforming processes are being developed. In this study, the ammonia reforming characteristics according to Ni content of the alumina pellet supported catalyst in the mid-temperature region were investigated under different space velocity. 20 Ni and 3,000 h^-1 showed the best catalytic activity with ammonia conversion of 63% among all conditions.

• 공업화학
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• 제28권6호
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• pp.705-713
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• 2017

독창적 물질인 $Bi_2WO_6-GO-TiO_2$ 나노복합체를 쉬운 수열법에 의해 성공적으로 합성하였다. 수열반응을 하는 동안, 그래핀 시트 위에 $Bi_2WO_6$와 $TiO_2$를 도포하였다. 합성한 $Bi_2WO_6-GO-TiO_2$ 복합체형 광촉매는 X-선 회절법(XRD), 주사전자현미경(SEM), 에너지 분산 X-선(EDX) 분석, 투과전자현미경(TEM), 라만분광법, UV-Vis 확산반사 분광법(UV-vis-DRS), 및 X-선 광전자분광기(XPS)에 의하여 특성화하였다. $Bi_2WO_6$ 나노입자는 불규칙한 dark-square block 나노 플페이트 형상을 보였으며, 이산화티탄 나노입자는 퀜텀 도트 사이즈로 그래핀 시트 위 표면을 덮고 있었다. 로다민 비의 분해는 농도감소의 측정과 함께 UV 분광법에 의하여 관찰하였다. 합성된 물질의 광촉매 반응은 Langmuir-Hinshelwood 모델과 띠 이론으로 설명하였다.

• Korean Chemical Engineering Research
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• 제43권1호
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• pp.118-124
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• 2005

본 연구에서는 폴리피롤로 개질된 Nafion 막에 직접적으로 백금촉매를 담지하는 방법을 제시하고 PEMFC로의 응용을 검토하였다. 개시제로 $FeCl_3$ 및 $Na_2S_2O_8$을 사용하여 피롤을 Nafion 막에 중합하였다. 제저된 PPy/Nafion 복합체 막의 양이온 전도도와 함수율을 측정한 결과, $Na_2S_2O_8$을 사용하여 제조된 복합체 막은 피롤 중합시간이 증가할수록 양이온 전도도와 함수율은 감소하였고, $FeCl_3$의 경우 함수율은 감소하지만 양이온 전도도는 유지되었다. 폴리피롤로 개질된 Nafion 막에 백금 촉매를 화학적 환원법에 의해 함침한 결과, 폴리피롤의 전자 전도성 특성에 의해 백금 담지가 향상됨을 알 수 있었다. 또한 Pt/PPy/Nafion 전극촉매와 확산 전극으로 구성된 MEA를 단위 연료전지 성능평가를 행한 결과, 0.3 V의 전위에서 $569mA/cm^2$의 전류밀도 값을 갖는 연료전지 성능을 얻을 수 있었다.