• 한국신재생에너지학회:학술대회논문집
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• 한국신재생에너지학회 2006년도 추계학술대회
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• pp.443-446
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• 2006

Carbon-supported Platinum (Pt) is the potential electro-catalyst material for anodic and cathodic reactions in fuel cell. Catalytic activity of the metal strongly depends on the particle shape, size and distribution of the metal in the porous supportive network. Conventional preparation techniques based on wet impregnation and chemical reduction of the metal precursors often do not provide adequate control of particle size and shape. We have proposed a novel route for preparing nano sized Pt colloidal particles in solution by oxidation of ethylene glycol. These Pt nano particles were deposited on large surface area carbon support. The process of nano Pt colloid formation involves the oxidation of solvent ethylene glycol to mainly glycolic acid and the presence of its anion glycolate depends on the solution pH. In the process of colloidal Pt formation glycolate actsas stabilizer for the Pt colloidal particle and prevents the agglomeration of colloidal Pt particles. These mono disperse Pt particles in carbon support are found uniformly distributed in nearly spherical shape and the size distribution was narrow for both supported and unsupported metals. The average diameter of the Pt nano particle was controlled in the range off to 3 nm by optimizing reaction parameters. Transmission electron microscopy, CV and RRDE experiments were used to compliment the results.

• Carbon letters
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• 제25권
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• pp.33-42
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• 2018

Activated carbon (AC) was modified by ammonium persulphate or nitric acid, respectively. AC and the modified materials were used as catalyst supports. The oxygen groups were introduced in the supports during the modifications. All the supports were characterized by $N_2$-physisorption, Raman, X-ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM), and thermogravimetric analysis. Methanol synthesis catalysts were prepared through wet impregnation of copper nitrate and zinc nitrate on the supports followed by thermal decomposition. These catalysts were measured by the means of $N_2$-physisorption, X-ray diffraction, XPS, temperature programmed reduction and TEM tests. The catalytic performances of the prepared catalysts were compared with a commercial catalyst (CZA) in this work. The results showed that the methanol production rate of AC-CZ ($23mmol-CH_3OH/(g-Cu{\cdot}h)$) was higher, on Cu loading basis, than that of CZA ($9mmol-CH_3OH/(g-Cu{\cdot}h)$). We also found that the modification methods produced strong metal-support interactions leading to poor catalytic performance. AC without any modification can prompt the catalytic performance of the resulted catalyst.

• Carbon letters
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• 제11권4호
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• pp.336-342
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• 2010

Different oxidation treatments on CNTs using diluted 4.0 M $H_2SO_4$ solution at room temperature and or at $90^{\circ}C$ reflux conditions were investigated to elucidate the physical and chemical changes occurring on the treated CNTs, which might have significant effects on their performance as catalyst supports in PEM fuel cells. Raman spectroscopy, X-ray diffraction and transmission electron microscope analyses were made for the acid treated CNTs to determine the particle size and distribution of the CNT-supported Pt-Ru nanoparticles. These CNT-supported Pt-based nanoparticles were then employed as anode catalysts in PEMFC to investigate their catalytic activity and single-cell performance towards $H_2$ oxidation. Based on PEMFC performance results, refluxed Pt-Ru/CNT catalysts prepared using CNTs treated at $90^{\circ}C$ for 0.5 h as anode have shown better catalytic activity and PEMFC polarization performance than those of the commercially available Pt-Ru/C catalyst from ETEK and other Pt-Ru/CNT catalysts developed using raw CNT, thus demonstrating the importance of acid treatment in improving and optimizing the surface properties of catalyst support.

• Bulletin of the Korean Chemical Society
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• 제28권4호
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• pp.529-532
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• 2007

Combined temperature programmed reaction (TPR) and infrared (IR) spectroscopic studies for Fischer- Tropsch reaction have been performed over Ru/SiO2 and Ru-Ag/SiO2 supported catalysts. Reaction of linearly absorbed CO with hydrogen starts at 375 K over Ru/SiO2 catalyst and reaches maximum at 420 K accompanied with an intensity decrease of linear CO absorption. The reaction with bridged absorbed CO peaks around 510-535 K. Addition of Ag yields mixed Ru-Ag bimetallic sites while it suppresses the formation of bridged bonded CO. Formation of methane on this modified surface occurs at 390 K and reaches maximum at 444 K. Suppression of hydrogen on the Ag-doped surface also occurs resulting in the formation of unsaturated hydrocarbons and of CHx intermediates not observed with Ru/SiO2 catalyst. Such intermediates are believed to be the building blocks of higher hydrocarbons during the Fischer-Tropsch synthesis. Linearly absorbed CO is found to be more reactive as compared to bridged CO. The Ag-modified surface also produces CO2 and carbon. On this surface, hydrogenation of CO begins at 390 K and reaches maximum at 494 K. The high temperature for hydrogenation of absorbed CO and C over Ru-Ag/SiO2 catalyst as compared to Ru/SiO2 catalyst is due to the formation of Ru-Ag bimetallic surfaces impeding hydrogen adsorption.

• Korean Chemical Engineering Research
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• 제53권1호
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• pp.11-15
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• 2015

휴대용 고분자전해질 연료전지의 수소발생용으로써 $NaBH_4$는 많은 장점을 갖고 있다. 본 연구에서는 비담지 Co-B, Co-P-B 촉매의 $NaBH_4$ 가수분해 특성에 대해 연구하였다. 촉매의 BET 표면적, 수소 수율, $NaBH_4$ 농도 영향, 촉매 내구성 등을 실험하였다. 비담지 Co-B 촉매의 BET 표면적은 $75.7m^2/g$으로 FeCrAlloy에 담지한 Co-B 촉매에 비해 BET 면적이 18배 높았다. 회분식 반응기에서 비담지 촉매들은 $NaBH_4$ 20~25 wt% 사용조건에서 97.6~98.5%의 높은 수소 수율을 보였다. $NaBH_4$ 농도가 30 wt%로 증가하면서 수소수율은 95.3~97.0%로 감소하였다. 비담지 촉매의 촉매 손실율은 FeCrAlloy에 담지 촉매에 비해 낮았으며, $NaBH_4$ 농도가 증가하면서 촉매 손실율도 증가하였다. 연속 반응기에서 1.2 g 비담지 Co-P-B 촉매를 사용해서 약 $3{\ell}/min$ 발생속도로 가수분해 반응하여 90%의 수소 수율을 얻었다.

• 한국수소및신에너지학회논문집
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• 제14권1호
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• pp.69-80
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• 2003

Nickel catalyst has been used for natural gas reforming with carbon dioxide, In this study, catalyst support used was HY zeolite. The optimum loading of Ni in the catalysts was 13 wt%. The effect of promoters, such as Mg, Mn, and K, was also studied. The addition of promoters to Ni catalyst improved the stability of catalysts and carbon deposition on Ni catalyst was suppressed. The reforming reactivity of promoter-added Ni catalyst was higher than that of Ni catalyst without any promoters. SEM, XRD, BET, TGA and FTIR tests were tried to characterize the catalyst structure before and after reaction.

• 한국수소및신에너지학회논문집
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• 제22권4호
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• pp.415-423
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• 2011

HI decomposition step certainly demand catalytic reaction for efficient production of hydrogen in SI process. Platinum catalyst can apply to HI decomposition reaction as well as hydrogenation or dehydrogenation. Generally, noble metal is used as catalyst which is loaded form for getting high dispersion and wide active area. In this study, Pt was loaded onto zirconia, ceria, alumina, and silica by impregnation method. HI decomposition reaction was carried out under the condition of $450^{\circ}C$, 1atm, and $167.76h^{-1}$ (WHSV) in a fixed bed reactor for measuring catalytic activity. And property of a catalyst was observed by BET, TEM, XRD and chemisoption analysis. On the basis of experimental results, we discussed about conversion of HI according to physical properties of the loaded Pt catalyst onto each support.

• 한국수소및신에너지학회논문집
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• 제23권1호
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• pp.1-7
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• 2012

This study was performed to develop a low Pt content catalyst as a catalyst for HI decomposition in S-I process. Bimetallic catalysts added various amounts of Pt on a silica supported Ni catalyst were prepared by impregnation method. HI decomposition was carried out using a fixed bed reactor. As a result, Ni-Pt bimetallic catalyst showed enhanced catalytic activity compared with each monometallic catalyst. Deactivation of Ni-Pt catalyst was not observed while deactivation of Ni monometallic catalyst was rapidly occurred in HI decomposition. The HI conversion of Ni-Pt bimetallic catalyst was increased similar to Pt catalyst with increase of the reaction temperature over a temperature range 573K to 773K. From the TG analysis, it was shown that $NiI_2$ remained on the Ni(5.0)-Pt(0.5)/$SiO_2$ catalyst after the HI decomposition reaction was decomposed below 700K. It seems that small amount of Pt in bimetallic catalyst increase the decomposition of $NiI_2$ generated after the decomposition of HI. Consequently, it was considered that the activity of Ni-Pt bimetallic catalyst was kept during the HI decomposition reaction.

• Bulletin of the Korean Chemical Society
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• 제26권11호
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• pp.1743-1748
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• 2005

This work presents that carbon dioxide, which is a main contributor to the global warming effect, could be utilized as a selective oxidant in the oxidative dehydrogenation of ethylbenzene. The dehydrogenation of ethylbenzene over alumina-supported vanadium-antimony oxide catalyst has been studied under different atmospheres such as inert nitrogen, steam, oxygen or carbon dioxide as diluent or oxidant. Among them, the addition of carbon dioxide gave the highest styrene yield (up to 82%) and styrene selectivity (up to 97%) along with stable activity. Carbon dioxide could play a beneficial role of a selective oxidant in the improvement of the catalytic behavior through the oxidative pathway.

• Bulletin of the Korean Chemical Society
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• 제16권5호
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• pp.398-400
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• 1995

Selective oxidation of cyclohexane in acetone solution has been studied using iron catalysts with hydrogen peroxide in-situ produced by palladium catalyst. Iron tetraphenylporphyrin chloride shows the highest activity among the tested chlorides and porphyrin complexes of some metals of the first transiton series. Iron chloride and iron tetraphenylporphyrin chloride were supported on four kinds of 4-vinylpyridine copolymer with styrene or divinyl-benzene. Nitrogen 1s photoelectron spectra give the evidence that pyridyl nitrogens of the 4-vinyl pyridine copolymer act as ligands to bind iron species. The copolymer with styrene is the most efficient support for the binding because its solubility in catalyst preparation solvent (methylene chloride) gives the pyridyl group advantage to contact with the iron catalysts. However, better catalytic activity per iron atom could be obtained with a rigid crosslinked polymer due to active site isolation.