• 제목/요약/키워드: Catalytic properties

검색결과 677건 처리시간 0.025초

베릴리아-실리카 촉매의 특성과 산촉매성질 (Characterization and Acid Catalytic Properties of Beryllia-Silica Catalysts)

  • 손종락;박은희;장향자;김해원
    • 공업화학
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    • 제7권2호
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    • pp.245-251
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    • 1996
  • 일련의 $BeO-SiO_2$ 촉매를 염화베릴리움과 sodium silicate 혼합 용액을 공침전법으로 제조하였다. $SiO_2$에 BeO를 첨가하면 표면적, 산의 양, 산세기, 산촉매활성이 증가하여 BeO 함량이 20mol%일 때 최대를 나타내었다. X-선 회절로 조사한 결과 $400{\sim}500^{\circ}C$에서 소성된 촉매는 무정형으로 존재하였으며 $Br{\ddot{o}}nsted$ 산점과 Lewis 산점 모두를 가지고 있었다. Cumene의 dealkylation 반응에 대한 촉매활성은 촉매의 산의 양과 밀접한 관계를 가졌다.

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Evaluation of thermally and chemically reduced graphene oxide films as counter electrodes on dye-sensitized solar cells

  • Rodriguez-Perez, Manuel;Villanueva-Cab, Julio;Pal, Umapada
    • Advances in nano research
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    • 제5권3호
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    • pp.231-244
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    • 2017
  • Graphene oxide (GO) was prepared by modified Hummer's method to produce reduced graphene oxide (RGO) following standard thermal and chemical reduction processes. Prepared RGO colloids were utilized to fabricate RGO films over glass and FTO coated glass substrates through drop-coating. A systematic study was performed to evaluate the effect of reduction degree on the optical and electrical properties of the RGO film. We demonstrate that both the reduction process (thermal and chemical) produce RGO films of similar optical and electrical behaviors. However, the RGO films fabricated using chemically reduced GO colloid render better performance in dye sensitized solar cells (DSSCs), when they are used as counter electrodes (CEs). It has been demonstrated that RGO films of optimum thicknesses fabricated using RGO colloids prepared using lower concentration of hydrazine reducer have better catalytic performance in DSSCs due to a better catalytic interaction with redox couple. The better catalytic performance of the RGO films fabricated at optimal hydrazine concentration is associated to their higher available surface area and lower grain boundaries.

촉매 처리된 코디어라이트 필터의 제조 및 그 특성 (Preparation and Characteristics of Catalyst Coated Cordierite Filter)

  • 김영배;조을훈;장윤영;신민철;이희수;최덕균
    • 한국재료학회지
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    • 제12권2호
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    • pp.129-134
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    • 2002
  • The optimum condition for fabricating cordierite disc type filter element was deduced. Cordierite monolith was used as starting material for filter element because it has many advantages such as high thermal shock resistance and good catalytic activity compared with $TiO_2$and SiC. The contents of organic additives and foaming agent were optimized to control the porosity and mechanical strength of cordierite filter. Among the required properties to be adopted as filter elements, the pressure drop and NOx removal efficiency were investigated depending on processing variables. It was found that pressure drop depends on particle size distribution of cordierite monolith and organic additives added as forming agent. The pressure drop at 5cm/sec of face velocity was in the range of 15~655mm$H_2O$ at room temperature. The NOx removal efficiency of catalytic filter with $V_2O_5$ as catalyst was over 85% at $450^{\circ}C$.

광촉매 공정에 따른 이부프로펜의 분해 특성 (Degradation Properties of Ibuprofen Using Photocatalytic Process)

  • 채금화;나승민;안윤경;이세반;김지형
    • 한국환경과학회지
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    • 제21권4호
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    • pp.411-419
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    • 2012
  • In this study, Ibuprofen (IBP) degradation by the photo catalytic process was investigated under various parameters, such as UV intensity, optimum dosage of $TiO_2$, alkalinity, temperature and pH of bulk solution. The pseudo-first order degradation rate constants were in the order of $10^{-1}$ to $10^{-4}min^{-1}$ depending on each condition. The Photocatalytic IBP degradation rate increased with an increase in the applied UV power. At high UV intensity a high rate of tri-iodide ($I_3{^-}$) ion formation was also observed. Moreover, in order to avoid the use of an excess catalyst, the optimum dosage of catalyst under the various UV intensities (30 and 40 W/L) was examined and ranged from approximately 0.1 $gL^{-1}$. The photo catalytic IBP degradation rate was changed depending on the alkalinity and temperature and pH in the aqueous solution. This study demonstrated the potential of photo catalytic IBP degradation under different conditions.

Catalytic Growth and Properties of Carbon Nanotubes from Fe-Mo/MgO by Chemical Vapor Deposition

  • Woo, Jong-Chang;Kim, Kyoung-Tae;Kim, Gwan-Ha;Kim, Jong-Sik;Kim, Jong-Gyu;Kim, Chang-Il
    • Transactions on Electrical and Electronic Materials
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    • 제8권5호
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    • pp.206-210
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    • 2007
  • Carbon nanotubes(CNTs) are largely synthesized on Fe catalysts by catalytic chemical vapor deposition. The various shapes and compositions of these nanostructure CNTs were obtained by controlled parameters such as the reaction temperature, gas-mixing ratio. The influence of these parameters is investigated, together with observations of the produced materials after the purification processes. A diameter of CNTs, range from 2 to 10 nm, closely correlated with the size of the catalyst particle found attached to the tube end. The yield of CNTs was estimated to be 88.5 % and the purities of CNTs thus obtained were more than 80 %. The experimental results were documented with field emission scanning electron microscopy and raman spectroscopy and transmission electron microscopy, both before and after the purification.

Synthesis of diameter-controlled carbon nanotubes via structural modification of Al2O3 supporting layer

  • Kim, Soo-Youn;Song, Woo-Seok;Kim, Min-Kook;Jung, Woo-Sung;Choi, Won-Chel;Park, Chong-Yun
    • 한국진공학회:학술대회논문집
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    • 한국진공학회 2010년도 제39회 하계학술대회 초록집
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    • pp.286-286
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    • 2010
  • The lack of homogeneously sized single-walled carbon nanotubes (SWNTs) hinders their many applications because properties of SWNTs, in particular electrical conduction, are highly dependent on the diameter and chirality. Therefore, the preferential growth of SWNTs with predetermined diameters is an ultimate objective for applications of SWNTs-based nanoelectronics. It has been previously emphasized that a catalyst size is the one crucial factor to determine the CNTs diameter in chemical vapor deposition (CVD) process, giving rise to several attempts to obtain size-controllable catalyst by diverse methods, such as solid supported catalyst, metal-containing molecular nanoclusters, and nanostructured catalytic layer. In this work, diameter-controlled CNTs were synthesized using a nanostructured catalytic layer consisting of Fe/Al2O3/Si substrate. The CNTs diameter was controlled by structural modification of Al2O3 supporting layer, because Al2O3 supporting layer can affect agglomeration phenomenon induced by heat-driven surface diffusion of Fe catalytic nanoparticles at growth temperature.

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Palladium Layers on an Au(111) Nanoparticle and Their Catalytic Activity to Formic Acid Oxidation

  • 김병권;서대하;송현준;곽주현
    • 한국진공학회:학술대회논문집
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    • 한국진공학회 2011년도 제41회 하계 정기 학술대회 초록집
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    • pp.206-206
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    • 2011
  • Nanoparticles have been received great attention from many researchers for several decades because of their good and unique properties. In particular, researches in the field of synthesis of bimetallic nanoparticles showed good results for the past ten years. In this research, Pd thinlayer on Au nanoparticles were synthesized by electrochemical deposition method. Well-defined Au(111) nanoparticles were synthesized by solution based reduction method. Electrochemical deposition conditions for Pd thinlayer on Au(111) nanoparticles surface were carefully regulated by controlling parameters of cyclic voltammetry. To calculate exact mass and surface area catalytic activities of deposited Pd thinlayer on Au(111) nanoparticle, electrochemically active surface area (ECSA) and mass of the deposited Pd thinlayer were measured by cyclic voltammetry in 0.1 M HClO4 solution. Afterward, catalytic activities of the deposited Pd thinlayer were measured in 0.1 M HClO4 + 0.2 M formic acid solution. In case of less negative deposition potential, the amounts of deposited Pd mass and surface area were small. However, mass and ECSA activity of the deposited Pd to oxidize formic acid were increased.

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Hydrogen Production Through Catalytic Dehydrogenation of Decalin over Pt/C Catalyst Using Activated Carbon Aerogel

  • Lee, Gihoon;Kang, Ji Yeon;Jeong, Yeojin;Jung, Ji Chul
    • 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.

Electroless Nickel Plating on Fibers for the Highly Porous Electrode

  • Cheon, So-Young;Park, So-Yeon;Rhym, Young-Mok;Kim, Doo-Hyun;Koo, Yeon-Soo;Lee, Jae-Ho
    • Journal of Electrochemical Science and Technology
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    • 제1권2호
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    • pp.117-120
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    • 2010
  • Materials used as fuel cell electrode should be light, high conductive, high surface area for reaction, catalytic surface and uniformity of porous structure. Nickel is widely used in electrode materials because it itself has catalytic properties. When used as electrode materials, nickel of only a few im on the surface may be sufficient to conduct the catalytic role. To manufacture the nickel with porous structure, Electroless nickel plating on carbon fiber be conducted. Because electroless nickel plating is possible to do uniform coating on the surface of substrate with complex shape. Acidic bath and alkaline bathe were used in electroless nickel plating bath, and pH and temperature of bath were controlled. The rate of electroless plating in alkaline bath was faster than that in acidic bath. As increasing pH and temperature, the rate of electrolee plating was increased. The content of phosphorous in nickel deposit was higher in acidic bath than that in alkaline bath. As a result, the uniform nickel deposit on porous carbon fiber was conducted.

Correlations between Electrical Properties and Process Parameters of Silicon Nitride Films Prepared by Low Temperature (100℃) Catalytic CVD

  • Noh, Se Myoung;Hong, Wan-Shick
    • 한국세라믹학회지
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    • 제52권3호
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    • pp.209-214
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    • 2015
  • Silicon nitride films were deposited at $100^{\circ}C$ by using the catalytic chemical vapor deposition technique. The source gas mixing ratio, $R_N=[NH_3]/[SiH_4]$, was varied from 10 to 30, and the hydrogen dilution ratio, $R_H=[H_2]/[SiH_4]$, was varied from 20 to 100. The breakdown field strength reached a maximum value at $R_N=20$ and $R_H=20$, whereas the resistivity decreased in the same sample. The relative permittivity had a positive correlation with the breakdown field strength. The capacitance-voltage threshold curve showed an asymmetric hysteresis loop, which became more squared as $R_H$ increased. The width of the hysteresis window showed a negative correlation with the slope of the transition region, implying that the combined effect of $R_N$ and $R_H$ overides the interface defects while creating charge storage sites in the bulk region.