• 제목/요약/키워드: ruthenium dioxide

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Ruthenium을 도입한 Titanium Dioxide의 합성과 산화반응 연구

  • 김영용;권기영
    • 한국진공학회:학술대회논문집
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    • 한국진공학회 2014년도 제46회 동계 정기학술대회 초록집
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    • pp.199.2-199.2
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    • 2014
  • Titanium과 Ruthenium의 비율(Ru/Ti = 0.01, 0.03, 0.05, 0.07)을 조절하여 Ruthenium이 도입된 산화타이타늄($TiO_2$)를 수열합성법을 이용하여 합성하였다. TEM 이미지를 통하여 네모난 형태의 나노입자를 확인하였으며 XRD 패턴과 ICP 원소 분석을 통하여 Anatase 형태와 각각 다른 양의 Ruthenium이 도입된 것을 확인하였다. 본 연구에서는 Ruthenium이 도입된 산화타이타늄을 이종상촉매로 사용하여 Benzyl alcohol 및 Benzyl amine의 산화반응에 적용하였으며 특히, Ru/Ti = 0.03인 촉매가 가장 우수한 활성을 보였다.

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염료감응 태양전지용 루테늄 금속착체 염료의 이산화티타늄 전극에 대한 동적 흡착 연구 (Adsorption Kinetic Study of Ruthenium Complex Dyes onto TiO2 Anodes for Dye-sensitized Solar Cells (DSSCs))

  • 안병관
    • 한국전기전자재료학회논문지
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    • 제24권11호
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    • pp.929-934
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    • 2011
  • The adsorption kinetic study of ruthenium complex, N3, onto nanoporous titanium dioxide ($TiO_2$) photoanodes has been carried out by measuring dye uptake in-situ. Three simplified kinetic models including a pseudo first-order equation, pseudo second-order equation and intraparticle diffusion equation were chosen to follow the adsorption process. Kinetic parameters, rate constant, equilibrium adsorption capacities and related coefficient coefficients for each kinetic model were calculated and discussed. It was shown that the adsorption kinetics of N3 dye molecules onto porous $TiO_2$ obeys pseudo second-order kinetics with chemisorption being the rate determining step. Additionally the heterogeneous surface and the pore size distribution of porous $TiO_2$ adsorbents were also discussed.

Electrochemical Oxidation of Amoxicillin in Its Commercial Formulation on Thermally Prepared RuO2/Ti

  • Auguste, Appia Foffie Thiery;Quand-Meme, Gnamba Corneil;Ollo, Kambire;Mohamed, Berte;Sahi placide, Sadia;Ibrahima, Sanogo;Lassine, Ouattara
    • Journal of Electrochemical Science and Technology
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    • 제7권1호
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    • pp.82-89
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    • 2016
  • In this work, a ruthenium dioxide electrode has been prepared by thermal decomposition at 400 ℃ then used for the oxidation of commercial amoxicillin. The physical characterization showed that RuO2 electrode presents a mud cracked structure. Its electrochemical characterization has revealed an increase of the voltammetric charge in acid electrolyte compared to neutral electrolyte indicating the importance of protons in its surface redox processes. The voltammetric study of the oxidation of amoxicillin has been investigated. It has been obtained that the oxidation of amoxicillin is controlled by both adsorption and diffusion processes. Moreover, the oxidation of amoxicillin occurs via direct and indirect processes in free or electrolyte containing chlorides. Through preparative electrolysis, enhancement of amoxicillin oxidation was observed in the presence of chloride where the amoxicillin degradation yield reached more than 50 % compared to less than 5% in the absence of chlorides. Spectrophotometric investigations have revealed the degradation of intermediates absorbing at 350 nm.

Formation and stability of a ruthenium-oxide thin film made of the $O_2$/Ar gas-mixture sputtering

  • Moonsup Han;Jung, Min-Cherl;Kim, H.-D.;William Jo
    • Journal of Korean Vacuum Science & Technology
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    • 제5권2호
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    • pp.47-51
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    • 2001
  • To obtain high remnant polarization and good crystalinity of ferroelectric thin films in non-volatile memory devices, the high temperature treatment in oxygen ambient is inevitable. Severe problems that occur in this process are oxygen diffusion into substrate, oxidation of electrode and buffer layer, degradation of microstructure and so on. We made ruthenium dioxide thin film by reactive sputtering with oxygen and argon mixture atmosphere. Comparing quantitatively the core-level spectra of Ru and RuO$_2$ obtained by x-ray photoelectron spectroscopy(XPS), we found that chemical state of RuO$_2$ is very stable and of good resistance to oxygen diffusion and oxidation of adjacent layers. It opens the use of RuO$_2$ thin film as a multifunctional layer of good conducting electrode and resistive barrier for the diffusion and the oxidation. We also suggest a correct understanding of Ru 3d core-level spectrum for RuO$_2$ based on the scheme of final state screening and charge transfer satellites.

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Ru/$Al_2O_3$ 촉매를 이용한 바이오매스 타르 개질 특성 (Tar Reforming for Biomass Gasification by Ru/$Al_2O_3$ catalyst)

  • 박영수;김우현;길상인;윤진한;민태진;노선아
    • 한국신재생에너지학회:학술대회논문집
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    • 한국신재생에너지학회 2008년도 춘계학술대회 논문집
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    • pp.247-250
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    • 2008
  • Biomass gasification is a promising technology for producing a fuel gas which is useful for power generation systems. In biomass gasification processes, tar formation often causes some problems such as pipeline plugging. Thus, proper tar treatment is necessary. So far, nickel (Ni)-based catalysts have been intensively studied for the catalytic tar removal. However, the deactivation of Ni-based catalysts takes place because of coke deposition and sintering of Ni metal particles. To overcome these problems, we have been using ruthenium (Ru)-based catalyst for tar removal. It is reported by Okada et al., that a Ru/$Al_2O_3$ catalyst is very effective for preventing the carbon deposition during the steam reforming of hydrocarbons. Also, this catalyst is more active than the Ni-based catalyst at a low steam to carbon ratio (S/C). Benzene was used for the tar model compound because it is the main constituent of biomass tar and also because it represents a stable aromatic structure apparent in tar formed in biomass gasification processes. The steam reforming process transforms hydrocarbons into gaseous mixtures constituted of carbon dioxide ($CO_2$), carbon monoxide (CO), methane ($CH_4$) and hydrogen ($H_2$).

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Effect of TiO2 Coating Thickness on Photovoltaic Performance of Dye-sensitized Solar Cells Prepared by Screen-printing Using TiO2 Powders

  • Lee, Deuk Yong;Cho, Hun;Kang, Daejun;Kang, Jong-Ho;Lee, Myung-Hyun;Kim, Bae-Yeon;Cho, Nam-Ihn
    • 한국세라믹학회지
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    • 제51권4호
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    • pp.362-366
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    • 2014
  • Dye-sensitized solar cells (DSSCs) were synthesized using a $0.25cm^2$ area of a $TiO_2$ nanoparticle layer as the electrode and platinum (Pt) as the counter electrode. The $TiO_2$ nanoparticle layers (12 to 22 ${\mu}m$) were screen-printed on fluorine-doped tin oxide glass. Glancing angle X-ray diffraction results indicated that the $TiO_2$ layer is composed of pure anatase with no traces of rutile $TiO_2$. The Pt counter electrode and the ruthenium dye anchored $TiO_2$ electrode were then assembled. The best photovoltaic performance of DSSC, which consists of a $18{\mu}m$ thick $TiO_2$ nanoparticle layer, was observed at a short circuit current density ($J_{sc}$) of $14.68mA{\cdot}cm^{-2}$, an open circuit voltage ($V_{oc}$) of 0.72V, a fill factor (FF) of 63.0%, and an energy conversion efficiency (${\eta}$) of 6.65%. It can be concluded that the electrode thickness is attributed to the energy conversion efficiency of DSSCs.

The Role of the Surface Oxide Layer on Ru Nanoparticles in Catalytic Activity of CO Oxidation

  • Kim, Sun-Mi;Qadir, Kamran;Jin, Sook-Young;Jung, Kyeong-Min;Reddy, A. Satyanarayana;Joo, Sang-Hoon;Park, Jeong-Young
    • 한국진공학회:학술대회논문집
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    • 한국진공학회 2010년도 제39회 하계학술대회 초록집
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    • pp.304-304
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    • 2010
  • The study on the catalytic oxidation of carbon monoxide (CO) to carbon dioxide ($CO_2$) using the noble metals has long been the interest subject and the recent progress in nanoscience provides the opportunity to develop new model systems of catalysts in this field. Of the noble metal catalysts, we selected ruthenium (Ru) as metal catalyst due to its unusual catalytic behavior. The size of colloid Ru NPs was controlled by the concentration of Ru precursor and the final reduction temperatures. For catalytic activity of CO oxidation, it was found that the trend is dependent on the size of Ru NPs. In order to explain this trend, the surface oxide layer surrounding the metal core has been suggested as the catalytically active species through several studies. In this poster, we show the influence of surface oxide on Ru NPs on the catalytic activity of CO oxidation using chemical treatments including oxidation, reduction and UV-Ozone surface treatment. The changes occurring to UV-Ozone surface treatment will be characterized with XPS and SEM. The catalytic activity before and after the chemical modification were measured. We discuss the trend of catalytic activity in light of the formation of core-shell type oxide on nanoparticles surfaces.

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반응표면분석법을 이용한 루테늄 알루미나 메탈모노리스 코팅촉매의 암모니아 분해 최적화 (Optimization for Ammonia Decomposition over Ruthenium Alumina Catalyst Coated on Metallic Monolith Using Response Surface Methodology)

  • 최재형;이성찬;이준혁;김경민;임동하
    • 청정기술
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    • 제28권3호
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    • pp.218-226
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    • 2022
  • 최근 선진국들은 수소경제 및 탄소중립 사회로의 전환을 위해 수소에너지의 수요가 급격히 증가하고 있으며, 이산화탄소(CO2)를 배출이 없는 친환경적인 수소(H2) 생산 기술에 대한 관심이 높아지고 있다. 본 연구에서는 암모니아(NH3) 분해 수소 제조를 위해 루테늄 알루미나(Ru/Al2O3) 분말 촉매와 함께 알루미나 졸(alumina sol)의 무기바인더(inorganic binder)와 메틸 셀룰로오스(methyl cellulose)의 유기바인더(organic binder)를 사용하여 딥 코팅(dip coating) 방법으로 루테늄 알루미나 메탈 모노리스 코팅 촉매를 제조하였다. 딥 코팅을 위한 촉매 슬러리의 최적 비율로 촉매와 무기바인더의 중량 비율을 1:1로 고정하여 유기바인더 0.1일 때 1회 딥 코팅 시 촉매 코팅양은 61.6 g L-1이다. 이때 메탈모노리스 표면에 코팅된 촉매 층의 균일한 두께 (약 42 ㎛)와 결정상을 주사전자현미경(Scanning Electron Microscope, SEM)과 X-ray 회절분석(X ray diffraction, XRD)을 통해 확인하였다. 또한, 암모니아 분해 수소 제조의 최적 공정조건을 찾고자 반응표면분석법(Response Surface Method, RSM)을 이용하여 반응온도와 공간속도의 독립변수에 따른 암모니아 전환율에 대한 수치 최적화 회귀식 모델을 계산하였다. 이러한 결과로부터 암모니아 분해 수소생산을 위한 상업적 규모의 공정운전 기본설계 자료로 활용이 가능하다.