• 제목/요약/키워드: electrochemical reduction

검색결과 793건 처리시간 0.029초

수소연료를 이용하는 원자층증착 박막전해질 세라믹연료전지의 초기성능 저하에 관한 연구 (A Study on the Initial Performance Degradation of Hydrogen-Fueled Ceramic Fuel Cell with Atomic Layer-Deposited Thin-Film Electrolyte)

  • 지상훈
    • 한국수소및신에너지학회논문집
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    • 제32권5호
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    • pp.410-416
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    • 2021
  • The initial electrochemical performance of ceramic fuel cell with thin-film electrolyte was evaluated in terms of peak power density ratio, open circuit voltage ratio, and activation/ohmic resistance ratios at 500℃. Hydrogen and air were used as anode fuel and cathode fuel, respectively. The peak power density ratio reduced as ~17% for 40 minutes, which rapidly decreased in the early stage of the performance evaluation but gradually decreased. The open circuit voltage ratio decreased with respect time; however, its time behavior was remarkably different with the reduction behavior of the peak power density ratio. The activation resistance ratio increased as ~15% for 40 minutes, which was almost similar with the time behavior of the peak power density ratio.

경량골재의 종류에 따른 시멘트 경화체의 강도 특성 평가 (Compressive Strength Property of Cement Matrix According to the Type of Lightweight Aggregate)

  • 편명장;정수미;김주성;김호진;박선규
    • 한국건축시공학회:학술대회논문집
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    • 한국건축시공학회 2022년도 봄 학술논문 발표대회
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    • pp.111-112
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    • 2022
  • Lightweight aggregate is a porous material that has a lower density than natural aggregate and is a lightweight construction material. Lightweight Aggregate has a suitable purpose because it is effective in reducing the heavy unit mass in high-rise buildings. However, since lightweight aggregate has weak strength and high water absorption compared to natural aggregate, it is difficult to control the quality of concrete. Although lightweight aggregate has disadvantages such as high water absorption, it is expected that the demand for lightweight aggregate concrete will continue to use in the future because the advantage of being able to reduce the weight of concrete is greater. In this study, we conducted an experimantal study on the compressive strength property of cement matrix according to the type of lightweight aggregate.

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시멘트 모르타르에 매립된 철근의 생태학적 부식방지제로서 폐기물 바이오매스의 적용 (Application of waste biomass as ecological corrosion inhibitors for steel rebar embedded in cement mortar)

  • 카르틱 수비아;이한승
    • 한국건축시공학회:학술대회논문집
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    • 한국건축시공학회 2022년도 가을 학술논문 발표대회
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    • pp.111-112
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    • 2022
  • In this present study, the corrosion mitigation effect of conifer cone extract (CC) was examined in the cement mortar to improve the steel rebar (SR) corrosion resistance. The corrosion inhibition properties of the SR embedded in cement mortar (CM) admixed with different percentage (0, 0.5, 1.0, 1.5, 2.0 %) of CC was studied by open circuit potential (OCP) and electrochemical impedance spectroscopy (EIS) tests. This result confirms that the CM with 0.5% of CC added has better corrosion resistance than the blank specimen (0 % of CC). Although, the percentage of CC increase above 0.5%, the CC could yield a negative impact on CM properties in terms of reducing the corrosion resistance due to the reduction of cement hydration reaction. It was highlighted that the SR embedded in CM containing 0.5% of CC had increased corrosion resistance.

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여러 자리 산소-질소계 시프염기 리간드 니켈(II)착물의 전기화학적 특성 (Electrochemical Properties of Nickel(II) Complexes with Multidentate N, O-Schiff Base Ligands)

  • 김선덕;김준광;노수균
    • 분석과학
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    • 제10권4호
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    • pp.246-255
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    • 1997
  • 산소-질소계를 포함하는 여러 자리 시프염기 리간드인 비스-살리실알데히드-에틸렌디아민(SED), 비스-살리실알데히드-프로필렌디아민(SPD), 비스-살리실알데히드-디에틸렌트리아민(SDT) 및 비스-살리실알데히드-트리에틸렌테트라아민(STT)들과 니켈(II) 착물을 합성하여 원소분석법, 적외선분광법, 자외-가시흡광분광법 및 질량분석법을 이용하여 확인하였다. 이들 리간드를 70% 디옥산-30% 물 혼합 용매 및 에탄올 용매에서 전위차법으로 니켈(II)-시프염기 착물들의 안정도상수값을 각각 구하였다. 안정도상수값의 크기는 Ni(II)-SPD

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Photocatalytic Systems of Pt Nanoparticles and Molecular Co Complexes for NADH Regeneration and Enzyme-coupled CO2 Conversion

  • Kim, Ellen;Jeon, Minkyung;Kim, Soojin;Yadav, Paras Nath;Jeong, Kwang-Duk;Kim, Jinheung
    • Rapid Communication in Photoscience
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    • 제2권2호
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    • pp.42-45
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    • 2013
  • Natural photosynthesis utilizes solar energy to convert carbon dioxide and water to energy-rich carbohydrates. Substantial use of sunlight to meet world energy demands requires energy storage in useful fuels via chemical bonds because sunlight is intermittent. Artificial photosynthesis research focuses the fundamental natural process to design solar energy conversion systems. Nicotinamide adenine dinucleotide ($NAD^+$) and $NADP^+$ are ubiquitous as electron transporters in biological systems. Enzymatic, chemical, and electrochemical methods have been reported for NADH regeneration. As photochemical systems, visible light-driven catalytic activity of NADH regeneration was carried out using platinum nanoparticles, molecular rhodium and cobalt complexes in the presence of triethanolamine as a sacrificial electron donor. Pt nanoparticles showed photochemical NADH regeneration activity without additional visible light collector molecules, demonstrating that both photoactivating and catalytic activities exist together in Pt nanoparticles. The NADH regeneration of the Pt nanoparticle system was not interfered with the reduction of $O_2$. Molecular cobalt complexes containing dimethylglyoxime ligands also transfer their hydrides to $NAD^+$ with photoactivation of eosin Y in the presence of TEOA. In this photocatalytic reaction, the $NAD^+$ reduction process competed with a proton reduction.

Aliphatic Acetylenic Alcohol의 電極反應過程 (Electorchemical Reduction Behavior of Aliphatic Acetylenic Alcohol)

  • 김원택;김진일;곽태영;이주성
    • 대한화학회지
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    • 제23권3호
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    • pp.180-185
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    • 1979
  • 각종 陰極, 卽 Ti, Zr, Ni, Pt, Cu, Ag, Au, Zn, Hg, Pb 및 흑연의 사용으로 2-butyne-1, 4-diol (BID)로부터 2-butene-1,4-diol (BED)까지의 電氣化學的 還元擧動에 관하여 연구하였다. IB族 金屬을 陰極으로 사용한 陰極分極曲線은 알칼리용액중에서 BID에 對해 한개의 還元波가 생기나 BED의 경우는 지지전해질내에서와 마찬가지로 還元波가 생기지 않았다. 고로 BID환원반응에 가장 적당한 陰極은 Cu, Ag, Au임을 알았다. 알칼리性 BID용액에서 銀電極을 사용한 電位走査法에서 peak電流는 電位走査速度의 제곱근과 BID농도에 比例하였다. 限界電流의 對數와 絶對溫度의 逆數의 관계로부터 구한 BID의 活性化에너지는 3.75kcal/mole였다. 고로 알칼리용액중 銀電極을 사용한 BID의 還元電流는 自己擴散에 의한 擴散電流임을 알았다.

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Chemical Stability of Conductive Ceramic Anodes in LiCl-Li2O Molten Salt for Electrolytic Reduction in Pyroprocessing

  • Kim, Sung-Wook;Kang, Hyun Woo;Jeon, Min Ku;Lee, Sang-Kwon;Choi, Eun-Young;Park, Wooshin;Hong, Sun-Seok;Oh, Seung-Chul;Hur, Jin-Mok
    • Nuclear Engineering and Technology
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    • 제48권4호
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    • pp.997-1001
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    • 2016
  • Conductive ceramics are being developed to replace current Pt anodes in the electrolytic reduction of spent oxide fuels in pyroprocessing. While several conductive ceramics have shown promising electrochemical properties in small-scale experiments, their long-term stabilities have not yet been investigated. In this study, the chemical stability of conductive $La_{0.33}Sr_{0.67}MnO_3$ in $LiCl-Li_2O$ molten salt at $650^{\circ}C$ was investigated to examine its feasibility as an anode material. Dissolution of Sr at the anode surface led to structural collapse, thereby indicating that the lifetime of the $La_{0.33}Sr_{0.67}MnO_3$ anode is limited. The dissolution rate of Sr is likely to be influenced by the local environment around Sr in the perovskite framework.

Co(Ⅱ)$(dimethyl bipyridine)_3(ClO_4)_2$의 전기화학적 성질과 산소환원에 대한 전극 촉매 효과 (Electrocatalytic Effect on the Oxygen Reduction and Electrochemical Properties of Co(Ⅱ)-dimethyl Bipyridine Perchlorate)

  • 김일광;박종술;한완수;김윤근;전일철
    • 대한화학회지
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    • 제41권8호
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    • pp.385-391
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    • 1997
  • Co$(dimethyl bipyridine)_3(ClO_4)_2$의 확산계수$(D_0)$와 전극반응속도상수$(K_0)$를 순환전압전류법과 대시간전류법으로 구하였다. 확산계수에 대한 용매, 농도, 주사속도 등의 영향과 반응속도상수에 대한 온도변화의 영향을 조사하였다. 25$^{\circ}C$에서 확산계수는 $5.54{\times}10^{-6 }cm^2/sec$이었고, 반응속도상수는 $2.39{\times}10^{-3 }/s$ 이었으며, 용매의 점도가 커질수록 봉우리전류값과 확산계수는 감소하였다. 반응속도상수에 대한 온도의 영향으로부터, ${\Delta}G^{\neq},\;{\Delta}H^{\neq},\;{\Delta}S$ 등의 열역학적 파라미터를 구하였다. 이 화합물은 $O_2$분자의 환원에서 봉우리전류를 크게 증가시키고, 환원전위를 양(+)전위방향으로 이동시키는 열역학적 전극촉매현상을 보였다.

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다중벽 탄소 나노 튜브에 담지한 PtxM(1-x)(M = Co, Cu, Ni) 합금촉매의 제조 및 고분자 전해질 연료전지에서 산소환원 특성 (Synthesis and Oxygen Reduction Reaction Characteristics of Multi-Walled Carbon Nanotubes Supported PtxM(1-x) (M = Co, Cu, Ni) Alloy Catalysts for Polymer Electrolyte Membrane Fuel Cell)

  • 정동원;박순;안치영;최성호;김준범
    • 한국재료학회지
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    • 제19권12호
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    • pp.667-673
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    • 2009
  • The electrocatalytic characteristics of oxygen reduction reaction of the $PtxM_{(1-x)}$ (M = Co, Cu, Ni) supported on multi-walled carbon nanotubes (MWNTs) have been evaluated in a Polymer Electrolyte Membrane Fuel Cell (PEMFC). The $Pt_xM_{(1-x)}$/MWNTs catalysts with a Pt : M atomic ratio of about 3 : 1 were synthesized and applied to the cathode of PEMFC. The crystalline structure and morphology images of the $Pt_xM_{(1-x)}$ particles were characterized by X-ray diffraction and transmission electron microscopy, respectively. The results showed that the crystalline structure of the Pt alloy particles in Pt/MWNTs and $Pt_xM_{(1-x)}$/MWNTs catalysts are seen as FCC, and synthesized $Pt_xM_{(1-x)}$ crystals have lattice parameters smaller than the pure Pt crystal. According to the electrochemical surface area (ESA) calculated with cyclic voltammetry analysis, $Pt_{0.77}Co_{0.23}$/MWNTs catalyst has higher ESA than the other catalysts. The evaluation of a unit cell test using Pt/MWNTs or $Pt_xM_{(1-x)}$/MWNTs as the cathode catalysts demonstrated higher cell performance than did a commercial Pt/C catalyst. Among the MWNTs-supported Pt and $Pt_xM_{(1-x)}$ (M = Co, Cu, Ni) catalysts, the $Pt_{0.77}Co_{0.23}$/MWNTs shows the highest performance with the cathode catalyst of PEMFC because they had the largest ESA.

아연-공기전지용 페롭스카이트 산화물 촉매의 산소환원반응 특성 (Characterization of LaCoO3 Perovskite Catalyst for Oxygen Reduction Reaction in Zn-air Rechargeable Batteries)

  • 선호정;조명연;안정철;엄승욱;박경세;심중표
    • 한국수소및신에너지학회논문집
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    • 제25권4호
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    • pp.436-442
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    • 2014
  • $LaCoO_3$ powders synthesized by Pechini process were pulverized by planetary ball-milling to decrease particle size and characterized as a catalyst in alkaline solution for oxygen reduction and evolution reaction (ORR & OER). The changes of physical properties, such as particle size distribution, surface area and electric conductivity, were analyzed as a function of ball-milling time. Also, the variations of the crystal structure and surface morphology of ball-milled powders were examined by X-ray diffraction (XRD) and scanning electron microscopy (SEM), respectively. The electrochemically catalytic activities of the intrinsic $LaCoO_3$ powders decreased with increasing ball-milling time, but their electrochemical performance as an electrode improved by the increase of the surface area of the powder.