• 제목/요약/키워드: Co-electrolysis

검색결과 150건 처리시간 0.021초

Ni-Fe-Co 박막도금층의 조성, 우선배향 및 자기적 성질 (Composition, preferred orientation and magnetic properties of Ni-Fe-Co alloy electrodeposits)

  • 예길촌;김선윤;문근호;김용웅
    • 한국표면공학회지
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    • 제28권6호
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    • pp.352-360
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    • 1995
  • The effect of electrolysis conditions on the composition, the magnetic properties and the preferred orientation of Ni-Fe-Co alloy deposits was investigated using the sulfate-chloride bath paddle agitated. Cathode current efficiency increases with the current density, showing the different tendency of the variation from that of the Ni-Fe electrodeposits. The Co content of the deposits decreases with increasing current density, while the content of Ni and Fe is shown to be minimum or maximum at 3A/$dm^2$ respectively. The Ni/Fe ratio of the alloy deposits is lower than that of Ni-Fe deposits. The coercive force($H_c$) of the deposits increases with the Co content in deposit, showing the relatively low value in the range of 1.8~5.0Wt.% Co. The anisotropy field ($H_k$) of the deposits is higher than that of Ni-Fe alloy deposits, The preferred orientation of the deposits is generally (200), but the orientation factor(R) changes with both the increase of current density and the magnetic field applied during deposition.

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Ni Foam-Supported Ni Nanoclusters for Enhanced Electrocatalytic Oxygen Evolution Reaction

  • Hoeun Seong;Jinhee Kim;Kiyoung Chang;Hyun-woo Kim;Woojun Choi;Dongil Lee
    • Journal of Electrochemical Science and Technology
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    • 제14권3호
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    • pp.243-251
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    • 2023
  • Developing oxygen evolution reaction (OER) electrocatalysts is essential to accomplish viable CO2 and water electrolysis. Herein, we report the fabrication and OER performance of Ni-foam (NF)-immobilized Ni6 nanoclusters (NCs) (Ni6/NF) prepared by a dip-coating process. The Ni6/NF electrode exhibited a high current density of 500 mA/cm2 for the OER at an overpotential as low as 0.39 V. Ni6/NF exhibited high durability in an alkaline solution without corrosion. Electrokinetic studies revealed that OER can be easily initiated on Ni6 NC with fast electron-transfer rates. Finally, we demonstrated stable CO2-to-CO electroreduction using an NC-based zero-gap CO2 electrolyzer operated at a current density of 100 mA/cm2 and a full-cell potential of 2.0 V for 12 h.

분무열분해로 합성한 수전해용 Co3O4의 입자형태에 따른 산소발생 활성에 관한 연구 (A Study on Oxygen Evolution Activity of Co3O4 with different morphology prepared by Ultrasonic Spray Pyrolysis for Water Electrolysis)

  • 김인겸;나인욱;박세규
    • Korean Chemical Engineering Research
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    • 제54권6호
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    • pp.854-862
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    • 2016
  • 최근 화석연료를 대체할 친환경 신재생에너지에 대한 요구가 증가하면서 수소에너지가 미래 대체에너지원으로서 주목받고 있다. 수소를 생산하는 방법 중 수전해 기술은 에너지효율과 안정성이 뛰어난 장점이 있지만, 산소발생반응시 발생하는 높은 과전압은 여전히 단점으로 지적되고 있다. 본 연구에서는 분무열분해 공정을 통하여 Co 전구체로부터 $Co_3O_4$를 제조하였다. 또한, urea, sucrose, citric acid의 유기물첨가제를 사용하여 다양한 입자 크기와 표면형상을 가지는 $Co_3O_4$를 제조하였고, 필요에 따라 추가로 열처리를 실시하였다. 합성한 $Co_3O_4$의 물리적 특성을 분석하기 위해 X-선 회절 분석(XRD)으로 결정성을 조사하였고, 주사전자현미경(SEM)과 투과전자현미경(TEM)으로 입자형상 및 표면을 분석하였다. 질소 흡 탈착 시험을 통해 촉매의 비표면적 및 기공부피를 측정하였고, 질소도핑을 확인하기 위해 X-선 광전자 분광법(XPS)을 사용하였다. 촉매의 산소발생반응 활성을 알아보기 위해 3전극 셀에서 선형주사전위법(LSV)으로 전기화학적 거동을 분석하였다. 첨가제를 사용하지 않은 $Co_3O_4$가 가장 우수한 활성을 보였고, 이는 분무열분해법을 통하여 상대적으로 작은 입자형성과 높은 비표면적의 영향인 것으로 판단된다.

Fe-Co-Ni합금박막의 조성 및 자기적 성질 (Composition and Coercivity of Fe-Co-Ni Alloy Electrodeposits)

  • 예길촌;김용웅;문근호
    • 한국표면공학회지
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    • 제29권3호
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    • pp.195-202
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    • 1996
  • The composition, the microstructure and the magnetic properties(HC and Hk) of Fe-Co-Ni alloy electrodeposits were investigated according to the electrolysis conditions using sulfate bath paddle agitated. The current efficiency of the alloys electrodeposition was considerably low in the range of 16∼50%. The Fe content(wt.%) of the alloy increased from 20% to 57% with current density, while Ni content of them decreased in the range of 70∼24% respectively, and Co content was nearly constant. As a result, Fe/Ni ratio of the alloy increased from 0.3 to 2.0 showing the anomalous codeposition. The structure of the alloy changed from fcc to the mixed one of fcc+bcc with the increase of Fe/Ni ratio. The preferred orientation of the alloy with fcc and bcc structure were (220) and (110) respectively. The alloy with Fe/Ni ratio(0.3∼l.2) had the lowest coercivity of 0.4∼0.8 Oe.

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Air Pollution Protection onboard by Seawater and Electrolyte

  • An Suk-Heon
    • Journal of Advanced Marine Engineering and Technology
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    • 제30권1호
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    • pp.93-101
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    • 2006
  • This research makes a new attempt to apply the activated seawater by electrolysis in the development of two-stage wet scrubber system to control the exhaust gas of large marine diesel engines. First, with using only seawater that is naturally alkaline (pH typically around 8.1). the $SO_2\;and\;SO_3$ are absorbed by relatively high solubility compared to other components of exhaust pollutants, and PM (Particulate Matter) is removed through direct contact with sprayed seawater droplets. Besides, the electrolyzed alkaline seawater by electrolysis, which contains mainly NaOH together with alkali metal ions $(i.e.\;Na^+,\;Mg^{2+},\;Ca^{2+})$, is used as the absorption medium of NOx and $CO_2$. Especially, to increase NOx absorption rate into the alkaline seawater. nitric oxide (NO) is adequately oxidized to nitrogen dioxide $(NO_2)$ in the acidic seawater, which means both volume fractions are adjusted to identical proportion. The results found that the strong acidic seawater was a valid oxidizer from NO to $NO_2$ and the strong alkaline seawater was effective in $CO_2$ absorption In the scrubber test, the SOx reduction of nearly $100\%$ could be achieved and also led to a sufficientPM reduction. Hence, the author believes that applying seawater and its electrolyte would bring the marine air pollution control system to an economical measure. Additionally it is well known that NOx and SOx concentration has a considerable influence on the $N_2O$ emission of green house gas. Although the $N_2O$ concentration exhausted from diesel engines is not as high, the green house gas effect is around 300 times greater than an equivalent volume of $CO_2$. Therefore, we investigated the $N_2O$ removal efficiency with using the electrolyzed seawater too. Finally this research would also plan to treat the effluent by applying electro-dialysis and electro-flotation technique s in the future.

수전해용 Pt/공유가교 SPEEK-HPA 복합막/Pt-Ru MEA의 전기화학적 특성 (The Electrochemical Characteristics of MEA with Pt/Cross-Linked SPEEK-HPA Composite Membranes/Pt-Ru for Water Electrolysis)

  • 황용구;우제영;이광문;정장훈;문상봉;강안수
    • 한국수소및신에너지학회논문집
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    • 제20권3호
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    • pp.194-201
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    • 2009
  • The e1ectrocatalytic properties of heteropolyacids(HPAs) entrapped in covalently cross-linked sulfonated polyetheretherketone(CL-SPEEK/HPA) membranes have been studied for water electrolysis. The HPAs, including tungstophosphoric acid(TPA), molybdophosphoric acid(MoPA), and tungstosilicic acid(TSiA) were used as additives in the composite membranes. The MEA was prepared by a non-equilibrium impregnation-reduction(I-R) method, using reducing agent, sodium borohydride(NaBH4) and tetraamineplatinum(II) chloride(pt(NH$_3$)$_4$Cl$_2$). The electrocatalytic properties of composite membranes such as the cell voltage were in the order of magnitude CL-SPEEKlMoPA40 (wt%) > /TPA30 > /TSiA40. In the optimum cell applications for water electrolysis, the cell voltage of PtlPEM/Pt-Ru MEA with CL-SPEEKlTPA30 membrane was 1.75 V at 80$^{\circ}$C and I A/cm$^2$ and this voltage carried lower than that of 1.81 V of Nafion 117. Consequently, in regards of electrochemical and mechanical characteristics and oxidation durability, the newly developed CL-SPEEKITPA30 composite membrane exhibited a better performance than the others, but CLSPEEKlMoPA40 showed the best electrocatalytic activity (1.71 Vat 80$^{\circ}$C and 1 A/cm$^2$) among the composite membranes.

고로슬래그 및 전기분해한 알칼리 수용액을 사용한 하이볼륨 시멘트 경화체의 수화특성 (Hydration Properties of High Volume Cement Matrix Using Blast Furnace Slag and Alkaline Aqueous by Electrolysis)

  • 김선아;박선규
    • 한국건설순환자원학회논문집
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    • 제5권1호
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    • pp.8-13
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    • 2017
  • 본 연구는 $CO_2$를 다량 발생시키는 시멘트의 사용량을 줄이기 위한 일련의 연구로서, 산업부산물인 고로슬래그 미분말을 다량 치환하고 기존 알칼리 자극제를 대체하여 전기분해한 알칼리 수용액을 사용한 하이볼륨 시멘트 경화체의 개발을 위한 기초적인 연구를 수행하였다. 즉, 일반적인 시멘트를 사용한 시험체와 고로슬래그 미분말 40%, 60%에 일반적인 물과 전기분해 알칼리 수용액을 사용한 시험체에 대하여 압축강도, XRD 및 SEM을 측정하였다. 그 결과, 고로슬래그 미분말을 사용하는 경화체에 있어서 알칼리 수용액을 사용할 시 강도가 증가하고 입자 표면에 수화물이 다량 생성되는 결과를 얻었다. 특히, 고로슬래그 미분말을 40% 치환하고 알칼리 수용액을 사용한 경우, 일반적인 시멘트 경화체 보다 높은 압축강도를 발현하였다. 그러나 본 연구는 재령 10일에 한정하여 실시한 연구로서, 고로슬래그 및 전기분해 알칼리 수용액을 사용한 시험체에 대한 추가적인 연구가 필요하다고 판단된다.

수전해용 공유가교 SPEEK 고분자 전해질 막의 전기 화학적 및 기계적 특성 (Electrochemical and Mechanical Characteristics of Covalently Cross-Linked SPEEK Polymer Electrolyte Membrane for Water Electrolysis)

  • 김경언;장인영;권오환;황용구;문상봉;강안수
    • 한국수소및신에너지학회논문집
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    • 제18권4호
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    • pp.391-398
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    • 2007
  • The covalently cross-linked sulfonated polyetheretherketone (CL-SPEEK) membrane was prepared by four-step synthesis of sulfonation-sulfochlorination, partial reduction, lithiation, and cross-linking, and its electrochemical and mechanical properties were investigated for water electrolysis application. The prepared ion exchange membranes showed good electrochemical and mechanical properties; proton conductivity of 0.116 S/cm at $80^{\circ}C$, water uptake of 44.6%, ion exchange capacity of 1.75 meq/g-dry-memb., tensile strength of 64.25 MPa and elongation of 61.11%. The membrane electrode assembly (MEA) with homemade membranes were prepared by non-equilibrium impregnation-reduction (I-R) method. Especially, the electrochemical surface area (ESA) and roughness factor of CL-SPEEK electrolyte by cyclic voltammetry method were 23.46 $m^2/g$ and 307.3 $cm^2-Pt/cm^2$, respectively. The prepared MEA was used in the unit cell of water electrolysis and the cell voltage was 1.81 V at 1 A/$cm^2$ and $80^{\circ}C$, with platinum loadings of 1.31 mg/$cm^2$.

극전환 전해 반응기를 이용한 양식 폐수 내 암모니아 제거 (Removal of Ammonia in Aquaculture Wastewater by Electrolysis with Switching Poles)

  • 강기문;김아람;원용선;이제근;임준혁
    • 청정기술
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    • 제21권1호
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    • pp.45-52
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    • 2015
  • 본 연구에서는 양식 폐수 중 암모니아를 제거하는 전기분해 공정에 극전환을 도입하여 전극 표면에 불용성 금속화합물이 형성되는 오염 현상을 방지하고자 하였다. 한편 극전환으로 인한 전류 손실이 유리염소 이온의 생성에 미치는 영향을 파악함으로서 최적의 극전환 주기를 찾고자 하였다. 먼저 극전환 주기가 짧아지면서 전류손실로 인해 유리염소 이온의 형성 효율이 떨어지는 것을 확인하였으며 이는 암모니아 제거 효율이 감소함을 의미한다. 이에 극전환 주기에 따른 폐수 중의 칼슘과 마그네슘의 농도를 측정해 본 결과 극전환 주기를 60초 이하로 유지하면 극전환에 의한 불용성 금속화합물의 분해를 통해 전극 표면의 오염 현상을 충분한 수준에서 방지할 수 있음을 확인하였다. 따라서 높은 유리염소 이온의 생성효율 유지와 전극 오염 방지라는 두 가지 운전목적 사이에서 최적의 극전환 주기는 60초이었다.

알칼리 전해액의 상호작용에 의한 Stainless Steel 주성분의 변화 분석 (Analysis on Variation of Primary Elements of Stainless Steel Interacting with Alkali Solution)

  • 변창섭;임수곤;김수곤;최호상;신훈규
    • 한국전기전자재료학회논문지
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    • 제26권7호
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    • pp.522-527
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    • 2013
  • In this paper, We studied the change of surface and variation of elements on both electrodes of hydrogen generator of alkaline electrolysis in use of FE-SEM and SIMS. We used the stainless steel 316(600 ${\mu}m$) as electrode in condition of 25%KOH, $60^{\circ}C$ Temperature. The results show that the intensity of elements (C, Si, P, S, Ti, Cr, Mn, Fe, Ni, Mo) of Positive Electrode are decreased as much as about $10^1{\sim}10^3 $than the original electrode. Thickness of Positive Electrode is decreased about 40 ${\mu}m$ after chemical reaction. The negative electrode, however, shows a slight variation in the intensity of elements (C, Si, P, Fe, Ni, Mn, Mo) but Change of thickness and surface' shape of electrode show nothing after chemical reaction. The change in thickness and variation of Stainless Steel 316 cause the lifetime of electrode to be shorted. We also observed hydrogen, oxygen, potassium in both electrodes. Especially, The potassium is increased in proportional with depth of positive electrode. this means the concentration of alkali solutions is changed. and so we have to supply alkaline solution to generator in order to produce same quantity of hydrogen gas continuously. we hope that this study gives a foundation to develop the electrode for hydrogen generator of alkaline electrolysis.