• Title/Summary/Keyword: electrolytic cell

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Continuous Decomposition of Ammonia by a Multi Cell-Stacked Electrolyzer with a Self-pH Adjustment Function (자체 pH 조정 기능을 갖는 다단 전해조에 의한 암모니아의 연속식 분해)

  • Kim, Kwang-Wook;Kim, Young-Jun;Kim, In-Tae;Park, Geun-Il;Lee, Eil-Hee
    • Korean Chemical Engineering Research
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    • v.43 no.3
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    • pp.352-359
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    • 2005
  • This work has studied the changes of pH in both of anodic and cathodic chambers of a divided cell due to the electrolytic split of water during the ammonia decomposition to nitrogen, and has studied the continuous decomposition characteristics of ammonia in a multi-cell stacked electrolyzer. The electrolytic decomposition of ammonia was much affected by the change of pH of ammonia solution which was caused by the water split reactions. The water split reaction occurred at pH of less than 8 in the anodic chamber with producing proton ions, and occurred at pH of more than 11 in the cathodic chamber with producing hydroxyl ions. The pH of the anodic chamber using an anion exchange membrane was sustained to be higher than that using a cation exchange membrane, which resulted in the higher decomposition of ammonia in the anodic chamber. By using the electrolytic characteristics of the divided cell, a continuous electrolyzer with a self-pH adjustment function was newly devised, where a portion of the ammonia solution from a pHadjustment tank was circulated through the cathodic chambers of the electrolyzer. It enhanced the pH of the ammonia solution fed from the pH-adjustment tank into the anodic chambers of the electrolyzer, which caused a higher decomposition yield of ammonia. And then, based on the electrolyzer, a salt-free ammonia decomposition process was suggested. In that process, ammonia solution could be continuously decomposed into the environmentally-harmless nitrogen gas up to 83%, when chloride ion was added into the ammonia solution.

Electrical and Optical Properties of Electrochromic Window with Both Lithium and Proton Conducting Polymer Electrolytic Media (리튬 및 프로톤 전도성 고분자전해질을 사용하여 제작한 Electrochromic 창의 전기 및 광학적 특성)

  • 박성용;이철환;김형선;조원일;조병원;윤경석;안춘호;우경근
    • Journal of the Korean institute of surface engineering
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    • v.28 no.1
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    • pp.46-54
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    • 1995
  • An electrochromic(EC) cell was constructed using $WO_3$ as a electrochromic material and NiO as a counter electrode, deposited onto ITO-coated glass by the implementation of electron beam evaporation. The electrolytic media were both lithium and proton conducting polymers such as poly-acrylonitrile(PAN)-$LiClO_4$, poly-ethylene oxide(PEO)-$LiClO_4$, poly-vinyl butyral(PVB)-LiCl and PVB-H$_3$$PO_4$. Potentiodynamic cycling of the cells using PAN-$LiClO_4$, or PVB-$H_3$$PO_4$ electrolyte yielded a transmission variation of more than 40% at the wavelength of 632.8 nm within less than 10 sec response time at room temperature. These results indicate that these electrolytes, transparent in gel type, are premising for the application in large area electrochromic windows.

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A Fully Optimized Electrowinning Cell for Achieving a Uniform Current Distribution at Electrodes Utilizing Sampling-Based Sensitivity Approach

  • Choi, Nak-Sun;Kim, Dong-Wook;Cho, Jeonghun;Kim, Dong-Hun
    • Journal of Electrical Engineering and Technology
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    • v.10 no.2
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    • pp.641-646
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    • 2015
  • In this paper, a zinc electrowinning cell is fully optimized to achieve a uniform current distribution at electrode surfaces. To effectively deal with an electromagnetically coupled problem with multi-dimensional design variables, a sampling-based sensitivity approach is combined with a highly tuned multiphysics simulation model. The model involves the interrelation between electrochemical reactions and electromagnetic phenomena so as to predict accurate current distributions in the electrowinning cell. In the sampling-based sensitivity approach, Kriging-based surrogate models are generated in a local window, and accordingly their sensitivity values are extracted. Such unique design strategy facilitates optimizing very complicated multiphysics and multi-dimensional design problems. Finally, ten design variables deciding the electrolytic cell structure are optimized, and then the uniformity of current distribution in the optimized cell is examined through the comparison with existing cell designs.

Development of a continuous electrolytic system with an ion exchange membrane for pH-control with only one discharge of electrolytic solution and its characteristics (단일 전해액 배출만을 가지는 pH조절용 연속식 이온 교환막 전해 시스템의 개발과 그 특성)

  • Kim Kwang-Wook;Kim In-Tae;Park Geun-Il;Lee Eil-Hee
    • Journal of Nuclear Fuel Cycle and Waste Technology(JNFCWT)
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    • v.3 no.4
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    • pp.269-278
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    • 2005
  • In order to produce only a pH-controlled solution without discharging any unwanted solution, this work has developed a continuous electrolytic system with a pH-adjustment reservoir being placed before an ion exchange membrane-equipped electrolyzer, where as a target solution was fed into the pH-adjustment reservoir, some portion of the solution in the pH-adjustment reservoir was circulated through the cathodic or anodic chamber of the electrolyzer depending on the type of the ion exchange membrane used, and some other portion of the solution in the pH-adjustment reservoir was discharged from the electrolytic system through the other counter chamber with its pH being controlled. The internal circulation of the pH-adjustment reservoir solution through the anodic chamber in the case of using a cation exchange membrane and that through the cathodic chamber in the case of using an anion exchange membrane could make the solution discharged from the other counter chamber effectively acidic and basic, respectively. The phenomena of the pH being controlled in the system could be explained by the electro-migration of the ion species in the solution through the ion exchange membrane under a cell potential difference between anode and cathode and its consequently-occurring non-charge equilibriums and electrolytic water- split reactions in the anodic and cathodic chambers.

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Advanced Lake Water Treatment with Bipolar Packed Bed Electrode Cell(II) (3차원 전극(Bipolar Packed Bed Electrode)을 이용한 호소수 처리(II))

  • 장철현;박상우;최창수
    • Journal of Environmental Science International
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    • v.11 no.4
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    • pp.355-360
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    • 2002
  • This study was to analyze the right of wrong of gray-water treatment by applying BPBE electrode cell to the effluence water in the terminal disposal plant of sewage. The results were as follows : The best result was obtained with applied voltage 40V and detention time 6 minutes for the BPBE electrode cell which has the graphite-plate in main electro-de, packing coconut activated carbon. The elimination rate of COD of Al-plate was higher than that of graphite-plate in main electrode. The result of electrolysis for 3 hour in parallel circuit showed the using possibility of gray-water according to each elimination rate : COD 59%, T-N 69 %, T-P 69%. The BPBE electrode cell with the Al-plate in main electrode made the best effect for the elimination of algae in lake water and algae were not occurred in electrolytic water.

Current characteristics of Cu/NaCl electrolyte/Zn electrochemical cell (구리/NaCl 전해질/아연 전기화학전지의 전류특성)

  • Kim, Yong-Hyuk
    • The Transactions of The Korean Institute of Electrical Engineers
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    • v.59 no.9
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    • pp.1626-1631
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    • 2010
  • The characteristics of electric current for the voltaic cell are important for electric power applications. In this paper, an electrical equivalent model consist of three resisters and a capacitance for the Cu/NaCl solution/Zn electrochemical cell is proposed. The capacitance which exists in the Zn electrode/electrolytic interface increased according to Zn electrode area, but cannot affect almost in electric current. Complex impedance plot was used to analysis the interface effect for Zn/electrolyte. This result shows that the interface is similar with the electric transmission line. The short current measurements were conducted to investigate the effects of hydrogen peroxide, the watery sulfuric acid and NaCl aqueous solution. As the hydrogen peroxide increased, the electric current increased because the hydrogen gas being converted with the water. Also electric current increased significantly with increase of the hydrogen ion with the watery sulfuric acid and increased with increase of $Na^+$ ion and $Cl^-$ion in the NaCl electrolyte.

Cell Activity of ELID-Machined Titanium Surface (ELID 경면 연삭 가공된 티타늄 표면의 세포 활성도)

  • Kang, Jong-Ho;Lee, Myung-Hyun;Seo, Won-Seon;Lee, Suk-Won;Kwak, Tae-Soo;Choi, Heon-Jin
    • Journal of the Korean Society of Manufacturing Process Engineers
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    • v.11 no.3
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    • pp.13-18
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    • 2012
  • We investigated the cell activity of controlled titanium surface using various grinding methods including ELID (Electrolytic In-Process Dressing) grinding method. The influence of titanium surface condition by each grinding process on the cell activity was evaluated by ALP activity of MSC(Mesenchymal Stem Cells). The ALP activity of controlled surface by ELID grinding process using # 2000 wheel was higher than that of other titanium surface. The morphological, chemical properties of machined surface by grinding method was observed using various analytical method.

A Study of Mercury-Cathode Membrane Cells for the Electrolytic Reduction of Uranyl Solutions (膈膜電解槽와 水銀陰極에 依한 Uranyl 溶液의 電解還元)

  • Kim, Jae-Won;Simard, R.
    • Journal of the Korean Chemical Society
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    • v.6 no.1
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    • pp.1-9
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    • 1962
  • Bench-scale horizontal cation-permeable membrane cells were constructed to study the effect of cell dimensions on the efficiency of electrolytic reduction of uranyl sulphate solutions flowing continuously over a mercury cathode. Current efficiencies were determined for various cells having length-to-width ratios of 10/1 to 40/1, and for catholyte solutions containing from 20 to 100g $U_3O_8/l$ in sulphuric acid. Optimum current density and solution flowrate were determined under these conditions. The effects of the nitrate and chloride ions were briefly examined.

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Development of a Continuous Electrolytic System for pH-control with Only One Discharge of Electrolytic Solution by Using Non-equilibrium Steady State Transfer of Ions across Ion Exchange Membranes (이온 교환막에서 이온의 비 평형 정상상태 이동을 이용한 단일 전해액의 배출만을 가지는 pH 조절용 연속식 전해 반응기 개발)

  • Kim Kwang-Wook;Lyu Je-Wook;Kim In-Tae;Park Geun-Il;Lee Eil-Hee
    • Proceedings of the Korean Radioactive Waste Society Conference
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    • 2005.06a
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    • pp.101-109
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    • 2005
  • In order to produce only a pH-controlled solution without discharging any unused solution, this work has developed a continuous electrolytic system with a pH-adjustment reservoir being placed before an ion exchange membrane-equipped electrolyzer, where as a target solution was fed into the pH-adjustment reservoir, some portion of the solution in the pH-adjustment reservoir was circulated through the cathodic or anodic chamber of the electrolyzer depending on the type of the ion exchange membrane used, and some other portion of the solution in the pH-adjustment reservoir was discharged from the electrolytic system through other counter chamber with its pH being controlled as acid or base. The phenomena of the pH being controlled in the system could be explained by the electro-migration of the ion species in the solution through the ion exchange membrane under a cell potential difference between anode and cathode and its consequently-occurring non-charge equilibriums and electrolytic water- split reactions in the anodic and cathodic chambers.

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Electrolytic Conductance Measurement using Four-Electrode Cell and Potentiometric Circuit (포텐티오메트릭 4-전극 용기에 의한 전도도 측정)

  • Jung-Kyoon Chon;Woon-kie Paik
    • Journal of the Korean Chemical Society
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    • v.20 no.2
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    • pp.129-135
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    • 1976
  • A direct-reading conductance measuring system using a potentiostatic circuit and a four-electrode conductance cell was devised. The difficulties with the traditional method of using the Wheatston bridge and a two-electrode cell due to the complicated nature of the electrochemical system, the double layer capacitance and the Faradaic impedance at the electrodes, etc., could be avoided in this method. The devised instrument proved to be convenient and suitable for precise measurements. The results of measured conductivities of KCl and HCl solutions are reported.

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