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首页> 外文期刊>Journal of power sources >Performance evaluation of a membraneless divergent electrode-flow-through (DEFT) alkaline electrolyser based on optimisation of electrolytic flow and electrode gap
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Performance evaluation of a membraneless divergent electrode-flow-through (DEFT) alkaline electrolyser based on optimisation of electrolytic flow and electrode gap

机译:基于电解流量和电极间隙优化的无膜发散式流通式(DEFT)碱性电解槽性能评估

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摘要

A membraneless divergent electrode-flow-through (DEFT) alkaline electrolysis design and operating principle is investigated, which allows for the ohmic drop contribution and performance threshold limitations of a conventional membrane barrier to be overcome. Employing mesh electrodes of 30 mm diameter, operation of the electrolyser at an electrolytic flow velocity of 0.075-0.1 m s(-1), resulted in an optimal electrode gap of similar to 2.5 mm, while operating at greater velocities (>0.1-0.2 m s(-1)) allows for the employment of a smaller optimal gap of similar to 0.8 mm. At an electrode gap of 2.5 mm and current densities of 3500 mA cm(-2), hydrogen purity of 99.83% has been recorded. With pure nickel electrodes current densities of 101.19 mA cm(-2) (at 1.80 VDC) and 326.33 mA cm(-2) (at 2 VDC) have been achieved, while the use of superior catalysts, namely, RuO2/IrO2/TiO2 and Pt for the anode and cathode respectively, resulted in the current densities to increase to 219.99 mA cm(-2) (at 1.8 VDC) and 474.40 mA cm(-2) (at 2 VDC) at an electrode gap of 2.5 mm and a minimum flow velocity of 0.075 m s(-1). The test rig is capable of generating hydrogen at a rate of 63.6 L/hr at normal temperature and pressure (NW). The production rate follows current density linearly at high overpotentials. (C) 2015 Elsevier B.V. All rights reserved.
机译:研究了无膜发散电极流通(DEFT)碱性电解的设计和工作原理,它可以克服常规膜屏障的欧姆滴贡献和性能阈值限制。使用直径为30 mm的网状电极,以0.075-0.1 ms(-1)的电解流速运行电解槽,可产生类似于2.5 mm的最佳电极间隙,同时以更高的速度(> 0.1-0.2 ms)运行(-1))允许采用更小的最佳间隙,该间隙类似于0.8 mm。在2.5 mm的电极间隙和3500 mA cm(-2)的电流密度下,记录到的氢纯度为99.83%。使用纯镍电极,电流密度分别为101.19 mA cm(-2)(在1.80 VDC时)和326.33 mA cm(-2)(在2 VDC时),同时使用了优良的催化剂RuO2 / IrO2 / TiO2阳极和阴极的Pt和Pt分别导致在2.5 mm的电极间隙下电流密度增加到219.99 mA cm(-2)(在1.8 VDC下)和474.40 mA cm(-2)(在2 VDC)下最小流速为0.075 ms(-1)。在正常温度和压力(NW)下,该试验台能够以63.6 L / hr的速度产生氢气。生产率在高过电势下线性地遵循电流密度。 (C)2015 Elsevier B.V.保留所有权利。

著录项

  • 来源
    《Journal of power sources 》 |2015年第20期| 228-235| 共8页
  • 作者单位

    Demcotech Engn, ZA-1613 Edenglen, South Africa;

    North West Univ, Res Focus Area Chem Resource Beneficiat CRS, Electrochem Energy & Environm Grp, ZA-2520 Potchefstroom, South Africa;

    North West Univ, Res Focus Area Chem Resource Beneficiat CRS, Electrochem Energy & Environm Grp, ZA-2520 Potchefstroom, South Africa;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Alkaline water electrolysis; Membraneless; Hydrogen production;

    机译:碱性水电解;无膜;制氢;

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