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New Catalysts for a Zero-Gap Type Gas-Diffusion Electrode in Chlor-Alkali Membrane Process

机译:氯碱膜过程中零间隙型气扩散电极的新催化剂

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Newly developed gas-diffusion electrodes (GDE) with binary catalyst composed of Ag and Pd were evaluated in a zero-gap type chlor-alkali cell. It was found that the cell voltage was 2.06V at 6kAm{sup}(-2), which was 120mV smaller than those of composed of single Ag catalyst or Pd catalyst. The increase of the cell voltage with the binary catalyst after 600days of operation was only around 20mV, which is one third of that of Ag catalyst. The particles sizes of the former catalyst were not changed after the electrolysis, but the size of Ag in the latter became large, which quantitatively corresponded to the increase of overvoltage predicted by a porous GDE model calculation. It was suggested that the agglomeration of the Ag catalyst could be inhibited by the existence of Pd.
机译:在零间隙型氯碱细胞中评价具有由Ag和Pd组成的二元催化剂的新开发的气体扩散电极(GDE)。发现电池电压在6kam {sup}( - 2)时为2.06V,比由单Ag催化剂或Pd催化剂组成的120mV。在600天的操作后,具有二元催化剂的电池电压的增加仅为20mV,这是Ag催化剂的三分之一。在电解后,前催化剂的颗粒尺寸不会改变,但是后者的AG的尺寸变大,该尺寸变得大,其定量相应于通过多孔GDE模型计算预测的过电压的增加。建议可以通过Pd的存在抑制Ag催化剂的附聚。

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