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New insights into the relationship between anode material, supporting electrolyte and applied current density in anodic oxidation processes

机译:阳极材料与阳极氧化过程中施加电解质和施加电流密度的新见解

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Taking Acid orange-II (AO II) as pollutant model, the relationship between anode material, supporting electrolyte and applied current density was quantitatively investigated with the aid of a statistical tool, factorial design methodology. Boron-doped diamond (BDD), mixed metal oxide (MMO) and platinum (Pt) used as anode materials were examined with Na2SO4 and NaCI as supporting electrolytes. Analysis of result showed that AO II degradation efficiency was strongly linked to the anode-electrolyte-current interaction. The differing performances recorded in these anode/electrolyte systems could be explained in terms of oxygen evolution over-potential and electro-generated oxidants, and BDD/NaCI system outperformed other systems in terms of decolorization and mineralization efficiency. Further kinetic study indicated that the electrochemical degradation of AO II might follow different reaction orders, depending on the anode material and supporting electrolytes adopted. As a consequence, the new results recorded above were mainly consistent with the low electrolyte concentrations employed (1.0 similar to 10.0 mM). Thus, we highlighted the importance of operating level selections in anodic oxidation processes, especially when different concentrations of supporting electrolytes were present in the reaction system. (C) 2017 Elsevier Ltd. All rights reserved.
机译:服用酸性橙色-II(AO II)作为污染物模型,借助于统计工具,因子设计方法,定量地研究了阳极材料之间的关系,支持电解质和施加的电流密度。用作阳极材料的硼掺杂的金刚石(BDD),混合金属氧化物(MMO)和铂(Pt)用Na 2 SO 4和NaCl检查作为支撑电解质。结果分析表明,AO II降解效率与阳极电解质电流相互作用强烈连接。在这些阳极/电解质系统中记录的不同性能可以在氧气进化过电位和电生氧化剂方面解释,并且BDD / NACI系统在脱色和矿化效率方面优于其他系统。进一步的动力学研究表明,取决于阳极材料和所采用的支撑电解质,AO II的电化学降解可能遵循不同的反应顺序。因此,上述新结果主要与所用的低电解质浓度一致(1.0类似于10.0mm)。因此,我们强调了阳极氧化过程中操作水平选择的重要性,特别是当在反应体系中存在不同浓度的支撑电解质时。 (c)2017 Elsevier Ltd.保留所有权利。

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