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Composite nanoscale electrodes for the study of electrocatalytic hydrogenation at palladium.

机译:用于研究钯电催化氢化反应的复合纳米电极。

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Well-ordered, nanoscale composite electrodes using template synthesis have been successfully constructed. The electrodes consisted of organic (alkyl carboxylic acids), inorganic (aluminum oxide) and metallic (palladium) components. Maximal homogeneity of the palladium deposits was obtained through manipulation of the metal precursor concentration, solution pH and the application of pulsed applied current waveforms rather than constant applied currents. Fabricated electrodes were characterized using scanning electron microscopy and the variability of pore-filling depths in the template was found to be less than 20%, which compares well with values reported in the literature.;Fabricated well-ordered Pd/Al203 composite electrodes were used to successfully convert phenol to cyclohexanone by electrocatalytic hydrogenation in an organic carboxylic acid buffer solution. Production of the secondary hydrogenation product cyclohexanol from the produced cyclohexanone was not observed. In contrast to powdered composite electrode systems reported in the literature, the functionalization of the alumina support with organic acids was found to have no effect on the reaction efficiency. This suggests that the fabricated ordered composite electrodes do not operate under the same constraints as the powdered-catalyst system upon which the model we were studying was based.
机译:已经成功地构建了使用模板合成的有序的纳米级复合电极。电极由有机(烷基羧酸),无机(氧化铝)和金属(钯)组成。通过控制金属前驱物的浓度,溶液的pH值和施加脉冲施加的电流波形而不是恒定施加的电流,可以获得钯沉积的最大均匀性。使用扫描电子显微镜对制备的电极进行表征,发现模板中孔填充深度的变化小于20%,与文献报道的值相比具有很好的可比性;使用制备良好的有序Pd / Al2O3复合电极通过在有机羧酸缓冲溶液中进行电催化氢化,成功地将苯酚转化为环己酮。没有观察到由生产的环己酮生产第二氢化产物环己醇。与文献中报道的粉末状复合电极系统相反,发现用有机酸对氧化铝载体进行官能化对反应效率没有影响。这表明,所制造的有序复合电极不能在与我们所研究的模型所基于的粉末催化剂体系相同的约束下运行。

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