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Enhanced Electroreductive Removal of Bromate by a Supported Pd-In Bimetallic Catalyst: Kinetics and Mechanism Investigation

机译:负载型Pd-In双金属催化剂增强的溴酸盐的电还原去除:动力学和机理研究

摘要

In this work, the electroreductive removal of bromate by a Pd-1-In-4/Al2O3 catalyst in a three-dimensional electrochemical reactor was investigated. A total of 96.4% of bromate could be efficiently reduced and completely converted into bromide within 30 min under optimized conditions. On the basis of the characterization results and kinetics analysis, a synergistic effect of Pd and In was observed, andPd(1)-In-4/Al2O3 had the highest reaction rate constant of 0.1275 min-1 (vs 0.0413, 0.0328, and 0.0253 min-1 for In/Al2O3, Pd/Al2O3, and Al2O3). The results of electron spin resonance and scavenger experiments confirmed that both direct electron transfer and indirect reduction by atomic H* were involved in the bromate removal process, while the direct reduction played a more important role. Moreover, the introduction of In could increase the zeta potential of Pd-1-In-4/Al2O3, facilitating bromate adsorption and its subsequent reduction on the catalyst. Finally, a reaction mechanism for bromate reduction by Pd-1-In-4/Al2O3 was proposed based on all the experimental results.
机译:在这项工作中,研究了在三维电化学反应器中通过Pd-1-In-4 / Al2O3催化剂对溴酸盐的电还原去除。在最佳条件下,可在30分钟内有效还原96.4%的溴酸盐,并将其完全转化为溴化物。根据表征结果和动力学分析,观察到Pd和In的协同作用,Pd(1)-In-4 / Al2O3的最高反应速率常数为0.1275 min-1(vs 0.0413、0.0328和0.0253) In / Al2O3,Pd / Al2O3和Al2O3的min-1)。电子自旋共振和清除剂实验的结果证实,直接电子转移和原子H *间接还原都参与了溴酸盐的去除过程,而直接还原起着更重要的作用。此外,In的引入可以增加Pd-1-In-4 / Al2O3的Zeta电位,从而促进溴酸盐的吸附及其随后在催化剂上的还原。最后,根据所有实验结果,提出了Pd-1-In-4 / Al2O3还原溴酸盐的反应机理。

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