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首页> 外文期刊>Electroanalysis >In situ FTIR spectroelectrochemical investigations on Cu2+-ZSM-5 modified electrodes. Reactivity of the electrogenerated species towards NO in aqueous solution
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In situ FTIR spectroelectrochemical investigations on Cu2+-ZSM-5 modified electrodes. Reactivity of the electrogenerated species towards NO in aqueous solution

机译:Cu2 + -ZSM-5修饰电极的原位FTIR光谱电化学研究。电生成物质对水溶液中NO的反应性

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摘要

In situ FTIR spectroelectrochemical experiments have been carried out on Cu2+-ZSM-5 with 40 and 100% ion exchange level with Nafion films coated on glassy carbon electrodes, and on the application of these electrodes to the interaction of NO with the electrogenerated species in aqueous solution. Voltammetric results revealed that the reduction of Cu2+-exchanged zeolites proceeds by two successive quasireversible one-electron steps. The first electron gain resulted in the formation of Cu+-ZSM-5. Cathodic peak potential shifts observed in NO-saturated aqueous solution indicated electrogenerated Cu+-ZSM-5-NO interactions. FTIR measurements showed that the Cu+ ions in the electroreduced Cu2+-ZSM-5 form with NO, among others products, Cu+-ZSM-5-nitrosylic complexes. [References: 41]
机译:在涂覆有玻璃碳电极上的Nafion膜上,以40%和100%的离子交换水平对Cu2 + -ZSM-5进行了原位FTIR光谱电化学实验,以及将这些电极应用于NO与水溶液中电生成物质的相互作用解。伏安法结果表明,Cu2 +交换沸石的还原过程通过两个连续的准可逆单电子步骤进行。第一次电子增益导致形成Cu + -ZSM-5。在NO饱和水溶液中观察到的阴极峰电位变化表明电生成的Cu + -ZSM-5-NO相互作用。 FTIR测量表明,电还原的Cu2 + -ZSM-5中的Cu +离子与NO形成了Cu + -ZSM-5-亚硝基配合物。 [参考:41]

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