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Electrochemical Degradation of Methyl Red Using Ti/Ru_(0.3)Ti_(0.7)O2: Fragmentation of Azo Group

机译:Ti / Ru_(0.3)Ti_(0.7)O2电化学降解甲基红:偶氮基团的断裂

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In this work, anodic oxidation of methyl red (MR) using Ti/Ru_(0.3)4Ti_(0.66)O2 as anode was.investigated for understanding of the fragmentation of chromophore group, as initial stage of MR degradation. Cyclic voltammetry was employed to evaluate the behavior of electrode in absence and presence of organic compound, indicating that the oxidation of MR occurs approximately at 1.45-1.55 V. UV-vis spectra showed that the color removal is attained independently of current density applied. The changes on absorbance band of MR indicated that a possible fragmentation of azo group was attained. The analysis of inorganic species released during MR degradation suggested that the release of nitrogen inorganic ions like NO3~- as well as NO2~- ions is a consequence of chromophore group cleavage, as it also observed by the changes of the band at 1,451 cm~(-1) (-N double bond), during the initial electrolysis times, achieved by Fourier-transform infrared spectrometry analyses. The findings presented herein are described and discussed in the light of the existing literature data.
机译:在这项工作中,以Ti / Ru_(0.3)4Ti_(0.66)O2为阳极进行了甲基红(MR)的阳极氧化研究,以了解发色团的断裂,这是MR降解的初始阶段。循环伏安法用于评估在不存在和存在有机化合物的情况下电极的行为,表明MR的氧化大约发生在1.45-1.55V。UV-vis光谱表明,脱色与施加的电流密度无关。 MR吸光度带的变化表明偶氮基可能断裂。对MR降解过程中释放的无机物的分析表明,氮无机离子(如NO3〜-以及NO2〜-)的释放是发色团裂解的结果,这也可以通过在1,451 cm〜处的谱带变化观察到。 (-1)(-N双键)在最初的电解时间内,通过傅里叶变换红外光谱分析获得。本文介绍的发现将根据现有文献数据进行描述和讨论。

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