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Electrochemical investigations of reactive dyes; cathodic stripping voltammetric determination of anthraquinone-based chlorotriazine dyes at a hanging mercury drop electrode

机译:活性染料的电化学研究;悬挂式汞滴电极上的阴极溶出伏安法测定蒽醌类氯三嗪染料

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摘要

Two anthraquinone-based chlorotriazine reactive dyes, Procion Blue MX-R and Cibacron Blue 3GA, have been determined at nanomolar levels using cathodic stripping voltammetry. When the differential pulse voltammetric stripping mode is used no peak is obtained for the reduction of the anthraquinone moiety in these dyes, although the signal is present when the linear sweep mode is used. The absence of this peak in the differential pulse mode is believed to occur because, when this group is reduced in the adsorbed state on application of the potential pulse, it is reduced so rapidly that reduction is complete before the current is monitored at the end of the pulse. The differential pulse signal is present for the reduction of the chlorotriazine active groups. The differential pulse peak for the anthraquinone reduction process does appear when boric acid is present in the supporting electrolyte, and it is also present when the chlorotriazine groups are hydrolysed or reacted with other hydroxy compounds. This means that hydrolysis or similar reactions of these dyes can be monitored by observing both the appearance of the anthraquinone peak and the disappearance of the chlorotriazine peak.
机译:两种基于蒽醌的氯三嗪活性染料Procion Blue MX-R和Cibacron Blue 3GA已通过阴极溶出伏安法在纳摩尔浓度下测定。当使用差分脉冲伏安剥离模式时,尽管在使用线性扫描模式时存在信号,但在这些染料中未获得用于还原蒽醌部分的峰。认为在差动脉冲模式下不存在该峰是因为,当在施加电势脉冲时该基团在吸附状态下被还原时,该基团被如此迅速地还原,以至于还原在电流结束时被监测之前就已经完成。脉冲。存在差分脉冲信号以还原氯三嗪活性基团。当硼酸存在于支持电解质中时,确实会出现蒽醌还原过程的微分脉冲峰,并且当氯三嗪基团水解或与其他羟基化合物反应时也会出现。这意味着可以通过观察蒽醌峰的出现和氯三嗪峰的消失来监视这些染料的水解或类似反应。

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