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In situ FTIR studies on the electrochemical hydrodechlorination of 3,4,5,6-tetrachloropicolinic acid on Ag cathode

机译:Ag阴极上3,4,5,6-四氯吡啶甲酸的电化学加氢氯化的原位FTIR研究

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摘要

The electrochemical hydrodechlorination reaction from starting material 3,4,5,6-tetrachloropicolinic acid (3,4,5,6-TCP) to the end product 3,6-dichloropicolinic acid (3,6-DCP) was investigated by cyclic voltammetry and in situ Fourier transform infrared spectroscopy (in situ FTIR). Compared with copper and glassy carbon, Ag cathode showed a high electrocatalytic activity for the irreversible reduction process of 3,4,5,6-TCP in NaOH aqueous solution. In situ FTIR results suggested that electrochemical hydrodechlorination took place in the 4- or 5-position of 3,4,5,6-TCP on Ag cathode after receiving an electron to get mixed trichloropicolinic acid free radical, which could receive another electron and give 3,5,6-trichloropicolinic acid (3,5,6-TCP) and 3,4,6-trichloropicolinic acid (3,4,6-TCP) at the potential more positive than -1000 mV afterwards. Finally, 3,5,6-TCP and 3,4,6-TCP were further dechlorinated to produce 3,6-dichloropicolinic acid (3,6-DCP) at the potential more negative than -1000mV. Further studies of preparative electrolysis experiments by constant current electrolysis were carried out. The results were in good agreement with those from in situ FTIR investigations.
机译:通过循环伏安法研究了从原料3,4,5,6-四氯吡啶甲酸(3,4,5,6-TCP)到最终产物3,6-二氯吡啶甲酸(3,6-DCP)的电化学加氢脱氯反应和原位傅里叶变换红外光谱(原位FTIR)。与铜和玻璃碳相比,Ag阴极对NaOH水溶液中3,4,5,6-TCP的不可逆还原过程表现出较高的电催化活性。原位FTIR结果表明电化学加氢脱氯反应是在接收电子后在Ag阴极的3,4,5,6-TCP的4位或5位发生的,从而得到混合的三氯吡啶甲酸自由基,该自由基可以接受另一个电子并产生之后,3,5,6-三氯吡啶甲酸(3,5,6-TCP)和3,4,6-三氯吡啶甲酸(3,4,6-TCP)之后的电位大于-1000 mV。最后,将3,5,6-TCP和3,4,6-TCP进一步脱氯,以产生比-1000mV负电势更大的3,6-二氯吡啶甲酸(3,6-DCP)。通过恒流电解进行制备性电解实验的进一步研究。结果与现场FTIR调查的结果非常吻合。

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