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Photo-electrochemical Degradation Of Some Chlorinated Organic Compounds On N-tio_2 Electrode

机译:N-tio_2电极上某些氯化有机物的光电化学降解

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摘要

The electrolysis of some chlorinated organic compounds such as chloroacetic acids, chloromethanes and chloroethenes were carried out on a photo-irradiated n-TiO_2 electrode applied a constant potential, 1.0 V vs. Ag/AgCl, and the alternated pulse potentials of +1.0 V and various negative potentials, -1.0,-1.2 and -1.4 V vs. Ag/AgCl in 0.1 mol dm~(-3) Na_2SO_4 solutions saturated with oxygen or with nitrogen. These compounds were degraded on the n-TiO_2 electrode by the photo-electrolysis and mineralized to carbon dioxide, carbon monoxide and chloride ion. When the alternated pulse potentials were applied, the mineralization yields were increased for these compounds, especially for trichloroacetic acid and carbon tetrachloride, both of which were comparatively stable to the degradation in the constant potential electrolysis. The presence of oxygen in the solution was effective for the mineralization of these compounds, while little effective for that of trichloroacetic acid and of carbon tetrachloride.
机译:某些氯化有机化合物(如氯乙酸,氯甲烷和氯乙烯)的电解是在光照射的n-TiO_2电极上进行的,该电极施加的恒定电位为1.0 V(相对于Ag / AgCl),交替脉冲电位为+1.0 V和相对于Ag / AgCl在0.1 mol dm〜(-3)Na_2SO_4溶液中充满氧或氮的各种负电势-1.0,-1.2和-1.4V。这些化合物通过光电解在n-TiO_2电极上降解,并矿化为二氧化碳,一氧化碳和氯离子。当施加交替的脉冲电势时,这些化合物的矿化产率提高,尤其是三氯乙酸和四氯化碳,它们在恒定电势电解中对于降解而言相对稳定。溶液中氧的存在对于这些化合物的矿化是有效的,而三氯乙酸和四氯化碳的矿化却几乎没有。

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