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首页> 外文期刊>Applied Catalysis, B. Environmental: An International Journal Devoted to Catalytic Science and Its Applications >Photocatalytic degradation of thiocarbamate herbicide active ingredients in water
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Photocatalytic degradation of thiocarbamate herbicide active ingredients in water

机译:水中硫代氨基甲酸酯类除草剂有效成分的光催化降解

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It has been shown that a wide range of organic compounds in aqueous solutions is photocatalytically oxidized to carbon dioxide in the presence of titanium dioxide with near-UV radiation. The photocatalytic mineralization of thiocarbamate derivative pesticides (EPTC, butylate, molinate, vernolate and cycloate) in water by illuminated TiO_2 has been studied. The determination of the effects of various kinetic factors on the photocatalytic degradation and the determination of the nature of the principal intermediates form part of the focus of this study. The degradation rate of these thiocarbamates in a continuous recirculation mode approximates first-order kinetics. It was demonstrated that photocatalyzed degradation of thiocarbamate active ingredients does not occur instantaneously to form carbon dioxide, but through the formation of long-lived intermediate species. Photocatalytic intermediates detected during the degradation of thiocarbamates were identified by GC/MS techniques. Intermediates detected in the photocatalytic oxidation of thiocarbamates in water solutions are in excellent agreement with products identified from the atmospherically important reactions of OH radical with thiocarbamates. Particular attention will be paid to the carbon dioxide formed from the illuminated suspension in order to demonstrate not only apparent destruction but also complete mineralization. The degradation of a two-component mixture was carried out and compared to results obtained with single-component studies.
机译:已经表明,在二氧化钛的存在下,在近紫外辐射下,水溶液中的多种有机化合物被光催化氧化为二氧化碳。研究了光照下TiO_2对水中硫代氨基甲酸酯类农药(EPTC,丁酸酯、,酸酯,戊酸酯和环酸酯)的光催化矿化作用。确定各种动力学因素对光催化降解的影响以及确定主要中间体的性质是本研究的重点。这些硫代氨基甲酸酯在连续再循环模式下的降解速率接近一级动力学。已经证明,硫代氨基甲酸酯活性成分的光催化降解不是立即发生以形成二氧化碳,而是通过形成长寿命的中间物种而发生。通过GC / MS技术鉴定了硫代氨基甲酸酯降解过程中检测到的光催化中间体。在水溶液中硫代氨基甲酸酯的光催化氧化中检测到的中间体与从OH自由基与硫代氨基甲酸酯的大气重要反应中鉴定出的产物高度吻合。将特别注意由照亮的悬浮液形成的二氧化碳,以证明不仅表观破坏而且还显示出完全矿化。进行了两组分混合物的降解,并将其与单组分研究获得的结果进行了比较。

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