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Degradation of Dibutyl Phthalate in Aqueous Solution by a Combined Ferrate and Photocatalytic Oxidation Process

机译:高铁酸盐与光催化氧化联合降解水溶液中邻苯二甲酸二丁酯

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摘要

The aim of the present work was to study the interaction of ferrate oxidation and photocatalytic oxidation in terms of dibutyl phthalate (DBP) degradation in aqueous solution, in which three sets of experiments were carried out, including (1) ferrate oxidation alone, (2) photocatalytic oxidation alone, and (3) the combination of ferrate oxidation and photocatalytic oxidation. Laboratory experiments demonstrated that ferrate oxidation and phtotocatalytic oxidation of DBP in aqueous solution are relatively slow processes. However, the presence of TiO_2 and ferrate together under UV illumination accelerated the DBP degradation significantly. Since ferrate was reduced quickly due to the presence of TiO_2 and UV irradiation, the DBP degradation reaction can be divided into two phases. During the first 30 min (Phase 1) the DBP was degraded by both photocatalytic oxidation and ferrate oxidation, and by interactive reactions. After 30 min (Phase 2), the ferrate residual had declined to a very low level and the photocatalytic reaction was the dominant mechanism of further DBP degradation. The influence of three main factors, ferrate dosage, TiO_2 dosage and pH, on the DBP degradation were investigated in order to understand the reaction mechanism and kinetics.
机译:本工作的目的是研究邻苯二甲酸二丁酯(DBP)在水溶液中降解时高铁酸盐氧化与光催化氧化的相互作用,其中进行了三组实验,包括(1)仅高铁酸盐氧化,(2 )单独进行光催化氧化,以及(3)高铁酸盐氧化和光催化氧化的结合。实验室实验表明,水溶液中DBP的高铁酸盐氧化和光催化氧化是相对缓慢的过程。然而,在紫外线照射下,TiO_2和高铁酸盐一起存在显着加速了DBP的降解。由于高铁酸盐由于存在TiO_2和紫外线而迅速还原,因此DBP降解反应可分为两个阶段。在最初的30分钟内(第1阶段),DBP被光催化氧化和高铁酸盐氧化以及相互作用引起的降解。 30分钟后(第2阶段),高铁酸盐残留量已降至非常低的水平,光催化反应是DBP进一步降解的主要机理。研究了高铁酸盐用量,TiO_2用量和pH值这三个主要因素对DBP降解的影响,以了解其反应机理和动力学。

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  • 会议地点 San Francisco CA(US);San Francisco CA(US)
  • 作者单位

    Department of Civil and Structural Engineering, The Hong Kong Polytechnic University, Hong Kong, People's Republic of China;

    rnDepartment of Civil and Structural Engineering, The Hong Kong Polytechnic University, Hong Kong, People's Republic of China Department of Environmental Science and Engineering, Fuzhou University, Fuzhou, Fujian, 350002 People's Republic of China;

    rnDepartment of Civil and Environmental Engineering, Imperial College London, South Kensington Campus, London SW7 2AZ, United Kingdom;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 工业用水、水的处理;
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