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Photocatalytic degradation of organic contaminants in water.

机译:光催化降解水中的有机污染物。

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This dissertation concerns the elucidation of degradation mechanisms of organic contaminants in aqueous suspension of TiO2, and extending understanding of photo catalysis condition to optimize degradation efficiency.; The degradation mechanism of maleic acid, an important intermediate from the photocatalytic degradation of aromatic contaminants, was investigated via product distribution study and control experiments. The understanding of the mechanism of degradation of these compounds can assist us for the ascertaining of the better conditions to perform the mineralization of recalcitrant organic compounds.; The challenge to degrade a cyanyric acid, a recalcitrant species, by modifying TiO2 suspension was carried out. The addition of fluoride to aqueous suspensions of TiO2 has proved to be an important mechanistic tool in unraveling a long-standing conundrum in photocatalytic degradation. By using this method in parallel with other methods for producing homogeneous hydroxyl-type reagents, it is shown that cyanuric acid is susceptible to degradation under easily accessible conditions.; There are isotope studies of photocatalysis of dimethyl phenyl phosphonate, a simple and safe form of organic phosphonate. Exposure of DMMP and related simple phosphonates to TiO2-mediated photocatalytic conditions results first in the loss of one of the methyl esters. An important unsettled mechanistic point is the mechanism by which the methyl is removed. Through the isotope studies of TiO2-mediated photocatalytic degradation of phosphonates, now we can understand removal of the alkyl ester portion of the compounds to produce phosphonic acid monoesters among the primary steps. The retention of 18O in the formation of MMPP clearly demonstrates that the dealkylation mechanism involves degradation of the methyl group exclusively, and neither attack at phosphorus by HO·ads or a related species, nor photoinduced hydrolysis.; With an attempt to activate the modified TiO2 photo catalysts by the visible light and decrease the rapid recombination of excited electrons/holes during photoreaction, WOx-TiO2 powder was prepared by a sol-gel method. The WOx-TiO2 catalysts were characterized by XRD, XPS, and SEM-EDX. The degradation of 4-methoxyresorcinol by using WOx-TiO2 under visible light irradiation was observed.
机译:本文的目的在于阐明TiO2水悬浮液中有机污染物的降解机理,并扩展对光催化条件的理解,以优化降解效率。通过产物分布研究和控制实验研究了马来酸的降解机理,马来酸是芳香族污染物光催化降解的重要中间体。对这些化合物降解机理的理解可以帮助我们确定进行顽固有机化合物矿化的更好条件。进行了通过修饰TiO2悬浮液来降解难分解的氰基酸的挑战。事实证明,向TiO2的水悬浮液中添加氟化物是解决光催化降解中长期存在的难题的重要机制。通过与其他生产均相羟基型试剂的方法并行使用该方法,表明氰尿酸在易于接近的条件下易于降解。有对光催化二甲基苯基膦酸酯(一种简单而安全的有机膦酸酯形式)的同位素研究。 DMMP和相关的简单膦酸酯暴露于TiO2介导的光催化条件下,首先会导致其中一种甲酯的损失。一个重要的未解决的机理是除去甲基的机理。通过TiO2介导的膦酸酯的光催化降解的同位素研究,现在我们可以理解在主要步骤中除去化合物的烷基酯部分以生产膦酸单酯的方法。 MMPP形成中18 O的保留清楚地表明,脱烷基化机理仅涉及甲基的降解,既不被HO·ads或相关物种攻击磷,也不进行光诱导水解。为了通过可见光活化改性的TiO 2光催化剂并减少光反应过程中激发电子/空穴的快速复合,采用溶胶-凝胶法制备了WOx-TiO 2粉末。通过XRD,XPS和SEM-EDX对WOx-TiO2催化剂进行了表征。在可见光照射下,通过使用WOx-TiO2观察到了4-甲氧基间苯二酚的降解。

著录项

  • 作者

    Oh, Youn-Chul.;

  • 作者单位

    Iowa State University.;

  • 授予单位 Iowa State University.;
  • 学科 Chemistry Organic.; Chemistry Inorganic.
  • 学位 Ph.D.
  • 年度 2004
  • 页码 173 p.
  • 总页数 173
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 有机化学;无机化学;
  • 关键词

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