首页> 外文学位 >Photocatalytic destruction of halogenated organic compounds in water with a new photocatalysts.
【24h】

Photocatalytic destruction of halogenated organic compounds in water with a new photocatalysts.

机译:用新型光催化剂光催化破坏水中的卤代有机化合物。

获取原文
获取原文并翻译 | 示例

摘要

In this research, a newly developed high surface area semiconductor porous material was synthesized from potassium titanium niobium mixed oxide (KTiNbO5) to be used as a photo catalyst in the presence of UV light to degrade halogenated organic compounds in water. The goal of the project was to investigate the catalytic activity of the material for its effectiveness in the degradation of the halogenated organic compounds, and it is the first investigation of this new photocatalyst with halogenated compounds. Model compounds dichloromethane, 1-chlorobutane, chlorobenzene, and trifluoroacetic acid in aqueous solutions were tested with the photocatalyst under ultraviolet light irradiation, using a batch photolysis reactor system. An improved process for preparing the photocatalysts was developed, which is more effective, faster, and less wasteful for rinsing the catalysts with a solvent exchange done in five hours instead of the original 6 days. The porous material was characterized by X-ray diffraction, scanning electron microscopy, transmission electron microscopy, nitrogen adsorption surface area analysis (BET), inductively coupled plasma optical emission spectroscopy, and X-ray fluorescence spectrometry. The project also involved researching a practical way to follow the reaction progress using the product concentrations of Cl- and F- in solution. Photo degradation kinetics was followed via titration, ion selective electrodes, ion chromatography, and total organic carbon analysis. In a mixture of the three chlorinated compounds, about 84% of the chlorine present in the compounds was released as chloride ions after 8.0 hours of irradiation with the catalyst. This was concomitant with a decrease in the pH of the solution. Loss of samples via vaporization and escape into the air was responsible for incomplete photolyzation. Several attempts to create a catalyst system using a flow-through reactive catalyst bed were not successful, and therefore a batch process was used. The photocatalytic activity of the new porous material towards halogenated organic compounds in stirred water reactors is demonstrated to be a promising alternative to TiO2 nano powders. The new catalyst had much better sedimentation characteristics than TiO2 nano powders and it can be filtered easily, qualities that TiO2 nano powders do not have.
机译:在这项研究中,由钾钛铌混合氧化物(KTiNbO5)合成了一种新开发的高表面积半导体多孔材料,可在紫外光存在下用作光催化剂以降解水中的卤代有机化合物。该项目的目的是研究该材料在卤代有机化合物降解中的催化活性,这是这种新型含卤代化合物的光催化剂的首次研究。使用间歇光解反应器系统,在紫外线照射下,用光催化剂测试水溶液中的模型化合物二氯甲烷,1-氯丁烷,氯苯和三氟乙酸。开发了一种改进的制备光催化剂的方法,该方法通过用五小时而不是最初的六天进行的溶剂交换来冲洗催化剂更有效,更快且浪费更少。通过X射线衍射,扫描电子显微镜,透射电子显微镜,氮吸附表面积分析(BET),电感耦合等离子体发射光谱法和X射线荧光光谱法表征多孔材料。该项目还涉及研究使用溶液中Cl-和F-的产物浓度跟踪反应进程的实用方法。通过滴定,离子选择性电极,离子色谱和总有机碳分析来跟踪光降解动力学。在三种氯化化合物的混合物中,用催化剂照射8.0小时后,化合物中存在的约84%的氯以氯离子的形式释放。这伴随溶液的pH降低。样品由于汽化而损失并逃逸到空气中是造成不完全光解的原因。使用流通式反应性催化剂床创建催化剂体系的几次尝试均未成功,因此使用了分批工艺。在搅拌水反应器中,新型多孔材料对卤代有机化合物的光催化活性被证明是TiO2纳米粉的有前途的替代品。该新型催化剂具有比TiO2纳米粉更好的沉降特性,并且易于过滤,这是TiO2纳米粉所不具备的。

著录项

  • 作者

    Hadidan, Mabruka.;

  • 作者单位

    The University of Texas at El Paso.;

  • 授予单位 The University of Texas at El Paso.;
  • 学科 Chemistry Molecular.;Chemistry Organic.
  • 学位 M.S.
  • 年度 2011
  • 页码 78 p.
  • 总页数 78
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 语言学;
  • 关键词

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号