期刊文献+

具有优异热稳定性的磷修饰氧化钛及其对水中污染物的降解(英文) 被引量:2

Phosphorous-Modified TiO_2 with Excellent Thermal Stability and Its Application to the Degradation of Pollutants in Water
下载PDF
导出
摘要 通过水热法制得磷修饰氧化钛,它在亚甲基蓝和对氯苯酚的降解以及消除大肠杆菌的实验中都表现出高于纯氧化钛的优异活性,甚至优于商品化催化剂P25.在捕获剂中降解亚甲基蓝的实验证实羟基自由基是最主要的活性氧物种,并且磷修饰氧化钛在光照下拥有较强的产生羟基自由基的能力.同时,磷修饰氧化钛具有非常高的热稳定性,直到950oC才会发生从锐钛矿到金红石的相变,这是因为粒子表面的磷酸根阻止了金红石在界面的成核因而抑制了相变发生.磷修饰氧化钛的这种优异性质使得它即使在900oC焙烧后也能有效地降解水中污染物. The phosphorous-modified TiO2(P-TiO2) was synthesized by a hydrothermal method. The as-prepared P-TiO2 was evaluated for the degradation of methylene blue,the dechlorination of 4-chlorophenol,and the inactivation of Escherichia coli. In all these experiments,P-TiO2 shows superior activity compared with pure TiO2 and even better activity than the commercially available P25 in most cases. By carrying out methylene blue degradation in the presence of different scavengers,OH radicals were found to be the dominant reactive oxidizing species. The excellent performance of P-TiO2 was correlated with its pronounced ability to generate ?OH radicals under illumination. We also found that P-TiO2 is extraordinarily stable against annealing. Its transformation from anatase to rutile does not occur until calcination as high as 950 oC. This phase transformation is retarded since the phosphate species on the surface of the particles acts as a barrier to grain boundary nucleation. This peculiar feature of P-TiO2 gives it reliable performance during water decontamination even after calcination at 900 oC since it retains a 100% anatase phase at this stage.
出处 《催化学报》 SCIE EI CAS CSCD 北大核心 2011年第7期1173-1179,共7页
基金 国家自然科学基金(20973012) 国家重点基础研究发展计划(973计划,2011CB808702)~~
关键词 磷修饰 氧化钛 光催化 热稳定性 抗菌 phosphorous modification titanium dioxide photocatalysis thermal stability antibacterial
  • 相关文献

参考文献35

  • 1Legrini O, Oliveros E, Brauna A M. Chem Rev, 1993, 93: 671.
  • 2Hoffmann M R, Martin S T, Choi W, Bahnemann D W. Chem Rev, 1995, 95:69.
  • 3Andreozzi A R, Caprio V, Insola A, Marotta R. Catal Today, 1999, 53:51.
  • 4Linsebigler A L, Lu G, Yates J T. Chem Rev, 1995, 95:735.
  • 5Lawless D, Serpone N, Meisel D. J Phys Chem, 1991, 95: 5166.
  • 6Cho M, Chung H, Choi W, Yoon J. Water Res, 2004, 38:1069.
  • 7Gandhe A R, Naik S P, Femandes J B. Microporous Mesoporous Mater, 2005, 87:103.
  • 8Kumar K N P, Keizer K, Burggraaf A J, Okubo T, Nagamoto H, Morooka S. Nature, 1992, 358:48.
  • 9Shannon R D, Pask J A. JAm Ceram Soc, 1965, 48:391.
  • 10Gouma P I, Dutta P K, Mills M J. Nano Mat, 1999, 11:1231.

同被引文献34

  • 1张金涛,胡吉明,张鉴清,曹楚南.LY12铝合金/钝化膜/环氧涂层复合电极的腐蚀电化学行为[J].金属学报,2006,42(5):528-532. 被引量:21
  • 2Xie Y B,Zhou L M,Lu J.Photoelectrochemical behavior of titania nanotube array grown on nanocrystalline titanium[J].Journal of Materials Science,2009,44 (11):2907-2915.
  • 3Alivov Y,Fan Z Y,Johnstone D.Titanium nanotubes grown by titanium anodization[J].Journal of Applied Physics,2009,106 (3):034314-034318.
  • 4Kang X W,Chen S W.Photocatalytic reduction of mrethylene blue by TiO2 nanotube arrays:Effects of TiO2 crystalline phase[J].Journal of Materials Science,2010.45(10):2696-2702.
  • 5Hu K H,Hu X G,Xu Y F,et al.Synthesis of nano-MoS2/TiO2 composite and its catalytic degradation effect on methyl orange[J].Journal of Materials Science,2010,45(10):2640-2648.
  • 6Archana P S,Jose R,Jin T M,et al.Structural and electrical properties of Nb-doped anatase TiO2 nanowires by electrospinning[J].J Am Ceram Soc,2010,93(12):4096-4102.
  • 7Fadl-Allah S A,El-Sherief R M,Badawy W A.Electrochemical formation and characterization of porous titania (TiO2) films on Ti[J].J Appl Electrochem,2008,38(10):1459-1466.
  • 8Diamanti M V,Bolzoni F,Ormellese M,et al.Characterisation of titanium oxide films by potentiodynamic polarisation and electrochemical impedance spectroscopy[J].Corrosion Engineering,Science and Technology,2010,45(6):428-434.
  • 9丁海洋,冯玉杰,吕江维,刘峻峰.钛基二氧化锡电极电解过程中羟基自由基检测及电催化机理[J].分析化学,2007,35(10):1395-1399. 被引量:23
  • 10庄惠芳,赖跃坤,李静,孙岚,林昌健.高度有序的二氧化钛纳米管阵列的制备及其光催化活性的研究[J].化学学报,2007,65(21):2363-2369. 被引量:24

引证文献2

二级引证文献45

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部