PREPARATION OF γ -Fe2O3/SiO2/TiO2 UNDER THE LOW-TEMPERATURE AND THE PHOTO-CATALYTIC DEGRADATION OF SULFAMETHAZINE IN WATER

被引:0
|
作者
Jia, Qingzhu [1 ]
Jia, Xiaochen [1 ]
Chen, Hui [1 ]
机构
[1] Tianjin Univ Sci & Technol, Sch Marine & Environm Sci, Tianjin 300457, Peoples R China
来源
FRESENIUS ENVIRONMENTAL BULLETIN | 2017年 / 26卷 / 10期
关键词
Photo-catalyst; TiO2; SiO2; Sulfadimidine; Degradation pathway; PHOTOCATALYTIC DEGRADATION; ACTIVATED CARBON; PHOTODEGRADATION; MICROSPHERES; SULFONAMIDES; ANTIBIOTICS; IRRADIATION; BLUE;
D O I
暂无
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
In this work, the magnetic gamma-Fe2O3/SiO2/TiO2 microspheres of core shell structure with convenient recyclability were prepared by using the ultrasonic-assisted modified Stober method and sol-gel approach, and the photo-activity of which was evaluated by through the photo-degradation of sulfamethazine in aqueous solution. Results suggested that the good superparamagnetic properties of gamma-Fe2O3/SiO2/TiO2 could be reserved by the formation of gamma-Fe2O3. The photo-degradation of sulfamethazine results demonstrated that the prepared gamma-Fe2O3/SiO2/TiO2 could provide the same high UV-photo-activity as that of P25 TiO2 because of their similar constitutes of anatase and rutile types. And the higher UV-photo-degradation rate for sulfamethazine of gamma-Fe2O3/SiO2/TiO2 than that of gamma-Fe2O3/TiO2 further demonstrated that the SiO2 interlining could not only block the contact of TiO2 shell and magnetic core gamma-Fe2O3, but also enhance the photo catalytic reactivity. Moreover, this easily recoverable gamma-Fe2O3/SiO2/TiO2 could be reused at least for five times without any appreciable reduction of photo-catalytic efficiency. In combination with HPLC/ESI-MS analysis and density functional theory, photo-degradation pathway of sulfamethazine had been speculated, and some key reaction processes as the hydroxyl oxide, ammonia oxidation, splitting decomposition and open loop reactions might have occurred during the photo-degradation of sulfamethazine.
引用
收藏
页码:6272 / 6285
页数:14
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