Fabrication of High Surface Area TiO2-MoO3 Nanocomposite as a Photocatalyst for Organic Pollutants Removal from Water Bodies

被引:10
作者
Abla, Fatima [1 ]
Elsayed, Yehya [2 ]
Abu Farha, Nedal [3 ]
Obaideen, Khaled [4 ]
Mohamed, Ahmed A. [1 ]
Lee, Haesung [5 ]
Han, Changseok [5 ,6 ]
Egilmez, Mehmet [7 ]
Kanan, Sofian [3 ]
机构
[1] Univ Sharjah, Dept Chem, Sharjah 27272, U Arab Emirates
[2] Donaldson Co, Bloomington, MN 55431 USA
[3] Amer Univ Sharjah, Dept Biol Chem & Environm Sci, Sharjah 26666, U Arab Emirates
[4] Univ Sharjah, Sustainable Energy & Power Syst Res Ctr, RISE, Sharjah 27272, U Arab Emirates
[5] INHA Univ, Grad Sch, Program Environm & Polymer Engn, 100 Inha Ro, Incheon 22212, South Korea
[6] INHA Univ, Dept Environm Engn, 100 Inha Ro, Incheon 22212, South Korea
[7] Amer Univ Sharjah, Dept Phys, Sharjah 26666, U Arab Emirates
基金
新加坡国家研究基金会;
关键词
Ti-Mo NC; carbaryl; fenoxycarb; methylene blue; photocatalyst; HYDROTHERMAL SYNTHESIS; PHOTODEGRADATION; DEGRADATION; ADSORPTION; FENOXYCARB; TIO2/MOO3; GROWTH;
D O I
10.3390/catal13020362
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A nanocomposite (NC) of titanium (IV) oxide (TiO2) and molybdenum (VI) oxide (MoO3) was synthesized using a hydrothermal route. Detailed analyses using transmission electron microscopy, X-ray diffraction, X-ray fluorescence (XRF), Brunauer-Emmett-Teller (BET) isotherms, X-ray photoelectron spectroscopy, Raman, and diffuse reflectance infrared Fourier transform spectroscopy were carried out and confirmed the successful formation of pure TiO2-MoO3 (Ti-Mo) NC. The Ti-Mo NC possesses sizes in the range of 150-500 nm. XPS, Raman, and DRIFT shift measurements confirmed the formation of mixed oxide linkage in the form of Ti-O-Mo. Sorption of nitrogen isotherms revealed a significant increase in the number and pore widths of mesopores in the NC. Water sorption isotherms revealed enhanced affinity of the nanocomposites for water relative to the pure metal oxides. The BET surface area for Ti-Mo NC from the nitrogen adsorption isotherm was 129.3 m(2)/g which is much higher than the pure metal oxides (i.e., 37.56 m(2)/g for TiO2 and 2.21 m(2)/g for MoO3). The Ti-Mo NC provided suitable adsorption sites that captured the studied carbamates from the solution and promoted their photodegradation process. The photocatalytic degradation of MB in the presence of the catalyst was enhanced by 2.9 and 5.5 folds upon irradiation with white LED and 302 nm UV light sources, respectively.
引用
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页数:17
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