A low-cost photoactive composite quartz sand/TiO2

被引:32
作者
Tokarsky, Jonas [1 ]
Matejka, Vlastimil [1 ]
Neuwirthova, Lucie [1 ]
Vontorova, Jirina [2 ]
Mamulova Kutlakova, Katerina [1 ]
Kukutschova, Jana [1 ]
Capkova, Pavla [3 ]
机构
[1] VSB Tech Univ Ostrava, Nanotechnol Ctr, Ostrava 70833, Czech Republic
[2] VSB Tech Univ Ostrava, Fac Met & Mat Testing, Dept Analyt Chem & Mat Testing, Ostrava 70833, Czech Republic
[3] Univ JE Purkyne, Fac Sci, Usti Nad Labem 40096, Czech Republic
关键词
Quartz sand; TiO2; Nanocomposite; Photoactivity; PHOTOCATALYTIC DEGRADATION; TITANIUM-DIOXIDE; TIO2; SILICA; NANOCOMPOSITE; PARAMETERS; RUTILE; FILMS; OXIDE;
D O I
10.1016/j.cej.2013.02.056
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The photoactive quartz sand/TiO2 composites were prepared by thermal hydrolysis of the suspension obtained by addition of quartz sand to a titanyl sulfate solution. The required amount of TiO2 in the prepared composites (i.e. 9,22 and 45 wt.%, respectively) was achieved using a variable titanyl sulfate/quartz ratio. As reference materials, pure TiO2 was prepared using the thermal hydrolysis of the titanyl sulfate solution under the same condition as used during the preparation of composite quartz/TiO2. The composite samples, dried at 105 degrees C and calcined at temperatures of 500-900 degrees C were investigated using X-ray fluorescence spectroscopy, X-ray powder diffraction analysis, transmission electron microscopy, and Fourier transform infrared spectroscopy. Structural ordering of TiO2 particles on the quartz surface was studied using atomistic simulations in a Material Studio modeling environment. Photodegradation activity of the composites was evaluated by the discoloration of Acid Orange 7 aqueous solution. The composite containing 22 wt.% of TiO2 and calcined at 800 degrees C exhibits the highest photoactivity. Higher and lower amounts of TiO2 led to worse results. The quartz/TiO2 composite is a promising material able to replace pure TiO2 in a wide range of building materials. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:488 / 497
页数:10
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