کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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148599 | 456419 | 2013 | 10 صفحه PDF | دانلود رایگان |

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 °C and calcined at temperatures of 500–900 °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 °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.
A low-cost photoactive composite prepared from quartz sand and titanyl sulfate solution exhibits the highest photoactivity when containing 22 wt.% of TiO2 and after the calcination at 800 °C.Figure optionsDownload as PowerPoint slideHighlights
► Quartz sand/TiO2 composite exhibits photocatalytic properties.
► The quartz sand was used as received, without any further treatment.
► TiOSO4 was used as a low-cost precursor of TiO2.
► Calcination caused significant increase in the photodegradation activity.
► Prepared composite is suitable for use in wide range of building materials.
Journal: Chemical Engineering Journal - Volume 222, 15 April 2013, Pages 488–497