کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
146476 456371 2015 7 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Silica supported SO42-/TiO2 for photocatalytic decomposition of acrylonitrile under simulant solar light irradiation
موضوعات مرتبط
مهندسی و علوم پایه مهندسی شیمی مهندسی شیمی (عمومی)
پیش نمایش صفحه اول مقاله
Silica supported SO42-/TiO2 for photocatalytic decomposition of acrylonitrile under simulant solar light irradiation
چکیده انگلیسی


• SO42-/TiO2/SiO2 solid acids were prepared by a simple impregnation method.
• Sulfur was highly dispersed in TiO2 crystals in the form of SO42-.
• Surface acid sites were responsible for improving photocatalytic activity.
• Excess coverage of SO42- on TiO2/SiO2 surface reduced the photocatalytic activity.
• The SO42-/TiO2/SiO2 solid acids were effective for acrylonitrile removal.

The SO42-/TiO2/SiO2 solid acids were prepared by impregnation method. The prepared powders were characterized by scanning electron microscope (SEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Brunauer–Emmett–Teller (BET), Fourier transform infrared spectroscopy (FT-IR), and UV spectrophotometer. The photocatalytic activities of the powders were investigated using acrylonitrile as a probe molecule. The results showed that sulfur was highly dispersed in TiO2 crystals in the form of SO42-. In situ IR and UV spectrophotometer showed that the higher photocatalytic activity of SO42-/TiO2/SiO2 solid acid was due to the increase of the surface Bronsted and Lewis acid sites. However, excess coverage of SO42- on TiO2/SiO2 surface decreased the photocatalytic activity due to inhibition of light absorption. The optimum synthesis conditions were calcination temperature at 450 °C for 2 h and 7.04 wt.% SO42- content. The degradation ratio of acrylonitrile reached to 97% with 1.0 g SO42-/TiO2/SiO2 solid acid for 30 min irradiation, indicating the effectiveness of photocatalytic degradation of acrylonitrile using the prepared catalyst.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Chemical Engineering Journal - Volume 270, 15 June 2015, Pages 590–596
نویسندگان
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