کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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42765 | 45940 | 2009 | 11 صفحه PDF | دانلود رایگان |
![عکس صفحه اول مقاله: Photocatalytic activity of Ag-substituted and impregnated nano-TiO2 Photocatalytic activity of Ag-substituted and impregnated nano-TiO2](/preview/png/42765.png)
Ag-substituted (Ag sub) and Ag-impregnated (Ag imp), anatase phase nano-TiO2 have been synthesized by solution combustion technique and reduction technique, respectively. The catalysts were characterized extensively by powder XRD, TEM, XPS, FT-Raman, UV absorption, FT-IR, TGA, photoluminescence, BET surface area and isoelectric pH measurements. These catalysts were used for the photodegradation of dyes and for the selective photooxidation of cyclohexane to cyclohexanone. The photoactivities of the combustion-synthesized catalysts were compared with those of commercial Degussa P 25 (DP 25) TiO2, and Ag-impregnated DP 25 (Ag DP). For the photocatalytic degradation of dyes, unsubstituted combustion-synthesized TiO2 (CS TiO2) exhibited the highest activity, followed by 1% Ag imp and 1% Ag sub. For the photoconversion of cyclohexane, the total conversion of cyclohexane and the selectivity of cyclohexanone followed the order: 1% Ag sub > DP 25 > CS TiO2 > 1% Ag imp > 1% Ag DP. The kinetics of the photodegradation of dyes and of the photooxidation of cyclohexane were modeled using Langmuir–Hinshelwood rate equation and a free radical mechanism, respectively, and the rate coefficients were determined. The difference in activity values of the catalysts observed for these two reactions and the detailed characterization of these catalysts are described in this study.
The photocatalytic activities of Ag-substituted, Ag-impregnated and unsubstituted combustion-synthesized nano-TiO2 were evaluated for the degradation of dyes and the selective conversion of cyclohexane to cyclohexanone. The activities of these catalysts for the above reactions are correlated with the surface area, band gap, hydroxyl content, photoluminescence intensity and oxide ion vacancy.Figure optionsDownload as PowerPoint slide
Journal: Applied Catalysis A: General - Volume 366, Issue 1, 15 September 2009, Pages 130–140