Back to Search Start Over

Synthesis of Mg-Doped TiO2 Nanoparticles under Different Conditions and its Photocatalytic Activity.

Authors :
Behnajady, Mohammad A.
Alizade, Bahare
Modirshahla, Nasser
Source :
Photochemistry & Photobiology; Nov2011, Vol. 87 Issue 6, p1308-1314, 7p, 2 Black and White Photographs, 3 Charts, 8 Graphs
Publication Year :
2011

Abstract

In this study, TiO<subscript>2</subscript>- and Mg-doped TiO<subscript>2</subscript> nanoparticles with different dopant contents were prepared by sol-gel method. The prepared photocatalysts were characterized with X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), Brunauer-Emmett-Teller (BET) and diffuse reflectance spectroscopy (DRS) techniques. The results of BET analysis indicated a pore diameter of 8 nm and surface area of 48.5 m<superscript>2</superscript> g<superscript>−1</superscript>. XRD patterns of pure and doped TiO<subscript>2</subscript> nanoparticles at 450°C revealed that all phases are anatase. The particle size obtained from TEM was less than 20 nm. The band gap energy of Mg-doped TiO<subscript>2</subscript> nanoparticles was lower than that of TiO<subscript>2</subscript>. The photocatalytic activity of the pure and doped nanoparticles has been compared in the removal of C.I. Acid Red 27 (AR27). The photocatalytic activity of Mg-doped (0.2 mol%) TiO<subscript>2</subscript> for the degradation of AR27 was higher than that of bare TiO<subscript>2</subscript> nanoparticles. Results of total organic carbon analysis and changes in the AR27 UV-Vis peaks indicated 99% mineralization and extinguishing of all peaks in UV and visible regions is possible with Mg-doped TiO<subscript>2</subscript> nanoparticles. Removal efficiency of AR27 was sensitive to the parameters such as catalyst dose, pollutant concentration and light intensity. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00318655
Volume :
87
Issue :
6
Database :
Complementary Index
Journal :
Photochemistry & Photobiology
Publication Type :
Academic Journal
Accession number :
66746406
Full Text :
https://doi.org/10.1111/j.1751-1097.2011.01002.x