Title of article :
Highly photoactive and stable TiO2 coatings on sintered glass Original Research Article
Author/Authors :
M.C. Hidalgo، نويسنده , , S. Sakthivel، نويسنده , , D. Bahnemann، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2004
Pages :
7
From page :
183
To page :
189
Abstract :
TiO2 coatings on sintered borosilicate glass (100–160 μm pore size) were prepared employing a synthetic route based on the hydrolysis of titanium oxysulfate (TiOSO4). The morphology of the coatings was studied by scanning electron microscopy (SEM), showing TiO2 layers with a smooth and homogeneous structure covering the entire surface of the particles forming the sintered glass. The photocatalytic activity of the TiO2 coatings was analysed employing the photooxidation of glucose in water as test reaction. The influence of the preparation conditions of the coatings on their photoactivities was studied. It was found that the starting concentration of precursor and the ageing time were two parameters of significant relevance for the final properties of the catalysts. With specific preparation parameters, photonic efficiencies up to 4% for the total mineralisation of glucose in water could be reached.The effect of the reaction pH during the photocatalytic tests on the efficiency of these coatings was also studied, with the glucose degradation being more favourable at high values of pH.The effect of the reaction pH during the photocatalytic tests on the efficiency of these coatings was also studied, with the glucose degradation being more favourable at high values of pH.Stability and lifetime of the coatings were tested following the evolution of their photocatalytic activity for more than 4000 h of continuous operation. No appreciable degradation of the coatings could be observed during this time.
Keywords :
TiO2 , Titanium oxysulfate , Sintered glass , Photocatalysis , Coatings , Glucose
Journal title :
Applied Catalysis A:General
Serial Year :
2004
Journal title :
Applied Catalysis A:General
Record number :
1151820
Link To Document :
بازگشت