Title of article :
Efficient adsorption and photocatalytic degradation of organic pollutants diluted in water using the fluoride-modified hydrophobic titanium oxide photocatalysts: Ti-containing Beta zeolite and TiO2 loaded on HMS mesoporous silica
Author/Authors :
Hiromi Yamashita، نويسنده , , Shinichi Kawasaki، نويسنده , , Shuai Yuan، نويسنده , , Kazuhiro Maekawa، نويسنده , , Masakazu Anpo، نويسنده , , Michio Matsumura )، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2007
Pages :
7
From page :
375
To page :
381
Abstract :
Using the F− media, the hydrophobic zeolite and mesoporous silica can be synthesized. These hydrophobic porous materials exhibit the high ability for the adsorption of organic compounds diluted in water and become the useful supports of photocatalyst. The hydrophobic Ti-Beta(F) zeolite prepared in the F− media exhibited high efficiency than the hydrophilic Ti-Beta(OH) zeolite prepared in OH− media for the liquid-phase photocatalytic degradation of 2-propanol diluted in water to produce CO2 and H2O. The TiO2 loaded on the hydrophobic mesoporous silica HMS(F) (TiO2/HMS(F)), which was synthesized using tetraethyl orthosilicate, tetraethylammonium fluoride as the source of the fluoride and dodecylamine as templates, also exhibited the efficient photocatalytic performance for the degradation. The amount of adsorption of 2-propanol and the photocatalytic reactivity for the degradation increased with increasing the content of fluoride ions on these photocatalysts. The efficient photocatalytic degradation of 2-propanol diluted in water on Ti-Beta(F) zeolite and TiO2/HMS(F) mesoporous silica can be attributed to the larger affinity for the adsorption of propanol molecules on the titanium oxide species depending on the hydrophobic surface properties of these photocatalysts.
Keywords :
photocatalysis , Titanium oxide , Zeolite , Mesoporous silica degradation , Hydrophobic property
Journal title :
CATALYSIS TODAY
Serial Year :
2007
Journal title :
CATALYSIS TODAY
Record number :
1236064
Link To Document :
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