Preparation of TiO2-nitrogen-doped photocatalyst active under visible light

Abstract

This study examined the photocatalytic degradation of phenol and azo dyes such as Reactive Red 198 and Direct Green 99 by photocatalysis over amorphous hydrated titanium dioxide (TiO2 · H2O) obtained directly from the sulphate technology installation modified in gaseous ammonia atmosphere. The photocatalysts were used in the solution and coated on the glass plate after sandblasting. The highest rate of phenol degradation in the solution was obtained for catalysts calcinated at 700°C (6.5% wt.), and the highest rate of dye decolorization was found for catalysts calcinated at 500°C and 600°C (ca. 40%–45%). Some TOC measurements of dye solutions were performed to check the rate of mineralization. On the glass plate, the decomposition of DG99 on TiO2/N 500 contrary to TiO2-P25 proceeded completely after 120 hours of visible light irradiation. The prolongation of the time of irradiation did not enhance DG99 degradation on TiO2-P25. The decomposition of the Direct Green 99 on TiO2/N 500 coated on the glass plate covered with liquid glass took place up to 24 hours of irradiation. The liquid layer on the glass plate which was covered with the photocatalyst reduced its activity. The nitrogen doping during calcinations under ammonia atmosphere is a new way of obtaining a photocatalyst which could have a practical application in water treatment system under broadened solar light spectrum as well as self-cleaning coatings.