Methylene blue dye (MB) was degraded photocatalytically in aqueous solution using Ag(+) doped TiO(2) under UV irradiation. The degradations of the dye using untreated TiO(2) and Ag(+) doped TiO(2) were compared. Ag(+) doped TiO(2) was found to be more efficient. Using Ag(+) doped TiO(2) the filtration process was eliminated, as the particles became more settleable. The effect of various parameters such as catalyst loading, initial dye concentration, depth of solution, degree of adsorption, pH and O(2) on dye degradation was studied. The extent of mineralization was studied by observing the COD removal at different time intervals. The effects of various interfering ions such as Cl(-), NO(3) (-), CO(3) (2-), SO(4) (2-), Ca(2+) and Fe(3+) and electron acceptors such as H(2)O(2), KBrO(3) and (NH(4))(2)S(2)O(8) on the dye degradation was also studied. The degradation kinetics fitted well to Langmuir-Hinshelwood pseudo first order rate law. An aqueous solution of MB (20ppm) degraded by more than 99% after UV irradiation for 180 min with Ag(+) doped TiO(2) (2 g/L) and by more than 95% with untreated TiO(2) (2 g/L)(.) The COD removal was more than 91% with Ag(+)doped TiO(2) and more than 86% with untreated TiO(2) after 240 min. The degradation and COD removal of 5 times diluted textile wastewater was more than 98% and 79% respectively with 1 g/L Ag(+) doped TiO(2) after UV irradiation for 420 min.

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Real textile wastewater collected from the cotton dyeing bath of a fabric dyeing and finishing plant was subjected to heterogeneous photocatalysis using Ag(+) doped TiO(2) under UV irradiation in a batch reactor. The photocatalysts were characterized by FESEM, XRD, EDS, FTIR, DRS and BET analyses. The kinetics of the reaction was also evaluated. Colour removal was more than 88%, 94% and 99%, respectively for undiluted, 2 times diluted and 5 times diluted wastewater with Ag(+) doped TiO(2) (2.5 g/L) after UV irradiation for 360 minutes. The COD removal for undiluted, 2 times diluted and 5 times diluted wastewater was 47%, 70% and 92%, respectively under similar conditions. The reaction followed Langmuir-Hinshelwood pseudo first order kinetic model and the data fitted well to polynomial regression analysis.

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