Method for attachment of TiO2 using design of experiments: application to the photocatalysis of a model pollutant methylene blue dye
Author(s) -
Abdenour Aıt Atmane,
Saliha Bourouına-Bacha
Publication year - 2020
Publication title -
water science and technology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.406
H-Index - 137
eISSN - 1996-9732
pISSN - 0273-1223
DOI - 10.2166/wst.2020.490
Subject(s) - methylene blue , calcination , photocatalysis , titanium dioxide , catalysis , degradation (telecommunications) , pollutant , central composite design , chemistry , response surface methodology , nuclear chemistry , chemical engineering , titanium oxide , deposition (geology) , materials science , chromatography , composite material , organic chemistry , computer science , engineering , telecommunications , paleontology , sediment , biology
The preparation of titanium dioxide (TiO 2 ) supported on a glass plate by heat attachment method is presented. With the use of response surface methodology based on a central composite design we investigated the influence of the experiment parameters of the TiO 2 deposition (temperature of calcination (T), time of calcination (ts) and the concentration of TiO 2 ((TiO 2 ))) on photocatalytic activity of the semiconductor for the degradation of a model pollutant: methylene blue. The analysis of variance results showed that the selected quadratic model with interaction (R 2 = 0.9802) was statistically significant. The experimental results showed that the degradation quantity of methylene blue increased when the ts value increased and T decreased. We have evaluated the photocatalytic activity of this supported catalyst (TiO 2 -GP) with a laboratory reactor under natural condition; the maximum removal (96.03%) was obtained at ts = 331 min, T = 559 °C and (TiO 2 ) = 2.38 g/l. The method of desirability function was used to obtain the best combination of factor settings for achieving the maximum of degradation quantity ((TiO 2 ) = 2.6 (g/l), T = 600 (°C) and ts = 240 (min)). The additional tests on the catalyst plates confirmed that the deposits keep their catalytic activity for several cycles of use.
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