Author(s)

Veronica Camargo¹, Elba Ortiz^1*, Hugo Solis¹, Carlos M. Cortes-Romero², Sandra Loera-Serna¹, Carlos J. Perez¹

¹Department of Basic Sciences, Universidad Autónoma Metropolitana Azcapotzalco, Mexico City, Mexico.
²Division of Industrial and Systems Engineering, Universidad Politecnica del Valle de México, Estado de Mexico, Mexico.

The experimental degradation of a water soluble dye, potassium indigo tetrasulfonate salt, has been studied using stand-alone ozonation and photocatalytic oxidation process. Progress of the dye oxidation was followed by UV-VIS spectrophotometric measurements at controlled operating conditions. The organic content of reaction samples was measured to verify the process efficiency in dye mineralization. According to current results, almost complete color removal was obtained for ozonation within about 1 h reaction time. The reduction of the organic load was almost 80% from its original while initial sulphur content decreased to 32.5%. Dye conversion of 100% was obtained by means of a photocatalytic process using TiO₂ as catalyst at 294 nm irradiated UV light. This complete color removal for the catalytic process was observed within 7 min of reaction time. The calculated initial rate of reaction of photocatalysis treatment was 8 times faster than that of ozonolysis. However, the remaining organic load of photocatalysis was almost 88% from its original while the final sulphur content was 27.3%. This contrasting behavior of the performance of the type of oxidation process stressed importance of physicochemical phenomena and intermediates molecules present during dye degradation. An insightful and mechanistic aspect of the dye oxidation was developed by performing quantumchemical calculations.

Indigo Potassium Tetrasulfonate, Advanced Oxidation Processes, Chemical Degradation, Theoretical Calculations

Camargo, V. , Ortiz, E. , Solis, H. , Cortes-Romero, C. , Loera-Serna, S. and Perez, C. (2014) Chemical Degradation of Indigo Potassium Tetrasulfonate Dye by Advanced Oxidation Processes. Journal of Environmental Protection, 5, 1342-1351. doi: 10.4236/jep.2014.513128.