Kinetics of Decolorization of Reactive Textile Dye via Heterogeneous Photocatalysis Using Titanium Dioxide

Author:

Carrasco-Venegas Luis Américo1ORCID,Castañeda-Pérez Luz Genara2,Martínez-Hilario Daril Giovani3,Medina-Collana Juan Taumaturgo4ORCID,Calderón-Cruz Julio Cesar3,Gutiérrez-Cuba César3,Cuba-Torre Héctor Ricardo5ORCID,Núñez Alex Pilco6ORCID,Herrera-Sánchez Sonia Elizabeth3

Affiliation:

1. Bioenergy Research Center, Callao National University, Callao 07011, Peru

2. Postgraduate School, International Research, Development, Innovation and Entrepreneurship Network, RIDIEP, Federico Villarreal National University, Lima 15001, Peru

3. Faculty Chemical Engineering, National University of Callao, Callao 07011, Peru

4. Water Treatment Process Engineering Research Center, Faculty of Chemical Engineering, Callao National University, Callao 07011, Peru

5. Postgraduate EPG, La Molina National University, La Molina, Lima 15001, Peru

6. Faculty of Chemical and Textile Engineering, National University of Engineering, Rimac, Lima 15001, Peru

Abstract

The textile industry is known for its excessive water consumption and environmental impact. One of the major challenges it faces is managing pollution generated by dyes, particularly bifunctional dyes, such as sumireact supra yellow s-hbu, with a red appearance and sumifix supra lemon-yellow e-xf, with a yellow appearance. This study aimed to investigate the decolorization kinetics of synthetic solutions of said bifunctional dyes, which comprise triazine and vinylsulfon. We conducted various tests, including modifications of pH, the addition of TiO2 P-50 nanoparticles, exposure to solar radiation, limited contact with oxygen, and eolic agitation. The initial solutions had a concentration of 1000 ppm of textile dye. The study showed that the reaction order for the “red” solutions in the R6 and R9 reactors and all the yellow solutions was ½. The concentration of nanoparticles and pH had a significant impact on the reaction rate. The yellow solutions with a concentration of 800 ppm and pH levels of 3.15, 4.13, and 2.25 demonstrated 100% color discoloration, followed by solutions with a concentration of 400 ppm and pH levels of 3.15, 2.25, and 4.13. The analysis of variance confirmed the reaction rate constants for the yellow solutions and emphasized the significance of pH in this process.

Funder

Universidad Nacional del Callao, Lima Perú

Publisher

MDPI AG

Reference53 articles.

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