Multistep Removal System of Gaseous Toluene: Adsorption, Electrochemical, and Photolytic Treatments

A large amount of atmospheric emissions result from various anthropogenic activities worldwide. Given the complexity of volatile organic compounds (VOCs) and their different adsorption capacities, redox potentials, and photolytic properties, an air purification system for the removal of VOCs that combines multiple physical processes was proposed in this study using toluene as an example. These processes include, in the first step, an adsorption treatment (AT) with activated carbon (AC), where toluene adsorption results from the insertion of aromatic rings (nonpolar groups) between the graphitic carbon planes, as demonstrated by the Raman spectroscopy; in the second step, electrochemical treatment (ECT) using TiO<sub>2,nt</sub>|Ti||SS-304 electrodes applying an electric field to accelerate the oxidation of toluene through the production of free radicals (⋅OH), hydroperoxyl radicals and benzyl groups, followed by the rupture of aromatic rings to generate aliphatic compounds and the consequent mineralization to CO, CO<sub>2</sub>, and H<sub>2</sub>O; in the third step, photolytic treatment (PT) with a 254-nm UV lamp for toluene degradation is used, which is influenced by the addition of radicals, such as ⋅OH or ⋅O<sup>-</sup> <sub>2ad</sub>, to transform toluene into either benzene or phenol. The multistep system integrating AT, ECT and PT was more efficient overall (99.58 %) than the individual treatments (AT=50.29 %, ECT=44.38 %, and PT=52.71 %) as evaluated by gas chromatography with a BID detector; it showed enhanced efficiency enabled by the synergistic effects of combining multiple technologies to enhance the overall toluene degradation efficiency and flexibility. The multistage systems can be adapted to specific contamination conditions and process requirements with the generation of residual toluene, phenol, and aliphatic compounds and possible mineralization to molecules such as CO<sub>2</sub>, CO, and H<sub>2</sub>O. This small and portable multistep system provides a novel approach for treating outdoor and/or indoor air contaminated with toluene.

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Journal
ChemPlusChem
Published
2024-12-03
DOI
https://doi.org/10.1002/cplu.202400532
Primary Topic
Gas Sensing Nanomaterials and Sensors
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article
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article

Multistep Removal System of Gaseous Toluene: Adsorption, Electrochemical, and Photolytic Treatments

Erika Bustos, J. Manríquez, Joaquín Rodríguez‐López, Antonia Sandoval‐González et al.
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article

Multistep Removal System of Gaseous Toluene: Adsorption, Electrochemical, and Photolytic Treatments

Erika Bustos, J. Manríquez, Joaquín Rodríguez‐López, Antonia Sandoval‐González, Goldie Oza, Issis C. Romero‐Ibarra, Karla Verónica Bolaños-Romero, Roberto Fernando Frausto‐Castillo, Rosa Luz López-Carbajal, Susana Citlaly Gaucin-Gutiérrez
article en

Abstract

A large amount of atmospheric emissions result from various anthropogenic activities worldwide. Given the complexity of volatile organic compounds (VOCs) and their different adsorption capacities, redox potentials, and photolytic properties, an air purification system for the removal of VOCs that combines multiple physical processes was proposed in this study using toluene as an example. These processes include, in the first step, an adsorption treatment (AT) with activated carbon (AC), where toluene adsorption results from the insertion of aromatic rings (nonpolar groups) between the graphitic carbon planes, as demonstrated by the Raman spectroscopy; in the second step, electrochemical treatment (ECT) using TiO<sub>2,nt</sub>|Ti||SS-304 electrodes applying an electric field to accelerate the oxidation of toluene through the production of free radicals (⋅OH), hydroperoxyl radicals and benzyl groups, followed by the rupture of aromatic rings to generate aliphatic compounds and the consequent mineralization to CO, CO<sub>2</sub>, and H<sub>2</sub>O; in the third step, photolytic treatment (PT) with a 254-nm UV lamp for toluene degradation is used, which is influenced by the addition of radicals, such as ⋅OH or ⋅O<sup>-</sup> <sub>2ad</sub>, to transform toluene into either benzene or phenol. The multistep system integrating AT, ECT and PT was more efficient overall (99.58 %) than the individual treatments (AT=50.29 %, ECT=44.38 %, and PT=52.71 %) as evaluated by gas chromatography with a BID detector; it showed enhanced efficiency enabled by the synergistic effects of combining multiple technologies to enhance the overall toluene degradation efficiency and flexibility. The multistage systems can be adapted to specific contamination conditions and process requirements with the generation of residual toluene, phenol, and aliphatic compounds and possible mineralization to molecules such as CO<sub>2</sub>, CO, and H<sub>2</sub>O. This small and portable multistep system provides a novel approach for treating outdoor and/or indoor air contaminated with toluene.

ChemPlusChemVol. 90(3)
University of Illinois Urbana-Champaign (US), Instituto Tecnológico de Querétaro (MX), Center of Research and Technologic Development in Electrochemistry (MX), Instituto Politécnico Nacional (MX)
Clean water and sanitation
Openalex Percentile: Top 80%
Gas Sensing Nanomaterials and Sensors
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