Cavitation intensifying bags improve ultrasonic advanced oxidation with Pd/Al2O3 catalyst

[Display omitted] •Cavitation Intensification Bags with Pd/Al2O3 catalyst improve oxidation processes.•Mass transport and thermal gradients improved near cavitating bubbles.•Intensification Factor analysis and ultrasonic reaction kinetics are unveiled. Advanced oxidation processes can potentially el...

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Veröffentlicht in:Ultrasonics sonochemistry 2021-01, Vol.70, p.105324-105324, Article 105324
Hauptverfasser: Pappaterra, Maria, Xu, Pengyu, van der Meer, Walter, Faria, Jimmy A., Fernandez Rivas, David
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Sprache:eng
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Zusammenfassung:[Display omitted] •Cavitation Intensification Bags with Pd/Al2O3 catalyst improve oxidation processes.•Mass transport and thermal gradients improved near cavitating bubbles.•Intensification Factor analysis and ultrasonic reaction kinetics are unveiled. Advanced oxidation processes can potentially eliminate organic contaminants from industrial waste streams as well as persistent pharmaceutical components in drinking water. We explore for the first time the utilization of Cavitation Intensifying Bags (CIB) in combination with Pd/Al2O3 catalyst as possible advanced oxidation technology for wastewater streams, oxidizing terephthalic acid (TA) to 2-hydroxyterephthalic acid (HTA). The detailed characterization of this novel reaction system reveals that, during sonication, the presence of surface pits of the CIB improves the reproducibility and thus the control of the sonication process, when compared to oxidation in non-pitted bags. Detailed reaction kinetics shows that in the CIB reactor the reaction order to TA is zero, which is attributed to the large excess of TA in the system. The rate of HTA formation increased ten-fold from ~0.01 μM*min−1 during sonication in the CIB, to ~0.10 μM*min−1 for CIB in the presence of the Pd/Al2O3 catalyst. This enhancement was ascribed to a combination of improved mass transport, the creation of thermal gradients, and Pd/Al2O3 catalyst near the cavitating bubbles. Further analysis of the kinetics of HTA formation on Pd/Al2O3 indicated that initially the reaction underwent through an induction period of 20 min, where the HTA concentration was ~0.3 μM. After this, the reaction rate increased reaching HTA concentrations ~6 μM after 40 min. This behavior resembled that observed during oxidation of hydrocarbons on metal catalysts, where the slow rate formation of hydroperoxides on the metal surface is followed by rapid product formation upon reaching a critical concentration. Finally, a global analysis using the Intensification Factor (IF) reveals that CIB in combination with the Pd/Al2O3 catalyst is a desirable option for the oxidation of TA when considering increased oxidation rates and costs.
ISSN:1350-4177
1873-2828
DOI:10.1016/j.ultsonch.2020.105324