P–nitrophenol degradation by hybrid advanced oxidation process of heterogeneous Fenton assisted hydrodynamic cavitation: Discernment of synergistic interactions and chemical mechanism. (November 2021)

• Record Type: Journal Article
• Authors: Roy, Kuldeep; Moholkar, Vijayanand S.
• Is Part Of: Chemosphere. Volume 283(2021)
• Publication Date: 2021-11
• Subjects: Hydrodynamic cavitation -- Advanced oxidation processes -- Heterogeneous fenton reagent -- Kinetic modelling -- Density functional theory; Pollution -- Periodicals; Pollution -- Physiological effect -- Periodicals; Environmental sciences -- Periodicals; Atmospheric chemistry -- Periodicals; 551.511
• DOI: 10.1016/j.chemosphere.2021.131114
• Languages: English
• ISSNs: 0045-6535

Abstract

Abstract: The present study has investigated p -nitrophenol (PNP) degradation by hybrid advanced oxidation process (AOP) of hydrodynamic cavitation with heterogenous Fe3 O4 nanoparticles. 78.8 ± 1.2% of PNP degradation was obtained at optimum operational conditions: inlet pressure = 8 atm, pH = 3, initial concentration of PNP = 20 mg L −1, Fe3 O4 :H2 O2 = 1:100. PNP degradation profiles were analyzed using a kinetic model based on the reaction network. The closest match between the simulated and experimental degradation profiles was obtained for the initial concertation of [H2 O2 ] = 0.6 M, which was far higher than concentration of externally added H2 O2 . This was attributed to in-situ generation of H2 O2 through transient cavitation. Intense shear and turbulence generated in cavitating flow caused surface leaching of Fe3 O4 particles that released Fe 2+ /Fe 3+ ions. The synergy in the hybrid AOP was in-situ Fenton reactions between leached Fe 2+ /Fe 3+ ions and H2 O2 present in the reaction mixture. The mechanism in OH mediated oxidative degradation of PNP was further explored with Density Functional Theory (DFT) simulations. Both OH addition on benzene ring and H–abstraction reactions were simulated to identify the possible pathways for the degradation. On the basis of activation free energy analysis, degradation pathways initiating with both OH addition and H abstraction were determined to be feasible. The ortho −C of benzene ring was the most favourable site for OH addition, while H atom of phenolic hydroxyl group was more susceptible (or more reactive) for H-atom abstraction route. Graphical abstract: Image 1 Highlights: 78% of PNP degradation using hybrid hydrodynamic cavitation with Fe3 O4 nanoparticles. Kinetic modelling of the degradation of PNP using a reaction network. Leaching of Fe ions and generation of H2 O2 in hydrodynamic cavitation flow. In-situ Fenton reactions in cavitating flow enhance the PNP degradation. DFT simulations reveal H abstraction and. OH addition as possible degradation pathways