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• W1997253809 abstract "An expanded reaction kinetic model, including 17 surface reactions, is proposed to explain the yields of PCDD/F obtained in an experimental study of the reaction of 2-chlorophenol over a CuO/silica surface. The mechanism is loosely based on the gas-phase mechanism for PCDD/F formation widely discussed in the literature. The principal differences are the impact of chemisorption of 2-chlorophenols to metal oxides on radical formation and the steric hindrance of oxygen-centered radicals on the surface inhibiting radical–radical reaction pathways that lead to formation of dibenzo-p-dioxin (DD). Gas-phase molecule–surface-bound adsorbate reactions are the preferred route of DD formation, while radical–radical surface reactions are the main channel for dichloro-dibenzofuran (DCDF) formation. These results suggest that the Langmuir–Hinshelwood (LH) mechanism, involving radical–radical surface reactions, and the Eley–Rideal mechanism, involving a gas-phase molecule and surface-bound adsorbate, are responsible for PCDF and PCDD formation on surfaces, respectively. The calculated yields of DCDF and DD are in reasonable agreement with experimental results." @default.
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• W1997253809 date "2007-08-01" @default.
• W1997253809 modified "2023-10-17" @default.
• W1997253809 title "An expanded reaction kinetic model of the CuO surface-mediated formation of PCDD/F from pyrolysis of 2-chlorophenol" @default.
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• W1997253809 doi "https://doi.org/10.1016/j.chemosphere.2007.03.042" @default.
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