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Title: Catalytic liquid-phase oxidation of phenol aqueous solutions: A kinetic investigation

Journal Article · · Industrial and Engineering Chemistry Research; (United States)
DOI:https://doi.org/10.1021/ie00036a023· OSTI ID:6593282
 [1];  [2]
  1. National Inst. of Chemistry, Ljubljana (Slovenia). Lab. of Catalysis and Chemical Reaction Engineering
  2. Univ. of Ljubljana (Slovenia). Dept. of Chemical Engineering

Catalytic oxidation of aqueous phenol solutions was studied in a differential, liquid-full operated fixed-bed reactor. A proprietary catalyst comprised of supported copper, zinc, and cobalt oxides was found to be effective for converting phenol to benzenedioles and benzoquinones, the C-4 intermediates in total oxidation route, and carbon dioxide. The proposed intrinsic rate expression for the phenol disappearance is based on the Langmuir-Hinshelwood kinetic approach, considering both equilibrium phenol and dissociative oxygen adsorption processes on different types of active sites and assuming a bimolecular surface reaction between adsorbed reactant species to be the rate-controlling step. Apparent activation energies for catalytic phenol oxidation and heat of phenol adsorption, in the temperature range 150--180 C, were found to be 139 and [minus]62 kJ/mol, respectively. It is believed that the liquid-phase oxidation of an aqueous phenol solution undergoes a combined redox and heterogeneous free-radical mechanism. The involvement of a free-radical mechanism is indicated by the intermediates formed and by a pH as well as radical initiator effects on observed phenol disappearance rates.

OSTI ID:
6593282
Journal Information:
Industrial and Engineering Chemistry Research; (United States), Vol. 33:12; ISSN 0888-5885
Country of Publication:
United States
Language:
English