Bulk MnO2 was used as a catalyst for phenol oxidation in supercritical wate
r at 380-420 degrees C and 219-300 atm in a flow reactor. The bulk MnO2 cat
alyst enhances both the phenol disappearance and CO2 formation rates during
supercritical water oxidation (SCWO), but it does not affect the selectivi
ty to CO2 or to the phenol dimers at a given phenol conversion. The role of
the catalyst appears to be accelerating the rate of formation of phenoxy r
adicals, which then react in the fluid phase by the same mechanism operativ
e for noncatalytic SCWO of phenol. The rates of phenol disappearance and CO
2 formation are sensitive to the phenol and Oz concentrations but independe
nt of the water density. Both power-law and dual site Langmuir-Hinshelwood-
Hougen-Watson (LHHW) rate laws were developed to correlate the catalytic ki
netics. Our results show that SCWO reactor volumes can be reduced by an ord
er of magnitude if bulk MnO2 is used as the catalyst and by yet another ord
er of magnitude if a supported oxidation catalyst is used.