Thermal decomposition of substituted phenols in supercritical water

The thermal decomposition of cresols, hydroxybenzaldehydes, nitrophenols, and benzenediols was studied in dilute aqueous solutions and in the absence of oxygen at 460 degrees C and 250 atm for residence times around 10 s. Thermolysis under these conditions produced conversions of less than 10% for o-, m-, and p-cresol, whereas hydroxybenzaldehydes and nitrophenols were much more reactive. Global rate expressions are reported for the thermolysis of each hydroxybenzaldehyde and nitrophenol isomer. Phenol was a major product from the decomposition of all of the substituted phenols studied. For a given substituent, ortho-substituted phenols reacted more rapidly than the other isomers. For a given substituted position, nitrophenols reacted more rapidly than hydroxybenzaldehydes, which in turn reacted more rapidly than cresols. These results demonstrate that the treatment of CHO- and NO2-substituted phenols by oxidation in supercritical water will involve the oxidation of thermal decomposition products in addition to the oxidation of the original compounds.