Nitroaromatic hydrocarbon ozonation in water. 1. Single ozonation

Single ozonation of two nitroaromatic hydrocarbons (nitrobenzene and 2,6-dinitrololuene) under different experimental conditions (ozone feed rate, pH, temperature, hydroxyl radical scavengers) has been studied. The absence of hydroxyl radical scavengers, pHs 7-9, and temperatures below 30 degrees C are optimum conditions for nitroaromatic removal. Due to the importance of hydroxyl radical reactions, removal rates in natural water are much lower than those observed in laboratory ultrapure water. Rate constants of the direct reaction between ozone and nitroaromatic hydrocarbons at 20 degrees C have been found to be lower than 6 M-1 s(-1). More than 99% of nitroaromatic removal is due to hydroxyl radical oxidation. Single ozonation of nitroaromatics can then be classified as a real advanced oxidation technology. Nitrophenols, compounds very reactive toward ozone and hydroxyl radicals, and 2,6-dinitrobenzaldehyde, identified in the single ozonation of nitrobenzene and 2,6-dinitrotoluene, respectively, are some of the first intermediates of single ozonation.