Mineralization of naphtenic acids with thermally-activated persulfate: The important role of oxygen

Abstract

This study reports on the mineralization of model naphtenic acids (NAs) in aqueous solution by catalyst-free thermally-activated persulfate (PS) oxidation. These species are found to be pollutants in oil sands process-affected waters. The NAs tested include saturated-ring (cyclohexanecarboxylic and cyclohexanebutyric acids) and aromatic (2-naphthoic and 1,2,3,4-tetrahydro-2-naphthoic acids) structures, at 50mgL−1starting concentration. The effect of PS dose within a wide range (10–100% of the theoretical stoichiometric) and working temperature (40–97°C) was investigated. At 80°C and intitial pH=8 complete mineralization of the four NAs was achieved with 40–60% of the stoichiometric PS dose. This is explained because of the important contribution of oxygen, which was experimentally verified and was found to be more effective toward the NAs with a single cyclohexane ring than for the bicyclic aromatic-ring-bearing ones. The effect of chloride and bicarbonate was also checked. The former showed negative effect on the degradation rate of NAs whereas it was negligible or even positive for bicarbonate. The rate of mineralization was well described by simple pseudo-first order kinetics with values of the rate constants normalized to the PS dose within the range of 0.062–0.099h−1. Apparent activation energy values between 93.7–105.3kJmol−1 were obtained.