The mineralization of aqueous solutions of antipyrine, an emerging contaminant, using an innovative homogeneous sono-photocatalytic oxidation process (H2O2/UV/Fe/Ultrasound) was evaluated in an artificial UV lamp. At the selected operation conditions [H2O2] = 1500 ppm, pH = 2.7, amplitude = 100%, pulse length (cycles) = 0.3 during 15 min and then 1, 92% of TOC is removed after 50 min treating an aqueous solution containing 50 ppm of antipyrine. An important synergistic effect between sonolysis and photoFenton (UV/H2O2/Fe) of 45.4% was quantified using the first order rate constants for TOC. Comparison experiments of scavenger-loaded conditions demonstrate that the antipyirine photodegradation proceeds mainly through a radical mechanism probably beginning by the cleavage of the N-N bond of penta heterocycle leading to the formation of aromatic acids (anthranilic and 1,4-benzenedicarboxylic acids) then followed by the opening of phenyl ring to form small molecular organic acids (mainly 2-butenedioic, 4-oxo-pentanoic and butanedioic acids), which may be decomposed further into CO2. (c) 2013 Elsevier B.V. All rights reserved.