Extraction of tetrachloroaurate or tetrabromoaurate anions has been carried out at acidic pHs (1 and 4) with several ionic liquids bearing halide or bis(trifluoromethanesulfonyl)imide NTf 2 − anions and cations 1-octyl-3-methylimidazolium, 1-octylpyridinium or 1-methyl-1-octylpyrrolidinium. The removal of gold anionic moieties from water was first studied by mixing aqueous solutions containing gold complexes and water soluble halide (chloride or bromide) ionic liquids. This lead to the formation of either a solid precipitate or a liquid phase corresponding to a hydrophobic ionic liquid based on a tetrahalogenoaurate anion. Values below 10 −6 for the solubility products of gold-bearing ionic liquids were obtained. Liquidliquid extraction of anionic gold complexes with hydrophobic ionic liquids was also carried out. Gold was successfully extracted from water whatever the pH and the ionic liquid used. Distribution coefficients ranged from 3 × 10 2 to 3 × 10 4 . Investigation on the extraction mechanism revealed an anion exchange between one anionic gold complex and one NTf 2 − anion.− , X representing a chloride or a bromide anion accordingly, is studied using IL. In order to study the influence of the cation ring (size and aromaticity of the ring, charge delocalization) on the removal of

Ultrasonic frequency is a key parameter determining multibubble sonoluminescence (MBSL) spectra of water saturated with Ar/O2 gas mixtures. At 20 kHz, the MBSL is quenched by oxygen. By contrast, at high-frequency ultrasound the maximal MBSL intensity is observed in the presence of Ar/20%O2 gas mixture. Nevertheless, oxygen has no influence on the shape of MBSL spectra. The effect of oxygen on MBSL is explained by oxygen dissociation inside the collapsing bubble which is much more effective at high ultrasonic frequency compared to 20 kHz ultrasound. In contrast to MBSL, a higher yield of H2O2 is observed in Ar/20%O2 gas mixture whatever the ultrasonic frequency. At 20°C and 20% of oxygen the maximal yield of H2O2 is observed at 204-362 kHz. The maximal yield of H2O2 is shifted to 613kHz when the bulk temperature is raised up to 40°C. Coupling of high-frequency ultrasound with mechanical stirring and intensive Ar/O2 bubbling improves H2O2 production. Comparison of MBSL and sonochemistry allowed to conclude that H2O2 is formed from non-excited OH (X(2)Π) and HO2 radicals. Finally, it was shown that at the studied conditions the efficiency of ultrasonic degassing is hardly influenced by frequency.