a b s t r a c tIn this study, heterogeneous Fenton-like degradation of reactive azo dye Rhodamine 6G in water was investigated over a CuFeZSM-5 zeolite catalyst prepared by hydrothermal synthesis. At initial pH of 3.4, a color removal of 100% was achieved after a reaction time of 45 min. TOC elimination was measured to be 51.8% after 2 h of oxidation. Initial decolorization rate was described by an equation of −r A0 = 4.56 × 10 2 e −24.83/RT C R6G,0 C 0.35 H 2 O 2 ,0 where R is in kJ/mol. The leaching of iron and copper cations from zeolite structure into the solution during oxidation was dependent on pH strongly. The regulation of pH from 6.5 (dye solution pH) to 3.4, increased leaching for iron from 0.7 to 0.8 mg/dm 3 and for copper from 1.4 to 2.1 mg/dm 3 . The copper was totally leached from the catalyst during the process at pH 3.4.

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This paper describes the ultrasonic degradation of oxalic acid. The effects of ultrasonic power, H(2)O(2), NaCl, external gases on the degradation of oxalic acid were investigated. Reactor flask containing oxalic acid was immersed in the ultrasonic bath with water as the coupling fluid. Representative samples withdrawn were analysed by volumetric titration. Degradation degree of oxalic acid increased with increasing ultrasonic power. It was observed that H(2)O(2) has negative contribution on the degradation of oxalic acid and there was an optimum concentration of NaCl for enhancing the degradation degree of oxalic acid. Although bubbling nitrogen gave higher degradation than that for bubbling air, both gases (for 20 min before sonication and during sonication together) could not help to enhance the degradation of oxalic acid when compared with the degradation without gas passage.

The removal of Orange II (O-II) from aqueous solution under irradiation at 850 kHz has been studied. The effects of both homogeneous (with FeSO4/H2O2), and heterogeneous (Fe containing ZSM-5 zeolite/H2O2) Fenton type reagents are reported together with the effect of UV irradiation in combination with ultrasound both alone and with homogeneous Fenton-type reagent. Degrees of decolourisation of 6.5% and 28.9% were observed using UV radiation and ultrasound, respectively, whereas under the simultaneous irradiation of ultrasound and UV light, the decolourisation degree reached 47.8%, indicating a synergetic effect of ultrasound and UV light. The decolourisation was increased with the addition of Fenton's reagent with an optimal Fenton molar reagent ratio, Fe(2+):H2O2 of 1:50. In the combined process of ultrasound and UV light with the homogeneous Fenton system 80.8% decolourisation could be achieved after 2h indicating that UV improves this type of Orange II degradation. The degree of decolourisation obtained using the heterogeneous sono-Fenton system (Fe containing ZSM-5 zeolite catalysts+H2O2+ultrasound) were consistently lower than the traditional homogeneous ultrasound Fenton system. This can be attributed to the greater difficulty of the reaction between Fe ions and hydrogen peroxide. In all cases the Orange II ultrasonic decolourisation was found to follow first order kinetics.

This study presents an evaluation of the catalytic performances of Fe and Cu containing ZSM-5 zeolites for oxidation of Rhodamine 6G. Fe and Cu were loaded by ion exchange or through hydrothermal synthesis. The catalytic process was carried out in an aqueous solution using H2O2 as an oxidant. The catalyst prepared by hydrothermal synthesis showed the highest activity (100% decolorization, 59.1% aromatic degradation and 51.8% TOC removal at initial pH of 3.5). This catalyst was stable against leaching even at low pH. The change in activity of the catalysts prepared was attributed to incorporation of the Fe and Cu species with ZSM-5. Fe and Cu were in structural locations - in the framework - in the catalyst prepared by hydrothermal synthesis while there were extraframework cations or species in catalysts prepared by ion exchange. Incoporation of Cu into FeZSM-5 increased its catalytic activity. © 2010 Elsevier B.V. All rights reserved.TÜBİTAK and NASU project number 107M62

In this study, degradation of Rhodamine 6G (Rh6G) was investigated with ultrasound-assisted heterogeneous photoFenton process by iron-containing TiO2 catalysts. The catalysts were prepared by incipient wetness impregnation method and characterized by XRD, SEM, FT-IR, nitrogen adsorption, and ICP-AES measurements. Almost complete color removal (99.9 %) was achieved after a reaction time of 90 min while chemical oxygen demand (COD) could be removed by 24 % only with the 1 wt% iron-containing TiO2 catalyst. Initial color removal after 15 min of reaction and total COD abatement after 90 min of reaction decreased with increasing calcination temperature of the catalyst from 573 to 973 K. This indicated that the catalytic activity of the catalyst depend on the percentage of anatase phase in the TiO2, which was decreased with increasing calcination temperature.

The Fenton-like oxidation of CI Reactive Red 141 was investigated over iron-containing ZSM-5 zeolites. Iron was loaded by ion exchange or through hydrothermal synthesis. The oxidation process was carried out in an aqueous solution using hydrogen peroxide as the oxidant. The catalyst prepared by ion exchange with a silicon/aluminium ratio of 42 zeolite showed the highest activity (97% decolorisation and 52% chemical oxygen demand reduction at an initial pH of 3.5) after an oxidation duration of 2 h. The chemical oxygen demand reduction increased with the increasing amount of iron loaded to the zeolite. The FeZSM-5 catalyst, prepared by hydrothermal synthesis in the presence of oxalic acid, showed very good activity in terms of mineralisation (99% of chemical oxygen demand reduction). The iron leaching was noticeably low (below the European Union directives of 2 mg dm À3 ) for the above-mentioned catalysts.

Oxidation of bisphenol-A (BPA) was investigated using a sonophoto Fenton-like hybrid process under visible light irradiation in the presence of iron-containing perovskite LaFeO 3 catalysts. For this purpose, firstly the perovskite catalyst (LaFeO 3) was prepared by the sol-gel method and calcined at different temperatures (500, 700, and 800 • C). The prepared catalysts were characterized using XRD, SEM, FTIR, nitrogen adsorption, UV-vis DRS, and ICP/OES measurements. Among the prepared catalysts the catalyst that was calcined at 500 • C showed better catalytic activity with respect to degradation and chemical oxygen demand (COD) reduction (of 21.8% and 11.2%, respectively, after 3 h of reaction duration) than the other catalysts calcined at 700 • C and 800 • C. The catalytic activity of the LaFeO 3 perovskite catalyst calcined at 500 • C was compared with that of a TiO 2 photocatalyst containing Fe and prepared by the sol-gel method. Better photocatalytic activity in terms of degradation of BPA, total organic carbon (TOC), and COD reductions was observed with the LaFeO 3 perovskite catalyst under visible light. The degradation, COD, and TOC reductions after 6 h of oxidation were 34.8%, 26.9%, and 8.8% for the LaFeO 3 perovskite catalyst, and 33.1%, 19.7%, and 4.9% for the Fe/TiO 2 catalyst, respectively.