Response of Rhodococcus cerastii IEGM 1278 to toxic effects of ibuprofen

The article expands our knowledge on the variety of biodegraders of ibuprofen, one of the most frequently detected non-steroidal anti-inflammatory drugs in the environment. We studied the dynamics of ibuprofen decomposition and its relationship with the physiological status of bacteria and with additional carbon and energy sources. The involvement of cytoplasmic enzymes in ibuprofen biodegradation was confirmed. Within the tested actinobacteria, Rhodococcus cerastii IEGM 1278 was capable of complete oxidation of 100 μg/L and 100 mg/L of ibuprofen in 30 h and 144 h, respectively, in the presence of an alternative carbon source (n-hexadecane). Besides, the presence of ibuprofen induced a transition of rhodococci from single- to multicellular lifeforms, a shift to more negative zeta potential values, and a decrease in the membrane permeability. The initial steps of ibuprofen biotransformation by R. cerastii IEGM 1278 involved the formation of hydroxylated and decarboxylated derivatives with higher phytotoxicity than the parent compound (ibuprofen). The data obtained indicate potential threats of this pharmaceutical pollutant and its metabolites to biota and natural ecosystems.

Effects of Fe(OH)3 and MnO2 Flocs on Iron/Manganese Removal and Fouling in Aerated Submerged Membrane Systems

Many treatment methods are used to remove iron and manganese from water. Aeration and membrane filtration are two of these methods. In this study, Fe2+ and Mn2+ removal by aeration with different catalysts and instead of simple membrane filtration applied in other studies, the aerated-submerged membrane systems were evaluated separately. When Fe(OH)3 was applied in the aeration step and complete oxidation of Fe2+ was obtained after 27 min, while complete Mn2+ oxidation was obtained in 76 min. However, when MnO2 was applied in the aeration step, complete oxidation of Fe2+ and Mn2+ was relatively slow (36 and 110 min, respectively). According to the results obtained from the aerated membrane system, Fe2+ and Mn2+ removal were extended by Fe(OH)3 via adsorption/surface oxidation. It is clearly shown from the flux, resistance results, scanning electron microscope (SEM) and Fourier transform infrared (FT/IR) spectroscopy observation that manganese oxides were deposited mainly in membrane pores forming membrane fouling by small flocs, while iron oxide particles were deposited on the membrane surface. Although the flux performance of PT PES membrane was higher than HF PP membrane, fouling resistance of HF PP membrane was higher than PT PES.

Modified Red Mud Catalyst for Volatile Organic Compounds Oxidation

Red mud waste from the aluminium industry was modified by leaching using hydrochloric acid or oxalic acid with additives, followed by precipitation or evaporation. The prepared catalysts were characterized in detail and tested for toluene total oxidation. The samples prepared by precipitation of the leachate by adding a base gave a much better performance in catalytic oxidation than the ones prepared by just evaporating the leachate. These improved performances can be correlated to the enhanced textural and redox properties of the catalysts due to the better dispersion and higher enrichment of Fe oxides at their surface. The best performing catalyst had a light-off temperature of around 310 °C and complete oxidation took place at around 380 °C.