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Fe 2 O 3 -TiO 2 -clay heterostructures have been prepared using an organo-bentonite as support, which organophilic character favored the fixation of TiO 2 . Furthermore, Fe 2 O 3 was successfully anchored by wet impregnation. The resulting materials are characterized by a disordered layered structure and a mesoporous texture. The heterostructures were employed as catalysts for the removal of two pharmaceuticals, acetaminophen (ACE) and antipyrine (ANT), by heterogeneous Fenton and photo-Fenton processes. ACE removal under different operation conditions was studied in detail to establish structure-performance relationships, being the TiO 2 formation and the developed texture the main factors controlling the activity. ANT showed a higher refractory behavior in oxidation by Fenton. Among the technologies studied, heterogeneous photo-Fenton achieved the best catalytic performance and higher kinetic rate and mineralization degree. Iron leaching was very low, lower than 5% of the initial iron load in all cases. This work demonstrates the potential application of these heterostructures for the removal of emerging pollutants of different nature.

The purpose of this study was to evaluate the incidence of surgical site infections in total knee arthroplasty patients using a preadmission cutaneous skin preparation protocol compared with a cohort of patients undergoing standard in-hospital perioperative preparation only. Records between 2007 and 2010 were reviewed to identify deep incisional and periprosthetic infections among patients using the chlorhexidine protocol (478 patients) and patients who did not use the protocol (1,735 patients). Patients using the chlorhexidine cloths were given two packets of six chlorhexidine gluconate-impregnated cloths, with instructions for use, the evening before and morning of surgery. A statistically lower incidence of surgical site infection was found in patients using the chlorhexidine cloths (0.6%) compared with patients undergoing in-hospital perioperative skin preparation only (2.2%). On the basis of the results of this study, a preadmission chlorhexidine protocol seems to be an effective method to prevent surgical site infections in total knee arthroplasty procedures., (Thieme Medical Publishers 333 Seventh Avenue, New York, NY 10001, USA.)

Bimetallic Pd-Rh catalysts supported on pillared clays have been prepared and tested for aqueous-phase hydrodechlorination (HDC) using 4-chlorophenol (4-CP) as target compound. These bimetallic catalysts combine the higher activity of Rh with the better stability of Pd found in previous works with monometallic catalysts. Different combinations of Pd and Rh amounting to 1 wt% total metal load were tested and the catalyst with 0.75 wt% Pd and 0.25 wt% Rh yielded the best results. Ecotoxicity and biodegradability (measured as BOD(5)/COD ratio) of the effluents were checked. A significant decrease of ecotoxicity was observed while biodegradability was dramatically improved from 0.02 for the initial 4-CP solution up to values higher than 0.6.

Catalysts based on pillared clays with Al-Fe have been synthesised from a commercial bentonite and tested for catalytic wet peroxide oxidation (CWPO) of aqueous 4-Chlorophenol (4-CP) solution and industrial wastewater from cosmetics manufacture. The effect of the synthesis procedure, the iron load and reaction temperature on the catalytic activity was studied using 4-CP as target compound. A lower temperature in the preparation of the pillaring solution, as well as a higher Fe load, gave rise to a higher catalytic activity, but also a higher leaching of the active phase. The best catalyst, in terms of catalytic activity, was also tested for treating cosmetic wastewater by CWPO. Experiments were carried out at 90 degrees C and atmospheric pressure and the influence of Fe load, catalyst concentration and H(2)O(2)/COD ratio (between 0.5 and 2 times the stoichiometric ratio) were analysed. Higher values of these parameters favour COD reduction. The Fe leaching in all cases was lower than 1.2 mg/L, indicating that these catalysts have a high stability under these experimental conditions.

Catalysts based on pillared clays with Pd-Al were synthesized from a commercial bentonite and tested for catalytic hydrodechlorination (HDC) using 4-chlorophenol (4-CPhOH) as target compound and formic acid as hydrogen source. Stable Pd-Al pillared clays, with a strong fixation of the active phase to the solid support were obtained since no Pd was detected in the reaction media. The incorporation of Pd to the pillared clay structure yielded catalysts with high activity in the reaction studied reaching a complete removal of the 4-CPhOH under mild conditions of temperature (50-70 degrees C). Phenol was not the only reaction product formed, since a more hydrogenated product such as cyclohexanone was detected in the effluent, which indicates additional hydrogenation of phenol. The influence of the method of introduction of Pd in the pillared clay (ion-exchange or impregnation) and Pd concentration in the catalytic activity were studied as well as other important operating variables such as reaction temperature, catalyst concentration, 4-CPhOH initial concentration and formic acid to 4-CPhOH molar ratio. The catalysts prepared suffered deactivation after three consecutive runs, probably due to carboneous deposits formation since no appreciable Pd leaching was observed.

This work deals with the evolution of intermediates and ecotoxicity upon Fenton's oxidation of phenol in aqueous solution. The EC50 values of the intermediates identified in the oxidation pathway of phenol have been measured. Some of these compounds, mainly hydroquinone and p-benzoquinone, showed toxicity levels much higher than phenol itself. Depending on the operating conditions, these intermediates could be completely transformed into organic acids, mainly oxalic and formic. Ecotoxicity values substantially lower than those expected from the chemical composition were measured in the reaction samples. This is explained by a reduction of the concentration of aromatic intermediates when the pH was adjusted at 6-8 (according to what is required by the standard bioassay ISO 11348-3). Formation of complexes between hydroquinone and p-benzoquinone at increasing pH can remove from solution those highly toxic intermediates whose very low EC50 values give rise to a high ecotoxicity even at fairly low concentrations. This together with the enhanced decomposition of residual H202 at increasing pH represent important beneficial effects of the neutralization step following Fenton treatment which allow a complementary cleaning of the effluent.