Modified diatomites for Fenton-like oxidation of phenol

Raw diatomites were modified by acid or base treatments; addition of Fe or Cu species through the incipient wet impregnation method (IWI) and calcination at 700 °C. Samples were characterized by X-ray powder diffraction (XRD), scanning electron microscopy (SEM-EDX), Mossbauer spectroscopy, point of zero charge (PZC), pyridine temperature programme desorption (TPD), themogravimetric analysis (TGA) and BET surface area determination. According to characterization results, four samples were selected: simply calcined Diatom (D), iron added (Fe-D), acid treated Fe reimpregnated (H-Fe-D) and copper added (Cu/Fe-D). Materials were tested as catalysts for the peroxidation of phenol solutions (1000 mg/L) in a batch laboratory reactor, at different operating conditions in 5 h tests. D, Fe-D and H-Fe-D samples allowed complete phenol removal under all the operating range studied. At optimum conditions, TOC conversions of 50–55% were obtained. Metal ions added through the IWI procedure resulted more labile than metal present originally. The acidic treatment favored the initiation of the reaction showing a reduction of the induction period at almost neutral initial pH. The Fe-D catalyst exhibited poor performance, lower reactions rates and higher Fe leaching. Conversely, high TOC conversions (80%) were achieved with Cu/Fe-D, however, Cu leaching was excessive (12.7%). D and H-Fe-D samples were used in consecutive runs (up to 20 h) maintaining phenol conversion and TOC reduction. Overall, a good performance was obtained, even comparable to more sophisticated Fe catalysts.Fil: Inchaurrondo, Natalia Soledad. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mar del Plata. Instituto de Investigaciones en Ciencia y Tecnología de Materiales. Universidad Nacional de Mar del Plata. Facultad de Ingeniería. Instituto de Investigaciones en Ciencia y Tecnología de Materiales; ArgentinaFil: Ramos, Cinthia Paula. Comisión Nacional de Energía Atómica. Gerencia del Área de Seguridad Nuclear y Ambiente. Gerencia de Química (CAC); Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Zerjav, G.. National Institute Of Chemistry; EsloveniaFil: Font, J.. Universitat Rovira I Virgili; EspañaFil: Pintar, A.. National Institute Of Chemistry; EsloveniaFil: Haure, Patricia Monica. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mar del Plata. Instituto de Investigaciones en Ciencia y Tecnología de Materiales. Universidad Nacional de Mar del Plata. Facultad de Ingeniería. Instituto de Investigaciones en Ciencia y Tecnología de Materiales; Argentin

Investigating the activity of modified TiO2 photocatalysts used for the photoreforming of biomass derivatives

Different TiO2 modified (with Pt, Cu2O, Nb) photocatalysts have been compared for the photo-reforming of glucose and fructose at ambient conditions with the aim of linking the photoactivity to some structural and surface characteristics. A different degree of conversion, distribution of intermediates and H2 production were observed with the various photocatalysts. Moreover, the results obtained with the same catalysts were slightly different with the two substrates, highlighting the importance of the interaction between the catalyst surface and the organic compound. Bare TiO2 was inactive towards H2 production, Cu2O was effective in replacing Pt for hydrogen generation, and the presence of Pt/Nb was beneficial for both H2 production and selective oxidation. Moreover, Pt not only works as a sink for the photoproduced electrons, as it is well known in the literature, but also modifies the surface acid-base properties of catalysts as revealed by DRIFT and TPD measurements

Pt-Nb2O5-TiO2 based semiconductors for photo-reforming of glucose and fructose aqueous solutions

The conversion of biomass derivatives into fuels and valuable compounds under green conditions is increasingly attracting the attention of the scientific community. In this study, the photo-reforming of aqueous glucose and fructose solutions in the presence of 0.5 wt% Pt-loaded homemade bare and Nb2O5-TiO2 catalysts was investigated to maximize the activity of titania for both hydrogen production and valuable chemical production. The most efficient sample was the home-prepared Pt-4 %Nb2O5-HP, for both glucose and fructose conversion, with the highest H2 productivity and the highest selectivity towards partially oxidized compounds. The behaviour of the Pt-4 %Nb2O5-HP derives from a favourable compromise of some surface and intrinsic electronic properties as, for instance, photoluminescence, zeta potential and surface acidity. The presence of Nb2O5 decreased the recombination rate of photoproduced charges. Photo-deposition of Pt was essential for H2 production and, surprisingly, also increased the basicity of the TiO2 surface; an increase in surface acidity was measured when only niobium oxide was added, whereas stronger basic sites were observed in the simultaneous presence of Pt and niobium oxide

Catalytic ozonation of an azo-dye using a natural aluminosilicate

Catalytic ozonation of Orange II (100 mg/L) was studied using aluminosilicate Montanit300® (M) modified with H2SO4 (MS) and HCl (MH). Characterization of these samples was performed through several techniques: SEM/EDX, FTIR, XRD, FRX, TPD pyridine, surface area, pHPZC. Acid treatment increased surface area, Si:Al ratio and quantity of acid sites, but reduced pHPZC and Fe and Mn content. Ozonation experiments achieved complete decoloration and remarkable TOC conversions of 66, 65, 88 and 91 % by single ozonation and catalytic ozonation with MH, MS and M, respectively. Higher M and MS activity under acidic pH was attributed to Mn leaching. Decreased mineralization efficiency in the presence of tert-butanol suggested a radical mechanism. At neutral pH, M showed no activity, while MS presented mild activity owing to its enlarged hydrophobicity. The M sample sustained mineralization levels over 20 h. Lower O3 dose caused quick MS deactivation. However, it was reversed through calcination and prevented with a higher oxidant dose. Mn is naturally found in Montanit300®, thus making it an inexpensive catalyst. The development of a dynamic cycle combining reduced and oxidized forms of Mn was key to the outstanding activity observed.Fil: Inchaurrondo, Natalia Soledad. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mar del Plata. Instituto de Investigaciones en Ciencia y Tecnología de Materiales. Universidad Nacional de Mar del Plata. Facultad de Ingeniería. Instituto de Investigaciones en Ciencia y Tecnología de Materiales; ArgentinaFil: Di Luca, Carla. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mar del Plata. Instituto de Investigaciones en Ciencia y Tecnología de Materiales. Universidad Nacional de Mar del Plata. Facultad de Ingeniería. Instituto de Investigaciones en Ciencia y Tecnología de Materiales; ArgentinaFil: Zerjav, G.. Department For Environmental Sciences And Engineering; EsloveniaFil: Grau, Javier Mario. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera". Universidad Nacional del Litoral. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera"; ArgentinaFil: Pintar, A.. Department For Environmental Sciences And Engineering; EsloveniaFil: Haure, Patricia Monica. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mar del Plata. Instituto de Investigaciones en Ciencia y Tecnología de Materiales. Universidad Nacional de Mar del Plata. Facultad de Ingeniería. Instituto de Investigaciones en Ciencia y Tecnología de Materiales; Argentin

The prevalence and risk of hepatitis flares in a Serbian cohort of HIV and HCV co-infected patients treated with HAART

Despite substantial benefits of HAART treatment of HIV-infected patients, cumulative long-term toxicity, including drug-induced hepatotoxicity, has emerged as an important complication. Thus, to examine the prevalence and risk of developing severe hepatic injury during HAART, we conducted a retrospective study in a cohort of 364 HIV-infected patients treated with HAART between January 1998 and May 2006, for whom data on alanine aminotransferase activity were available both before and during HAART. HCV co-infection was recorded in 35.4% of the series, but was found not to influence either the efficacy of HAART or survival. (P gt 0.05). Severe hepatotoxicity occurred in a total of 24 patients' (6.6%). Multivariate logistic regression defined HCV co-infection (OR 16.6, 95% CI 3.8-46.0, P lt 0.0001), and the use of SQV/RTV and d4T (OR 3.1, 95% CI 1.2-8.16, P = 0.02, and OR 7.1, 95% CI 1.0-54.5, P = 0.05, respectively) as independent risk factors for,aggravation-of hepatitis. In addition, there was a significant increase,in the probability of developing liver damage over years of treatment (Log rank, P lt 0.01). Conversely, the probability of developing hepatotoxicity was not associated with an increase, in the CD4 cell count to values,greater than 350/mu L (Log rank, P = 0.59). In conclusion, in the setting of chronic viral hepatitis, hepatotoxicity during HAART may be attributed to the cumulative toxicity of drugs that induce mitochondrial toxicity, along with particular PIs and/or NNRTIs. Furthermore, our data suggest prudent use of D-drugs, still common in resource-limited countries, in HCV co-infected patients.(c) 2006 Elsevier Masson SAS. All rights reserved

Synthesis and adsorption behavior of mesoporous alumina and Fe-doped alumina for the removal of dominant arsenic species in contaminated waters

Ordered mesoporous Al 2 O 3 and Fe-Al 2 O 3 materials were synthesized at room temperature by an easy and environmentally friendly self-assembly sol-gel route, to be tested for arsenic removal. Solid samples were thoroughly characterized by several techniques. Synthetized and commercial alumina samples were evaluated as adsorbents for the removal of dominant arsenic species under a wide pH range (3.6-11.5). The mesoporous alumina showed higher adsorption capacity (90 mg/g As(V), pH eq 4) than commercial alumina (54 mg/g As(V), pH eq 4), due to its amorphous structure, uniform accessible mesopores and higher surface acidity. The Fe bearing material exhibited strong As affinity. As(III) adsorption resulted much lower than for arsenate (maximum uptake of 16 mg/g, at pH 8), since As(III)-adsorbent interaction is only based on weak Van der Waals force. Arsenic isotherms adjusted well to the Freundlich model and more accurately to the three parameters Siṕs model. The kinetics results fitted the Elovich model. As pH increased, adsorption capacity decreased due to the reduction of electrostatic interactions. Under alkaline conditions arsenic desorption was achieved, although the stability of the material was compromised. The presence of several interfering ions was evaluated. Phosphate ions showed the highest interference. The use of a tap water matrix increased As(V) adsorption, encouraging the use of these materials in the treatment of real polluted waters.Fil: Inchaurrondo, Natalia Soledad. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mar del Plata. Instituto de Investigaciones en Ciencia y Tecnología de Materiales. Universidad Nacional de Mar del Plata. Facultad de Ingeniería. Instituto de Investigaciones en Ciencia y Tecnología de Materiales; ArgentinaFil: Di Luca, Carla. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mar del Plata. Instituto de Investigaciones en Ciencia y Tecnología de Materiales. Universidad Nacional de Mar del Plata. Facultad de Ingeniería. Instituto de Investigaciones en Ciencia y Tecnología de Materiales; ArgentinaFil: Mori, Maria Fernanda. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera". Universidad Nacional del Litoral. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera"; ArgentinaFil: Pintar, A.. Department For Environmental Sciences And Engineering;Fil: Zerjav, G.. Department For Environmental Sciences And Engineering;Fil: Valiente, M.. Gts, Universitat Autònoma de Barcelona;Fil: Palet, C.. Gts, Universitat Autónoma de Barcelona

Clinical onset and course, response to treatment and outcome in 24 patients with the cblE or cblG remethylation defect complemented by genetic and in vitro enzyme study data

BACKGROUND: The cobalamin E (cblE) (MTRR, methionine synthase reductase) and cobalamin G (cblG) (MTR, methionine synthase) defects are rare inborn errors of cobalamin metabolism leading to impairment of the remethylation of homocysteine to methionine. METHODS: Information on clinical and laboratory data at initial full assessment and during the course of the disease, treatment, outcome and quality of life was obtained in a survey-based, retrospective study from physicians caring for patients with the CblE or CblG defect. In addition, data on enzyme studies in cultured skin fibroblasts and mutations in the MTRR and MTR gene were analysed. RESULTS: In 11 cblE and 13 cblG patients, failure to thrive, feeding problems, delayed milestones, muscular hypotonia, cognitive impairment and macrocytic anaemia were the most frequent symptoms. Delay in diagnosis depended on age at first symptom and clinical pattern at presentation and correlated significantly with impaired communication abilities at follow-up. Eighteen/22 patients presented with brain atrophy or white matter disease. Biochemical response to treatment with variable combinations of betaine, cobalamin, folate was significant. The overall course was considered improving (n = 8) or stable (n = 15) in 96 % of patients, however the average number of CNS symptoms per patient increased significantly over time and 16 of 23 patients were classified as developmentally delayed or severely handicapped. In vitro enzyme analysis data showed no correlation with outcome. Predominantly private mutations were detected and no genotype- phenotype correlations evident. CONCLUSIONS: The majority of patients with the cblE and cblG defect show limited clinical response to treatment and have neurocognitive impairment