Photodegradation applied to the treatment of phenol and derived substances catalyzed by TiO2/BiPO4 and biological toxicity analysis.

For this work, a phenol solution model was treated by an advanced oxidation process (AOPs), using the heterogeneous catalyst TiO2/BiPO4 and hydrogen peroxide combined with UVA for 240 min. An annular reactor containing a UVA lamp (80 W) was employed. A central composite rotacional design was developed employing a TiO2/BiPO4 concentration of 87 mg L-1 and a hydrogen peroxide concentration of 1800 mg L-1, being evaluated by the degradation percentage and phenol mineralization percentage as responses; 94.30 and 67.00 % were obtained for the phenol degradation and total organic carbon (TOC) conversion, respectively. The lumped kinetic model (LKM) was applied and a satisfactory profile of the residual fractions of the organic compounds present in the liquid phase as a time function with a determination coefficient (R 2 = 0.9945). The toxicity tests employing microbiological species indicated that the organisms tested for the evaluation of the toxic compounds present in the contaminated samples presented a practical low cost test, rapid execution, and high sensibility as an indicator of the presence of toxic substances in liquid effluents.

Extraction and recovery of chromium from electroplating sludge.

This work reports a study of the extraction and recovery of chromium from the wastes (class I dangerous) generated by a galvanic manufacturer. Commercial HCl at room temperature was employed, and the conditions of the extraction process were optimized according to a sequential experimental design, which also included the acid concentration and contact time as variables. The best extraction conditions (80% v/v; 30 min; 97.6% Cr) for the chromic sludge were chosen in order to make the recovery process economically feasible. After each extraction, the residue was submitted to leaching essays, to assess environmental risks. It was found that sludge could be characterized as no longer dangerous. In the recovery study, a simple and low-cost technique was evaluated for selectivity based on an oxidation step with hydrogen peroxide. A 2(3) factorial design to assess the influence of oxidation time (min), temperature ( degrees C) and peroxide amount (mol/L) was employed. The best conditions, yielding a chromium recovery of about 92%, were a time of 60 min, a temperature of 60 degrees C and 2.1 mol/L peroxide. Additional essays revealed that the same result could be obtained with more economic conditions (40 min, 1.4 mol/L peroxide and 60 degrees C). This technique proved not only effective in comparison with existing alternatives, but also low costing.

A flow-batch internal standard procedure for iron determination in hydrated ethanol fuel by flame atomic absorption spectrometry.

A flow-batch manifold coupled to a flame atomic absorption spectrometer was evaluated to assess the iron content by the internal standard method in hydrated ethanol used as fuel in automotive industry. For this assessment official methods require calibration procedures with matrix matching, making it difficult to obtain accurate results for samples adulterated by the addition of water. Nickel was selected as the internal standard since it is usually absent in samples and because it requires similar conditions of atomization. After procedure optimization, which requires about 4.25mL of sample and standard per measurement, it was possible to get linear analytical response for iron concentrations between 0.12 and 1.40mgL(-1) and a detection limit of 0.04mgL(-1). Eighteen samples were collected randomly from fuel stations in Pernambuco (Brazil) and iron concentration was determined using the proposed procedure. Comparison of results obtained (0.20-1.50mgL(-1)) showed a mean standard error of 3.9%, with 3.8% and 2.3% calculated for the mean variation coefficients of the proposed method and the reference procedure, respectively. For adulterated samples (0.12-0.64mgL(-1)), the mean standard error was 4.8% when compared with the standard addition method. These results allowed concluding that the proposed procedure is adequate to accomplish the determination of iron in ethanol fuel in a large scale basis with a sampling rate of about 10h(-1).

Flow-injection amperometric determination of dopamine in pharmaceuticals using a polyphenol oxidase biosensor obtained from soursop pulp.

The amperometric determination of dopamine (Do) in pharmaceuticals formulations by flow injection analysis (FIA) is proposed. An enzymatically modified carbon paste electrode constituted by 25% (w/w) of polyphenol oxidase obtained from Annona muricata L. tissue, 30% (w/w) of graphite, 30% (w/w) of silicone and 15% (w/w) of 7,7,8,8 tetracyanoquinodimethane (TCNQ), was used as flow-through detector. The flow amperometric detection was carried out at a potential of 0.10 V (vs. Ag/AgCl) when an injected sample volume of 250 microl was inserted on a 0.3 M phosphate buffer carrier solution (pH 7.8) flowing at 2.5 ml/min. The developed biosensor showed good stability and reproducibility, enabling up to 500 determinations in 60 days, without considerable loss of enzymatic activity. The FIA system presented a linear response to Do concentrations in the interval from 2 x 10(-2) to 2 x 10(-4) M, with relative standard deviations lower than 1.5%. The kinetic parameter K(M) for the soluble and immobilized enzyme was 1.45 x 10(-2) and 1.91 x 10(-2) M, respectively. In the analyses of different commercially pharmaceutical formulations a relative deviation lower than about 3.4% was obtained.

Partial characterization of proteases from Spretomyces clavuligerus using an inexpensive medium

The partial characterization of extracellular proteases from Streptomyces clavuligerus NRRL 3585 and 644 mutant was investigated. The enzyme production was carried out in batch fermentation using soy bean filtrate as nitrogen source. Maximum activity was obtained after 96h of fermentation with an initial pH of 7.0. The enzyme was partially purified by ammonium sulphate precipitation. Enzymes from the two strains retained 37 per cent of their initial activities at pH 8.0 after 2 h incubation at 25§C. Enzyme half-life at pH 8.0 and 60§C was 40.30 and 53.32 min, respectively for both strains (partially purified extract). The optimum pH was obtained at pH 7.0-8.0 and 8.4 for enzymes produced for 3585 and 644 strains (crude extract), respectively, and 8.4 and 8.0 for enzymes from the partially purified extract 3585 and 644 strains, respectively. The optimum temperature for the crude extract was 21§C for both strains. However, for the partially preparation the optimum temperature was 50§C and 40ºC for S. clavuligerus NRRL 3585 and 644 strains respectively.

Avaliaçäo microbiológica da água do Riacho Cavouco, Recife - PE / Evaluation of microbiological water of the Cavouco stream, Recife - PE

A água, essencial à vida de todo ser humano, atua também como importante veículo de contaminaçäo de inúmeras doenças, seja em decorrência de excretos humanos ou de outros animais, seja pela presença de substâncias químicas nocivas à saúde humana. As águas do Riacho Cavouco, no munícipio de Recife - PE, säo classificadas como águas doces, classe 04, destinadas à navegaçäo, à harmonia paisagística e aos usos menos exigentes. O nível de contaminaçäo microbiológica de cada ponto de contribuiçäo do Riacho Cavouco, no "campus" da Universidade Federal de Pernambuco, foi avaliado durante um período de 6 (seis) meses. Em alguns pontos de contribuiçäo, essas águas residuárias näo säo constituídas essencialmente de esgoto bruto. Foi detectada uma variaçäo de 100 mil a 10 bilhöes no NMP de coliformes totais e 10 mil a 1 milhäo no NMP de coliformes fecais. Os testes realizados confirmaram a presença de Eschirichia coli, Enterobacter aerogenes, Pseudomonas aeruginosa, Serratia sp., Staphylococcus aureus e Streptococcus faecalis. As águas desse Riacho precisam ser tratadas para que possam ser utilizadas para criaçäo de peixes, dentre outros objetivos incluídos na revitalizaçäo e urbanizaçäo desse riacho, como também para evitar poluiçäo de lençóis de água subterrâneos.