An improved analytical method was developed and validated for the determination of the monosaccharide anhydrides levoglucosan, mannosan, and galactosan in atmospheric aerosol samples. The method uses an external recovery standard, extraction in dichloromethane, trimethylsilylation, addition of an internal standard (1-phenyl dodecane), and analysis by gas chromatography with flame ionization detection (GC-FID) and gas chromatography/mass spectrometry (GC/MS). As external recovery standard, we selected 1,2,3-trihydroxyhexane, which has a similar polarity as the monosaccharide anhydrides; furthermore, it was ensured that the trimethylsilylation step leads to complete derivatization into trimethylsilyl ethers. The reproducibility of the combined trimethylsilylation and analysis of levoglucosan was about 2% for standard solutions, whereas the precision of the entire method for the sum of all three monosaccharide anhydrides (MAs) in real aerosol filter samples was about 5%. The method was applied to aerosol samples from urban and tropical locations. The atmospheric concentration of the MAs in fine (<2.5 microm) aerosols at a primary forest site in Rondĵnia, Brazil, was on average 2.15 microg m(-3) during the dry season when intensive biomass burning occurs, which was almost 400 times higher than during the wet (nonburning) season. Urban total aerosols collected in Gent, Belgium, showed an average atmospheric concentration of MAs of 0.56 microg m(-3) for the winter season, which was a factor of 20 higher than for the summer season. The carbon in the MAs accounted on average for about 5.1% and 1.8% of the organic carbon in the Brazilian dry season and Gent winter aerosols, respectively. Levoglucosan was the major MA, with a relative abundance in the range of 76-93%.

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Cytotoxic activity of eight plant extracts, native from the MidWest of Brazil comprising Cerrado, Pantanal and semideciduous forest, was evaluated for MDA-MB-435, SF-295, and HCT-8 cancer cell strains. A single 100 µg.mL -1 dose of each extract was employed with 72 h of incubation for all tests. Doxorubicin (1 µg.mL -1 ) was used as the positive control and the MTT method was used to detect the activity. Cytotoxicity of distinct polarities was observed in thirty extracts (46%), from different parts of the following species: Tabebuia heptaphylla (Vell.) Toledo, Bignoniaceae, Tapirira guianensis Aubl., Anacardiaceae, Myracrodruon urundeuva Allemão, Anacardiaceae, Schinus terebinthifolius Raddi, Anacardiaceae, Gomphrena elegans Mart., Amaranthaceae, Attalea phalerata Mart. ex Spreng., Arecaceae, Eugenia uniflora L., Myrtaceae, and Annona dioica A. St.-Hil., Annonaceae. Extracts of at least two tested cell strains were considered to be highly active since their inhibition rate was over 75%.

This study evaluated the potential bioconversion of crude glycerol from biodiesel production, applying used cooking oil for biohydrogen production by fermentative bacteria consortia. The pretreatment of crude glycerol was made by pH adjustment. Heat treatment of the inocula and initial pH 5.5 were applied to select hydrogen-producing bacteria and inactivate hydrogen-consumers microorganisms. The inocula tested were: (I) granular sludge from the thermophilic UASB reactor used on the treatment of vinasse and (II) granular sludge from the UASB reactor used on the treatment of sanitary sludge for the assays (1) and (2), respectively. The characterization of crude glycerol presented high levels of alkalinity, methanol and soap that may be inhibitory to biologic processes of H 2 production. The assays were carried in anaerobic batch reactors in order to verify the efficiencies of crude glycerol to H 2 generations by the microbial consortia (20%) at 37 C, initial pH 5.5, with 20.0 g COD L À1 glycerol. The cumulative production of hydrogen for the assays (1) and (2) were, respectively, (mmol H 2 L À1) 28.49 ± 1.55 and 19.14 ± 1.67. The subsequent yields were obtained as follows: 2.2 moL H 2 mol À1 glycerol and 1.1 moL H 2 mol À1 glycerol, respectively. The used cooking oil was an efficient waste for bioconversion of crude glycerol to H 2 production.

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