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Airborne particulate matter (PM 10 ) samples were collected daily, indoors and outdoors, in a primary school at Aveiro, Portugal, from February 28 to May 27, 2011. The carbonaceous content (organic and elemental carbon) was determined by a thermo-optical technique. The organic speciation of PM 10 was performed by gas chromatography-mass spectrometry. Mean PM 10 levels of 107 and 36 µg/m 3 were obtained in the schoolroom and outdoors, respectively. On average, organic carbon accounted for 30.0% of the mass of PM 10 indoors, whereas a lower mass fraction of 21.3% was found outdoors. The lack of correlation between indoor and outdoor organic carbon and the much higher indoor levels suggest significant contributions by indoor sources. The most abundant organic compound classes were acids, sugars, polyols and n-alkanes. Infiltration of outdoor particles leads to contamination of the schoolroom with vehicle emissions, as well as emissions related to the burning of biofuel in nearby restaurants and bakeries. However, the much higher indoor concentrations than in the outdoor air for the majority of compounds suggest that the origin of much of the particulate matter is from within the school building (due to school activities and materials, skin debris, microorganisms, and so on), and this also includes the formation of secondary organic aerosols. Based on the concentrations of polycyclic aromatic hydrocarbons, a negligible cancer risk was estimated in relation to the air within the school.

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Objectives To determine the concentration of calcium, iron, manganese and zinc ions after the application of chelator to Enterococcus faecalis biofilms.Material and Methods Fifty bovine maxillary central incisors were prepared and inoculated with E. faecalis for 60 days. The following were used as irrigation solutions: 17% EDTA (pH 3, 7 and 10), 2.5% sodium hypochlorite (NaOCl) combined with 17% EDTA (pH 3, 7 and 10), distilled water (pH 3, 7 and 10), and 2.5% NaOCl. Each solution was kept in the root canal for five minutes. Fifteen uncontaminated root canals were irrigated with 17% EDTA (pH 3, 7 and 10). Six teeth were used as bacterial control. The number of calcium, iron, manganese and zinc ions was determined using flame atomic absorption spectrometry. Mean ± standard deviation (SD) values were used for descriptive statistics.Results Calcium chelation using 17% EDTA at pH 7 was higher than at pH 3 and 10, regardless of whether bacterial biofilm was present. The highest concentration of iron occurred at pH 3 in the presence of bacterial biofilm. The highest concentration of manganese found was 2.5% NaOCl and 17% EDTA at pH 7 in the presence of bacterial biofilm. Zinc levels were not detectable.Conclusions The pH of chelating agents affected the removal of calcium, iron, and manganese ions. The concentration of iron ions in root canals with bacterial biofilm was higher after the use of 17% EDTA at pH 3 than after the use of the other solutions at all pH levels.

The proposed new sensor combines low cost, sensitivity, selectivity, portability and suitability for the speciation analysis of copper in natural waters.

This work describes the optimization of an extraction method for the determination of polycyclic aromatic hydrocarbons (PAHs) and their nitro- and oxy-PAH derivatives in atmospheric particulate matter (PM) samples, and demonstrates that this method is also effective for the determination of levoglucosan. The optimization of the extraction solvents was performed using a three-component mixture design with the solvents dichloromethane, methanol, and acetonitrile. The number of extractions, volume of solvent, and duration of extraction in an ultrasonic bath were optimized using a full factorial design followed by a central composite design. The analyses were performed by gas chromatography coupled with mass spectrometry. The optimized conditions of the method were three extractions using 4.0 ml of acetonitrile, with ultrasonication for 34 min. The proposed method presented good linearity (r > 0.990) and acceptable precision for low (100 ng ml−1, RSD: 1–16%), medium (300 ng ml−1, RSD: 1–19%), and high (500 ng ml−1, RSD: 2–16%) concentrations of PAHs. The limits of quantification for different PAHs ranged from 10 to 50 ng ml−1, which were suitable for atmospheric PM. Assessment of the method using sample matrix spiking/recovery assays, as well as use of a reference method, showed good recoveries for levoglucosan and for most of the PAHs and their derivatives, except for the most volatile compounds, which were lost during the evaporation of the solvent. The results for PM samples extracted by the optimized method and the reference method were in good agreement. The proposed method required 97% less solvent than the reference method, shortened the analysis time by 85%, and proved to be accurate and precise for the determination of at least 27 PAHs and their derivatives present in PM samples collected with a low-volume sampler.