Adaptation of a cold vapour mercury analyser to flow injection analysis

Minor modifications to a Coleman MAS-50A Mercury Analyser System allowed the determination of mercury by flow injection analysis. Using sample volumes of 600 μl it was possible to analyse up to 120 samples per hour, with a detection limit of 0.2 μg. l-1 (120 pg) of mercury. The authors also report on a simple digestion procedure which replaces the time- and reagent-consuming EPA procedure, when the sample content permits

Seasonal behavior of mercury species in waters and sediments from the Negro River Basin, Amazon, Brazil

Total (HgT), reactive (HgR) and organic (Hg ORG) mercury species have been quantified in non-filtered waters collected from the Negro River Basin, Amazon (from January/2002 through January/2004), in both black and white water bodies. Black waters presented the highest HgT, HgORG and HgR concentration (29.1 ng L-1, 1.63 ng L-1 and 3.9 ng L-1, respectively), while, white waters presented the lowest HgT, Hg ORG and HgR concentration (8.8 ng L-1, 0.49 ng L-1 and 1.2 ng L-1, respectively). An inverse correlation between HgT and the water level over the basin was obtained, although the HgORG concentration has increased in the first rainy months and then decreased as the water level rose. Total mercury in surface sediments (0-10 cm) ranged from 70 to 271 mg kg-1 being the methylmercury 0.47-1.79 % of this stock. The results indicate that HgR and the labile dissolved organic matter were introduced into the aquatic environment during the flooding season, especially in the earlier stages, thus contributing to mercury methylation. ©2007 Sociedade Brasileira de Química

Endocrine disruptors in the enviroment

Although the hypothesis that environmental chemicals may exhibit endocrine disrupting effects is not new, the issue has been a growing level of concern due to reports of increased incidences of endocrine-related disease in humans, including declining male fertility, and more significantly, to adverse physiological effects observed in wildlife where cause and effect relationships are more evident. The list of endocrine disrupting chemicals (EDCs) includes a range of anthropogenic compounds, phytoestrogens, naturally occurring sex steroids and synthetic estrogens. Within the aquatic environment, the presence of EDCs has concerned many scientists and water quality regulators. Discharge of effluents from treatment facilities is likely to be a significant source of input of contaminants to many systems, and the potential for concentration of hydrophilic compounds and transformation products within sludges has implications for their disposal. Then, understanding the processes and the fate of EDCs on the environment, as well as the mechanisms of endocrine disruption, may facilitate controlling or limiting exposure of both humans and the environment to these compounds.695706Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP

Automatic determination of mercury in samples of environmental interest

An automatic flow injection (FI) system for the determination of mercury was developed using a commercial Gold vapour atomic absorption spectrophotometer (CVAAS). Control and data acquisition in the FI system was done with an IBM-PC 286 XI compatible microcomputer and a home-made interface, using software written in QuickBasic 4.5. Mercury content was determined by: sampling using a combination of four electromechanical three-way poly(tetrafluoroethylene) valves; separation of the dissolved reduced mercury in a gas/liquid separation cell using nitrogen as carrier, followed by amalgamation of the stripped metal on a gold wire column; after stripping the metal, cleaning the separation cell using vacuum, which was controlled by a three-way electromechanical valve; heating the gold wire column automatically to release the amalgamated mercury using an external nichrome wire coil; storing the output signals automatically to calculate the final mercury concentration, using commercially available software. The optimized system presents a detection limit of 5.3 ng l(-1) of mercury (30 pg absolute) using 5.7 ml (three injections of 1900 mu l of the sample) with an analytical frequency of six samples per hour and reproducibility of 5%. The procedure was used to determine mercury in fish, hair and natural water samples.18619319

Factors affecting Hg (II) adsorption in soils from the Rio Negro basin (Amazon)

Mercury (II) adsorption studies in top soils (top 10 cm) from the Rio Negro basin show this process depends strongly on some selected parameters of the aqueous phase in contact with the soils. Maximum adsorption occurred in the pH range 3.0-5.0 (>90%). Dissolved organic matter shows an inhibitory effect on the availability of Hg (II) to be adsorbed by the soils, whereas a higher chloride content of the solution resulted in a lower adsorption of Hg (II) at pH 5.0. Soils with higher organic matter content were less affected by changes in the salinity. An increase in the initial Hg (II) concentration increased the amount of Hg (II) adsorbed by the soil and decreased the time needed to reach equilibrium. A Freundlich isotherm provided a good model for Hg (II) adsorption in the two types of soil studied. The kinetics of Hg (II) adsorption on Amazonian soils showed to be very fast and followed pseudo-second order kinetics. An environmental implication of these results is discussed under the real scenario present in the Negro River basin, where acidic waters are in contact with a soil naturally rich in mercury.438443Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP

Synchronous-scan fluorescence and the complexation of copper (II) ions by humic substances

Two fluorescence bands were detected using synchronous-scan fluorescence on samples of terrestrially derived humic substances (lex/lem 380/398, 440/458 nm) without the addition of copper. A third band (lex/lem 502/520 nm) was detected after severe quenching of the second band (lex/lem 440/458 nm) caused by additions of copper. A more energetic band (lex/lem 333/351 nm) is present in marine DOM, but absent in the terrestrial material. The effects of copper on both the intensity and shape of the synchronous-scan fluorescence spectra and this technique s potential use as a tracer are discussed.A fluorescência de substâncias húmicas de origem terrestre foi investigada através da técnica de fluorescência sincronizada, e as amostras mostraram duas bandas principais (lex/lem 380/398, 440/458 nm) quando analisadas sem adição do metal paramagnético cobre. Uma terceira banda (lex/lem 502/520 nm) foi detectada após severa extinção de fluorescência da segunda banda causada pela adição de cobre. Uma outra banda, mais energética (lex/lem 333/351 nm) foi detectada em amostras marinhas, porém ausente do material de origem terrestre. Os efeitos de cobre sobre a intensidade e forma do espectro de fluorescência sincronizado e a utilização desta técnica como marcadores são discutidas.339342Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq