Oxidative co-treatment using hydrogen peroxide with anaerobic digestion of excess municipal sludge.

The effect of an oxidative co-treatment on anaerobic digestion of a mixture of primary and waste activated sludge was investigated. The oxidant used in this study was hydrogen peroxide (H2O2). A maximum improvement in solid destruction of 15.2% was achieved in the overall process, with a dosage of 2.0 g H2O2/g influent volatile suspended solids (VSS(influent)). All configurations operated at this dosage also showed statistically significant increases in solids removal. A statistically significant enhancement in overall solids destruction was observed for the lower oxidant dosage (0.5 H2O2/g VSS(influent)). Surprisingly, for 1.0 g H2O2/g VSS(influent), only one of the three configurations involving oxidative co-treatment showed significant increases in solids destruction. Special attention was paid to the performance of this process relative to fecal coliforms destruction. Class A biosolids were obtained for all the different hydrogen peroxide dosages used when oxidative co-treatment is combined with a two-stage anaerobic digestion process.     

Biosorption of Reactive Black 5 from aqueous solutions by chitosan: Column studies

Fixed-bed column studies were carried out to investigate the dynamic sorption of Reactive Black 5 (RB5) onto chitosan. The effect of operating parameters such as initial dye concentration, superficial flow velocity, bed height and particle size on the sorption of RB5 onto chitosan was studied. Column regeneration, dye recovery and the possibility of reusing the regenerated chitosan were also investigated. The results show that both the breakthrough curves and the adsorption parameters of the column were strongly affected by the operating parameters studied. An analysis of the breakthrough curves indicated that adsorption was affected by mass transfer limitations, probably due to intraparticle diffusion. An empirical model was applied to describe the breakthrough curves, while the Bohart–Adams and BDST models were used to determine the operating parameters useful in the process design. Elution of the column with 0.01 mol L^?1 NaOH allowed the chitosan to be regenerated and the dye to be recovered and concentrated. The concentration factor was 10. Several cycles of adsorption–elution showed that the regenerated chitosan retained good adsorption efficiency and the elution efficiency was always higher than 80%.     

Validation of a multiclass multiresidue method and monitoring results for 210 pesticides in fruits and vegetables by gas chromatography-triple quadrupole mass spectrometry

A rapid, sensitive, accurate and reliable multiresidue method for the identification and quantification of 210 relevant pesticides in four representative fruit and vegetable commodities (tomato, potato, spring onion and orange) has been developed and validated by gas chromatography in tandem with triple quadrupole mass spectrometry. The method has been fully validated and applied to 292 samples from different countries. Prior to instrumental analysis, an extraction procedure based on a sample extraction of multiclass analytes, using the ethyl acetate method was employed. Mass spectrometric conditions were individually optimized for each compound in the selected reaction monitoring (SRM) mode to achieve maximum sensitivity. The pesticides were separated in less than 25 min. This was followed by an exhaustive control of the retention times. The Retention Time Locking Method was applied, working at a constant pressure throughout the analysis. System maintenance was reduced by using a purged capillary flow device that provided backflush capabilities by reversing column flow immediately after elution of the last compound of interest. Istotopically labelled internal standards were employed to improve the quality of the analytical results.     

Mercury, lead and cadmium in human milk in relation to diet, lifestyle habits and sociodemographic variables in Madrid (Spain)

Background

Although breastfeeding is the ideal way of nurturing infants, it can be a source of exposure to toxicants. This study reports the concentration of Hg, Pb and Cd in breast milk from a sample of women drawn from the general population of the Madrid Region, and explores the association between metal levels and socio-demographic factors, lifestyle habits, diet and environmental exposures, including tobacco smoke, exposure at home and occupational exposures.

Methods

Breast milk was obtained from 100 women (20 mL) at around the third week postpartum. Pb, Cd and Hg levels were determined using Atomic Absorption Spectrometry. Metal levels were log-transformed due to non-normal distribution. Their association with the variables collected by questionnaire was assessed using linear regression models. Separate models were fitted for Hg, Pb and Cd, using univariate linear regression in a first step. Secondly, multivariate linear regression models were adjusted introducing potential confounders specific for each metal. Finally, a test for trend was performed in order to evaluate possible dose-response relationships between metal levels and changes in variables categories.

Results

Geometric mean Hg, Pb and Cd content in milk were 0.53 μg L⁻¹, 15.56 μg L⁻¹, and 1.31 μg L⁻¹, respectively. Decreases in Hg levels in older women and in those with a previous history of pregnancies and lactations suggested clearance of this metal over lifetime, though differences were not statistically significant, probably due to limited sample size. Lead concentrations increased with greater exposure to motor vehicle traffic and higher potato consumption. Increased Cd levels were associated with type of lactation and tended to increase with tobacco smoking.

Conclusions

Surveillance for the presence of heavy metals in human milk is needed. Smoking and dietary habits are the main factors linked to heavy metal levels in breast milk. Our results reinforce the need to strengthen national food safety programs and to further promote avoidance of unhealthy behaviors such as smoking during pregnancy.     

Coupled hydromechanical modeling of CO2 sequestration in deep saline aquifers

Sequestration of carbon dioxide (CO₂) in deep saline aquifers has emerged as an option for reducing greenhouse gas emissions to the atmosphere. The large amounts of supercritical CO₂ that need to be injected into deep saline aquifers may cause large fluid pressure increases. The resulting overpressure may promote reactivation of sealed fractures or the creation of new ones in the caprock seal. This could lead to escape routes for CO₂. In order to assess the probability of such an event, we model an axisymmetric horizontal aquifer–caprock system, including hydromechanical coupling. We study the failure mechanisms, using a viscoplastic approach. Simulations illustrate that, depending on boundary conditions, the least favorable moment takes place at the beginning of injection. Initially, fluid pressure rises sharply because of a reduction in permeability due to desaturation. Once CO₂ fills the pores in the vicinity of the injection well and a capillary fringe is fully developed, the less viscous CO₂ displaces the brine and the capillary fringe laterally. The overpressure caused by the permeability reduction within the capillary fringe due to desaturation decreases with distance from the injection well. This results in a drop in fluid pressure buildup with time, which leads to a safer situation. Nevertheless, in the presence of low-permeability boundaries, fluid pressure continues to rise in the whole aquifer. This occurs when the radius of influence of the injection reaches the outer boundary. Thus, caprock integrity might be compromised in the long term.