The aim of this study is to determine the solubility rate of tantalum contained in pyrochlore, columbite-tantalite and columbite in simulant lung fluid. The International Commission on Radiological Protection (ICRP), in its recommendation for limiting intakes of radionuclide by workers, has consistently recognized that the biological behavior of any specific material after incorporation can significantly diverge from model prevision. Model parameters should be adjusted to adapt the model for each specific substance material in order to estimate the dose due to this element intake. The most recent ICRP publication 66, respiratory tract dosimetry model, point out that information as data like particle size, aerosols solubility and the material chemical compounds are important parameters in the dose coefficients calculation. This paper studies the solubility in Simulant Lung Fluid (SLF) of Ta present in mineral dust particles. For this study 3 minerals were selected: pyrochlore, columbite-tantalite and columbite. Tantalum dissolution in vitro samples were obtained using the Gamble solution and PIXE (Particle Induced X-ray Emission) as analytical technique. In order to characterize the worker exposure to Ta bearing particles, one Brazilian niobium mine was selected. The mineral dust particles were collected using a six-stage cascade impactor and the elemental mass concentrations and the MMAD (Mass Median Aerodynamic Diameter) were determined. Concentrations of radionuclides from natural series of thorium and uranium were also determined. The results show that the workers are exposed to Ta bearing particles in the respirable fraction of aerosols (aerodynamic diameter (d aer) <2.5 μm) during the mineral processing to obtain Fe-Nb alloy. The solubility in Simulant Lung Fluid (SLF) of Ta present in mineral dust particles depends on the mineral characteristics. The solubility half-time varies between 34 and 62 h depending on the associated mineral.

Sewage sludge is a cost-effective media for the production of Bacillus thuringiensis (Bt) based biopesticides. To enhance the entomotoxicity of the fermentation broth, pretreatments of sewage sludge by alkali and ultrasonic were applied in this study. Effects of alkaline and ultrasonic pretreatments on the soluble COD (SCOD) and total COD (TCOD) were evaluated by altering the alkali addition dose and the ultrasonic specific energy. Suitable pretreatment conditions were optimized with 5 g l-¹ sodium hydroxide (NaOH) for alkaline treatment and 1.2 x 10⁵ kJ kg-¹ of total solid for ultrasonic treatment. Fermentations of raw and pretreated sludge for biopesticides were carried out in a bench scale fermentor. Results revealed that both pretreatments were effective for Bt growth and metabolism. Higher viable cells (VC) and viable spores (VS) counts, δ-endotoxin yields and entomotoxicity were achieved in the pretreated sludge. The enhancement was attributed to more available nutrients and better oxygen transfer. Moreover, ultrasonic pretreated sludge was superior to alkaline pretreated sludge for δ-endotoxin production and entomotoxicity owing to its higher soluble C/N ratio and finer particles.

We studied the seasonal cycle of the coupling between atmospheric denoxification processes and in-situ daytime formation of gas phase HNO₃ using a photochemical air pollution model. The model is constrained with urban atmospheric boundary layer observations of O₃, NO₂ and NO made in Ciudad Real, central Spain. The highest daytime HNO₃ mixing ratio of 0.3 ppbv was predicted to occur in summer, following a modelled OH concentration peak of ∼1.4 × 10⁶ molecules cm⁻³ and subsequent reaction with NO₂. During winter, calculated values of HNO₃ are lower due to less incoming radiation and higher wet removal of atmospheric HNO₃. The predicted mixing ratios are in good agreement with observations of atmospheric HNO₃ at similar urban environments in central Spain. Additionally, a marked seasonal cycle is predicted with minimum HNO₃ concentrations occurring in winter, indicative that traffic emissions and photochemistry dominate the in-situ formation of gas phase HNO₃ at this location. This process has implications in the removal of NOₓ from the urban atmosphere.

Lake Victoria and its basin supports more than 30 million people, while its fishes are exported the world over. This second largest fresh water body is however experiencing stress due to eutrophication, sedimentation, declining levels and more recently the motor vehicle sector. This contribution examines the general pollution from motor vehicle and gives an in-depth analysis of motor vehicle washing along the lakeshore. The results indicate the water samples from the motor vehicle washing and urban runoff points to be slightly acidic (i.e., average pH of 6.7) and average Total Phosphorus levels of 0.4 and 2.4 ppm respectively. This implies that there was high soap input at these points. The conductivity for the motor vehicle washing points averaged at 150 μS/cm, while the urban runoffs point was more varied ranging from below 150 μS/cm to over 400 μS/cm (average 301 μS/cm). A positive correlation coefficient of more than 0.7 is obtained between the total daily count of vehicles and each of the water quality parameter tested. This signifies a strong correlation between motor vehicle related activities and the pollution of the lake. In general, the motor vehicle industry is found to have a noticeable negative effect on the Lake.

In principle, conventional lysimeters are suitable for the investigation of vertical water and solute fluxes. Lateral fluxes in water-saturated fen sites are characterized by heterogeneities and abnormities due to anisotropic layering. But due to lack of adequate monitoring techniques, these fluxes have been insufficiently analyzed. The newly developed large weighable fen lysimeter (LWFL) overcomes the limitations of conventional lysimetry and enables the measurement of vertical and horizontal transport processes in undisturbed large volume soil monoliths. The LWFL has a volume of 6 m³ (4 m length, 1 m width and 1.5 m depth) and was tested by filling the lysimeter with an undisturbed fen monolith. A special extraction procedure for the horizontal sliding of the lysimeter vessel through the natural fen was developed. In front of the vessel a converted cutting tool assisted in carving the soil monolith out of the peat, both vertically and horizontally. Inlet and outlet of the LWFL was constructed to allow the adjustment of a wide range of hydraulic gradients to depict natural occurring lateral transport processes. The LWFL including the measurement techniques was tested successfully for 3 years. On the basis of these tests, we conclude that complex physical and biogeochemical research problems involving lateral flows can be tackled now with multiphase observations and measurements at high spatial and temporal resolution, transdisciplinary data evaluation and numerical modelling approaches.

This study qualifies and quantifies the effects of pH, hardness, alkalinity, salinity and bone calcination temperature related with the adsorption of As(V) onto biogenic hydroxyapatite (HAPb) obtained from cow-charred bones. Arsenic contamination of surface and subsurface waters is widely extended in Argentina. It is a problem of major concern, particularly in rural and suburban areas where there are not water treatment plants for supplying of drinking water. HAPb is a natural material, whose absorbent properties can be used for the design of low-cost technologies for As(V) abatement in water. In this work HAPb has been characterized by physical and chemical analysis (XRD, SEM, EDAX, BET, and electrophoretic mobility). A Plackett–Burman screening experimental design allowed us to determine the main variables affecting the efficiency of As(V) sorption onto HAPb. Based on these variables and with a design of higher order we developed a model of the system to study its behaviour. Data collection was planned through a Doehlert experimental design and a back propagation artificial neural network was used to work it out. Results showed that salinity is the major variable affecting the efficiency of the As(V) immobilization process but pH and hardness should be taken into account because of associations among them.

The quantification of arsenic biovolatilization by microscopic filamentous fungi Aspergillus clavatus, A. niger, Trichoderma viride and Penicillium glabrum under laboratory conditions is discussed in this article. The fungi were cultivated on a liquid medium enriched with inorganic arsenic in pentavalent form (H₃AsO₄). Filamentous fungi volatilized 0.010 mg to 0.067 mg and 0.093 mg to 0.262 mg of arsenic from cultivation systems enriched with 0.25 mg (5 mg.l-¹ of arsenic in culture media) and 1.00 mg of arsenic (20 mg.l-¹ of arsenic in culture media), respectively. These results represent the loss of arsenic after a 30-day cultivation from cultivation systems. The production of volatile arsenic derivatives by the A. niger and A. clavatus strains was also determined by hourly sorption using the sorbent Anasorb (CSC) on the 29th day of cultivation.

During the period from July 2002 to June 2004, the chemical characteristics of the rainwater samples collected in downtown São Paulo were investigated. The analysis of 224 wet-only precipitation samples included pH and electrical conductivity, as well as major ions (Na⁺, [graphic removed] , K⁺, Ca²⁺, Mg²⁺, Cl-, [graphic removed] , [graphic removed] ) and carboxylic acids (acetic, formic and oxalic) using ion chromatography. The volume weighted mean, VWM, of the anions [graphic removed] , [graphic removed] and Cl- was, respectively, 20.3, 12.1 and 10.7 μmol l-¹. Rainwater in São Paulo was acidic, with 55% of the samples exhibiting a pH below 5.6. The VWM of the free H⁺ was 6.27 μmol l-¹), corresponding to a pH of 5.20. Ammonia (NH₃), determined as [graphic removed] (VWM = 32.8 μmol l-¹), was the main acidity neutralizing agent. Considering that the H⁺ ion is the only counter ion produced from the non-sea-salt fraction of the dissociated anions, the contribution of each anion to the free acidity potential has the following profile: [graphic removed] (31.1%), [graphic removed] (26.0%), CH₃COO- (22.0%), Cl- (13.7%), HCOO- (5.4%) and [graphic removed] (1.8%). The precipitation chemistry showed seasonal differences, with higher concentrations of ammonium and calcium during autumn and winter (dry period). The marine contribution was not significant, while the direct vehicular emission showed to be relevant in the ionic composition of precipitation.

European critical loads and novel dynamic modelling data have been compiled under the LRTAP Convention by the Coordination Centre for Effects. In 2000 9.8% of the pan-European and 20.8% of the EU25 ecosystem area were at risk of acidification. For eutrophication (nutrient N) the areas at risk were 30.1 and 71.2%, respectively. Dynamic modelling results reveal that 95% of the area at risk of acidification could recover by 2030 provided acid deposition is reduced according to present legislation. Insight into the timing of effects of exceedances of critical loads for nutrient N necessitates the further development of dynamic models.

In this study critical load functions and target load functions of nitrogen and sulphur deposition with respect to acidity and minimum base cation to aluminium ratio were calculated with the SAFE model using three different averaging strategies: (1) averaging based on current forest generation, (2) averaging based on next generation and (3) averaging based on the entire simulation period. From the results it is evident that although target load calculation and indeed critical load calculation is straight forward, there is a problem in translating a predicted recovery according to the target load calculation back to a site-specific condition. We conclude that a policy strategy for emission reductions that ensures recovery, according to calculated target load functions, is likely to be beneficial from an ecosystem point of view. However, such a strategy may not be sufficient to achieve actual non-violation of the chemical criteria throughout the seasonal or rotational variations. To address this issue we propose a method for calculating dynamic critical loads which ensures that the chosen criteria is not violated.