A laboratory study of the transfer of U-234 and U-238 during water-rock interactions in the Carnmenellis granite (Cornwall, England) and implications for the interpretation of field data

Laboratory time-scale experiments were conducted on gravels from the Carnmenellis granite, Cornwall, England, with the purpose of evaluating the release of natural uranium isotopes to the water phase. The implications of these results for the production of enhanced U-234/U-238 activity ratios in Cornish groundwaters are discussed. It is suggested that the U-234/U-238 lab data can be used to interpret activity ratios from Cornwall, even when the observed inverse relationship between dissolved U and U-234/U-238 in leachates/etchates is taken into account. (C) 2001 Elsevier B.V. Ltd. All rights reserved.

Dissolved radioelements in (oil) water wells in Parana basin, Brazil

This paper describes the results of a study on groundwaters from Tubarao Group at the Parana sedimentary basin, São Paulo State, Brazil. The purpose of this study was to integrate chemical and U-isotopes data in order to evaluate the models for quantifying different relative volumes of mixing waters in a resultant water. Despite it was possible to generate a typical triangle involving U-238 and its daughter U-234, the U-isotopes model failed to interpret the major hydrochemical facies observed in the studied localities.

Radon in groundwaters from Guarany aquifer, South America: environmental and exploration implications

Groundwater and sandstone samples were analyzed for radon in Guarany aquifer, Parana sedimentary basin, South America. The dissolved radon ranged between 3 and 3303 pCi/l, being lognormally distributed, with a modal value of 1315 pCi/l, and a median value of 330 pCi/l. Rn-222 leakage experiments for sandstones yielded a theoretical value of 1390 pCi/l for Rn-222 in water, showing that theoretical modeling can reliably be used to interpret laboratory and field data. (C) 2002 Elsevier B.V. Ltd. All rights reserved.

Hydrochemical relationships in groundwater from central São Paulo State, Brazil

Groundwater samples from different aquifers occurring at center/northeast portion of São Paulo State, Brazil, were collected and chemically analyzed. The waters leaching Mesozoic sediments are generally more acid (pH(average) = 5.9) and have lower values for total dissolved solids (TDSaverage = 105 mg/L) than those obtained for waters leaching Paleozoic sediments of Tubarao Group. First-degree trend surfaces revealed that the deeper tubular wells occur towards east/southeast and exploit Paleozoic sediments as well fractured/fissured diabases/basalts, whereas the tubular wells in the west/northwest region are shallower. Piper diagrams indicated that the majority of the waters are a blend of waters from different lithologies. Significant correlations were found among nitrate, chloride and bicarbonate, suggesting the occurrence of some anthropogenic inputs, whereas elevated alpha activity of geogenic Ra-226 indicated the need of a broad radiometric survey in the area.

The use of U-isotopes on the study of a weathered cover in Parana basin, Brazil

This paper describes the results of a study involving the sampling of a soil profile developed over sandstone from Itarare Sub-Group at the Parana sedimentary basin, Brazil. It was carried out to integrate chemical and U-isotopes data in order to improve the knowledge of the weathering processes acting in the area. U-238 and its daughter U-234 proved to be important tools for evaluating physical and chemical alteration, allowing to suggest a possible timescale for the development of the more superficial soil horizons.

Hidrogeoquímica do aqüífero guarani na área urbana de ribeirão preto (SP)

This work evaluated the hydrogeochemistry of the Guarani Aquifer in the urban area of Ribeirão Preto, São Paulo State. Thirty one sampling points were established and it was carried out field campaigns in 7 and 8 July 2005, analyzing the following parameters: conductivity, temperature, pH, turbidity, color, dry residue, dissolved oxygen, Ca2+, Mg2+, Na+, K+, Fe3+, Al3+, HCO3-, SO42-, PO43-, NO3-, Cl- and F-. The results indicated that the groundwaters in the urban area of Ribeirão Preto pH possess slightly acid, low conductivity, turbidity, color and dissolved oxygen inside the limits established for drinking waters. The ionic composition indicated that the groundwaters have low cations and anions concentration, being they classified as soft water and calcium-bicarbonated. Statistical tests suggested that conductivity and pH are controlled for the calcite dissolution (CaCO3) during the water/rock interaction process. Besides, it is possible to conclude that the high NO3- and PO43- concentrations found in the groundwater in the urban area of Ribeirão Preto are originated due to anthropogenic activities.

A comparative study of aquifer systems occurring at the Paraná sedimentary basin, Brazil: U-isotopes contribution

The radioactivity due to 238U and 234U in three aquifer systems occurring within the Paraná sedimentary basin, South America, has been investigated. Uranium is much less dissolved from fractured igneous rocks than from the porous sedimentary rocks as indicated by the U-mobility coefficients between 7. 6 × 10-6 and 1. 2 × 10-3 g cm-3. These values are also compatible with the U preference ratios relative to Na, K, Ca, Mg and SiO2, which showed that U is never preferentially mobilized in the liquid phase during the flow occurring in cracks, fissures, fractures and faults of the igneous basaltic rocks. Experimental dissolution of diabase grains on a time-scale laboratory has demonstrated that the U dissolution appeared to be a two-stage process characterized by linear and second-order kinetics. The U dissolution rate was 8 × 10-16 mol m-2 s-1 that is within the range of 4 × 10-16-3 × 10-14 mol m-2 s-1 estimated for other rock types. The 234U/238U activity ratio of dissolved U in solutions was higher than unity, a typical result expected during the water-rock interactions when preferential 234U-leach from the rock surfaces takes place. Some U-isotopes data allowed estimating 320 ka for the groundwater residence time in a sector of a transect in São Paulo State. A modeling has been also realized considering all U-isotopes data obtained in Bauru (35 samples), Serra Geral (16 samples) and Guarani (29 samples) aquifers. The results indicated that the Bauru aquifer waters may result from the admixture of waters from Guarani (1. 5 %) and Serra Geral (98. 5 %) aquifers. © 2012 Springer-Verlag.

Radon emissions related to the granitic Precambrian shield in southern Brazil

The equivalent uranium (eU) activity concentration was analysed in selected granite samples at several sites in Porto Alegre, Southern Brazil, to obtain information on the radon (222Rn) generation by the aquifer rock matrices. Radon analyses of ground water and soil samples were also performed. Several samples exhibited a dissolved 222Rn activity concentration exceeding the World Health Organization maximum limit of 100 Bq l-1. The dissolved radon content in ground waters from the Fractured Precambrian Aquifer System exhibited a direct significant correlation with the eU in the rock matrices, which is a typical result of water-rock interactions. Variation in the soil's porosity was confirmed as an important factor for 222Rn release, as expected, due to its gaseous nature. Thus, although the calcic-alkaline to alkaline Precambrian granitoid rocks of the study area are important reservoirs for underground resources, they can release high amounts of radon gas into the liquid phase. © 2013 Copyright Taylor and Francis Group, LLC.

Hidrogeoquímica do aquífero Bauru na área urbana do município de Marília (SP)

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)

Hidrogeoquímica do aquífero Adamantina na área urbana do município de Bauru/SP

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)

Influências naturais e antrópicas na qualidade da água subterrânea de poços de abastecimento público na área urbana de Marília (SP)

This work evaluated the natural and anthropogenic influences on the quality of groundwater from public supply wells in the urban area of Marília, São Paulo State. Sixteen sampling points were established in the Adamantina Aquifer, Bauru Aquifer System, analyzing the following parameters: electrical conductivity, temperature, pH, total suspended solids, HCO3 - , PO4 3-, SO4 2-, Cl- , F- , N-NO3 - , Ca2+, Na+ , K+ , Mg2+, Si4+, Fe3+ and Al3+. The results indicated that the groundwater in the urban area of Marília has a slightly acid pH and low conductivity, with the ionic composition presenting a low cation and anion concentration and is classified as soft water and calciumbicarbonated water. Natural sources of elements/compounds can be attributed to the dissolution of carbonates during the water/rock interaction, controlling pH, alkalinity and electrical conductivity, and hydrolysis of other mineral constituents of sedimentary rocks from Adamantina Formation, with the exception of quartz. High concentrations of N-NO3 - found in some public supply wells in urban Marilia were due to sewage.

Study of water and dimethylformamide interaction by computer simulation

Monte Carlo simulations of water-dimethylformamide (DMF) mixtures were performed in the isothermal and isobaric ensemble at 298.15 K and 1 atm. The intermolecular interaction energy was calculated using the classical 6-12 Lennard-Jones pairwise potential plus a Coulomb term. The TIP4P model was used for simulating water molecules, and a six-site model previously optimised by us was used to represent DMF. The potential energy for the water-DMF interaction was obtained via standard geometric combining rules using the original potential parameters for the pure liquids. The radial distribution functions calculated for water-DMF mixtures show well characterised hydrogen bonds between the oxygen site of DMF and hydrogen of water. A structureless correlation curve was observed for the interaction between the hydrogen site of the carbonyl group and the oxygen site of water. Hydration effects on the stabilisation of the DMF molecule in aqueous solution have been investigated using statistical perturbation theory. The results show that energetic changes involved in the hydration process are not strong enough to stabilise another configuration of DMF than the planar one.

Interaction between the septal area and the subfornical organ in the control of water intake induced by thirst-eliciting procedures

Rats bearing lesions in the septal area followed by lesions in the subfornical organ were submitted to various thirst-eliciting procedures. The rats with hyperdipsia induced by lesions of the septal area drank more water than either during the control period or after lesion of the subfornical organ under the same thirst-eliciting or angiotensin-liberating stimuli (polyethyleneglycol, isoproterenol, water deprivation and ligation of the inferior vena cava). The overdrinking elicited by lesions in the septal area was blocked after lesion of the subfornical organ. Neither hypovolemia, nor hypotension or water deprivation could elicit increased water intake in animals whose subfornical organ had been destroyed. Animals with lesions in the subfornical organ showed decreased water intake after cellular dehydration. The results obtained suggest that the subfornical organ acts as a more important structure than the septal area in the regulation of water intake elicited by angiotensin, with two opposite effects: a direct one facilitating water intake, and an indirect one inhibiting the septal area. The septal area has an inhibitory effect on the subfornical organ and on water intake. © 1980.

Theoretical studies of liquids by computer simulations: the water-acetone mixture.

Monte Carlo simulation results for pure liquid acetone and water-acetone mixtures calculated in the isothermal and isobaric (NPT) ensemble at T=298K and p=1.0atm are presented. The TIP4P model was used for water and optimized potential for liquid simulation (OPLS) force field parameters used for acetone. The results obtained for the average configurational energy as a function of the mole fraction are in good accord with experimental data. Energy partitioning and co-ordination numbers results calculated for equimolar water-acetone solution are compared to similar data obtained for other water-organic liquid mixtures. These results show an increase in water-water interaction energy and co-ordination numbers when the interaction between water and organic liquid molecules decrease. Distribution functions for pure liquid acetone and water-acetone mixtures are presented. Dipole-dipole angular correlation functions obtained for pure liquid acetone show a predominance of dimers with parallel alignment of dipole moments. Radial distribution functions from water-acetone interaction show characteristic features of hydrogen bonded liquids. Radial and angular distribution functions for water-water correlation calculated in pure water and in equimolar water-acetone mixture are compared, showing very similar features in both systems. (C) 1999 Elsevier B.V. B.V. All rights reserved.