A literature survey on the dissolution mechanism of spent fuel under disposal conditions

International Nuclear Information System (INIS)

Ollila, Kaija

1989-06-01

In Finland spent nuclear fuel is planned to be disposed of at large depths in crystalline bedrock. As part of the YJT (Nuclear Waste Commission of Finnish Power Companies) - program, the solubiliy and dissolution mechanisms of unirradiated UO 2 are experimentally investigated as a function of groundwater conditions. This study is a literature survey on the leaching and dissolution studies carried out with spent fuel. It consists first a review on characterization studies of spent fuel. Then the solubilities and release mechanisms of the radionuclides from spent fuel in granitic or related groundwaters are discussed, including the dissolution of UO 2 matrix, and the leaching of fission products and actinides. Lastly approaches to modelling the dissolution of spent fuel are shortly discussed

Hydrogeochemistry and isotope geochemistry of Velenje Basin groundwater

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Tjaša Kanduč

2016-08-01

Full Text Available The geochemical and isotopic composition of groundwater in the Velenje Basin, Slovenia, was investigated between the years 2014 to 2015 to identify the geochemical processes in the major aquifers (Pliocene and Triassic and the water–rock interactions. Thirty-eight samples of groundwater were taken from the aquifers, 19 in the mine and 19 from the surface. Groundwater in the Triassic aquifer is dominated by HCO3–, Ca2+ and Mg2+ with δ13C DIC values in the range from -19.3 to -2.8 ‰, indicating degradation of soil organic matter and dissolution of carbonate minerals. In contrast, groundwater in the Pliocene aquifers is enriched in Mg2+, Na+, Ca2+, K+, and Si, and has high alkalinity, with δ13CDIC values in the range of -14.4 to +4.6 ‰. Based on the δ13CDIC values in all the aquifers (Pliocene and Triassic, both processes inflence the dissolution of carbonate minerals and dissolution of organic matter and in the Pliocene aquifers, methanogenesis as well. Based on Principal Component Analysis (PCA, and on geochemical and isotopic data we conclude that the following types of groundwater in Velenje Basin are present: Triassic aquifers with higher pH and lower conductivity and chloride, Pliocene, Pliocene 1 and Pliocene 2 aquifers with lower pH and higher conductivity and chloride contents, and Pliocene 3 and Pliocene 2, 3 aquifers with the highest pH values and lowest conductivities and chloride contents. 87Sr/86Sr tracer was used for the fist time in Slovenia to determine geochemical processes (dissolution of silicate versus carbonate fraction in Velenje Basin groundwater of different aquifers dewatering Pliocene and Triassic strata. 87Sr/86Sr values range from 0.70820 to 0.71056 in groundwater of Pliocene aquifers and from 0.70808 to 0.70910 in groundwater of the Triassic aquifer. This indicates that dissolution of the carbonate fraction prevails in both aquifers, while in Pliocene aquifers, an additional silicate weathering prevails with

Dissolution of UO2 in redox conditions

International Nuclear Information System (INIS)

Casas, I.; Pablo de, J.; Rovira, M.

1998-01-01

The performance assessment of the final disposal of the spent nuclear fuel in geological formations is strongly dependent on the spent fuel matrix dissolution. Unirradiated uranium (IV) dioxide has shown to be very useful for such purposes. The stability of UO 2 is very dependent on vault redox conditions. At reducing conditions, which are expected in deep groundwaters, the dissolution of the UO 2 -matrix can be explained in terms of solubility, while under oxidizing conditions, the UO 2 is thermodynamically unstable and the dissolution is kinetically controlled. In this report the parameters which affect the uranium solubility under reducing conditions, basically pH and redox potential are discussed. Under oxidizing conditions, UO 2 dissolution rate equations as a function of pH, carbonate concentration and oxidant concentration are reported. Dissolution experiments performed with spent fuel are also reviewed. The experimental equations presented in this work, have been used to model independent dissolution experiments performed with both unirradiated and irradiated UO 2 . (Author)

Waste dissolution with chemical reaction, diffusion and advection

International Nuclear Information System (INIS)

Chambre, P.L.; Kang, C.H.; Lee, W.W.L.; Pigford, T.H.

1987-06-01

This paper extends the mass-transfer analysis to include the effect of advective transport in predicting the steady-state dissolution rate, with a chemical-reaction-rate boundary condition at the surface of a waste form of arbitrary shape. This new theory provides an analytic means of predicting the ground-water velocities at which dissolution rate in a geologic environment will be governed entirely to the chemical reaction rate. As an illustration, we consider the steady-state potential flow of ground water in porous rock surrounding a spherical waste solid. 3 refs., 2 figs

The dissolution of unirradiated UO2 fuel pellets under simulated disposal conditions

International Nuclear Information System (INIS)

Ollila, K.; Leino-Forsman, H.

1993-03-01

The dissolution behaviour of unirradiated UO 2 pellets was studied as a function of water composition under oxidizing and reducing conditions at 25 deg C. The waters included deionized water as the reference water, sodium bicarbonate solutions with varying bicarbonate content, and two different synthetic groundwaters. The release of uranium was measured during static batch dissolution experiments of long duration (3-4 years)

Composition and Dissolution of a Migratory, Weathered Coal Tar Creosote DNAPL

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Kerstin E. Scherr

2016-09-01

Full Text Available Opaque, viscous tars derived from the carbonization of fossile carbon feedstocks, such coal tars and creosote, are long-term sources of groundwater contamination, predominantly with poly- and heterocyclic aromatic hydrocarbons (PAH. The dissolution, ageing and migratory behavior of dense, non aqueous phase liquid (DNAPL coal tar blobs and pools forming at the aquitard is not sufficiently understood to estimate the risk and adequately design groundwater treatment measures at a contaminated site. In this study, we investigate the composition and dissolution of a migrated, aged creosote DNAPL and corresponding experimental and groundwater profiles using comprehensive two-dimensional gas chromatography (GCxGC-MS. GC-FID unresolved compounds were attributed to methylated homocyclic species using GCxGC-MS in the Methylanthracene weight range. Equilibrium concentrations were estimated using Raoult’s law, assuming non-ideal behavior. Low molecular weight compounds were found to be prevalent even after decades of weathering, with Naphthalene (8% by mass representing the most abundant identified compound, contrary to the expected preferential depletion of hydrophilic compounds. Morevoer, dimethylnaphthalenes were relatively more abundant in the aqueous boundary layer than in the DNAPL. DNAPL migration over 400m with the groundwater flow effected lower viscosity and specific gravity of the migrated phase body in a superposition of weathering, transport and aquifer chromatography effects. Based on a decomposition of analysed and estimated constituents using the group contribution approach, reference DNAPL values for activity coefficients γi were used to model aqueous solubilities for selected compounds. Anthracene was close to its theoretical precipitation limit in the bulk DNAPL. While laboratory and modelled DNAPL dissolution behavior agree well, field data imply the presence of specific interfacial in situ processes significantly impacting dissolution

Factors affecting the differences in reactivity and dissolution rates between UO2 and spent nuclear fuel

International Nuclear Information System (INIS)

Shoesmith, D.W.; Tait, J.C.; Sunder, S.; Steward, S.; Russo, R.E.; Rudnicki, J.D.

1996-08-01

Strategies for the permanent disposal of spent nuclear fuel are being investigated by the U.S. Department of Energy at the Yucca Mountain site and by Atomic Energy of Canada Limited (AECL) in plutonic rock formations in the Canadian Shield. Uranium dioxide is the primary constituent of spent nuclear fuel and dissolution of the matrix is regarded as a necessary step for the release of radionuclides to repository groundwaters. In order to develop models to describe the dissolution of the U0 2 fuel matrix and subsequent release of radionuclides, it is necessary to understand both chemical and oxidative dissolution processes and how they can be affected by parameters such as groundwater composition, pH, temperature, surface area, radiolysis and redox potential. This report summarizes both published and on-going dissolution studies of U0 2 and both LWR and CANDU spent fuels being conducted at the Pacific Northwest Laboratory, Lawrence Livermore National Laboratory and Lawrence Berkeley Laboratory in the U.S. and at AECL's Whiteshell Laboratories in Canada. The studies include both dissolution tests and electrochemical experiments to measure uranium dissolution rates. The report focuses on identifying differences in reactivity towards aqueous dissolution between U0 2 and spent fuel samples as well as estimating bounding values for uranium dissolution rates. This review also outlines the basic tenets for the development of a dissolution model that is based on electrochemical principles. (author). 49 refs., 2 tabs., 11 figs

A multiphase interfacial model for the dissolution of spent nuclear fuel

Energy Technology Data Exchange (ETDEWEB)

Jerden, James L., E-mail: jerden@anl.gov [Argonne National Laboratory, 9700 South Cass Ave., Argonne, IL 60439 (United States); Frey, Kurt [University of Notre Dame, Notre Dame, IN 46556 (United States); Ebert, William [Argonne National Laboratory, 9700 South Cass Ave., Argonne, IL 60439 (United States)

2015-07-15

Highlights: • This model accounts for chemistry, temperature, radiolysis, U(VI) minerals, and hydrogen effect. • The hydrogen effect dominates processes determining spent fuel dissolution rate. • The hydrogen effect protects uranium oxide spent fuel from oxidative dissolution. - Abstract: The Fuel Matrix Dissolution Model (FMDM) is an electrochemical reaction/diffusion model for the dissolution of spent uranium oxide fuel. The model was developed to provide radionuclide source terms for use in performance assessment calculations for various types of geologic repositories. It is based on mixed potential theory and consists of a two-phase fuel surface made up of UO{sub 2} and a noble metal bearing fission product phase in contact with groundwater. The corrosion potential at the surface of the dissolving fuel is calculated by balancing cathodic and anodic reactions occurring at the solution interfaces with UO{sub 2} and NMP surfaces. Dissolved oxygen and hydrogen peroxide generated by radiolysis of the groundwater are the major oxidizing agents that promote fuel dissolution. Several reactions occurring on noble metal alloy surfaces are electrically coupled to the UO{sub 2} and can catalyze or inhibit oxidative dissolution of the fuel. The most important of these is the oxidation of hydrogen, which counteracts the effects of oxidants (primarily H{sub 2}O{sub 2} and O{sub 2}). Inclusion of this reaction greatly decreases the oxidation of U(IV) and slows fuel dissolution significantly. In addition to radiolytic hydrogen, large quantities of hydrogen can be produced by the anoxic corrosion of steel structures within and near the fuel waste package. The model accurately predicts key experimental trends seen in literature data, the most important being the dramatic depression of the fuel dissolution rate by the presence of dissolved hydrogen at even relatively low concentrations (e.g., less than 1 mM). This hydrogen effect counteracts oxidation reactions and can limit

Dissolution rates of DWPF glasses from long-term PCT

International Nuclear Information System (INIS)

Ebert, W.L.; Tam, S.W.

1996-01-01

We have characterized the corrosion behavior of several Defense Waste Processing Facility (DWPF) reference waste glasses by conducting static dissolution tests with crushed glasses. Glass dissolution rates were calculated from measured B concentrations in tests conducted for up to five years. The dissolution rates of all glasses increased significantly after certain alteration phases precipitated. Calculation of the dissolution rates was complicated by the decrease in the available surface area as the glass dissolves. We took the loss of surface area into account by modeling the particles to be spheres, then extracting from the short-term test results the dissolution rate corresponding to a linear decrease in the radius of spherical particles. The measured extent of dissolution in tests conducted for longer times was less than predicted with this linear dissolution model. This indicates that advanced stages of corrosion are affected by another process besides dissolution, which we believe to be associated with a decrease in the precipitation rate of the alteration phases. These results show that the dissolution rate measured soon after the formation of certain alteration phases provides an upper limit for the long-term dissolution rate, and can be used to determine a bounding value for the source term for radionuclide release from waste glasses. The long-term dissolution rates measured in tests at 20,000 per m at 90 degrees C in tuff groundwater at pH values near 12 for the Environmental Assessment glass and glasses made with SRL 131 and SRL 202 frits, respectively

A multiphase interfacial model for the dissolution of spent nuclear fuel

Science.gov (United States)

Jerden, James L.; Frey, Kurt; Ebert, William

2015-07-01

The Fuel Matrix Dissolution Model (FMDM) is an electrochemical reaction/diffusion model for the dissolution of spent uranium oxide fuel. The model was developed to provide radionuclide source terms for use in performance assessment calculations for various types of geologic repositories. It is based on mixed potential theory and consists of a two-phase fuel surface made up of UO2 and a noble metal bearing fission product phase in contact with groundwater. The corrosion potential at the surface of the dissolving fuel is calculated by balancing cathodic and anodic reactions occurring at the solution interfaces with UO2 and NMP surfaces. Dissolved oxygen and hydrogen peroxide generated by radiolysis of the groundwater are the major oxidizing agents that promote fuel dissolution. Several reactions occurring on noble metal alloy surfaces are electrically coupled to the UO2 and can catalyze or inhibit oxidative dissolution of the fuel. The most important of these is the oxidation of hydrogen, which counteracts the effects of oxidants (primarily H2O2 and O2). Inclusion of this reaction greatly decreases the oxidation of U(IV) and slows fuel dissolution significantly. In addition to radiolytic hydrogen, large quantities of hydrogen can be produced by the anoxic corrosion of steel structures within and near the fuel waste package. The model accurately predicts key experimental trends seen in literature data, the most important being the dramatic depression of the fuel dissolution rate by the presence of dissolved hydrogen at even relatively low concentrations (e.g., less than 1 mM). This hydrogen effect counteracts oxidation reactions and can limit fuel degradation to chemical dissolution, which results in radionuclide source term values that are four or five orders of magnitude lower than when oxidative dissolution processes are operative. This paper presents the scientific basis of the model, the approach for modeling used fuel in a disposal system, and preliminary

Groundwater fluoride contamination: A reappraisal

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Amlan Banerjee

2015-03-01

Full Text Available Dissolution of fluorite (CaF2 and/or fluorapatite (FAP [Ca5(PO43F], pulled by calcite precipitation, is thought to be the dominant mechanism responsible for groundwater fluoride (F− contamination. Here, one dimensional reactive–transport models are developed to test this mechanism using the published dissolution and precipitation rate kinetics for the mineral pair FAP and calcite. Simulation results correctly show positive correlation between the aqueous concentrations of F− and CO32− and negative correlation between F− and Ca2+. Results also show that precipitation of calcite, contrary to the present understanding, slows down the FAP dissolution by 106 orders of magnitude compared to the FAP dissolution by hydrolysis. For appreciable amount of fluoride contamination rock–water interaction time must be long and of order 106 years.

Groundwater evolution of the granite area, Korea

International Nuclear Information System (INIS)

Kim, C.S.; Bae, D.S.; Koh, Y.K.; Kim, K.S.; Kim, G.Y.

2001-01-01

The geochemistry and environmental isotopes of groundwater in the Cretaceous granite of the Yeongcheon area has been investigated. The hydrochemistry of groundwater belongs to the Ca-HCO 3 type. The oxygen-18 and deuterium data are clustered along the meteoric water line, indicating that the groundwater is of meteoric water origin. Tritium data show that the groundwaters were mostly recharged before pre-thermonuclear period and have been mixed with younger surface water flowing rapidly along fractured zones. Based on the mass balance and reaction simulation approaches using both the hydrochemistry of groundwater and the secondary mineralogy of fracture-filling materials, the low-temperature hydrogeochemical evolution of groundwater in the area has been modeled. The results of geochemical simulation show that the concentrations of Ca, Na and HCO 3 and pH of waters increase progressively owing to the dissolution of reactive minerals in flow paths. The concentrations of Mg and K first increase with the dissolution of reactant minerals, but later decrease when montmorillonite and illitic material are precipitated respectively. The continuous adding of reactive minerals, i. e. the progressively larger degrees of water/rock interaction, causes the formation of secondary minerals with the following sequence: hematite > gibbsite > kaolinite > montmorillonite > illitic material > microcline. The results of reaction simulation agree well with the observed water chemistry and secondary mineralogy, indicating the successful applicability of this simulation technique to delineate the complex hydrogeochemistry of bedrock groundwaters. (author)

Affinity functions for modeling glass dissolution rates

Energy Technology Data Exchange (ETDEWEB)

Bourcier, W.L. [Lawrence Livermore National Lab., CA (United States)

1997-07-01

Glass dissolution rates decrease dramatically as glass approach ''saturation'' with respect to the leachate solution. Most repository sites are chosen where water fluxes are minimal, and therefore the waste glass is most likely to dissolve under conditions close to ''saturation''. The key term in the rate expression used to predict glass dissolution rates close to ''saturation'' is the affinity term, which accounts for saturation effects on dissolution rates. Interpretations of recent experimental data on the dissolution behaviour of silicate glasses and silicate minerals indicate the following: 1) simple affinity control does not explain the observed dissolution rate for silicate minerals or glasses; 2) dissolution rates can be significantly modified by dissolved cations even under conditions far from saturation where the affinity term is near unity; 3) the effects of dissolved species such as Al and Si on the dissolution rate vary with pH, temperature, and saturation state; and 4) as temperature is increased, the effect of both pH and temperature on glass and mineral dissolution rates decrease, which strongly suggests a switch in rate control from surface reaction-based to diffusion control. Borosilicate glass dissolution models need to be upgraded to account for these recent experimental observations. (A.C.)

Study of groundwater salinization in Chaj Doab using environmental isotopes

International Nuclear Information System (INIS)

Hussain, S.D.; Sajjid, M.I.; Akram, W.; Ahmad, M.; Rafiq, M.

1991-09-01

Environmental isotopes and chemical composition of water have been used to study the origin of groundwater salinity in Chaj Doab. Three important possible processes of salinization i.e. enrichment of salt content of water by evaopration, mixing with connate marine water and dissolution of salts from soil sediments have been investigated. No evidence for mixing with connate maine water could be found. The process of evaporation too does not seem to apply any significant role in salinization of groundwater. The dissolution of salts from soil sediments appears as dominant mechanism for increasing the salt content of water in this area. (author)

Spent fuel dissolution studies FY 1991 to 1994

International Nuclear Information System (INIS)

Gray, W.J.; Wilson, C.N.

1995-12-01

Dissolution and transport as a result of groundwater flow are generally accepted as the primary mechanisms by which radionuclides from spent fuel placed in a geologic repository could be released to the biosphere. To help provide a source term for performance assessment calculations, dissolution studies on spent fuel and unirradiated uranium oxides have been conducted over the past few years at Pacific Northwest National Laboratory (PNNL) in support of the Yucca Mountain Site Characterization Project. This report describes work for fiscal years 1991 through 1994. The objectives of these studies and the associated conclusions, which were based on the limited number of tests conducted so far, are described in the following subsections

Brahmaputra river basin groundwater: Solute distribution, chemical evolution and arsenic occurrences in different geomorphic settings

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Swati Verma

2015-09-01

New hydrological insights for the region: Most groundwater solutes of RCD and YA terrains were derived from both silicate weathering and carbonate dissolution, while silicate weathering process dominates the solute contribution in OA groundwater. Groundwater samples from all terrains are postoxic with mean pe values between Fe(III and As(V–As(III reductive transition. While, reductive dissolution of (Fe–MnOOH is the dominant mechanism of As mobilization in RCD and YA aquifers, As in OA and PD aquifers could be mobilized by combined effect of pH dependent sorption and competitive ion exchange. The present study focuses on the major ion chemistry as well as the chemistry of the redox sensitive solutes of the groundwater in different geomorphic settings and their links to arsenic mobilization in groundwater.

Effect of metallic iron on the oxidative dissolution of UO2 doped with a radioactive alpha emitter in synthetic Callovian-Oxfordian groundwater

Science.gov (United States)

Odorowski, Mélina; Jegou, Christophe; De Windt, Laurent; Broudic, Véronique; Jouan, Gauthier; Peuget, Sylvain; Martin, Christelle

2017-12-01

In the hypothesis of direct disposal of spent fuel in a geological nuclear waste repository, interactions between the fuel mainly composed of UO2 and its environment must be understood. The dissolution rate of the UO2 matrix, which depends on the redox conditions on the fuel surface, will have a major impact on the release of radionuclides into the environment. The reducing conditions expected for a geological disposal situation would appear to be favorable as regards the solubility and stability of the UO2 matrix, but may be disturbed on the surface of irradiated fuel. In particular, the local redox conditions will result from a competition between the radiolysis effects of water under alpha irradiation (simultaneously producing oxidizing species like H2O2, hydrogen peroxide, and reducing species like H2, hydrogen) and those of redox active species from the environment. In particular, Fe2+, a strongly reducing aqueous species coming from the corrosion of the iron canister or from the host rock, could influence the dissolution of the fuel matrix. The effect of iron on the oxidative dissolution of UO2 was thus investigated under the conditions of the French disposal site, a Callovian-Oxfordian clay formation chosen by the French National Radioactive Waste Management Agency (Andra), here tested under alpha irradiation. For this study, UO2 fuel pellets doped with a radioactive alpha emitter (238/239Pu) were leached in synthetic Callovian-Oxfordian groundwater (representative of the French waste disposal site groundwater) in the presence of a metallic iron foil to simulate the steel canister. The pellets had varying levels of alpha activity, in order to modulate the concentrations of species produced by water radiolysis on the surface and to simulate the activity of aged spent fuel after 50 and 10,000 years of alpha radioactivity decay. The experimental data showed that whatever the sample alpha radioactivity, the presence of iron inhibits the oxidizing dissolution of

Arsenic species and chemistry in groundwater of southeast Michigan

International Nuclear Information System (INIS)

Kim, M.-J.; Nriagu, Jerome; Haack, Sheridan

2002-01-01

Most of the arsenic detected was arsenite [As(III)]. - Groundwater samples, taken from 73 wells in 10 counties of southeast Michigan in 1997 had arsenic concentrations in the range of 0.5 to 278 μg/l, the average being 29 μg/l. About 12% of these wells had arsenic concentrations that exceeded the current USEPA's maximum contaminant level of 50 μg/l. Most (53-98%) of the arsenic detected was arsenite [As(III)] and other observations supported the arsenic species distribution (low redox potential and DO). In shallow groundwater ( 15 m), the concentration of arsenic is possibly controlled by reductive dissolution of arsenic-rich iron hydroxide/oxyhydroxide and dissolution of arsenic sulfide minerals

Hydrogeochemical and isotopic characterization of the groundwater ...

African Journals Online (AJOL)

POSTE7

water for both human consumption and agriculture is. *Corresponding author. ..... groundwater of Dababa (Figure 2) shows that the highest conductivities are found in .... comes from the dissolution of CO2 by plants and micro- organisms that ...

Chemical Dissolution of Simulant FCA Cladding and Plates

Energy Technology Data Exchange (ETDEWEB)

Daniel, G. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Pierce, R. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); O' Rourke, P. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL)

2017-11-08

The Savannah River Site (SRS) has received some fast critical assembly (FCA) fuel from the Japan Atomic Energy Agency (JAEA) for disposition. Among the JAEA FCA fuel are approximately 7090 rectangular Stainless Steel clad fuel elements. Each element has an internal Pu-10.6Al alloy metal wafer. The thickness of each element is either 1/16 inch or 1/32 inch. The dimensions of each element ranges from 2 inches x 1 inch to 2 inches x 4 inches. This report discusses the potential chemical dissolution of the FCA clad material or stainless steel. This technology uses nitric acid-potassium fluoride (HNO₃-KF) flowsheets of H-Canyon to dissolve the FCA elements from a rack of materials. Historically, dissolution flowsheets have aimed to maximize Pu dissolution rates while minimizing stainless steel dissolution (corrosion) rates. Because the FCA cladding is made of stainless steel, this work sought to accelerate stainless steel dissolution.

Oxidative corrosion of spent UO2 fuel in vapor and dripping groundwater at 900C

International Nuclear Information System (INIS)

Finch, R. J.

1999-01-01

Corrosion of spent UO 2 fuel has been studied in experiments conducted for nearly six years. Oxidative dissolution in vapor and dripping groundwater at 90 C occurs via general corrosion at fuel-fragment surfaces. Dissolution along fuel-grain boundaries is also evident in samples contacted by the largest volumes of groundwater, and corroded grain boundaries extend at least 20 or 30 grains deep (> 200 microm), possibly throughout millimeter-sized fragments. Apparent dissolution of fuel along defects that intersect grain boundaries has created dissolution pits that are 50 to 200 nm in diameter. Dissolution pits penetrate 1-2 microm into each grain, producing a ''worm-like'' texture along fuel-grain-boundaries. Sub-micrometer-sized fuel shards are common between fuel grains and may contribute to the reactive surface area of fuel exposed to groundwater. Outer surfaces of reacted fuel fragments develop a fine-grained layer of corrosion products adjacent to the fuel (5-15 microm thick). A more coarsely crystalline layer of corrosion products commonly covers the fine-grained layer, the thickness of which varies considerably among samples (from less than 5 microm to greater than 40 microm). The thickest and most porous corrosion layers develop on fuel fragments exposed to the largest volumes of groundwater. Corrosion-layer compositions depend strongly on water flux, with uranyl oxy-hydroxides predominating in vapor experiments, and alkali and alkaline earth uranyl silicates predominating in high drip-rate experiments. Low drip-rate experiments exhibit a complex assemblage of corrosion products, including phases identified in vapor and high drip-rate experiments

Carbonate mineral dissolution kinetics in high pressure experiments

Science.gov (United States)

Dethlefsen, F.; Dörr, C.; Schäfer, D.; Ebert, M.

2012-04-01

The potential CO2 reservoirs in the North German Basin are overlain by a series of Mesozoic barrier rocks and aquifers and finally mostly by Tertiary and Quaternary close-to-surface aquifers. The unexpected rise of stored CO2 from its reservoir into close-to-surface aquifer systems, perhaps through a broken well casing, may pose a threat to groundwater quality because of the acidifying effect of CO2 dissolution in water. The consequences may be further worsening of the groundwater quality due to the mobilization of heavy metals. Buffer mechanisms counteracting the acidification are for instance the dissolution of carbonates. Carbonate dissolution kinetics is comparably fast and carbonates can be abundant in close-to-surface aquifers. The disadvantages of batch experiments compared to column experiments in order to determine rate constants are well known and have for instance been described by v. GRINSVEN and RIEMSDIJK (1992). Therefore, we have designed, developed, tested, and used a high-pressure laboratory column system to simulate aquifer conditions in a flow through setup within the CO2-MoPa project. The calcite dissolution kinetics was determined for CO2-pressures of 6, 10, and 50 bars. The results were evaluated by using the PHREEQC code with a 1-D reactive transport model, applying a LASAGA (1984) -type kinetic dissolution equation (PALANDRI and KHARAKA, 2004; eq. 7). While PALANDRI and KHARAKA (2004) gave calcite dissolution rate constants originating from batch experiments of log kacid = -0.3 and log kneutral = -5.81, the data of the column experiment were best fitted using log kacid = -2.3 and log kneutral = -7.81, so that the rate constants fitted using the lab experiment applying 50 bars pCO2 were approximately 100 times lower than according to the literature data. Rate constants of experiments performed at less CO2 pressure (pCO2 = 6 bars: log kacid = -1.78; log kneutral = -7.29) were only 30 times lower than literature data. These discrepancies in the

Multivariate analysis of the heterogeneous geochemical processes controlling arsenic enrichment in a shallow groundwater system.

Science.gov (United States)

Huang, Shuangbing; Liu, Changrong; Wang, Yanxin; Zhan, Hongbin

2014-01-01

The effects of various geochemical processes on arsenic enrichment in a high-arsenic aquifer at Jianghan Plain in Central China were investigated using multivariate models developed from combined adaptive neuro-fuzzy inference system (ANFIS) and multiple linear regression (MLR). The results indicated that the optimum variable group for the AFNIS model consisted of bicarbonate, ammonium, phosphorus, iron, manganese, fluorescence index, pH, and siderite saturation. These data suggest that reductive dissolution of iron/manganese oxides, phosphate-competitive adsorption, pH-dependent desorption, and siderite precipitation could integrally affect arsenic concentration. Analysis of the MLR models indicated that reductive dissolution of iron(III) was primarily responsible for arsenic mobilization in groundwaters with low arsenic concentration. By contrast, for groundwaters with high arsenic concentration (i.e., > 170 μg/L), reductive dissolution of iron oxides approached a dynamic equilibrium. The desorption effects from phosphate-competitive adsorption and the increase in pH exhibited arsenic enrichment superior to that caused by iron(III) reductive dissolution as the groundwater chemistry evolved. The inhibition effect of siderite precipitation on arsenic mobilization was expected to exist in groundwater that was highly saturated with siderite. The results suggest an evolutionary dominance of specific geochemical process over other factors controlling arsenic concentration, which presented a heterogeneous distribution in aquifers. Supplemental materials are available for this article. Go to the publisher's online edition of the Journal of Environmental Science and Health, Part A, to view the supplemental file.

Improving groundwater management in rural India using simple modeling tools with minimal data requirements

Science.gov (United States)

Moysey, S. M.; Oblinger, J. A.; Ravindranath, R.; Guha, C.

2008-12-01

shortly after the start of the monsoon and villager water use is small compared to the other fluxes. Groundwater fluxes were accounted for by conceptualizing the contributing areas upstream and downstream of the reservoir as one dimensional flow tubes. This description of the flow system allows for the definition of physically-based parameters making the model useful for investigating WHS infiltration under a variety of management scenarios. To address concerns regarding the uniqueness of the model parameters, 10,000 independent model calibrations were performed using randomly selected starting parameters. Based on this Monte Carlo analysis, it was found that the mean volume of water contributed by the WHS to infiltration over the study period (Sept.-Dec., 2007) was 48.1x103m3 with a 95% confidence interval of 43.7-53.7x103m3. This volume represents 17-21% of the total natural groundwater recharge contributed by the entire watershed, which was determined independently using a surface water balance. Despite the fact that the model is easy to use and requires minimal data, the results obtained provide a powerful quantitative starting point for managing groundwater withdrawals in the dry season.

Dissolution studies with pilot plant and actual INTEC calcines

International Nuclear Information System (INIS)

Herbst, R.S.; Garn, T.G.

1999-01-01

The dissolution of Idaho Nuclear Technology and Engineering Center (INTEC) pilot plant calcines was examined to determine solubility of calcine matrix components in acidic media. Two representatives pilot plant calcine types were studied: Zirconia calcine and Zirconia/Sodium calcine. Dissolution of these calcines was evaluated using lower initial concentrations of nitric acid than used in previous tests to decrease the [H+] concentration in the final solutions. Lower [H+] concentrations contribute to more favorable TRUEX/SREX solvent extraction flowsheet performance. Dissolution and analytical results were also obtained for radioactive calcines produced using high sodium feeds blended with non-radioactive Al(NO 3 ) 3 solutions to dilute the sodium concentration and prevent bed agglomeration during the calcination process. Dissolution tests indicated >95 wt.% of the initial calcine mass can be dissolved using the baseline dissolution procedure, with the exception that higher initial nitric acid concentrations are required. The higher initial acid concentration is required for stoichiometric dissolution of the oxides, primarily aluminum oxide. Statistically designed experiments using pilot plant calcine were performed to determine the effect of mixing rate on dissolution efficiency. Mixing rate was determined to provide minimal effects on wt.% dissolution. The acid/calcine ratio and temperature were the predominate variables affecting the wt.% dissolution, a result consistent with previous studies using other similar types of pilot plant calcines

Groundwater recharge and discharge scenarios for a nuclear waste repository in bedded salt

International Nuclear Information System (INIS)

Carpenter, D.W.; Steinborn, T.L.; Thorson, L.D.

1979-01-01

Twelve potential scenarios have been identified whereby groundwater may enter or exit a nuclear waste repository in bedded salt. The 12 scenarios may be grouped into 4 categories or failure modes: dissolution, fracturing, voids, and penetration. Dissolution modes include breccia pipe and breccia blanket formation, and dissolution around boreholes. Fracture modes include flow through preexisting or new fractures and the effects of facies changes. Voids include interstitial voids (pores) and fluid inclusions. Penetration modes include shaft and borehole sealing failures, undetected boreholes, and new mines or wells constructed after repository decommissioning. The potential importance of thermal effects on groundwater flow patterns and on the recharge-discharge process is discussed. The appropriate levels of modeling effort, and the interaction between the adequacy of the geohydrologic data base and the warranted degree of model complexity are also discussed

An autoclave system for uranium oxide dissolution experiments

International Nuclear Information System (INIS)

Nykyri, Mikko

1985-05-01

According to the decision in principle of the Council of State of Finland the nuclear energy producers must provide preparedness for carrying out the final disposal of spent nuclear fuel in Finland. By the present principal concept the spent fuel will be disposed deep into the granitic bedrock. A parameter needed by risk analysis models is the dissolution rate of the uranium oxide matrix in the fuel pellets. In order to approach conditions prevailing deep in the groundwater, and autoclave system for dissolution experiments was developed at the Technical Research Centre of Finland. The low oxygen content and high pressure at elevated temperatures are simulated in the system. 20 MPa and 100 deg C are the upper operation limits of pressure and temperature. Water can be changed in the experiment autoclave without remarkable pressure and temperature variations. This has been arranged by using three pressure vessels: a supply vessel, a dissolution vessel and a depletion vessel. The extreme vessels serve pressure balancing purposes during water exchange. The water is deoxygenated during a preparation phase in the supply vessel by flushing it with nitrogen gas. Polytetrafluoroethylene is the principal material in contact with the water. A redox electrode couple was developed for potential measurements inside the dissolution vessel. The reference electrode is of Ag/AgCl-type with saturated KC1 electrolyte. A platinum wire operates as a measuring electrode

Dissolution of minerals with rough surfaces

Science.gov (United States)

de Assis, Thiago A.; Aarão Reis, Fábio D. A.

2018-05-01

We study dissolution of minerals with initial rough surfaces using kinetic Monte Carlo simulations and a scaling approach. We consider a simple cubic lattice structure, a thermally activated rate of detachment of a molecule (site), and rough surface configurations produced by fractional Brownian motion algorithm. First we revisit the problem of dissolution of initial flat surfaces, in which the dissolution rate rF reaches an approximately constant value at short times and is controlled by detachment of step edge sites. For initial rough surfaces, the dissolution rate r at short times is much larger than rF ; after dissolution of some hundreds of molecular layers, r decreases by some orders of magnitude across several time decades. Meanwhile, the surface evolves through configurations of decreasing energy, beginning with dissolution of isolated sites, then formation of terraces with disordered boundaries, their growth, and final smoothing. A crossover time to a smooth configuration is defined when r = 1.5rF ; the surface retreat at the crossover is approximately 3 times the initial roughness and is temperature-independent, while the crossover time is proportional to the initial roughness and is controlled by step-edge site detachment. The initial dissolution process is described by the so-called rough rates, which are measured for fixed ratios between the surface retreat and the initial roughness. The temperature dependence of the rough rates indicates control by kink site detachment; in general, it suggests that rough rates are controlled by the weakest microscopic bonds during the nucleation and formation of the lowest energy configurations of the crystalline surface. Our results are related to recent laboratory studies which show enhanced dissolution in polished calcite surfaces. In the application to calcite dissolution in alkaline environment, the minimal values of recently measured dissolution rate spectra give rF ∼10-9 mol/(m2 s), and the calculated rate

Geochemical investigation of groundwater in the Tono area, Japan. Chemical characteristics and groundwater evolution

International Nuclear Information System (INIS)

Iwatsuki, Teruki; Hama, Katsuhiro; Yoshida, Hidekazu

1997-01-01

Geochemical investigations form an important part of the R and D program at the Tono study site, central Japan. Detailed geological structure and groundwater chemistry have been studied to understand the geochemical environment in the sedimentary and crystalline rocks distributed in this area. The chemical evolution of the groundwater in the sedimentary rocks is characterized with the variation in Na + , Ca 2+ and HCO 3 - concentrations, and ion exchange and dissolution of calcite are dominant reactions in the evolution of groundwater. Geological investigation shows that a fracture system of crystalline rock can be classified into:intact zone, moderately fractured zone and intensely fractured zone, according to the frequency and the width of fractures and fractured zones. The groundwater in the intact and fractured zones of crystalline rock are characterized by Na + -Ca 2+ -HCO 3 - or Na + -HCO 3 - dominated water, and Na + -Ca 2+ -Fe 2+ -HCO 3 - dominated water. The chemical evolution of groundwater is, generally, controlled by water-rock interaction between plagioclase, iron minerals and groundwater. The groundwater at depth of G.L.-186m in the crystalline rock at the Tono area is characterized by the mixture between the oxidized surface water and the reduced groundwater. The investigation based on correlation between geological structures and groundwater chemistry can be applied to understand the geochemical environment in deep crystalline rock, and will support the development of a realistic hydrogeochemical model. (author)

The effect of fuel chemistry on UO{sub 2} dissolution

Energy Technology Data Exchange (ETDEWEB)

Casella, Amanda, E-mail: amanda.casella@pnnl.gov [Pacific Northwest National Laboratory, PO Box 999, MSIN P7-25, Richland, WA 99352 (United States); Hanson, Brady, E-mail: brady.hanson@pnnl.gov [Pacific Northwest National Laboratory, PO Box 999, MSIN P7-27, Richland, WA 99352 (United States); Miller, William [University of Missouri Research Reactor, 1513 Research Park Drive, Columbia, MO 65211 (United States)

2016-08-01

The dissolution rate of both unirradiated UO{sub 2} and used nuclear fuel has been studied by numerous countries as part of the performance assessment of proposed geologic repositories. In the scenario of waste package failure and groundwater contact with the fuel, the effects of variables such as temperature, dissolved oxygen, and water and fuel chemistry on the dissolution rates of the fuel are necessary to provide a quantitative estimate of the potential release over geologic time frames. The primary objective of this research was to determine the influence these parameters, with primary focus on the fuel chemistry, have on the dissolution rate of unirradiated UO{sub 2} under oxidizing repository conditions and compare them to the rates predicted by current dissolution models. Both unirradiated UO{sub 2} and UO{sub 2} doped with varying concentrations of Gd{sub 2}O{sub 3}, to simulate used fuel composition after long time periods when radiolysis has minor contributions to dissolution, were examined. In general, a rise in temperature increased the dissolution rate of UO{sub 2} and had a larger effect on pure UO{sub 2} than on those doped with Gd{sub 2}O{sub 3}. Oxygen dependence was observed in the UO{sub 2} samples with no dopant and increased as the temperature rose; in the doped fuels less dependence was observed. The addition of gadolinia into the UO{sub 2} matrix resulted in a significant decrease in the dissolution rate. The matrix stabilization effect resulting from the dopant proved even more beneficial in lowering the dissolution rate at higher temperatures and dissolved O{sub 2} concentrations in the leachate where the rates would typically be elevated. - Highlights: • UO{sub 2} dissolution rates were measured for a matrix of repository relevant conditions. • Dopants in the UO{sub 2} matrix lowered the dissolution rate. • Reduction in rates by dopants were increased at elevated temperature and O{sub 2} levels. • UO{sub 2} may be overly

Hydrogeochemical analysis and evaluation of groundwater in the reclaimed small basin of Abu Mina, Egypt

Science.gov (United States)

Salem, Zenhom E.; Atwia, Mohamed G.; El-Horiny, Mohamed M.

2015-12-01

Agricultural reclamation activities during the last few decades in the Western Nile Delta have led to great changes in the groundwater levels and quality. In Egypt, changing the desert land into agricultural land has been done using transferred Nile water (through irrigation canal systems) or/and groundwater. This research investigates the hydrogeochemical changes accompanying the reclamation processes in the small basin of Abu Mina, which is part of the Western Nile Delta region. In summer 2008, 23 groundwater samples were collected and groundwater levels were measured in 40 observation wells. Comparing the groundwater data of the pre-reclamation (1974) and the post-reclamation (2008) periods, groundwater seems to have been subjected to many changes: rise in water level, modification of the flow system, improvement of water quality, and addition of new salts through dissolution processes. Generally, Abu Mina basin is subdivided into two areas, recharge and discharge. The dissolution and mixing were recognized in the recharge areas, while the groundwater of the discharge region carries the signature of the diluted pre-reclamation groundwater. The salts of soil and aquifer deposits play an important role in the salt content of the post and pre-reclamation groundwater. NaCl was the predominant water type in the pre-reclamation groundwater, while CaSO4, NaCl and MgSO4 are the common chemical facies in the post-reclamation groundwater. The post-reclamation groundwater mostly indicates mixing between the pre-reclamation groundwater and the infiltrated freshwater with addition of some ions due to interaction with soil and sediments.

Pavement Subsidence in the Cumberland Gap Tunnel, USA: A Story of Groundwater Chemistry

Science.gov (United States)

Zhu, J.; Currens, J. C.; Webb, S. E.; Rister, B. W.

2014-12-01

Cumberland Gap Tunnel was constructed in 1996 to improve highway travel between southeastern Kentucky and northeastern Tennessee and to restore Cumberland Gap to its historical appearance. About five years after construction, the concrete pavement in the tunnel began to exhibit noticeable signs of subsidence. Ground penetrating radar surveys detected voids in many areas of the limestone roadbed aggregate beneath the pavement. Field investigations conducted by the Kentucky Geological Survey and Kentucky Transportation Center from 2006 to 2008 discovered that groundwater was flowing from the bedrock invert into the aggregate along many parts of the tunnel. Average groundwater discharge from the tunnel was measured at approximately 1700 m3/d. We analyzed 265 groundwater samples collected from aggregate in different parts of the tunnel roadbed during low and high flow conditions. Calculated calcite saturation indices indicated that the groundwater was geochemically aggressive and capable of continuously dissolving calcite in the limestone aggregate although pH values of these water samples were near neutral. We also conducted an in-situ dissolution experiment by placing eight baskets filled with limestone aggregate beneath the roadbed in different locations in the tunnel for 178 days. At the end of the experiment, the limestone aggregate in contact with groundwater exhibited visual signs of dissolution and lost mass, and the highest mass loss recorded was 3.4 percent. Mass loss calculations based on kinetic models of calcite mineral and water samples taken near the baskets matched well with the actual measured mass losses, confirming that dissolution of calcite by the groundwater was the primary cause of the roadbed subsidence problem. Based on these findings, we suggested the limestone aggregate be replaced with noncarbonate (granite) aggregate to mitigate future road subsidence. The suggestion was adopted, and the repair was completed in early 2014.

Dissolution characteristics of chalcedony under alkaline condition. Study for changes in mineral composition of engineered barrier composed by bentonite

International Nuclear Information System (INIS)

Watanabe, Yasutaka; Yokoyama, Shingo

2016-01-01

In the engineered barrier of radioactive waste disposal facilities, it is expected that bentonite is exposed to alkaline groundwater which arise from leaching of cementations materials. Minerals contained in the bentonite will be dissolved by reactions of the alkaline groundwater. Some bentonite contains silica such as quartz and chalcedony. Chalcedony is categorized in intermediate silica which is microcrystalline. It is known that dissolution of silica influences to the dissolution of smectite by means of solubility. However, dissolution kinetics of chalcedony in the alkaline condition has not been investigated, which is an uncertainty in geochemical simulations to evaluate a long-term stability of the engineered barrier. Therefore, this study performed flow-through experiments in alkaline conditions using chalcedony in order to obtain the dissolution rate of the chalcedony. The flow-through experiments was performed using NaOH-NaCl solution adjusted to 0.3 mol/L of ionic strength. Initial pH of the solution was from 8.9 to 13.5. As a result, higher pH and higher temperature showed higher Si ion concentrations of reacted solutions. The dissolution rate of the samples was calculated using Si ion concentrations at steady state of the experiment. Note that, the dissolution rate of the chalcedony was almost same as that of quartz at same temperature. After the experiments, SEM observation showed that rough surface of the chalcedony partly changed to smooth surface like quartz. It is supposed that rough surface of chalcedony was rapidly dissolved because of low degree of crystallization. The dissolution rate obtained is supposedly applicable to highly crystalline SiO 2 of chalcedony. (author)

Kinetics and thermodynamics of the dissolution of Th1-xMxO2 solid solutions (M = U, Pu)

International Nuclear Information System (INIS)

Hubert, S.; Heisbourg, G.; Dacheux, N.; Moisy, Ph.; Purans, J.

2004-01-01

Kinetics of the dissolution of Th 1-x M x O 2 (M = U, Pu) solid solutions was investigated as a function of several chemical parameters such as pH, substitution ratio, temperature, ionic strength, and electrolyte. Several compositions of Th 1-x U x O 2 and Th 1-x Pu x O 2 were synthesized and characterized before and after leaching by using several methods such as XRD, EXAFS, BET, PIXE, SEM, and XPS. Leaching tests were performed in nitric, hydrochloric or sulfuric media and groundwater. The normalized dissolution rates were evaluated for Th 1-x U x O 2 , and Th 0.88 Pu 0.12 O 2 leading to the determination of the partial order related to the proton concentration, n, and to the corresponding normalized dissolution rate constant at pH = 0, k'T. While for Th enriched solids, the solid solutions Th 1-x U x O 2 have the same dissolution behaviour than ThO 2 with a partial order n ∼ 0.3, in the case of uranium enriched solids, Th 1-x U x O 2 has the same dissolution behaviour than UO 2 with a partial order of n = 1, indicating that uranium oxidation rate becomes the limiting step of the dissolution process. The stoichiometry of the release of both actinides (U or Pu, Th) was verified until the precipitation of thorium occurred in the leachate for pH > 2, while uranium was released in the solution as an uranyl form. For uranium enriched solid solutions, thermodynamic equilibrium was reached after 100 days, and solubility constant of secondary phase was determined. In the case of Th 1-x Pu x O 2 , the dissolution behaviour is similar to that of ThO 2 , but only kinetic aspect of the dissolution can be studied. From the analysis of XPS and EXAFS data on leached and un-leached Th 1-x U x O 2 samples, the dissolution mechanism of solid solutions was explained and will be discussed. The role of the electrolytes on the dissolution of the solid solutions is discussed. Kinetics parameters of dissolution are also given in groundwater and in neutral media

Geochemistry of groundwater in the Beaver and Camas Creek drainage basins, eastern Idaho

Science.gov (United States)

Rattray, Gordon W.; Ginsbach, Michael L.

2014-01-01

The U.S. Geological Survey (USGS), in cooperation with the U.S. Department of Energy, is studying the fate and transport of waste solutes in the eastern Snake River Plain (ESRP) aquifer at the Idaho National Laboratory (INL) in eastern Idaho. This effort requires an understanding of the natural and anthropogenic geochemistry of groundwater at the INL and of the important physical and chemical processes controlling the geochemistry. In this study, the USGS applied geochemical modeling to investigate the geochemistry of groundwater in the Beaver and Camas Creek drainage basins, which provide groundwater recharge to the ESRP aquifer underlying the northeastern part of the INL. Data used in this study include petrology and mineralogy from 2 sediment and 3 rock samples, and water-quality analyses from 4 surface-water and 18 groundwater samples. The mineralogy of the sediment and rock samples was analyzed with X-ray diffraction, and the mineralogy and petrology of the rock samples were examined in thin sections. The water samples were analyzed for field parameters, major ions, silica, nutrients, dissolved organic carbon, trace elements, tritium, and the stable isotope ratios of hydrogen, oxygen, carbon, sulfur, and nitrogen. Groundwater geochemistry was influenced by reactions with rocks of the geologic terranes—carbonate rocks, rhyolite, basalt, evaporite deposits, and sediment comprised of all of these rocks. Agricultural practices near and south of Dubois and application of road anti-icing liquids on U.S. Interstate Highway 15 were likely sources of nitrate, chloride, calcium, and magnesium to groundwater. Groundwater geochemistry was successfully modeled in the alluvial aquifer in Camas Meadows and the ESRP fractured basalt aquifer using the geochemical modeling code PHREEQC. The primary geochemical processes appear to be precipitation or dissolution of calcite and dissolution of silicate minerals. Dissolution of evaporite minerals, associated with Pleistocene Lake

Test Objectives for the Saltcake Dissolution Retrieval Demonstration

International Nuclear Information System (INIS)

DEFIGH PRICE, C.

2000-01-01

This document describes the objectives the Saltcake Dissolution Retrieval Demonstration. The near term strategy for single-shell tank waste retrieval activities has shifted from focusing on maximizing the number of tanks entered for retrieval (regardless of waste volume or content) to a focus on scheduling the retrieval of wastes from those single-shell tanks with a high volume of contaminants of concern. These contaminants are defined as mobile, long-lived radionuclides that have a potential of reaching the groundwater and the Columbia River. This strategy also focuses on the performance of key retrieval technology demonstrations, including the Saltcake Dissolution Retrieval Demonstration, in a variety of waste forms and tank farm locations to establish a technical basis for future work. The work scope will also focus on the performance of risk assessment, retrieval performance evaluations (RPE) and incorporating vadose zone characterization data on a tank-by-tank basis, and on updating tank farm closure/post closure work plans. The deployment of a retrieval technology other than Past-Practice Sluicing (PPS) allows determination of limits of technical capabilities, as well as, providing a solid planning basis for future SST retrievals. This saltcake dissolution technology deployment test will determine if saltcake dissolution is a viable retrieval option for SST retrieval. CH2M Hill Hanford Group (CHG) recognizes the SST retrieval mission is key to the success of the River Protection Project (RPP) and the overall completion of the Hanford Site cleanup. The objectives outlined in this document will be incorporated into and used to develop the test and evaluation plan for saltcake dissolution retrievals. The test and evaluation plan will be developed in fiscal year 2001

Acid groundwater in an anoxic aquifer: Reactive transport modelling of buffering processes

International Nuclear Information System (INIS)

Franken, Gudrun; Postma, Dieke; Duijnisveld, Wilhelmus H.M.; Boettcher, Juergen; Molson, John

2009-01-01

The acidification of groundwater, due to acid rain, was investigated in a Quaternary sandy aquifer in the Fuhrberger Feld, near Hannover, Germany. The groundwater, recharged through an area covered by a coniferous forest, had a pH in the range 4-5 down to a depth of 5 m. The evolution in groundwater chemistry along the flow path was investigated in a transect of multisamplers. A 2D groundwater flow model was established delineating the groundwater flow field and a groundwater flow velocity of around 80 m/a along the flow path was derived. Speciation calculations showed the groundwater to be close to equilibrium with the mineral jurbanite (AlOHSO 4 ) over the pH range 4.0-6.5. This suggests an accumulation of acid rain derived SO 4 2- in the aquifer sediment during the decades with high atmospheric S deposition. The groundwater has a pH of around 4.5 in the upstream part of the flow path increasing to near 6 further downstream. 1D reactive transport modelling, using PHREEQC, was used to analyze different combinations of buffering processes. The first model contains ion exchange in combination with jurbanite dissolution. At the ion exchange front Al 3+ is adsorbed leading to the dissolution of jurbanite and an increase in pH. Comparison with field data showed that the simulated increases in pH and alkalinity are much lower than observed in the field. The second model includes organic matter degradation. In addition to ion exchange and jurbanite dissolution, the model included the reduction of SO 4 2- and Fe-oxides as well as the precipitation of Fe sulfide. This model matches the field data well and illustrates the importance of redox processes for pH buffering in the Fuhrberg aquifer. The current progress of the acidification front is about 4 m/a. This corresponds to an average value of 150 a of acid input, which covers large historical variations. Remediation is expected to take the same time span because it requires desorption and neutralization of adsorbed Al 3

Geochemical evolution of groundwater in the Mud Lake area, eastern Idaho, USA

Science.gov (United States)

Rattray, Gordon W.

2015-01-01

Groundwater with elevated dissolved-solids concentrations—containing large concentrations of chloride, sodium, sulfate, and calcium—is present in the Mud Lake area of Eastern Idaho. The source of these solutes is unknown; however, an understanding of the geochemical sources and processes controlling their presence in groundwater in the Mud Lake area is needed to better understand the geochemical sources and processes controlling the water quality of groundwater at the Idaho National Laboratory. The geochemical sources and processes controlling the water quality of groundwater in the Mud Lake area were determined by investigating the geology, hydrology, land use, and groundwater geochemistry in the Mud Lake area, proposing sources for solutes, and testing the proposed sources through geochemical modeling with PHREEQC. Modeling indicated that sources of water to the eastern Snake River Plain aquifer were groundwater from the Beaverhead Mountains and the Camas Creek drainage basin; surface water from Medicine Lodge and Camas Creeks, Mud Lake, and irrigation water; and upward flow of geothermal water from beneath the aquifer. Mixing of groundwater with surface water or other groundwater occurred throughout the aquifer. Carbonate reactions, silicate weathering, and dissolution of evaporite minerals and fertilizer explain most of the changes in chemistry in the aquifer. Redox reactions, cation exchange, and evaporation were locally important. The source of large concentrations of chloride, sodium, sulfate, and calcium was evaporite deposits in the unsaturated zone associated with Pleistocene Lake Terreton. Large amounts of chloride, sodium, sulfate, and calcium are added to groundwater from irrigation water infiltrating through lake bed sediments containing evaporite deposits and the resultant dissolution of gypsum, halite, sylvite, and bischofite.

Dissolution chemistry and biocompatibility of silicon- and germanium-based semiconductors for transient electronics.

Science.gov (United States)

Kang, Seung-Kyun; Park, Gayoung; Kim, Kyungmin; Hwang, Suk-Won; Cheng, Huanyu; Shin, Jiho; Chung, Sangjin; Kim, Minjin; Yin, Lan; Lee, Jeong Chul; Lee, Kyung-Mi; Rogers, John A

2015-05-06

Semiconducting materials are central to the development of high-performance electronics that are capable of dissolving completely when immersed in aqueous solutions, groundwater, or biofluids, for applications in temporary biomedical implants, environmentally degradable sensors, and other systems. The results reported here include comprehensive studies of the dissolution by hydrolysis of polycrystalline silicon, amorphous silicon, silicon-germanium, and germanium in aqueous solutions of various pH values and temperatures. In vitro cellular toxicity evaluations demonstrate the biocompatibility of the materials and end products of dissolution, thereby supporting their potential for use in biodegradable electronics. A fully dissolvable thin-film solar cell illustrates the ability to integrate these semiconductors into functional systems.

Effect of compositional heterogeneity on dissolution of non-ideal LNAPL mixtures

Science.gov (United States)

Vasudevan, M.; Johnston, C. D.; Bastow, T. P.; Lekmine, G.; Rayner, J. L.; Nambi, I. M.; Suresh Kumar, G.; Ravi Krishna, R.; Davis, G. B.

2016-11-01

The extent of dissolution of petroleum hydrocarbon fuels into groundwater depends greatly on fuel composition. Petroleum fuels can consist of thousands of compounds creating different interactions within the non-aqueous phase liquid (NAPL), thereby affecting the relative dissolution of the components and hence a groundwater plume's composition over long periods. Laboratory experiments were conducted to study the variability in the effective solubilities and activity coefficients for common constituents of gasoline fuels (benzene, toluene, p-xylene and 1,2,4-trimethylbenzene) (BTX) in matrices with an extreme range of molar volumes and chemical affinities. Four synthetic mixtures were investigated comprising BTX with the bulk of the NAPL mixtures made up of either, ethylbenzene (an aromatic like BTX with similar molar volume); 1,3,5-trimethylbenzene (an aromatic with a greater molar volume); n-hexane (an aliphatic with a low molar volume); and n-decane (an aliphatic with a high molar volume). Equilibrium solubility values for the constituents were under-predicted by Raoult's law by up to 30% (higher experimental concentrations) for the mixture with n-hexane as a filler and over-predicted by up to 12% (lower experimental concentrations) for the aromatic mixtures with ethylbenzene and 1,3,5-trimethylbenzene as fillers. Application of PP-LFER (poly-parameter linear free energy relationship) model for non-ideal mixtures also resulted in poor correlation between experimentally measured and predicted concentrations, indicating that differences in chemical affinities can be the major cause of deviation from ideal behavior. Synthetic mixtures were compared with the dissolution behavior of fresh and naturally weathered unleaded gasoline. The presence of lighter aliphatic components in the gasoline had a profound effect on estimating effective solubility due to chemical affinity differences (estimated at 0.0055 per percentage increase in the molar proportion of aliphatic) as

High-resolution InSAR constraints on flood-related subsidence and evaporite dissolution along the Dead Sea shores: Interplay between hydrology and rheology

Science.gov (United States)

Shviro, Maayan; Haviv, Itai; Baer, Gidon

2017-09-01

Sinkhole generation and land subsidence are commonly attributed to dissolution of subsurface layers by under-saturated groundwater and formation of cavities. Along the Dead Sea (DS) shorelines, this process also involves seasonal flash floods that are drained into the subsurface by existing and newly formed sinkholes. We quantify the contribution of flash-floods to salt dissolution and land subsidence using high-resolution interferometric synthetic aperture radar (InSAR). Subsidence rates during a 3-year period (2012-2015) were calculated from 57 COSMO SkyMed X-band interferograms bracketing major flood events and intra-flood periods in 21 sinkhole sites. The sites are located within channels and alluvial fans along the western shores of the Dead Sea, Israel. The observed subsidence reaches maximum rates of 2.5 mm/day, accumulating in specific sites to 500 mm/year. In most of the sinkhole sites a gradual increase in the annual subsidence rate is observed during the 3-year study period. Three different modes of response to floods were observed: (1) sites where floodwater is not directly channeled into sinkholes do not respond to floods; (2) sites adjacent to active channels with sinkholes are unaffected by specific floods but their subsidence rates increase gradually from early winter to mid-summer, and decay gradually until the following winter; and (3) sites in active channels with sinkholes are characterized by an abrupt increase in subsidence rates immediately after each flood (by a factor of up to 20) and by a subsequent quasi-exponential subsidence decay over periods of several months. In these latter sites, subsidence rates after each flood are temporally correlated with alternating groundwater levels in adjacent boreholes. The rapid rise in groundwater head following floods increases the hydraulic gradient of the under-saturated groundwater and hence also the groundwater discharge and the dissolution rate of the subsurface salt layer. A subsequent quasi

Biogeochemistry of Arsenic in Groundwater Flow Systems: The Case of Southern Louisiana

Science.gov (United States)

Johannesson, K. H.; Yang, N.; Datta, S.

2017-12-01

Arsenic (As) is a highly toxic and carcinogenic metalloid that can cause serious health effects, including increased risk of cancers, infant mortality, and reduced intellectual and motor function in children to populations chronically exposed to As. Recent estimates suggest that more than 140 million people worldwide are drinking As-contaminated groundwater (i.e., As ≥ 10 µg kg-1), and the most severely affected region is the Ganges-Brahmaputra-Meghna delta in Bangladesh and India (i.e., Bengal Basin). Arsenic appears to be mobilized to Bengal Basin groundwaters by reductive dissolution of Fe oxides in aquifer sediments with the source of the labile organic matter occurring in the aquifer sediments. Studies within the lower Mississippi River delta of southern Louisiana (USA) also reveal high As concentrations (up to 640 µg kg-1) in shallow groundwaters. It is not known what affects, if any, the elevated groundwater As has had on local communities. The regional extent of high As shallow groundwaters is controlled, in part, by the distribution of Holocene sediments, deltaic deposits, and organic-rich sediments, similar to the Bengal Basin. Field and laboratory studies suggest that As is largely of geogenic origin, and further that microbial reduction of Fe(III)/Mn(IV) oxides/oxyhydroxides within the sediments contributes the bulk of the As to the groundwaters. Incubation studies are supported by biogeochemical reactive transport modeling, which also indicates reductive dissolution of metal oxides/oxyhydroxides as the likely source of As to these groundwaters. Finally, reactive transport modeling of As in shallow groundwaters suggests that sorption to aquifer mineral surfaces limits the transport of As after mobilization, which may explain, in part, the heterogeneous distribution of As in groundwaters of southern Louisiana and, perhaps, the Bengal Basin.

Modeling dissolution and volatilization of LNAPL sources migrating on the groundwater table.

Science.gov (United States)

Kim, Jeongkon; Corapcioglu, M Yavuz

2003-08-01

A vertically averaged two-dimensional model was developed to describe areal spreading and migration of light nonaqueous-phase liquids (LNAPLs) introduced into the subsurface by spills or leaks from underground storage tanks. The NAPL transport model was coupled with two-dimensional contaminant transport models to predict contamination of soil gas and groundwater resulting from a LNAPL migrating on the water table. Numerical solutions were obtained by using the finite-difference method. Simulations and sensitivity analyses were conducted with a LNAPL of pure benzene to study LNAPL migration and groundwater contamination. The model was applied to subsurface contamination by jet fuel. Results indicated that LNAPL migration were affected mostly by volatilization. The generation and movement of the dissolved plume was affected by the geology of the site and the free-product plume. Most of the spilled mass remained as a free LNAPL phase 20 years after the spill. The migration of LNAPL for such a long period resulted in the contamination of both groundwater and a large volume of soil.

Effect of clayey groundwater on the dissolution rate of SON68 simulated nuclear waste glass at 70 °C

Science.gov (United States)

De Echave, T.; Tribet, M.; Jollivet, P.; Marques, C.; Gin, S.; Jégou, C.

2018-05-01

To predict the long-term behavior of high-level radioactive waste glass, it is necessary to study aqueous dissolution of the glass matrix under geological repository conditions. The present article focuses on SON68 (an inactive surrogate of the R7T7 glass) glass alteration in synthetic clayey groundwater at 70 °C. Experiments in deionized water as reference were also performed in the same conditions. Results are in agreement with those of previous studies showing that magnesium present in the solution is responsible for higher glass alteration. This effect is transient and pH-dependent: Once all the magnesium is consumed, the glass alteration rate diminishes. Precipitation of magnesium silicate of the smectite group seems to be the main factor for the increased glass alteration. A pH threshold of 7.5-7.8 was found, above which precipitation of these magnesium silicates at 70 °C is possible. TEM observations reveal that magnesium silicates grow at the expense of the passivating gel, which partly dissolves, forming large pores which increase mass transfer between the reacting glass surface and the bulk solution.

Double porosity model to describe both permeability change and dissolution processes

International Nuclear Information System (INIS)

Niibori, Yuichi; Usui, Hideo; Chida, Taiji

2015-01-01

Cement is a practical material for constructing the geological disposal system of radioactive wastes. The dynamic behavior of both permeability change and dissolution process caused by a high pH groundwater was explained using a double porosity model assuming that each packed particle consists of the sphere-shaped aggregation of smaller particles. This model assumes two kinds of porosities between the particle clusters and between the particles, where the former porosity change mainly controls the permeability change of the bed, and the latter porosity change controls the diffusion of OH"- ions inducing the dissolution of silica. The fundamental equations consist of a diffusion equation of spherical coordinates of OH"- ions including the first-order reaction term and some equations describing the size changes of both the particles and the particle clusters with time. The change of over-all permeability of the packed bed is evaluated by Kozeny-Carman equation and the calculated radii of particle clusters. The calculated result well describes the experimental result of both permeability change and dissolution processes. (author)

The role of evapotranspiration in the groundwater hydrochemistry of an arid coastal wetland (Península Valdés, Argentina)

International Nuclear Information System (INIS)

Alvarez, María del Pilar; Carol, Eleonora; Dapeña, Cristina

2015-01-01

Coastal wetlands are complex hydrogeological systems, in which saline groundwater usually occurs. Salinity can be attributed to many origins, such as dissolution of minerals in the sediments, marine contribution and evapotranspiration, among others. The aim of this paper is to evaluate the processes that condition the hydrochemistry of an arid marsh, Playa Fracasso, located in Patagonia, Argentina. A study of the dynamics and geochemistry of the groundwater was carried out in each hydrogeomorphological unit, using major ion and isotope ( 18 O and 2 H) data, soil profiles descriptions and measurements, and recording of water tables in relation to the tidal flow. Water balances and analytical models based on isotope data were used to quantify the evaporation processes and to define the role of evaporation in the chemical composition of water. The results obtained show that the groundwater salinity of the marsh comes mainly from the tidal inflow, to which the halite and gypsum dissolution is added. These mineral facies are the result of the total evaporation of the marine water flooding that occurs mostly at the spring high tides. The isotope relationships in the fan and bajada samples show the occurrence of evaporation processes. Such processes, however, are not mainly responsible for the saline content of groundwater, which is actually generated by the dissolution of the typical evaporite facies of the arid environment sediments. It is concluded that the evapotranspiration processes condition groundwater quality. This is not only due to the saline enrichment caused by the evapotranspiration of shallow water, but also because such processes are the main drivers of the formation of soluble salts, which are then incorporated into the water by groundwater or tidal flow. - Highlights: • Tidal inflow and evapotranspiration processes condition the salinity of the marsh. • The total evaporation of marine water led the halite and gypsum precipitation. • The dissolution

Insights on surface-water/groundwater exchange in the upper Floridan aquifer, north-central Florida (USA), from streamflow data and numerical modeling

Science.gov (United States)

Sutton, James E.; Screaton, Elizabeth J.; Martin, Jonathan B.

2015-03-01

Surface-water/groundwater exchange impacts water quality and budgets. In karst aquifers, these exchanges also play an important role in dissolution. Five years of river discharge data were analyzed and a transient groundwater flow model was developed to evaluate large-scale temporal and spatial variations of exchange between an 80-km stretch of the Suwannee River in north-central Florida (USA) and the karstic upper Floridan aquifer. The one-layer transient groundwater flow model was calibrated using groundwater levels from 59 monitoring wells, and fluxes were compared to the exchange calculated from discharge data. Both the numerical modeling and the discharge analysis suggest that the Suwannee River loses water under both low- and high-stage conditions. River losses appear greatest at the inside of a large meander, and the former river water may continue across the meander within the aquifer rather than return to the river. In addition, the numerical model calibration reveals that aquifer transmissivity is elevated within this large meander, which is consistent with enhanced dissolution due to river losses. The results show the importance of temporal and spatial variations in head gradients to exchange between streams and karst aquifers and dissolution of the aquifers.

Coupled multiphase reactive flow and mineral dissolution-precipitation kinetics: Examples of long-term CO2 sequestration in Utsira Sand, Norway and Mt. Simon Formation, Midwest USA

Science.gov (United States)

Zhang, Y.; Zhang, G.; Lu, P.; Hu, B.; Zhu, C.

2017-12-01

The extent of CO2 mineralization after CO2 injection into deep saline aquifers is a result of the complex coupling of multiphase fluid flow, mass transport, and brine-mineral reactions. The effects of dissolution rate laws and groundwater flow on the long-term fate of CO2 have been seriously overlooked. To investigate these effects, we conducted multiphase (CO2 and brine) coupled reactive transport modeling of CO2 storage in two sandy formations (Utsira Sand, Norway1,2 and Mt. Simon formation, USA 3) using ToughReact and simulated a series of scenarios. The results indicated that: (1) Different dissolution rate laws for feldspars can significantly affect the amount of CO2 mineralization. Increased feldspar dissolution will promote CO2 mineral trapping through the coupling between feldspar dissolution and carbonate mineral precipitation at raised pH. The predicted amount of CO2 mineral trapping when using the principle of detailed balancing-based rate law for feldspar dissolution is about twice as much as that when using sigmoidal rate laws in the literature. (2) Mineral trapping is twice as much when regional groundwater flow is taken into consideration in long-term simulations (e.g., 10,000 years) whereas most modeling studies neglected the regional groundwater flow back and effectively simulated a batch reactor process. Under the influence of regional groundwater flow, the fresh brine from upstream continuously dissolves CO2 at the tail of CO2 plume, generating a large acidified area where large amount of CO2 mineralization takes place. The upstream replenishment of groundwater results in ˜22% mineral trapping at year 10,000, compared to ˜4% when this effect is ignored. Refs: 1Zhang, G., Lu, P., Wei, X., Zhu, C. (2016). Impacts of Mineral Reaction Kinetics and Regional Groundwater Flow on Long-Term CO2 Fate at Sleipner. Energy & Fuels, 30(5), 4159-4180. 2Zhu, C., Zhang, G., Lu, P., Meng, L., Ji, X. (2015). Benchmark modeling of the Sleipner CO2 plume

Dissolution processes

International Nuclear Information System (INIS)

Silver, G.L.

1976-01-01

This review contains more than 100 observations and 224 references on the dissolution phenomenon. The dissolution processes are grouped into three categories: methods of aqueous attack, fusion methods, and miscellaneous observations on phenomena related to dissolution problems

Groundwater arsenic concentrations in Vietnam controlled by sediment age

DEFF Research Database (Denmark)

Postma, Dieke; Larsen, Flemming; Thai, Nguyen Thi

2012-01-01

Arsenic contamination of groundwater continues to threaten the health of millions of people in southeast Asia. The oxidation of organic carbon, coupled to the reductive dissolution of arsenic-bearing iron oxides, is thought to control the release of sediment-bound arsenic into groundwater. However......, the cause of the high spatial variability in groundwater arsenic concentrations—which can range from 5 to 500 μg l−1 within distances of a few kilometres—has been uncertain. Here, we combine measurements of sediment age, organic-matter reactivity and water chemistry at four locations along a cross......-section of the arsenic-contaminated Red River floodplain in Vietnam to determine the origin of variations in groundwater arsenic concentrations. The burial age of the aquifer sediments, determined using optical stimulated luminescence, ranged from 460 years near the course of the present-day river to 5,900 years...

Chemical alteration of cement hydrates by dissolution

International Nuclear Information System (INIS)

Sugiyama, Daisuke; Fujita, Tomonari; Nakanishi, Kiyoshi

2000-01-01

Cementitious material is a potential waste packaging and backfilling material for the radioactive waste disposal, and is expected to provide both physical and chemical containment. In particular, the sorption of radionuclides onto cementitious material and the ability to provide a high pH condition are very important parameters when considering the release of radionuclides from radioactive wastes. For the long term, in the geological disposal environment, cement hydrates will be altered by, for example, dissolution, chemical reaction with ions in the groundwater, and hydrothermal reaction. Once the composition or crystallinity of the constituent minerals of a cement hydrate is changed by these processes, the pH of the repository buffered by cementitious material and its sorption ability might be affected. However, the mechanism of cement alteration is not yet fully understood. In this study, leaching experiments of some candidate cements for radioactive waste disposal were carried out. Hydrated Ordinary Portland Cement (OPC), Blast Furnace Slag blended cement (OPC/BFS) and Highly containing Flyash and Silicafume Cement (HFSC) samples were contacted with distilled water at liquid:solid ratios of 10:1, 100:1 and 1000:1 at room temperature for 200 days. In the case of OPC, Ca(OH) 2 dissolved at high liquid:solid ratios. The specific surface area of all cement samples increased by leaching process. This might be caused by further hydration and change of composition of constituent minerals. A model is presented which predicts the leaching of cement hydrates and the mineral composition in the hydrated cement solid phase, including the incongruent dissolution of CSH gel phases and congruent dissolution of Ca(OH) 2 , Ettringite and Hydrotalcite. Experimental results of dissolution of Ca-O-H and Ca-Si-O-H phases were well predicted by this model. (author)

Modelling the incongruent dissolution of hydrated cement minerals

International Nuclear Information System (INIS)

Berner, U.R.

1988-01-01

Hydrated calciumsilicates are the main constituents of hydrated portland cements. Their chemistry will strongly influence the longterm behaviour of a concrete system envisioned in use in radioactive waste repositories. Experimental data show that hydrated calciumsilicates dissolve incongruently, depending on the calcium/silicon ratio of the solid. A model that simulates the incongruent dissolution behaviour of these hydrated calciumsilicates is presented. In the model the hydrated calciumcilicates are represented as a mixture of two congruently soluble components. The dissolution of the particular components is described using the concept of variable activities in the solid state. Each component's activity in the solid state is obtained from a large body of solubility data by applying the Gibbs-Duhem equation for nonideal mixtures. Using this approach a simplified set of equations, which describe the solubility of the components as a function of the calcium/silicon ratio of the solid, is derived. As an application, the degradation of a standard portland cement in pure water and in a carbonate-rich groundwater is modelled. (orig.)

Groundwater salinity study in the Mekong Delta using isotope techniques

International Nuclear Information System (INIS)

Le Van Khoi, Nguyen Kien Chinh; Do Tien Hung

2002-01-01

Environmental isotopes D, 18 O and chemical composition were used for study of recharge and salinization of groundwater in the are located between Bassac and Mekong Rivers. The results showed that: (a) Pleistocene aquifers are recharged through flood plains and outcrops located at the same altitude. The sanility of groundwater in these aquifers is mostly due to dissolution of the aquifer material, (b) Pliocene and Miocene aquifers receive recharge through outcrops located at the higher altitude on the northeast extension of the Delta and Cambodia. The salinity of groundwater in the coastal region of the aquifer is attributable to sea water intrusion. There appears to be significant retention of sea water in the coastal sediment during intrusion. (Author)

Hydrogeochemical investigations of groundwater in Ziarat valley, Baluchistan

International Nuclear Information System (INIS)

Akram, W.; Ahmad, M.; Rafiq, M.

2010-03-01

Present study was undertaken in Ziarat Valley, Baluchistan to investigate recent trends of groundwater chemistry (geochemical facies, geochemical evolution) and assess the groundwater quality for drinking and irrigation purposes. For this purpose samples of groundwater (open wells, tube wells, karezes, springs) were periodically collected from different locations and analyzed for dissolved chemical constituents such as sodium, potassium, magnesium, calcium, carbonate, bicarbonate, chloride and sulphate. The data indicated that concentrations of sodium, potassium, calcium and magnesium vary from 5 to 113,0.3 to 3,18 to 62 and 27 to 85 mg/l respectively. Values of anions i. e. bicarbonate, chloride and sulphate lie in the range of 184 to 418, 14 to 77 and 8 to 318 mg/l respectively. Hydrogeochemical facies revealed that groundwater in the study area belongs to Mg-HCO/sub 3/ type at 72% surveyed locations. Dissolution and calcite precipitation were found to be the main processes controlling the groundwater chemistry. Chemical quality was assessed for drinking use by comparing with WHO, Indian and proposed national standards, and for irrigation use using empirical indices such as SAR and RSC. The results show that groundwater is quite suitable for irrigation and drinking purposes. (author)

A critical evaluation of the local-equilibrium assumption in modeling NAPL-pool dissolution

Science.gov (United States)

Seagren, Eric A.; Rittmann, Bruce E.; Valocchi, Albert J.

1999-07-01

An analytical modeling analysis was used to assess when local equilibrium (LE) and nonequilibrium (NE) modeling approaches may be appropriate for describing nonaqueous-phase liquid (NAPL) pool dissolution. NE mass-transfer between NAPL pools and groundwater is expected to affect the dissolution flux under conditions corresponding to values of Sh'St (the modified Sherwood number ( Lxkl/ Dz) multiplied by the Stanton number ( kl/ vx))≈400, the NE and LE solutions converge, and the LE assumption is appropriate. Based on typical groundwater conditions, many cases of interest are expected to fall in this range. The parameter with the greatest impact on Sh'St is kl. The NAPL pool mass-transfer coefficient correlation of Pfannkuch [Pfannkuch, H.-O., 1984. Determination of the contaminant source strength from mass exchange processes at the petroleum-ground-water interface in shallow aquifer systems. In: Proceedings of the NWWA/API Conference on Petroleum Hydrocarbons and Organic Chemicals in Ground Water—Prevention, Detection, and Restoration, Houston, TX. Natl. Water Well Assoc., Worthington, OH, Nov. 1984, pp. 111-129.] was evaluated using the toluene pool data from Seagren et al. [Seagren, E.A., Rittmann, B.E., Valocchi, A.J., 1998. An experimental investigation of NAPL-pool dissolution enhancement by flushing. J. Contam. Hydrol., accepted.]. Dissolution flux predictions made with kl calculated using the Pfannkuch correlation were similar to the LE model predictions, and deviated systematically from predictions made using the average overall kl=4.76 m/day estimated by Seagren et al. [Seagren, E.A., Rittmann, B.E., Valocchi, A.J., 1998. An experimental investigation of NAPL-pool dissolution enhancement by flushing. J. Contam. Hydrol., accepted.] and from the experimental data for vx>18 m/day. The Pfannkuch correlation kl was too large for vx>≈10 m/day, possibly because of the relatively low Peclet number data used by Pfannkuch [Pfannkuch, H.-O., 1984. Determination

The groundwater regime of the Harwell region

International Nuclear Information System (INIS)

Alexander, J.

1983-12-01

A regional hydrogeological assessment has been undertaken in the Harwell area utilizing currently available geological information and water level data. Since the dissolution and transport of any disposed waste would be controlled by the rate and direction of groundwater movement through a potential repository, a detailed knowledge of regional and local hydrogeology is essential. This study is based on the tenet that very slow groundwater movement, through a sequence of clay lithologies, is measurable at widely separated points within intervening high permeability systems. The analysis of available data from high permeability units within a regional groundwater flow-system provides a general flow model which takes into account inter-lithology water movement in general and vertical water movement across low permeability formations in particular. Groundwater contour maps have been constructed for the Chalk, Upper Greensand, Corallian and Great Oolite lithologies. These show that in the Cretaceous and Jurassic formations of the Harwell area, groundwater movement is predominantly in the horizontal direction with a smaller proportion of vertical flow taking place between adjacent formations. The potential for vertical movement, both upwards and downwards through intervening low permeability clay lithologies is evident. The results are discussed. (author)

Groundwater recharge and agricultural contamination

Science.gov (United States)

Böhlke, J.K.

2002-01-01

Agriculture has had direct and indirect effects on the rates and compositions of groundwater recharge and aquifer biogeochemistry. Direct effects include dissolution and transport of excess quantities of fertilizers and associated materials and hydrologic alterations related to irrigation and drainage. Some indirect effects include changes in water–rock reactions in soils and aquifers caused by increased concentrations of dissolved oxidants, protons, and major ions. Agricultural activities have directly or indirectly affected the concentrations of a large number of inorganic chemicals in groundwater, for example NO3–, N2, Cl, SO42–, H+, P, C, K, Mg, Ca, Sr, Ba, Ra, and As, as well as a wide variety of pesticides and other organic compounds. For reactive contaminants like NO3–, a combination of chemical, isotopic, and environmental-tracer analytical approaches might be required to resolve changing inputs from subsequent alterations as causes of concentration gradients in groundwater. Groundwater records derived from multi-component hydrostratigraphic data can be used to quantify recharge rates and residence times of water and dissolved contaminants, document past variations in recharging contaminant loads, and identify natural contaminant-remediation processes. These data indicate that many of the world's surficial aquifers contain transient records of changing agricultural contamination from the last half of the 20th century. The transient agricultural groundwater signal has important implications for long-term trends and spatial heterogeneity in discharge.

Factors controlling groundwater quality in the Yeonjegu District of Busan City, Korea, using the hydrogeochemical processes and fuzzy GIS.

Science.gov (United States)

Venkatramanan, Senapathi; Chung, Sang Yong; Selvam, Sekar; Lee, Seung Yeop; Elzain, Hussam Eldin

2017-10-01

The hydrogeochemical processes and fuzzy GIS techniques were used to evaluate the groundwater quality in the Yeonjegu district of Busan Metropolitan City, Korea. The highest concentrations of major ions were mainly related to the local geology. The seawater intrusion into the river water and municipal contaminants were secondary contamination sources of groundwater in the study area. Factor analysis represented the contamination sources of the mineral dissolution of the host rocks and domestic influences. The Gibbs plot exhibited that the major ions were derived from the rock weathering condition. Piper's trilinear diagram showed that the groundwater quality was classified into five types of CaHCO 3 , NaHCO 3 , NaCl, CaCl 2 , and CaSO 4 types in that order. The ionic relationship and the saturation mineral index of the ions indicated that the evaporation, dissolution, and precipitation processes controlled the groundwater chemistry. The fuzzy GIS map showed that highly contaminated groundwater occurred in the northeastern and the central parts and that the groundwater of medium quality appeared in most parts of the study area. It suggested that the groundwater quality of the study area was influenced by local geology, seawater intrusion, and municipal contaminants. This research clearly demonstrated that the geochemical analyses and fuzzy GIS method were very useful to identify the contaminant sources and the location of good groundwater quality.

Variable infiltration and river flooding resulting in changing groundwater quality - A case study from Central Europe

Science.gov (United States)

Miotliński, Konrad; Postma, Dieke; Kowalczyk, Andrzej

2012-01-01

SummaryThe changes in groundwater quality occurring in a buried valley aquifer following a reduction in groundwater exploitation and enhanced infiltration due to extensive flooding of the Odra River in 1997 were investigated. Long-time series data for the chemical composition of groundwater in a large well field for drinking water supply indicated the deterioration of groundwater quality in the wells capturing water from the flooded area, which had been intensively cultivated since the 1960s. Infiltration of flooded river water into the aquifer is suggested by an elevated chloride concentration, although salt flushing from the rewatered unsaturated zone due to the enhanced recharge event is much more feasible. Concomitantly with chloride increases in the concentrations of sulphate, ferrous iron, manganese, and nickel imply the oxidation of pyrite (FeS 2) which is abundant in the aquifer. The proton production resulting from pyrite oxidation is buffered by the dissolution of calcite, while the Ca:SO 4 stoichiometry of the groundwater indicates that pyrite oxidation coupled with nitrate reduction is the dominant process occurring in the aquifer. The pyritic origin of SO42- is confirmed by the sulphur isotopic composition. The resultant Fe 2+ increase induces Mn-oxide dissolution and the mobilisation of Ni 2+ previously adsorbed to Mn-oxide surfaces. The study has a major implication for groundwater quality prediction studies where there are considerable variations in water level associated with groundwater management and climate change issues.

Dissolution of aluminium

International Nuclear Information System (INIS)

Uriarte Hueda, A.; Berberana Eizmendi, M.; Pereira Sanchez, G.

1968-01-01

The dissolution of aluminum with acid solutions ( nitric acid-mercuric nitrate) and alkaline solutions (sodium hydroxide-sodium nitrate) has been studied. The instantaneous dissolution rate (IDR) has been studied in function of the concentration of the used reagents and the dissolution temperature. The complete dissolution has been included in the second part of this report, to know the total dissolution time, the consume of reagents and the stability of the resultant solutions. (Author)

The anodic dissolution of SIMFUEL (UO2) in slightly alkaline sodium carbonate/bicarbonate solutions

International Nuclear Information System (INIS)

Keech, P.G.; Goldik, J.S.; Qin, Z.; Shoesmith, D.W.

2011-01-01

The corrosion of nuclear fuel under waste disposal conditions is likely to be influenced by the bicarbonate/carbonate content of the groundwater since it increases the solubility of the U VI corrosion product, [UO 2 ] 2+ . As one of the half reactions involved in the corrosion process, the anodic dissolution of SIMFUEL (UO 2 ) has been studied in bicarbonate/carbonate solutions (pH 9.8) using voltammetric and potentiostatic techniques and electrochemical impedance spectroscopy. The reaction proceeds by two consecutive one electron transfer reactions (U IV → U V → U VI ). At low potentials (≤250 mV (vs. SCE) the rate of the first electron transfer reaction is rate determining irrespective of the total carbonate concentration. At potentials >250 mV (vs. SCE) the formation of a U VI O 2 CO 3 surface layer begins to inhibit the dissolution rate and the current becomes independent of potential indicating rate control by the chemical dissolution of this layer.

Hydrochemistry of urban groundwater, Seoul, Korea: the impact of subway tunnels on groundwater quality.

Science.gov (United States)

Chae, Gi-Tak; Yun, Seong-Taek; Choi, Byoung-Young; Yu, Soon-Young; Jo, Ho-Young; Mayer, Bernhard; Kim, Yun-Jong; Lee, Jin-Yong

2008-10-23

Hydrogeologic and hydrochemical data for subway tunnel seepage waters in Seoul (Republic of Korea) were examined to understand the effect of underground tunnels on the degradation of urban groundwater. A very large quantity of groundwater (up to 63 million m3 year(-1)) is discharged into subway tunnels with a total length of 287 km, resulting in a significant drop of the local groundwater table and the abandonment of groundwater wells. For the tunnel seepage water samples (n = 72) collected from 43 subway stations, at least one parameter among pathogenic microbes (total coliform, heterotrophic bacteria), dissolved Mn and Fe, NH4+, NO3(-), turbidity, and color exceeded the Korean Drinking Water Standards. Locally, tunnel seepage water was enriched in dissolved Mn (avg. 0.70 mg L(-1), max. 5.58 mg L(-1)), in addition to dissolved Fe, NH4+, and pathogenic microbes, likely due to significant inflow of sewage water from broken or leaking sewer pipes. Geochemical modeling of redox reactions was conducted to simulate the characteristic hydrochemistry of subway tunnel seepage. The results show that variations in the reducing conditions occur in urban groundwater, dependent upon the amount of organic matter-rich municipal sewage contaminating the aquifer. The organic matter facilitates the reduction and dissolution of Mn- and Fe-bearing solids in aquifers and/or tunnel construction materials, resulting in the successive increase of dissolved Mn and Fe. The present study clearly demonstrates that locally significant deterioration of urban groundwater is caused by a series of interlinked hydrogeologic and hydrochemical changes induced by underground tunnels.

Heterogeneous redox conditions, arsenic mobility, and groundwater flow in a fractured-rock aquifer near a waste repository site in New Hampshire, USA

Science.gov (United States)

Anthropogenic sources of carbon from landfill or waste leachate can promote reductive dissolution of in situ arsenic (As) and enhance the mobility of As in groundwater. Groundwater from residential-supply wells in a fractured crystalline-rock aquifer adjacent to a Superfund site ...

A Study on the Oxidative-dissolution Leaching of Fission Product Oxides in the carbonate solution

International Nuclear Information System (INIS)

Lee, Eil Hee; Kim, Kwang Wook; Lim, Jae Gwan; Chung, Dong Yong; Yang, Han Beom; Joe, Kih Soo; Seo, Heui Seung; Kim, Yeon Hwa; Lee, Se Yoon

2009-07-01

This study was carried out to investigate the characteristics of an oxidativedissolution leaching of FP co-dissolved with U in a carbonate solution of Na 2 CO 3 - H 2 O 2 and (NH 4 ) 2 CO 3 -H 2 O 2 , respectively. Simulated FP-oxides which contained 12 components have been added to the solution to examine their oxidative dissolution characteristics. It was found that H 2 O 2 was an effective oxidant to minimize the dissolution of FP in a carbonate solution. In 0.5M Na 2 CO 3 -0.5M H 2 O 2 and 0.5M (NH 4 ) 2 CO 3 -0.5M H 2 O 2 solution, some elements such as Re, Te, Cs and Mo seem to be dissolved together with U. It is revealed that dissolution rates of Re, Te and Cs are high (completely dissolved within 10∼20 minutes) due to their high solubility in Na 2 CO 3 and (NH 4 ) 2 CO 3 solution regardless of the addition of H 2 O 2 , and independent of the concentrations of Na 2 CO 3 and H 2 O 2 . However, Mo was slowly dissolved by an oxidative dissolution with H 2 O 2 . It is found that the most important factor for the oxidative dissolution of FP is the pH of the solution and an effective oxidative dissolution is achieved at a pH between 10∼12 for Na 2 CO 3 and a pH between 9∼10 for (NH 4 ) 2 CO 3 , respectively, in order to minimize the dissolution of FP

Assessment of groundwater contamination by leachate near a ...

African Journals Online (AJOL)

The results show that the leachate from the landfill has a minimal impact on the groundwater resource and this can be attributed to the existing soil stratigraphy at the site consisting of clay which is deduced to have a significant influence on the natural attenuation of leachate into groundwater. Keywords: Groundwater ...

Major ion chemistry and quality assessment of groundwater in Haripur area

International Nuclear Information System (INIS)

Akram, W.; Tariq, J.A.; Ahmad, M.

2011-07-01

Study was conducted for investigating chemical composition of groundwater, identifying the compositional types of groundwater, delineating the processes controlling the groundwater chemistry and assessing the groundwater quality for drinking / irrigation uses. Groundwater samples collected from shallow (hand pumps, open well, motor pumps) and deep (tube wells) aquifers were analyzed for major cations (Na/sup +/,K/sup +, Ca/sup 2+/, Mg/sup 2+/) and anions (HCO/sub 3/, Cl/sup '/, SO/sub 4/). The data indicated that Ca/sub 2/ is the dominant cation in most of the samples followed by Mg/sup 2+/ whereas HCO/sub 3/ is the most abundant anion in all samples. Hydrochemistry provides a clear indication of active recharge of shallow and deep aquifers by modern meteoric water. Carbonate dissolution was found to be the prevailing process controlling the groundwater chemistry. Chemical quality was assessed for drinking purpose by comparing with WHO, Indian and national standards, and for irrigation purpose using empirical indices such as SAR and RSC. The results show that groundwater meets the norms of good quality drinking water and can be safely used for irrigation. (author)

Transient changes in shallow groundwater chemistry during the MSU ZERT CO2 injection experiment

Science.gov (United States)

Apps, J.A.; Zheng, Lingyun; Spycher, N.; Birkholzer, J.T.; Kharaka, Y.; Thordsen, J.; Kakouros, E.; Trautz, R.

2011-01-01

Food-grade CO2 was injected into a shallow aquifer through a perforated pipe placed horizontally 1-2 m below the water table at the Montana State University Zero Emission Research and Technology (MSU-ZERT) field site at Bozeman, Montana. The possible impact of elevated CO2 levels on groundwater quality was investigated by analyzing 80 water samples taken before, during, and following CO2 injection. Field determinations and laboratory analyses showed rapid and systematic changes in pH, alkalinity, and conductance, as well as increases in the aqueous concentrations of trace element species. The geochemical data were first evaluated using principal component analysis (PCA) in order to identify correlations between aqueous species. The PCA findings were then used in formulating a geochemical model to simulate the processes likely to be responsible for the observed increases in the concentrations of dissolved constituents. Modeling was conducted taking into account aqueous and surface complexation, cation exchange, and mineral precipitation and dissolution. Reasonable matches between measured data and model results suggest that: (1) CO2 dissolution in the groundwater causes calcite to dissolve. (2) Observed increases in the concentration of dissolved trace metals result likely from Ca+2-driven ion exchange with clays (smectites) and sorption/desorption reactions likely involving Fe (hydr)oxides. (3) Bicarbonate from CO2 dissolution appears to compete for sorption with anionic species such as HAsO4-2, potentially increasing dissolved As levels in groundwater. ?? 2011 Published by Elsevier Ltd.

Calcite Dissolution Kinetics

Science.gov (United States)

Berelson, W.; Subhas, A.; Dong, S.; Naviaux, J.; Adkins, J. F.

2016-12-01

A geological buffer for high atmospheric CO2 concentrations is neutralization via reaction with CaCO3. We have been studying the dissolution kinetics of carbonate minerals using labeled 13C calcite and Picarro-based measurements of 13C enrichments in solution DIC. This methodology has greatly facilitated our investigation of dissolution kinetics as a function of water carbonate chemistry, temperature and pressure. One can adjust the saturation state Omega by changing the ion activity product (e.g. adjusting carbonate ion concentration), or by changing the solubility product (e.g. adjusting temperature or pressure). The canonical formulation of dissolution rate vs. omega has been refined (Subhas et al. 2015) and shows distinct non-linear behavior near equilibrium and rates in sea water of 1-3 e-6 g/cm2day at omega = 0.8. Carbonic anhydrase (CA), an enzyme that catalyzes the hydration of dissolved CO2 to carbonic acid, was shown (in concentrations 500x. This result points to the importance of carbonic acid in enhancing dissolution at low degrees of undersaturation. CA activity and abundance in nature must be considered regarding the role it plays in catalyzing dissolution. We also have been investigating the role of temperature on dissolution kinetics. An increase of 16C yields an order of magnitude increase in dissolution rate. Temperature (and P) also change Omega critical, the saturation state where dissolution rates change substantially. Increasing pressure (achieved in a pressure reaction chamber we built) also shifts Omega critical closer to equilibrium and small pressure increases have large impact on dissolution kinetics. Dissolution rates are enhanced by an order of magnitude for a change in pressure of 1500 psi relative to the dissolution rate achieved by water chemistry effects alone for an omega of 0.8. We've shown that the thermodynamic determination of saturation state does not adequately describe the kinetics of dissolution. The interplay of mineral

Geochemical modelling baseline compositions of groundwater

DEFF Research Database (Denmark)

Postma, Diederik Jan; Kjøller, Claus; Andersen, Martin Søgaard

2008-01-01

and variations in water chemistry that are caused by large scale geochemical processes taking place at the timescale of thousands of years. The most important geochemical processes are ion exchange (Valreas and Aveiro) where freshwater solutes are displacing marine ions from the sediment surface, and carbonate......Reactive transport models, were developed to explore the evolution in groundwater chemistry along the flow path in three aquifers; the Triassic East Midland aquifer (UK), the Miocene aquifer at Valreas (F) and the Cretaceous aquifer near Aveiro (P). All three aquifers contain very old groundwaters...... dissolution (East Midlands, Valreas and Aveiro). Reactive transport models, employing the code PHREEQC, which included these geochemical processes and one-dimensional solute transport were able to duplicate the observed patterns in water quality. These models may provide a quantitative understanding...

Strontium isotope geochemistry of alluvial groundwater: a tracer for groundwater resources characterisation

Directory of Open Access Journals (Sweden)

P. Négrel

2004-01-01

Full Text Available This study presents strontium isotope and major ion data of shallow groundwater and river water from the Ile du Chambon catchment, located on the Allier river in the Massif Central (France. There are large variations in the major-element contents in the surface- and groundwater. Plotting of Na vs. Cl contents and Ca, Mg, NO3, K, SO4, HCO3, Sr concentrations reflect water–rock interaction (carbonate dissolution for Ca, Mg, HCO3 and Sr because the bedrock contains marly limestones, agricultural input (farming and fertilising and sewage effluents (for NO3, K, SO4, although some water samples are unpolluted. Sr contents and isotope ratios (87Sr/86Sr vary from 0.70892 to 0.71180 along the hydrological cycle in the groundwater agree with previous work on groundwater in alluvial aquifers in the Loire catchment. The data plot along three directions in a 87Sr/86Sr v. 1/Sr diagram as a result of mixing, involving at least three geochemical signatures–Allier river water, and two distinct signatures that might be related to different water-rock interactions in the catchment. Mixing proportions are calculated and discussed. The alluvial aquifer of the Ile du Chambon catchment is considered, within the Sr isotope systematic, in a larger scheme that includes several alluvial aquifers of the Loire Allier catchment. Keywords: : Loire river, major and trace elements, Sr isotopic ratio, alluvial aquifer, hydrology

Determination of the origin of dissolved inorganic carbon in groundwater around a reclaimed landfill in Otwock using stable carbon isotopes

Energy Technology Data Exchange (ETDEWEB)

Porowska, Dorota, E-mail: dorotap@uw.edu.pl

2015-05-15

Highlights: • Research showed the origin of DIC in the groundwater around a reclaimed landfill. • Carbon isotope was used to evaluate the contributions of carbon from different sources. • The leachate-contaminated water was isotopically distinct from the natural groundwater. • DIC in the natural groundwater comes from organic matter and dissolution of carbonates. • In the contaminated water, DIC comes from organic matter in the aquifer and landfill. - Abstract: Chemical and isotopic analyses of groundwater from piezometers located around a reclaimed landfill in Otwock (Poland) were performed in order to trace the origin of dissolved inorganic carbon (DIC) in the groundwater. Due to differences in the isotopic composition of carbon from different sources, an analysis of stable carbon isotopes in the groundwater, together with the Keeling plot approach and a two-component mixing model allow us to evaluate the relative contributions of carbon from these sources in the groundwater. In the natural (background) groundwater, DIC concentrations and the isotopic composition of DIC (δ{sup 13}C{sub DIC}) comes from two sources: decomposition of organic matter and carbonate dissolution within the aquifer sediments, whereas in the leachate-contaminated groundwater, DIC concentrations and δ{sup 13}C{sub DIC} values depend on the degradation of organic matter within the aquifer sediments and biodegradation of organic matter stored in the landfill. From the mixing model, about 4–54% of the DIC pool is derived from organic matter degradation and 96–46% from carbonate dissolution in natural conditions. In the leachate-contaminated groundwater, about 20–53% of the DIC is derived from organic matter degradation of natural origin and 80–47% from biodegradation of organic matter stored in the landfill. Partial pressure of CO{sub 2} (P CO{sub 2}) was generally above the atmospheric, hence atmospheric CO{sub 2} as a source of carbon in DIC pool was negligible in the

Genesis of the gossan at the Las Cruces Ore Deposit (SW Spain). Groundwater-Rock Interaction.

Science.gov (United States)

Scheiber, L.; Ayora, C.; Vázquez-Suñé, E.; Soler, A.

2016-12-01

The Las Cruces deposit has sparked an interest in the scientific community due to the exceptional genesis and mineralogical composition. The original gossan formed by goethite and hematite has been replaced by siderite and galena rock. The current gossan composition is as the result of the interaction of groundwater that circulates through the Niebla-Posadas aquifer and a gossan formed by Fe-oxyhydroxides. The groundwater conditions promoted the reductive dissolution of Pb-bearing goethite by the organic matter degradation and the formation of siderite and galena. Hydrochemical and isotopic characteristics of groundwater endorses this hypothesis. Thus, negative Eh values, the existence of H2S and the tendency to light sulfate isotope values show the reducing conditions of groundwater. The key role of the organic matter degradation is marked by the high ammonium, boron and dissolved organic carbon (DOC) concentrations together the light δ13C values, both in groundwater and siderite. The siderite precipitation is confirmed by the high pH values (up to 10), the low amount of Fe (<10ppb) and the thermodynamic calculations. The Fe-oxyhydroxides are a high adsorption capacity which is capable of absorbing metals as arsenic, lead and antimony. The reductive dissolution of these minerals involves the release of these metal to groundwater. Then, the groundwater rich in sulfur and an excess of lead produce the galena precipitation. The likeness between the δ34S values, both the gossan and groundwater, reveals that the sulfur of the galena come from the currently groundwater. A reactive transport model confirm that the present day groundwater flux and composition is able to form the siderite rock in less than 1Ma, with no external supply of reactants. The limiting factor of the process is the Dissolved Organic Carbon (DOC) concentration in groundwater, i.e., higher concentrations would decrease the formation time, whereas the result is not sensitive to flow conditions.

The dissolution rate of UO2 in the alkaline regime under oxidizing conditions using a simplified ground water analog

International Nuclear Information System (INIS)

Leider, H.R.; Nguyen, S.N.; Weed, H.C.; Steward, S.A.

1992-01-01

The major factor controlling the long term release of radionuclides from spent fuel in a geologic repository is the leaching/dissolution by groundwater of the UO 2 matrix, since more than 90% of the radionuclide waste is contained in the fuel matrix. The objective of this investigation is to provide experimental dissolution rates for UO 2 samples which can be used to develop a mechanistic release model (or models) for UO 2+x (x≥0) under repository conditions. Several types of data will be obtained from this study: (1) the dissolution rates of UO 2 as a function of pI-L temperature, carbonate and oxygen fugacity; (2) the comparison of the steady state dissolution rates of ''not-reduced'' versus ''reduced'' UO 2 samples and of single crystal versus polycrystalline UO 2 under identical experimental conditions; (3) the pre- and post-test surface analyses of the samples to provide information on the surface phases that may be formed under experimental conditions

Cl/Br ratios and chlorine isotope evidences for groundwater salinization and its impact on groundwater arsenic, fluoride and iodine enrichment in the Datong basin, China.

Science.gov (United States)

Li, Junxia; Wang, Yanxin; Xie, Xianjun

2016-02-15

In order to identify the salinization processes and its impact on arsenic, fluoride and iodine enrichment in groundwater, hydrogeochemical and environmental isotope studies have been conducted on groundwater from the Datong basin, China. The total dissolved solid (TDS) concentrations in groundwater ranged from 451 to 8250 mg/L, and 41% of all samples were identified as moderately saline groundwater with TDS of 3000-10,000 mg/L. The results of groundwater Cl concentrations, Cl/Br molar ratio and Cl isotope composition suggest that three processes including water-rock interaction, surface saline soil flushing, and evapotranspiration result in the groundwater salinization in the study area. The relatively higher Cl/Br molar ratio in groundwater from multiple screening wells indicates the contribution of halite dissolution from saline soil flushed by vertical infiltration to the groundwater salinization. However, the results of groundwater Cl/Br molar ratio model indicate that the effect of saline soil flushing practice is limited to account for the observed salinity variation in groundwater. The plots of groundwater Cl vs. Cl/Br molar ratio, and Cl vs δ(37)Cl perform the dominant effects of evapotranspiration on groundwater salinization. Inverse geochemical modeling results show that evapotranspiration may cause approximately 66% loss of shallow groundwater to account for the observed hydrochemical pattern. Due to the redox condition fluctuation induced by irrigation activities and evapotranspiration, groundwater salinization processes have negative effects on groundwater arsenic enrichment. For groundwater iodine and fluoride enrichment, evapotranspiration partly accounts for their elevation in slightly saline water. However, too strong evapotranspiration would restrict groundwater fluoride concentration due to the limitation of fluorite solubility. Copyright © 2015. Published by Elsevier B.V.

The impact of river infiltration on the chemistry of shallow groundwater in a reclaimed water irrigation area.

Science.gov (United States)

Yin, Shiyang; Wu, Wenyong; Liu, Honglu; Bao, Zhe

2016-10-01

Reclaimed water reuse is an effective method of alleviating agricultural water shortages, which entails some potential risks for groundwater. In this study, the impacts of wastewater reuse on groundwater were evaluated by combination of groundwater chemistry and isotopes. In reclaimed water infiltration, salt composition was affected not only by ion exchange and dissolution equilibrium but also by carbonic acid equilibrium. The dissolution and precipitation of calcites and dolomites as well as exchange and adsorption between Na and Ca/Mg were simultaneous, leading to significant changes in Na/Cl, (Ca+Mg)/Cl, electrical conductivity (EC) and sodium adsorption ratio (SAR). The reclaimed water was of the Na-Mg-Ca-HCO 3 -Cl type, and groundwater recharged by reclaimed water was of the Na-Mg-HCO 3 and Mg-Na-HCO 3 types. The hydrogeological conditions characterized by sand-clay alternation led to both total nitrogen (TN) and total phosphorus (TP) removal efficiencies >95%, and there was no significant difference in those contents between aquifers recharged by precipitation and reclamation water. >40years of long-term infiltration and recharge from sewage and reclaimed water did not cause groundwater contamination by nitrogen, phosphorus and heavy metals. These results indicate that characteristics of the study area, such as the lithologic structure with sand-clay alternation, relatively thick clay layer, and relatively large groundwater depth have a significant role in the high vulnerability. Copyright © 2016 Elsevier B.V. All rights reserved.

Environmental impacts of open loop geothermal system on groundwater

Science.gov (United States)

Kwon, Koo-Sang; Park, Youngyun; Yun, Sang Woong; Lee, Jin-Yong

2013-04-01

Application of renewable energies such as sunlight, wind, rain, tides, waves and geothermal heat has gradually increased to reduce emission of CO2 which is supplied from combustion of fossil fuel. The geothermal energy of various renewable energies has benefit to be used to cooling and heating systems and has good energy efficiency compared with other renewable energies. However, open loop system of geothermal heat pump system has possibility that various environmental problems are induced because the system directly uses groundwater to exchange heat. This study was performed to collect data from many documents such as papers and reports and to summarize environmental impacts for application of open loop system. The environmental impacts are classified into change of hydrogeological factors such as water temperature, redox condition, EC, change of microbial species, well contamination and depletion of groundwater. The change of hydrogeological factors can induce new geological processes such as dissolution and precipitation of some minerals. For examples, increase of water temperature can change pH and Eh. These variations can change saturation index of some minerals. Therefore, dissolution and precipitation of some minerals such as quartz and carbonate species and compounds including Fe and Mn can induce a collapse and a clogging of well. The well contamination and depletion of groundwater can reduce available groundwater resources. These environmental impacts will be different in each region because hydrogeological properties and scale, operation period and kind of the system. Therefore, appropriate responses will be considered for each environmental impact. Also, sufficient study will be conducted to reduce the environmental impacts and to improve geothermal energy efficiency during the period that a open loop system is operated. This work was supported by the Energy Efficiency and Resources of the Korea Institute of Energy Technology Evaluation and Planning

Inverse Modeling of Water-Rock-CO2 Batch Experiments: Potential Impacts on Groundwater Resources at Carbon Sequestration Sites.

Science.gov (United States)

Yang, Changbing; Dai, Zhenxue; Romanak, Katherine D; Hovorka, Susan D; Treviño, Ramón H

2014-01-01

This study developed a multicomponent geochemical model to interpret responses of water chemistry to introduction of CO2 into six water-rock batches with sedimentary samples collected from representative potable aquifers in the Gulf Coast area. The model simulated CO2 dissolution in groundwater, aqueous complexation, mineral reactions (dissolution/precipitation), and surface complexation on clay mineral surfaces. An inverse method was used to estimate mineral surface area, the key parameter for describing kinetic mineral reactions. Modeling results suggested that reductions in groundwater pH were more significant in the carbonate-poor aquifers than in the carbonate-rich aquifers, resulting in potential groundwater acidification. Modeled concentrations of major ions showed overall increasing trends, depending on mineralogy of the sediments, especially carbonate content. The geochemical model confirmed that mobilization of trace metals was caused likely by mineral dissolution and surface complexation on clay mineral surfaces. Although dissolved inorganic carbon and pH may be used as indicative parameters in potable aquifers, selection of geochemical parameters for CO2 leakage detection is site-specific and a stepwise procedure may be followed. A combined study of the geochemical models with the laboratory batch experiments improves our understanding of the mechanisms that dominate responses of water chemistry to CO2 leakage and also provides a frame of reference for designing monitoring strategy in potable aquifers.

A synthesis of hydrochemistry with an integrated conceptual model for groundwater in the Hexi Corridor, northwestern China

Science.gov (United States)

Wang, Liheng; Dong, Yanhui; Xu, Zhifang

2017-09-01

Although many studies have investigated the recharge and evolution of groundwater in the Hexi Corridor, northwestern (NW) China, they describe individual sites such as Jinchang, Jiuquan, Dunhuang, and others. Considering the similarity of these sites, a systematic review of the entire Hexi Corridor is lacking. This paper compares and summarizes previous studies in the Hexi Corridor to provide a regional perspective of the isotopic characteristics and hydrochemical composition of groundwater. In unconfined aquifers, groundwater is recharged by snow and ice melt water from the Qilian Mountains; local precipitation can be neglected. Therefore, the groundwater belongs to a unique hydrological cycle model in the Hexi Corridor, referred to as snow and ice melt water-groundwater system. The dominant anion species changes from HCO3- in front of the mountains to SO42- in the middle basin and Cl- at the basin boundary along the groundwater flow direction, and TDS increases gradually owing to evaporation. A major hydrogeochemical process is the dissolution of minerals from the aquifer in the recharge area changing to cation exchange reactions in the discharge area. Confined groundwater was recharged mainly in the late Pleistocene and middle Holocene at colder temperatures than those of modern times; thus, it is non-renewable. In addition to dissolution, the hydrochemical composition of confined groundwater is also affected by cation exchange reactions. The hydrogeochemical categories of the confined groundwater are simple and stable. In the present study, a conceptual model is established on the basis of the analyses presented, which has important implications for water resource management in the Hexi Corridor. The inter-basin water allocation program should continue in order to achieve optimal utilization of water resources, but groundwater exploitation should be limited as much as possible. Additionally, on the basis of the review and integration of previous research, the

The anodic dissolution of SIMFUEL (UO{sub 2}) in slightly alkaline sodium carbonate/bicarbonate solutions

Energy Technology Data Exchange (ETDEWEB)

Keech, P.G.; Goldik, J.S.; Qin, Z. [Department of Chemistry, University of Western Ontario, 1151 Richmond St, London ON, N6A 5B7 (Canada); Shoesmith, D.W., E-mail: dwshoesm@uwo.ca [Department of Chemistry, University of Western Ontario, 1151 Richmond St, London ON, N6A 5B7 (Canada)

2011-09-30

The corrosion of nuclear fuel under waste disposal conditions is likely to be influenced by the bicarbonate/carbonate content of the groundwater since it increases the solubility of the U{sup VI} corrosion product, [UO{sub 2}]{sup 2+}. As one of the half reactions involved in the corrosion process, the anodic dissolution of SIMFUEL (UO{sub 2}) has been studied in bicarbonate/carbonate solutions (pH 9.8) using voltammetric and potentiostatic techniques and electrochemical impedance spectroscopy. The reaction proceeds by two consecutive one electron transfer reactions (U{sup IV} {yields} U{sup V} {yields} U{sup VI}). At low potentials ({<=}250 mV (vs. SCE) the rate of the first electron transfer reaction is rate determining irrespective of the total carbonate concentration. At potentials >250 mV (vs. SCE) the formation of a U{sup VI}O{sub 2}CO{sub 3} surface layer begins to inhibit the dissolution rate and the current becomes independent of potential indicating rate control by the chemical dissolution of this layer.

Ground-water protection activities of the US Nuclear Regulatory Commission

International Nuclear Information System (INIS)

1987-02-01

This report evaluates the internal consistency of NRC's ground-water protection programs. These programs have evolved consistently with growing public concerns about the significance of ground-water contamination and environmental impacts. Early NRC programs provided for protection of the public health and safety by minimizing releases of radionuclides. More recent programs have included provisions for minimizing releases of nonradiological constituents, mitigating environmental impacts, and correcting ground-water contamination. NRC's ground-water protection programs are categorized according to program areas, including nuclear materials and waste management (NMSS), nuclear reactor operation (NRR), confirmatory research and standards development (RES), inspection and enforcement (IE), and agreement state programs (SP). Based on analysis of existing ground-water protection programs within NRC, the interoffice Ground-water Protection Group has identified several inconsistencies between and within program areas. These inconsistencies include: (1) different definitions of the term ''ground-water,'' (2) variable regulation of nonradiological constituents in ground water, (3) different design periods for ground-water protection, and (4) different scopes and rigor of ground-water assessments. The second inconsistency stems from differences in statutory authority granted to the NRC. The third inconsistency is rationalized by recognizing differences in perceived risks associated with nuclear facilities. The Ground-water Protection Group will document its analysis of the remaining inconsistencies and make recommendations to reconcile or eliminate them in a subsequent report

Ground-water monitoring under RCRA

International Nuclear Information System (INIS)

Coalgate, J.

1993-11-01

In developing a regulatory strategy for the disposal of hazardous waste under the Resource Conservation and Recovery Act (RCRA), protection of ground-water resources was the primary goal of the Environmental Protection Agency (EPA). EPA's ground-water protection strategy seeks to minimize the potential for hazardous wastes and hazardous constituents in waste placed in land disposel units to migrate into the environment. This is achieved through liquids management (limiting the placement of liquid wastes in or on the land, requiring the use of liners beneath waste, installing leachate collection systems and run-on and run-off controls, and covering wastes at closure). Ground-water monitoring serves to detect any failure in EPA's liquids management strategy so that ground-water contamination can be detected and addressed as soon as possible

HIV status awareness, partnership dissolution and HIV transmission in generalized epidemics.

Science.gov (United States)

Reniers, Georges; Armbruster, Benjamin

2012-01-01

HIV status aware couples with at least one HIV positive partner are characterized by high separation and divorce rates. This phenomenon is often described as a corollary of couples HIV Testing and Counseling (HTC) that ought to be minimized. In this contribution, we demonstrate the implications of partnership dissolution in serodiscordant couples for the propagation of HIV. We develop a compartmental model to study epidemic outcomes of elevated partnership dissolution rates in serodiscordant couples and parameterize it with estimates from population-based data (Rakai, Uganda). Via its effect on partnership dissolution, every percentage point increase in HIV status awareness reduces HIV incidence in monogamous populations by 0.27 percent for women and 0.63 percent for men. These effects are even larger when the assumption of monogamy can be relaxed, but are moderated by other behavior changes (e.g., increased condom use) in HIV status aware serodiscordant partnerships. When these behavior changes are taken into account, each percentage point increase in HIV status awareness reduces HIV incidence by 0.13 and 0.32 percent for women and men, respectively (assuming monogamy). The partnership dissolution effect exists because it decreases the fraction of serodiscordant couples in the population and prolongs the time that individuals spend outside partnerships. Our model predicts that elevated partnership dissolution rates in HIV status aware serodiscordant couples reduce the spread of HIV. As a consequence, the full impact of couples HTC for HIV prevention is probably larger than recognized to date. Particularly high partnership dissolution rates in female positive serodiscordant couples contribute to the gender imbalance in HIV infections.

Solubility limits on radionuclide dissolution

Energy Technology Data Exchange (ETDEWEB)

Kerrisk, J.F.

1984-12-31

This paper examines the effects of solubility in limiting dissolution rates of a number of important radionuclides from spent fuel and high-level waste. Two simple dissolution models were used for calculations that would be characteristics of a Yucca Mountain repository. A saturation-limited dissolution model, in which the water flowing through the repository is assumed to be saturated with each waste element, is very conservative in that it overestimates dissolution rates. A diffusion-limited dissolution model, in which element-dissolution rates are limited by diffusion of waste elements into water flowing past the waste, is more realistic, but it is subject to some uncertainty at this time. Dissolution rates of some elements (Pu, Am, Sn, Th, Zr, Sm) are always limited by solubility. Dissolution rates of other elements (Cs, Tc, Np, Sr, C, I) are never solubility limited; their release would be limited by dissolution of the bulk waste form. Still other elements (U, Cm, Ni, Ra) show solubility-limited dissolution under some conditions. 9 references, 3 tables.

Cl/Br ratios and chlorine isotope evidences for groundwater salinization and its impact on groundwater arsenic, fluoride and iodine enrichment in the Datong basin, China

Energy Technology Data Exchange (ETDEWEB)

Li, Junxia; Wang, Yanxin, E-mail: yx.wang@cug.edu.cn; Xie, Xianjun

2016-02-15

In order to identify the salinization processes and its impact on arsenic, fluoride and iodine enrichment in groundwater, hydrogeochemical and environmental isotope studies have been conducted on groundwater from the Datong basin, China. The total dissolved solid (TDS) concentrations in groundwater ranged from 451 to 8250 mg/L, and 41% of all samples were identified as moderately saline groundwater with TDS of 3000–10,000 mg/L. The results of groundwater Cl concentrations, Cl/Br molar ratio and Cl isotope composition suggest that three processes including water-rock interaction, surface saline soil flushing, and evapotranspiration result in the groundwater salinization in the study area. The relatively higher Cl/Br molar ratio in groundwater from multiple screening wells indicates the contribution of halite dissolution from saline soil flushed by vertical infiltration to the groundwater salinization. However, the results of groundwater Cl/Br molar ratio model indicate that the effect of saline soil flushing practice is limited to account for the observed salinity variation in groundwater. The plots of groundwater Cl vs. Cl/Br molar ratio, and Cl vs δ{sup 37}Cl perform the dominant effects of evapotranspiration on groundwater salinization. Inverse geochemical modeling results show that evapotranspiration may cause approximately 66% loss of shallow groundwater to account for the observed hydrochemical pattern. Due to the redox condition fluctuation induced by irrigation activities and evapotranspiration, groundwater salinization processes have negative effects on groundwater arsenic enrichment. For groundwater iodine and fluoride enrichment, evapotranspiration partly accounts for their elevation in slightly saline water. However, too strong evapotranspiration would restrict groundwater fluoride concentration due to the limitation of fluorite solubility. - Highlights: • Natural high arsenic, fluoride and iodine groundwater co-occur with saline water. �

Cl/Br ratios and chlorine isotope evidences for groundwater salinization and its impact on groundwater arsenic, fluoride and iodine enrichment in the Datong basin, China

International Nuclear Information System (INIS)

Li, Junxia; Wang, Yanxin; Xie, Xianjun

2016-01-01

In order to identify the salinization processes and its impact on arsenic, fluoride and iodine enrichment in groundwater, hydrogeochemical and environmental isotope studies have been conducted on groundwater from the Datong basin, China. The total dissolved solid (TDS) concentrations in groundwater ranged from 451 to 8250 mg/L, and 41% of all samples were identified as moderately saline groundwater with TDS of 3000–10,000 mg/L. The results of groundwater Cl concentrations, Cl/Br molar ratio and Cl isotope composition suggest that three processes including water-rock interaction, surface saline soil flushing, and evapotranspiration result in the groundwater salinization in the study area. The relatively higher Cl/Br molar ratio in groundwater from multiple screening wells indicates the contribution of halite dissolution from saline soil flushed by vertical infiltration to the groundwater salinization. However, the results of groundwater Cl/Br molar ratio model indicate that the effect of saline soil flushing practice is limited to account for the observed salinity variation in groundwater. The plots of groundwater Cl vs. Cl/Br molar ratio, and Cl vs δ"3"7Cl perform the dominant effects of evapotranspiration on groundwater salinization. Inverse geochemical modeling results show that evapotranspiration may cause approximately 66% loss of shallow groundwater to account for the observed hydrochemical pattern. Due to the redox condition fluctuation induced by irrigation activities and evapotranspiration, groundwater salinization processes have negative effects on groundwater arsenic enrichment. For groundwater iodine and fluoride enrichment, evapotranspiration partly accounts for their elevation in slightly saline water. However, too strong evapotranspiration would restrict groundwater fluoride concentration due to the limitation of fluorite solubility. - Highlights: • Natural high arsenic, fluoride and iodine groundwater co-occur with saline water. • Groundwater

Colloid-facilitated effects on migration of radionuclides in fractured rock with a kinetic solubility-limited dissolution model

International Nuclear Information System (INIS)

Jen Chunping; Tien Nengchuan

2010-01-01

Nuclides can move with groundwater either as solutes or colloids, where the latter mechanism generally results in much shorter traveling time as the nuclides interact strongly with solid phases, such as actinides. In the performance assessment, it is therefore essential to assess the relative importance of these two transport mechanisms for different nuclides. The relative importance of colloids depends on the nature and concentration of the colloids in groundwater. Plutonium (Pu), neptunium (Np), uranium (U) and americium (Am) are four nuclides of concern for the long-term emplacement of nuclear wastes at potential repository sites. These four actinides have a high potential for migrating if attached to iron oxide, clay or silica colloids in the groundwater.Strong sorption of the actinides by colloids in the groundwater may facilitate the transport of these nuclides along potential flow paths. The solubility-limited dissolution model can be used to assess the safety of the release of nuclear waste in geological disposal sites. Usually, it has been assumed that the solubility of the waste form is constant. If a nuclide reaches its solubility limit at an inner location near the waste form, it is unlikely that the same nuclide will reach its solubility limit at an outer location unless this nuclide has a parent nuclide. It is unlikely that the daughter nuclides will exceed their solubility limit due to decay of their parent nuclide. The present study investigates the effect of colloids on the transport of solubility-limited nuclides under the kinetic solubility-limited dissolution (KSLD) boundary condition in fractured media. The release rate of the nuclides is proportional to the difference between the saturation concentration and the inlet aqueous concentration of the nuclides. The presence of colloids decreases the aqueous concentration of nuclides and, thus, increases the release flux of nuclides from the waste form. (authors)

Hydrochemistry and Isotope Hydrology for Groundwater Sustainability of the Coastal Multilayered Aquifer System (Zhanjiang, China

Directory of Open Access Journals (Sweden)

Pengpeng Zhou

2017-01-01

Full Text Available Groundwater sustainability has become a critical issue for Zhanjiang (China because of serious groundwater level drawdown induced by overexploitation of its coastal multilayered aquifer system. It is necessary to understand the origins, material sources, hydrochemical processes, and dynamics of the coastal groundwater in Zhanjiang to support its sustainable management. To this end, an integrated analysis of hydrochemical and isotopic data of 95 groundwater samples was conducted. Hydrochemical analysis shows that coastal groundwater is fresh; however, relatively high levels of Cl−, Mg2+, and total dissolved solid (TDS imply slight seawater mixing with coastal unconfined groundwater. Stable isotopes (δ18O and δ2H values reveal the recharge sources of groundwater in the multilayered aquifer system. The unconfined groundwater originates from local modern precipitation; the confined groundwater in mainland originates from modern precipitation in northwestern mountain area, and the confined groundwater in Donghai and Leizhou is sourced from rainfall recharge during an older period with a colder climate. Ionic relations demonstrate that silicate weathering, carbonate dissolutions, and cation exchange are the primary processes controlling the groundwater chemical composition. Declining trends of groundwater level and increasing trends of TDS of the confined groundwater in islands reveal the landward extending tendency of the freshwater-seawater mixing zone.

Hydrochemical characterization of groundwater in the Akyem area, Ghana

Science.gov (United States)

Banoeng-Yakubo, B.; Yidana, S.M.; Anku, Y.; Akabzaa, T.; Asiedu, D.

2008-01-01

The Akyem area is a small farming community located in southeastern Ghana. Groundwater samples from wells in the area were analyzed for concentrations of the major ions, silica, electrical conductivity and pH. The objective was to determine the main controls on the hydrochemistry of ground-water. Mass balance modeling was used together with multivariate R-mode hierarchical cluster analysis to determine the significant sources of variation in the hydrochemistry. Two water types exist in this area. The first is influenced most by the weathering of silicate minerals from the underlying geology, and is thus rich in silica, sodium, calcium, bicarbonate, and magnesium ions. The second is water that has been influenced by the effects of fertilizers and other anthropogenic activities in the area. Mineral speciation and silicate mineral stability diagrams suggest that montmorillonite, probably derived from the incongruent dissolution of feldspars and micas, is the most stable silicate phase in the groundwaters. The apparent incongruent weathering of silicate minerals in the groundwater system has led to the enrichment of sodium, calcium, magnesium and bicarbonate ions as well as silica, leading to the supersaturation of calcite, aragonite, dolomite and quartz. Stability in the montmorillonite field suggests restricted flow conditions and a long groundwater residence time, leading to greater exposure of the rock to weathering. Cation exchange processes appear to play minor roles in the hydrochemistry of groundwater.

CHARACTERIZATION AND ALUMINUM DISSOLUTION DEMONSTRATION WITH A 3 LITER TANK 51H SAMPLE

International Nuclear Information System (INIS)

Hay, M; John Pareizs, J; Cj Bannochie, C; Michael Stone, M; Damon Click, D; Daniel McCabe, D

2008-01-01

A 3-liter sludge slurry sample was sent to SRNL for demonstration of a low temperature aluminum dissolution process. The sludge was characterized before and after the aluminum dissolution. Post aluminum dissolution sludge settling and the stability of the decanted supernate were also observed. The characterization of the as-received 3-liter sample of Tank 51H sludge slurry shows a typical high aluminum HM sludge. The XRD analysis of the dried solids indicates Boehmite is the predominant crystalline form of aluminum in the sludge solids. However, amorphous phases of aluminum present in the sludge would not be identified using this analytical technique. The low temperature (55 C) aluminum dissolution process was effective at dissolving aluminum from the sludge. Over the three week test, ∼42% of the aluminum was dissolved out of the sludge solids. The process appears to be selective for aluminum with no other metals dissolving to any appreciable extent. At the termination of the three week test, the aluminum concentration in the supernate had not leveled off indicating more aluminum could be dissolved from the sludge with longer contact times or higher temperatures. The slow aluminum dissolution rate in the test may indicate the dissolution of the Boehmite form of aluminum however; insufficient kinetic data exists to confirm this hypothesis. The aluminum dissolution process appears to have minimal impact on the settling rate of the post aluminum dissolution sludge. However, limited settling data were generated during the test to quantify the effects. The sludge settling was complete after approximately twelve days. The supernate decanted from the settled sludge after aluminum dissolution appears stable and did not precipitate aluminum over the course of several months. A mixture of the decanted supernate with Tank 11 simulated supernate was also stable with respect to precipitation

Formulation strategy towards minimizing viscosity mediated negative food effect on disintegration and dissolution of immediate release tablets.

Science.gov (United States)

Zaheer, Kamran; Langguth, Peter

2018-03-01

Food induced viscosity can delay disintegration and subsequent release of API from solid dosage form which may lead to severe reduction in the bioavailability of BCS type III compounds. Formulations of such tablets need to be optimized in view of this postprandial viscosity factor. In this study, three super disintegrants, croscarmellose sodium (CCS), cross-linked polyvinylpolypyrrolidone (CPD), and sodium starch glycolate (SSG) were assessed for their efficiency under simulated fed state. Tablets containing these disintegrants were compressed at 10 and 30 KN, while taking lactose as a soluble filler. In addition to other compendial tests, disintegration force of these formulations was measured by texture analysis. Comparison of parameters derived from force - time curves revealed a direct relation of maximum disintegration force (F max ) and disintegration force development rate (DFDR) with compressional force in fasted state, whereas an inverse relationship of F max and DFDR with compressional force was observed in fed state. The gelling tendency of disintegrants influenced the rate of release of API in simulated fed and fasted states when compressional force was changed. These observations recommend the evaluation of formulations in simulated fed state, in the development stage, with an objective of minimizing the negative impact of food induced viscosity on disintegration. Use of disintegrants that act without gelling or can counteract the effect of gelling is recommended for tablet formulations with reduced disintegration time (DT) and mean dissolution time (MDT) in fed state, respectively.

Hydrothermal waste package interactions with methane-containing basalt groundwater

International Nuclear Information System (INIS)

McGrail, B.P.

1984-11-01

Hydrothermal waste package interaction tests with methane-containing synthetic basalt groundwater have shown that in the absence of gamma radiolysis, methane has little influence on the glass dissolution rate. Gamma radiolysis tests at fluxes of 5.5 x 10 5 and 4.4 x 10 4 R/hr showed that methane-saturated groundwater was more reducing than identical experiments where Ar was substituted for CH 4 . Dissolved methane, therefore, may be beneficial to the waste package in limiting the solubility of redox sensitive radionuclides such a 99 Tc. Hydrocarbon polymers known to form under the irradiation conditions of these tests were not produced. The presence of the waste package constituents apparently inhibited the formation of the polymers, however, the mechanism which prevented their formation was not determined

Hydrochemical and multivariate analysis of groundwater quality in the northwest of Sinai, Egypt.

Science.gov (United States)

El-Shahat, M F; Sadek, M A; Salem, W M; Embaby, A A; Mohamed, F A

2017-08-01

The northwestern coast of Sinai is home to many economic activities and development programs, thus evaluation of the potentiality and vulnerability of water resources is important. The present work has been conducted on the groundwater resources of this area for describing the major features of groundwater quality and the principal factors that control salinity evolution. The major ionic content of 39 groundwater samples collected from the Quaternary aquifer shows high coefficients of variation reflecting asymmetry of aquifer recharge. The groundwater samples have been classified into four clusters (using hierarchical cluster analysis), these match the variety of total dissolvable solids, water types and ionic orders. The principal component analysis combined the ionic parameters of the studied groundwater samples into two principal components. The first represents about 56% of the whole sample variance reflecting a salinization due to evaporation, leaching, dissolution of marine salts and/or seawater intrusion. The second represents about 15.8% reflecting dilution with rain water and the El-Salam Canal. Most groundwater samples were not suitable for human consumption and about 41% are suitable for irrigation. However, all groundwater samples are suitable for cattle, about 69% and 15% are suitable for horses and poultry, respectively.

Assessment of groundwater salinization mechanisms in Santiago Island - Cabo Verde: An environmental isotopic approach

International Nuclear Information System (INIS)

Carreira, P.M.; Nunes, D.; Marques, J.M.; Pina, A.; Mota Gomes, A.; Almeida, E.; Goncalves, R.; Monteiro Santos, F.

2007-01-01

Two sampling campaigns were carried out at Santiago Island - Cabo Verde under the scope of an isotopic and geochemical research study. An evaluation of the groundwater systems was carried out through the application of environmental isotopes and geochemical data in order to answer questions such as: origin and mechanisms of groundwater recharge; relation between the hydrochemical evolution of the groundwater systems with the geological matrix (minerals dissolution) or mixture with seawater and aerosol marine influence; identification of seawater intrusion mechanisms and, determination of the apparent groundwater 'age'. The results obtained so far are not conclusive on the identification of the process responsible for the increase of salinity. In general, all the data obtained seems to indicate that the waters have the same isotopic history but different geochemical evolution, which depends on the weathering and permeability of the rocks. (author)

In-situ radionuclide transport and preferential groundwater flows at INEEL (Idaho): Decay-series disequilibrium studies

International Nuclear Information System (INIS)

Luo, S.; Ku, T.L.; Roback, R.; Murrell, M.; McLing, T.L.

2000-01-01

Uranium and thorium-decay series disequilibria in groundwater occur as a result of water-rock interactions, and they provide site-specific, natural analog information for assessment of in-situ, long-term migration of radionuclides in the far field of a nuclear waste disposal site. In this study, a mass balance model was used to relate the decay-series radionuclide distributions among solution, sorbed and solid phases in an aquifer system to processes of water transport, sorption-desorption, dissolution-precipitation, radioactive ingrowth-decay, and α recoil. Isotopes of U and Rn were measured in 23 groundwater samples collected from a basaltic aquifer at the Idaho National Engineering and Environmental Laboratory (INEEL), Idaho. The results show that groundwater activities of Th and Ra isotopes are 2--4 orders lower than those of their U progenitors. Modeling of the observed disequilibria places the following constraints on the time scale of radionuclide migration and water-rock interaction at INEEL: (1) Time for sorption is minutes for Ra and Th; time for desorption is days for Ra and years for Th; and time for precipitation is days for Th, years for Ra, and centuries for U. (2) Retardation factors due to sorption average > 10 6 for 232 Th, approximately10 4 for 226 Ra, and approximately10 3 for 238 U. (3) Dissolution rates of rocks are approximately70 to 800 mg/L/y. (4) Ages of groundwater range from 222 Rn occur near the groundwater recharging sites as well as in the major flow pathways. Decay of the sorbed parent radionuclides (e.g., 226 Ra and 228 Ra) on micro-fracture surfaces constitutes an important source of their daughter ( 222 Rn and 228 Th) activities in groundwater

Impact of leachable sulfate on the quality of groundwater in the Pocatello aquifer

International Nuclear Information System (INIS)

Meehan, C.; Welhan, J.

1994-01-01

During the summer of 1993, groundwaters and surface waters were found to have anomalous sulfate concentrations in the Southern Pocatello municipal aquifer in an area known as the Highway Ponds. Leach tests performed on a large pile of road aggregate stockpiled near the Highway Ponds have been identified as the most likely source for the sulfate. Correlating trends of sulfate and chloride concentrations can be found both in the main Pocatello aquifer and in Pocatello Creek groundwaters. The chloride contamination at Pocatello Creek has previously been suggested to be derived from road salt. It is hypothesized that aggregate used in roadbed construction may be responsible for elevated sulfate in the areas groundwater. Chemical modeling has eliminated carbonate precipitation/dissolution reactions in buffering the chemistry of sulfate-impacted groundwater. Ion-exchange with clays is hypothesized to be a more significant process and is being investigated further. 12 refs., 3 figs

Geochemistry and environmental isotope of groundwater from the upper Cretaceous aquifer of Orontes basin (Syria)

International Nuclear Information System (INIS)

Al-Charideh, A.

2010-03-01

Chemical and environmental isotopes have been used for studying the Upper Cretaceous aquifer systems in the Middle Orontes basin. The results indicate that the salinity of groundwater (0.2 to 2 g/l) reveals the dissolution of evaporate rocks is the main factor of high salinity especially in the Homes depression. The degree of salinity and its spaces distribution are basically related to the pattern of groundwater movement in the Upper cretaceous aquifer. The stable isotopes composition of groundwater in the Homes depression are more depleted by -2.5% and -17.0% for δ 18 O and δ 2 H respectively, than the groundwater from Hama elevation, suggested different origin and recharge time between this two groundwater groups. Estimates of their mean subsurface residence times have been constrained on the basis of 14 C D IC. The corrected ages of groundwater are recent and less to 10 thousand years in Hama uplift. However, the corrected age of groundwater in the Homs depression range between 10 to 25 thousand years indicate late Pleistocene recharge period. (author)

Water-rock interaction and geochemistry of groundwater from the Ain Azel aquifer, Algeria.

Science.gov (United States)

Belkhiri, Lazhar; Mouni, Lotfi; Tiri, Ammar

2012-02-01

Hydrochemical, multivariate statistical, and inverse geochemical modeling techniques were used to investigate the hydrochemical evolution within the Ain Azel aquifer, Algeria. Cluster analysis based on major ion contents defined 3 main chemical water types, reflecting different hydrochemical processes. The first group water, group 1, has low salinity (mean EC = 735 μS/cm). The second group waters are classified as Cl-HCO(3)-alkaline earth type. The third group is made up of water samples, the cation composition of which is dominated by Ca and Mg with anion composition varying from dominantly Cl to dominantly HCO(3) plus SO(4). The varifactors obtained from R-mode FA indicate that the parameters responsible for groundwater quality variations are mainly related to the presence and dissolution of some carbonate, silicate, and evaporite minerals in the aquifer. Inverse geochemical modeling along groundwater flow paths indicates the dominant processes are the consumption of CO(2), the dissolution of dolomite, gypsum, and halite, along with the precipitation of calcite, Ca-montmorillonite, illite, kaolinite, and quartz. © Springer Science+Business Media B.V. 2011

Hydrogeochemical characterization of groundwater in the Outaouais Region (Québec, Canada) - A regional scale study

Science.gov (United States)

Montcoudiol, N.; Molson, J. W.; Lemieux, J.

2013-12-01

As part of the Québec regional groundwater characterization program (PACES), a detailed groundwater quality survey was undertaken in the Outaouais Region (Québec, Canada). During the summers of 2011 and 2012, 139 samples were taken from municipal and private wells which were analysed for major ions, nutrients, metals and sulphides. About 70% of the samples were obtained from bedrock wells, mainly in the Canadian Shield and the remainder from wells screened in Quaternary deposit aquifers. Hydrogeochemical facies were determined for 127 samples which had anion-cation charge balance errors within ×10 %. Ca-HCO3 is the dominant water type (65%) which was mainly found in unconfined aquifers, especially Quaternary deposits, and is typical of recently infiltrated rainwater. Other relevant water types are Na-HCO3 and Na-Cl (17 and 6% respectively), characteristic of confined aquifers. This classification by water type is supported by multivariate statistical analysis, namely Principal Component Analysis (PCA) and Hierarchical Clustering Analysis (HCA). PCA allows the identification of three factors controlling groundwater chemistry: salinity, silicate dissolution and F-bearing mineral dissolution. HCA results show that the samples can be grouped into seven clusters. Clusters 1 to 4 are mostly Ca-HCO3 water type and are representative of the enrichment in major ions due to carbonate and silicate dissolution, cluster 1 being closer to rainwater and cluster 4 the most evolved. Cluster 5, made of one sample with a particular chemistry, is not yet fully understood. Samples from cluster 6 present various degrees of Na-Ca exchange, a consequence of remnant Champlain Sea water (some samples from cluster 7 in confined zones) being replaced by infiltrating recharge water. Samples from cluster 7 are evolved waters with high Total Dissolved Solid (TDS) concentrations: they are remnants of the Champlain Sea in confined aquifers (bromide detected) or diluted/mixed by infiltrating

HIV status awareness, partnership dissolution and HIV transmission in generalized epidemics.

Directory of Open Access Journals (Sweden)

Georges Reniers

Full Text Available HIV status aware couples with at least one HIV positive partner are characterized by high separation and divorce rates. This phenomenon is often described as a corollary of couples HIV Testing and Counseling (HTC that ought to be minimized. In this contribution, we demonstrate the implications of partnership dissolution in serodiscordant couples for the propagation of HIV.We develop a compartmental model to study epidemic outcomes of elevated partnership dissolution rates in serodiscordant couples and parameterize it with estimates from population-based data (Rakai, Uganda.Via its effect on partnership dissolution, every percentage point increase in HIV status awareness reduces HIV incidence in monogamous populations by 0.27 percent for women and 0.63 percent for men. These effects are even larger when the assumption of monogamy can be relaxed, but are moderated by other behavior changes (e.g., increased condom use in HIV status aware serodiscordant partnerships. When these behavior changes are taken into account, each percentage point increase in HIV status awareness reduces HIV incidence by 0.13 and 0.32 percent for women and men, respectively (assuming monogamy. The partnership dissolution effect exists because it decreases the fraction of serodiscordant couples in the population and prolongs the time that individuals spend outside partnerships.Our model predicts that elevated partnership dissolution rates in HIV status aware serodiscordant couples reduce the spread of HIV. As a consequence, the full impact of couples HTC for HIV prevention is probably larger than recognized to date. Particularly high partnership dissolution rates in female positive serodiscordant couples contribute to the gender imbalance in HIV infections.

Assessment of groundwater contamination by gypsum dissolution in San Luis Potosí (México) using geoelectrical characterization

Science.gov (United States)

Arango-Galvan, C.; Ramos-Leal, J. A.; Yáñez-Rodríguez, M. A.; Corbo-Camargo, F.

2017-12-01

The Cerritos and Río Verde aquifers in San Luis Potosí (central México) make up a very complex aquifer system that is seriously affected by the overexploitation and the high concentration of sulphates. Currently, it is partially closed for extraction causing a substantial decrease in per capita drinking water availability affecting to more than 50,000 inhabitants in the region. Therefore, a very comprehensive study has been proposed in order to evaluate not only the groundwater contamination distribution but also to better know the aquifer configuration and its main hydrogeological characteristics as well. These studies include a detailed geological reconnaissance, hydrogeochemical analyses and a geoelectrical characterization. The main goal is to assess the aquifer geometry and to identify the gypsum horizons causing the presence of higher concentrations of sulphates in drinking water. A total of 26 audiomagnetotelluric soundings were measured and modelled along profiles following a perpendicular direction to the NW regional trending. Two-dimensional resistivity models suggest the presence of a shallow conductive layer (C1) with resistivity values ranging from 10 to 20 Ohm.m. It is related to the upper aquifer with a very low exploitation potential. A less conductive horizon (C2; 50 Ohm.m) underlying the shallow aquifer could be related to a very fractured limestone horizon forming a confined aquifer in the middle of the valley. A very resistive layer (R1) is observed underlying C1 and C2 units. This strata shows higher resistivity values (>100 Ohm.m) and could be associated with a reefal limestone identified as El Abra Formation. Finally, a conductive layer (<100 Ohm.m) observed beneath this horizon could be related to the oldest stratigraphic unit outcropping on the region, the Guaxcamá Formation, a gypsum-enriched unit, that contributes to the presence of sulphates in the upper aquifers by dissolution processes.

New isotopic evidence for the origin of groundwater from the Nubian Sandstone Aquifer in the Negev, Israel

Science.gov (United States)

Vengosh, A.; Hening, S.; Ganor, J.; Mayer, B.; Weyhenmeyer, C.E.; Bullen, T.D.; Paytan, A.

2007-01-01

The geochemistry and isotopic composition (H, O, S, Osulfate, C, Sr) of groundwater from the Nubian Sandstone (Kurnub Group) aquifer in the Negev, Israel, were investigated in an attempt to reconstruct the origin of the water and solutes, evaluate modes of water-rock interactions, and determine mean residence times of the water. The results indicate multiple recharge events into the Nubian sandstone aquifer characterized by distinctive isotope signatures and deuterium excess values. In the northeastern Negev, groundwater was identified with deuterium excess values of ???16???, which suggests local recharge via unconfined areas of the aquifer in the Negev anticline systems. The ??18OH2O and ??2H values (-6.5??? and -35.4???) of this groundwater are higher than those of groundwater in the Sinai Peninsula and southern Arava valley (-7.5??? and -48.3???) that likewise have lower deuterium excess values of ???10???. Based on the geochemical differences between groundwater in the unconfined and confined zones of the aquifer, a conceptual geochemical model for the evolution of the groundwater in the Nubian sandstone aquifer has been reconstructed. The isotopic composition of shallow groundwater from the unconfined zone indicates that during recharge oxidation of pyrite to SO4 (??34SSO4 ???-13???; ??18OSO4 ???+7.7???) and dissolution of CaCO3 (87Sr/86Sr ???0.70787; ??13CDIC = -3.7???) occur. In the confined zone of the aquifer, bacterial SO4 reduction removes a significant part of dissolved SO42 -, thereby modifying its isotopic composition (??34SSO4 ???-2???; ??18OSO4 ???+8.5???) and liberating dissolved inorganic C that contains little or no radiocarbon (14C-free) with low ??13CDIC values (contribution of external groundwater sources to the Nubian Sandstone aquifer, resulting in further modifications of the groundwater chemical and isotopic signatures. In the northeastern Negev, it is shown that SO4-rich groundwater from the underlying Jurassic aquifer contributes

Evaluation of processes controlling the geochemical constituents in deep groundwater in Bangladesh: Spatial variability on arsenic and boron enrichment

International Nuclear Information System (INIS)

Halim, M.A.; Majumder, R.K.; Nessa, S.A.; Hiroshiro, Y.; Sasaki, K.; Saha, B.B.; Saepuloh, A.; Jinno, K.

2010-01-01

Forty-six deep groundwater samples from highly arsenic affected areas in Bangladesh were analyzed in order to evaluate the processes controlling geochemical constituents in the deep aquifer system. Spatial trends of solutes, geochemical modeling and principal component analysis indicate that carbonate dissolution, silicate weathering and ion exchange control the major-ion chemistry. The groundwater is dominantly of Na-Cl type brackish water. Approximately 17% of the examined groundwaters exhibit As concentrations higher than the maximum acceptable limit of 10 μg/L for drinking water. Strong correlation (R 2 = 0.67) of Fe with dissolved organic carbon (DOC) and positive saturation index of siderite suggests that the reductive dissolution of Fe-oxyhydroxide in presence of organic matter is considered to be the dominant process to release high content of Fe (median 0.31 mg/L) in the deep aquifer. In contrast, As is not correlated with Fe and DOC. Boron concentration in the 26% samples exceeds the standard limit of 500 μg/L, for water intended for human consumption. Negative relationships of B/Cl ratio with Cl and boron with Na/Ca ratio demonstrate the boron in deep groundwater is accompanied by brackish water and cation exchange within the clayey sediments.

Minimizing Characterization - Derived Waste at the Department of Energy Savannah River Site, Aiken, South Carolina

Energy Technology Data Exchange (ETDEWEB)

Van Pelt, R. S.; Amidon, M. B.; Reboul, S. H.

2002-02-25

Environmental restoration activities at the Department of Energy Savannah River Site (SRS) utilize innovative site characterization approaches and technologies that minimize waste generation. Characterization is typically conducted in phases, first by collecting large quantities of inexpensive data, followed by targeted minimally invasive drilling to collect depth-discrete soil/groundwater data, and concluded with the installation of permanent multi-level groundwater monitoring wells. Waste-reducing characterization methods utilize non-traditional drilling practices (sonic drilling), minimally intrusive (geoprobe, cone penetrometer) and non-intrusive (3-D seismic, ground penetration radar, aerial monitoring) investigative tools. Various types of sensor probes (moisture sensors, gamma spectroscopy, Raman spectroscopy, laser induced and X-ray fluorescence) and hydrophobic membranes (FLUTe) are used in conjunction with depth-discrete sampling techniques to obtain high-resolution 3-D plume profiles. Groundwater monitoring (short/long-term) approaches utilize multi-level sampling technologies (Strata-Sampler, Cone-Sipper, Solinst Waterloo, Westbay) and low-cost diffusion samplers for seepline/surface water sampling. Upon collection of soil and groundwater data, information is portrayed in a Geographic Information Systems (GIS) format for interpretation and planning purposes. At the SRS, the use of non-traditional drilling methods and minimally/non intrusive investigation approaches along with in-situ sampling methods has minimized waste generation and improved the effectiveness and efficiency of characterization activities.

Minimizing Characterization - Derived Waste at the Department of Energy Savannah River Site, Aiken, South Carolina

International Nuclear Information System (INIS)

Van Pelt, R. S.; Amidon, M. B.; Reboul, S. H.

2002-01-01

Environmental restoration activities at the Department of Energy Savannah River Site (SRS) utilize innovative site characterization approaches and technologies that minimize waste generation. Characterization is typically conducted in phases, first by collecting large quantities of inexpensive data, followed by targeted minimally invasive drilling to collect depth-discrete soil/groundwater data, and concluded with the installation of permanent multi-level groundwater monitoring wells. Waste-reducing characterization methods utilize non-traditional drilling practices (sonic drilling), minimally intrusive (geoprobe, cone penetrometer) and non-intrusive (3-D seismic, ground penetration radar, aerial monitoring) investigative tools. Various types of sensor probes (moisture sensors, gamma spectroscopy, Raman spectroscopy, laser induced and X-ray fluorescence) and hydrophobic membranes (FLUTe) are used in conjunction with depth-discrete sampling techniques to obtain high-resolution 3-D plume profiles. Groundwater monitoring (short/long-term) approaches utilize multi-level sampling technologies (Strata-Sampler, Cone-Sipper, Solinst Waterloo, Westbay) and low-cost diffusion samplers for seepline/surface water sampling. Upon collection of soil and groundwater data, information is portrayed in a Geographic Information Systems (GIS) format for interpretation and planning purposes. At the SRS, the use of non-traditional drilling methods and minimally/non intrusive investigation approaches along with in-situ sampling methods has minimized waste generation and improved the effectiveness and efficiency of characterization activities

Dissolution Methods Database

Data.gov (United States)

U.S. Department of Health & Human Services — For a drug product that does not have a dissolution test method in the United States Pharmacopeia (USP), the FDA Dissolution Methods Database provides information on...

Investigation on Microbial Dissolution of Uranium (VI) from Autunite Mineral - 13421

International Nuclear Information System (INIS)

Sepulveda, Paola; Katsenovich, Yelena; Lagos, Leonel

2013-01-01

Precipitating autunite minerals by polyphosphate injection was identified as a feasible remediation strategy for sequestering uranium in contaminated groundwater and soil in situ at the Hanford Site. Autunite stability under vadose and saturated zone environmental conditions can help to determine the long-term effectiveness of this remediation strategy. The Arthrobacter bacteria are one of the most common groups in soils and are found in large numbers in Hanford soil as well as other subsurface environments contaminated with radionuclides. Ubiquitous in subsurface microbial communities, these bacteria can play a significant role in the dissolution of minerals and the formation of secondary minerals. The main objective of this investigation was to study the bacterial interactions under oxidizing conditions with uranium (VI); study the potential role of bicarbonate, which is an integral complexing ligand for U(VI) and a major ion in groundwater compositions; and present data from autunite dissolution experiments using Arthrobacter strain G968, a less U(VI)-tolerant strain. Sterile 100 mL glass mixed reactors served as the major bioreactor for initial experimentation. These autunite-containing bioreactors were injected with bacterial cells after the autunite equilibrated with the media solution amended with 0 mM, 3 mM 5 mM and 10 mM concentrations of bicarbonate. G968 Arthrobacter cells in the amount of 10 6 cells/mL were injected into the reactors after 27 days, giving time for the autunite to reach steady state. Abiotic non-carbonate controls were kept without bacterial inoculation to provide a control for the biotic samples. Samples of the solution were analyzed for dissolved U(VI) by means of kinetic phosphorescence analyzer KPA-11 (Chemcheck Instruments, Richland, WA). Analysis showed that as [HCO 3 - ] increases, a diminishing trend on the effect of bacteria on autunite leaching is observed. Viability of cells was conducted after 24 hours of cell incubation with

Investigation on Microbial Dissolution of Uranium (VI) from Autunite Mineral - 13421

Energy Technology Data Exchange (ETDEWEB)

Sepulveda, Paola; Katsenovich, Yelena; Lagos, Leonel [Applied Research Center, Florida International University. 10555 West Flagler St. Suite 2100, Miami Fl 33175 (United States)

2013-07-01

Precipitating autunite minerals by polyphosphate injection was identified as a feasible remediation strategy for sequestering uranium in contaminated groundwater and soil in situ at the Hanford Site. Autunite stability under vadose and saturated zone environmental conditions can help to determine the long-term effectiveness of this remediation strategy. The Arthrobacter bacteria are one of the most common groups in soils and are found in large numbers in Hanford soil as well as other subsurface environments contaminated with radionuclides. Ubiquitous in subsurface microbial communities, these bacteria can play a significant role in the dissolution of minerals and the formation of secondary minerals. The main objective of this investigation was to study the bacterial interactions under oxidizing conditions with uranium (VI); study the potential role of bicarbonate, which is an integral complexing ligand for U(VI) and a major ion in groundwater compositions; and present data from autunite dissolution experiments using Arthrobacter strain G968, a less U(VI)-tolerant strain. Sterile 100 mL glass mixed reactors served as the major bioreactor for initial experimentation. These autunite-containing bioreactors were injected with bacterial cells after the autunite equilibrated with the media solution amended with 0 mM, 3 mM 5 mM and 10 mM concentrations of bicarbonate. G968 Arthrobacter cells in the amount of 10{sup 6} cells/mL were injected into the reactors after 27 days, giving time for the autunite to reach steady state. Abiotic non-carbonate controls were kept without bacterial inoculation to provide a control for the biotic samples. Samples of the solution were analyzed for dissolved U(VI) by means of kinetic phosphorescence analyzer KPA-11 (Chemcheck Instruments, Richland, WA). Analysis showed that as [HCO{sub 3}{sup -}] increases, a diminishing trend on the effect of bacteria on autunite leaching is observed. Viability of cells was conducted after 24 hours of cell

100-N pilot project: Proposed consolidated groundwater monitoring program

International Nuclear Information System (INIS)

Borghese, J.V.; Hartman, M.J.; Lutrell, S.P.; Perkins, C.J.; Zoric, J.P.; Tindall, S.C.

1996-11-01

This report presents a proposed consolidated groundwater monitoring program for the 100-N Pilot Project. This program is the result of a cooperative effort between the Hanford Site contractors who monitor the groundwater beneath the 100-N Area. The consolidation of the groundwater monitoring programs is being proposed to minimize the cost, time, and effort necessary for groundwater monitoring in the 100-N Area, and to coordinate regulatory compliance activities. The integrity of the subprograms requirements remained intact during the consolidation effort. The purpose of this report is to present the proposed consolidated groundwater monitoring program and to summarize the process by which it was determined

The origin of groundwater composition in the Pampeano Aquifer underlying the Del Azul Creek basin, Argentina.

Science.gov (United States)

Zabala, M E; Manzano, M; Vives, L

2015-06-15

The Pampean plain is the most productive region in Argentina. The Pampeano Aquifer beneath the Pampean plain is used mostly for drinking water. The study area is the sector of the Pampeano Aquifer underlying the Del Azul Creek basin, in Buenos Aires province. The main objective is to characterize the chemical and isotopic compositions of groundwater and their origin on a regional scale. The methodology used involved the identification and characterization of potential sources of solutes, the study of rain water and groundwater chemical and isotopic characteristics to deduce processes, the development of a hydrogeochemical conceptual model, and its validation by hydrogeochemical modelling with PHREEQC. Groundwater samples come mostly from a two-depth monitoring network of the "Dr. Eduardo J. Usunoff" Large Plains Hydrology Institute (IHLLA). Groundwater salinity increases from SW to NE, where groundwater is saline. In the upper basin groundwater is of the HCO3-Ca type, in the middle basin it is HCO3-Na, and in the lower basin it is ClSO4-NaCa and Cl-Na. The main processes incorporating solutes to groundwater during recharge in the upper basin are rain water evaporation, dissolution of CO2, calcite, dolomite, silica, and anorthite; cationic exchange with Na release and Ca and Mg uptake, and clay precipitation. The main processes modifying groundwater chemistry along horizontal flow at 30 m depth from the upper to the lower basin are cationic exchange, dissolution of silica and anorthite, and clay precipitation. The origin of salinity in the middle and lower basin is secular evaporation in a naturally endorheic area. In the upper and middle basins there is agricultural pollution. In the lower basin the main pollution source is human liquid and solid wastes. Vertical infiltration through the boreholes annular space during the yearly flooding stages is probably the pollution mechanism of the samples at 30 m depth. Copyright © 2015 Elsevier B.V. All rights reserved.

Reactive transport modelling of groundwater chemistry in a chalk aquifer at the watershed scale.

Science.gov (United States)

Mangeret, A; De Windt, L; Crançon, P

2012-09-01

This study investigates thermodynamics and kinetics of water-rock interactions in a carbonate aquifer at the watershed scale. A reactive transport model is applied to the unconfined chalk aquifer of the Champagne Mounts (France), by considering both the chalk matrix and the interconnected fracture network. Major element concentrations and main chemical parameters calculated in groundwater and their evolution along flow lines are in fair agreement with field data. A relative homogeneity of the aquifer baseline chemistry is rapidly reached in terms of pH, alkalinity and Ca concentration since calcite equilibrium is achieved over the first metres of the vadose zone. However, incongruent chalk dissolution slowly releases Ba, Mg and Sr in groundwater. Introducing dilution effect by rainwater infiltration and a local occurrence of dolomite improves the agreement between modelling and field data. The dissolution of illite and opal-CT, controlling K and SiO(2) concentrations in the model, can be approximately tackled by classical kinetic rate laws, but not the incongruent chalk dissolution. An apparent kinetic rate has therefore been fitted on field data by inverse modelling: 1.5×10(-5) mol(chalk)L (-1) water year (-1). Sensitivity analysis indicates that the CO(2) partial pressure of the unsaturated zone is a critical parameter for modelling the baseline chemistry over the whole chalk aquifer. Copyright © 2012 Elsevier B.V. All rights reserved.

Dry Stream Reaches in Carbonate Terranes: Surface Indicators of Ground-Water Reservoirs

Science.gov (United States)

Brahana, J.V.; Hollyday, E.F.

1988-01-01

In areas where dry stream reaches occur, subsurface drainage successfully competes with surface drainage, and sheet-like dissolution openings have developed parallel to bedding creating the ground-water reservoir. Union Hollow in south-central Tennessee is the setting for a case study that illustrates the application of the dry stream reach technique. In this technique, dry stream reach identification is based on two types of readily acquired information: remotely sensed black and white infrared aerial photography; and surface reconnaissance of stream channel characteristics. Test drilling in Union Hollow subsequent to identification of the dry reach proved that a localized ground-water reservoir was present.

A kinetic model for borosilicate glass dissolution based on the dissolution affinity of a surface alteration layer

International Nuclear Information System (INIS)

Bourcier, W.L.; Peiffer, D.W.; Knauss, K.G.; McKeegan, K.D.; Smith, D.K.

1989-11-01

A kinetic model for the dissolution of borosilicate glass is used to predict the dissolution rate of a nuclear waste glass. In the model, the glass dissolution rate is controlled by the rate of dissolution of an alkali-depleted amorphous surface (gel) layer. Our model predicts that all components concentrated in the surface layer, affect glass dissolution rates. The good agreement between predicted and observed elemental dissolution rates suggests that the dissolution rate of the gel layer limits the overall rate of glass dissolution. The model predicts that the long-term rate of glass dissolution will depend mainly on ion concentrations in solution, and therefore on the secondary phases which precipitate and control ion concentrations. 10 refs., 5 figs., 1 tab

From laboratory experiments to a geological disposal vault: calculation of used nuclear fuel dissolution rates

International Nuclear Information System (INIS)

Sunder, S.; Shoesmith, D.W.; Kolar, M.; Leneveu, D.M.

1998-01-01

Calculation of used nuclear fuel dissolution rates in a geological disposal vault requires a knowledge of the redox conditions in the vault. For redox conditions less oxidizing than those causing UO 2 oxidation to the U 3 O 7 , stage, a thermodynamically-based model is appropriate. For more oxidizing redox conditions a kinetic or an electrochemical model is needed to calculate these rates. The redox conditions in a disposal vault will be affected by the radiolysis of groundwater by the ionizing radiation associated with the fuel. Therefore, we have calculated the alpha-, beta- and gamma-dose rates in water in contact with the reference used fuel in the Canadian Nuclear Fuel Waste Management Program (CNFWMP) as a function of cooling time. Also, we have determined dissolution rates of UO 2 fuel as a function of alpha and gamma dose rates from our electrochemical measurements. These room-temperature rates are used to calculate the dissolution rates of used fuel at 100 o C, the highest temperature expected in a container in the CNFWMP, as a function of time since emplacement. It is shown that beta radiolysis of water will be the main cause of oxidation of used CANDU fuel in a failed container. The use of a kinetic or an electrochemical corrosion model, to calculate fuel dissolution rates, is required for a period of ∼1000 a following emplacement of copper containers in the geologic disposal vault envisaged in the CNFWMP. Beyond this time period a thermodynamically-based model adequately predicts the fuel dissolution rates. The results presented in this paper can be adopted to calculate used fuel dissolution rates for other used UO 2 fuels in other waste management programs. (author)

Modelling of the UO2 dissolution mechanisms in synthetic groundwater. Experiments carried out under anaerobic and reducing conditions

International Nuclear Information System (INIS)

Cera, E.; Grive, M.; Bruno, J.; Ollila, K.

2000-07-01

The experimental data generated under anaerobic and reducing conditions within the EU R and D programme 1996-1998 entitled 'Source term for performance assessment of spent fuel as a waste form' and published as a POSIVA report (Ollila, 1999) have been modelled in the present work. The dissolution data available, mainly U in the aqueous phase as a function of time and redox potentials have been used to elucidate the redox pairs controlling the redox potential of the systems studied. Dissolution experiments carried out under anaerobic conditions have shown the important role of the uranium system on buffering the redox capacity of these systems. In the presence of carbonates in the system, the redox control has been given by the UO 2 (c)/U(VI) aqueous redox couple while in absence of carbonates in the system, the redox control has been governed by the UO 2 (c)/UO 2+x transition. In addition dissolution rates have been satisfactorily modelled by assuming an oxidative dissolution mechanism consisting in an initial oxidation of the surface of the uranium dioxide, binding of the HCO 3 or H+ at the U(VI) sites of the oxidised surface layer and detachment of these surface complexes. The redox controls in the experiments carried out under reducing conditions have been exerted by the different reducing agents added in the systems. Therefore, the addition of Fe 2+ lead to a redox control exerted by the Fe 2+ /Fe(OH) 3 (s) redox pair, while the addition of sulphide lead to a different redox control governed by the HS/SO 3 2- redox pair. (orig.)

Minimal groundwater leakage restricts salinity in a hydrologically terminal basin of northwest Australia

Science.gov (United States)

Skrzypek, Grzegorz; Dogramaci, Shawan; Rouillard, Alexandra; Grierson, Pauline

2016-04-01

The Fortescue Marsh (FM) is one of the largest wetlands of arid northwest Australia (~1200 km2) and is thought to act as a terminal basin for the Upper Fortescue River catchment. Unlike the playa lake systems that predominate in most arid regions, where salinity is driven by inflow and evaporation of groundwater, the hydrological regime of the FM is driven by inundation from irregular cyclonic events [1]. Surface water of the FM is fresh to brackish and the salinity of the deepest groundwater (80 m b.g.l.) does not exceed 160 g/L; salt efflorescences are rarely present on the surface [2]. In this study, we tested the hypothesis that persistent but low rates of groundwater outflow have restricted the accumulation of salt in the FM over time. Using hydrological, hydrochemical data and dimensionless time evaporation modelling along with the water and salt budget, we calculated the time and the annual groundwater discharge volume that would be required to achieve and maintain the range of salinity levels observed in the Marsh. Groundwater outflow from alluvial and colluvial aquifers to the Lower Fortescue catchment is limited by an extremely low hydraulic gradient of 0.001 and is restricted to a relatively small 'alluvial window' of 0.35 km2 because of the elevation of the basement bedrock at the Marsh outflow. We show that if the Marsh was 100% "leakage free" i.e., a true terminal basin for the Upper Fortescue Catchment, the basin water would have achieved salt saturation after ~45 ka. This is not the case and only a very small outflow of saline groundwater of water volume) is needed to maintain the current salinity conditions. The minimum time required to develop the current hydrochemical composition of the water in the Marsh and the steady-state conditions for salt concentration is between 58 and 164 ka. This is a minimum age of the Marsh but it can be much older as nearly steady-state conditions could be maintained infinitely. Our approach using a combined water

Groundwater geochemistry of the Yucatan Peninsula, Mexico: Constraints on stratigraphy and hydrogeology

Science.gov (United States)

Perry, Eugene; Paytan, Adina; Pedersen, Bianca; Velazquez-Oliman, Guadalupe

2009-03-01

SummaryWe report 87Sr/ 86Sr and ion concentrations of sulfate, chloride, and strontium in the groundwater of the northern and central Yucatan Peninsula, Mexico. Correlation between these data indicates that ejecta from the 65.95 m.y. old Chicxulub impact crater have an important effect on hydrogeology, geomorphology, and soil development of the region. Ejecta are present at relatively shallow subsurface depths in north-central Yucatan and at the surface along the Rio Hondo escarpment in southeast Quintana Roo, where they are referred to as the Albion Formation. Anhydrite/gypsum (and by inference celestite) are common in impact ejecta clasts and in beds and cements of overlying Paleocene and Lower Eocene rocks cored around the margin of the crater. The sulfate-rich minerals that are found in rocks immediately overlying the impact ejecta blanket, may either be partially mobilized from the ejecta layer itself or may have been deposited after the K/T impact event in an extensive pre-Oligocene shallow sea. These deposits form a distinctive sedimentary package that can be easily traced by the Eocene-Cretaceous 87Sr/ 86Sr signal. A distinct Sr isotopic signature and high SO 4/Cl ratios are observed in groundwater of northwestern and north-central Yucatan that interacts with these rocks. Moreover, the distribution of the gypsum-rich stratigraphic unit provides a solution-enhanced subsurface drainage pathway for a broad region characterized by dissolution features (poljes) extending from Chetumal, Quintana Roo to Campeche, Campeche. The presence of gypsum quarries in the area is also consistent with a sulfate-rich stratigraphic "package" that includes ejecta. The distinctive chemistry of groundwater that has been in contact with evaporite/ejecta can be used to trace flow directions and confirms a groundwater divide in the northern Peninsula. Information about groundwater flow directions and about deep subsurface zones of high permeability is useful for groundwater and

Arsenic in Holocene aquifers of the Red River floodplain, Vietnam: Effects of sediment-water interactions, sediment burial age and groundwater residence time

Science.gov (United States)

Sø, Helle Ugilt; Postma, Dieke; , Mai Lan, Vi; Pham, Thi Kim Trang; Kazmierczak, Jolanta; Dao, Viet Nga; Pi, Kunfu; Koch, Christian Bender; Pham, Hung Viet; Jakobsen, Rasmus

2018-03-01

Water-sediment interactions were investigated in arsenic contaminated Holocene aquifers of the Red River floodplain, Vietnam, in order to elucidate the origin of the spatial variability in the groundwater arsenic concentration. The investigated aquifers are spread over an 8 × 13 km field area with sediments that varied in burial age from V) redox couple was found in disequilibrium with the other redox couples. Using the pe calculated from the CH4/CO2 redox couple we show that the groundwater has a reducing potential towards Fe-oxides ranging from ferrihydrite to poorly crystalline goethite, but not for well crystalline goethite or hematite. Hematite and poorly crystalline goethite were identified as the Fe-oxides present in the sediments. Reductive dissolution experiments identify two phases releasing Fe(II); one rapidly dissolving that also contains As and a second releasing Fe(II) more slowly but without As. The initial release of Fe and As occurs at a near constant As/Fe ratio that varied from site to site between 1.2 and 0.1 mmol As/mol Fe. Siderite (FeCO3) is the main sink for Fe(II), based on saturation calculations as well as the identification of siderite in the sediment. Most of the carbonate incorporated in siderite originates from the dissolution of sedimentary CaCO3. Over time the CaCO3 content of the sediments diminishes and FeCO3 appears instead. No specific secondary phases that incorporate arsenite could be identified. Alternatively, the amount of arsenic mobilized during the dissolution of reactive phases can be contained in the pool of adsorbed arsenite. Combining groundwater age with aquifer sediment age allows the calculation of the total number of pore volumes flushed through the aquifer. Comparison with groundwater chemistry shows the highest arsenic concentration to be present within the first 200 pore volumes flushed through the aquifer. These results agree with reactive transport modeling combining a kinetic description of reductive

Optimization of Dissolution Compartments in a Biorelevant Dissolution Apparatus Golem v2, Supported by Multivariate Analysis

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Ivan Stupák

2017-11-01

Full Text Available Biorelevant dissolution instruments represent an important tool for pharmaceutical research and development. These instruments are designed to simulate the dissolution of drug formulations in conditions most closely mimicking the gastrointestinal tract. In this work, we focused on the optimization of dissolution compartments/vessels for an updated version of the biorelevant dissolution apparatus—Golem v2. We designed eight compartments of uniform size but different inner geometry. The dissolution performance of the compartments was tested using immediate release caffeine tablets and evaluated by standard statistical methods and principal component analysis. Based on two phases of dissolution testing (using 250 and 100 mL of dissolution medium, we selected two compartment types yielding the highest measurement reproducibility. We also confirmed a statistically ssignificant effect of agitation rate and dissolution volume on the extent of drug dissolved and measurement reproducibility.

The origin of groundwater composition in the Pampeano Aquifer underlying the Del Azul Creek basin, Argentina

International Nuclear Information System (INIS)

Zabala, M.E.; Manzano, M.; Vives, L.

2015-01-01

The Pampean plain is the most productive region in Argentina. The Pampeano Aquifer beneath the Pampean plain is used mostly for drinking water. The study area is the sector of the Pampeano Aquifer underlying the Del Azul Creek basin, in Buenos Aires province. The main objective is to characterize the chemical and isotopic compositions of groundwater and their origin on a regional scale. The methodology used involved the identification and characterization of potential sources of solutes, the study of rain water and groundwater chemical and isotopic characteristics to deduce processes, the development of a hydrogeochemical conceptual model, and its validation by hydrogeochemical modelling with PHREEQC. Groundwater samples come mostly from a two-depth monitoring network of the “Dr. Eduardo J. Usunoff” Large Plains Hydrology Institute (IHLLA). Groundwater salinity increases from SW to NE, where groundwater is saline. In the upper basin groundwater is of the HCO 3 -Ca type, in the middle basin it is HCO 3 -Na, and in the lower basin it is ClSO 4 –NaCa and Cl–Na. The main processes incorporating solutes to groundwater during recharge in the upper basin are rain water evaporation, dissolution of CO 2 , calcite, dolomite, silica, and anorthite; cationic exchange with Na release and Ca and Mg uptake, and clay precipitation. The main processes modifying groundwater chemistry along horizontal flow at 30 m depth from the upper to the lower basin are cationic exchange, dissolution of silica and anorthite, and clay precipitation. The origin of salinity in the middle and lower basin is secular evaporation in a naturally endorheic area. In the upper and middle basins there is agricultural pollution. In the lower basin the main pollution source is human liquid and solid wastes. Vertical infiltration through the boreholes annular space during the yearly flooding stages is probably the pollution mechanism of the samples at 30 m depth. - Highlights: • The work studies the

The origin of groundwater composition in the Pampeano Aquifer underlying the Del Azul Creek basin, Argentina

Energy Technology Data Exchange (ETDEWEB)

Zabala, M.E., E-mail: mzabala@faa.unicen.edu.ar [Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Av. Rivadavia 1917, C1033AAJ Ciudad Autónoma de Buenos Aires (Argentina); Instituto de Hidrología de Llanuras “Dr. Eduardo J. Usunoff”, Av. República Italia 780, 7300 Azul, Provincia Buenos Aires (Argentina); Manzano, M., E-mail: marisol.manzano@upct.es [Escuela de Ingeniería de Caminos, Canales y Puertos y de Ingeniería de Minas, Universidad Politécnica de Cartagena, P° de Alfonso XIII 52, E-30203 Cartagena (Spain); Vives, L., E-mail: lvives@faa.unicen.edu.ar [Instituto de Hidrología de Llanuras “Dr. Eduardo J. Usunoff”, Av. República Italia 780, 7300 Azul, Provincia Buenos Aires (Argentina)

2015-06-15

The Pampean plain is the most productive region in Argentina. The Pampeano Aquifer beneath the Pampean plain is used mostly for drinking water. The study area is the sector of the Pampeano Aquifer underlying the Del Azul Creek basin, in Buenos Aires province. The main objective is to characterize the chemical and isotopic compositions of groundwater and their origin on a regional scale. The methodology used involved the identification and characterization of potential sources of solutes, the study of rain water and groundwater chemical and isotopic characteristics to deduce processes, the development of a hydrogeochemical conceptual model, and its validation by hydrogeochemical modelling with PHREEQC. Groundwater samples come mostly from a two-depth monitoring network of the “Dr. Eduardo J. Usunoff” Large Plains Hydrology Institute (IHLLA). Groundwater salinity increases from SW to NE, where groundwater is saline. In the upper basin groundwater is of the HCO{sub 3}-Ca type, in the middle basin it is HCO{sub 3}-Na, and in the lower basin it is ClSO{sub 4}–NaCa and Cl–Na. The main processes incorporating solutes to groundwater during recharge in the upper basin are rain water evaporation, dissolution of CO{sub 2}, calcite, dolomite, silica, and anorthite; cationic exchange with Na release and Ca and Mg uptake, and clay precipitation. The main processes modifying groundwater chemistry along horizontal flow at 30 m depth from the upper to the lower basin are cationic exchange, dissolution of silica and anorthite, and clay precipitation. The origin of salinity in the middle and lower basin is secular evaporation in a naturally endorheic area. In the upper and middle basins there is agricultural pollution. In the lower basin the main pollution source is human liquid and solid wastes. Vertical infiltration through the boreholes annular space during the yearly flooding stages is probably the pollution mechanism of the samples at 30 m depth. - Highlights: • The

PCR detection of groundwater bacteria associated with colloidal transport

Energy Technology Data Exchange (ETDEWEB)

Cruz-Perez, P.; Stetzenbach, L.D.; Alvarez, A.J.

1996-02-29

Colloidal transport may increase the amount of contaminant material than that which could be transported by water flow alone. The role of colloids in groundwater contaminant transport is complicated and may involve many different processes, including sorption of elements onto colloidal particles, coagulation/dissolution, adsorption onto solid surfaces, filtration, and migration. Bacteria are known to concentrate minerals and influence the transport of compounds in aqueous environments and may also serve as organic colloids, thereby influencing subsurface transport of radionuclides and other contaminants. The initial phase of the project consisted of assembling a list of bacteria capable of sequestering or facilitating mineral transport. The development and optimization of the PCR amplification assay for the detection of the organisms of interest, and the examination of regional groundwaters for those organisms, are presented for subsequent research.

PCR detection of groundwater bacteria associated with colloidal transport

International Nuclear Information System (INIS)

Cruz-Perez, P.; Stetzenbach, L.D.; Alvarez, A.J.

1996-01-01

Colloidal transport may increase the amount of contaminant material than that which could be transported by water flow alone. The role of colloids in groundwater contaminant transport is complicated and may involve many different processes, including sorption of elements onto colloidal particles, coagulation/dissolution, adsorption onto solid surfaces, filtration, and migration. Bacteria are known to concentrate minerals and influence the transport of compounds in aqueous environments and may also serve as organic colloids, thereby influencing subsurface transport of radionuclides and other contaminants. The initial phase of the project consisted of assembling a list of bacteria capable of sequestering or facilitating mineral transport. The development and optimization of the PCR amplification assay for the detection of the organisms of interest, and the examination of regional groundwaters for those organisms, are presented for subsequent research

Current Status of Groundwater Monitoring Networks in Korea

Directory of Open Access Journals (Sweden)

Jin-Yong Lee

2016-04-01

Full Text Available Korea has been operating groundwater monitoring systems since 1996 as the Groundwater Act enacted in 1994 enforces nationwide monitoring. Currently, there are six main groundwater monitoring networks operated by different government ministries with different purposes: National Groundwater Monitoring Network (NGMN, Groundwater Quality Monitoring Network (GQMN, Seawater Intrusion Monitoring Network (SIMN, Rural Groundwater Monitoring Network (RGMN, Subsidiary Groundwater Monitoring Network (SGMN, and Drinking Water Monitoring Network (DWMN. The Networks have a total of over 3500 monitoring wells and the majority of them are now equipped with automatic data loggers and remote terminal units. Most of the monitoring data are available to the public through internet websites. These Networks have provided scientific data for designing groundwater management plans and contributed to securing the groundwater resource particularly for recent prolonged drought seasons. Each Network, however, utilizes its own well-specifications, probes, and telecommunication protocols with minimal communication with other Networks, and thus duplicate installations of monitoring wells are not uncommon among different Networks. This mini-review introduces the current regulations and the Groundwater Monitoring Networks operated in Korea and provides some suggestions to improve the sustainability of the current groundwater monitoring system in Korea.

Determination of the origin of dissolved inorganic carbon in groundwater around a reclaimed landfill in Otwock using stable carbon isotopes.

Science.gov (United States)

Porowska, Dorota

2015-05-01

Chemical and isotopic analyses of groundwater from piezometers located around a reclaimed landfill in Otwock (Poland) were performed in order to trace the origin of dissolved inorganic carbon (DIC) in the groundwater. Due to differences in the isotopic composition of carbon from different sources, an analysis of stable carbon isotopes in the groundwater, together with the Keeling plot approach and a two-component mixing model allow us to evaluate the relative contributions of carbon from these sources in the groundwater. In the natural (background) groundwater, DIC concentrations and the isotopic composition of DIC (δ(13)CDIC) comes from two sources: decomposition of organic matter and carbonate dissolution within the aquifer sediments, whereas in the leachate-contaminated groundwater, DIC concentrations and δ(13)CDIC values depend on the degradation of organic matter within the aquifer sediments and biodegradation of organic matter stored in the landfill. From the mixing model, about 4-54% of the DIC pool is derived from organic matter degradation and 96-46% from carbonate dissolution in natural conditions. In the leachate-contaminated groundwater, about 20-53% of the DIC is derived from organic matter degradation of natural origin and 80-47% from biodegradation of organic matter stored in the landfill. Partial pressure of CO2 (P CO2) was generally above the atmospheric, hence atmospheric CO2 as a source of carbon in DIC pool was negligible in the aquifer. P CO2 values in the aquifer in Otwock were always one to two orders of magnitude above the atmospheric P CO2, and thus CO2 escaped directly into the vadose zone. Copyright © 2015 Elsevier Ltd. All rights reserved.

Dissolution of nuclear fuels

International Nuclear Information System (INIS)

Uriarte Hueda, A.; Berberana Eizmendi, M.; Rainey, R.

1968-01-01

A laboratory study was made of the instantaneous dissolution rate (IDR) for unirradiated uranium metal rods and UO 2 , PuO 2 and PuO 2 -UO 2 pellets in boiling nitric acid alone and with additives. The uranium metal and UO 2 dissolved readily in nitric acid alone; PuO 2 dissolved slowly even with the addition of fluoride; PuO 2 -UO 2 pellets containing as much as 35% PuO 2 in UO 2 gave values of the instantaneous dissolution rate to indicate can be dissolved with nitric acid alone. An equation to calculate the time for complete dissolution has been determinate in function of the instantaneous dissolution rates. The calculated values agree with the experimental. Uranium dioxide pellets from various sources but all having a same density varied in instantaneous dissolution rate. All the pellets, however, have dissolved ved in the same time. The time for complete dissolution of PuO 2 -UO 2 pellets, having the same composition, and the concentration of the used reagents are function of the used reagents are function of the fabrication method. (Author) 8 refs

Mapping groundwater renewability using age data in the Baiyang alluvial fan, NW China

Science.gov (United States)

Huang, Tianming; Pang, Zhonghe; Li, Jie; Xiang, Yong; Zhao, Zhijiang

2017-05-01

Groundwater age has been used to map renewability of water resources within four groups: strong, partial, and rare renewability, and non-renewable. The Baiyang alluvial fan in NW China is a representative area for examining groundwater recharge from river infiltration and for mapping groundwater renewability, and it has been investigated using multiple isotopes and water chemistry. Systematic sampling included 52 samples for 2H and 18O analysis and 32 samples for 3H, 13C and 14C analysis. The δ13C compositions remain nearly constant throughout the basin (median -12.7‰) and indicate that carbonate dissolution does not alter 14C age. The initial 14C activity of 80 pmC, obtained by plotting 3H and 14C activity, was used to correct groundwater 14C age. The results show that areas closer to the river consist of younger groundwater ages; this suggests that river infiltration is the main recharge source to the shallow groundwater system. However, at distances far away from the river, groundwater ages become older, i.e., from modern water (less than 60 year) to pre-modern water (from 60 to 1,000 years) and paleowater (more than 1,000 yeas). The four classifications of groundwater renewability have been associated with different age ranges. The area of shallow groundwater with strong renewability accounts for 74% of the total study area. Because recharge condition (river infiltration) controls overall renewability, a groundwater renewability map is of significant importance to the management of groundwater exploitation of this area as well as other arid groundwater basins.

Integration of ground-water and vadose-zone geochemistry to investigate hydrochemical evolution

International Nuclear Information System (INIS)

Fisher, R.S.; Mullican, W.F.

1990-01-01

This paper summarizes the results of an extensive groundwater-sampling program conducted in the Hueco Bolson and Diablo Plateau area of West Texas. The origin, hydrochemical evolution, and age of groundwater in arid lands of Trans-Pecos Texas were investigated by combining mineralogic analyses of soils and aquifer matrix, chemical analyses of readily soluble materials in soils and water extracted from the thick, unsaturated zone, and chemical and isotopic analyses of groundwater from three principal aquifers, the Diablo Plateau, Hueco Bolson, and Rio Grande alluvial aquifers. Repeated groundwater sampling over a 3-year period and quarterly sampling of selected wells revealed no significant short-term chemical or isotopic variability. Groundwater ages range from recent to nearly 28,000 years; the distribution of ages reflects relative permeability (transmissivity) of the aquifers. Most groundwaters evolve from calcium-bicarbonate to sodium-sulfate types because of carbonate and sulfate mineral dissolution coupled with exchange of aqueous calcium and magnesium for sodium on clay minerals. Water in the Rio Grande alluvial aquifer evolved to a sodium-chloride type as a result of extensive evapotranspiration on irrigated fields. The appendices list detailed results of field measurements of temperature, pH, Eh, dissolved oxygen, and major ion concentrations

Standard practice for measurement of the glass dissolution rate using the single-pass flow-through test method

CERN Document Server

American Society for Testing and Materials. Philadelphia

2010-01-01

1.1 This practice describes a single-pass flow-through (SPFT) test method that can be used to measure the dissolution rate of a homogeneous silicate glass, including nuclear waste glasses, in various test solutions at temperatures less than 100°C. Tests may be conducted under conditions in which the effects from dissolved species on the dissolution rate are minimized to measure the forward dissolution rate at specific values of temperature and pH, or to measure the dependence of the dissolution rate on the concentrations of various solute species. 1.2 Tests are conducted by pumping solutions in either a continuous or pulsed flow mode through a reaction cell that contains the test specimen. Tests must be conducted at several solution flow rates to evaluate the effect of the flow rate on the glass dissolution rate. 1.3 This practice excludes static test methods in which flow is simulated by manually removing solution from the reaction cell and replacing it with fresh solution. 1.4 Tests may be conducted wit...

Evaluation of a three compartment in vitro gastrointestinal simulator dissolution apparatus to predict in vivo dissolution.

Science.gov (United States)

Takeuchi, Susumu; Tsume, Yasuhiro; Amidon, Gregory E; Amidon, Gordon L

2014-11-01

In vitro dissolution tests are performed for new formulations to evaluate in vivo performance, which is affected by the change of gastrointestinal (GI) physiology, in the GI tract. Thus, those environmental changes should be introduced to an in vitro dissolution test. Many studies have successfully shown the improvement of in vitro-in vivo correlations (IVIVC) by introducing those physiological changes into dissolution tests. The gastrointestinal simulator (GIS), a multicompartment in vitro dissolution apparatus, was developed to evaluate in vivo drug dissolution. A gastric-emptying rate along with transit rate are key factors to evaluate in vivo drug dissolution and, hence, drug absorption. Dissolution tests with the GIS were performed with Biopharmaceutical Classification System class I drugs at five different gastric-emptying rates in the fasted state. Computational models were used to determine in vivo gastric-emptying time for propranolol and metoprolol based on the GIS dissolution results. Those were compared with published clinical data to determine the gastric half-emptying time. In conclusion, the GIS is a practical tool to assess dissolution properties and can improve IVIVC. © 2014 Wiley Periodicals, Inc. and the American Pharmacists Association.

Analysis of americium, plutonium and technetium solubility in groundwater

International Nuclear Information System (INIS)

Takeda, Seiji

1999-08-01

Safety assessments for geologic disposal of radioactive waste generally use solubilities of radioactive elements as the parameter restricting the dissolution of the elements from a waste matrix. This study evaluated americium, plutonium and technetium solubilities under a variety of geochemical conditions using the geochemical model EQ3/6. Thermodynamic data of elements used in the analysis were provided in the JAERI-data base. Chemical properties of both natural groundwater and interstitial water in buffer materials (bentonite and concrete) were investigated to determine the variations in Eh, pH and ligand concentrations (CO 3 2- , F - , PO 4 3- , SO 4 2- , NO 3 - and NH 4 + ). These properties can play an important role in the complexation of radioactive elements. Effect of the groundwater chemical properties on the solubility and formation of chemical species for americium, plutonium and technetium was predicted based on the solubility analyses under a variety of geochemical conditions. The solubility and speciation of the radioactive elements were estimated, taking into account the possible range of chemical compositions determined from the groundwater investigation. (author)

Human impact on regional groundwater composition through intervention in natural flow patterns and changes in land use

Science.gov (United States)

Schot, P. P.; van der Wal, J.

1992-06-01

The relations between groundwater composition, land use, soil conditions and flow patterns on a regional scale are studied for the Gooi and Vechtstreek area in the Netherlands. This densely populated area consists of a glacier-created ridge with dry sand soils bordered by the Vecht and Eem River plains with wet peat and clay soils. R-mode factor analysis and Q-mode cluster analysis were applied to a set of 1349 groundwater analyses to determine the factors controlling groundwater composition and the main resulting water types. The results indicate that groundwater composition in the study area is affected on a regional scale by human activities through changes in land use and intervention in natural flow patterns. On the ridge, ground water is recharged by precipitation, which dissolves carbonates from the matrix of the sandy aquifer. Increased solute concentrations in shallow ground water, especially of nitrate, sulphate and potassium, indicate increased pollution resulting from urbanization and increasingly intensive agricultural activity over the past decades. In the Vecht River plain infiltration occurs as a result of drainage of polders and groundwater extraction on the ridge. Recharge occurs by precipitation and from polluted surface water to which ammonium, organic complexes and carbonic acid are added through decomposition of organic matter in the peat and clay soils. The carbonic acid results in enhanced dissolution of carbonates present in the soil and the underlying sandy aquifer. Oxygen depletion and subsequent low redox potentials result in denitrification, dissolution of manganese and iron oxides, and sulphate reduction. The flow of ground water from high-level to low-level polders causes displacement of a former stagnant brakish groundwater body under the Vecht River plain accompanied by increased mixing of fresh and brackish ground water.

Plutonium oxide dissolution

International Nuclear Information System (INIS)

Gray, J.H.

1992-01-01

Several processing options for dissolving plutonium oxide (PuO 2 ) from high-fired materials have been studied. The scoping studies performed on these options were focused on PuO 2 typically generated by burning plutonium metal and PuO 2 produced during incineration of alpha contaminated waste. At least two processing options remain applicable for dissolving high-fired PuO 2 in canyon dissolvers. The options involve solid solution formation of PuO 2 With uranium oxide (UO 2 ) and alloying incinerator ash with aluminum. An oxidative dissolution process involving nitric acid solutions containing a strong oxidizing agent, such as cerium (IV), was neither proven nor rejected. This uncertainty was due to difficulty in regenerating cerium (IV) ions during dissolution. However, recent work on silver-catalyzed dissolution of PuO 2 with persulfate has demonstrated that persulfate ions regenerate silver (II). Use of persulfate to regenerate cerium (IV) or bismuth (V) ions during dissolution of PuO 2 materials may warrant further study

Spent fuel dissolution mechanisms

International Nuclear Information System (INIS)

Ollila, K.

1993-11-01

This study is a literature survey on the dissolution mechanisms of spent fuel under disposal conditions. First, the effects of radiolysis products on the oxidative dissolution mechanisms and rates of UO 2 are discussed. These effects have mainly been investigated by using electrochemical methods. Then the release mechanisms of soluble radionuclides and the dissolution of the UO 2 matrix including the actinides, are treated. Experimental methods have been developed for measuring the grain-boundary inventories of radionuclides. The behaviour of cesium, strontium and technetium in leaching tests shows different trends. Comparison of spent fuel leaching data strongly suggests that the release of 90 Sr into the leachant can be used as a measure of the oxidation/dissolution of the fuel matrix. Approaches to the modelling UO 2 , dissolution are briefly discussed in the next chapter. Lastly, the use of natural material, uraninite, in the evaluation of the long-term performance of spent fuel is discussed. (orig.). (81 ref., 37 figs., 8 tabs.)

Looking for the Self: Phenomenology, Neurophysiology and Philosophical Significance of Drug-induced Ego Dissolution

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Raphaël Millière

2017-05-01

Full Text Available There is converging evidence that high doses of hallucinogenic drugs can produce significant alterations of self-experience, described as the dissolution of the sense of self and the loss of boundaries between self and world. This article discusses the relevance of this phenomenon, known as “drug-induced ego dissolution (DIED”, for cognitive neuroscience, psychology and philosophy of mind. Data from self-report questionnaires suggest that three neuropharmacological classes of drugs can induce ego dissolution: classical psychedelics, dissociative anesthetics and agonists of the kappa opioid receptor (KOR. While these substances act on different neurotransmitter receptors, they all produce strong subjective effects that can be compared to the symptoms of acute psychosis, including ego dissolution. It has been suggested that neuroimaging of DIED can indirectly shed light on the neural correlates of the self. While this line of inquiry is promising, its results must be interpreted with caution. First, neural correlates of ego dissolution might reveal the necessary neurophysiological conditions for the maintenance of the sense of self, but it is more doubtful that this method can reveal its minimally sufficient conditions. Second, it is necessary to define the relevant notion of self at play in the phenomenon of DIED. This article suggests that DIED consists in the disruption of subpersonal processes underlying the “minimal” or “embodied” self, i.e., the basic experience of being a self rooted in multimodal integration of self-related stimuli. This hypothesis is consistent with Bayesian models of phenomenal selfhood, according to which the subjective structure of conscious experience ultimately results from the optimization of predictions in perception and action. Finally, it is argued that DIED is also of particular interest for philosophy of mind. On the one hand, it challenges theories according to which consciousness always involves

Looking for the Self: Phenomenology, Neurophysiology and Philosophical Significance of Drug-induced Ego Dissolution

Science.gov (United States)

Millière, Raphaël

2017-01-01

There is converging evidence that high doses of hallucinogenic drugs can produce significant alterations of self-experience, described as the dissolution of the sense of self and the loss of boundaries between self and world. This article discusses the relevance of this phenomenon, known as “drug-induced ego dissolution (DIED)”, for cognitive neuroscience, psychology and philosophy of mind. Data from self-report questionnaires suggest that three neuropharmacological classes of drugs can induce ego dissolution: classical psychedelics, dissociative anesthetics and agonists of the kappa opioid receptor (KOR). While these substances act on different neurotransmitter receptors, they all produce strong subjective effects that can be compared to the symptoms of acute psychosis, including ego dissolution. It has been suggested that neuroimaging of DIED can indirectly shed light on the neural correlates of the self. While this line of inquiry is promising, its results must be interpreted with caution. First, neural correlates of ego dissolution might reveal the necessary neurophysiological conditions for the maintenance of the sense of self, but it is more doubtful that this method can reveal its minimally sufficient conditions. Second, it is necessary to define the relevant notion of self at play in the phenomenon of DIED. This article suggests that DIED consists in the disruption of subpersonal processes underlying the “minimal” or “embodied” self, i.e., the basic experience of being a self rooted in multimodal integration of self-related stimuli. This hypothesis is consistent with Bayesian models of phenomenal selfhood, according to which the subjective structure of conscious experience ultimately results from the optimization of predictions in perception and action. Finally, it is argued that DIED is also of particular interest for philosophy of mind. On the one hand, it challenges theories according to which consciousness always involves self-awareness. On

Analysis of the Erosion Law of Karst Groundwater Using Hydrogeochemical Theory in Liulin Spring Area, North China

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Xiuqing Zheng

2018-05-01

Full Text Available The comprehensive geological, hydrogeological and hydrogeochemical model of the Liulin karstic spring area in the eastern limb of the Ordos syncline was established by a combination of chemical thermodynamics, chemical kinetics and hydrogeology. The study area was divided into four zones based on the saturation indices of calcite, dolomite and gypsum, which were computed by the groundwater-chemical simulation software PHREEQC (a computer program for speciation, batch-reaction, one-dimensional transport, and inverse geochemical calculations, with consideration of the geological and hydrogeological conditions and hydro-geochemical reactions. The weight and volume modulus of carbonate rocks and sulphate rocks in each zone were calculated by the method of correlation analysis to evaluate the dissolution law of karst groundwater. The results showed that in the zone I (saturation index of calcite βc ≤ 1 the dissolution of calcite was the major geochemical reaction, the weight modulus of calcite was higher than that of dolomite and gypsum, and the pore space generated by the dissolution of calcite was one order of magnitude larger than that of dolomite and gypsum. In zone II (saturation index of calcite βc > 1 to saturation index of dolomite βd ≤ 1 the corrosion moduli were all smaller than that in zone I, the solubility of dolomite and gypsum increased, and calcite reached saturation. The space occupied by the calcite sediment was less than that dissolved by dolomite and gypsum. In zone III (saturation index of dolomite βd > 1 to saturation index of gypsum βg ≤ 1, calcite and dolomite had reached saturation, accompanied by dedolomitization, and the amount of gypsum dissolution increased obviously. The conclusions indicate that the hydrogeochemical environment plays an important role in mineral dissolution.

Dissolution of aluminium; Disolucion de aluminio

Energy Technology Data Exchange (ETDEWEB)

Uriarte Hueda, A; Berberana Eizmendi, M; Pereira Sanchez, G

1968-07-01

The dissolution of aluminum with acid solutions ( nitric acid-mercuric nitrate) and alkaline solutions (sodium hydroxide-sodium nitrate) has been studied. The instantaneous dissolution rate (IDR) has been studied in function of the concentration of the used reagents and the dissolution temperature. The complete dissolution has been included in the second part of this report, to know the total dissolution time, the consume of reagents and the stability of the resultant solutions. (Author)

Hydrogeochemical quality and suitability studies of groundwater in northern Bangladesh.

Science.gov (United States)

Islam, M J; Hakim, M A; Hanafi, M M; Juraimi, Abdul Shukor; Aktar, Sharmin; Siddiqa, Aysha; Rahman, A K M Shajedur; Islam, M Atikul; Halim, M A

2014-07-01

Agriculture, rapid urbanization and geochemical processes have direct or indirect effects on the chemical composition of groundwater and aquifer geochemistry. Hydro-chemical investigations, which are significant for assessment of water quality, were carried out to study the sources of dissolved ions in groundwater of Dinajpur district, northern Bangladesh. The groundwater samplish were analyzed for physico-chemical properties like pH, electrical conductance, hardness, alkalinity, total dissolved solids and Ca2+, Mg2+, Na+, K+, CO3(2-), HCO3(-), SO4(2-) and Cl- ions, respectively. Based on the analyses, certain parameters like sodium adsorption ratio, soluble sodium percentage, potential salinity, residual sodium carbonate, Kelly's ratio, permeability index and Gibbs ratio were also calculated. The results showed that the groundwater of study area was fresh, slightly acidic (pH 5.3-6.4) and low in TDS (35-275 mg I(-1)). Ground water of the study area was found suitable for irrigation, drinking and domestic purposes, since most of the parameters analyzed were within the WHO recommended values for drinking water. High concentration of NO3- and Cl- was reported in areas with extensive agriculture and rapid urbanization. Ion-exchange, weathering, oxidation and dissolution of minerals were major geochemical processes governing the groundwater evolution in study area. Gibb's diagram showed that all the samples fell in the rock dominance field. Based on evaluation, it is clear that groundwater quality of the study area was suitable for both domestic and irrigation purposes.

Strontium isotopes as an indicator for groundwater salinity sources in the Kirkuk region, Iraq

Energy Technology Data Exchange (ETDEWEB)

Sahib, Layth Y. [Institute for Applied Geosciences, Technische Universität Darmstadt, Schnittspahnstraße 9, 64287 Darmstadt (Germany); Geology Department, College of Science, University of Baghdad, Jadreya, Baghdad (Iraq); Marandi, Andres; Schüth, Christoph [Institute for Applied Geosciences, Technische Universität Darmstadt, Schnittspahnstraße 9, 64287 Darmstadt (Germany)

2016-08-15

The Kirkuk region in northern Iraq hosts some of the largest oil fields in the Middle East. Several anticline structures enabled vertical migration and entrapment of the oil. Frequently, complex fracture systems and faults cut across the Eocene and middle Oligocene reservoirs and the cap rock, the Fatha Formation of Miocene age. Seepage of crude oil and oil field brines are therefore a common observation in the anticline axes and contamination of shallow groundwater resources is a major concern. In this study, 65 water samples were collected in the Kirkuk region to analyze and distinguish mixing processes between shallow groundwater resources, uprising oil field brines, and dissolution of gypsum and halite from the Fatha Formation. Hydrochemical analyses of the water samples included general hydrochemistry, stable water isotopes, as well as strontium concentrations and for 22 of the samples strontium isotopes ({sup 87}Sr/{sup 86}Sr). Strontium concentrations increased close to the anticline axes with highest concentrations in the oil field brines (300 mg/l). Strontium isotopes proved to be a valuable tool to distinguish mixing processes as isotope signatures of the oil field brines and of waters from the Fatha Formation are significantly different. It could be shown, that mixing of shallow groundwater with oil field brines is occurring close to the major fault zones in the anticlines but high concentrations of strontium in the water samples are mainly due to dissolution from the Fatha Formation. - Highlights: • This field study evaluates the salinity sources in the groundwater in Kirkuk region. • Salinity is related to evaporates dissolving and/or mixing with oil field brine. • Strontium isotopes proved to be a valuable tool to distinguish mixing processes.

Cation exchange and CaCO 3 dissolution during artificial recharge of effluent to a calcareous sandstone aquifer

Science.gov (United States)

Goren, Orly; Gavrieli, Ittai; Burg, Avihu; Lazar, Boaz

2011-03-01

SummaryThis research describes a field study and laboratory simulations of the geochemical evolution of groundwater following a recharge of effluent into aquifers. The study was conducted in the soil aquifer treatment (SAT) system of the Shafdan sewage reclamation plant, Israel. The SAT system recharges secondary effluent into the calcareous sandstone sediments of the Israeli Coastal Aquifer as a tertiary treatment. The reclaimed effluent is recovered ca. 500 m off the recharge basin and is used for unlimited irrigation. The laboratory simulations in which effluent was pumped through experimental columns packed with pristine Shafdan sediment showed that the chemical composition of the outflowing water was controlled mainly by cation exchange and CaCO 3 dissolution. Na +, K + and Mg 2+ were adsorbed and Ca 2+ was desorbed during the initial stage of recharge. The equilibrium distribution of the adsorbed cations was: Ca 2+ ˜ 60%, Mg 2+ ˜ 20%, and Na + and K + ˜ 10% each. The Ca 2+ in the Shafdan production wells and in the experimental columns outflow (˜5 meq L -1) was always higher than the Ca 2+ in the recharged effluent (˜3.5 meq L -1), indicating continuous CaCO 3 dissolution. This study demonstrates that besides mixing, a suite of geochemical processes should be considered when assessing groundwater quality following artificial recharge of aquifers.

JSS project phase 4: Experimental and modelling studies of HLW glass dissolution in repository environments

International Nuclear Information System (INIS)

1987-10-01

A goal of the JSS project was to develop a scientific basis for understanding the effects of waste package components, groundwater chemistry, and other repository conditions on glass dissolution behaviour, and to develop and refine a model for the processes governing glass dissolution. The fourth phase of the project, which was performed by the Hahn-Meitner-Institut, Berlin, FRG, dealt specifically with model development and application. Phase 4 also adressed whether basaltic glasses could serve as natural analogues for nuclear waste glasses, thus providing a means to test the capability of the model for long-term predictions. Additional experiments were performed in order to complete the data base necessary to model interactions between the glass and bentonite and between glass and steel corrosion products. More data on temperature, S/V, and pH dependence of the glass/water reaction were also collected. In this report, the data acquired during phase 4 are presented and discussed. (orig./DG)

Contribution To The HYDROGEOCHEMISTRY Of Groundwater In The Northwest Coastal Plain, Egypt

International Nuclear Information System (INIS)

EL-SAYED, S.A.

2010-01-01

The present study aims to investigate the deterioration of water resources in the studied area using the hydrogeochemical and isotopic tools as complementary techniques. Fourteen water samples from the available groundwater and surface water bodies and from rainwater were collected to execute this study. The main source for groundwater recharge is the rainwater falling on the area in winter season (150 mm/year). The quality of this water has been changed in the Pleistocene and Middle Miocene aquifers and excavations due to the effect of different hydrogeochemical processes, leaching, dissolution, evaporation and mixing with sea water. The classic hydrochemical tool alone was not enough to delineate these processes while the stable isotope investigation was very useful in discriminating them. Water from wells tapping the Middle Miocene aquifer, from wells nos. 6 and 9, penetrating the Pleistocene aquifer and from excavation no. 11 have not been influenced by sea water intrusion. Its high salinity and other chemical constituents were due to the effect of leaching and dissolution of rocks and soil salts. The higher salinity, chemical constituents and stable isotopic composition of water from wells 6 and 9 and from excavation no. 10 were attributed to the mixing with sea water. The presence of water levels of these points under mean sea level confirms the intrusion of sea water. Water of Al-Agara spring was highly affected by evaporation process. As a result of this study, the coastal aquifers were vulnerable to sea water invasion. Groundwater over exploitation and drilling of more water wells in the area should be managed wisely

Modelling of the UO{sub 2} dissolution mechanisms in synthetic groundwater. Experiments carried out under anaerobic and reducing conditions

Energy Technology Data Exchange (ETDEWEB)

Cera, E.; Grive, M.; Bruno, J. [EnvirosQuantiSci (Spain); Ollila, K. [VTT Chemical Technology, Espoo (Finland)

2000-07-01

The experimental data generated under anaerobic and reducing conditions within the EU R and D programme 1996-1998 entitled 'Source term for performance assessment of spent fuel as a waste form' and published as a POSIVA report (Ollila, 1999) have been modelled in the present work. The dissolution data available, mainly U in the aqueous phase as a function of time and redox potentials have been used to elucidate the redox pairs controlling the redox potential of the systems studied. Dissolution experiments carried out under anaerobic conditions have shown the important role of the uranium system on buffering the redox capacity of these systems. In the presence of carbonates in the system, the redox control has been given by the UO{sub 2}(c)/U(VI) aqueous redox couple while in absence of carbonates in the system, the redox control has been governed by the UO{sub 2}(c)/UO{sub 2+x} transition. In addition dissolution rates have been satisfactorily modelled by assuming an oxidative dissolution mechanism consisting in an initial oxidation of the surface of the uranium dioxide, binding of the HCO{sub 3} or H+ at the U(VI) sites of the oxidised surface layer and detachment of these surface complexes. The redox controls in the experiments carried out under reducing conditions have been exerted by the different reducing agents added in the systems. Therefore, the addition of Fe{sup 2+} lead to a redox control exerted by the Fe{sup 2+}/Fe(OH){sub 3}(s) redox pair, while the addition of sulphide lead to a different redox control governed by the HS/SO{sub 3}{sup 2-} redox pair. (orig.)

Hydrogeochemistry and Stable Isotope Studies of Groundwater in the Ga West Municipal Area, Ghana

International Nuclear Information System (INIS)

Saka, David

2011-07-01

This study assesses groundwater in the Ga West Municipal Area of Ghana using hydrogeochemistry and stable isotope approaches. High salinity groundwaters are obtained in the municipality which poses problems for current and future domestic water supply exploitation. The increase in salinity is related to the dissolution of minerals in the host rocks and the evaporative concentration of solutes. The dominant groundwater composition in both shallow and deep wells sampled is Na-Cl, with concentration increasing substantially with well depths. The mixing process between freshwater and saline water was observed in the shift from CaHCO3 facies to Ca-Cl facies. Schoeller diagrams showed that groundwater movement in the study area is mostly vertical, moving from the shallow groundwaters towards the deep groundwaters. There were however few exceptions where no relationship was established between the shallow and the deep groundwaters. The oxygen and hydrogen isotope compositions in the groundwater samples suggest that groundwater recharge is of meteoric origin, with few samples showing evidence of evaporation. An average deuterium excess of rainfall of 14.2‰ was observed, which indicates the significance of kinetic evaporation due to low humidity conditions prevalent in the study area. The d-excess also indicates modern recharge along the Akwapim-Togo Ranges. Groundwater analysis for trace metals indicates that 93% of the groundwaters have Iron concentration above recommended limits. However, Cu, Zn, Pb, Cd and Cr have values within the acceptable limits. Generally, about 40% of the groundwaters sampled are not suitable for drinking and domestic purposes based on comparison with international standards for drinking water. (au)

Arsenic mobilization in a freshening groundwater system formed within glaciomarine deposits

International Nuclear Information System (INIS)

Cavalcanti de Albuquerque, R.; Kirste, D.

2012-01-01

Arsenic release to groundwater and conditions favoring As mobility are investigated in a system of aquifers formed within unconsolidated Quaternary sediments. The studied groundwater system is comprised of unconfined aquifers formed in glaciofluvial sediments with Ca–Mg–HCO 3 groundwater, and confined aquifers formed within glaciomarine sediments with high As (above 10 μg/L) Na–HCO 3 or Na–Cl groundwater. A positive relationship of As concentrations with the Na/(Ca + Mg) ratio of groundwater indicates that As release occurs in glaciomarine sediments concurrent to cation exchange reactions related to groundwater freshening. Arsenic is mobile in confined aquifers as a result of groundwater basic pH which prevents arsenate from adsorbing to mineral surfaces, and reducing conditions that favor speciation to arsenite. Selected extractions applied to sediment core samples indicate that As occurs in sediments predominantly in sulfide minerals and in Mn oxides and/or Fe oxyhydroxides. General positive relationships between As and the reduced species Fe 2+ , NH 3 and dissolved S 2− suggest that As release occurs at increasingly reducing conditions. Despite likely As release via Fe oxyhydroxide reductive dissolution, Fe remains at relatively low concentrations in groundwater (up to 0.37 mg/L) as a result of possible Fe adsorption and Fe reprecipitation as carbonate minerals favored by basic pH and high alkalinity. The presence of S 2− in some samples, a negative relationship between δ 34 S of SO 4 and SO 4 2- concentrations, and a positive relationship between δ 34 S and δ 18 O of SO 4 indicate that groundwater in confined aquifers is undergoing bacterial SO 4 reduction.

Development and application of a biorelevant dissolution method using USP apparatus 4 in early phase formulation development.

Science.gov (United States)

Fang, Jiang B; Robertson, Vivian K; Rawat, Archana; Flick, Tawnya; Tang, Zhe J; Cauchon, Nina S; McElvain, James S

2010-10-04

Dissolution testing is frequently used to determine the rate and extent at which a drug is released from a dosage form, and it plays many important roles throughout drug product development. However, the traditional dissolution approach often emphasizes its application in quality control testing and usually strives to obtain 100% drug release. As a result, dissolution methods are not necessarily biorelevant and meaningful application of traditional dissolution methods in the early phases of drug product development can be very limited. This article will describe the development of a biorelevant in vitro dissolution method using USP apparatus 4, biorelevant media, and real-time online UV analysis. Several case studies in the areas of formulation selection, lot-to-lot variability, and food effect will be presented to demonstrate the application of this method in early phase formulation development. This biorelevant dissolution method using USP apparatus 4 provides a valuable tool to predict certain aspects of the in vivo drug release. It can be used to facilitate the formulation development/selection for pharmacokinetic (PK) and clinical studies. It may also potentially be used to minimize the number of PK studies, and to aid in the design of more efficient PK and clinical studies.

Effect of sodium lauryl sulfate in dissolution media on dissolution of hard gelatin capsule shells.

Science.gov (United States)

Zhao, Fang; Malayev, Vyacheslav; Rao, Venkatramana; Hussain, Munir

2004-01-01

Sodium lauryl sulfate (SLS) is a commonly used surfactant in dissolution media for poorly water soluble drugs. However, it has occasionally been observed that SLS negatively impacts the dissolution of drug products formulated in gelatin capsules. This study investigated the effect of SLS on the dissolution of hard gelatin capsule shells. The USP paddle method was used with online UV monitoring at 214 nm (peptide bond). Empty size #0 capsule shells were held to the bottom of the dissolution vessel by magnetic three-prong sinkers. SLS significantly slowed down the dissolution of gelatin shells at pH < 5. Visually, the gelatin shells transformed into some less-soluble precipitate under these conditions. This precipitate was found to contain a higher sulfur content than the gelatin control sample by elemental analysis, indicating that SLS is part of the precipitate. Additionally, the slowdown of capsule shell dissolution was shown to be dependent on the SLS concentration and the ionic strength of the media. SLS interacts with gelatin to form a less-soluble precipitate at pH < 5. The use of SLS in dissolution media at acidic pH should be carefully evaluated for gelatin capsule products.

Geochemical tracing and hydrogeochemical modelling of water-rock interactions during salinization of alluvial groundwater (Upper Rhine Valley, France)

Energy Technology Data Exchange (ETDEWEB)

Lucas, Y., E-mail: yann.lucas@eost.u-strasbg.fr [Universite de Strasbourg et CNRS, Laboratoire d' Hydrologie et de Geochimie de Strasbourg, Ecole et Observatoire des Sciences de la Terre, 1, rue Blessig, 67084 Strasbourg Cedex (France); Schmitt, A.D., E-mail: anne-desiree.schmitt@univ-fcomte.fr [Universite de Strasbourg et CNRS, Laboratoire d' Hydrologie et de Geochimie de Strasbourg, Ecole et Observatoire des Sciences de la Terre, 1, rue Blessig, 67084 Strasbourg Cedex (France)] [Universite de Franche-Comte et CNRS-UMR 6249, Chrono-Environnement, 16, Route de Gray, 25030 Besancon Cedex (France); Chabaux, F., E-mail: francois.chabaux@eost.u-strasbg.fr [Universite de Strasbourg et CNRS, Laboratoire d' Hydrologie et de Geochimie de Strasbourg, Ecole et Observatoire des Sciences de la Terre, 1, rue Blessig, 67084 Strasbourg Cedex (France); Clement, A.; Fritz, B. [Universite de Strasbourg et CNRS, Laboratoire d' Hydrologie et de Geochimie de Strasbourg, Ecole et Observatoire des Sciences de la Terre, 1, rue Blessig, 67084 Strasbourg Cedex (France); Elsass, Ph. [BRGM, GEODERIS, 1, rue Claude Chappe, 57070 Metz (France); Durand, S. [Universite de Strasbourg et CNRS, Laboratoire d' Hydrologie et de Geochimie de Strasbourg, Ecole et Observatoire des Sciences de la Terre, 1, rue Blessig, 67084 Strasbourg Cedex (France)

2010-11-15

Research highlights: {yields} Major and trace elements along with strontium and uranium isotopic ratios show that groundwater geochemical characteristics along the saline plumes cannot reflect a conservative mixing. {yields} A coupled hydrogeochemical model demonstrates that cationic exchange between alkalis from polluted waters and alkaline-earth elements from montmorillonite present in the host rock of the aquifer is the primary process. {yields} The model requires only a small amount of montmorillonite. {yields} It is necessary to consider the pollution history to explain the important chloride, sodium and calcium concentration modifications. {yields} The model shows that the rapidity of the cationic exchange reactions insures a reversibility of the cation fixation on clays in the aquifer. - Abstract: In the southern Upper Rhine Valley, groundwater has undergone intensive saline pollution caused by the infiltration of mining brines, a consequence of potash extraction carried out during the 20th century. Major and trace elements along with Sr and U isotopic ratios show that groundwater geochemical characteristics along the saline plumes cannot reflect conservative mixing between saline waters resulting from the dissolution of waste heaps and one or more unpolluted end-members. The results imply the occurrence of interactions between host rocks and polluted waters, and they suggest that cationic exchange mechanisms are the primary controlling process. A coupled hydrogeochemical model has been developed with the numerical code KIRMAT, which demonstrates that cationic exchange between alkalis from polluted waters and alkaline-earth elements from montmorillonite present in the host rock of the aquifer is the primary process controlling the geochemical evolution of the groundwater. The model requires only a small amount of montmorillonite (between 0.75% and 2.25%), which is in agreement with the observed mineralogical composition of the aquifer. The model also proves

Hydrogeochemistry of co-occurring geogenic arsenic, fluoride and iodine in groundwater at Datong Basin, northern China

Energy Technology Data Exchange (ETDEWEB)

Pi, Kunfu; Wang, Yanxin, E-mail: yx.wang@cug.edu.cn; Xie, Xianjun, E-mail: xjxie@cug.edu.cn; Su, Chunli; Ma, Teng; Li, Junxia; Liu, Yaqing

2015-12-30

Highlights: • Co-mobilization of As, F and I was identified at Datong Basin. • Both As and I are released via reductive dissolution of Fe minerals. • Some amounts of As and I may be sequestered by FeS precipitates. • Intensive evaporation promotes retention of As but mobilization of F and I. - Abstract: Abnormal levels of co-occurring arsenic (As), fluorine (F) and iodine (I) in groundwater at Datong Basin, northern China are geochemically unique. Hydrochemical, {sup 18}O and {sup 2}H characteristics of groundwater were analyzed to elucidate their mobilization processes. Aqueous As, F and I ranged from 5.6 to 2680 μg/L, 0.40 to 3.32 mg/L and 10.1 to 186 μg/L, respectively. High As, F and I groundwater was characterized by moderately alkaline, high HCO{sub 3}{sup −}, Fe(II), HS{sup −} and DOC concentrations with H{sub 3}AsO{sub 3}, F{sup −} and I{sup −} as the dominant species. The plots of δ{sup 18}O values and Cl/Br ratios versus Cl{sup −} concentration demonstrate build-up of more oxidizing conditions and precipitation of carbonate minerals induced by vertical recharge and intensive evaporation facilitate As retention to Fe (hydr) oxides, but enhance F and I mobilization from host minerals. Under reducing conditions, As and I can be simultaneously released via reductive dissolution of Fe (hydr) oxides and reduction of As(V) and I(V) while F migration may be retarded due to effects of dissolution-precipitation equilibria between carbonate minerals and fluorite. With the prevalence of sulfate-reducing condition and lowering of HCO{sub 3}{sup −} concentration, As and I may be sequestered by Fe(II) sulfides and F is retained to fluorite and on clay mineral surfaces.

Hydrogeochemistry of co-occurring geogenic arsenic, fluoride and iodine in groundwater at Datong Basin, northern China

International Nuclear Information System (INIS)

Pi, Kunfu; Wang, Yanxin; Xie, Xianjun; Su, Chunli; Ma, Teng; Li, Junxia; Liu, Yaqing

2015-01-01

Highlights: • Co-mobilization of As, F and I was identified at Datong Basin. • Both As and I are released via reductive dissolution of Fe minerals. • Some amounts of As and I may be sequestered by FeS precipitates. • Intensive evaporation promotes retention of As but mobilization of F and I. - Abstract: Abnormal levels of co-occurring arsenic (As), fluorine (F) and iodine (I) in groundwater at Datong Basin, northern China are geochemically unique. Hydrochemical, "1"8O and "2H characteristics of groundwater were analyzed to elucidate their mobilization processes. Aqueous As, F and I ranged from 5.6 to 2680 μg/L, 0.40 to 3.32 mg/L and 10.1 to 186 μg/L, respectively. High As, F and I groundwater was characterized by moderately alkaline, high HCO_3"−, Fe(II), HS"− and DOC concentrations with H_3AsO_3, F"− and I"− as the dominant species. The plots of δ"1"8O values and Cl/Br ratios versus Cl"− concentration demonstrate build-up of more oxidizing conditions and precipitation of carbonate minerals induced by vertical recharge and intensive evaporation facilitate As retention to Fe (hydr) oxides, but enhance F and I mobilization from host minerals. Under reducing conditions, As and I can be simultaneously released via reductive dissolution of Fe (hydr) oxides and reduction of As(V) and I(V) while F migration may be retarded due to effects of dissolution-precipitation equilibria between carbonate minerals and fluorite. With the prevalence of sulfate-reducing condition and lowering of HCO_3"− concentration, As and I may be sequestered by Fe(II) sulfides and F is retained to fluorite and on clay mineral surfaces.

Hydrochemical and isotopic characteristics of groundwater in the northeastern Tennger Desert, northern China

Science.gov (United States)

Wang, Liheng; Dong, Yanhui; Xu, Zhifang; Qiao, Xiaojuan

2017-12-01

Groundwater is typically the only water source in arid regions, and its circulation processes should be better understood for rational resource exploitation. Stable isotopes and major ions were investigated in the northeastern Tengger Desert, northern China, to gain insights into groundwater recharge and evolution. In the northern mountains, Quaternary unconsolidated sediments, exposed only in valleys between hills, form the main aquifer, which is mainly made of aeolian sand and gravel. Most of the mountain groundwater samples plot along the local meteoric water line (LMWL), with a more depleted signature compared to summer precipitation, suggesting that mountain groundwater was recharged by local precipitation during winter. Most of the groundwater was fresh, with total dissolved solids less than 1 g/L; dominant ions are Na+, SO4 2- and Cl-, and all mineral saturation indices are less than zero. Evaporation, dissolution and cation exchange are the major hydrogeochemical processes. In the southern plains, however, the main aquifers are sandstone. The linear regression line of δD and δ 18O of groundwater parallels the LMWL but the intercept is lower, indicating that groundwater in the plains has been recharged by ancient precipitation rather than modern. Both calcite and dolomite phases in the plains groundwater are close to saturation, while gypsum and halite can still be dissolved into the groundwater. Different recharge mechanisms occur in the northern mountains and the southern plains, and the hydraulic connection between them is weak. Because of the limited recharge, groundwater exploitation should be limited as much as possible.

Can hydrate dissolution experiments predict the fate of a natural hydrate system?

Energy Technology Data Exchange (ETDEWEB)

Hester, K.C.; Peltzer, E.T.; Dunk, R.M.; Walz, P.M.; Brewer, P.G. [Monterey Bay Aquarium Research Inst., Moss Landing, CA (United States); Dendy Sloan, E. [Colorado School of Mines, Golden, CO (United States). Center for Hydrate Research

2008-07-01

Gas hydrates are naturally occurring compounds found in permafrost regions and in oceans. In the natural environment, sufficient temperature and pressure conditions for hydrate formation exist over a significant portion of the ocean. However, in addition to pressure and temperature, the chemical potential of the gas in the hydrate must be equal to the surrounding waters. If the concentration of the gas in surrounding water is under-saturated with respect to the gas in the hydrate, the hydrate will dissolve to drive the system towards chemical equilibrium. This paper presented a dissolution study of exposed hydrate from outcrops at Barkley Canyon, located off Vancouver Island, British Columbia. A previous field experiment on synthetic methane hydrate samples had demonstrated that mass transfer controlled dissolution in under-saturated seawater. However, seafloor hydrate outcrops have been shown to have significant longevity compared to expected dissolution rates based upon convective boundary layer diffusion calculations. An in-situ dissolution experiment was performed on two distinct natural hydrate fabrics in order to help resolve this apparent disconnect between the dissolution rates of synthetic and natural hydrate. The paper presented a map of Barkley Canyon and discussed the field measurements and methods for the study. Exposed outcrops of gas hydrates were cored using a specially constructed stainless steel coring device and a hydraulic ram was located inside the corer. Hydrate samples were cored directly using the a manipulator arm and then injected into a sampling cell. The hydrate was then added to an open mesh exposure container, which allowed for exposure to ambient benthic currents with minimal disturbance. As well, in order to observe the slow dissolution of the hydrate in seawater at Barkley Canyon, time-lapse photography was employed. Last, the paper presented the results of the hydrate fabric porosities and hydrate dissolution rates. It was

Dissolution of targets for the production of Mo-99: Part 1. Influence of NaOH concentration and the addition of NaNO3 and NaNO2 on the dissolution time

International Nuclear Information System (INIS)

Camilo, Ruth L.; Araujo, Izilda da C.; Mindrisz, Ana C.; Forbicini, Christina A.L.G. de O.

2011-01-01

Faced with global crisis in the production of radioisotope 99 Mo, which product of decay, 99 mTc, is the tracer element most often used in nuclear medicine and accounts for about 80% of all diagnostic procedures in vivo, since September 2008 Brazil is developing the project called Brazilian Multipurpose Reactor (RMB). Within the Brazilian Nuclear Program (PNB) the construction of the RMB, is seen as a long term solution to meet all domestic demand relative to the supply of radioisotopes and radiopharmaceuticals. In the process to be studied to obtain 99 Mo from irradiated UA1 x -A1 LEU targets employing alkaline dissolution, processing time should be minimized, considering the short half life of 99 Mo and 99 mTc, about 66 h and 6 h, respectively. That makes dissolution time a significant factor in the development of the process. This paper presents the results of alkaline dissolution of scraps of Al, used to simulate the dissolution process of UA1 x -A1 targets. Al corresponds to about 79% of the total weight of the UA1 x -A1 target. The effect of NaOH concentration on dissolution time for the interval of 1 to 3.5 mol.L-1 was studied, keeping the molar ratio in 1Al:2.16NaOH and the initial temperature of 88 degree C. The influence of reagent composition over dissolution time was studied using three different solutions: a) 3 mol.L -1 NaOH, b) 3 mol.L -1 NaOH/NaNO 3 and c) 3 mol.L -1 NaOH/NaNO 2 , keeping the same molar ratio and temperature. The results showed that the dissolution time decreases with increasing NaOH concentration and the addition of NaNO 3 or NaNO 2 in the NaOH solution reduces both dissolution time and volume of gases released. (author)

Structural analysis of S-wave seismics around an urban sinkhole: evidence of enhanced dissolution in a strike-slip fault zone

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S. H. Wadas

2017-12-01

Full Text Available In November 2010, a large sinkhole opened up in the urban area of Schmalkalden, Germany. To determine the key factors which benefited the development of this collapse structure and therefore the dissolution, we carried out several shear-wave reflection-seismic profiles around the sinkhole. In the seismic sections we see evidence of the Mesozoic tectonic movement in the form of a NW–SE striking, dextral strike-slip fault, known as the Heßleser Fault, which faulted and fractured the subsurface below the town. The strike-slip faulting created a zone of small blocks ( < 100 m in size, around which steep-dipping normal faults, reverse faults and a dense fracture network serve as fluid pathways for the artesian-confined groundwater. The faults also acted as barriers for horizontal groundwater flow perpendicular to the fault planes. Instead groundwater flows along the faults which serve as conduits and forms cavities in the Permian deposits below ca. 60 m depth. Mass movements and the resulting cavities lead to the formation of sinkholes and dissolution-induced depressions. Since the processes are still ongoing, the occurrence of a new sinkhole cannot be ruled out. This case study demonstrates how S-wave seismics can characterize a sinkhole and, together with geological information, can be used to study the processes that result in sinkhole formation, such as a near-surface fault zone located in soluble rocks. The more complex the fault geometry and interaction between faults, the more prone an area is to sinkhole occurrence.

Assessment of fluoride contaminations in groundwater of hard rock aquifers in Madurai district, Tamil Nadu (India)

Science.gov (United States)

Thivya, C.; Chidambaram, S.; Rao, M. S.; Thilagavathi, R.; Prasanna, M. V.; Manikandan, S.

2017-05-01

The fluoride contamination in drinking water is already gone to the alarming level and it needs the immediate involvement and attention of all people to solve this problem. Fluoride problem is higher in hard rock terrains in worldwide and Madurai is such type of hard rock region. Totally 54 samples were collected from the Madurai district of Tamilnadu with respect to lithology. The samples collected were analysed for major cations and anions using standard procedures. The higher concentration of fluoride is noted in the Charnockite rock types of northern part of the study area. 20 % of samples are below 0.5 ppm and 6 % of samples are above 1.5 ppm exceeding the permissible limit. The affinity between the pH and fluoride ions in groundwater suggests that dissolution of fluoride bearing minerals in groundwater. The higher concentration of fluoride ions are observed in the lower EC concentration. The isotopic study suggests that fluoride is geogenic in nature. In factor scores, fluoride is noted in association with pH which indicates the dissolution process.

Origin of increased sulfate in groundwater at the ETF disposal site

International Nuclear Information System (INIS)

Thornton, E.C.

1997-09-01

Treated effluent being discharged to the vadose zone from the C-018H Effluent Treatment Facility (ETF) at the Hanford Site has infiltrated vertically to the unconfined aquifer, as indicated by increasing tritium activity levels in the groundwater. Well 699-48-77A, in particular, exhibits increased levels of tritium and also sulfate in the groundwater. The origin of increased sulfate levels in the groundwater is attributed to the dissolution of gypsum as the effluent flows through the vadose zone. This is supported by the observation that sulfate was found to be present in soils collected from the vadose zone at an average value of about 10.6 ppm. The maximum observed sulfate concentration of 190 mg/L from well 699-48-77A was observed on August 6, 1996, and is less than the maximum value of 879 mg/L that potentially could be achieved if water in the vadose zone was to attain saturation with respect to gypsum and calcite. It is suggested that infiltration rates were high enough that the effluent did not completely equilibrate with gypsum in the vadose zone, and thus, sulfate levels remained below gypsum saturation levels. Sulfate levels appear to be dropping, which may be attributed to the completion of the dissolution of the bulk of gypsum present along the vadose zone flow path traversed by the effluent. Geochemical modeling was undertaken to evaluate the influence of effluent chemistry on sulfate concentration levels in the presence of excess calcite and gypsum. In general, the effect is fairly minor for dilute solutions, but becomes more significant for concentrated solutions

Coupled S and Sr isotope evidences for elevated arsenic concentrations in groundwater from the world's largest antimony mine, Central China

Science.gov (United States)

Wen, Bing; Zhou, Aiguo; Zhou, Jianwei; Liu, Cunfu; Huang, Yuliu; Li, Ligang

2018-02-01

The Xikuangshan(XKS) mine, the world's largest antimony mine, was chosen for a detailed arsenic hydrogeochemical study because of the elevated arsenic in bedrock aquifers used by local residents. Hydrochemical data, δ34S values of dissolved SO42- and 87Sr/86Sr ratios have been analyzed to identify the predominant geochemical processes that control the arsenic mobilization within the aquifers. Groundwater samples can be divided into three major types: low arsenic groundwater (0-50 μg/L), high arsenic groundwater (50-1000 μg/L) and anomalous high arsenic groundwater (>1000 μg/L). Arsenic occurs under oxidizing conditions at the XKS Sb mine as the HAsO42- anion. The Ca/Na ratio correlates significantly with HCO3-/Na and Sr/Na ratios, indicating that carbonate dissolution and silicate weathering are the dominant processes controlling groundwater hydrochemistry. The δ34S values of the groundwater indicate that dissolved SO42- in groundwater is mainly sourced from the oxidation of sulfide minerals, and elevated As concentrations in groundwater are influenced by the mixing of mine water and surface water. Furthermore, the δ34S values are not correlated with dissolved As concentrations and Fe concentrations, suggesting that the reduction dissolution of Fe(III) hydroxides is not the dominant process controlling As mobilization. The 87Sr/86Sr ratios imply that elevated As concentrations in groundwater are primarily derived from the interaction with the stibnite and silicified limestone. More specifically, the excess-Na ion, the feature of Ca/Na ratio, and the spatial association of elevated As concentrations in groundwater collectively suggest that high and anomalous high arsenic groundwater are associated with smelting slags and, in particular, the arsenic alkali residue. In general, the hydrochemistry analysis, especially the S and Sr isotope evidences elucidate that elevated As concentrations and As mobilization are influenced by several geochemical processes

Mathematical modeling of drug dissolution.

Science.gov (United States)

Siepmann, J; Siepmann, F

2013-08-30

The dissolution of a drug administered in the solid state is a pre-requisite for efficient subsequent transport within the human body. This is because only dissolved drug molecules/ions/atoms are able to diffuse, e.g. through living tissue. Thus, generally major barriers, including the mucosa of the gastro intestinal tract, can only be crossed after dissolution. Consequently, the process of dissolution is of fundamental importance for the bioavailability and, hence, therapeutic efficacy of various pharmaco-treatments. Poor aqueous solubility and/or very low dissolution rates potentially lead to insufficient availability at the site of action and, hence, failure of the treatment in vivo, despite a potentially ideal chemical structure of the drug to interact with its target site. Different physical phenomena are involved in the process of drug dissolution in an aqueous body fluid, namely the wetting of the particle's surface, breakdown of solid state bonds, solvation, diffusion through the liquid unstirred boundary layer surrounding the particle as well as convection in the surrounding bulk fluid. Appropriate mathematical equations can be used to quantify these mass transport steps, and more or less complex theories can be developed to describe the resulting drug dissolution kinetics. This article gives an overview on the current state of the art of modeling drug dissolution and points out the assumptions the different theories are based on. Various practical examples are given in order to illustrate the benefits of such models. This review is not restricted to mathematical theories considering drugs exhibiting poor aqueous solubility and/or low dissolution rates, but also addresses models quantifying drug release from controlled release dosage forms, in which the process of drug dissolution plays a major role. Copyright © 2013 Elsevier B.V. All rights reserved.

Preliminary study on the corrosion behavior of carbon steel in Horonobe groundwater environment

International Nuclear Information System (INIS)

Taniguchi, Naoki; Kogawa, Noritaka; Maeda, Kazuto

2006-08-01

It is necessary to understand the corrosion behavior of candidate overpack materials to plan the in-situ engineered barrier test at underground laboratory constructing at Horonobe and to design the overpacks suitable to Horonobe environment. The preliminary corrosion tests of carbon steel which is a candidate material for overpacks were carried out using artificial groundwater and actual groundwater sampled at Horonobe. As the results of anodic polarization experiments, the anodic polarization curves of carbon steel in buffer material were active dissolution type, and the corrosion type of carbon steel in Horonobe groundwater environment was expected to be general corrosion. The results of immersion test under air equilibrium condition showed that the degrees of corrosion localization were not exceeded the data obtained in previous studies. The trend of corrosion rates in buffer material under anaerobic condition were similar to the data obtained in previous studies. Based on the experimental results, it was confirmed that the corrosion assessment model and assumed corrosion rate in second progress report (H12 report) can be applied to the assessment for Horonobe groundwater condition. (author)

Dissolution of two NWCF calcines: Extent of dissolution and characterization of undissolved solids

International Nuclear Information System (INIS)

Brewer, K.N.; Herbst, R.S.; Tranter, T.J.

1995-01-01

A study was undertaken to determine the dissolution characteristics of two NWCF calcine types. A two-way blended calcine made from 4 parts nonradioactive aluminum nitrate and one part WM-102 was studied to determine the extent of dissolution for aluminum-type calcines. A two-way blend of 3.5 parts fluorinel waste from WM-187 and 1 part sodium waste from WM-185 was used to determine the extent of dissolution for zirconium-type calcines. This study was necessary to develop suitable aqueous separation flowsheets for the partitioning of actinides and fission products from ICPP calcines and to determine the disposition of the resulting undissolved solids (UDS). The dissolution flowsheet developed by Herbst was used to dissolve these two NWCF calcine types. Results show that greater than 95 wt% of aluminum and zirconium calcine types were dissolved after a single batch contact with 5 M HNO 3 . A characterization of the UDS indicates that the weight percent of TRU elements in the UDS resulting from both calcine type dissolutions increases by approximately an order of magnitude from their concentrations prior to dissolution. Substantial activities of cesium and strontium are also present in the UDS resulting from the dissolution of both calcine types. Multiple TRU, Cs, and Sr analyses of both UDS types show that these solids are relatively homogeneous. From this study, it is estimated that between 63.5 and 635 cubic meters of UDS will be generated from the dissolution of 3800 M 3 of calcine. The significant actinide and fission product activities in these UDS will preclude their disposal as low-level waste. If the actinide and fission activity resulting from the UDS is the only considered source in the dissolved calcine solutions, an estimated 99.9 to 99.99 percent of the solids must be removed from this solution for it to meet non-TRU Class A low-level waste

Evolutionary analysis of groundwater flow: Application of multivariate statistical analysis to hydrochemical data in the Densu Basin, Ghana

Science.gov (United States)

Yidana, Sandow Mark; Bawoyobie, Patrick; Sakyi, Patrick; Fynn, Obed Fiifi

2018-02-01

An evolutionary trend has been postulated through the analysis of hydrochemical data of a crystalline rock aquifer system in the Densu Basin, Southern Ghana. Hydrochemcial data from 63 groundwater samples, taken from two main groundwater outlets (Boreholes and hand dug wells) were used to postulate an evolutionary theory for the basin. Sequential factor and hierarchical cluster analysis were used to disintegrate the data into three factors and five clusters (spatial associations). These were used to characterize the controls on groundwater hydrochemistry and its evolution in the terrain. The dissolution of soluble salts and cation exchange processes are the dominant processes controlling groundwater hydrochemistry in the terrain. The trend of evolution of this set of processes follows the pattern of groundwater flow predicted by a calibrated transient groundwater model in the area. The data suggest that anthropogenic activities represent the second most important process in the hydrochemistry. Silicate mineral weathering is the third most important set of processes. Groundwater associations resulting from Q-mode hierarchical cluster analysis indicate an evolutionary pattern consistent with the general groundwater flow pattern in the basin. These key findings are at variance with results of previous investigations and indicate that when carefully done, groundwater hydrochemical data can be very useful for conceptualizing groundwater flow in basins.

Geochemical Characteristics of Shallow Groundwater in Jiaoshiba Shale Gas Production Area: Implications for Environmental Concerns

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Yiman Li

2016-11-01

Full Text Available The geochemical characteristics of shallow groundwater are essential for environmental impact studies in the shale gas production area. Jiaoshiba in the Sichuan basin is the first commercial-scale shale gas production area in China. This paper studied the geochemical and isotopic characteristics of the shallow groundwater of the area for future environmental concerns. Results show that the average pH of the shallow groundwater is 7.5 and the total dissolved solids (TDS vary from 150 mg/L to 350 mg/L. The main water types are HCO3-Ca and HCO3-Ca·Mg due to the carbonates dissolution equilibrium in karst aquifers. The concentrations of major ions and typical toxic elements including Mn, Cr, Cu, Zn, Ba, and Pb are below the drinking water standard of China and are safe for use as drinking water. The high nitrate content is inferred to be caused by agricultural pollution. The shallow groundwater is recharged by local precipitation and flows in the vertical circulation zone. Evidences from low TDS, water isotopes, and high 3H and 14C indicate that the circulation rate of shallow groundwater is rapid, and the lateral groundwater has strong renewability. Once groundwater pollution from deep shale gas production occurs, it will be recovered soon by enough precipitation.

Minimizing transient influence in WHPA delineation: An optimization approach for optimal pumping rate schemes

Science.gov (United States)

Rodriguez-Pretelin, A.; Nowak, W.

2017-12-01

For most groundwater protection management programs, Wellhead Protection Areas (WHPAs) have served as primarily protection measure. In their delineation, the influence of time-varying groundwater flow conditions is often underestimated because steady-state assumptions are commonly made. However, it has been demonstrated that temporary variations lead to significant changes in the required size and shape of WHPAs. Apart from natural transient groundwater drivers (e.g., changes in the regional angle of flow direction and seasonal natural groundwater recharge), anthropogenic causes such as transient pumping rates are of the most influential factors that require larger WHPAs. We hypothesize that WHPA programs that integrate adaptive and optimized pumping-injection management schemes can counter transient effects and thus reduce the additional areal demand in well protection under transient conditions. The main goal of this study is to present a novel management framework that optimizes pumping schemes dynamically, in order to minimize the impact triggered by transient conditions in WHPA delineation. For optimizing pumping schemes, we consider three objectives: 1) to minimize the risk of pumping water from outside a given WHPA, 2) to maximize the groundwater supply and 3) to minimize the involved operating costs. We solve transient groundwater flow through an available transient groundwater and Lagrangian particle tracking model. The optimization problem is formulated as a dynamic programming problem. Two different optimization approaches are explored: I) the first approach aims for single-objective optimization under objective (1) only. The second approach performs multiobjective optimization under all three objectives where compromise pumping rates are selected from the current Pareto front. Finally, we look for WHPA outlines that are as small as possible, yet allow the optimization problem to find the most suitable solutions.

Chlorine stable isotope studies of old groundwater, southwestern Great Artesian Basin, Australia

International Nuclear Information System (INIS)

Zhang Min; Frape, Shaun K.; Love, Andrew J.; Herczeg, Andrew L.; Lehmann, B.E.; Beyerle, U.; Purtschert, R.

2007-01-01

Stable Cl isotope ratios ( 37 Cl/ 35 Cl) were measured in groundwater samples from the southwestern flow system of the Great Artesian Basin, Australia to gain a better understanding of the Cl - sources and transport mechanisms. δ 37 Cl values range from 0 per mille to -2.5 per mille (SMOC), and are inversely correlated with Cl - concentration along the inferred flow direction. The Cl isotopic compositions, in conjunction with other geochemical parameters, suggest that Cl - in groundwaters is not derived from salt dissolution. Mixing of the recharge water with saline groundwater cannot explain the relationship between δ 37 Cl and Cl - concentration measured. Marine aerosols deposited via rainfall and subsequent evapotranspiration appear to be responsible for the Cl - concentrations observed in wells that are close to the recharge area, and in groundwaters sampled along the southern transect. δ 37 Cl values measured in the leachate of the Bulldog shale suggest that the aquitard is the subsurface source of Cl - for the majority of groundwater samples studied. Diffusion is likely the mechanism through which Cl - is transported from the pore water of the Bulldog shale to the aquifer. However, a more detailed study of the aquitard rocks is required to verify this hypothesis

Fluoride contamination in groundwater resources of Alleppey, southern India

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Dhanya Raj

2017-01-01

Full Text Available Alleppey is one of the thickly populated coastal towns of the Kerala state in southern India. Groundwater is the main source of drinking water for the 240,991 people living in this region. The groundwater is being extracted from a multi-layer aquifer system of unconsolidated to semi-consolidated sedimentary formations, which range in age from Recent to Tertiary. The public water distribution system uses dug and tube wells. Though there were reports on fluoride contamination, this study reports for the first time excess fluoride and excess salinity in the drinking water of the region. The quality parameters, like Electrical Conductivity (EC ranges from 266 to 3900 μs/cm, the fluoride content ranges from 0.68 to 2.88 mg/L, and the chloride ranges between the 5.7 to 1253 mg/L. The main water types are Na-HCO3, Na-CO3 and Na-Cl. The aqueous concentrations of F− and CO32− show positive correlation whereas F− and Ca2+ show negative correlation. The source of fluoride in the groundwater could be from dissolution of fluorapatite, which is a common mineral in the Tertiary sediments of the area. Long residence time, sediment–groundwater interaction and facies changes (Ca-HCO3 to Na-HCO3 during groundwater flow regime are the major factors responsible for the high fluoride content in the groundwater of the area. High strontium content and high EC in some of the wells indicate saline water intrusion that could be due to the excess pumping from the deeper aquifers of the area. The water quality index computation has revealed that 62% of groundwater belongs to poor quality and is not suitable for domestic purposes as per BIS and WHO standards. Since the groundwater is the only source of drinking water in the area, proper treatment strategies and regulating the groundwater extraction are required as the quality deterioration poses serious threat to human health.

HB-Line Dissolution of Glovebox Floor Sweepings

International Nuclear Information System (INIS)

Gray, J.H.

1998-02-01

Two candidate flowsheets for dissolving glovebox floor sweepings in the HB-Line Phase I geometrically favorable dissolver have been developed.Dissolving conditions tested and modified during the laboratory program were based on the current processing scheme for dissolving high-fired Pu-238 oxide in HB-Line. Subsequent adjustments made to the HB-Line flowsheet reflected differences in the dissolution behavior between high-fired Pu-238 oxide and the MgO sand/PuF 4 /PuO 2 mixture in glovebox floor sweepings. Although both candidate flowsheets involved two separate dissolving steps and resulted incomplete dissolution of all solids, the one selected for use in HB-Line will require fewer processing operations and resembles the initial flowsheet proposed for dissolving sand, slag, and crucible material in F-Canyon dissolvers. Complete dissolution of glovebox floor sweepings was accomplished in the laboratory by initially dissolving between 55 and 65 degree in a 14 molar nitric acid solution. Under these conditions, partial dissolution of PuF 4 and complete dissolution of PuO 2 and MgO sand were achieved in less than one hour. The presence of free fluoride in solution,uncomplexed by aluminum, was necessary for complete dissolution of the PuO 2 .The remaining PuF 4 dissolved following addition of aluminum nitrate nonahydrate (ANN) to complex the fluoride and heating between 75 and 85 degree C for an additional hour. Precipitation of magnesium and/or aluminum nitrates could occur before, during, and after transfer of product solutions. Both dilution and/or product solution temperature controls may be necessary to prevent precipitation of these salts. Corrosion of the dissolver should not be an issue during these dissolving operations. Corrosion is minimized when dissolving at 55-65 degree C for one to three hours at a maximum uncomplexed free fluoride concentration of 0.07 molar and by dissolving at 75-85 degree C at a one to one aluminum to fluoride mole ratio for another

Arsenic release and geochemical evolution of groundwater in an alluvial aquitard, West Bengal, India.

Science.gov (United States)

Desbarats, A. J.; Pal, T.; Mukherjee, P. K.; Beckie, R. D.

2017-12-01

According to the World Health Organization, contamination of groundwater by geogenic arsenic (As) represents the largest mass poisoning in history. At a field site in West Bengal, India, the source of As affecting a shallow aquifer was traced to silty sediments filling an abandoned river meander. Along with As-bearing phases, these sediments also contain 0.46 % organic carbon. The release of As within the channel fill is investigated using a geochemical mass balance model supported by detailed field observations of aqueous chemistry, sequential extraction analyses of sediment chemistry, and analyses of sediment mineralogy. The model explores the evolution of groundwater chemistry along a flow path extending from its recharge point in an abandoned channel pond, through the channel-fill sequence, to the underlying aquifer. Variations in groundwater composition within the host sediments are explained in terms of mineral weathering driven by organic carbon decay. The model yields reaction coefficients expressing amounts of minerals (and gases) reacting or precipitating along the flow path. Arsenic and phosphorus cycles appear closely linked as these species are hosted by goethite, Fe-rich chlorite, and vivianite. Arsenic is released through the rapid reductive dissolution of goethite and the slower weathering of chlorite. Concomitantly, some As is sequestered in precipitating vivianite. These competing processes reach equilibrium deeper in the channel-fill sequence as groundwater As concentrations stabilize. Using groundwater residence time in channel fill obtained from a numerical flow model and the calculated reaction coefficients, rates of organic carbon oxidation, goethite dissolution, and net As release are estimated at 1.15 mmol C L-1 a-1, 0.18 mmol L-1 a-1, and 4.57 10-4 mmol L-1 a-1, respectively. Fine-grained yet slightly permeable deposits such as channel-fill silts containing reactive organic carbon and As-bearing goethite and phyllosilicates are localized

Assessment of groundwater quality using geographical information system (GIS), at north-east Cairo, Egypt.

Science.gov (United States)

El-Shahat, M F; Sadek, M A; Mostafa, W M; Hagagg, K H

2016-04-01

The present investigation has been conducted to delineate the hydrogeochemical and environmental factors that control the water quality of the groundwater resources in the north-east of Cairo. A complementary approach based on hydrogeochemistry and a geographical information system (GIS) based protectability index has been employed for conducting this work. The results from the chemical analysis revealed that the groundwater of the Quaternary aquifer is less saline than that of the Miocene aquifer and the main factors that control the groundwater salinity in the studied area are primarily related to the genesis of the original recharging water modified after by leaching, dissolution, cation exchange, and fertilizer leachate. The computed groundwater quality index (WQI) falls into two categories: fair for almost all the Miocene groundwater samples, while the Quaternary groundwater samples are all have a good quality. The retarded flow and non-replenishment of the Miocene aquifer compared to the renewable active recharge of the Quaternary aquifer can explain this variation of WQI. The index and overlay approach exemplified by the DUPIT index has been used to investigate the protectability of the study aquifers against diffuse pollutants. Three categories (highly protectable less vulnerable, moderately protectable moderately vulnerable and less protectable highly vulnerable) have been determined and areally mapped.

Dissolution of Monocrystalline Silicon Nanomembranes and Their Use as Encapsulation Layers and Electrical Interfaces in Water-Soluble Electronics.

Science.gov (United States)

Lee, Yoon Kyeung; Yu, Ki Jun; Song, Enming; Barati Farimani, Amir; Vitale, Flavia; Xie, Zhaoqian; Yoon, Younghee; Kim, Yerim; Richardson, Andrew; Luan, Haiwen; Wu, Yixin; Xie, Xu; Lucas, Timothy H; Crawford, Kaitlyn; Mei, Yongfeng; Feng, Xue; Huang, Yonggang; Litt, Brian; Aluru, Narayana R; Yin, Lan; Rogers, John A

2017-12-26

The chemistry that governs the dissolution of device-grade, monocrystalline silicon nanomembranes into benign end products by hydrolysis serves as the foundation for fully eco/biodegradable classes of high-performance electronics. This paper examines these processes in aqueous solutions with chemical compositions relevant to groundwater and biofluids. The results show that the presence of Si(OH) 4 and proteins in these solutions can slow the rates of dissolution and that ion-specific effects associated with Ca 2+ can significantly increase these rates. This information allows for effective use of silicon nanomembranes not only as active layers in eco/biodegradable electronics but also as water barriers capable of providing perfect encapsulation until their disappearance by dissolution. The time scales for this encapsulation can be controlled by introduction of dopants into the Si and by addition of oxide layers on the exposed surfaces.The former possibility also allows the doped silicon to serve as an electrical interface for measuring biopotentials, as demonstrated in fully bioresorbable platforms for in vivo neural recordings. This collection of findings is important for further engineering development of water-soluble classes of silicon electronics.

Hydrochemical Characteristics and Evolution Laws of Drinking Groundwater in Pengyang County, Ningxia, Northwest China

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Li Peiyue

2011-01-01

Full Text Available The purpose of the paper is to identify the chemical characteristics of drinking groundwater and its distribution patterns in Pengyang County and to discover the hydrochemical evolution laws of groundwater. The temporal and spatial variation of groundwater hydrochemical characteristics and evolution laws were comprehensively and systematically studied based on the understanding of the geological, hydrogeological, meteorological and hydrological conditions. Many analytical methods such as descriptive statistics, geostatistical analysis, ionic ratio coefficient method and correlation analysis were adopted based on the underground water quality analysis data. Study results showed that variation coefficients of chemical parameters of pore water in unconsolidated rocks were relatively high which indicated that water chemical compositions are vulnerable to topography, meteorology, hydrology and human activities. TDS variation was in accordance with the changes in Ca2+, Mg2+ and SO42- concentration. Hydrochemical type varied from HCO3•SO4-Na•Ca•Mg type and HCO3•SO4-Ca•Mg type at the upper reaches towards gradually to HCO3-Na type at the lower reaches. Ionic ratio coefficient analysis showed that the hydrodynamic conditions of the pore water in loose rocks were better than that of pore-fissure water in clastic rocks and groundwater was non-marine deposited water. Its formation effects include the weathering leaching effects of the formation containing rock salt, water-rock interaction and cation exchange reaction. Hydrochemical characteristics were mainly controlled by geological and hydrogeological conditions. Correlation analysis showed that the dissolution of rock salt and sodium sulfate salt as well as calcite precipitation occurred in pore water and in pore-crack water in clastic rocks the dissolution of albite, K-feldspar and the precipitation of dolomite were also important effects.

Optimization of the solvent-based dissolution method to sample volatile organic compound vapors for compound-specific isotope analysis.

Science.gov (United States)

Bouchard, Daniel; Wanner, Philipp; Luo, Hong; McLoughlin, Patrick W; Henderson, James K; Pirkle, Robert J; Hunkeler, Daniel

2017-10-20

The methodology of the solvent-based dissolution method used to sample gas phase volatile organic compounds (VOC) for compound-specific isotope analysis (CSIA) was optimized to lower the method detection limits for TCE and benzene. The sampling methodology previously evaluated by [1] consists in pulling the air through a solvent to dissolve and accumulate the gaseous VOC. After the sampling process, the solvent can then be treated similarly as groundwater samples to perform routine CSIA by diluting an aliquot of the solvent into water to reach the required concentration of the targeted contaminant. Among solvents tested, tetraethylene glycol dimethyl ether (TGDE) showed the best aptitude for the method. TGDE has a great affinity with TCE and benzene, hence efficiently dissolving the compounds during their transition through the solvent. The method detection limit for TCE (5±1μg/m 3 ) and benzene (1.7±0.5μg/m 3 ) is lower when using TGDE compared to methanol, which was previously used (385μg/m 3 for TCE and 130μg/m 3 for benzene) [2]. The method detection limit refers to the minimal gas phase concentration in ambient air required to load sufficient VOC mass into TGDE to perform δ 13 C analysis. Due to a different analytical procedure, the method detection limit associated with δ 37 Cl analysis was found to be 156±6μg/m 3 for TCE. Furthermore, the experimental results validated the relationship between the gas phase TCE and the progressive accumulation of dissolved TCE in the solvent during the sampling process. Accordingly, based on the air-solvent partitioning coefficient, the sampling methodology (e.g. sampling rate, sampling duration, amount of solvent) and the final TCE concentration in the solvent, the concentration of TCE in the gas phase prevailing during the sampling event can be determined. Moreover, the possibility to analyse for TCE concentration in the solvent after sampling (or other targeted VOCs) allows the field deployment of the sampling

Optimized remedial groundwater extraction using linear programming

International Nuclear Information System (INIS)

Quinn, J.J.

1995-01-01

Groundwater extraction systems are typically installed to remediate contaminant plumes or prevent further spread of contamination. These systems are expensive to install and maintain. A traditional approach to designing such a wellfield uses a series of trial-and-error simulations to test the effects of various well locations and pump rates. However, the optimal locations and pump rates of extraction wells are difficult to determine when objectives related to the site hydrogeology and potential pumping scheme are considered. This paper describes a case study of an application of linear programming theory to determine optimal well placement and pump rates. The objectives of the pumping scheme were to contain contaminant migration and reduce contaminant concentrations while minimizing the total amount of water pumped and treated. Past site activities at the area under study included disposal of contaminants in pits. Several groundwater plumes have been identified, and others may be present. The area of concern is bordered on three sides by a wetland, which receives a portion of its input budget as groundwater discharge from the pits. Optimization of the containment pumping scheme was intended to meet three goals: (1) prevent discharge of contaminated groundwater to the wetland, (2) minimize the total water pumped and treated (cost benefit), and (3) avoid dewatering of the wetland (cost and ecological benefits). Possible well locations were placed at known source areas. To constrain the problem, the optimization program was instructed to prevent any flow toward the wetland along a user-specified border. In this manner, the optimization routine selects well locations and pump rates so that a groundwater divide is produced along this boundary

The dissolution phenomenon of lysozyme crystals

Energy Technology Data Exchange (ETDEWEB)

Mueller, C.; Ulrich, J. [Martin Luther University Halle-Wittenberg, Department of Thermal Separation Processes, Centre of Engineering Science, Halle/Saale (Germany)

2012-02-15

Dissolution studies on lysozyme crystals were carried out since the observed dissolution pattern look different from non-protein dissolved crystals. The Tetragonal, High Temperature and Low Temperature Orthorhombic morphologies, crystallized using sodium chloride, were chosen and the influence of different pH, salt and protein concentration on their dissolution was investigated. An increase in pH and/or salt concentration can modify the dissolution behaviour. The pattern of the crystals during the dissolution process will, therefore, develop differently. Frequently a skeleton like crystal pattern followed by a falling apart of the crystals is observed. The multi-component character of the lysozyme crystal (protein, water, buffer, salt) as well as ''solvatomorphism'' gives first insights in the phenomena happening in the dissolution process. (copyright 2012 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

Investigation of Processes Controlling Elution of Solutes from Nonaqueous Phase Liquid (NAPL) Pools into Groundwater

Science.gov (United States)

Seyedabbasi, M.; Pirestani, K.; Holland, S. B.; Imhoff, P. T.

2005-12-01

Two major processes influencing the elution of solutes from porous media contaminated with nonaqueous phase liquids (NAPLs) are external mass transfer between the NAPL and groundwater and internal diffusion through NAPL ganglia and pools. There is a relatively large body of literature on the dissolution of single-species NAPLs. Less is known about the rates of elution of compounds dissolving from multicomponent NAPLs. We examined the mass transfer of one solute, 2,3-dimethyl-2-butanol (DMB) - a partitioning tracer, between groundwater and a dense NAPL - trichloroethylene (TCE). Diffusion cell experiments were used to measure the molecular diffusion coefficient of DMB in pure TCE and in porous media contaminated with a TCE pool. Measured diffusion coefficients were compared with empirical correlations (pure TCE) and a parallel resistance model (TCE pool). Based on the results from these analyses, a dimensionless Biot number was derived to express the ratio of the external rate of mass transfer from a NAPL pool to the internal rate of diffusion within the pool, which varies with NAPL saturation and NAPL-water partition coefficient. Biot numbers were then estimated for several laboratory scale experiments involving DMB transport between NAPL pools and groundwater. The estimated Biot numbers were in good agreement with experimental results. The expression for the Biot number developed here may be used to assess the processes controlling the elution of solutes from NAPL pools, which has implications on long-term predictions of solute dissolution from NAPLs in the field.

Identification of hydrogeochemical processes and pollution sources of groundwater nitrate in Leiming Basin of Hainan island, Southern China

Science.gov (United States)

Shaowen, Y.; Zhan, Y., , Dr; Li, Q.

2017-12-01

Identifying the evolution of groundwater quality is important for the control and management of groundwater resources. The main aims of the present study are to identify the major factors affecting hydrogeochemistry of groundwater resources and to evaluate the potential sources of groundwater nitrate in Leiming basin using chemical and isotopic methods. The majority of samples belong to Na-Cl water type and are followed by Ca-HCO3 and mixed Ca-Na-HCO3. The δ18O and δ2H values in groundwater indicate that the shallow fissure groundwater is mainly recharged by rainfall. The evaporated surface water is another significant origin of groundwater. The weathering and dissolution of different rocks and minerals, input of precipitation, evaporation, ion exchange and anthropogenic activities, especially agricultural activities, influence the hydrogeochemistry of the study area. NO- 3 concentration in the groundwater varies from 0.7 to 51.7 mg/L and high values are mainly occurred in the densely populated area. The combined use of isotopic values and hydrochemical data suggests that the NO- 3 load in Leiming basin is not only derived from agricultural activities but also from other sources such as waste water and atmospheric deposition. Fertilizer is considered as the major source of NO- 3 in the groundwater in Leiming basin.

Groundwater characteristics in Elminia governorate, Egypt by hydro chemistry and environmental tritium

International Nuclear Information System (INIS)

Awad, M.A.; Hamza, M.S.; Elbakri, A.; Tantawi, M.

1993-01-01

El-Minia governorate is located along the Nile valley between latitudes 27 degree 30' and 28 degree 45'N and longitudes 30 degree 30' and 31 degree 00'E. The investigated area is essentially occupied by sedimentary rocks belonging to tertiary and quaternary period. The valley on both sides is bounded by faulted steep slopes made up of eocene limestone. The quaternary alluvial aquifer is the most important aquifer in the area, its recharge takes place from infiltration of the surface Nile waters after the irrigation processes, and also from the upward leakage from deep fissured limestone and Nubian sandstone aquifers through the fault planes present in the area and from extensive pumping. Seventy four representative wells as well as twenty surface water from Nile water, main irrigation canals and drainage system were selected for chemical and isotopic analysis in the study area. The chemical composition of water along the valley is heterogeneous. The groundwater types are mainly sodium bicarbonate Na H C O 3 and calcium bicarbonate Ca(H C O 3 ) 2 , while the surface water is magnesium bicarbonate Mg(H CO 3 ) 2 water type. The sources of salinity in groundwater are due to contributions of: 1. halite and gypsum dissolution, 2. calcium carbonate dissolution, and 3. weathering of silicate minerals. With respect to (T.D.S.) content, the quality in most of Elminia groundwater was found to be good to moderate as a supply for drinking purposes. The hardness values of the surface and groundwater could be classified as 'SOFT' which makes it suitable for house-cleaning purposes. Based on the total dissolved salts (T.D.S.), sodium adsorption ratio (SAR) and the sodium percentage (Na %), the majority of Elminia groundwater might also be considered suitable for irrigation uses. The very low tritium content in a considerable part of Elminia wells, proves no direct contact with surface water recharge for more than four decades. These preserved water are free from pathogenic

Dissolution of targets for the production of Mo-99: Part 1. Influence of NaOH concentration and the addition of NaNO{sub 3} and NaNO{sub 2} on the dissolution time

Energy Technology Data Exchange (ETDEWEB)

Camilo, Ruth L.; Araujo, Izilda da C.; Mindrisz, Ana C.; Forbicini, Christina A.L.G. de O., E-mail: rcamilo@ipen.br, E-mail: icaraujo@ipen.br, E-mail: acmindri@ipen.br, E-mail: cforbici@ipen.br [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN/SP), Sao Paulo, SP (Brazil)

2011-07-01

Faced with global crisis in the production of radioisotope {sup 99}Mo, which product of decay, {sup 99}mTc, is the tracer element most often used in nuclear medicine and accounts for about 80% of all diagnostic procedures in vivo, since September 2008 Brazil is developing the project called Brazilian Multipurpose Reactor (RMB). Within the Brazilian Nuclear Program (PNB) the construction of the RMB, is seen as a long term solution to meet all domestic demand relative to the supply of radioisotopes and radiopharmaceuticals. In the process to be studied to obtain {sup 99}Mo from irradiated UA1{sub x}-A1 LEU targets employing alkaline dissolution, processing time should be minimized, considering the short half life of {sup 99}Mo and {sup 99}mTc, about 66 h and 6 h, respectively. That makes dissolution time a significant factor in the development of the process. This paper presents the results of alkaline dissolution of scraps of Al, used to simulate the dissolution process of UA1{sub x}-A1 targets. Al corresponds to about 79% of the total weight of the UA1{sub x}-A1 target. The effect of NaOH concentration on dissolution time for the interval of 1 to 3.5 mol.L-1 was studied, keeping the molar ratio in 1Al:2.16NaOH and the initial temperature of 88 degree C. The influence of reagent composition over dissolution time was studied using three different solutions: a) 3 mol.L{sup -1} NaOH, b) 3 mol.L{sup -1} NaOH/NaNO{sub 3} and c) 3 mol.L{sup -1} NaOH/NaNO{sub 2}, keeping the same molar ratio and temperature. The results showed that the dissolution time decreases with increasing NaOH concentration and the addition of NaNO{sub 3} or NaNO{sub 2} in the NaOH solution reduces both dissolution time and volume of gases released. (author)

Groundwater geochemistry of a Mio-Pliocene aquifer in the northeastern Algerian Sahara (Djamaa region)

Science.gov (United States)

Houari, Idir Menad; Nezli, Imed Eddine; Belksier, Mohamed Salah

2018-05-01

The groundwater resources in the Northern Sahara are represented by two superimposed major aquifer systems: the Intercalary Continental (CI) and the Terminal Complex (CT). The waters of these aquifers pose serious physical and chemical quality problems; they are highly mineralized and very hard. The present work aims to describe the water's geochemical evolution of sand groundwater (Mio-Pliocene) of the Terminal Complex in the area of Djamaa, by the research of the relationship between water's chemical composition and lithology of aquifer formations through. The results obtained show that the water's chemistry is essentially governed by the dissolution of evaporate formations, which gives to, waters an excessive mineralization expressed by high concentrations of sulfates, chlorides and sodium.

Innovative technique for assessment of groundwater quality

International Nuclear Information System (INIS)

Ahmad, N.; Ahmad, M.; Sajjad, M.I.

2001-07-01

Groundwater quality of a part of Chaj Doab has been assessed with innovative techniques which are not reported in literature. The concept of triangular coordinates is modified by multi-rectangular ones for the classification of major cations and anions analysed in the ground water. A Multi-Rectangular Diagram (MRD) has been developed with the combination of rectangular coordinates by virtue of which milli-equivalent per liter percentages (meq/1%) of major cations and anions could be classified into different categories more efficiently as compared to classical trilinear diagrams. Both Piper diagram and MRD are used for the assessment of 259 data sets analysed from ground water of Chaj Doab area, Pakistan. The differentiated ground water types with MRD in the study area are calcium bicarbonate, magnesium bicarbonate, sodium bicarbonate and sodium sulfate. Sodium bicarbonate type emerges as the most abundant type of ground water in the study area. A map showing spatial variation of groundwater quality has been constructed with the help of MRD. This map shows that, in the vicinity of rivers Chenab and Jhelum, calcium bicarbonate type of waters occur while the central area is mainly covered by sodium bicarbonate dominant waters. Groundwaters near the upper Jhelum canal are dominant in sodium sulfate. An important relation between calcium and sodium is proposed which explains the movement history of groundwater in the aquifer. Hydrogeochemical processes have been evaluated with new methods. Ion exchange between calcium and sodium, precipitation of calcium bicarbonate and dissolution of rock forming minerals are the major delineated hydrogeochemical processes. (author)

Effects of the proposed EPA groundwater standards on the Uranium Mill Tailings Remedial Action Project

International Nuclear Information System (INIS)

Titus, F.B.

1988-01-01

Potential groundwater contamination beneath the 24 tailings piles that are to be stabilized under the UMTRA Project was intended in early project plans to be minimized by placing disposal piles over thick stratigraphic sequences of tight (minimally permeable) formations, and by designing covers that contained low permeability soil/clay infiltration barriers. The court-ordered revision of the UMTRA groundwater standards by EPA (proposed standards of September 1987) include very low Maximum Concentration Limits (MCLs), which are based mostly on Primary Drinking Water Standards. EPA also mandates that the designs should control radioactivity and hazardous constituents...for up to one thousand years, to the extends reasonably achievable, and, in any case, for at least two hundred years.... In order to accommodate this stipulation, transport modeling of water and contaminants in both the vadose and saturated zones beneath the piles is run until steady state conditions are reached. The early decision to locate stabilized piles over tight formations now exacerbates the problem of complying with the standards, since the contaminants percolate to groundwater that moves only slowly through strata having low permeabilities. Innovative solutions have been evaluated that are aimed at further minimizing long-term infiltration, geochemically fixing contaminants in place before they reach groundwater, or otherwise minimizing contaminant flux

Recent and old groundwater in the Niebla-Posadas regional aquifer (southern Spain): Implications for its management

Science.gov (United States)

Scheiber, Laura; Ayora, Carlos; Vázquez-Suñé, Enric; Cendón, Dioni I.; Soler, Albert; Custodio, Emilio; Baquero, Juan Carlos

2015-04-01

The Niebla-Posadas (NP) aquifer in southern Spain is one of the main groundwater sources for the lower Guadalquivir Valley, a semiarid region supporting an important population, agriculture and industry. To contribute to the understanding of this aquifer the assessment of sustainable use of groundwater, the residence time of groundwater in the NP aquifer has been estimated using 3H, 14C and 36Cl. Along the flow paths, recharged groundwater mixes with NaCl-type waters and undergoes calcite dissolution and is further modified by cation exchange (Ca-Na). Consequently, the water loses most of its calcium and the residual δ13CDIC in the groundwater is isotopically enriched. Further modifications take place along the flow path in deeper zones, where depleted δ13CDIC values are overprinted due to SO42- and iron oxide reduction, triggered by the presence of organic matter. Dating with 3H, 14C and 36Cl has allowed the differentiation of several zones: recharge zone (30 ky). An apparent link between the tectonic structure and the groundwater residence time zonation can be established. Regional faults clearly separates deep zone 1 from the distinctly older age (>30 ky) deep zone 2. From the estimated residence times, two groundwater areas of different behavior can be differentiated within the aquifer.

The evolution of redox conditions and groundwater geochemistry in recharge-discharge environments on the Canadian Shield

International Nuclear Information System (INIS)

Gascoyne, M.

1996-10-01

Groundwater composition evolves along flow paths from recharge to discharge in response to interactions with bedrock and fracture-filling minerals, and dissolution of soluble (Cl-rich) salts in the rock matrix. The groundwater redox potential changes from oxidizing to reducing conditions due, initially, to rapid consumption of dissolved oxygen by organics in the upper ∼100 m of bedrock and, subsequently, interaction with Fe (II)-containing minerals. Measured Eh values of groundwaters at depth in the granitic Lac du Bonnet batholith indicate that biotite and chlorite control groundwater redox potential. This is supported by other geochemical characteristics such as absence of CH 4 , H 2 S, H 2 , NO 3 , low concentrations of Fe (II), and abundance of SO 4 . Further evidence of evolution of redox conditions is given by variations in U concentration ranging from up to 1000 μg/L in dilute near-surface waters to <1 μg/L in some deep, saline groundwaters. Groundwaters at about 400 m depth in a recharge area on the Lac du Bonnet batholith contain significantly more U than groundwaters further along the flow path or near surface in discharge areas. Uranium concentration is found to be a useful and sensitive indicator of redox conditions. (author)

Assessing the effect of dissolved organic ligands on mineral dissolution rates: An example from calcite dissolution

International Nuclear Information System (INIS)

DeMaio, T.; Grandstaff, D.E.

1997-01-01

Experiments suggest that dissolved organic ligands may primarily modify mineral dissolution rates by three mechanisms: (1) metal-ligand (M-L) complex formation in solution, which increases the degree of undersaturation, (2) formation of surface M-L complexes that attack the surface, and (3) formation of surface complexes which passivate or protect the surface. Mechanisms (1) and (2) increase the dissolution rate and the third decreases it compared with organic-free solutions. The types and importance of these mechanisms may be assessed from plots of dissolution rate versus degree of undersaturation. To illustrate this technique, calcite, a common repository cementing and vein-filling mineral, was dissolved at pH 7.8 and 22 C in Na-Ca-HCO 3 -Cl solutions with low concentrations of three organic ligands. Low citrate concentrations (50 microM) increased the dissolution rate consistent with mechanism (1). Oxalate decreased the rate, consistent with mechanism (3). Low phthalate concentration (<50 microM) decreased calcite dissolution rates; however, higher concentrations increased the dissolution rates, which became faster than in inorganic solutions. Thus, phthalate exhibits both mechanisms (2) and (3) at different concentrations. In such cases linear extrapolations of dissolution rates from high organic ligand concentrations may not be valid

Trace elements in groundwater used for water supply in Latvia

Science.gov (United States)

Retike, Inga; Kalvans, Andis; Babre, Alise; Kalvane, Gunta; Popovs, Konrads

2014-05-01

Latvia is rich with groundwater resources of various chemical composition and groundwater is the main drinking source. Groundwater quality can be easily affected by pollution or overexploitation, therefore drinking water quality is an issue of high importance. Here the first attempt is made to evaluate the vast data base of trace element concentrations in groundwater collected by Latvian Environment, Geology and Meteorology Centre. Data sources here range from National monitoring programs to groundwater resources prospecting and research projects. First available historical records are from early 1960, whose quality is impossible to test. More recent systematic research has been focused on the agricultural impact on groundwater quality (Levins and Gosk, 2007). This research was mainly limited to Quaternary aquifer. Monitoring of trace elements arsenic, cadmium and lead was included in National groundwater monitoring program of Latvia in 2008 and 2009, but due to lack of funding the monitoring was suspended until 2013. As a result there are no comprehensive baseline studies regarding the trace elements concentration in groundwater. The aim of this study is to determine natural major and trace element concentration in aquifers mainly used for water supply in Latvia and to compare the results with EU potable water standards. A new overview of artesian groundwater quality will be useful for national and regional planning documents. Initial few characteristic traits of trace element concentration have been identified. For example, elevated fluorine, strontium and lithium content can be mainly associated with gypsum dissolution, but the highest barium concentrations are found in groundwaters with low sulphate content. The groundwater composition data including trace element concentrations originating from heterogeneous sources will be processed and analyzed as a part of a newly developed geologic and hydrogeological data management and modeling system with working name

Hydrogeochemical characterization and groundwater quality assessment in intruded coastal brine aquifers (Laizhou Bay, China).

Science.gov (United States)

Zhang, Xiaoying; Miao, Jinjie; Hu, Bill X; Liu, Hongwei; Zhang, Hanxiong; Ma, Zhen

2017-09-01

The aquifer in the coastal area of the Laizhou Bay is affected by salinization processes related to intense groundwater exploitation for brine resource and for agriculture irrigation during the last three decades. As a result, the dynamic balances among freshwater, brine, and seawater have been disturbed and the quality of groundwater has deteriorated. To fully understand the groundwater chemical distribution and evolution in the regional aquifers, hydrogeochemical and isotopic studies have been conducted based on the water samples from 102 observation wells. Groundwater levels and salinities in four monitoring wells are as well measured to inspect the general groundwater flow and chemical patterns and seasonal variations. Chemical components such as Na + , K + , Ca 2+ , Mg 2+ , Sr 2+ , Cl - , SO 4 2- , HCO 3 - , NO 3 - , F - , and TDS during the same period are analyzed to explore geochemical evolution, water-rock interactions, sources of salt, nitrate, and fluoride pollution in fresh, brackish, saline, and brine waters. The decreased water levels without typical seasonal variation in the southeast of the study area confirm an over-exploitation of groundwater. The hydrogeochemical characteristics indicate fresh-saline-brine-saline transition pattern from inland to coast where evaporation is a vital factor to control the chemical evolution. The cation exchange processes are occurred at fresh-saline interfaces of mixtures along the hydraulic gradient. Meanwhile, isotopic data indicate that the brine in aquifers was either originated from older meteoric water with mineral dissolution and evaporation or repeatedly evaporation of retained seawater with fresher water recharge and mixing in geological time. Groundwater suitability for drinking is further evaluated according to water quality standard of China. Results reveal high risks of nitrate and fluoride contamination. The elevated nitrate concentration of 560 mg/L, which as high as 28 times of the standard content

U-ages in soils and groundwater evidencing wet periods 400-600 kyr ago in southeast Brazil

International Nuclear Information System (INIS)

Bonotto, D.M.; Jimenez-Rueda, J.R.

2007-01-01

238 U and its radiogenic daughter 234 U have been utilized for dating soil formation and groundwater residence time during the last 1.5 million years, in this case based on the U-dissolution/precipitation occurring during modifications of the oxidation-reduction conditions. In this paper, we report a 400-600 kyr proxy of wet periods from sediments occurring in a soil profile developed over rocks outcropping at the Parana sedimentary basin in Brazil, and from groundwater exploited of Guarani aquifer at the same basin. The approaches indicated successful use of the U-modeled ages for suggesting wet periods exceeding the past 116-210 kyr from previous studies

H-O isotopic and chemical characteristics of a precipitation-lake water-groundwater system in a desert area

Science.gov (United States)

Jin, Ke; Rao, Wenbo; Tan, Hongbing; Song, Yinxian; Yong, Bin; Zheng, Fangwen; Chen, Tangqing; Han, Liangfeng

2018-04-01

The recharge mechanism of groundwater in the Badain Jaran Desert, North China has been a focus of research and still disputable in the past two decades. In this study, the chemical and hydrogen (H) and oxygen (O) isotopic characteristics of shallow groundwater, lake water and local precipitation in the Badain Jaran Desert and neighboring areas were investigated to reveal the relationships between various water bodies and the recharge source of shallow groundwater. Isotopic and hydrogeochemical results show that (1) shallow groundwater was associated with local precipitation in the Ayouqi and Yabulai regions, (2) lake water was mainly recharged by groundwater in the desert hinterland, (3) shallow groundwater of the desert hinterland, Yabulai Mountain and Gurinai Grassland had a common recharge source. Shallow groundwater of the desert hinterland had a mean recharge elevation of 1869 m a.s.l. on the basis of the isotope-altitude relationship and thus originated chiefly from lateral infiltration of precipitation in the Yabulai Mountain. It is further concluded that shallow groundwater flowed towards the Gurinai Grassland according to the groundwater table contour map. Along the flow pathway, the H-O isotopic variations were primarily caused by the evaporation effect but chemical variations of shallow groundwater were affected by multiple factors, e.g., evaporation effect, dilution effect of occasional heavy-precipitation and dissolution of aquifer evaporites. Our findings provide new insight into the groundwater cycle and benefit the management of the limited water resources in the arid desert area.

Hydrochemical and Isotopic Investigation of Groundwater in the Hammamet-Nabeul Aquifer System, North-Eastern Tunisia

Energy Technology Data Exchange (ETDEWEB)

Ben Moussa, A.; Zouari, K. [Laboratory of Radio-Analysis and Environment, ENIS, Sfax (Tunisia); Kurttas, T. [Isotope Hydrology Section, International Atomic Energy Agency, Vienna (Austria)

2013-07-15

The combination of major element geochemistry, stable ({delta}{sup 18}O, {delta}{sup 2}H) and radioactive ({sup 3}H, {sup 14}C) isotopes has provided a comprehensive understanding of the natural and anthropogenic processes that control groundwater mineralization as well as the sources of different groundwater bodies within the Hammamet-Nabeul unconfined aquifer (Cap Bon peninsula, northeastern Tunisia). The geochemical examination shows the dominance of Na-Cl and Ca-SO{sub 4} water types resulting from the dissolution of halite and gypsum, the dedolomitization and the cation exchange process. Additionally, the return flow process in relation with the long term flood irrigation practice contributes to the mineralization by producing high amounts of nitrate. The stable isotope signatures reveal the existence of two groundwater groups. The non-evaporated groundwaters with relatively depleted contents, reflecting recharge at higher altitudes; and evaporated groundwaters with enriched contents highlighting the influence of return flow of irrigation waters. Tritium contents in these two groups provide evidence of the presence of pre- 1950 and post-1960 recharge periods. Carbon-14 activities in shallow wells, in spite of their contamination by organic {sup 14}C, confirm the recent origin of the groundwaters in the study area. (author)

Surface controlled dissolution rates of gypsum in aqueous solutions exhibit nonlinear dissolution kinetics

Science.gov (United States)

Jeschke, Alexander A.; Vosbeck, Katrin; Dreybrodt, Wolfgang

2001-01-01

The effective dissolution rates of gypsum are determined by mixed kinetics, where the rate constants of dissolution at the surface and the transport constant of molecular diffusion of dissolved material are similar. To obtain the surface reaction rate law it is necessary to know the transport constant. We have determined the surface rate law for monocrystalline selenite by using a rotating disc set-up, where the transport coefficients are well known. As a result, up to a calcium concentration of 0.6 · ceq, we find a nearly linear rate law Rs = ksl (1- cs/ ceq) n1, where cs is the total calcium concentration at the surface and ceq the equilibrium concentration with respect to gypsum, n1 = 1.2 ± 0.2, and ksl = 1.1 · 10 -4 mmol cm -2 s -1 ± 15%. We also employed batch-experiments for selenite, alabaster and gypsum rock samples. The result of these experiments were interpreted by using a transport constant determined by NaCl dissolution experiments under similar physical conditions. The batch experiments reveal a dissolution rate law Rs = ksl (1- cs/ ceq) n1, ksl = 1.3 · 10 -4 mmol · cm -2 s -1, n1 = 1.2 ± 0.2 for c ≤ 0.94 · ceq. Close to equilibrium a nonlinear rate law, Rs = ks2 (1- cs/ ceq) n2, is observed, where ks2 is in the order of 10 mmol · cm -2 s -1 and n2 ≈ 4.5. The experimentally observed gypsum dissolution rates from the batch experiments could be accurately fitted, with only minor variations of the surface reaction constant obtained from the rotating disk experiment and the transport coefficient from the NaCl dissolution batch experiment. Batch experiments on pure synthetic gypsum, reveal a linear rate law up to equilibrium. This indicates inhibition of dissolution in natural samples close to equilibrium, as is known also for calcite minerals.

Evaluating data worth for ground-water management under uncertainty

Science.gov (United States)

Wagner, B.J.

1999-01-01

A decision framework is presented for assessing the value of ground-water sampling within the context of ground-water management under uncertainty. The framework couples two optimization models-a chance-constrained ground-water management model and an integer-programing sampling network design model-to identify optimal pumping and sampling strategies. The methodology consists of four steps: (1) The optimal ground-water management strategy for the present level of model uncertainty is determined using the chance-constrained management model; (2) for a specified data collection budget, the monitoring network design model identifies, prior to data collection, the sampling strategy that will minimize model uncertainty; (3) the optimal ground-water management strategy is recalculated on the basis of the projected model uncertainty after sampling; and (4) the worth of the monitoring strategy is assessed by comparing the value of the sample information-i.e., the projected reduction in management costs-with the cost of data collection. Steps 2-4 are repeated for a series of data collection budgets, producing a suite of management/monitoring alternatives, from which the best alternative can be selected. A hypothetical example demonstrates the methodology's ability to identify the ground-water sampling strategy with greatest net economic benefit for ground-water management.A decision framework is presented for assessing the value of ground-water sampling within the context of ground-water management under uncertainty. The framework couples two optimization models - a chance-constrained ground-water management model and an integer-programming sampling network design model - to identify optimal pumping and sampling strategies. The methodology consists of four steps: (1) The optimal ground-water management strategy for the present level of model uncertainty is determined using the chance-constrained management model; (2) for a specified data collection budget, the monitoring

Groundwater Discharges to Rivers in the Western Canadian Oil Sands Region

Science.gov (United States)

Ellis, J.; Jasechko, S.

2016-12-01

Groundwater discharges into rivers impacts the movement and fate of nutrients and contaminants in the environment. Understanding groundwater-surface water interactions is especially important in the western Canadian oil sands, where groundwater contamination risks are elevated and baseline water chemistry data is lacking, leading to substantial uncertainties about anthropogenic influences on local river quality. High salinity groundwater springs sourced from deep aquifers, comprised of Pleistocene-aged glacial meltwater, are known to discharge into many rivers in the oil sands. Understanding connections between deep aquifers and surficial waterways is important in order to determine natural inputs into these rivers and to assess the potential for injected wastewater or oil extraction fluids to enter surface waters. While these springs have been identified, their spatial distribution along rivers has not been fully characterized. Here we present river chemistry data collected along a number of major river corridors in the Canadian oil sands region. We show that saline groundwater springs vary spatially along the course of these rivers and tend to be concentrated where the rivers incise Devonian- or Cretaceous-aged aquifers along an evaporite dissolution front. Our results suggest that water sourced from Devonian aquifers may travel through bitumen-bearing Cretaceous units and discharge into local rivers, implying a strong groundwater-surface water connection in specialized locations. These findings indicate that oil sands process-affected waters that are injected at depth have the potential to move through these aquifers and reach the rivers at the surface at some time in the future. Groundwater-surface water interactions remain key to understanding the risks oil sands activities pose to aquatic ecosystems and downstream communities.

Concentrations and speciation of arsenic along a groundwater flow-path in the Upper Floridan aquifer, Florida, USA

Science.gov (United States)

Haque, S. E.; Johannesson, K. H.

2006-05-01

Arsenic (As) concentrations and speciation were determined in groundwaters along a flow-path in the Upper Floridan aquifer (UFA) to investigate the biogeochemical “evolution“ of As in this relatively pristine aquifer. Dissolved inorganic As species were separated in the field using anion-exchange chromatography and subsequently analyzed by inductively coupled plasma mass spectrometry. Total As concentrations are higher in the recharge area groundwaters compared to down-gradient portions of UFA. Redox conditions vary from relatively oxic to anoxic along the flow-path. Mobilization of As species in UFA groundwaters is influenced by ferric iron reduction and subsequent dissolution, sulfate reduction, and probable pyrite precipitation that are inferred from the data to occur along distinct regions of the flow-path. In general, the distribution of As species are consistent with equilibrium thermodynamics, such that arsenate dominates in more oxidizing waters near the recharge area, and arsenite predominates in the progressively reducing groundwaters beyond the recharge area.

Geology of groundwater occurrences of the Lower Cretaceus sandstone aquifer in East Central Sinai, Egypt

Directory of Open Access Journals (Sweden)

Saad Younes Ghoubachi

2017-01-01

Full Text Available The present study focused on investigating the impact of geological setting on the groundwater occurrences of the Lower Cretaceous sandstone aquifer (Malha. The Lower Cretaceous sandstone aquifer is subdivided into 3 units according to their lithological characters for the first time in this present work. The study area is dissected by normal faults with their downthrown sides due north direction. The groundwater flows from southeast recharge area (outcrop to the northwest direction with an average hydraulic gradient of 0.0035. The hydraulic parameters of the Lower Cretaceous sandstone aquifer were determined and evaluated through 7 pumping tests carried out on productive wells. The Lower Cretaceous aquifer in the study area is characterized by moderate to high potential. The calculated groundwater volume of the Lower Cretaceous aquifer (6300 km2 in the study area attains about 300 bcm, while the estimated recharge to the same aquifer reaches about 44,500 m3/day with an annual recharge of 16 mcm/year. Expended Durov diagram plot revealed that the groundwater has been evolved from Mg-SO4 and Mg-Cl dissolution area types that eventually reached a final stage of evolution represented by a Na-Cl water type. This diagram helps also in identifying groundwater flow direction. The groundwater salinity ranges from 1082 ppm (Shaira to 1719 ppm (Nakhl, in the direction of groundwater movement towards north.

Leaching Tc-99 from SRP glass in simulated tuff and salt groundwaters

International Nuclear Information System (INIS)

Bibler, N.E.; Jurgensen, A.R.

1987-01-01

Results of leach tests with Tc-99 doped SRP borosilicate waste glass are presented. The glass was prepared by melting a mixture of SRP 165 powdered frit doped with a carrier free solution of Tc-99 at 1150 0 C. Dissolution of portions of the resulting glass indicated that the Tc-99 was distributed homogeneously throughout the glass. Static leach tests up to 90 days were performed at 90 0 C in J-13 tuff groundwater or WIPP brine A at a SA/V of 100m -1 . Normalized mass losses were calculated for Tc-99 as well as all the major elements in the glass. Results indicated that under ambient oxidizing conditions Tc-99 leached no faster than the glass-forming elements of the glass. In J-13 water, Tc-99 leached congruently with B. In WIPP brine A, it leached congruently with Si. Leach rates for Li were higher in both groundwaters, probably due to a contribution from an ion exchange mechanism. Leach tests were performed under reducing conditions in J-13 water by adding Zn/Hg amalgam to the leachate. In these tests the pH increased significantly, probably because of the reaction of the amalgam with the water. In a 21-day test, the pH increased to 13 and leach rates for the glass were very high. Even though there was signifcant dissolution of the glass, the normalized mass loss based on Tc-99 was only 0.02g/m 2 . This result and the fact that reducing conditions at normal pH values do not significantly affect the dissolution of the glass, indicate that the low concentrations for Tc-99 obtained under reducing conditions are due to is solubility and not due to an increased durability of the glass. 14 refs., 2 figs., 5 tabs

Dissolution process for advanced-PWR-type fuels

International Nuclear Information System (INIS)

Black, D.E.; Decker, L.A.; Pearson, L.G.

1979-01-01

The new Fluorinel Dissolution Process and Fuel Storage (FAST) Facility at ICPP will provide underwater storage of spent PWR fuel and a new head-end process for fuel dissolution. The dissolution will be two-stage, using HF and HNO 3 , with an intermittent H 2 SO 4 dissolution for removing stainless steel components. Equipment operation is described

The dissolution of chalcopyrite in chloride media

International Nuclear Information System (INIS)

Ibanez, T.; Velasquez, L.

2013-01-01

The aim of this investigation is to determinate the effects of parameters and additives on the kinetics of dissolution of chalcopyrite on moderated conditions by means of dissolutions test with chalcopyrite concentrate and pure chalcopyrite in shake flasks and instrumented stirred reactors. A study of the dissolution of chalcopyrite in chloride solutions has demonstrated that the rate of dissolution of chalcopyrite is strongly dependent on the potential of the solution within a range of 540 to 630 mV (versus SHE). Leaching at pH around 2.5 results in increased rates of copper dissolution suggesting the possibility to keep the solution potential within the range. Both pyrite and silver ions enhance the dissolution of chalcopyrite and this effect increases when both species are present. The MnO 2 has a negative effect on the dissolution increasing the solution potential to values where the rate decreases considerably. (Author)

Hydrogeochemical interpretation of the groundwater at the Haestholmen site, Finland

International Nuclear Information System (INIS)

Nordstrom, D.K.

1986-11-01

This investigation forms a part of the research aimed at marking an assessment of the suitability of rapakivi granite at Haestholmen, an island off the southeastern coast of Finland, for the storage of reactor waste from the Loviisa nuclear power plant. The purpose of this study is to provide preliminary interpretations of the groundwater chemistry based on analyses of groundwater samples taken from several drillholes down to depths of 200 m, as well as other hydrogeological studies made on the site. Chemical analyses of grounfwaters at Haestholmen have demonstrated a fresh-water/saline-water interface at 60-150 m depth, depending on the distance from the coast. The main conclusions from this study are that (1) the saline water has a seawater origin, (2) the saline water is most likely old Baltic seawater from the early to middle Holocene, (3) this seawater has been chemically modified by at least four processes: calcite precipitation, fluorite dissolution and precipitation, Na-K-Mg-Ca cation exchange and sulfate reduction, (4) the saline groundwaters are not chemically uniform with depth and (5) the saline water chemistry reflects a structural control by the bedrock

Dissolution glow curve in LLD

International Nuclear Information System (INIS)

Haverkamp, U.; Wiezorek, C.; Poetter, R.

1990-01-01

Lyoluminescence dosimetry is based upon light emission during dissolution of previously irradiated dosimetric materials. The lyoluminescence signal is expressed in the dissolution glow curve. These curves begin, depending on the dissolution system, with a high peak followed by an exponentially decreasing intensity. System parameters that influence the graph of the dissolution glow curve, are, for example, injection speed, temperature and pH value of the solution and the design of the dissolution cell. The initial peak does not significantly correlate with the absorbed dose, it is mainly an effect of the injection. The decay of the curve consists of two exponential components: one fast and one slow. The components depend on the absorbed dose and the dosimetric materials used. In particular, the slow component correlates with the absorbed dose. In contrast to the fast component the argument of the exponential function of the slow component is independent of the dosimetric materials investigated: trehalose, glucose and mannitol. The maximum value, following the peak of the curve, and the integral light output are a measure of the absorbed dose. The reason for the different light outputs of various dosimetric materials after irradiation with the same dose is the differing solubility. The character of the dissolution glow curves is the same following irradiation with photons, electrons or neutrons. (author)

Modeling of geochemical processes related to uranium mobilization in the groundwater of a uranium mine

International Nuclear Information System (INIS)

Gomez, P.; Garralon, A.; Buil, B.; Turrero, Ma.J.; Sanchez, L.; Cruz, B. de la

2006-01-01

This paper describes the processes leading to uranium distribution in the groundwater of five boreholes near a restored uranium mine (dug in granite), and the environmental impact of restoration work in the discharge area. The groundwater uranium content varied from < 1 μg/L in reduced water far from the area of influence of the uranium ore-containing dyke, to 104 μg/L in a borehole hydraulically connected to the mine. These values, however, fail to reflect a chemical equilibrium between the water and the pure mineral phases. A model for the mobilization of uranium in this groundwater is therefore proposed. This involves the percolation of oxidized waters through the fractured granite, leading to the oxidation of pyrite and arsenopyrite and the precipitation of iron oxyhydroxides. This in turn leads to the dissolution of the primary pitchblende and, subsequently, the release of U(VI) species to the groundwater. These U(VI) species are retained by iron hydroxides. Secondary uranium species are eventually formed as reducing conditions are re-established due to water-rock interactions

Role of competing ions in the mobilization of arsenic in groundwater of Bengal Basin: insight from surface complexation modeling.

Science.gov (United States)

Biswas, Ashis; Gustafsson, Jon Petter; Neidhardt, Harald; Halder, Dipti; Kundu, Amit K; Chatterjee, Debashis; Berner, Zsolt; Bhattacharya, Prosun

2014-05-15

This study assesses the role of competing ions in the mobilization of arsenic (As) by surface complexation modeling of the temporal variability of As in groundwater. The potential use of two different surface complexation models (SCMs), developed for ferrihydrite and goethite, has been explored to account for the temporal variation of As(III) and As(V) concentration, monitored in shallow groundwater of Bengal Basin over a period of 20 months. The SCM for ferrihydrite appears as the better predictor of the observed variation in both As(III) and As(V) concentrations in the study sites. It is estimated that among the competing ions, PO4(3-) is the major competitor of As(III) and As(V) adsorption onto Fe oxyhydroxide, and the competition ability decreases in the order PO4(3-) ≫ Fe(II) > H4SiO4 = HCO3(-). It is further revealed that a small change in pH can also have a significant effect on the mobility of As(III) and As(V) in the aquifers. A decrease in pH increases the concentration of As(III), whereas it decreases the As(V) concentration and vice versa. The present study suggests that the reductive dissolution of Fe oxyhydroxide alone cannot explain the observed high As concentration in groundwater of the Bengal Basin. This study supports the view that the reductive dissolution of Fe oxyhydroxide followed by competitive sorption reactions with the aquifer sediment is the processes responsible for As enrichment in groundwater. Copyright © 2014 Elsevier Ltd. All rights reserved.

Sampling and treatment of rock cores and groundwater under reducing environments of deep underground

International Nuclear Information System (INIS)

Ebashi, Katsuhiro; Yamaguchi, Tetsuji; Tanaka, Tadao

2005-01-01

A method of sampling and treatment of undisturbed rock cores and groundwater under maintained reducing environments of deep underground was developed and demonstrated in a Neogene's sandy mudstone layer at depth of GL-100 to -200 m. Undisturbed rock cores and groundwater were sampled and transferred into an Ar gas atmospheric glove box with minimized exposure to the atmosphere. The reducing conditions of the sampled groundwater and rock cores were examined in the Ar atmospheric glove box by measuring pH and Eh of the sampled groundwater and sampled groundwater contacting with disk type rock samples, respectively. (author)

Modeling of groundwater using the isotopic technique in the sedimentary aquifer of the Mahafaly basin, southwestern Madagascar

International Nuclear Information System (INIS)

Fareze, L.H.

2016-01-01

The Mahafaly sedimentary basin, southwest of Madagascar belongs to the region where the water resources management problem, such as high groundwater mineralization and dry wells lingers. In this research work, hydrochemistry and isotopes techniques are used to assess the groundwater characteristics, to determine the groundwater origin and to understand their geochemical evolution. The development of an hydrological model using Modflow software contribute to control the groundwater flow and predict the dissolved particles evolution and travel time according to their flow direction. Dissolution of halite, calcite and gypsum and cation exchange are the main sources of the groundwater mineralization in the study area. The groundwater isotopic composition indicates that the groundwaters are directly recharged by local precipitation, having a mean time of 25 years. A mixture of groundwater and Onilahy river water occurs in adjacent aquifers, of which residence time is about 60 years. A mixture of recent and old groundwaters by the upwelling of the deep waters is observed in the southern aquifer of Isalo, confirmed by the tritium concentration value, which is lower than 0,5UT. The model established indicates a high groundwater flow rate from the recharge area, located in Betioky hill. This is due to a steep slope with a hydraulic conductivity of about 10 -5 m.s -1 , although other flow directions have been identified. The model predicts a decrease of the hydraulic head during the last decades. [fr

Stable isotopic data for inferring source of groundwater recharge in the Anekal Taluk, Karnataka

International Nuclear Information System (INIS)

Ansari, Md. Arzoo; Deodhar, Archana; Jaryal, Ajay; Mendhekar, G.N.; Sinha, U.K.; Dash, Ashutosh; Davis, Deljo

2015-01-01

Occurrence of groundwater mainly depends on recharge area characteristics such as slope of the topography, surface cover characteristics, geology of the area and the permeability of top soil etc. Most of the tube wells located in the study area are in unconfined aquifer and the hydrology of them is mainly influenced by rainfall and surrounding catchments area characteristics. Isotope techniques provide a unique tool for establishing the recharge areas of groundwater. The stable Isotopes of O and H in water behave chemically conservative below 60 - 80°C and their concentrations are not affected by geochemical reactions in normal aquifers. Therefore, groundwater preserves its isotopic fingerprint, reflecting the history and origin before infiltration. This makes it an useful tool to interpret recharge mechanisms and the flow system. Therefore, an isotope hydrological technique has been applied in Anekal (12 deg 47 min 44 sec N; 77 deg 41 min 29 sec E) to identify the groundwater recharge area. Groundwater samples were collected from the study areas and analyzed for environmental Isotope (δ 2 H, δ 18 O) by a Isotope ratio mass spectrometer (IsoPrime-100) using gas equilibration method. Physico-chemical parameters (Temperature, EC, pH) were measured insitu. Electrical conductivity (EC) of the groundwater ranges from 668 to 2139 μS/cm, which is dependent on their travel path and the associated rock-water interaction (dissolution of rock minerals)

IMPACT OF THE JAKUŠEVEC-PRUDINEC WASTE DISPOSAL SITE ON GROUNDWATER QUALITY

Directory of Open Access Journals (Sweden)

Zoran Nakić

2007-12-01

Full Text Available The main goal of the research shown in this paper is to investigate the cause and effect relation of the Jakuševec-Prudinec waste disposal site and the groundwater pollution. The recovery of the Jakuševec-Prudinec waste disposal site by the end of 2003 did not have any significant impact on the pollution reduction in groundwater. Very high values of the pollution index defined in the area southeastern from the waste disposal site show spreading of the pollution toward Mičevec village. The analysis of the hydrogeochemical characteristics showed that in the waste disposal site area the local geochemical anomalies of the partial CO2 pressure exist, indicating that the intensive carbonate dissolution processes and HCO3- enrichment dominate in this area. Near the border of the waste disposal site groundwater with high ammonium ion (NH4+ and chloride ion (Cl- dominates. The high concentrations of the heavy metals and very strong geochemical bonds determined from the correlation coefficients show that in the reductive aquifer conditions heavy metals strongly release (the paper is published in Croatian.

Review: Optimization methods for groundwater modeling and management

Science.gov (United States)

Yeh, William W.-G.

2015-09-01

Optimization methods have been used in groundwater modeling as well as for the planning and management of groundwater systems. This paper reviews and evaluates the various optimization methods that have been used for solving the inverse problem of parameter identification (estimation), experimental design, and groundwater planning and management. Various model selection criteria are discussed, as well as criteria used for model discrimination. The inverse problem of parameter identification concerns the optimal determination of model parameters using water-level observations. In general, the optimal experimental design seeks to find sampling strategies for the purpose of estimating the unknown model parameters. A typical objective of optimal conjunctive-use planning of surface water and groundwater is to minimize the operational costs of meeting water demand. The optimization methods include mathematical programming techniques such as linear programming, quadratic programming, dynamic programming, stochastic programming, nonlinear programming, and the global search algorithms such as genetic algorithms, simulated annealing, and tabu search. Emphasis is placed on groundwater flow problems as opposed to contaminant transport problems. A typical two-dimensional groundwater flow problem is used to explain the basic formulations and algorithms that have been used to solve the formulated optimization problems.

The use of commercial microwave dissolution equipment for the fast and reliable dissolution of high-fired POX and MOX samples

International Nuclear Information System (INIS)

Tushingham, J.; McInnes, C.; Firkin, S.

1998-09-01

The use of commercially available microwave dissolution equipment for the fast and reliable dissolution of high-fired plutonium dioxide (POX) and mixed oxide (MOX) samples has been evaluated for application to Safeguards Analysis. Under the auspices of the UK R and D Support Programme to the IAEA, equipment has been purchased and tested for the high-pressure microwave dissolution of POX samples fired to 1250 deg. C and MOX samples fired to 1600 deg. C, in concentrated nitric acid and hydrofluoric acid mixture. Considerable problems were encountered during development of procedures for microwave dissolution, resulting largely from sudden changes in pressure within dissolution vessels, which resulted in actuation of safety interlocks designed to prevent overpressurisation. These difficulties were alleviated by controlling the microwave power to reduce the reaction temperature and pressure, and also by introducing additional safety valves into the digestion vessels. Using microwave digestion, dissolution times for high fired POX and MOX samples were substantially reduced. Samples which required ca. 10 hours to dissolve by conventional means could be dissolved in ca. 80 minutes by microwave digestion. Whilst a similar performance in terms of plutonium recovery was achieved for some materials by microwave and conventional dissolution, for other materials microwave dissolution gave higher plutonium recoveries but with poorer precision. This suggests the possible presence of some plutonium oxide within high-fired materials which is more difficult to dissolve than the bulk, and which is perhaps dissolved to an additional but variable degree by the current microwave dissolution procedure. Microwave dissolution has been demonstrated to increase the speed of dissolution of high-fired POX and MOX materials, compared with conventional dissolution. However, the technique has not yet proved satisfactory for the complete dissolution of all high-fired materials tested because of

Groundwater regimes and isotopic studies, Ranger mine area, Northern Territory

Energy Technology Data Exchange (ETDEWEB)

Ahmad, M; Green, D C

1986-12-01

Three types of groundwater occur in the area of the Ranger mine. Type A groundwater occurs in the loose sands and gravels occupying the present day stream channels, Type B in the weathering profile and Type C occurs in relatively fresh fractured bedrock occupying open fractures and other cavities. The three types of groundwater can be distinguished both chemically and isotopically. Light stable isotope data suggest that most early rains are lost by evapotranspiration and have no imprint on the groundwater. Later in the wet season, the ground is saturated and groundwater recharge occurs on a regional scale. This younger groundwater sits on the older waters. Mixing is probably minimal as before any large scale mixing could occur, most younger waters are lost by evapotranspiration. Stable isotope data suggest that Type B groundwater in certain areas has some connection with evaporated surface water bodies. Stable isotope measurements for the pollution monitoring bores around the tailings dam do not indicate any connection with the polluted pond waters at the time of sample collection.

Concentration and size distribution of particles in abstracted groundwater.

Science.gov (United States)

van Beek, C G E M; de Zwart, A H; Balemans, M; Kooiman, J W; van Rosmalen, C; Timmer, H; Vandersluys, J; Stuyfzand, P J

2010-02-01

Particle number concentrations have been counted and particle size distributions calculated in groundwater derived by abstraction wells. Both concentration and size distribution are governed by the discharge rate: the higher this rate the higher the concentration and the higher the proportion of larger particles. However, the particle concentration in groundwater derived from abstraction wells, with high groundwater flow velocities, is much lower than in groundwater from monitor wells, with minimal flow velocities. This inconsistency points to exhaustion of the particle supply in the aquifer around wells due to groundwater abstraction for many years. The particle size distribution can be described with the help of a power law or Pareto distribution. Comparing the measured particle size distribution with the Pareto distribution shows that particles with a diameter >7 microm are under-represented. As the particle size distribution is dependent on the flow velocity, so is the value of the "Pareto" slope beta. (c) 2009 Elsevier Ltd. All rights reserved.

Groundwater chemical baseline values to assess the Recovery Plan in the Matanza-Riachuelo River basin, Argentina.

Science.gov (United States)

Zabala, M E; Martínez, S; Manzano, M; Vives, L

2016-01-15

The two most exploited aquifers in the Matanza-Riachuelo River basin are being monitored in the framework of the Integrated Environmental Sanitation Plan that implements the Basin Authority, Autoridad de Cuenca Matanza Riachuelo. In this context, this work identifies the groundwater chemical types and the natural processes behind them; determines spatial and temporal changes; establishes ranges of variation for chemical components, and proposes concentration values for the upper limit of the natural chemical background. A total of 1007 samples from three aquifer-layers (Upper Aquifer, top and bottom of Puelche Aquifer) have been studied. As concrete guidelines for practical determination of baseline values are not available in the region, the methodology used follows the proposals of European projects which assessed European water directives. The groundwater composition is very stable in terms of both chemical facies and mineralization degree, and the changes observed in the dry and wet periods analysed are subtle in general. Most of the groundwater is Na-HCO3 type, except a few samples that are Ca-HCO3, Na-ClSO4 and Na-Cl types. The Ca-HCO3 waters are the result of calcium carbonate dissolution, Na-HCO3 waters result from cation exchange and carbonate dissolution, while in the Na-ClSO4 and Na-Cl waters, mixing with connate and with encroached old marine water from the underlying and overlying sediments are the most relevant processes. The proposed values for the upper limit of the natural background consider the influence of geology and Holocene marine ingressions in the baseline of coastal groundwater. This study allowed to know the initial chemical conditions of the groundwater system of the Matanza-Riachuelo River basin and to establish the reference from which Basin Authority can start to evaluate trends and monitor the recovery plan. At the same time, it sets a precedent for future studies in the region. Copyright © 2015 Elsevier B.V. All rights reserved.

Development of Dissolution Test Method for Drotaverine ...

African Journals Online (AJOL)

Development of Dissolution Test Method for Drotaverine ... Methods: Sink conditions, drug stability and specificity in different dissolution media were tested to optimize a dissolution test .... test by Prism 4.0 software, and differences between ...

Mechanistic Basis of Cocrystal Dissolution Advantage.

Science.gov (United States)

Cao, Fengjuan; Amidon, Gordon L; Rodríguez-Hornedo, Naír; Amidon, Gregory E

2018-01-01

Current interest in cocrystal development resides in the advantages that the cocrystal may have in solubility and dissolution compared with the parent drug. This work provides a mechanistic analysis and comparison of the dissolution behavior of carbamazepine (CBZ) and its 2 cocrystals, carbamazepine-saccharin (CBZ-SAC) and carbamazepine-salicylic acid (CBZ-SLC) under the influence of pH and micellar solubilization. A simple mathematical equation is derived based on the mass transport analyses to describe the dissolution advantage of cocrystals. The dissolution advantage is the ratio of the cocrystal flux to drug flux and is defined as the solubility advantage (cocrystal to drug solubility ratio) times the diffusivity advantage (cocrystal to drug diffusivity ratio). In this work, the effective diffusivity of CBZ in the presence of surfactant was determined to be different and less than those of the cocrystals. The higher effective diffusivity of drug from the dissolved cocrystals, the diffusivity advantage, can impart a dissolution advantage to cocrystals with lower solubility than the parent drug while still maintaining thermodynamic stability. Dissolution conditions where cocrystals can display both thermodynamic stability and a dissolution advantage can be obtained from the mass transport models, and this information is useful for both cocrystal selection and formulation development. Copyright © 2018 American Pharmacists Association®. Published by Elsevier Inc. All rights reserved.

URANIUM-SERIES CONSTRAINTS ON RADIONUCLIDE TRANSPORT AND GROUNDWATER FLOW AT NOPAL I URANIUM DEPOSIT, SIERRA PENA BLANCA, MEXICO

Energy Technology Data Exchange (ETDEWEB)

S. J. Goldstein, S. Luo, T. L. Ku, and M. T. Murrell

2006-04-01

Uranium-series data for groundwater samples from the vicinity of the Nopal I uranium ore deposit are used to place constraints on radionuclide transport and hydrologic processes at this site, and also, by analogy, at Yucca Mountain. Decreasing uranium concentrations for wells drilled in 2003 suggest that groundwater flow rates are low (< 10 m/yr). Field tests, well productivity, and uranium isotopic constraints also suggest that groundwater flow and mixing is limited at this site. The uranium isotopic systematics for water collected in the mine adit are consistent with longer rock-water interaction times and higher uranium dissolution rates at the front of the adit where the deposit is located. Short-lived nuclide data for groundwater wells are used to calculate retardation factors that are on the order of 1,000 for radium and 10,000 to 10,000,000 for lead and polonium. Radium has enhanced mobility in adit water and fractures near the deposit.

URANIUM-SERIES CONSTRAINTS ON RADIONUCLIDE TRANSPORT AND GROUNDWATER FLOW AT NOPAL I URANIUM DEPOSIT, SIERRA PENA BLANCA, MEXICO

International Nuclear Information System (INIS)

S. J. Goldstein, S. Luo, T. L. Ku, and M. T. Murrell

2006-01-01

Uranium-series data for groundwater samples from the vicinity of the Nopal I uranium ore deposit are used to place constraints on radionuclide transport and hydrologic processes at this site, and also, by analogy, at Yucca Mountain. Decreasing uranium concentrations for wells drilled in 2003 suggest that groundwater flow rates are low (< 10 m/yr). Field tests, well productivity, and uranium isotopic constraints also suggest that groundwater flow and mixing is limited at this site. The uranium isotopic systematics for water collected in the mine adit are consistent with longer rock-water interaction times and higher uranium dissolution rates at the front of the adit where the deposit is located. Short-lived nuclide data for groundwater wells are used to calculate retardation factors that are on the order of 1,000 for radium and 10,000 to 10,000,000 for lead and polonium. Radium has enhanced mobility in adit water and fractures near the deposit

Kinetic Controls on the Desorption/Dissolution of Sorbed U(VI) and their Influence on Reactive Transport

International Nuclear Information System (INIS)

Zachara, John M.; Chongxuan Liu; Qafoku, Nikolla P.; McKinley, James P.; Catalano, Jeffrey G.; Brown, Gordon E. Jr.; Davis, James A.

2006-01-01

A number of published studies have sought to understand geochemical kinetic process of uranium (U) that are relevant to nuclear waste sites and repositories by studying the weathering of U ore bodies and downgradient transport of weathering products. Such studies have provided important insights on processes operative over many thousand to millions of years. This project also seeks knowledge on the geochemical kinetics of U, but for shorter in-ground time periods (e.g., 20-50 years) relevant to DOE legacy waste sites. Several representative field sites were selected for intense study at Hanford as part of EMSP research to provide: (1) fundamental insights on intermediate duration geochemical events of U controlling fate and transport, and (2) key scientific information needed for remedial action assessment and informed decision making. The site discussed in this poster is the 300 A uranium plume. This plume is located at the south end of Hanford and discharges directly to the Columbia River. The plume resulted from the discharge of fuels fabrication wastes (nitric acid solutions containing U and Cu) and cladding dissolution wastes (basic sodium aluminate) to the North and South Process Ponds between 1943 and 1975 near the Columbia River. A Kd-based remedial action assessment fifteen years ago predicted that the plume would dissipate to concentrations below the DWS within 10 y. As a result of this assessment, an interim, MNA remedial decision was agreed to by DOE and state/federal regulators. It has been 15 y since the above assessment, and groundwater concentrations have not decreased (attenuated) as projected. Stakeholders are now demanding remedial intervention, and DOE seeks science-based conceptual and numeric models for more accurate future projections. The objectives are: (1) Identify the chemical speciation (e.g., adsorption complexes precipitates), mineral residence, and physical location of contaminant U in a depth sequence of sediments from the disposal

Kinetic Controls on the Desorption/Dissolution of Sorbed U(VI) and Their Influence on Reactive Transport

International Nuclear Information System (INIS)

J. M. Zachara; C. Liu; N. Qafoku; J. P. McKinley; J. A. Davis; D. Stoliker; Y. Arai; J. G. Catalano; G. E. Brown, Jr.

2007-01-01

A number of published studies have sought to understand geochemical kinetic process of uranium (U) that are relevant to nuclear waste sites and repositories by studying the weathering of U ore bodies and downgradient transport of weathering products. Such studies have provided important insights on processes operative over many thousand to millions of years. This project also seeks knowledge on the geochemical kinetics of U, but for shorter in-ground time periods (e.g., 20-50 years) relevant to DOE legacy waste sites. Several representative field sites were selected for intense study at Hanford as part of EMSP research to provide: (1) fundamental insights on intermediate duration geochemical events of U controlling fate and transport, and (2) key scientific information needed for remedial action assessment and informed decision making. The site discussed in this poster is the 300 A uranium plume. This plume is located at the south end of Hanford and discharges directly to the Columbia River. The plume resulted from the discharge of fuels fabrication wastes (nitric acid solutions containing U and Cu) and cladding dissolution wastes (basic sodium aluminate) to the North and South Process Ponds between 1943 and 1975 near the Columbia River. A Kd-based remedial action assessment fifteen years ago predicted that the plume would dissipate to concentrations below the DWS within 10 y. As a result of this assessment, an interim, MNA remedial decision was agreed to by DOE and state/federal regulators. It has been 15 y since the above assessment, and groundwater concentrations have not decreased (attenuated) as projected. Stakeholders are now demanding remedial intervention, and DOE seeks science-based conceptual and numeric models for more accurate future projections. The objectives are: (1) Identify the chemical speciation (e.g., adsorption complexes or precipitates), mineral residence, and physical location of contaminant U in a depth sequence of sediments from the

Accelerated dissolution of iron oxides in ice

Directory of Open Access Journals (Sweden)

D. Jeong

2012-11-01

Full Text Available Iron dissolution from mineral dusts and soil particles is vital as a source of bioavailable iron in various environmental media. In this work, the dissolution of iron oxide particles trapped in ice was investigated as a new pathway of iron supply. The dissolution experiments were carried out in the absence and presence of various organic complexing ligands under dark condition. In acidic pH conditions (pH 2, 3, and 4, the dissolution of iron oxides was greatly enhanced in the ice phase compared to that in water. The dissolved iron was mainly in the ferric form, which indicates that the dissolution is not a reductive process. The extent of dissolved iron was greatly affected by the kind of organic complexing ligands and the surface area of iron oxides. The iron dissolution was most pronounced with high surface area iron oxides and in the presence of strong iron binding ligands. The enhanced dissolution of iron oxides in ice is mainly ascribed to the "freeze concentration effect", which concentrates iron oxide particles, organic ligands, and protons in the liquid like ice grain boundary region and accelerates the dissolution of iron oxides. The ice-enhanced dissolution effect gradually decreased when decreasing the freezing temperature from −10 to −196 °C, which implies that the presence and formation of the liquid-like ice grain boundary region play a critical role. The proposed phenomenon of enhanced dissolution of iron oxides in ice may provide a new pathway of bioavailable iron production. The frozen atmospheric ice with iron-containing dust particles in the upper atmosphere thaws upon descending and may provide bioavailable iron upon deposition onto the ocean surface.

Investigation of Geochemical Characteristics and Controlling Processes of Groundwater in a Typical Long-Term Reclaimed Water Use Area

Directory of Open Access Journals (Sweden)

Yong Xiao

2017-10-01

Full Text Available The usage of reclaimed water can efficiently mitigate water crises, but it may cause groundwater pollution. To clearly understand the potential influences of long-term reclaimed water usage, a total of 91 samples of shallow and deep groundwater were collected from a typical reclaimed water use area during the dry and rainy seasons. The results suggest both shallow and deep groundwater are mainly naturally alkaline freshwater, which are composed mainly of Ca-HCO3, followed by mixed types such as Ca-Na-HCO3 and Ca-Mg-HCO3. A seasonal desalination trend was observed in both shallow and deep aquifers due to dilution effects in the rainy season. Groundwater chemical compositions in both shallow and deep aquifers are still dominantly controlled by natural processes such as silicate weathering, minerals dissolution and cation exchange. Human activities are also the factors influencing groundwater chemistry. Urbanization has been found responsible for the deterioration of groundwater quality, especially in shallow aquifers, because of the relative thin aquitard. Reclaimed water usage for agricultural irrigation and landscape purposes has nearly no influences on groundwater quality in rural areas due to thick aquitards. Therefore, reclaimed water usage should be encouraged in arid and semiarid areas with proper hydrogeological condition.

In vitro dissolution methodology, mini-Gastrointestinal Simulator (mGIS), predicts better in vivo dissolution of a weak base drug, dasatinib.

Science.gov (United States)

Tsume, Yasuhiro; Takeuchi, Susumu; Matsui, Kazuki; Amidon, Gregory E; Amidon, Gordon L

2015-08-30

USP apparatus I and II are gold standard methodologies for determining the in vitro dissolution profiles of test drugs. However, it is difficult to use in vitro dissolution results to predict in vivo dissolution, particularly the pH-dependent solubility of weak acid and base drugs, because the USP apparatus contains one vessel with a fixed pH for the test drug, limiting insight into in vivo drug dissolution of weak acid and weak base drugs. This discrepancy underscores the need to develop new in vitro dissolution methodology that better predicts in vivo response to assure the therapeutic efficacy and safety of oral drug products. Thus, the development of the in vivo predictive dissolution (IPD) methodology is necessitated. The major goals of in vitro dissolution are to ensure the performance of oral drug products and the support of drug formulation design, including bioequivalence (BE). Orally administered anticancer drugs, such as dasatinib and erlotinib (tyrosine kinase inhibitors), are used to treat various types of cancer. These drugs are weak bases that exhibit pH-dependent and high solubility in the acidic stomach and low solubility in the small intestine (>pH 6.0). Therefore, these drugs supersaturate and/or precipitate when they move from the stomach to the small intestine. Also of importance, gastric acidity for cancer patients may be altered with aging (reduction of gastric fluid secretion) and/or co-administration of acid-reducing agents. These may result in changes to the dissolution profiles of weak base and the reduction of drug absorption and efficacy. In vitro dissolution methodologies that assess the impact of these physiological changes in the GI condition are expected to better predict in vivo dissolution of oral medications for patients and, hence, better assess efficacy, toxicity and safety concerns. The objective of this present study is to determine the initial conditions for a mini-Gastrointestinal Simulator (mGIS) to assess in vivo

Study of groundwater chemistry and salinization in Rechna Doab using hydrochemical and isotopic tools

International Nuclear Information System (INIS)

Sajjad, M.I.; Tasneem, M.A.; Akram, W.; Ahmad, M.; Hussain, S.D.; Khan, I.H.

1991-09-01

Isotopic and chemical characterization of groundwater in Rechna Doab were studied. Samples of water from existing shallow and deep wells, etc. were collected and analyzed for their major ionic and stable isotopic (/sup 2/H, /sup 18/O) contents. The chemical data was used to have a knowledge of various aspects of water chemistry. Different compositional types of water existing in the area were identified. It was observed that groundwater at most of the locations belongs to sodium bicarbonate type. The geochemical evaluation of groundwater was also studied. It is suggested that infiltering water picks up carbon dioxide during percolation through the soil zone. This CO/sub 2/rich water upon interaction with the sediments dissolves more soluble ions. With the increase in salinity soluble remains in solution. Chemical quality of water was evaluated for various uses and found satisfactory in most of the cases. Stable isotopic values in combination with conservative ion (Cl) concentration were used to identify the process of groundwater salinization. Three possible processes, mixing with connate marine water, concentration of salts by evaporation and dissolution of salts from sediments was found to be the operating mechanism under the prevailing conditions. (author)

Cycling of oxyanion-forming trace elements in groundwaters from a freshwater deltaic marsh

Science.gov (United States)

Telfeyan, Katherine; Breaux, Alexander; Kim, Jihyuk; Kolker, Alexander S.; Cable, Jaye E.; Johannesson, Karen H.

2018-05-01

Pore waters and surface waters were collected from a freshwater system in southeastern Louisiana to investigate the geochemical cycling of oxyanion-forming trace elements (i.e., Mo, W, As, V). A small bayou (Bayou Fortier) receives input from a connecting lake (Lac des Allemands) and groundwater input at the head approximately 5 km directly south of the Mississippi River. Marsh groundwaters exchange with bayou surface water but are otherwise relatively isolated from outside hydrologic forcings, such as tides, storms, and effects from local navigation canals. Rather, redox processes in the marsh groundwaters appear to drive changes in trace element concentrations. Elevated dissolved S(-II) concentrations in marsh groundwaters suggest greater reducing conditions in the late fall and winter as compared to the spring and late summer. The data suggest that reducing conditions in marsh groundwaters initiate the dissolution of Fe(III)/Mn(IV) oxide/hydroxide minerals, which releases adsorbed and/or co-precipitated trace elements into solution. Once in solution, the fate of these elements is determined by complexation with aqueous species and precipitation with iron sulfide minerals. The trace elements remain soluble in the presence of Fe(III)- and SO42-- reducing conditions, suggesting that either kinetic limitations or complexation with aqueous ligands obfuscates the correlation between V and Mo sequestration in sediments with reducing or euxinic conditions.

Investigation into the dissolution and direct assay of high-fired plutonium dioxide

International Nuclear Information System (INIS)

Patterson, J.K.

1976-01-01

A fusion-melt and dissolution assay method has been developed and tested for the quantitative analysis of high-fired plutonium dioxide. The method employs fusion of the plutonium dioxide at temperatures greater than the melting point of an eutectic mixture of potassium pyrosulfate plus sodium peroxide. The resultant melt is then titrated directly by either controlled potential coulometry or a gravimetric titration, using standardized ceric sulfate as the titrant. It has been concluded from these investigations that by using the techniques described, high-fired plutonium dioxide (stochiometric) can be quantitatively dissolved and assayed to a degree heretofore beyond the state-of-the-art, while showing direct traceability to the Federal standards. After fusion, the dissolution and direct assay is applicable to existing routine analytical procedures. The method was designed so as to minimize physical handling, simplify the chemical operations, and maximize the personal safety of the analyst at an appreciable cost savings per analysis

Arsenic mobilization in the Brahmaputra plains of Assam: groundwater and sedimentary controls.

Science.gov (United States)

Sailo, Lalsangzela; Mahanta, Chandan

2014-10-01

Arsenic (As) mobilization to the groundwater of Brahmaputra floodplains was investigated in Titabor, Jorhat District, located in the North Eastern part of India. The groundwater and the aquifer geochemistry were characterized in the study area. The range of As concentration in the groundwater varies from 10 to 440 μg/l with mean concentration 210 μg/l. The groundwaters are characterized by high dissolved Fe, Mn, and HCO₃(-) and low concentrations of NO₃(-) and SO₄(2-) indicating the reduced conditions prevailing in the groundwater. In order to understand the actual mobilization processes in the area, six core drilling surrounding the two target tube wells (T1 and T2) with high As concentration (three drill-cores surrounds each tube well closely) was done. The sediment was analyzed its chemical, mineralogical, and elemental compositions. A selective sequential extraction suggested that most of the As in the sediment is bound to Fe oxides fractions (32 to 50%) and the competition for adsorption site by anions (PO₄(3-)) also accounts to significant fractions of the total arsenic extracted. High variability in the extraction as well as properties of the sediment was observed due to the heterogeneity of the sediment samples with different chemical properties. The SEM and EDX results indicate the presence of Fe, Mn coating along with As for most of the sample, and the presence of As associated minerals were calculated using PHREEQC. The mobilization of As into the groundwater was anticipated to be largely controlled by the reductive dissolution of Fe oxides and partly by the competitive anions viz. PO₄(3-).

Evaluation of alkaline dissolution of Al 6061 and Al 1050 for the production of Mo-99 from LEU targets

International Nuclear Information System (INIS)

Mindrisz, Ana C.; Camilo, Ruth L.; Araujo, Izilda C.; Forbicini, Christina A.L.G. de O.

2013-01-01

Since 2008, due to the global crisis in the production of radioisotope 99 Mo, which product of decay, 99m Tc, is the tracer element most often used in nuclear medicine and accounts for about 80% of all diagnostic procedures in vivo. Studies on the alkaline dissolution to obtain 9 9M o from irradiated UAl x -Al LEU targets are under development. Processing time should be minimized, considering the short half-life of 99 Mo and 99m Tc, about 66 h and 6 h, respectively. This makes dissolution time a significant factor in the development of the process. This paper presents the results of alkaline dissolution of 'scraps' of Al 6061 and 1050, used to simulate the dissolution process of UAl x -Al targets. Dissolution time and gas releasing were evaluated using the following alkaline solutions: a) NaOH 3 mol.L -1 and NaNO 3 2 mol.L -1 , b) NaOH 3 mol.L -1 and NaNO 3 4 mol.L -1 . The initial temperature of dissolution was 85 deg C in all cases. Al 6061 showed values of dissolution time greater than that for Al 1050, 25% for NaNO 3 2 mol.L -1 and 104.55% for NaNO 3 4 mol.L -1 . The dissolution with NaNO 3 2 mol.L -1 showed that the gas releasing for Al 6061 was 2.7% greater than for Al 1050. However Al 1050 showed that gas releasing 9.92% greater than for Al 6061 during the dissolution with NaNO 3 4 mol.L -1 . The decision about what type of alloy has to be used, Al 1050 or Al 6061, it will be upto the group that will manufacture the targets for the RMB. (author)

Extent and severity of groundwater contamination based on hydrochemistry mechanism of sandy tropical coastal aquifer.

Science.gov (United States)

Isa, Noorain Mohd; Aris, Ahmad Zaharin; Sulaiman, Wan Nor Azmin Wan

2012-11-01

Small islands are susceptible to anthropogenic and natural activities, especially in respect of their freshwater supply. The freshwater supply in small islands may be threatened by the encroachment of seawater into freshwater aquifers, usually caused by over pumping. This study focused on the hydrochemistry of the Kapas Island aquifer, which controls the groundwater composition. Groundwater samples were taken from six constructed boreholes for the analysis and measurement of its in-situ and major ions. The experimental results show a positive and significant correlation between Na-Cl (r=0.907; paquifer bedrock. About 76% of collected data (n=108) were found to be in the dissolution process of carbonate minerals. Moreover, the correlation between total CEC and Ca shows a positive and strong relationship (r=0.995; pchemical composition. The output of this research explains the chemical mechanism attributed to the groundwater condition of the Kapas Island aquifer. Copyright © 2012 Elsevier B.V. All rights reserved.

Dissolution of metallic uranium and its alloys. Part 1. Review of analytical and process-scale metallic uranium dissolution

International Nuclear Information System (INIS)

Laue, C.A.; Gates-Anderson, D.; Fitch, T.E.

2004-01-01

This review focuses on dissolution/reaction systems capable of treating uranium metal waste to remove its pyrophoric properties. The primary emphasis is the review of literature describing analytical and production-scale dissolution methods applied to either uranium metal or uranium alloys. A brief summary of uranium's corrosion behavior is included since the corrosion resistance of metals and alloys affects their dissolution behavior. Based on this review, dissolution systems were recommended for subsequent screening studies designed to identify the best system to treat depleted uranium metal wastes at Lawrence Livermore National Laboratory (LLNL). (author)

Dissolution of uranium oxide TBP-HNO3 complex

International Nuclear Information System (INIS)

Mizuno, Mineo; Kosaka, Yuji; Mori, Yukihide; Shimada, Takashi

2002-12-01

As a head end process for the pulverization of the spent fuel, the mechanical method (the shredder method) and the pyro-chemical method (oxidisation heat-treatment) have been examined. UO 2 is a main ingredient of Uranium oxide powder by the mechanical method, and U 3 O 8 is that by the pyro-chemical method. Moreover, the particle size of the pulverized powder depend on the conditions of the pulverizing process. As it was considered that the difference of dissolution rates of samples was caused by the difference of sample chemical forms and dissolution temperature, parametric surveys on chemical form and particle size of powder and dissolution temperature were carried out, and the following results were obtained. 1) The remarkable difference of dissolution rate between U 3 O 8 powder (average particle size 3.7 μm) and UO 2 powder (average particle size 2.4 μm) which have comparatively similar particle size was not observed. 2) It was confirmed that the dissolution rate became lower according to the particle size increase (average particle size 2.4 μm-1 mm). And it was considered that dissolution rate had strong dependency on particle size, according to the results that the powder with 1 mm particle size did not dissolute completely after 5 hours test. 3) The temperature dependency of the dissolution rate was confirmed by dissolution test with UO 2 powder (average particle size 2.4 μm-1 mm). The higher dissolution rate was obtained in the higher dissolution temperature, and 11 kcal/mol was obtained as activation energy of dissolution. 4) In the dissolution test of UO 2 powder, the nitric acid concentration started to change earlier than that of U 3 O 8 powder and concentration change range became larger compared with that in the dissolution test of U 3 O 8 powder. It was considered that those differences were caused by difference in mole ratio of Uranium and nitric acid which are consumed in the dissolution reaction (3:7 for U 3 O 8 , 3:8 for UO 2 ). 5) In case

Dissolution rates of aluminum-based spent fuels relevant to geological disposal

International Nuclear Information System (INIS)

Mickalonis, J.I.

2000-01-01

The Department of Energy is pursuing the option of direct disposal of a wide variety of spent nuclear fuels under its jurisdiction. Characterization of the various types of spent fuel is required prior to licensing by the Nuclear Regulatory Commission and acceptance of the fuel at a repository site. One category of required data is the expected rate of radionuclide and fissile release to the environment as a result of exposure to groundwater after closure of the repository. To provide this type of data for four different aluminum-based spent fuels, tests were conducted using a flow through method that allows the dissolution rate of the spent fuel matrix to be measured without interference by secondary precipitation reactions that would muddle interpretation of the results. Similar tests had been conducted earlier with light water reactor spent fuel, thereby allowing direct comparisons

Dissolution rate enhancement of piroxicam by ordered mixing.

Science.gov (United States)

Saharan, Vikas Anand; Choudhury, Pratim Kumar

2012-07-01

Micronized piroxicam was mixed with lactose, mannitol, sorbitol, maltitol and sodium chloride to produce ordered mixture in a glass vial by manual hand shaking method. The effect of excipients, surfactant, superdisintegrant, drug concentration and carrier particle size on dissolution rate was investigated. Dissolution rate studies of the prepared ordered mixtures revealed that all water soluble excipients increased the dissolution rate of piroxicam when compared to the dissolution rate of piroxicam or its suspension. Ordered mixture formulation PLF4, consisting of lactose as water soluble excipient, SSG (8% w/s) and SLS (1% w/w), released piroxcam at a very fast rate so much so that about 90% of the composition had passed into solution within 2 min. The order of the dissolution rate enhancement for ordered mixtures of various water soluble excipients was: lactose > mannitol > maltitol > sorbitol > sodium chloride. Carrier granules of size 355-710 µm were most effective in increasing the dissolution rate of drug from ordered mixtures. Decreasing the carrier particle size reduced drug dissolution from ordered mixtures. The dissolution rate of ordered mixtures consisting of 1-5% w/w piroxicam was superior to dissolution rate of piroxicam suspension. The dissolution data fitting and the resulting regression parameters indicated Hixson Crowell, cube root law, as the best fit to drug release data of ordered mixtures.

Investigation of Groundwater transport using environmental isotopes along the north-eastern part of sinai peninsula

International Nuclear Information System (INIS)

Hamza, M.S.; Awad, M.A.; Nada, A.A.; Abd El-Samie, S.G.; Zaghloul, A.

1998-01-01

Fourteen groundwater samples were collected from the north-eastern part of sinai peninsula representing different eater bearing formations from younger to older: The sand and gravel interbeds (quaternary), the fissured and fracture limestone of eocene and upper cretaceous and the fractured sandstone (Lower cretaceous). The chemical and isotopic analysis reflected the changes in the meteoric origin of the groundwater in these aquifers with respect to the recharge sources and the rock types. The groundwater in the quaternary aquifer have the metric water type which are affected by evaporation and sea spray deposits. The majority of the wells tapping in the eocene aquifer have the fresh water character while the other have the marine water originated from two sources; the first is the dissolution of the host rock (mainly limestone) which increase the groundwater salinity without changes in the isotopic content. The second source is mixing with connote water seeped to the aquifer through cracks and causing isotopic enrichment in these samples. Otherwise, the depleted values of the stable isotopes in the groundwater of lower and Upper cretaceous represent mixing with palaeo water in these aquifers. High values of tritium content were detected in wells in the eastern part. Further survey is needed to follow up the tritium content

Subsurface Transport Behavior of Micro-Nano Bubbles and Potential Applications for Groundwater Remediation

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Hengzhen Li

2013-12-01

Full Text Available Micro-nano bubbles (MNBs are tiny bubbles with diameters on the order of micrometers and nanometers, showing great potential in environmental remediation. However, the application is only in the beginning stages and remains to be intensively studied. In order to explore the possible use of MNBs in groundwater contaminant removal, this study focuses on the transport of MNBs in porous media and dissolution processes. The bubble diameter distribution was obtained under different conditions by a laser particle analyzer. The permeability of MNB water through sand was compared with that of air-free water. Moreover, the mass transfer features of dissolved oxygen in water with MNBs were studied. The results show that the bubble diameter distribution is influenced by the surfactant concentration in the water. The existence of MNBs in pore water has no impact on the hydraulic conductivity of sand. Furthermore, the dissolved oxygen (DO in water is greatly increased by the MNBs, which will predictably improve the aerobic bioremediation of groundwater. The results are meaningful and instructive in the further study of MNB research and applications in groundwater bioremediation.

Improvement of database on glass dissolution

International Nuclear Information System (INIS)

Hayashi, Maki; Sasamoto, Hiroshi; Yoshikawa, Hideki

2008-03-01

In geological disposal system, high-level radioactive waste (HLW) glass is expected to retain radionuclide for the long term as the first barrier to prevent radionuclide release. The advancement of its performance assessment technology leads to the reliability improvement of the safety assessment of entire geological disposal system. For this purpose, phenomenological studies for improvement of scientific understanding of dissolution/alteration mechanisms, and development of robust dissolution/alteration model based on the study outcomes are indispensable. The database on glass dissolution has been developed for supporting these studies. This report describes improvement of the prototype glass database. Also, this report gives an example of the application of the database for reliability assessment of glass dissolution model. (author)

Development of a kinetic model for the dissolution of the UO2 spent nuclear fuel. Application of the model to the minor radionuclides

International Nuclear Information System (INIS)

Bruno, J.; Cera, E.; Duro, L.; Pon, J.; Pablo, J. de; Eriksen, Trygve

1998-05-01

A kinetic model has been developed in order to explain the evolution of the spent fuel matrix/groundwater system. Mass balance equations have been used to follow the evolution of the system with time. The model has been calibrated by using experimental dissolution data from spent fuel leaching tests from Studsvik and KTH and from synthetic unirradiated UO 2 dissolution tests from VTT. The results of the testing exercise indicate that the combination of mass balance equations together with the kinetic rate laws constitute a useful tool to model and explain experimental dissolution data available in the literature for UO 2 solid phases, including uraninites, unirradiated UO 2 and spent fuel. Although the key processes are well identified and understood, there are still some remaining uncertainties concerning some of the critical parameters of the model. This is particularly true for the density of UO 2 sites prone to oxidation and the rates and mechanisms of the hydrogen peroxide and the combined oxygen and bicarbonate promoted dissolution of UO 2 for oxidant concentration ranges relevant to the spent fuel disposal system. The mass balance kinetic model developed has been extended to minor radionuclides contained in the matrix, i.e. Pu, Tc and Sr. In the case of Pu, the model presented reproduces the behaviour of this critical radionuclide even at early contact times. As it would be expected, Tc seems to follow a different mechanism for its release with respect to the UO 2 matrix dissolution, which is probably linked to the rate of oxidation of Tc metallic inclusions in the fuel. A co- dissolution process of Sr with the UO 2 matrix reproduces the long term dissolution behaviour of this radionuclide, better than the initial Sr release rates

Formation, transformation and dissolution of phases formed on surfaces

International Nuclear Information System (INIS)

Shoesmith, D.W.

1983-03-01

The basic mechanisms of film growth, transformation, and dissolution of phases formed on surfaces are discussed. Film growth can occur via solid-state processes or via substrate (usally metal or alloy) dissolution, followed by local supersaturation and precipitation of an insoluble phase. The phase(s) formed may be metastable and transform to a more stable phase, via either solid-state or dissolution-reprecipitation processes. Film dissolution reactions can also occur via a variety of mechanisms, including: (i) direct chemical dissolution when no oxidation state change occurs; (ii) redox dissolution when the film dissolves via a redox reaction involving a reducing or oxidizing agent in solution; and (iii) autoreduction, where film dissolution is coupled to metal dissolution. Such film-growth and dissolution processes, which often produce complex multilayer films, are common in the nuclear industry. A number of examples are discussed

Groundwater management under uncertainty using a stochastic multi-cell model

Science.gov (United States)

Joodavi, Ata; Zare, Mohammad; Ziaei, Ali Naghi; Ferré, Ty P. A.

2017-08-01

The optimization of spatially complex groundwater management models over long time horizons requires the use of computationally efficient groundwater flow models. This paper presents a new stochastic multi-cell lumped-parameter aquifer model that explicitly considers uncertainty in groundwater recharge. To achieve this, the multi-cell model is combined with the constrained-state formulation method. In this method, the lower and upper bounds of groundwater heads are incorporated into the mass balance equation using indicator functions. This provides expressions for the means, variances and covariances of the groundwater heads, which can be included in the constraint set in an optimization model. This method was used to formulate two separate stochastic models: (i) groundwater flow in a two-cell aquifer model with normal and non-normal distributions of groundwater recharge; and (ii) groundwater management in a multiple cell aquifer in which the differences between groundwater abstractions and water demands are minimized. The comparison between the results obtained from the proposed modeling technique with those from Monte Carlo simulation demonstrates the capability of the proposed models to approximate the means, variances and covariances. Significantly, considering covariances between the heads of adjacent cells allows a more accurate estimate of the variances of the groundwater heads. Moreover, this modeling technique requires no discretization of state variables, thus offering an efficient alternative to computationally demanding methods.

The effect of sodium chloride on the dissolution of calcium silicate hydrate gels

International Nuclear Information System (INIS)

Hill, J.; Harris, A.W.; Manning, M.; Chambers, A.; Swanton, S.W.

2006-01-01

The use of cement based materials will be widespread in the long-term management of radioactive materials in the United Kingdom. One of the applications could be the Nirex reference vault backfill (NRVB) as an engineered barrier within a deep geological repository. NRVB confers alkaline conditions, which would provide a robust chemical barrier through the control of the solubility of some key radionuclides, enhanced sorption and minimised corrosion of steel containers. An understanding of the dissolution of C-S-H gels in cement under the appropriate conditions (e.g., saline groundwaters) is necessary to demonstrate the expected evolution of the chemistry over time and to provide sufficient cement to buffer the porewater conditions for the required time. A programme of experimental work has been undertaken to investigate C-S-H gel dissolution behaviour in sodium chloride solutions and the effect of calcium/silicon ratio (C/S), temperature and cation type on this behaviour. Reductions in calcium concentration and pH values were observed with samples equilibrated at 45 deg. C compared to those prepared at 25 deg. C. The effect of salt cation type on salt-concentration dependence of the dissolution of C-S-H gels was investigated by the addition of lithium or potassium chloride in place of sodium chloride for gels with a C/S of 1.0 and 1.8. With a C/S of 1.0, similar increases in dissolved calcium concentration with increasing ionic strength were recorded for the different salts. However, at a C/S of 1.8, anomalously high calcium concentrations were observed in the presence of lithium

Kinetics of oxidic phase dissolution in acids

International Nuclear Information System (INIS)

Gorichev, I.G.; Kipriyanov, N.A.

1981-01-01

The critical analysis of the experimental data on dissolution kinetics of metal oxides (BeO, V 2 O 5 , UO 2 , Nb 2 O 5 , Ta 2 O 5 etc.) in acid media is carried out. Kinetic peculiarities of oxide dissolution are explained on the basis of the notions of electron- proton theory. It is established that the surface nonstoichiometric ccomposition of oxide phase and potential jump, appearing on the interface of the oxide-electrolyte phase are the important factors, determining the dissolution rate of a solid phase. The dissolution rate of metal oxides is limited by the transition of protons into the solid oxide phase. Morphological models of heterogeneous kinetics are used when explaining kinetic regularities of oxide dissolution process [ru

Groundwater resources of Mosteiros basin, island of Fogo, Cape Verde, West Africa

Science.gov (United States)

Heilweil, Victor M.; Gingerich, Stephen B.; Plummer, Niel; Verstraeten, Ingrid M.

2010-01-01

Groundwater resources in Cape Verde provide water for agriculture, industry, and human consumption. These resources are limited and susceptible to contamination. Additional groundwater resources are needed for continued agricultural development, particularly during times of drought, but increased use and (or) climatic change may have adverse effects on the quantity and quality of freshwater available. In volcanic island aquifers such as those of Cape Verde, a lens of fresh groundwater typically ?floats? upon a layer of brackish water at the freshwater/saltwater boundary, and increased pumping may cause salt water intrusion or other contamination. A recent U.S. Geological Survey study assessed baseline groundwater conditions in watersheds on three islands of Cape Verde to provide the scientific basis for sustainably developing water resources and minimizing future groundwater depletion and contamination.

Using SDP to optimize conjunctive use of surface and groundwater in China

DEFF Research Database (Denmark)

Davidsen, Claus; Mo, X; Liu, S.

2014-01-01

A hydro-economic modelling approach to optimize conjunctive use of scarce surface water and groundwater resources under uncertainty is presented. Stochastic dynamic programming (SDP) is used to minimize the basin-wide total costs arising from allocations of surface water, head-dependent groundwater......, which includes surface water droughts and groundwater over-pumping. The head-dependent groundwater pumping costs will enable assessment of the long-term effects of increased electricity prices on the groundwater pumping. The optimization framework is used to assess realistic alternative development...... pumping costs, water allocations from the South-North Water Transfer Project and water curtailments of the users. Each water user group (agriculture, industry, domestic) is characterized by fixed demands and fixed water allocation and water supply curtailment costs. The non-linear one step-ahead sub...

Dissolution rate of BTEX contaminants in water

International Nuclear Information System (INIS)

Njobuenwu, D.O.; Amadi, S.A.; Ukpaka, P.C.

2005-01-01

Benzene, toluene, ethylbenzene and xylenes (BTEX) and substituted benzenes are the most common aromatic compounds in petroleum. BTEX components are the most soluble and mobile fraction of crude oil and many petroleum products, and frequently enter soil, sediments and aquatic environments because of accidental spills, leaks and improper oil waste disposal practices. The mass transfer process of hydrocarbons in aquatic mediums has received considerable attention in the literature. This paper focused on the molecular mass transfer rate of BTEX in water, with the aim of understanding and predicting contaminant fate and transport. A comprehensive model was developed to simulate the molecular dissolution rate of BTEX in a natural water stream. The model considered the physicochemical properties of the BTEX compounds and physical processes relevant to the spreading of contaminants in the sea. The dissolution rate was a function of oil slick area, dissolution mass transferability and oil solubility in water. The total dissolution rate N was calculated and the dissolution mass transfer coefficient K was given as the point value of mass transfer coefficient. Results for the dissolution rate based on the solubility of the components in the water were compared with analytical solutions from previous studies and showed good agreement. The model showed that benzene had the largest dissolution rate, while o-xylene had the lowest rate because of its lower fraction. Benzene dissolution rate was approximately 2.6, which was 20.6 times that of toluene and ethylbenzene. It was concluded that the model is useful in predicting and monitoring the dissolution rate of BTEX contaminants in soil and water systems. 22 refs., 2 tabs., 3 figs

Removal of the arsenic from contaminated groundwater with use of the new generation of MicroDrop Aqua system

DEFF Research Database (Denmark)

Kowalski, Krzysztof; Søgaard, Erik Gydesen

2012-01-01

The results from a new pilot scale plant of the MicroDrop Aqua arsenic removal technology are introduced. The technology is based on the employing of electrochemical iron dissolution and efficient aeration prior to sand filtration. The pilot treatment was used to study effectiveness of iron relea...... addition and easily to remove arsenic from contaminated groundwater.......The results from a new pilot scale plant of the MicroDrop Aqua arsenic removal technology are introduced. The technology is based on the employing of electrochemical iron dissolution and efficient aeration prior to sand filtration. The pilot treatment was used to study effectiveness of iron release...... in an electro-dissolution process that is taking place in an iron generator. It was found that there is a need of some extra time to reach a state of steady iron release and that could not be achieved within a short period of 10-20 minutes. The pilot plant proved to be able to remove arsenic to value below 5μg...

Geochemical modelling of groundwater evolution and residence time at the Kivetty site

Energy Technology Data Exchange (ETDEWEB)

Pitkaenen, P.; Luukkonen, A. [VTT Communities and Infrastructure, Espoo (Finland); Ruotsalainen, P. [Fintact Oy, Helsinki (Finland); Leino-Forsman, H.; Vuorinen, U. [VTT Chemical Technology, Espoo (Finland)

1998-12-01

groundwater are due to carbonate reactions: oxidising of organic carbon, and dissolution and precipitation of calcite. The carbonate reactions and slight hydrolysis of silicates stabilise the pH value at 8-9. In addition to aerobic oxidation of organic matter, oxidative dissolution of biotite seems to be an important oxygen consumer at shallow depth during recharge. The most important process controlling the redox state deeper in the bedrock was interpreted to be the microbially mediated sulphate reduction with simultaneous anaerobic respiration of organic carbon. This process buffers the redox level of about -200 - -300 mV depending on the pH. Even though the salinities of the groundwater samples and mass-transfer along flow paths remain low, the geochemical evolution was fully developed and has reached quite a stable thermodynamic state. The residence times of the groundwater samples cover the time span back to glaciation. Young ages seem to be limited to the upper part of bedrock, and any really dynamic natural flowpath with deep observed recently recharged water cannot be demonstrated. Deglacial or subglacial ages (over 9,700 years old at Kivetty) are typical below the 150-300m level in the bedrock. Subglacial waters are interpreted to derive from mixing of preglacial water and meltwater, the input of which is estimated to be about 20% at the most. Indications of elevated oxygen intrusion cannot be observed in groundwater having glacial signals. (orig.) 122 refs.

Geochemical modelling of groundwater evolution and residence time at the Kivetty site

International Nuclear Information System (INIS)

Pitkaenen, P.; Luukkonen, A.; Ruotsalainen, P.; Leino-Forsman, H.; Vuorinen, U.

1998-12-01

groundwater are due to carbonate reactions: oxidising of organic carbon, and dissolution and precipitation of calcite. The carbonate reactions and slight hydrolysis of silicates stabilise the pH value at 8-9. In addition to aerobic oxidation of organic matter, oxidative dissolution of biotite seems to be an important oxygen consumer at shallow depth during recharge. The most important process controlling the redox state deeper in the bedrock was interpreted to be the microbially mediated sulphate reduction with simultaneous anaerobic respiration of organic carbon. This process buffers the redox level of about -200 - -300 mV depending on the pH. Even though the salinities of the groundwater samples and mass-transfer along flow paths remain low, the geochemical evolution was fully developed and has reached quite a stable thermodynamic state. The residence times of the groundwater samples cover the time span back to glaciation. Young ages seem to be limited to the upper part of bedrock, and any really dynamic natural flowpath with deep observed recently recharged water cannot be demonstrated. Deglacial or subglacial ages (over 9,700 years old at Kivetty) are typical below the 150-300m level in the bedrock. Subglacial waters are interpreted to derive from mixing of preglacial water and meltwater, the input of which is estimated to be about 20% at the most. Indications of elevated oxygen intrusion cannot be observed in groundwater having glacial signals. (orig.)

Dissolution studies of natural analogues spent fuel and U(VI)-Silicon phases of and oxidative alteration process

International Nuclear Information System (INIS)

Perez Morales, I.

2000-01-01

In order to understand the long-term behavior of the nuclear spent fuel in geological repository conditions, we have performed dissolution studies with natural analogues to UO 2 as well as with solid phases representatives of the oxidative alteration pathway of uranium dioxide, as observed in both natural environment and laboratory studies. In all cases, we have studied the influence of the bicarbonate concentration in the dissolution process, as a first approximation to the groundwater composition of a granitic environment, where carbonate is one of the most important complexing agents. As a natural analogue to the nuclear spent fuel some uraninite samples from the Oklo are deposit in Gabon, where chain fission reactions took place 2000 millions years ago, as well as a pitchblende sample from the mine Fe ore deposit, in Salamanca (spain) have been studied. The studies have been performed at 25 and 60 deg C and 60 deg C, and they have focussed on the determination of both the thermodynamic and the kinetic properties of the different samples studied, using batch and continuous experimental methodologies, respectively. (Author)

Groundwater quality assessment for domestic and agriculture purposes in Puducherry region

Science.gov (United States)

Sridharan, M.; Senthil Nathan, D.

2017-11-01

Totally about 174 groundwater samples have been collected during pre-monsoon and post-monsoon season to study the suitability for domestic and agriculture purposes along the coastal aquifers of Puducherry region. Parameters such as pH, total dissolved solids (TDS), electrical conductivity (EC), sodium (Na), potassium (K), calcium (Ca), magnesium (Mg), bicarbonate (HCO3), chloride (Cl) and sulfate (SO4) were analyzed to assess the suitability of groundwater for domestic purposes. Sodium adsorption ratio (SAR), magnesium adsorption ratio (MAR), residual sodium bicarbonate (RSC), soluble sodium percentage (Na%), permeability index (PI) and chlorinity index were assessed for irrigation purposes. The higher concentration of ions such as Na, Ca, Cl and So4 indicates seawater intrusion, mineral dissolution, intense agricultural practices and improper sewage disposal. The level of EC, TDS and hardness in the water samples indicates that maximum of them are suitable for drinking and domestic purposes. The parameters such as SAR, Na%, PI, MAR and Chlorinity index indicates that majority of water sample are very good to moderately suitable for agriculture. In pre-monsoon, RSC of about 5.7% of samples was higher which when used for a longer time alter the soil properties and reduce crop production. Wilcox diagram suggests that water samples are of medium saline to low sodium type indicating that groundwater is suitable for irrigation. Temporal variation of groundwater quality shows significant increasing trend in EC, TDS and ions like Mg, K and Cl in the last decade, mainly due to anthropogenic activities with little geogenic impact in the quality of groundwater.

Formalization of the kinetics for autocatalytic dissolutions. Focus on the dissolution of uranium dioxide in nitric medium

International Nuclear Information System (INIS)

Charlier, F.; Canion, D.; Gravinese, A.; Magnaldo, A.; Lalleman, S.; Borda, G.; Schaer, E.

2017-01-01

Uranium dioxide dissolution in nitric acid is a complex reaction. On the one hand, the dissolution produces nitrous oxides (NOX), which makes it a triphasic reaction. On the other hand, one of the products accelerates the kinetic rate; the reaction is hence called autocatalytic.The kinetics for these kinds of reactions need to be formalized in order to optimize and design innovative dissolution reactors. In this work, the kinetics rates have been measured by optical microscopy using a single particle approach. The advantages of this analytical technique are an easier management of species transport in solution and a precise following of the dissolution rate. The global rate is well described by a mechanism considering two steps: a non-catalyzed reaction, where the catalyst concentration has no influence on the dissolution rate, and a catalyzed reaction. The mass transfer rate of the catalyst was quantified in order to discriminate when the reaction was influenced by catalyst accumulated in the boundary layer or uncatalyzed. This first approximation described well the sigmoid dissolution curve profile. Moreover, experiments showed that solutions filled with catalyst proved to lose reactivity over time. Results pointed out that the higher the liquid-gas exchanges, the faster the kinetic rate decreases with time. Thus, it was demonstrated, for the first time, that there is a link between catalyst and nitrous oxides. The outcome of this study leads to new ways for improving the design of dissolvers. Gas-liquid exchanges are indeed a lever to impact dissolution rates. Temperature and catalyst concentration can be optimized to reduce residence times in dissolvers. (authors)

Arsenic contamination of groundwater and drinking water in Vietnam: a human health threat.

Science.gov (United States)

Berg, M; Tran, H C; Nguyen, T C; Pham, H V; Schertenleib, R; Giger, W

2001-07-01

This is the first publication on arsenic contamination of the Red River alluvial tract in the city of Hanoi and in the surrounding rural districts. Due to naturally occurring organic matter in the sediments, the groundwaters are anoxic and rich in iron. With an average arsenic concentration of 159 micrograms/L, the contamination levels varied from 1 to 3050 micrograms/L in rural groundwater samples from private small-scale tubewells. In a highly affected rural area, the groundwater used directly as drinking water had an average concentration of 430 micrograms/L. Analysis of raw groundwater pumped from the lower aquifer for the Hanoi water supply yielded arsenic levels of 240-320 micrograms/L in three of eight treatment plants and 37-82 micrograms/L in another five plants. Aeration and sand filtration that are applied in the treatment plants for iron removal lowered the arsenic concentrations to levels of 25-91 micrograms/L, but 50% remained above the Vietnamese Standard of 50 micrograms/L. Extracts of sediment samples from five bore cores showed a correlation of arsenic and iron contents (r2 = 0.700, n = 64). The arsenic in the sediments may be associated with iron oxyhydroxides and released to the groundwater by reductive dissolution of iron. Oxidation of sulfide phases could also release arsenic to the groundwater, but sulfur concentrations in sediments were below 1 mg/g. The high arsenic concentrations found in the tubewells (48% above 50 micrograms/L and 20% above 150 micrograms/L) indicate that several million people consuming untreated groundwater might be at a considerable risk of chronic arsenic poisoning.

STATISTICAL INVESTIGATION OF THE GROUNDWATER SYSTEM IN DARB EL-ARBAEIN, SOUTHWESTERN DESERT, EGYPT

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Kashouty Mohamed El

2009-12-01

Full Text Available In Darb El Arbaein, the groundwater is the only water resources. The aquifer system starts from Paleozoic-Mesozoic to Upper Cretaceous sandstone rocks. They overlay the basement rocks and the aquifer is confined. In the present research, the performance of the statistical analyses to classify groundwater samples depending on their chemical characters has been tested. The hydrogeological and hydrogeochemical data of 92 groundwater samples was obtained from the GARPAD authority in northern, central, and southern Darb El Arbaein. A robust classification scheme for partitioning groundwater chemistry into homogeneous groups was an important tool for the characterization of Nubian sandstone aquifer. We test the performance of the many available graphical and statistical methodologies used to classify water samples. R-mode, Q-mode, correlation analysis, and principal component analysis were investigated. All the methods were discussed and compared as to their ability to cluster, ease of use, and ease of interpretation. The correlation investigation clarifies the relationship among the lithology, hydrogeology, and anthropogenic. Factor investigation revealed three factors namely; the evaporation process-agriculturalimpact-lithogenic dissolution, the hydrogeological characteristics of the aquifer system, and the surface meteoric water that rechargethe aquifer system. Two main clusters that subdivided into four sub clusters were identified in groundwater system based on hydrogeological and hydrogeochemical data. They reflect the impact of geomedia, hydrogeology, geographic position, and agricultural wastewater. The groundwater is undersaturated with respect to most selected minerals. The groundwater was supersaturated with respect to iron minerals in northern and southern Darb El Arbaein. The partial pressure of CO2 of the groundwater versus saturation index of calcite shows the gradual change in PCO2 from atmospheric to the present aquifer

Arsenic and Fluoride Mobilization Mechanism in Groundwater of Indus Delta and Thar Desert, Sindh, Pakistan

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VIQAR HUSAIN

2012-06-01

Full Text Available Indus deltaic plain consists of medium to fine grained sediments, rich in organic matter deposited during the Holocene period. Thar desert is covered with sand dunes and loess originated from transported sediments from Rann of Kutch or the Indus plain by monsoon winds or by the reworking of local alluvial deposits. Groundwater salinity and microbial pollution are common in both types of lanforms, but arsenic (AS and fluoride (F toxicity dominate in the groundwater of Indus delta and Thar desert, respectively. Arsenic concentration in Tando Mohammad Khan and Tando Allayar varies from 10-500 ppb and exhibits near neutral slightly alkaline pH ranging from 6.8 to 8.0. Arsenic distribution is patchy and seems to be related to the prsence of small scale redox zonation in the aquifer. High arsenic affected areas are densely populated and intensively cultivated and its hot spots are those from where the Indus river passed during the Holocene period including Tando Allayar and Tando Mohammad Khan. Extensive ground water irrigation has accelerated flow of groundwater that brought dissolved degraded organic matter in contact with arsenic bearing sediments, enhancing reduction processes and triggering release of arsenic from detrital bioitite and muscovite in the groundwater. Furthermore, unlined sanitation and microbial contamination contribute to degradation of organic matter that enhances the reduction of iron oxy-hydroxide leading to release of arsenic to groundwater. Fluoride is found in all the groundwater samples of Tharparkar district, in the range of 0.96-2.74mg/l. The pH of groundwater is alkaline (7.38-8.59, which is accelerating maximum (1.24%F dissolution in the groundwater. The favourable pH of groundwater and soil composition of Holocene sediments of Indus delta and slightly older alluvium of Thar desert, respectively are responsible for mobilization of arsenic and fluoride in groundwater of Sindh province of Pakistan.

Seasonal and Spatial Variability of Anthropogenic and Natural Factors Influencing Groundwater Quality Based on Source Apportionment

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Xueru Guo

2018-02-01

Full Text Available Globally, groundwater resources are being deteriorated by rapid social development. Thus, there is an urgent need to assess the combined impacts of natural and enhanced anthropogenic sources on groundwater chemistry. The aim of this study was to identify seasonal characteristics and spatial variations in anthropogenic and natural effects, to improve the understanding of major hydrogeochemical processes based on source apportionment. 34 groundwater points located in a riverside groundwater resource area in northeast China were sampled during the wet and dry seasons in 2015. Using principal component analysis and factor analysis, 4 principal components (PCs were extracted from 16 groundwater parameters. Three of the PCs were water-rock interaction (PC1, geogenic Fe and Mn (PC2, and agricultural pollution (PC3. A remarkable difference (PC4 was organic pollution originating from negative anthropogenic effects during the wet season, and geogenic F enrichment during the dry season. Groundwater exploitation resulted in dramatic depression cone with higher hydraulic gradient around the water source area. It not only intensified dissolution of calcite, dolomite, gypsum, Fe, Mn and fluorine minerals, but also induced more surface water recharge for the water source area. The spatial distribution of the PCs also suggested the center of the study area was extremely vulnerable to contamination by Fe, Mn, COD, and F−.

Chemistry of groundwater discharge inferred from longitudinal river sampling

Science.gov (United States)

Batlle-Aguilar, J.; Harrington, G. A.; Leblanc, M.; Welch, C.; Cook, P. G.

2014-02-01

We present an approach for identifying groundwater discharge chemistry and quantifying spatially distributed groundwater discharge into rivers based on longitudinal synoptic sampling and flow gauging of a river. The method is demonstrated using a 450 km reach of a tropical river in Australia. Results obtained from sampling for environmental tracers, major ions, and selected trace element chemistry were used to calibrate a steady state one-dimensional advective transport model of tracer distribution along the river. The model closely reproduced river discharge and environmental tracer and chemistry composition along the study length. It provided a detailed longitudinal profile of groundwater inflow chemistry and discharge rates, revealing that regional fractured mudstones in the central part of the catchment contributed up to 40% of all groundwater discharge. Detailed analysis of model calibration errors and modeled/measured groundwater ion ratios elucidated that groundwater discharging in the top of the catchment is a mixture of local groundwater and bank storage return flow, making the method potentially useful to differentiate between local and regional sourced groundwater discharge. As the error in tracer concentration induced by a flow event applies equally to any conservative tracer, we show that major ion ratios can still be resolved with minimal error when river samples are collected during transient flow conditions. The ability of the method to infer groundwater inflow chemistry from longitudinal river sampling is particularly attractive in remote areas where access to groundwater is limited or not possible, and for identification of actual fluxes of salts and/or specific contaminant sources.

Development of a kinetic model for the dissolution of the UO{sub 2} spent nuclear fuel. Application of the model to the minor radionuclides

Energy Technology Data Exchange (ETDEWEB)

Bruno, J.; Cera, E.; Duro, L.; Pon, J. [QuantiSci SL, Barcelona (Spain); Pablo, J. de [UPC, Barcelona (Spain). Dept. Enginyeria Quimica; Eriksen, Trygve [Royal Inst. of Tech., Stockholm (Sweden). Dept. of Nuclear Chemistry

1998-05-01

A kinetic model has been developed in order to explain the evolution of the spent fuel matrix/groundwater system. Mass balance equations have been used to follow the evolution of the system with time. The model has been calibrated by using experimental dissolution data from spent fuel leaching tests from Studsvik and KTH and from synthetic unirradiated UO{sub 2} dissolution tests from VTT. The results of the testing exercise indicate that the combination of mass balance equations together with the kinetic rate laws constitute a useful tool to model and explain experimental dissolution data available in the literature for UO{sub 2} solid phases, including uraninites, unirradiated UO{sub 2} and spent fuel. Although the key processes are well identified and understood, there are still some remaining uncertainties concerning some of the critical parameters of the model. This is particularly true for the density of UO{sub 2} sites prone to oxidation and the rates and mechanisms of the hydrogen peroxide and the combined oxygen and bicarbonate promoted dissolution of UO{sub 2} for oxidant concentration ranges relevant to the spent fuel disposal system. The mass balance kinetic model developed has been extended to minor radionuclides contained in the matrix, i.e. Pu, Tc and Sr. In the case of Pu, the model presented reproduces the behaviour of this critical radionuclide even at early contact times. As it would be expected, Tc seems to follow a different mechanism for its release with respect to the UO{sub 2} matrix dissolution, which is probably linked to the rate of oxidation of Tc metallic inclusions in the fuel. A co- dissolution process of Sr with the UO{sub 2} matrix reproduces the long term dissolution behaviour of this radionuclide, better than the initial Sr release rates 49 refs, 22 figs, 2 tables

On-line monitoring of lithium carbonate dissolution

Energy Technology Data Exchange (ETDEWEB)

Sun, Yuzhu; Song, Xingfu; Wang, Jin; Luo, Yan; Yu, Jianguo [National Engineering Research Center for Integrated Utilization Salt Lake Resources, East China University of Science and Technology, Shanghai (China)

2009-11-15

Dissolution of lithium carbonate (Li{sub 2}CO{sub 3}) in aqueous solution was investigated using three on-line apparatuses: the concentration of Li{sub 2}CO{sub 3} was measured by electrical conductivity equipment; CLD (Chord Length Distribution) was monitored by FBRM (Focused Beam Reflectance Measurement); crystal image was observed by PVM (Particle Video Microscope). Results show dissolution rate goes up with a decrease of particle size, and with an increase in temperature; stirring speed causes little impact on dissolution; ultrasound facilitates dissolution obviously. The CLD evolution and crystal images of Li{sub 2}CO{sub 3}powders in stirred fluid were observed detailedly by FBRM and PVM during dissolution. Experimental data were fitted to Avrami model, through which the activation energy was found to be 34.35 kJ/mol. PBE (Population Balance Equation) and moment transform were introduced to calculate dissolution kinetics, obtaining correlation equations of particle size decreasing rate as a function of temperature and undersaturation. (copyright 2009 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

Iodine mobilization in groundwater system at Datong basin, China: Evidence from hydrochemistry and fluorescence characteristics

Energy Technology Data Exchange (ETDEWEB)

Li, Junxia; Wang, Yanxin, E-mail: yx.wang@cug.edu.cn; Guo, Wei; Xie, Xianjun; Zhang, Liping; Liu, Yaqing; Kong, Shuqiong

2014-01-01

Characterizing the speciation of iodine in groundwater is essential for understanding its hydrogeochemical behavior in aquifer systems. To quantify the variations in iodine speciation and assess factors controlling the distribution and transformation of iodine, 82 groundwater samples and 1 rain water were collected from the Datong basin, northern China in this study. Factor analysis (FA) and excitation emission matrix with parallel factor analysis (EEM–PARAFAC) were used to clarify the potential relationships among iodine species and other hydrochemical parameters. The iodine concentrations of groundwater range from 6.23 to 1380 μg L{sup −1} with 47% of samples exceeding its drinking water level of 150 μg L{sup −1} as recommended by the Chinese government. 57% of samples have ratios of iodate to total iodine greater than 60%, while iodide as the major species in 22% of the samples. Significant amounts of organic iodine with concentrations higher than 100 μg L{sup −1} were observed in 9 groundwater samples. Redox conditions of groundwater system strongly affect iodine concentration and speciation of inorganic iodine in groundwater, and extremely reducing condition restricts the iodine release from sediments into groundwater. The results of FA show that iodine mobilization in groundwater is related to the nature of dissolved organic matter. EEM-PARAFAC model demonstrates the dominance of terrestrial DOM sources and the presence of microbial activities in groundwater system of the Datong basin. It is proposed that degradation of organic matter and reductive dissolution of iron oxyhydroxides are major hydrogeochemical processes responsible for the mobilization of iodine release and the genesis of organic iodine. - Highlights: • Iodine species in groundwater was studied from Datong basin, northern China. • Weakly alkaline environment favors the accumulation of iodine in groundwater. • Iodate is the major species of iodine in groundwater from Datong

Hydrochemical characterization and pollution sources identification of groundwater in Salawusu aquifer system of Ordos Basin, China.

Science.gov (United States)

Yang, Qingchun; Wang, Luchen; Ma, Hongyun; Yu, Kun; Martín, Jordi Delgado

2016-09-01

Ordos Basin is located in an arid and semi-arid region of northwestern China, which is the most important energy source bases in China. Salawusu Formation (Q3 s) is one of the most important aquifer systems of Ordos Basin, which is adjacent to Jurassic coalfield areas. A large-scale exploitation of Jurassic coal resources over ten years results in series of influences to the coal minerals, such as exposed to the oxidation process and dissolution into the groundwater due to the precipitation infiltration. Therefore, how these processes impact groundwater quality is of great concerns. In this paper, the descriptive statistical method, Piper trilinear diagram, ratios of major ions and canonical correspondence analysis are employed to investigate the hydrochemical evolution, determine the possible sources of pollution processes, and assess the controls on groundwater compositions using the monitored data in 2004 and 2014 (before and after large-scale coal mining). Results showed that long-term exploration of coal resources do not result in serious groundwater pollution. The hydrochemical types changed from HCO3(-)-CO3(2-) facies to SO4(2-)-Cl facies during 10 years. Groundwater hardness, nitrate and sulfate pollution were identified in 2014, which was most likely caused by agricultural activities. Copyright © 2016 Elsevier Ltd. All rights reserved.

Understanding the roles of ligand promoted dissolution, water column saturation and hydrological properties on intense basalt weathering using reactive transport and watershed-scale hydrologic modeling

Science.gov (United States)

Perez Fodich, A.; Walter, M. T.; Derry, L. A.

2016-12-01

The interaction of rocks with rainwater generates physical and chemical changes, which ultimately culminates in soil development. The addition of catalyzers such as plants, atmospheric gases and hydrological properties will result in more intense and/or faster weathering transformations. The intensity of weathering across the Island of Hawaii is strongly correlated with exposure age and time-integrated precipitation. Intense weathering has resulted from interaction between a thermodynamically unstable lithology, high water/rock ratios, atmospheric gases (O2, CO2) and biota as an organic acid and CO2 producer. To further investigate the role of different weathering agents we have developed 1-D reactive transport models (RTM) to understand mineralogical and fluid chemistry changes in the initially basaltic porous media. The initial meso-scale heterogeneity of porosity makes it difficult for RTMs to capture changes in runoff/groundwater partitioning. Therefore, hydraulic properties (hydraulic conductivity and aquifer depth) are modeled as a watershed parameter appropriate for this system where sub-surface hydraulic data is scarce(1). Initial results agree with field data in a broad sense: different rainfall regimes and timescales show depletion of mobile cations, increasingly low pH, congruent dissolution of olivine and pyroxene, incongruent dissolution of plagioclase and basaltic glass, precipitation of non-crystalline allophane and ferrihydrite, and porosity changes due to dissolution and precipitation of minerals; ultimately Al and Fe are also exported from the system. RTM is used to examine the roles of unsaturation in the soil profile, ligand promoted dissolution of Al- and Fe-bearing phases, and Fe-oxide precipitation at the outcrop scale. Also, we aim to test the use of recession flow analysis to model watershed-scale hydrological properties to extrapolate changes in the runoff/groundwater partitioning. The coupling between weathering processes and hydrologic

Hydrological and geochemical constraints on the mechanism of formation of arsenic contaminated groundwater in Sonargaon, Bangladesh

Energy Technology Data Exchange (ETDEWEB)

Itai, Takaaki [Institute for Study of the Earth' s Interior, Okayama University, Misasa, Tottori 682-0193 (Japan)], E-mail: itai-epss@hiroshima-u.ac.jp; Masuda, Harue [Department of Geosciences, Osaka-City University, Sugimoto-tyo, Sumiyoshi, Osaka 558-8585 (Japan); Seddique, Ashraf A. [Department of Geosciences, Osaka-City University, Sugimoto-tyo, Sumiyoshi, Osaka 558-8585 (Japan); Department of Geology, University of Dhaka, Dhaka 1000 (Bangladesh); Mitamura, Muneki [Department of Geosciences, Osaka-City University, Sugimoto-tyo, Sumiyoshi, Osaka 558-8585 (Japan); Maruoka, Teruyuki [Department of Integrative Environmental Science, University of Tsukuba, Tsukuba, Ibaraki 305-8572 (Japan); Li, Xiaodong [Department of Geosciences, Osaka-City University, Sugimoto-tyo, Sumiyoshi, Osaka 558-8585 (Japan); Kusakabe, Minoru [Institute for Study of the Earth' s Interior, Okayama University, Misasa, Tottori 682-0193 (Japan); Dipak, Biswas K. [Department of Geology, University of Dhaka, Dhaka 1000 (Bangladesh); Farooqi, Abida [Department of Geosciences, Osaka-City University, Sugimoto-tyo, Sumiyoshi, Osaka 558-8585 (Japan); Yamanaka, Toshiro [Department of Earth Systems Science, Okayama University, 3-1-1 Tsushima-naka Okayama 700-8530 (Japan); Nakaya, Shinji [Department of Civil Engineering, Shinshu University, Wakazato, Nagano 380-8553 (Japan); Matsuda, Jun-ichi [Department of Earth and Space Science, Osaka University, 1-1 Machikaneyama-tyo, Toyonaka-shi, Osaka 560-0043 (Japan); Ahmed, Kazi Matin [Department of Geology, University of Dhaka, Dhaka 1000 (Bangladesh)

2008-11-15

The geochemical characteristics and hydrological constraints of high As groundwater in Sonargaon, in mid-eastern Bangladesh were investigated in order to ascertain the mechanism of As release into the groundwaters from host sediments in the Ganges-Brahmaputra delta. Samples of groundwater were collected from ca. 230 tube wells in both the rainy and dry seasons. Similar to previous studies, high As groundwater was found in the Holocene unconfined aquifer but not in the Pleistocene aquifer. Groundwaters in the Holocene aquifer were of the Ca-Mg-HCO{sub 3} type with major solutes derived from chemical weathering of detrital minerals such as plagioclase and biotite. Groundwater with high As was generally characterized by high NH{sub 4}{sup +}, possibly derived from the agricultural application of fertilizer as suggested by the small variation of {delta}{sup 15}N{sub NH4} (mostly 2-4 per mille ). Concentrations of Fe changed between the rainy and dry seasons by precipitation/dissolution of Fe oxyhydroxide and siderite, whilst there was not an apparent concomitant change in As. Inhomogeneous spatial distribution of {delta}{sup 18}O in the Holocene unconfined aquifer indicates poor mixing of groundwater in the horizontal direction. Spatial variation of redox conditions is associated with localized variations in subsurface permeability and the recharge/discharge cycle of groundwater. Hydrogeochemical data presented in this paper suggest that reduction of Fe oxyhydroxide is not the only mechanism of As mobilization, and chemical weathering of biotite and/or other basic minerals in the Holocene aquifer could also be important as a primary cause of As mobilization.

Monitoring the hydrolyzation of aspirin during the dissolution testing for aspirin delayed-release tablets with a fiber-optic dissolution system

Directory of Open Access Journals (Sweden)

Yan Wang

2012-10-01

Full Text Available The purpose of this study was to investigate the hydrolyzation of aspirin during the process of dissolution testing for aspirin delayed-release tablets. Hydrolysis product of salicylic acid can result in adverse effects and affect the determination of dissolution rate assaying. In this study, the technique of differential spectra was employed, which made it possible to monitor the dissolution testing in situ. The results showed that the hydrolyzation of aspirin made the percentage of salicylic acid exceed the limit of free salicylic acid (4.0, and the hydrolyzation may affect the quality detection of aspirin delayed-release tablets. Keywords: Aspirin delayed-release tablets, Drug dissolution test, Fiber-optic dissolution system, UV–vis spectrum

Impact of Spatial Pumping Patterns on Groundwater Management

Science.gov (United States)

Yin, J.; Tsai, F. T. C.

2017-12-01

Challenges exist to manage groundwater resources while maintaining a balance between groundwater quantity and quality because of anthropogenic pumping activities as well as complex subsurface environment. In this study, to address the impact of spatial pumping pattern on groundwater management, a mixed integer nonlinear multi-objective model is formulated by integrating three objectives within a management framework to: (i) maximize total groundwater withdrawal from potential wells; (ii) minimize total electricity cost for well pumps; and (iii) attain groundwater level at selected monitoring locations as close as possible to the target level. Binary variables are used in the groundwater management model to control the operative status of pumping wells. The NSGA-II is linked with MODFLOW to solve the multi-objective problem. The proposed method is applied to a groundwater management problem in the complex Baton Rouge aquifer system, southeastern Louisiana. Results show that (a) non-dominated trade-off solutions under various spatial distributions of active pumping wells can be achieved. Each solution is optimal with regard to its corresponding objectives; (b) operative status, locations and pumping rates of pumping wells are significant to influence the distribution of hydraulic head, which in turn influence the optimization results; (c) A wide range of optimal solutions is obtained such that decision makers can select the most appropriate solution through negotiation with different stakeholders. This technique is beneficial to finding out the optimal extent to which three objectives including water supply concern, energy concern and subsidence concern can be balanced.

Use of partial dissolution techniques in geochemical exploration

Science.gov (United States)

Chao, T.T.

1984-01-01

Application of partial dissolution techniques to geochemical exploration has advanced from an early empirical approach to an approach based on sound geochemical principles. This advance assures a prominent future position for the use of these techniques in geochemical exploration for concealed mineral deposits. Partial dissolution techniques are classified as single dissolution or sequential multiple dissolution depending on the number of steps taken in the procedure, or as "nonselective" extraction and as "selective" extraction in terms of the relative specificity of the extraction. The choice of dissolution techniques for use in geochemical exploration is dictated by the geology of the area, the type and degree of weathering, and the expected chemical forms of the ore and of the pathfinding elements. Case histories have illustrated many instances where partial dissolution techniques exhibit advantages over conventional methods of chemical analysis used in geochemical exploration. ?? 1984.

Jarosite dissolution rates in perchlorate brine

Science.gov (United States)

Legett, Carey; Pritchett, Brittany N.; Elwood Madden, Andrew S.; Phillips-Lander, Charity M.; Elwood Madden, Megan E.

2018-02-01

Perchlorate salts and the ferric sulfate mineral jarosite have been detected at multiple locations on Mars by both landed instruments and orbiting spectrometers. Many perchlorate brines have eutectic temperatures bearing rocks and sediments may have been altered by perchlorate brines. Here we measured jarosite dissolution rates in 2 M sodium perchlorate brine as well as dilute water at 298 K to determine the effects of perchlorate anions on jarosite dissolution rates and potential reaction products. We developed a simple method for determining aqueous iron concentrations in high salinity perchlorate solutions using ultraviolet-visible spectrophotometry that eliminates the risk of rapid oxidation reactions during analyses. Jarosite dissolution rates in 2 M perchlorate brine determined by iron release rate (2.87 × 10-12 ±0.85 × 10-12 mol m-2 s-1) were slightly slower than the jarosite dissolution rate measured in ultrapure (18.2 MΩ cm-1) water (5.06 × 10-12 mol m-2 s-1) using identical methods. No additional secondary phases were observed in XRD analyses of the reaction products. The observed decrease in dissolution rate may be due to lower activity of water (ɑH2O = 0.9) in the 2 M NaClO4 brine compared with ultrapure water (ɑH2O = 1). This suggests that the perchlorate anion does not facilitate iron release, unlike chloride anions which accelerated Fe release rates in previously reported jarosite and hematite dissolution experiments. Since dissolution rates are slower in perchlorate-rich solutions, jarosite is expected to persist longer in perchlorate brines than in dilute waters or chloride-rich brines. Therefore, if perchlorate brines dominate aqueous fluids on the surface of Mars, jarosite may remain preserved over extended periods of time, despite active aqueous processes.

Evolution of chemical and isotopic composition of inorganic carbon in a complex semi-arid zone environment: Consequences for groundwater dating using radiocarbon

Science.gov (United States)

Meredith, K. T.; Han, L. F.; Hollins, S. E.; Cendón, D. I.; Jacobsen, G. E.; Baker, A.

2016-09-01

Estimating groundwater age is important for any groundwater resource assessment and radiocarbon (14C) dating of dissolved inorganic carbon (DIC) can provide this information. In semi-arid zone (i.e. water-limited environments), there are a multitude of reasons why 14C dating of groundwater and traditional correction models may not be directly transferable. Some include; (1) the complex hydrological responses of these systems that lead to a mixture of different ages in the aquifer(s), (2) the varied sources, origins and ages of organic matter in the unsaturated zone and (3) high evaporation rates. These all influence the evolution of DIC and are not easily accounted for in traditional correction models. In this study, we determined carbon isotope data for; DIC in water, carbonate minerals in the sediments, sediment organic matter, soil gas CO2 from the unsaturated zone, and vegetation samples. The samples were collected after an extended drought, and again after a flood event, to capture the evolution of DIC after varying hydrological regimes. A graphical method (Han et al., 2012) was applied for interpretation of the carbon geochemical and isotopic data. Simple forward mass-balance modelling was carried out on key geochemical processes involving carbon and agreed well with observed data. High values of DIC and δ13CDIC, and low 14CDIC could not be explained by a simple carbonate mineral-CO2 gas dissolution process. Instead it is suggested that during extended drought, water-sediment interaction leads to ion exchange processes within the top ∼10-20 m of the aquifer which promotes greater calcite dissolution in saline groundwater. This process was found to contribute more than half of the DIC, which is from a mostly 'dead' carbon source. DIC is also influenced by carbon exchange between DIC in water and carbonate minerals found in the top 2 m of the unsaturated zone. This process occurs because of repeated dissolution/precipitation of carbonate that is dependent on

Dissolution of metallic uranium in alkalis

International Nuclear Information System (INIS)

Mondino, Angel V.; Wilkinson, Maria V.; Manzini, Alberto C.

1999-01-01

The dissolution of U metallic foils has been studied in the framework of the development of an improved 99 Mo-production process. The best conditions for the dissolution of uranium foils of approximately 150 μm are the following: a) NaClO concentrations of 0.20 and 0.23 M with NaOH of 0.27 and 0.31 M respectively; b) temperature of the solution, 70 C degrees; c) volume of the solution, 15 ml / cm 2 of uranium foil; d) dissolution time, 30 minutes. (author)

Development and Validation of a Dissolution Test Method for ...

African Journals Online (AJOL)

Purpose: To develop and validate a dissolution test method for dissolution release of artemether and lumefantrine from tablets. Methods: A single dissolution method for evaluating the in vitro release of artemether and lumefantrine from tablets was developed and validated. The method comprised of a dissolution medium of ...

Groundwater impact assessment report for the 216-S-26 Crib, 200 West Area

Energy Technology Data Exchange (ETDEWEB)

Lindberg, J.W.; Evelo, S.D.; Alexander, D.J.

1993-11-01

This report assesses the impact of wastewater discharged to the 216-S-26 Crib on groundwater quality. The 216-S-26 Crib, located in the southern 200 West Area, has been in use since 1984 to dispose of liquid effluents from the 222-S Laboratory Complex. The 222-S Laboratory Complex effluent stream includes wastewater from four sources: the 222-S Laboratory, the 219-S Waste Storage Facility, the 222-SA Chemical Standards Laboratory, and the 291-S Exhaust Fan Control House and Stack. Based on assessment of groundwater chemistry and flow data, contaminant transport predictions, and groundwater chemistry data, the 216-S-26 Crib has minimal influence on groundwater contamination in the southern 200 West Area.

Groundwater impact assessment report for the 216-S-26 Crib, 200 West Area

International Nuclear Information System (INIS)

Lindberg, J.W.; Evelo, S.D.; Alexander, D.J.

1993-11-01

This report assesses the impact of wastewater discharged to the 216-S-26 Crib on groundwater quality. The 216-S-26 Crib, located in the southern 200 West Area, has been in use since 1984 to dispose of liquid effluents from the 222-S Laboratory Complex. The 222-S Laboratory Complex effluent stream includes wastewater from four sources: the 222-S Laboratory, the 219-S Waste Storage Facility, the 222-SA Chemical Standards Laboratory, and the 291-S Exhaust Fan Control House and Stack. Based on assessment of groundwater chemistry and flow data, contaminant transport predictions, and groundwater chemistry data, the 216-S-26 Crib has minimal influence on groundwater contamination in the southern 200 West Area

Low temperature dissolution flowsheet for plutonium metal

Energy Technology Data Exchange (ETDEWEB)

Daniel, W. E. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Almond, P. M. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Rudisill, T. S. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL)

2016-05-01

The H-Canyon flowsheet used to dissolve Pu metal for PuO₂ production utilizes boiling HNO₃. SRNL was requested to develop a complementary dissolution flowsheet at two reduced temperature ranges. The dissolution and H₂ generation rates of Pu metal were investigated using a dissolving solution at ambient temperature (20-30 °C) and for an intermediate temperature of 50-60 °C. Additionally, the testing included an investigation of the dissolution rates and characterization of the off-gas generated from the ambient temperature dissolution of carbon steel cans and the nylon bags that contain the Pu metal when charged to the dissolver.

Porewater and groundwater geochemistry at the Down Ampney fault research site

International Nuclear Information System (INIS)

Metcalfe, R.; Ross, C.A.M.; Cave, M.R.; Green, K.A.; Reeder, S.; Entwisle, D.C.

1993-01-01

This work is performed under contract with the Commission of the European Communities in the framework of its research programme on Management and Storage of Radioactive Wastes. The importance of faults in mudrocks as groundwater conduits, and as a control on solute transport, was assessed in a Jurassic mudrock, siltstone and limestone sequence at Down Ampney, Gloucestershire. Samples were taken from a borehole array crossing an east-west trending fault, of approximately 48 m northerly downthrow. Squeezing mudrock samples yielded 18.1 to 34.5% of total porewater, which was analyzed for major/trace elements and stable O/H isotope compositions. Fault-zone porewaters have greatly increased sulphate concentrations relative to those remote from the fault. Porewater cation concentrations are related to pH, which is correlated with sulphate concentrations, probably controlled by sulphide oxidation. Control of cation concentrations is largely by pH-dependent carbonate dissolution and cation exchange reactions. Porewater C1 and Br concentrations increase downwards, but at twice the rate away from the fault as near the fault, suggesting that although meteoric waters penetrate throughout the area, they are preferentially conducted by the fault. Comparisons are made between pore- and groundwater samples from each side of the fault, and from the fault zone. Pore- and groundwater compositions are not simply related, except in the case of sulphate which, in the fault zone, is more diluted in groundwaters. 14 refs. 20 figs., 17 tabs

Simulating the effects of a beaver dam on regional groundwater flow through a wetland

Directory of Open Access Journals (Sweden)

Kathleen Feiner

2015-09-01

New hydrological insights for the region: The construction of a beaver dam resulted in minimal changes to regional groundwater flow paths at this site, which is attributed to a clay unit underlying the peat, disconnecting this wetland from regional groundwater flow. However, groundwater discharge from the wetland pond increased by 90%. Simulating a scenario with the numerical model in which the wetland is connected to regional groundwater flow results in a much larger impact on flow paths. In the absence of the clay layer, the simulated construction of a beaver dam causes a 70% increase in groundwater discharge from the wetland pond and increases the surface area of both the capture zone and the discharge zone by 30% and 80%, respectively.

Geomorphic aspects of groundwater flow

Science.gov (United States)

LaFleur, Robert G.

The many roles that groundwater plays in landscape evolution are becoming more widely appreciated. In this overview, three major categories of groundwater processes and resulting landforms are considered: (1) Dissolution creates various karst geometries, mainly in carbonate rocks, in response to conditions of recharge, geologic setting, lithology, and groundwater circulation. Denudation and cave formation rates can be estimated from kinetic and hydraulic parameters. (2) Groundwater weathering generates regoliths of residual alteration products at weathering fronts, and subsequent exhumation exposes corestones, flared slopes, balanced rocks, domed inselbergs, and etchplains of regional importance. Groundwater relocation of dissolved salts creates duricrusts of various compositions, which become landforms. (3) Soil and rock erosion by groundwater processes include piping, seepage erosion, and sapping, important agents in slope retreat and headward gully migration. Thresholds and limits are important in many chemical and mechanical groundwater actions. A quantitative, morphometric approach to groundwater landforms and processes is exemplified by selected studies in carbonate and clastic terrains of ancient and recent origins. Résumé Les rôles variés joués par les eaux souterraines dans l'évolution des paysages deviennent nettement mieux connus. La revue faite ici prend en considération trois grandes catégories de processus liés aux eaux souterraines et les formes associées: (1) La dissolution crée des formes karstiques variées, surtout dans les roches carbonatées, en fonction des conditions d'alimentation, du cadre géologique, de la lithologie et de la circulation des eaux souterraines. Les taux d'érosion et de formation des grottes peuvent être estimés à partir de paramètres cinétiques et hydrauliques. (2) L'érosion par les eaux souterraines donne naissance à des régolites, résidus d'altération sur des fronts d'altération, et l'exhumation r

Physical heterogeneity control on effective mineral dissolution rates

Science.gov (United States)

Jung, Heewon; Navarre-Sitchler, Alexis

2018-04-01

Hydrologic heterogeneity may be an important factor contributing to the discrepancy in laboratory and field measured dissolution rates, but the governing factors influencing mineral dissolution rates among various representations of physical heterogeneity remain poorly understood. Here, we present multiple reactive transport simulations of anorthite dissolution in 2D latticed random permeability fields and link the information from local grid scale (1 cm or 4 m) dissolution rates to domain-scale (1m or 400 m) effective dissolution rates measured by the flux-weighted average of an ensemble of flow paths. We compare results of homogeneous models to heterogeneous models with different structure and layered permeability distributions within the model domain. Chemistry is simplified to a single dissolving primary mineral (anorthite) distributed homogeneously throughout the domain and a single secondary mineral (kaolinite) that is allowed to dissolve or precipitate. Results show that increasing size in correlation structure (i.e. long integral scales) and high variance in permeability distribution are two important factors inducing a reduction in effective mineral dissolution rates compared to homogeneous permeability domains. Larger correlation structures produce larger zones of low permeability where diffusion is an important transport mechanism. Due to the increased residence time under slow diffusive transport, the saturation state of a solute with respect to a reacting mineral approaches equilibrium and reduces the reaction rate. High variance in permeability distribution favorably develops large low permeability zones that intensifies the reduction in mixing and effective dissolution rate. However, the degree of reduction in effective dissolution rate observed in 1 m × 1 m domains is too small (equilibrium conditions reduce the effective dissolution rate by increasing the saturation state. However, in large domains where less- or non-reactive zones develop, higher

Integrating geochemical investigations and geospatial assessment to understand the evolutionary process of hydrochemistry and groundwater quality in arid areas.

Science.gov (United States)

El Alfy, Mohamed; Alharbi, Talal; Mansour, Basma

2018-04-12

Groundwater is the key for life in arid areas. Aquifer overexploitation and climatic conditions can significantly deteriorate groundwater quality. The Al-Qassim area in central Saudi Arabia is characterized by dense agricultural use and is irrigated mainly by fossil groundwater from the Saq Aquifer. Understanding the area's hydrochemistry, major factors governing groundwater quality, and alternative uses of the groundwater are the main goals of this study. Groundwater samples were collected and examined for major, minor, and trace elements. Ionic relationships, hydrochemical facies, geospatial distributions, and multivariate analyses were conducted to assess the hydrochemical processes at play. The salinity and nitrate concentrations of the Saq Aquifer's groundwater were found to increase in the outcrop areas more than the confined areas. The spatial distributions were fragmented by three main factors: (i) modern recharge by relatively brackish water, (ii) irrigation return flow in intensive farming areas, and (iii) overexploitation and draining of deep and relatively saline zones of the aquifer. Seven water types were found representing the alkaline water with a predominance of sulfate-chloride ions and earth alkaline water with a predominance of sulfate and chloride. Mixing between fresh and brackish water, dissolution of mineral phases, silicate weathering, and reverse ion exchange were recognized as the evolutionary processes, while evaporation played a minor role. Cluster analyses characterized the fresh groundwater zone, modern groundwater recharge zone, and anthropogenic influence zone. In the confined areas, nearly all the groundwater was appropriate for domestic use and irrigation. In the outcrop areas, some limitations were found due to unsuitable conditions.

The aquatic geochemistry of arsenic in volcanic groundwaters from southern Italy

International Nuclear Information System (INIS)

Aiuppa, Alessandro; D'Alessandro, Walter; Federico, Cinzia; Palumbo, Barbara; Valenza, Mariano

2003-01-01

This paper discusses the abundance, speciation and mobility of As in groundwater systems from active volcanic areas in Italy. Using literature data and new additional determinations, the main geochemical processes controlling the fate of As during gas-water-rock interaction in these systems are examined. Arsenic concentrations in the fluids range from 0.1 to 6940 μg/l, with wide differences observed among the different volcanoes and within each area. The dependence of As content on water temperature, pH, redox potential and major ions is investigated. Results demonstrate that As concentrations are highest where active hydrothermal circulation takes place at shallow levels, i.e. at Vulcano Island and the Phlegrean Fields. In both areas the dissolution of As-bearing sulphides is likely to be the main source of As. Mature Cl-rich groundwaters, representative of the discharge from the deep thermal reservoirs, are typically enriched in As with respect to SO 4 -rich ''steam heated groundwaters''. In the HCO 3 - groundwaters recovered at Vesuvius and Etna, aqueous As cycling is limited by the absence of high-temperature interactions and by high-Fe content of the host rocks, resulting in oxidative As adsorption. Thermodynamic modelling suggests that reducing H 2 S-rich groundwaters are in equilibrium with realgar, whereas in oxidising environments over-saturation with respect to Fe oxy-hydroxides is indicated. Under these oxidising conditions, As solubility decreases controlled by As co-precipitation with, or adsorption on, Fe oxy-hydroxides. Consistent with thermodynamic considerations, As mobility in the studied areas is enhanced in intermediate redox environments, where both sulphides and Fe hydroxides are unstable

Porewater and groundwater geochemistry at the Down Ampney fault research site

International Nuclear Information System (INIS)

Metcalfe, R.; Ross, C.A.M.; Cave, M.R.; Green, K.A.; Reeder, S.; Entwisle, D.C.

1990-12-01

A Jurassic sequence of mudrocks, siltstones and limestones, at Down Ampney, Gloucestershire, was investigated. The aim was to evaluate the importance of faults in mudrocks as conduits for direct groundwater flow, and the influence of such faults on solute transport. Chemical analysis of porewaters and groundwaters are reported. Porewaters were obtained for analysis by squeezing mudrock core samples, yielding 18.1-34.5% of the total porewater. The solutions were analysed for major and trace elements and stable O/H isotope compositions. These analyses are compared with analyses for conventional groundwater samples. Samples were taken from a borehole array which crossed a prominent east-west trending fault, with a northerly downthrow of c.48 m. Comparisons are made between pore- and ground- water samples from each side of the fault, and from the fault zone itself. Sulphate concentrations are greatly increased in porewaters from the fault zone in comparison with sulphate concentrations in porewaters remote from the fault. The concentrations of porewater cations are related to pH, which in turn can be related to sulphate concentrations, probably controlled by sulphide oxidation. Cation concentrations are controlled mainly by carbonate dissolution and cation exchange reactions, largely dependent upon pH. Porewater concentrations of Cl and Br increase downwards but away from the fault zones the concentration gradients with depth are twice those in the vicinity of the fault. This suggests that meteoric waters are conducted by the fault, although they also penetrate downwards throughout the area. Groundwater compositions bear no simple relationship to porewater compositions, except in the case of sulphate. In the fault zone this is invariably more dilute in groundwaters than in porewaters. (author)

Overview of chemical modeling of nuclear waste glass dissolution

International Nuclear Information System (INIS)

Bourcier, W.L.

1991-02-01

Glass dissolution takes place through metal leaching and hydration of the glass surface accompanied by development of alternation layers of varying crystallinity. The reaction which controls the long-term glass dissolution rate appears to be surface layer dissolution. This reaction is reversible because the buildup of dissolved species in solution slows the dissolution rate due to a decreased dissolution affinity. Glass dissolution rates are therefore highly dependent on silica concentrations in solution because silica is the major component of the alteration layer. Chemical modeling of glass dissolution using reaction path computer codes has successfully been applied to short term experimental tests and used to predict long-term repository performance. Current problems and limitations of the models include a poorly defined long-term glass dissolution mechanism, the use of model parameters determined from the same experiments that the model is used to predict, and the lack of sufficient validation of key assumptions in the modeling approach. Work is in progress that addresses these issues. 41 refs., 7 figs., 2 tabs

Development and validation of dissolution test for Metoprolol ...

African Journals Online (AJOL)

The dissolution method which uses USP apparatus I (Basket) with rotating at 100 rpm, 900 ml of different dissolution medium, ultra violet spectroscopy for quantification was demonstrated to be robust, discriminating and transferable. Dissolution tests conditions were selected after it was demonstrated that the Metoprolol ...

Interactions between a poorly soluble cationic drug and sodium dodecyl sulfate in dissolution medium and their impact on in vitro dissolution behavior.

Science.gov (United States)

Huang, Zongyun; Parikh, Shuchi; Fish, William P

2018-01-15

In the pharmaceutical industry, in vitro dissolution testing ofsolid oral dosage forms is a very important tool for drug development and quality control. However, ion-pairing interaction between the ionic drugand surfactants in dissolution medium often occurs, resulting in inconsistent and incomplete drug release. The aim of this study is toevaluate the effects ofsodium dodecyl sulfate (SDS) mediated medium onthe dissolution behaviors of a poorly soluble cationic drug (Drug B). The study was carried out by measuring solubility of Drug B substance and dissolution rate of Drug B product in media containing SDS.Desolubilization of Drug B substance was observed at pH 4.5 in the presence of SDS at concentrations below critical micelle concentration (CMC) which is attributed to the formation of an insoluble di-dodecyl sulfate salt between SDS and Drug B. This ion-pairing effect is less significant with increasing medium pH where Drug B is less ionized and CMC of SDS is lower. In medium at pH 4.5, dissolution of Drug B product was found incomplete with SDS concentration below CMC due to the desolubilization of Drug B substance. In media with SDS level above CMC, the dissolution rate is rather slower with higher inter-vessel variations compared to that obtained in pH 4.5 medium without SDS. The dissolution results demonstrate that the presence of SDS in medium generates unexpected irregular dissolution profiles for Drug B which are attributed to incompatible dissolution medium for this particular drug. Therefore, non-ionic surfactant was selected for Drug B product dissolution method and ion-pairing effect in SDS mediated medium should be evaluated when developing a dissolution method for any poorly soluble cationic drugs. Copyright © 2017 Elsevier B.V. All rights reserved.

Time scales for dissolution of calcite fracture fillings and implications for saturated zone radionuclide transport at Yucca Mountain, Nevada

International Nuclear Information System (INIS)

Winterle, J.R.; Murphy, W.M.

1999-01-01

An analysis was performed to estimate time scales for dissolution of calcite fracture fillings in the fractured tuff aquifer that underlies Yucca Mountain (YM), Nevada, where groundwater is chemically undersaturated with respect to calcite. The impetus for this analysis originates from speculation that undissolved calcite in the saturated zone is evidence for limited diffusive exchange between fracture and matrix waters. Assuming that matrix diffusion is the rate-limiting process, the time scale for dissolution of calcite fracture fillings depends on the amount of calcite initially deposited, the distance between flowing fractures, the degree of chemical disequilibrium, and the rate of diffusion. Assuming geochemistry of J-13 well water in free-flowing fractures, estimated time scales for complete dissolution of matrix-entrapped calcite range from about 10 4 yr for a 2 mm-thick deposit located 1 m from a flowing fracture, to over 10 7 yr for a 2 cm-thick deposit located 100 m from a flowing fracture. The authors conclude that, given the geochemical and hydrologic characteristics observed at YM, the persistence of calcite minerals over geologic time scales in aquifers where flowing water is under-saturated with calcite does not necessarily preclude matrix diffusion as a dilution mechanism. However, the model suggests that the effective spacing between flowing fractures may be large enough to diminish the overall benefit of matrix diffusion to proposed high-level waste repository performance

Groundwater quality assessment of urban Bengaluru using multivariate statistical techniques

Science.gov (United States)

Gulgundi, Mohammad Shahid; Shetty, Amba

2018-03-01

Groundwater quality deterioration due to anthropogenic activities has become a subject of prime concern. The objective of the study was to assess the spatial and temporal variations in groundwater quality and to identify the sources in the western half of the Bengaluru city using multivariate statistical techniques. Water quality index rating was calculated for pre and post monsoon seasons to quantify overall water quality for human consumption. The post-monsoon samples show signs of poor quality in drinking purpose compared to pre-monsoon. Cluster analysis (CA), principal component analysis (PCA) and discriminant analysis (DA) were applied to the groundwater quality data measured on 14 parameters from 67 sites distributed across the city. Hierarchical cluster analysis (CA) grouped the 67 sampling stations into two groups, cluster 1 having high pollution and cluster 2 having lesser pollution. Discriminant analysis (DA) was applied to delineate the most meaningful parameters accounting for temporal and spatial variations in groundwater quality of the study area. Temporal DA identified pH as the most important parameter, which discriminates between water quality in the pre-monsoon and post-monsoon seasons and accounts for 72% seasonal assignation of cases. Spatial DA identified Mg, Cl and NO3 as the three most important parameters discriminating between two clusters and accounting for 89% spatial assignation of cases. Principal component analysis was applied to the dataset obtained from the two clusters, which evolved three factors in each cluster, explaining 85.4 and 84% of the total variance, respectively. Varifactors obtained from principal component analysis showed that groundwater quality variation is mainly explained by dissolution of minerals from rock water interactions in the aquifer, effect of anthropogenic activities and ion exchange processes in water.

Arsenic and fluoride in the groundwater of Mexico.

Science.gov (United States)

Armienta, M A; Segovia, N

2008-08-01

Concentrations of arsenic and fluoride above Mexican drinking water standards have been detected in aquifers of various areas of Mexico. This contamination has been found to be mainly caused by natural sources. However, the specific processes releasing these toxic elements into groundwater have been determined in a few zones only. Many studies, focused on arsenic-related health effects, have been performed at Comarca Lagunera in northern México. High concentrations of fluoride in water were also found in this area. The origin of the arsenic there is still controversial. Groundwater in active mining areas has been polluted by both natural and anthropogenic sources. Arsenic-rich minerals contaminate the fractured limestone aquifer at Zimapán, Central México. Tailings and deposits smelter-rich fumes polluted the shallow granular aquifer. Arsenic contamination has also been reported in the San Antonio-El Triunfo mining zone, southern Baja California, and Santa María de la Paz, in San Luis Potosí state. Even in the absence of mining activities, hydrogeochemistry and statistical techniques showed that arsenopyrite oxidation may also contaminate water, as in the case of the Independencia aquifer in the Mexican Altiplano. High concentrations of arsenic have also been detected in geothermal areas like Los Azufres, Los Humeros, and Acoculco. Prevalence of dental fluorosis was revealed by epidemiological studies in Aguascalientes and San Luis Potosí states. Presence of fluoride in water results from dissolution of acid-volcanic rocks. In Mexico, groundwater supplies most drinking water. Current knowledge and the geology of Mexico indicate the need to include arsenic and fluoride determinations in groundwater on a routine basis, and to develop interdisciplinary studies to assess the contaminant's sources in all enriched areas.

Dissolution studies of spent nuclear fuels

International Nuclear Information System (INIS)

1991-02-01

To obtain quantitative data on the dissolution of high burnup spent nuclear fuel, dissolution study have been carried out at the Department of Chemistry, JAERI, from 1984 under the contract with STA entitled 'Reprocessing Test Study of High Burnup Fuel'. In this study PWR spent fuels of 8,400 to 36,100 MWd/t in averaged burnup were dissolved and the chemical composition and distribution of radioactive nuclides were measured for insoluble residue, cladding material (hull), off-gas and dissolved solution. With these analyses basic data concerning the dissolution and clarification process in the reprocessing plant were accumulated. (author)

The immigration model and its implications of natural radionuclides of coastal groundwater in Xiamen

International Nuclear Information System (INIS)

Cai Minggang; Huang Yipu; Chen Min; Liu Guangshan

2004-01-01

The natural radionuclides in groundwater systems are considered to reside in three pools: dissolved, sorbed (on rock surface), and solid. Transfer of radionuclides between the dissolved and solid pools is accomplished chiefly by dissolution, (co-)precipitation and/or a-recoil. The mass balance equations model of the natural radionuclides of dissolved and adsorbed phase reservoir in groundwater is established by setting certain conditions and parameters. The modeling equations form the basic of our assessment of the effects of sorption-desorption, dissolution-precipitation, and advection-diffusion in radionuclide transport in the groundwater. The interaction between groundwater and rock in Xiamen coastal aquifers were studied quantitatively using this model, which gave us reasonable explanation for the spatial distribution of natural radium, radon isotopes activities and their activities ratio. α-recoil supply rates of 222 Rn (P r,Rn-222 ) and 224 Ra (P α,Ra-224 ) range from 0.09 x 10 3 to 3.44 x 10 3 atoms·m -3 ·s -1 and from 0.13 x l0 3 to 4.91 x 10 3 atoms·m -3 ·s -1 , respectively. P α,Ra-224 is also found to be larger than P r,Rn-222 in every station, revealing that aquifer solids contain more thorium than uranium in studied area. Both of P r,Rn-222 and P α,Ra-224 of coastal groundwater decreased seaward, revealing a-recoil supplying rates of 222 Rn and 224 Ra by aquifers rock decreased gradually, which gave good explanation of the spatial distribution characters of above two nuclides. P r,Rn-222 /A Rn-222 increase seaward from 0.3 to 0.9 along the major paths, with the average value of 0.6. Such results reveal that the primary source of groundwater 222 Rn in these areas is α-recoil of 226 Ra decay in solid pool, and its relative increase along the paths. Another source of 222 Rn is 226 Ra decay in tile sorbed pool (R f,Ra-226 ·A Ra-226 ), which attributes about 40 percent of total source of coastal groundwater 222 Rn. P α,Ra-224 /A Ra-224 ranges

The immigration model and its implications of natural radionuclides of coastal groundwater in Xiamen

International Nuclear Information System (INIS)

Cai Minggang; Huang Yipu; Chen Min; Liu Guangshan

2005-01-01

The natural radionuclides in groundwater systems are considered to reside in three pools: dissolved, sorbed (on rock surface), and solid. Transfer of radionuclides between the dissolved and solid pools is accomplished chiefly by dissolution. (co-)precipitation and/or α-recoil. The mass balance equations model of the natural radionuclides of dissolved and adsorbed phase reservoir in groundwater is established by setting certain conditions and parameters. The modeling equations form the basic of our assessment of the effects of sorption-desorption, dissolution-precipitation, and advection-diffusion in radionuclide transport in the groundwater. The interaction between groundwater and rock in Xiamen coastal aquifers were studied quantitatively using this model, which gave us reasonable explanation for the spatial distribution of natural radium, radon isotopes activities and their activities ratio. α-recoil supply rates of 222 Rn (P r,Rn-22 -2) and 224 Ra (P a,Ra-224 ) range from 0.09 x l0 3 to 3.44 x 10 3 atoms·m -3 ·s -1 and from 0.13 x 10 3 to 4.91 x 10 3 x 10 3 atoms·m -3 ·s -1 , respectively. P a,Ra-224 is also found to be larger than P r,Rn-222 in every station, revealing that aquifer solids contain more thorium than uranium in studied area. Both of P r,Rn-222 and P a,Ra-224 of coastal groundwater decreased seaward, revealing α-recoil supplying rates of 222 Rn and 224 Ra by aquifers rock decreased gradually, which gave good explanation of the spatial distribution characters of above two nuclides. P r,Rn-222 /A Rn-222 increase seaward from 0.3 to 0.9 along the major paths, with the average value of 0.6, Such results reveal that the primary source of groundwater 222 Rn in these areas is α-recoil of 226 Ra decay in solid pool, and its relative increase along the paths. Another source of 222 Rn is 226 Ra decay in the sorbed pool (R f,Ra-226 ·A Ra-226 ), which attributes about 40 per cent of total source of coastal groundwater 222 Rn. P α,Ra-224 /A Ra-224

Groundwater mixing and mineralization processes in a mountain-oasis-desert basin, northwest China: hydrogeochemistry and environmental tracer indicators

Science.gov (United States)

Ma, Bin; Jin, Menggui; Liang, Xing; Li, Jing

2018-02-01

Hydrogeochemistry and environmental tracers (2H, 18O, 87Sr/86Sr) in precipitation, river and reservoir water, and groundwater have been used to determine groundwater recharge sources, and to identify mixing characteristics and mineralization processes in the Manas River Basin (MRB), which is a typical mountain-oasis-desert ecosystem in arid northwest China. The oasis component is artificial (irrigation). Groundwater with enriched stable isotope content originates from local precipitation and surface-water leakage in the piedmont alluvial-oasis plain. Groundwater with more depleted isotopes in the north oasis plain and desert is recharged by lateral flow from the adjacent mountains, for which recharge is associated with high altitude and/or paleo-water infiltrating during a period of much colder climate. Little evaporation and isotope exchange between groundwater and rock and soil minerals occurred in the mountain, piedmont and oasis plain. Groundwater δ2H and δ18O values show more homogeneous values along the groundwater flow direction and with well depths, indicating inter-aquifer mixing processes. A regional contrast of groundwater allows the 87Sr/86Sr ratios and δ18O values to be useful in a combination with Cl, Na, Mg, Ca and Sr concentrations to distinguish the groundwater mixing characteristics. Two main processes are identified: groundwater lateral-flow mixing and river leakage in the piedmont alluvial-oasis plain, and vertical mixing in the north oasis plain and the desert. The 87Sr/86Sr ratios and selected ion ratios reveal that carbonate dissolution and mixing with silicate from the southern mountain area are primarily controlling the strontium isotope hydrogeochemistry.

Dissolution testing of orally disintegrating tablets.

Science.gov (United States)

Kraemer, Johannes; Gajendran, Jayachandar; Guillot, Alexis; Schichtel, Julian; Tuereli, Akif

2012-07-01

For industrially manufactured pharmaceutical dosage forms, product quality tests and performance tests are required to ascertain the quality of the final product. Current compendial requirements specify a disintegration and/or a dissolution test to check the quality of oral solid dosage forms. These requirements led to a number of compendial monographs for individual products and, at times, the results obtained may not be reflective of the dosage form performance. Although a general product performance test is desirable for orally disintegrating tablets (ODTs), the complexity of the release controlling mechanisms and short time-frame of release make such tests difficult to establish. For conventional oral solid dosage forms (COSDFs), disintegration is often considered to be the prerequisite for subsequent dissolution. Hence, disintegration testing is usually insufficient to judge product performance of COSDFs. Given the very fast disintegration of ODTs, the relationship between disintegration and dissolution is worthy of closer scrutiny. This article reviews the current status of dissolution testing of ODTs to establish the product quality standards. Based on experimental results, it appears that it may be feasible to rely on the dissolution test without a need for disintegration studies for selected ODTs on the market. © 2012 The Authors. JPP © 2012 Royal Pharmaceutical Society.

Importance of surface structure on dissolution of fluorite

DEFF Research Database (Denmark)

Godinho, Jose; Piazolo, Sandra; Balic Zunic, Tonci

2014-01-01

forming the initial surface and its inclination to the closest stable planes, which are specific for each surface orientation. During an initial dissolution regime dissolution rates decrease significantly, even though the total surface area increases. During a second dissolution regime, some surfaces...... by the relative stability of the planes and type of edges that constitute a surface needs to be considered. Significant differences between dissolution rates calculated based on surface area alone, and based on surface reactivity are expected for materials with the fluorite structure....

Minimization of required model runs in the Random Mixing approach to inverse groundwater flow and transport modeling

Science.gov (United States)

Hoerning, Sebastian; Bardossy, Andras; du Plessis, Jaco

2017-04-01

Most geostatistical inverse groundwater flow and transport modelling approaches utilize a numerical solver to minimize the discrepancy between observed and simulated hydraulic heads and/or hydraulic concentration values. The optimization procedure often requires many model runs, which for complex models lead to long run times. Random Mixing is a promising new geostatistical technique for inverse modelling. The method is an extension of the gradual deformation approach. It works by finding a field which preserves the covariance structure and maintains observed hydraulic conductivities. This field is perturbed by mixing it with new fields that fulfill the homogeneous conditions. This mixing is expressed as an optimization problem which aims to minimize the difference between the observed and simulated hydraulic heads and/or concentration values. To preserve the spatial structure, the mixing weights must lie on the unit hyper-sphere. We present a modification to the Random Mixing algorithm which significantly reduces the number of model runs required. The approach involves taking n equally spaced points on the unit circle as weights for mixing conditional random fields. Each of these mixtures provides a solution to the forward model at the conditioning locations. For each of the locations the solutions are then interpolated around the circle to provide solutions for additional mixing weights at very low computational cost. The interpolated solutions are used to search for a mixture which maximally reduces the objective function. This is in contrast to other approaches which evaluate the objective function for the n mixtures and then interpolate the obtained values. Keeping the mixture on the unit circle makes it easy to generate equidistant sampling points in the space; however, this means that only two fields are mixed at a time. Once the optimal mixture for two fields has been found, they are combined to form the input to the next iteration of the algorithm. This

Geochemistry and arsenic behaviour in groundwater resources of the Pannonian Basin (Hungary and Romania)

International Nuclear Information System (INIS)

Rowland, Helen A.L.; Omoregie, Enoma O.; Millot, Romain; Jimenez, Cristina; Mertens, Jasmin; Baciu, Calin; Hug, Stephan J.; Berg, Michael

2011-01-01

Graphical abstract: Elevated As levels in the Pannonian Basin are mainly present in very old (Palaeo) groundwater of methanogenic Pliocene/Quaternary aquifers, which is in contrast to Asian regions where arsenic-enriched groundwater is generally much younger. Display Omitted Research highlights: → Arsenic originates from Late Pliocene/Quaternary aquifers and some very old waters. → Arsenic levels are controlled by both mobilisation and retention mechanisms. → Mobilisation is caused by biogeochemical reductive dissolution. → Sufficient sulfate supply triggers arsenic retention in sulfide precipitates. → Nearly 500,000 people are exposed to elevated arsenic in their drinking water. - Abstract: Groundwater resources in the Pannonian Basin (Hungary, Romania, Croatia and Serbia) are known to contain elevated naturally occurring As. Published estimates suggest nearly 500,000 people are exposed to levels greater than the EU maximum admissible concentration of 10 μg/L in their drinking water, making it the largest area so affected in Europe. In this study, a variety of groundwaters were collected from Romania and Hungary to elucidate the general geochemistry and identify processes controlling As behaviour. Concentrations ranged from 4 2- reduction containing low As levels ( 7 Li (an indicator of geothermal inputs) and As(tot) in geothermal/saline influenced waters indicate that elevated As is not from an external input, but is released due to an in-aquifer process. Geochemical reasoning, therefore, implies As mobilisation is controlled by redox processes, most likely microbially mediated reductive dissolution of As bearing Fe-oxides, known to occur in sediments from the area. More important is an overlying retention mechanism determined by the presence or absence of SO 4 2- . Ongoing SO 4 2- reduction will release S 2- , removing As from solution either by the formation of As-sulfides, or from sorption onto Fe-sulfide phases. In methanogenic waters, As released

Assessment of Long-Term Evolution of Groundwater Hydrochemical Characteristics Using Multiple Approaches: A Case Study in Cangzhou, Northern China

Directory of Open Access Journals (Sweden)

Wei Li

2015-03-01

Full Text Available Water shortage is severe in the North China Plain (NCP. In addition to a deficiency of water resources, deterioration of groundwater quality should be of great concern. In this study, hydrogeological analysis was conducted in combination with principal component analysis, correlation analysis and the co-kriging method to identify factors controlling the content of major ions and total dissolved solids (TDS in areal shallow and deep groundwater and to assess groundwater evolution in Cangzhou, China. The results suggested that groundwater quality degradation occurred and developed in the study area, as indicated by increasing concentrations of major ions, TDS and hardness in both shallow and deep groundwater. In shallow groundwater, whose hydrochemical water types changed from HCO3–Ca.Na.Mg and HCO3.Cl–Na in the west (Zone II to Cl.SO4–Na and Cl–Na in the east (Zone III. Areas with TDS concentrations between 1500 and 2000 mg/L occupied 79.76% of the total in the 1980s, while areas with a TDS concentration ranging from 2500 to 3000 mg/L comprised 59.11% of the total in the 2010s. In deep groundwater, the area with TDS over 1000 mg/L expanded from 5366.39 km2 in the 1960s to 7183.52 km2 in the 2010s. Natural processes (water-rock interactions and anthropogenic activities (groundwater exploitation were the dominant factors controlling the major ions’ content in local groundwater. Dissolution of dolomite, calcite, feldspar and gypsum were the primary sources of major ions in groundwater, and the ion exchange reaction had a strong effect on the cation content, especially for deep groundwater.

Investigation of Submarine Groundwater Discharge and Preferential Groundwater Flow-paths in a Coastal Karst Area using towed Marine and Terrestrial Electrical Resistivity

Science.gov (United States)

O'connell, Y.; Daly, E.; Duffy, G.; Henry, T.

2012-12-01

Large volumes of groundwater, containing nutrients and contaminants enter the coastal waters of southern Galway Bay on the west coast of Ireland through submarine groundwater discharge (SGD). The SGD occurs through karstified Carboniferous limestone in a major karst region comprising the Burren and Gort Lowlands. The Carboniferous limestones have experienced extensive dissolution resulting in the development of an underground network of conduits and fissures that define a trimodal groundwater flow pattern across the region. Groundwater discharge to the sea in this area is exclusively intertidal and submarine. Storage in the karst is limited and typical winter rainfall conditions result in the karst system becoming saturated. Temporary lakes (turloughs) form in lowlying areas and act as large reservoirs which provide storage to enable the transmission of the large volumes of water in the system to the sea. Between 2010 and 2012, terrestrial and shallow marine geophysical surveying has been undertaken to investigate preferential groundwater flow-paths and SGD locations in order to quantify the groundwater-seawater interactions in this coastal karst system. A report into the groundwater system of this karst region following a major flood event proposed a conceptual conduit model defined by extensive water tracing, water level monitoring, hydrochemical sampling, geological mapping and drilling. Limited information about the dimensions of the conduits was known. Electrical resistivity tomography (ERT) profiling to depths of 100m below ground level, with multiple array configurations, has been carried out to investigate the modes of groundwater flow in to and out of both temporary and permanent freshwater lakes in the system. Towed dipole-dipole profiles have been recorded to investigate conduits beneath a permanent lake exhibiting a tidal influence despite its location 5.5 km from the seashore. The ERT data indicates significant variations in subsurface resistivities

Possible effects of groundwater pumping on surface water in the Verde Valley, Arizona

Science.gov (United States)

Leake, Stanley A.; Haney, Jeanmarie

2010-01-01

The U.S. Geological Survey (USGS), in cooperation with The Nature Conservancy, has applied a groundwater model to simulate effects of groundwater pumping and artificial recharge on surface water in the Verde Valley sub-basin of Arizona. Results are in two sets of maps that show effects of locations of pumping or recharge on streamflow. These maps will help managers make decisions that will meet water needs and minimize environmental impacts.

Estimation of microbial respiration rates in groundwater by geochemical modeling constrained with stable isotopes

International Nuclear Information System (INIS)

Murphy, E.M.

1998-01-01

Changes in geochemistry and stable isotopes along a well-established groundwater flow path were used to estimate in situ microbial respiration rates in the Middendorf aquifer in the southeastern United States. Respiration rates were determined for individual terminal electron acceptors including O 2 , MnO 2 , Fe 3+ , and SO 4 2- . The extent of biotic reactions were constrained by the fractionation of stable isotopes of carbon and sulfur. Sulfur isotopes and the presence of sulfur-oxidizing microorganisms indicated that sulfate is produced through the oxidation of reduced sulfur species in the aquifer and not by the dissolution of gypsum, as previously reported. The respiration rates varied along the flow path as the groundwater transitioned between primarily oxic to anoxic conditions. Iron-reducing microorganisms were the largest contributors to the oxidation of organic matter along the portion of the groundwater flow path investigated in this study. The transition zone between oxic and anoxic groundwater contained a wide range of terminal electron acceptors and showed the greatest diversity and numbers of culturable microorganisms and the highest respiration rates. A comparison of respiration rates measured from core samples and pumped groundwater suggests that variability in respiration rates may often reflect the measurement scales, both in the sample volume and the time-frame over which the respiration measurement is averaged. Chemical heterogeneity may create a wide range of respiration rates when the scale of the observation is below the scale of the heterogeneity

Hydrogeochemical signatures and evolution of groundwater impacted by the Bayan Obo tailing pond in northwest China

Energy Technology Data Exchange (ETDEWEB)

Huang, Xiang [Institute of Water Sciences and College of Engineering, Peking University, Beijing (China); Shaanxi Key Laboratory of Comprehensive Utilization of Tailing Resources, Shangluo University, Shaanxi (China); Deng, Hailin, E-mail: hailin.deng@gmail.com [CSIRO Land and Water, Private Bag No. 5, Wembley, WA 6913 (Australia); Zheng, Chunmiao [Institute of Water Sciences and College of Engineering, Peking University, Beijing (China); School of Environmental Science and Engineering, South University of Science and Technology of China, Shenzhen (China); Department of Geological Science, University of Alabama, Tuscaloosa, AL (United States); Cao, Guoliang [Institute of Water Sciences and College of Engineering, Peking University, Beijing (China)

2016-02-01

Uncontrolled leakage from mine tailing ponds can pose a serious environmental threat. Groundwater quality in a semi-arid region with extensive worries about the leakage from one of world's largest tailing ponds is studied herein through an integrated hydrogeochemical analysis and multivariate statistical analysis. Results show that elevated concentrations of NO{sub 2}{sup −}, B, Mn, NH{sub 4}{sup +}, F{sup −}, and SO{sub 4}{sup 2−} in groundwater were probably caused by leakage from the tailing pond and transported with the regional groundwater flow towards downstream Yellow River. While NO{sub 2}{sup −} contamination is only limited to areas close to the pond, high B concentrations persist within the contaminated plume originating from the tailing pond. Our current study shows that there is no geochemical evidence for U and Th contamination in groundwater due to leakage from the Bayan Obo tailing pond. Combining effects which includes regional variations, pond leaking and downstream mixing, mineral precipitation and dissolution, redox processes, ion exchange processes and agricultural activities, controlled groundwater hydrogeochemical signatures in the studied area. This study demonstrate that an increase in knowledge of evolution of groundwater quality by integrating field hydrochemical data and multivariate statistical analysis will help understand major water–rock interactions and provide a scientific basis for protection and rational utilization of groundwater resources in this and other tailing-impacted areas. - Highlights: • Combining hydrogeochemical methods and multivariate statistical analysis. • First reporting geochemical processes in aquifers nearby Bayan Obo REE tailing pond. • No geochemical evidence for uranium and thorium contamination in shallow groundwater.

Effect of Domestic Waste Leachates on Quality Parameters of Groundwater

Directory of Open Access Journals (Sweden)

John Jiya MUSA

2014-02-01

Full Text Available Water is an elixir of life. Percolating groundwater provides a medium through which wastes particularly organics can undergo degradation into simpler substances through biochemical reactions involving dissolution, hydrolysis, oxidation and reduction processes. Ground water samples in and around dumpsite and landfills located in Kubuwa were studied to assess the effect of wastewater leachates on groundwater resources in the particular area. Groundwater samples were collected from 5 different bore-wells in and around relative distances from dumpsites. EC values ranged between 30 and 138 µS/cm, TDS ranged between 95 mg/L and 120 mg/L, SS ranged between 10 and 23 mg/L while that of the evening ranged between 11 and 15 mg/L, nitrate values ranged between 0.18 to 0.80 mg/L for the early morning samples while the late evening samples which ranged between 0.25 and 0.43 mg/L, while concentration of Sulphate in the morning water sample ranged between 168 and 213 mg/L while that of the evening ranged between 20 and 45 mg/L. The government of the Federal Republic of Nigeria should create landfills and dumpsites far away from residential homes and better still recycling plants should be put in place to recycle the various forms of waste products from homes.

In vivo in vitro correlations for a poorly soluble drug, danazol, using the flow-through dissolution method with biorelevant dissolution media

DEFF Research Database (Denmark)

Sunesen, Vibeke Hougaard; Pedersen, Betty Lomstein; Kristensen, Henning Gjelstrup

2005-01-01

The purpose of the study was to design dissolution tests that were able to distinguish between the behaviour of danazol under fasted and fed conditions, by using biorelevant media. In vitro dissolution of 100mg danazol capsules was performed using the flow-through dissolution method. Flow rates w...

Dissolution of FFTF vendor fuel

International Nuclear Information System (INIS)

Lerch, R.E.

1979-08-01

Dissolution experiments were performed on FFTF vendor fuel (both mechanically mixed and coprecipitated) during 1974, 1975, and 1976. A marked improvement was noted in the completeness of fuel dissolution from 1974 to 1976. The reason for this is unknown but may have been attributable to slight changes in fuel fabrication conditions. In general, the bulk of the fuel pellets tested dissolved to greater than 99.9% in nitric acid alone

Dissolution of FFTF vendor fuel

Energy Technology Data Exchange (ETDEWEB)

Lerch, R.E.

1979-08-01

Dissolution experiments were performed on FFTF vendor fuel (both mechanically mixed and coprecipitated) during 1974, 1975, and 1976. A marked improvement was noted in the completeness of fuel dissolution from 1974 to 1976. The reason for this is unknown but may have been attributable to slight changes in fuel fabrication conditions. In general, the bulk of the fuel pellets tested dissolved to greater than 99.9% in nitric acid alone.

Hydrogeochemistry of the groundwater in the Tarkwa area, Wasa west District of Ghana

International Nuclear Information System (INIS)

Yankey, R. K.

2008-06-01

The pH of the groundwater is acidic (4.3-6.7) and acidification of the groundwater is principally due to natural biogeochemical processes. Three main water types were delineated: Na-Cl (31.3%), Ca-Mg-HCO 3 (62.5%) and mixed type (6.3%) Major cation and anion concentrations dominance pattern observed in this study were generally in the order of Na > Ca > Mg > K and HCO 3 > CI > SO 4 and indicated partial cationic and anionic characteristics of fresh water. The chemistry of groundwater is controlled by mineral weathering, ion exchange and to some extent precipitation. Iron and manganese were the predominant trace elements in the groundwater and contributed substantially (93.1 %) to the metal load of the groundwater. The pollution index (HPI) for the groundwater came out to be 9.82; which is far below the critical value of 100 indicating that the groundwater is not critically contaminated. The anthropogenic influence on the groundwater is at present minimal. Water quality is good for the majority of the groundwater samples as the majority of samples were within the permissible drinking limits of World Health Organization (WHO, 1998). However the pH of the groundwater was disturbingly low. (au)

Towards sustainable groundwater management in Karst aquifers in semi-arid environments: Central West Bank, Palestine

Science.gov (United States)

Jebreen, H.; Banning, A.; Wohnlich, S.

2017-12-01

The Central West Bank (CWB) is characterized by karstified carbonate aquifers in the semiarid climate zone, where groundwater resources are frequently threatened by overexploitation and pollution. Despite often limited system knowledge, quantitative and qualitative factors such as groundwater recharge rate, aquifer parameters, flow and transport dynamics, anthropogenic impacts, and groundwater vulnerability need to be assessed. Therefore, sustainable groundwater use in the CWB is of critical importance. In the present study, we explore the scale of the groundwater problems in CWB as well as the possibility of sustainable management through different scenarios: 1) Managed aquifer recharge using a water balance model, stable isotopes (2H & 18O) and chloride mass balance, 2) Geochemical evolution and renewability of groundwater, and 3) Anthropogenic impacts. A total of 20 spring water samples were collected and analyzed for pH, electrical conductivity, total dissolved solids (TDS), hardness, major-ion chemistry (Cl-, HCO3-, SO42-, Na+, K+, Ca2+ and Mg2+), trace elements (Li, Be, Al, Ba, Tl, Pb, Bi, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Ga, Rb, Sr, Mo, Ag and Cd), microbiological data (total and fecal coliforms bacteria), and stable isotopes (2H & 18O). The results show a spatialized recharge rate, which ranges from 111-211 mm/year, representing 17-33 % of the long-term mean annual rainfall. The mean annual actual evapotranspiration was about 19-37 % of precipitation. The chemical composition of groundwater of the study area is strongly influenced by rock-water interaction, dissolution and deposition of carbonate and silicate minerals. Stable isotopes show that precipitation is the source of recharge to the groundwater system. All analyzed spring waters are suitable for irrigation but not for drinking purposes. This studýs results can serve as a basis for decision makers, and will lead to an increased understanding of the sustainable management of the Central West Bank

DISSOLUTION OF IRRADIATED MURR FUEL ASSEMBLIES

Energy Technology Data Exchange (ETDEWEB)

Kyser, E.

2010-06-17

A literature survey on the dissolution of spent nuclear fuel from the University of Missouri Research Reactor (MURR) has been performed. This survey encompassed both internal and external literature sources for the dissolution of aluminum-clad uranium alloy fuels. The most limiting aspect of dissolution in the current facility configuration involves issues related to the control of the flammability of the off-gas from this process. The primary conclusion of this work is that based on past dissolution of this fuel in H-Canyon, four bundles of this fuel (initial charge) may be safely dissolved in a nitric acid flowsheet catalyzed with 0.002 M mercuric nitrate using a 40 scfm purge to control off-gas flammability. The initial charge may be followed by a second charge of up to five bundles to the same dissolver batch depending on volume and concentration constraints. The safety of this flowsheet relies on composite lower flammability limits (LFL) estimated from prior literature, pilot-scale work on the dissolution of site fuels, and the proposed processing flowsheet. Equipment modifications or improved LFL data offer the potential for improved processing rates. The fuel charging sequence, as well as the acid and catalyst concentrations, will control the dissolution rate during the initial portion of the cycle. These parameters directly impact the hydrogen and off-gas generation and, along with the purge flowrate determine the number of bundles that may be charged. The calculation approach within provides Engineering a means to determine optimal charging patterns. Downstream processing of this material should be similar to that of recent processing of site fuels requiring only minor adjustments of the existing flowsheet parameters.

The combined use of 87Sr/86Sr and carbon and water isotopes to study the hydrochemical interaction between groundwater and lakewater in mantled karst

Science.gov (United States)

Katz, Brian G.; Bullen, Thomas D.

1996-12-01

The hydrochemical interaction between groundwater and lakewater influences the composition of water that percolates downward from the surficial aquifer system through the underlying intermediate confining unit and recharges the Upper Floridan aquifer along highlands in Florida. The 87Sr/86Sr ratio along with the stable isotopes, D, 18O, and 13C were used as tracers to study the interaction between groundwater, lakewater, and aquifer minerals near Lake Barco, a seepage lake in the mantled karst terrane of northern Florida. Upgradient from the lake, the 87Sr/86Sr ratio of groundwater decreases with depth (mean values of 0.71004, 0.70890, and 0.70852 for water from the surficial aquifer system, intermediate confining unit, and Upper Floridan aquifer, respectively), resulting from the interaction of dilute oxygenated recharge water with aquifer minerals that are less radiogenic with depth. The concentrations of Sr2+ generally increase with depth, and higher concentrations of Sr2+ in water from the Upper Floridan aquifer (20-35 μg/L), relative to water from the surficial aquifer system and the intermediate confining unit, result from the dissolution of Sr-bearing calcite and dolomite in the Eocene limestone. Dissolution of calcite [δ13C= -1.6permil(‰)] is also indicated by an enriched δ13CDIC(-8.8 to -11.4 ‰) in water from the Upper Floridan aquifer, relative to the overlying hydrogeologic units (δ13CDICaquifer material become less radiogenic and the Sr2+ concentrations generally increase with depth. However, Sr2+ concentrations are substantially less than in upgradient groundwaters at similar depths. The lower Sr2+ concentrations result from the influence of anoxic lakewater leakage on the mobility of Sr2+ from clays. Based on results from mass-balance modeling, it is probable that cation exchange plays the dominant role in controlling the 87Sr/86Sr ratio of groundwater, both upgradient and downgradient from Lake Barco. Even though groundwater from the three

Hydrogeochemical and Isotopic Studies of Groundwater in the Central Region of Ghana

Energy Technology Data Exchange (ETDEWEB)

Ganyaglo, S. Y.; Osae, S.; Fianko, J.R., E-mail: sganyaglo@yahoo.co.uk [National Nuclear Research Institute, Ghana Atomic Energy Commission and School of Nuclear Allied Sciences, University of Ghana, Legon-Accra (Ghana); Gibrilla, A.; Bam, E. [National Nuclear Research Institute, Ghana Atomic Energy Commission, Legon-Accra (Ghana)

2013-07-15

The hydrogeochemical and isotopic evolution of groundwater in the Central Region of Ghana has been studied in order to examine how hydrogeochemical processes control the overall groundwater chemistry in the study area. Two major hydrochemical facies have been identified as the Na-Cl and NaHCO{sub 3} water types. The Na/Cl molar ratio indicates that silicate weathering is one of the major hydrogeochemical processes controlling groundwater water chemistry in the area. This is further confirmed by a plot of TDS against the Na/Na+Ca ratio. The Br/Cl ratio ranges from 0.00148 to 0.7087, suggesting minimal seawater intrusion in the area. Stable isotope values of the groundwater samples ({sup 18}O and {sup 2}H) are found around the global meteoric water line (GMWL), suggesting a direct infiltration of rainwater into the groundwater system. Elevated Cl- concentrations of the groundwater is probably due to sea spray and marine aerosols deposited on the top soil, though further studies are needed to determine the cause. (author)

Dissolution of ion exchange resin by hydrogen peroxide

International Nuclear Information System (INIS)

Lee, S.C.

1981-08-01

The resin dissolution process was conducted successfully in full-scale equipment at the SRL Semiworks. A solution containing 0.001M Fe 2+ , or Fe 3+ , and 3 vol % H 2 O 2 in 0.1M HNO 3 is sufficient to dissolve up to 40 vol % resin slurry (Dowex 50W-X8). Foaming and pressurization can be eliminated by maintaining the dissolution temperature below 99 0 C. The recommended dissolution temperature range is 85 to 90 0 C. Premixing hydrogen peroxide with all reactants will not create a safety hazard, but operating with a continual feed of hydrogen peroxide is recommended to control the dissolution rate. An air sparging rate of 1.0 to 1.5 scfm will provide sufficient mixing. Spent resin from chemical separation contains DTPA (diethylenetriaminepentaacetic acid) residue, and the resin must be washed with 0.1M NH 4 OH to remove excess DTPA before dissolution. Gamma irradiation of resin up to 4 kW-hr/L did not change the dissolution rate significantly

Dissolution of mixed oxide spent fuel from FBR

International Nuclear Information System (INIS)

Sanyoshi, H.; Nishina, H.; Toyota, O.; Yamamoto, R.; Nemoto, S.; Okamoto, F.; Togashi, A.; Kawata, T.; Hayashi, S.

1991-01-01

At the Tokai Works of the Power Reactor and Nuclear Fuel Development Corporation (PNC), the Chemical Processing Facility (CPF) has been continuing operation since 1982 for laboratory scale hot experiments on reprocessing of FBR mixed oxide fuel. As a part of these experiments, dissolution experiments have been performed to define the key parameters affecting dissolution rates such as concentration of nitric acid, temperature and burnup and also to confirm the amount of insoluble residue. The dissolution rate of the irradiated fuel was determined to be in proportion to the 1.7 power of the nitric acid concentration. The activation energy determined from the experiments varied from 6 to 11 kcal/mol depending on the method of dissolution. The dissolution rate decreased as the fuel burnup increased in low nitric acid media below 5 mol/l. However, it was found that the effect of the burnup became negligible in a high concentration of nitric acid media. The amount of insoluble residue and its constituents were evaluated by changing the dissolution condition. (author)

Mathematical methods for quantification and comparison of dissolution testing data.

Science.gov (United States)

Vranić, Edina; Mehmedagić, Aida; Hadzović, Sabira

2002-12-01

In recent years, drug release/dissolution from solid dosage forms has been the subject of intense and profitable scientific developments. Whenever a new solid dosage form is developed or produced, it is necessary to ensure that drug dissolution occurs in an appropriate manner. The pharmaceutical industry and the registration authorities do focus, nowadays, on drug dissolution studies. The quantitative analysis of the values obtained in dissolution/release tests is easier when mathematical formulas that express the dissolution results as a function of some of the dosage forms characteristics are used. This work discusses the analysis of data obtained for dissolution profiles under different media pH conditions using mathematical methods of analysis described by Moore and Flanner. These authors have described difference factor (f1) and similarity factor (f2), which can be used to characterise drug dissolution/release profiles. In this work we have used these formulas for evaluation of dissolution profiles of the conventional tablets in different pH of dissolution medium (range of physiological variations).

Dissimilatory Arsenate Reduction and In Situ Microbial Activities and Diversity in Arsenic-rich Groundwater of Chianan Plain, Southwestern Taiwan.

Science.gov (United States)

Das, Suvendu; Liu, Chia-Chuan; Jean, Jiin-Shuh; Liu, Tsunglin

2016-02-01

Although dissimilatory arsenic reduction (DAsR) has been recognized as an important process for groundwater arsenic (As) enrichment, its characterization and association with in situ microbial activities and diversity in As-rich groundwater is barely studied. In this work, we collected As-rich groundwater at depths of 23, 300, and 313 m, respectively, from Yenshui-3, Budai-Shinwen, and Budai-4 of Chianan plain, southwestern Taiwan, and conducted incubation experiments using different electron donors, acceptors, and sulfate-reducing bacterial inhibitor (tungstate) to characterize DAsR. Moreover, bacterial diversity was evaluated using 454-pyrosequencing targeting bacterial 16S rRNAs. MPN technique was used to enumerate microorganisms with different in situ metabolic functions. The results revealed that DAsR in groundwater of Chianan plain was a biotic phenomenon (as DAsR was totally inhibited by filter sterilization), enhanced by the type of electron donor (in this case, lactate enhanced DAsR but acetate and succinate did not), and limited by the availability of arsenate. In addition to oxidative recycling of As(III), dissolution of As(V)-saturated manganese and iron minerals by indigenous dissimilatory Mn(IV)- and Fe(III)-reducing bacteria, and abiotic oxidation of As(III) with Mn(IV) regenerated As(V) in the groundwater. Sulfate-respiring bacteria contributed 7.4 and 28.2 % to the observed DAsR in groundwater of Yinshui-3 and Budai-Shinwen, respectively, whereas their contribution was negligible in groundwater of Budai-4. A noticeable variation in dominant genera Acinetobacter and Bacillus was observed within the groundwater. Firmicutes dominated in highly As-rich groundwater of Yenshui-3, whereas Proteobacteria dominated in comparatively less As-rich groundwater of Budai-Shinwen and Budai 4.

Oxidation and dissolution of UO{sub 2} in bicarbonate media: Implications for the spent nuclear fuel oxidative dissolution mechanism

Energy Technology Data Exchange (ETDEWEB)

Gimenez, J. [Department of Chemical Engineering, Universitat Politecnica de Catalunya, Diagonal 647, 08028 Barcelona (Spain)]. E-mail: francisco.javier.gimenez@upc.edu; Clarens, F. [Department of Chemical Engineering, Universitat Politecnica de Catalunya, Diagonal 647, 08028 Barcelona (Spain); Casas, I. [Department of Chemical Engineering, Universitat Politecnica de Catalunya, Diagonal 647, 08028 Barcelona (Spain); Rovira, M. [CTM Centre Tecnologic, Avda. Bases de Manresa 1. 08240 Manresa (Spain); Pablo, J. de [Department of Chemical Engineering, Universitat Politecnica de Catalunya, Diagonal 647, 08028 Barcelona (Spain); Bruno, J. [Enresa-Enviros Environmental Science and Waste Management Chair, UPC, Jordi Girona 1-3 B2, 08034 Barcelona (Spain)

2005-10-15

The objective of this work is to study the UO{sub 2} oxidation by O{sub 2} and dissolution in bicarbonate media and to extrapolate the results obtained to improve the knowledge of the oxidative dissolution of spent nuclear fuel. The results obtained show that in the studied range the oxygen consumption rate is independent on the bicarbonate concentration while the UO{sub 2} dissolution rate does depend on. Besides, at 10{sup -4} mol dm{sup -3} bicarbonate concentration, the oxygen consumption rate is almost two orders of magnitude higher than the UO{sub 2} dissolution rate. These results suggest that at low bicarbonate concentration (<10{sup -2} mol dm{sup -3}) the alteration of the spent nuclear fuel cannot be directly derived from the measured uranium concentrations in solution. On the other hand, the study at low bicarbonate concentrations of the evolution of the UO{sub 2} surface at nanometric scale by means of the SFM technique shows that the difference between oxidation and dissolution rates is not due to the precipitation of a secondary solid phase on UO{sub 2}.

Frogging It: A poetic Analysis of Relationship Dissolution

Directory of Open Access Journals (Sweden)

Sandra L. Faulkner

2012-10-01

Full Text Available Often, themes in work and life intertwine; the author recognized that a cadre of poems she had written during the past several years were about relationship dissolution. The poems concerned romantic and friendship dissolution and the aspects of identity creation and loss this entails. The author presents the poems and makes an explicit connection to interpersonal relationship dissolution literature through the technique of poetic analysis. This analysis serves as an exemplar for how poetry as performative writing offers a valuable addition to interpersonal communication research through the poeticizing of relational dissolution as an everyday relational challenge.

Assessment of seawater intrusion and nitrate contamination on the groundwater quality in the Korba coastal plain of Cap-Bon (North-east of Tunisia)

Science.gov (United States)

Zghibi, Adel; Tarhouni, Jamila; Zouhri, Lahcen

2013-11-01

In recent years, seawater intrusion and nitrate contamination of groundwater have become a growing concern for people in rural areas in Tunisia where groundwater is always used as drinking water. The coastal plain of Korba (north-east of Tunisia) is a typical area where the contamination of the aquifer in the form of saltwater intrusion and high nitrate concentrations is very developed and represents the major consequence of human activities. The objective of this study is to evaluate groundwater resource level, to determine groundwater quality and to assess the risk of NO3- pollution in groundwater using hydrogeochemical tools. Groundwater were sampled and analyzed for physic-chemical parameters: Ca2+, Mg2+, Na+, K+, Cl-, SO42-, HCO3-, NO3-, Total Dissolved Solid and of the physical parameters (pH, electrical conductivity and the temperature). The interpretation of the analytical results is shown numerically and graphically through the ionic deviations, Piper Diagram, seawater fractions and binary diagrams. Moreover, electrical conductivity investigations have been used to identify the location of the major intrusion plumes in this coastal area and to obtain new information on the spatial scales and dynamics of the fresh water-seawater interface. Those processes can be used as indicators of seawater intrusion progression. First, the hydrogeochemical investigation of this aquifer reveals the major sources of contamination, represented by seawater intrusion. Thus, the intensive extraction of groundwater from aquifer reduces freshwater outflow to the sea, creates several drawdown cones and lowering of the water table to as much as 12 m below mean sea level in the center part of the study area especially between Diarr El Hojjej and Tafelloun villages, causing seawater migration inland and rising toward the wells. Moreover, the results of this study revealed the presence of direct cation exchange linked to seawater intrusion and dissolution processes associated with

Uranium carbide dissolution in nitric solution: Sonication vs. silent conditions

International Nuclear Information System (INIS)

Virot, Matthieu; Szenknect, Stéphanie; Chave, Tony; Dacheux, Nicolas; Moisy, Philippe; Nikitenko, Sergey I.

2013-01-01

The dissolution of uranium carbide (UC) in nitric acid media is considered by means of power ultrasound (sonication) or magnetic stirring. The induction period required to initiate UC dissolution was found to be dramatically shortened when sonicating a 3 M nitric solution (Ar, 20 kHz, 18 W cm −2 , 20 °C). At higher acidity, magnetic stirring offers faster dissolution kinetics compared to sonication. Ultrasound-assisted UC dissolution is found to be passivated after ∼60% dissolution and remains incomplete whatever the acidity which is confirmed by ICP–AES, LECO and SEM–EDX analyses. In general, the kinetics of UC dissolution is linked to the in situ generation of nitrous acid in agreement with the general mechanism of UC dissolution; the nitrous acid formation is reported to be faster under ultrasound at low acidity due to the nitric acid sonolysis. The carbon balance shared between the gaseous, liquid, and solid phases is strongly influenced by the applied dissolution procedure and HNO 3 concentration

Uranium carbide dissolution in nitric solution: Sonication vs. silent conditions

Science.gov (United States)

Virot, Matthieu; Szenknect, Stéphanie; Chave, Tony; Dacheux, Nicolas; Moisy, Philippe; Nikitenko, Sergey I.

2013-10-01

The dissolution of uranium carbide (UC) in nitric acid media is considered by means of power ultrasound (sonication) or magnetic stirring. The induction period required to initiate UC dissolution was found to be dramatically shortened when sonicating a 3 M nitric solution (Ar, 20 kHz, 18 W cm-2, 20 °C). At higher acidity, magnetic stirring offers faster dissolution kinetics compared to sonication. Ultrasound-assisted UC dissolution is found to be passivated after ∼60% dissolution and remains incomplete whatever the acidity which is confirmed by ICP-AES, LECO and SEM-EDX analyses. In general, the kinetics of UC dissolution is linked to the in situ generation of nitrous acid in agreement with the general mechanism of UC dissolution; the nitrous acid formation is reported to be faster under ultrasound at low acidity due to the nitric acid sonolysis. The carbon balance shared between the gaseous, liquid, and solid phases is strongly influenced by the applied dissolution procedure and HNO3 concentration.

In vitro Dissolution Studies on Solid Dispersions of Mefenamic Acid.

Science.gov (United States)

Rao, K R S Sambasiva; Nagabhushanam, M V; Chowdary, K P R

2011-03-01

Solid dispersions of mefanamic acid with a water-soluble polymer polyvinyl pyrrolidine and a super disintegrant, primojel were prepared by common solvent and solvent evaporation methods employing methanol as the solvent. The dissolution rate and dissolution efficiency of the prepared solid dispersions were evaluated in comparison to the corresponding pure drug. Solid dispersions of mefenamic acid showed a marked enhancement in dissolution rate and dissolution efficiency. At 1:4 ratio of mefenamic acid-primojel a 2.61 fold increase in the dissolution rate of mefenamic acid was observed with solid dispersion. The solid dispersions in combined carriers gave much higher rates of dissolution than super disintegrants alone. Mefanamic acid-primojel-polyvinyl pyrrolidine (1:3.2:0.8) solid dispersion gave a 4.11 fold increase in the dissolution rate of mefenamic acid. Super disintegrants alone or in combination with polyvinyl pyrrolidine could be used to enhance the dissolution rate of mefenamic acid.

User's guide to PROTOCOL, a numerical simulator for the dissolution reactions of inorganic solids in aqueous solutions

International Nuclear Information System (INIS)

Pickrell, G.; Jackson, D.D.

1984-10-01

This report provides a user's manual for PROTOCOL, a comprehensive coupled kinetic/equilibrium computer program for analyzing the dissolution reactions of solids with aqueous solutions, specifically applied to the potential corrosion of vitrified nuclear waste by groundwater. The capabilities and available options are summarized as well as instructions for setting up and running problems. Also described in this report and included in the PROTOCOL software package are MASTER, a master file of species thermodynamic data, MANEQL, a preprocessor program and POSTP, a postprocessor. POSTP provides offline plotting using the CRAY-1 DISSPLA 9.0 graphics library. PROTOCOL is operational on the CDC-7600 and CRAY-1 computers at the Lawrence Livermore National Laboratory. 7 references, 10 figures, 2 tables

Assessment of hydro-geochemistry and groundwater quality of Rajshahi City in Bangladesh

Science.gov (United States)

Mostafa, M. G.; Uddin, S. M. Helal; Haque, A. B. M. H.

2017-12-01

The study was carried out to understand the hydro-geochemistry and ground water quality in the Rajshahi City of Bangladesh. A total of 240 groundwater samples were collected in 2 years, i.e., 2009 and 2010 covering the pre-monsoon, monsoon and post-monsoon seasons. Aquifer soil samples were collected from 30 locations during the monsoon in 2000. All the samples were analyzed for various physicochemical parameters according to standard methods of analysis, these includes pH, electrical conductivity, total dissolved solids, total hardness, and total alkalinity, major cations such as Na+, K+, Ca2+, Mg2+, and Fe2+, major anions such as HCO3 -, NO3 -, Cl-, and SO4 2- and heavy metals such as Mn, Zn, Cu, As, Cd and Pb. The results illustrated that the groundwater was slightly acidic to neutral in nature, total hardness observed in all samples fall under the hard to a very hard category. The bicarbonate and calcium concentration in the groundwater exceeded the permissible limits may be due to the dissolution of calcite. The concentration of calcium, iron, manganese, arsenic and lead were far above the permissible limit in most of the shallow tube well samples. The study found that the major hydrochemical facies was identified to be calcium-bicarbonate-type (CaHCO3). A higher concentration of metals including Fe, Mn, As and Pb was found indicating various health hazards. The rock-water interaction was the major geochemical process controlling the chemistry of groundwater in the study area. The study results revealed that the quality of the groundwater in Rajshahi City area was of great concern and not suitable for human consumption without adequate treatment.

TANK 12 SLUDGE CHARACTERIZATION AND ALUMINUM DISSOLUTION DEMONSTRATION

International Nuclear Information System (INIS)

Reboul, S.; Hay, Michael; Zeigler, Kristine; Stone, Michael

2009-01-01

A 3-L sludge slurry sample from Tank 12 was characterized and then processed through an aluminum dissolution demonstration. The dominant constituent of the sludge was found to be aluminum in the form of boehmite. The iron content was minor, about one-tenth that of the aluminum. The salt content of the supernatant was relatively high, with a sodium concentration of ∼7 M. Due to these characteristics, the yield stress and plastic viscosity of the unprocessed slurry were relatively high (19 Pa and 27 cP), and the settling rate of the sludge was relatively low (∼20% settling over a two and a half week period). Prior to performing aluminum dissolution, plutonium and gadolinium were added to the slurry to simulate receipt of plutonium waste from H-Canyon. Aluminum dissolution was performed over a 26 day period at a temperature of 65 C. Approximately 60% of the insoluble aluminum dissolved during the demonstration, with the rate of dissolution slowing significantly by the end of the demonstration period. In contrast, approximately 20% of the plutonium and less than 1% of the gadolinium partitioned to the liquid phase. However, about a third of the liquid phase plutonium became solubilized prior to the dissolution period, when the H-Canyon plutonium/gadolinium simulant was added to the Tank 12 slurry. Quantification of iron dissolution was less clear, but appeared to be on the order of 1% based on the majority of data (a minor portion of the data suggested iron dissolution could be as high as 10%). The yield stress of the post-dissolution slurry (2.5 Pa) was an order of magnitude lower than the initial slurry, due most likely to the reduced insoluble solids content caused by aluminum dissolution. In contrast, the plastic viscosity remained unchanged (27 cP). The settling rate of the post-dissolution slurry was higher than the initial slurry, but still relatively low compared to settling of typical high iron content/low salt content sludges. Approximately 40% of the

Groundwater and underground coal gasification in Alberta

International Nuclear Information System (INIS)

Haluszka, A.; MacMillan, G.; Maev, S.

2010-01-01

Underground coal gasification has potential in Alberta. This presentation provided background information on underground coal gasification and discussed groundwater and the Laurus Energy demonstration project. A multi-disciplined approach to project assessment was described with particular reference to geologic and hydrogeologic setting; geologic mapping; and a hydrogeologic numerical model. Underground coal gasification involves the conversion of coal into synthesis gas or syngas. It can be applied to mined coal at the surface or applied to non-mined coal seams using injection and production wells. Underground coal gasification can effect groundwater as the rate of water influx into the coal seams influences the quality and composition of the syngas. Byproducts created include heat as well as water with dissolved concentrations of ammonia, phenols, salts, polyaromatic hydrocarbons, and liquid organic products from the pyrolysis of coal. A process overview of underground coal gasification was also illustrated. It was concluded that underground coal gasification has the potential in Alberta and risks to groundwater could be minimized by a properly designed project. refs., figs.

34S and 18O in dissolved sulfate as tracers of hydrogeochemical evolution of the Triassic carbonate aquifer exposed to intense groundwater exploitation (Olkusz-Zawiercie region, southern Poland)

International Nuclear Information System (INIS)

Samborska, Katarzyna; Halas, Stanislaw

2010-01-01

Research highlights: → Groundwater table rebound in aquifer containing sulfide ore. → Degradation of water quality causes by the significant increase in sulfate concentrations. → Isotopic examinations of sulfate and sulfate concentrations along flow path. → Sulfate concentrations as a result of binary mixing of sources (sulfide and evaporate). → Changes in isotopic composition of sulfide in extended vadose zone. - Abstract: The objective of this study was to determine the sources of SO 4 2- in groundwater of the Olkusz-Zawiercie Major Groundwater Body. The quality of groundwater was relatively good in the past, but fluctuations of the water table level have caused degradation of water quality. Variations in the water table level and the formation of the depression cone have resulted from both groundwater withdrawal and Zn-Pb mine dewatering. As a result within the extended vadose zone of the aquifer, weathering of pyrite and accompanying sulfides has taken place. Since 1992 the water table has risen and this process has been associated with an increase in concentrations of SO 4 2- , Ca and Mg. At the same time, the pH has decreased and periodically high Fe concentrations have been detected. High concentrations of Mg and Sr have been observed and, since gypsum layers are known to be present, a de-dolomitisation process has been hypothesized. The PHREEQC program for Windows was used to estimate saturation indices for calcite, dolomite, gypsum and epsomite. Isotopic data for SO 4 2- dissolved in the groundwater and archival data on isotopic composition of ore sulfides were used to solve the isotope balance equation and to estimate the fraction of dissolved SO 4 2- that originated from pyrite oxidation and gypsum dissolution. The results have shown that dissolution of pyrite oxidation products has a significant influence on chemical composition of groundwater, especially in the southern part of the cone of depression. By solving the additional, combined mass

Natural spatial and temporal variations in groundwater chemistry in fractured, sedimentary rocks: scale and implications for solute transport

International Nuclear Information System (INIS)

Hoven, Stephen J. van der; Kip Solomon, D.; Moline, Gerilynn R.

2005-01-01

Natural tracers (major ions, δ 18 O, and O 2 ) were monitored to evaluate groundwater flow and transport to a depth of 20 m below the surface in fractured sedimentary (primarily shale and limestone) rocks. Large temporal variations in these tracers were noted in the soil zone and the saprolite, and are driven primarily by individual storm events. During nonstorm periods, an upward flow brings water with high TDS, constant δ 18 O, and low dissolved O 2 to the water table. During storm events, low TDS, variable δ 18 O, and high dissolved O 2 water recharges through the unsaturated zone. These oscillating signals are rapidly transmitted along fracture pathways in the saprolite, with changes occurring on spatial scales of several meters and on a time scale of hours. The variations decreased markedly below the boundary between the saprolite and less weathered bedrock. Variations in the bedrock units occurred on time scales of days and spatial scales of at least 20 m. The oscillations of chemical conditions in the shallow groundwater are hypothesized to have significant implications for solute transport. Solutes and colloids that adsorb onto aquifer solids can be released into solution by decreases in ionic strength and pH. The decreases in ionic strength also cause thermodynamic undersaturation of the groundwater with respect to some mineral species and may result in mineral dissolution. Redox conditions are also changing and may result in mineral dissolution/precipitation. The net result of these chemical variations is episodic transport of a wide range of dissolved solutes or suspended particles, a phenomenon rarely considered in contaminant transport studies

Dissolution behaviour of silicon nitride coatings for joint replacements

Energy Technology Data Exchange (ETDEWEB)

Pettersson, Maria [Materials in Medicine Group, Div. of Applied Materials Science, Dept. of Engineering Sciences, Uppsala University, Uppsala (Sweden); Bryant, Michael [Institute of Functional Surfaces (iFS), School of Mechanical Engineering, University of Leeds, Leeds (United Kingdom); Schmidt, Susann [Thin Film Physics, Department of Physics, Chemistry and Biology (IFM), Linköping University, Linköping (Sweden); Engqvist, Håkan [Materials in Medicine Group, Div. of Applied Materials Science, Dept. of Engineering Sciences, Uppsala University, Uppsala (Sweden); Hall, Richard M. [Institute of Medical and Biological Engineering (iMBE), School of Mechanical Engineering, University of Leeds, Leeds (United Kingdom); Neville, Anne [Institute of Functional Surfaces (iFS), School of Mechanical Engineering, University of Leeds, Leeds (United Kingdom); Persson, Cecilia, E-mail: cecilia.persson@angstrom.uu.se [Materials in Medicine Group, Div. of Applied Materials Science, Dept. of Engineering Sciences, Uppsala University, Uppsala (Sweden)

2016-05-01

In this study, the dissolution rate of SiN{sub x} coatings was investigated as a function of coating composition, in comparison to a cobalt chromium molybdenum alloy (CoCrMo) reference. SiN{sub x} coatings with N/Si ratios of 0.3, 0.8 and 1.1 were investigated. Electrochemical measurements were complemented with solution (inductively coupled plasma techniques) and surface analysis (vertical scanning interferometry and x-ray photoelectron spectroscopy). The dissolution rate of the SiN{sub x} coatings was evaluated to 0.2–1.4 nm/day, with a trend of lower dissolution rate with higher N/Si atomic ratio in the coating. The dissolution rates of the coatings were similar to or lower than that of CoCrMo (0.7–1.2 nm/day). The highest nitrogen containing coating showed mainly Si–N bonds in the bulk as well as at the surface and in the dissolution area. The lower nitrogen containing coatings showed Si–N and/or Si–Si bonds in the bulk and an increased formation of Si–O bonds at the surface as well as in the dissolution area. The SiN{sub x} coatings reduced the metal ion release from the substrate. The possibility to tune the dissolution rate and the ability to prevent release of metal ions encourage further studies on SiN{sub x} coatings for joint replacements. - Graphical abstract: Dissolution rates of SiN{sub 0.3}, SiN{sub 0.8}, and SiN{sub 1.1} coatings on CoCrMo compared to uncoated CoCrMo. Dissolution rates were obtained from i) electrochemical measurements of I{sub corr}, ii) the step height between covered and solution-exposed surfaces, measured using VSI, and iii) the ion concentration in the solution, measured with ICP. - Highlights: • The dissolution of SiN{sub x} coatings was investigated in comparison to (bulk) CoCrMo. • The coatings gave a lower or similar dissolution rate to CoCrMo, of 0.2–1.2 nm/day. • An increased nitrogen content in the coatings gave lower dissolution rates. • SiN{sub x} coatings on CoCrMo reduced the metal ion release

The application of parallel wells to support the use of groundwater for sustainable irrigation

Science.gov (United States)

Suhardi

2018-05-01

The use of groundwater as a source of irrigation is one alternative in meeting water needs of plants. Using groundwater for irrigation requires a high cost because of the discharge that can be taken is limited. In addition, the use of large groundwater can cause environmental damage and social conflict. To minimize costs, maintain quality of the environment and to prevent social conflicts, it is necessary to innovate in the groundwater taking system. The study was conducted with an innovation of using parallel wells. Performance is measured by comparing parallel wells with a single well. The results showed that the use of parallel wells to meet the water needs of rice plants and increase the pump discharge up to 100%. In addition, parallel wells can reduce the influence radius of taking of groundwater compared to single well so as to prevent social conflict. Thus, the use of parallel wells can support the achievement of the use of groundwater for sustainable irrigation.

Dissolution of nuclear fuels; Disolucion de combustibles Nucleares

Energy Technology Data Exchange (ETDEWEB)

Uriarte Hueda, A; Berberana Eizmendi, M; Rainey, R

1968-07-01

A laboratory study was made of the instantaneous dissolution rate (IDR) for unirradiated uranium metal rods and UO{sub 2}, PuO{sub 2} and PuO{sub 2}-UO{sub 2} pellets in boiling nitric acid alone and with additives. The uranium metal and UO{sub 2} dissolved readily in nitric acid alone; PuO{sub 2} dissolved slowly even with the addition of fluoride; PuO{sub 2}-UO{sub 2} pellets containing as much as 35% PuO{sub 2} in UO{sub 2} gave values of the instantaneous dissolution rate to indicate can be dissolved with nitric acid alone. An equation to calculate the time for complete dissolution has been determinate in function of the instantaneous dissolution rates. The calculated values agree with the experimental. Uranium dioxide pellets from various sources but all having a same density varied in instantaneous dissolution rate. All the pellets, however, have dissolved ved in the same time. The time for complete dissolution of PuO{sub 2}-UO{sub 2} pellets, having the same composition, and the concentration of the used reagents are function of the used reagents are function of the fabrication method. (Author) 8 refs.

Dissolution Model Development: Formulation Effects and Filter Complications

DEFF Research Database (Denmark)

Berthelsen, Ragna; Holm, Rene; Jacobsen, Jette

2016-01-01

This study describes various complications related to sample preparation (filtration) during development of a dissolution method intended to discriminate among different fenofibrate immediate-release formulations. Several dissolution apparatus and sample preparation techniques were tested. The fl....... With the tested drug–formulation combination, the best in vivo–in vitro correlation was found after filtration of the dissolution samples through 0.45-μm hydrophobic PTFE membrane filters....

Application of multivariate statistical technique for hydrogeochemical assessment of groundwater within the Lower Pra Basin, Ghana

Science.gov (United States)

Tay, C. K.; Hayford, E. K.; Hodgson, I. O. A.

2017-06-01

Multivariate statistical technique and hydrogeochemical approach were employed for groundwater assessment within the Lower Pra Basin. The main objective was to delineate the main processes that are responsible for the water chemistry and pollution of groundwater within the basin. Fifty-four (54) (No) boreholes were sampled in January 2012 for quality assessment. PCA using Varimax with Kaiser Normalization method of extraction for both rotated space and component matrix have been applied to the data. Results show that Spearman's correlation matrix of major ions revealed expected process-based relationships derived mainly from the geochemical processes, such as ion-exchange and silicate/aluminosilicate weathering within the aquifer. Three main principal components influence the water chemistry and pollution of groundwater within the basin. The three principal components have accounted for approximately 79% of the total variance in the hydrochemical data. Component 1 delineates the main natural processes (water-soil-rock interactions) through which groundwater within the basin acquires its chemical characteristics, Component 2 delineates the incongruent dissolution of silicate/aluminosilicates, while Component 3 delineates the prevalence of pollution principally from agricultural input as well as trace metal mobilization in groundwater within the basin. The loadings and score plots of the first two PCs show grouping pattern which indicates the strength of the mutual relation among the hydrochemical variables. In terms of proper management and development of groundwater within the basin, communities, where intense agriculture is taking place, should be monitored and protected from agricultural activities. especially where inorganic fertilizers are used by creating buffer zones. Monitoring of the water quality especially the water pH is recommended to ensure the acid neutralizing potential of groundwater within the basin thereby, curtailing further trace metal

Catalysed electrolytic metal oxide dissolution processes

International Nuclear Information System (INIS)

Machuron-Mandard, X.

1994-01-01

The hydrometallurgical processes designed for recovering valuable metals from mineral ores as well as industrial wastes usually require preliminary dissolution of inorganic compounds in aqueous media before extraction and purification steps. Unfortunately, most of the minerals concerned hardly or slowly dissolve in acidic or basic solutions. Metallic oxides, sulfides and silicates are among the materials most difficult to dissolve in aqueous solutions. They are also among the main minerals containing valuable metals. The redox properties of such materials sometimes permit to improve their dissolution by adding oxidizing or reducing species to the leaching solution, which leads to an increase in the dissolution rate. Moreover, limited amounts of redox promoters are required if the redox agent is regenerated continuously thanks to an electrochemical device. Nuclear applications of such concepts have been suggested since the dissolution of many actinide compounds (e.g., UO 2 , AmO 2 , PuC, PuN,...) is mainly based on redox reactions. In the 1980s, improvements of the plutonium dioxide dissolution process have been proposed on the basis of oxidation-reduction principles, which led a few years later to the design of industrial facilities (e.g., at Marcoule or at the french reprocessing plant of La Hague). General concepts and well-established results obtained in France at the Atomic Energy Commission (''Commissariat a l'Energie Atomique'') will be presented and will illustrate applications to industrial as well as analytical problems. (author)

Effect of pH on the dissolution kinetics of zero-valent iron in the presence of EDDHA and EDTA

International Nuclear Information System (INIS)

Lodge, Alexander M.; Pierce, Eric M.; Wellman, Dawn M.; Rodriguez, Elsa A.

2007-01-01

The effect of environmental factors (e.g., pH, solution composition, and temperature) that affect the longevity of Fe(0) barriers in the subsurface are difficult to quantify independently from changes that occur to the passivating layer. Therefore, to quantify the rate of Fe(0) dissolution under conditions which maintain the pO2 at a relatively constant level and minimize the formation of a passivating layer on the metal surface, a series of experiments have been conducted with the single-pass flow-through (SPFT) apparatus. These experiments were conducted over the pH range from 7.0 to 12.0 at 90 C in the presence of 5 mM EDDHA or 5 mM EDTA. The organic acids, EDDHA and EDTA, helped to maintain the aqueous Fe concentration below saturation with respect to Fe-bearing alteration phases and minimize the formation of a partially oxidized surface film. Results suggest the corrosion of Fe(0) is relatively insensitive to pH and the forward or maximum dissolution rate is 3 to 4 orders of magnitude higher than when a passive film and corrosion products are present

Effect of the mineral precipitation-dissolution at tunnel walls during the operational and post-operational phases

Energy Technology Data Exchange (ETDEWEB)

Domenech, Cristina; Arcos, David; Duro, Lara; Grandia, Fidel [Enviros Consul ting, Valldoreix, Barcelona (Spain)

2007-11-15

The extent of reversibility of the geochemical conditions disturbed during the construction and operational phases is of importance in order to assess the chemical evolution of the repository system. In this regard, it is essential to have a deep understanding of the chemical status of the repository system at closure in order to describe its immediate geochemical evolution beyond this point. This project assesses the dissolution and precipitation of minerals due to the interaction with groundwater in the deposition tunnel wall-rock during the operational phase (prior to tunnel backfilling) and during the saturation phase, also considering the effect on the backfill material. We have performed a 2D model in which a fracture intersecting the main tunnel has been considered. The project has been developed in two consecutive stages. The first stage simulates the precipitation and dissolution of minerals in the tunnel wall rock during the operational phase (100 years after excavation) when the tunnel is empty and filled with air. During this stage, water flows through fractures into the tunnel. The results of the model suggest that the interaction between groundwater, fracture-filling minerals, and atmospheric O{sub 2}(g) and CO{sub 2}(g) present in the tunnel leads to the precipitation of secondary minerals (calcite and iron(III) oxy-hydroxide) that do not significantly affect the porosity of the area surrounding the tunnel. The second stage starts after the operational phase, once the tunnel is backfilled, and simulates the interaction of groundwater with fracture-filling minerals and the backfill material. The model implemented assumes that the backfill is already water saturated and that water flows following the regional head gradient. Moreover, it also assumes that O2(g) is still present in the tunnel wall, as a result of the operational phase disturbances. The results show that oxygen will oxidise pyrite in the backfill and promote the precipitation of Fe

Etching of semiconductor cubic crystals: Determination of the dissolution slowness surfaces

Science.gov (United States)

Tellier, C. R.

1990-03-01

Equations of the representative surface of dissolution slowness for cubic crystals are determined in the framework of a tensorial approach of the orientation-dependent etching process. The independent dissolution constants are deduced from symmetry considerations. Using previous data on the chemical etching of germanium and gallium arsenide crystals, some possible polar diagrams of the dissolution slowness are proposed. A numerical and graphical simulation method is used to obtain the derived dissolution shapes. The influence of extrema in the dissolution slowness on the successive dissolution shapes is also examined. A graphical construction of limiting shapes of etched crystals appears possible using the tensorial representation of the dissolution slowness.

Effect of alteration phase formation on the glass dissolution rate

International Nuclear Information System (INIS)

Ebert, W.L.

1997-01-01

The dissolution rates of many glasses have been observed to increase upon the formation of certain alteration phases. While simulations have predicted the accelerating effect of formation of certain phases, the phases predicted to form in computer simulations are usually different than those observed to form in experiments. This is because kinetically favored phases form first in experiments, while simulations predict the thermodynamically favored phases. Static dissolution tests with crushed glass have been used to measure the glass dissolution rate after alteration phases form. Because glass dissolution rates are calculated on a per area basis, an important effect in tests conducted with crushed glass is the decrease in the surface area of glass that is available for reaction as the glass dissolves. This loss of surface area must be taken into account when calculating the dissolution rate. The phases that form and their effect on the dissolution rate are probably related to the glass composition. The impact of phase formation on the glass dissolution rate also varies according to the solubility products of the alteration phases and how the orthocilicic acid activity is affected. Insight into the relationship between the glass dissolution rate, solution chemistry and alteration phase formation is provided by the results of accelerated dissolution tests

Dissolution studies on Nickel ferrite in dilute chemical decontamination formulations

Energy Technology Data Exchange (ETDEWEB)

Ranganathan, S. [New Brunswick Univ., Fredericton, NB (Canada). Dept. of Chemical Engineering; Srinivasan, M.P. [Bhabha Atomic Research Centre (BARC) (India). Water and Steam Chemistry Laboratory; Raghavan, P.S. [Madras Christian College, Chennai (India); Narasimhan, S.V. [Bhabha Atomic Research Centre, Bombay (India); Gopalan, R. [Madras Christian College, Chennai (India). Department of Chemistry

2004-09-01

Nickel ferrite is one of the important corrosion products in the pipeline surfaces of water-cooled nuclear reactors. The dissolution of the nickel ferrite by chelating agents is very sensitive to the nature of the chelant, the nature of the reductant used in the formulation and the temperature at which the dissolution studies are performed. The dissolution is mainly controlled by the reductive dissolution of the ferrite particles, but complexing agents also play a significant role in the dissolution process. This study deals with the leaching of iron and nickel from nickel ferrite prepared by the solid-state method. The dissolution studies are performed in pyridine-2,6-dicarboxylic acid (PDCA), nitrilotriacetic acid (NTA), and ethylenediaminetetraacetic acid (EDTA) formulations containing organic reductants like ascorbic acid and low oxidation state transition metal ion reductants like Fe(II)-L (where L = PDCA, NTA, EDTA) at 85 C. The dissolution of nickel ferrite in PDCA, NTA and EDTA formulations is influenced by the presence of reductants in the formulations. The addition of Fe(II)-L in the formulation greatly enhances the dissolution of nickel ferrite. The preferential leaching of nickel over iron during the dissolution of nickel ferrite was observed in all the formulations. (orig.)

Dissolution studies on Nickel ferrite in dilute chemical decontamination formulations

International Nuclear Information System (INIS)

Ranganathan, S.; Narasimhan, S.V.; Gopalan, R.

2004-01-01

Nickel ferrite is one of the important corrosion products in the pipeline surfaces of water-cooled nuclear reactors. The dissolution of the nickel ferrite by chelating agents is very sensitive to the nature of the chelant, the nature of the reductant used in the formulation and the temperature at which the dissolution studies are performed. The dissolution is mainly controlled by the reductive dissolution of the ferrite particles, but complexing agents also play a significant role in the dissolution process. This study deals with the leaching of iron and nickel from nickel ferrite prepared by the solid-state method. The dissolution studies are performed in pyridine-2,6-dicarboxylic acid (PDCA), nitrilotriacetic acid (NTA), and ethylenediaminetetraacetic acid (EDTA) formulations containing organic reductants like ascorbic acid and low oxidation state transition metal ion reductants like Fe(II)-L (where L = PDCA, NTA, EDTA) at 85 C. The dissolution of nickel ferrite in PDCA, NTA and EDTA formulations is influenced by the presence of reductants in the formulations. The addition of Fe(II)-L in the formulation greatly enhances the dissolution of nickel ferrite. The preferential leaching of nickel over iron during the dissolution of nickel ferrite was observed in all the formulations. (orig.)

Effect of alteration phase formation on the glass dissolution rate

Energy Technology Data Exchange (ETDEWEB)

Ebert, W L [Argonne National Laboratory, Chemical Technology Div. (United States)

1997-07-01

The dissolution rates of many glasses have been observed to increase upon the formation of certain alteration phases. While simulations have predicted the accelerating effect of formation of certain phases, the phases predicted to form in computer simulations are usually different than those observed to form in experiments. This is because kinetically favored phases form first in experiments, while simulations predict the thermodynamically favored phases. Static dissolution tests with crushed glass have been used to measure the glass dissolution rate after alteration phases form. Because glass dissolution rates are calculated on a per area basis, an important effect in tests conducted with crushed glass is the decrease in the surface area of glass that is available for reaction as the glass dissolves. This loss of surface area must be taken into account when calculating the dissolution rate. The phases that form and their effect on the dissolution rate are probably related to the glass composition. The impact of phase formation on the glass dissolution rate also varies according to the solubility products of the alteration phases and how the orthocilicic acid activity is affected. Insight into the relationship between the glass dissolution rate, solution chemistry and alteration phase formation is provided by the results of accelerated dissolution tests.

Montmorillonite dissolution kinetics: Experimental and reactive transport modeling interpretation

Science.gov (United States)

Cappelli, Chiara; Yokoyama, Shingo; Cama, Jordi; Huertas, F. Javier

2018-04-01

The dissolution kinetics of K-montmorillonite was studied at 25 °C, acidic pH (2-4) and 0.01 M ionic strength by means of well-mixed flow-through experiments. The variations of Si, Al and Mg over time resulted in high releases of Si and Mg and Al deficit, which yielded long periods of incongruent dissolution before reaching stoichiometric steady state. This behavior was caused by simultaneous dissolution of nanoparticles and cation exchange between the interlayer K and released Ca, Mg and Al and H. Since Si was only involved in the dissolution reaction, it was used to calculate steady-state dissolution rates, RSi, over a wide solution saturation state (ΔGr ranged from -5 to -40 kcal mol-1). The effects of pH and the degree of undersaturation (ΔGr) on the K-montmorillonite dissolution rate were determined using RSi. Employing dissolution rates farthest from equilibrium, the catalytic pH effect on the K-montmorillonite dissolution rate was expressed as Rdiss = k·aH0.56±0.05 whereas using all dissolution rates, the ΔGr effect was expressed as a non-linear f(ΔGr) function Rdiss = k · [1 - exp(-3.8 × 10-4 · (|ΔGr|/RT)2.13)] The functionality of this expression is similar to the equations reported for dissolution of Na-montmorillonite at pH 3 and 50 °C (Metz, 2001) and Na-K-Ca-montmorillonite at pH 9 and 80 °C (Cama et al., 2000; Marty et al., 2011), which lends support to the use of a single f(ΔGr) term to calculate the rate over the pH range 0-14. Thus, we propose a rate law that also accounts for the effect of pOH and temperature by using the pOH-rate dependence and the apparent activation energy proposed by Rozalén et al. (2008) and Amram and Ganor (2005), respectively, and normalizing the dissolution rate constant with the edge surface area of the K-montmorillonite. 1D reactive transport simulations of the experimental data were performed using the Crunchflow code (Steefel et al., 2015) to quantitatively interpret the evolution of the released cations

Chrysotile dissolution rates: Implications for carbon sequestration

International Nuclear Information System (INIS)

Thom, James G.M.; Dipple, Gregory M.; Power, Ian M.; Harrison, Anna L.

2013-01-01

Highlights: • Uncertainties in serpentine dissolution kinetics hinder carbon sequestration models. • A pH dependent, far from equilibrium dissolution rate law for chrysotile. • F chrysotile (mol/m 2 /s) = 10 −0.21pH−10.57 at 22 °C over pH 2–10. • Laboratory dissolution rates consistent with mine waste weathering observations. • Potential for carbon sequestration in mine tailings and aquifers is assessed. - Abstract: Serpentine minerals (e.g., chrysotile) are a potentially important medium for sequestration of CO 2 via carbonation reactions. The goals of this study are to report a steady-state, far from equilibrium chrysotile dissolution rate law and to better define what role serpentine dissolution kinetics will have in constraining rates of carbon sequestration via serpentine carbonation. The steady-state dissolution rate of chrysotile in 0.1 m NaCl solutions was measured at 22 °C and pH ranging from 2 to 8. Dissolution experiments were performed in a continuously stirred flow-through reactor with the input solutions pre-equilibrated with atmospheric CO 2 . Both Mg and Si steady-state fluxes from the chrysotile surface, and the overall chrysotile flux were regressed and the following empirical relationships were obtained: F Mg =-0.22pH-10.02;F Si =-0.19pH-10.37;F chrysotile =-0.21pH-10.57 where F Mg , F Si , and F chrysotile are the log 10 Mg, Si, and molar chrysotile fluxes in mol/m 2 /s, respectively. Element fluxes were used in reaction-path calculations to constrain the rate of CO 2 sequestration in two geological environments that have been proposed as potential sinks for anthropogenic CO 2 . Carbon sequestration in chrysotile tailings at 10 °C is approximately an order of magnitude faster than carbon sequestration in a serpentinite-hosted aquifer at 60 °C on a per kilogram of water basis. A serpentinite-hosted aquifer, however, provides a larger sequestration capacity. The chrysotile dissolution rate law determined in this study has

Contributions of Phosphorus from Groundwater to Streams in the Piedmont, Blue Ridge, and Valley and Ridge Physiographic Provinces, Eastern United States

Science.gov (United States)

Denver, Judith M.; Cravotta,, Charles A.; Ator, Scott W.; Lindsey, Bruce D.

2011-01-01

Phosphorus from natural and human sources is likely to be discharged from groundwater to streams in certain geochemical environments. Water-quality data collected from 1991 through 2007 in paired networks of groundwater and streams in different hydrogeologic and land-use settings of the Piedmont, Blue Ridge, and Valley and Ridge Physiographic Provinces in the eastern United States were compiled and analyzed to evaluate the sources, fate, and transport of phosphorus. The median concentrations of phosphate in groundwater from the crystalline and siliciclastic bedrock settings (0.017 and 0.020 milligrams per liter, respectively) generally were greater than the median for the carbonate setting (less than 0.01 milligrams per liter). In contrast, the median concentrations of dissolved phosphate in stream base flow from the crystalline and siliciclastic bedrock settings (0.010 and 0.014 milligrams per liter, respectively) were less than the median concentration for base-flow samples from the carbonate setting (0.020 milligrams per liter). Concentrations of phosphorus in many of the stream base-flow and groundwater samples exceeded ecological criteria for streams in the region. Mineral dissolution was identified as the dominant source of phosphorus in the groundwater and stream base flow draining crystalline or siliciclastic bedrock in the study area. Low concentrations of dissolved phosphorus in groundwater from carbonate bedrock result from the precipitation of minerals and (or) from sorption to mineral surfaces along groundwater flow paths. Phosphorus concentrations are commonly elevated in stream base flow in areas underlain by carbonate bedrock, however, presumably derived from in-stream sources or from upland anthropogenic sources and transported along short, shallow groundwater flow paths. Dissolved phosphate concentrations in groundwater were correlated positively with concentrations of silica and sodium, and negatively with alkalinity and concentrations of calcium

Criticality safety in high explosives dissolution

International Nuclear Information System (INIS)

Troyer, S.D.

1997-01-01

In 1992, an incident occurred at the Pantex Plant in which the cladding around a fissile material component (pit) cracked during dismantlement of the high explosives portion of a nuclear weapon. Although the event did not result in any significant contamination or personnel exposures, concerns about the incident led to the conclusion that the current dismantlement process was unacceptable. Options considered for redesign, dissolution tooling design considerations, dissolution tooling design features, and the analysis of the new dissolution tooling are summarized. The final tooling design developed incorporated a number of safety features and provides a simple, self-contained, low-maintenance method of high explosives removal for nuclear explosive dismantlement. Analyses demonstrate that the tooling design will remain subcritical under normal, abnormal, and credible accident scenarios. 1 fig

Waste form dissolution in bedded salt

International Nuclear Information System (INIS)

Kaufman, A.M.

1980-01-01

A model was devised for waste dissolution in bedded salt, a hydrologically tight medium. For a typical Spent UnReprocessed Fuel (SURF) emplacement, the dissolution rate wll be diffusion limited and will rise to a steady state value after t/sub eq/ approx. = 250 (1+(1-epsilon 0 ) K/sub D//epsilon 0 ) (years) epsilon 0 is the overpack porosity and K/sub d/ is the overpack sorption coefficient. The steady state dissolution rate itself is dominated by the solubility of UO 2 . Steady state rates between 5 x 10 -5 and .5 (g/year) are achievable by SURF emplacements in bedded salt without overpack, and rates between 5 x 10 -7 and 5 x 10 -3 (g/year) with an overpack having porosity of 10 -2

Emotional and Cognitive Coping in Relationship Dissolution

Science.gov (United States)

Wrape, Elizabeth R.; Jenkins, Sharon Rae; Callahan, Jennifer L.; Nowlin, Rachel B.

2016-01-01

Dissolution of a romantic relationship can adversely affect functioning among college students and represents one primary reason for seeking campus counseling. This study examined the associations among common coping strategies and distress following relationship dissolution. Avoidance and repetitive negative thinking (RNT) were significantly…

CALCIUM CARBONATE DISSOLUTION RATE IN LIMESTONE CONTACTORS

Science.gov (United States)

The rate of carbonate mineral dissolution from limestone was studied using a rotating disk apparatus and samples of limestone of varied composition. The purpose of this study was to determine the effect of limestone composition on the kinetics of carbonate mineral dissolution. Th...

Speciation, Mobility and Fate of Actinides in the Groundwater at the Hanford Site

International Nuclear Information System (INIS)

Buesseler, K.O.; Dai, M.; Repeta, D.; Wacker, J.F.; Kelley, J.M.

2003-01-01

Plutonium and other actinides represent important contaminants in the groundwater and vadose zone at Hanford and other DOE sites. The distribution and migration of these actinides in groundwater must be understood so that these sites can be carefully monitored and effectively cleaned up, thereby minimizing risks to the public. The objective of this project was to obtain field data on the chemical and physical forms of plutonium in groundwater at the Hanford site. We focused on the 100-k and 100-n areas near the Columbia River, where prior reactor operations and waste storage was in close proximity to the river. In particular, a unique set of technical approaches were combined to look at the details of Pu speciation in groundwater, as thus its chemical affinity for soil surfaces and solubility in groundwater, as these impact directly the migration rates off site and possible mitigation possibilities one might undertake to control, or at least better monitor these releases

Assessing the hydrogeochemical processes affecting groundwater pollution in arid areas using an integration of geochemical equilibrium and multivariate statistical techniques.

Science.gov (United States)

El Alfy, Mohamed; Lashin, Aref; Abdalla, Fathy; Al-Bassam, Abdulaziz

2017-10-01

Rapid economic expansion poses serious problems for groundwater resources in arid areas, which typically have high rates of groundwater depletion. In this study, integration of hydrochemical investigations involving chemical and statistical analyses are conducted to assess the factors controlling hydrochemistry and potential pollution in an arid region. Fifty-four groundwater samples were collected from the Dhurma aquifer in Saudi Arabia, and twenty-one physicochemical variables were examined for each sample. Spatial patterns of salinity and nitrate were mapped using fitted variograms. The nitrate spatial distribution shows that nitrate pollution is a persistent problem affecting a wide area of the aquifer. The hydrochemical investigations and cluster analysis reveal four significant clusters of groundwater zones. Five main factors were extracted, which explain >77% of the total data variance. These factors indicated that the chemical characteristics of the groundwater were influenced by rock-water interactions and anthropogenic factors. The identified clusters and factors were validated with hydrochemical investigations. The geogenic factors include the dissolution of various minerals (calcite, aragonite, gypsum, anhydrite, halite and fluorite) and ion exchange processes. The anthropogenic factors include the impact of irrigation return flows and the application of potassium, nitrate, and phosphate fertilizers. Over time, these anthropogenic factors will most likely contribute to further declines in groundwater quality. Copyright © 2017 Elsevier Ltd. All rights reserved.

Hydrothermal evolution of repository groundwaters in basalt

International Nuclear Information System (INIS)

Apps, J.A.

1984-01-01

Groundwaters in the near field of a radioactive waste repository in basalt will change their chemical composition in response to reactions with the basalt. These reactions will be promoted by the heat generated by the decaying waste. It is important to predict both the rate and the extent of these reactions, and the secondary minerals produced, because the alteration process controls the chemical environment affecting the corrosion of the canister, the solubility and complexation of migrating radionuclides, the reactivity of the alteration products to radionuclides sorption, and the porosity and permeability of the host rock. A comprehensive review of the literature leads to the preliminary finding that hydrothermally altering basalts in geothermal regions such as Iceland lead to a secondary mineralogy and groundwater composition similar to that expected to surround a repository. Furthermore, laboratory experiments replicating the alteration conditions approximate those observed in the field and expected in a repository. Preliminary estimates were made of the rate of hydration and devitrification of basaltic glass and the zero-order dissolution rate of basaltic materials. The rates were compared with those for rhyolitic glasses and silicate minerals. Preliminary calculations made of mixed process alteration kinetics, involving pore diffusion and surface reaction suggest that at temperatures greater than 150 0 C, alteration proceeds so rapidly as to become pervasive in normally fractured basalt exposed to higher temperatures in the field. 70 references

Environmental Tritium (3H) and hydrochemical investigations to evaluate groundwater in Varahi and Markandeya river basins, Karnataka, India

International Nuclear Information System (INIS)

Ravikumar, P.; Somashekar, R.K.

2011-01-01

The present study aimed at assessing the activity of natural radionuclides ( 3 H) and hydrochemical parameters (viz., pH, EC, F - , NO 3 - , Cl - , Ca 2+ , Mg 2+ ) in the groundwater used for domestic and irrigation purposes in the Varahi and Markandeya river basins to understand the levels of hydrochemical parameters in terms of the relative age(s) of the groundwater contained within the study area. The recorded environmental 3 H content in Varahi and Markandeya river basins varied from 1.95 ± 0.25 T.U. to 11.35 ± 0.44 T.U. and 1.49 ± 0.75 T.U. to 9.17 ± 1.13 T.U. respectively. Majority of the samples in Varahi (93.34%) and Markandeya (93.75%) river basins being pre-modern water with modern recharge, significantly influenced by precipitation and river inflowing/sea water intrusion. The EC-Tritium and Tritium-Fluoride plots confirmed the existence of higher total dissolved solids (SEC > 500 μS/cm) and high fluoride (MAC > 1.5 mg/L) in groundwater of Markandeya river basin, attributed to relatively longer residence time of groundwater interacting with rock formations and vice versa in case of Varahi river basin. The tritium-EC and tritium-chloride plots indicated shallow and deep circulating groundwater types in Markandeya river basin and only shallow circulating groundwater type in Varahi river basin. Increasing Mg relative to Ca with decreasing tritium indicated the influence of incongruent dissolution of a dolomite phase. The samples with high nitrate (MAC > 45 mg/L) are waters that are actually mixtures of fresh water (containing very high nitrate, possibly from agricultural fertilizers) and older 'unpolluted' waters (containing low nitrate levels), strongly influenced by surface source. - Research highlights: → It is evident that majority of the samples in Varahi (93.34%) and Markandeya (93.75%) river basins exhibited radioactive decay (1-8 T.U.) having a mixture of pre-modern (viz., old water) water with modern (viz., new water) recharge, significantly

Co-occurrence of arsenic and fluoride in the groundwater of Punjab, Pakistan: source discrimination and health risk assessment.

Science.gov (United States)

Rasool, Atta; Xiao, Tangfu; Baig, Zenab Tariq; Masood, Sajid; Mostofa, Khan M G; Iqbal, Muhammad

2015-12-01

The present study discusses elevated groundwater arsenic (As) and fluoride (F(-)) concentrations in Mailsi, Punjab, Pakistan, and links these elevated concentrations to health risks for the local residents. The results indicate that groundwater samples of two areas of Mailsi, Punjab were severely contaminated with As (5.9-507 ppb) and F(-) (5.5-29.6 ppm), as these values exceeded the permissible limits of World Health Organization (10 ppb for As and 1.5 ppm for F(-)). The groundwater samples were categorized by redox state. The major process controlling the As levels in groundwater was the adsorption of As onto PO4 (3-) at high pH. High alkalinity and low Ca(2+) and Mg(2+) concentrations promoted the higher F(-) and As concentrations in the groundwater. A positive correlation was observed between F(-) and As concentrations (r = 0.37; n = 52) and other major ions found in the groundwater of the studied area. The mineral saturation indices calculated by PHREEQC 2.1 suggested that a majority of samples were oversaturated with calcite and fluorite, leading to the dissolution of fluoride minerals at alkaline pH. Local inhabitants exhibited arsenicosis and fluorosis after exposure to environmental concentration doses of As and F(-). Estimated daily intake (EDI) and target hazard quotient (THQ) highlighted the risk factors borne by local residents. Multivariate statistical analysis further revealed that both geologic origins and anthropogenic activities contributed to As and F(-) contamination in the groundwater. We propose that pollutants originate, in part, from coal combusted at brick factories, and agricultural activities. Once generated, these pollutants were mobilized by the alkaline nature of the groundwater.

Dissolution mechanisms of CO2 hydrate droplets in deep seawaters

International Nuclear Information System (INIS)

Gabitto, Jorge; Tsouris, Costas

2006-01-01

Carbon dioxide dissolution at intermediate ocean depths was studied using physical and mass transfer models. Particle density and hydrate layer thickness were determined using existing field data. Pseudo-homogeneous and heterogeneous mass transfer models were proposed to study the dissolution process. Pseudo-homogeneous models do not seem to represent the dissolution process well. Although heterogeneous models interpret the physical behavior better, unresolved issues related to hydrate dissolution still remain. For example, solid hydrate forms on one side of the hydrate film while it dissolves on the other. Dissolution is a complex process that comprises at least two sequential steps. The global process is controlled by mass transfer inside the hydrate layer or by a dissolution reaction at the hydrate-water interface

Hydro-chemo-mechanical coupling in sediments: Localized mineral dissolution

KAUST Repository

Cha, Minsu; Santamarina, Carlos

2016-01-01

Mineral dissolution is inherently a chemo-hydro-mechanical coupled process. Field evidence and laboratory results show that dissolution may localize and form open conduits in cohesive media such as carbonate rocks. This study focuses on the evolution of localized dissolution in soils (i.e., frictional and non-cohesive granular materials) under effective confining stresses. Experimental results show the development of localized dissolution (“pipe”) when a carbonate-quartz sand is subjected to reactive fluid flow: only loosely packed quartz grains remain within pipes, and the number of pipes decreases away from the inlet port. Concurrent shear wave velocity measurements show a decrease in stiffness during dissolution due to stress and fabric changes, and more complex signal codas anticipate the development of internal heterogeneity. The discrete element method is used to simulate localized vertical dissolution features in granular materials, under constant vertical stress and zero lateral strain far-field boundaries. As porosity increases along dissolution pipes, vertical load is transferred to the surrounding soils and marked force chains develop. In terms of equivalent stress, principal stress rotation takes place within pipes and the sediment reaches the Coulomb failure condition inside pipes and in the surrounding medium. Dissolution pipes alter the geo-plumbing of the subsurface, enhance fluid transport but limit the long term performance of storage systems, alter the fluid pressure and effective stress fields, soften the sediment and may trigger shear failures.

Hydro-chemo-mechanical coupling in sediments: Localized mineral dissolution

KAUST Repository

Cha, Minsu

2016-06-11

Mineral dissolution is inherently a chemo-hydro-mechanical coupled process. Field evidence and laboratory results show that dissolution may localize and form open conduits in cohesive media such as carbonate rocks. This study focuses on the evolution of localized dissolution in soils (i.e., frictional and non-cohesive granular materials) under effective confining stresses. Experimental results show the development of localized dissolution (“pipe”) when a carbonate-quartz sand is subjected to reactive fluid flow: only loosely packed quartz grains remain within pipes, and the number of pipes decreases away from the inlet port. Concurrent shear wave velocity measurements show a decrease in stiffness during dissolution due to stress and fabric changes, and more complex signal codas anticipate the development of internal heterogeneity. The discrete element method is used to simulate localized vertical dissolution features in granular materials, under constant vertical stress and zero lateral strain far-field boundaries. As porosity increases along dissolution pipes, vertical load is transferred to the surrounding soils and marked force chains develop. In terms of equivalent stress, principal stress rotation takes place within pipes and the sediment reaches the Coulomb failure condition inside pipes and in the surrounding medium. Dissolution pipes alter the geo-plumbing of the subsurface, enhance fluid transport but limit the long term performance of storage systems, alter the fluid pressure and effective stress fields, soften the sediment and may trigger shear failures.

Dissolution Threats and Legislative Bargaining

DEFF Research Database (Denmark)

Becher, Michael; Christiansen, Flemming Juul

2015-01-01

Chief executives in many parliamentary democracies have the power to dissolve the legislature. Despite a well-developed literature on the endogenous timing of parliamentary elections, political scientists know remarkably little about the strategic use of dissolution power to influence policymaking....... To address this gap, we propose and empirically evaluate a theoretical model of legislative bargaining in the shadow of executive dissolution power. The model implies that the chief executive's public support and legislative strength, as well as the time until the next constitutionally mandated election...

Sodium tetraphenylborate solubility and dissolution rates

International Nuclear Information System (INIS)

Barnes, M.J.; Peterson, R.A.; Swingle, R.F.; Reeves, C.T.

1995-01-01

The rate of solid sodium tetraphenylborate (NaTPB) dissolution in In-Tank Precipitation salt solutions has been experimentally determined. The data indicates that the dissolution rate of solid NaTPB is a minor contributor the lag time experienced in the 1983 Salt Decontamination Demonstration Test and should not be considered as the rate determining step. Current analytical models for predicting the time to reach the composite lower flammability limit assume that the lag time is not more than 6 hours, and the data supports this assumption (i.e., dissolution by itself requires much less than 6 hours). The data suggests that another step--such as mass transport, the reaction of a benzene precursor or the mixing behavior--is the rate determining factor for benzene release to the vapor space in Tank 48H. In addition, preliminary results from this program show that the degree of agitation employed is not a significant parameter in determining the rate of NaTPB dissolution. As a result of this study, an improved equation for predicting equilibrium tetraphenylborate solubility with respect to temperature and sodium ion concentration has been determined

Geochemistry of shale groundwaters: Results of preliminary laboratory leaching experiments

International Nuclear Information System (INIS)

Von Damm, K.L.; Johnson, K.O.

1987-09-01

Twelve shales were reacted with distilled water at 20 0 C and 100 0 C; the composition of the waters and the mineralogy were determined before and after reaction. The experiments were conducted in a batch mode over a period of approximately 40 days. Major changes occurred in the solution chemistry; in most cases sulfate became the dominant anion while either sodium or calcium was the major cation. The high sulfate is most likely a result of the oxidation of pyrite in the samples. In the 100 0 C experiments some of the solutions became quite acidic. Examination of the observed mineralogy and comparison to the mineral assemblage calculated to be in equilibrium with the experimentally determined waters, suggests that the acidic waters are generated when no carbonate minerals remain to buffer the groundwaters to a more neutral pH. The pH of shale waters will be determined by the balance between the oxidation of pyrite and organic matter and the dissolution of carbonate minerals. The experimental data are helping to elucidate the chemical reactions that control the pH of shale groundwaters, a critical parameter in determining other water-rock and waste-water-rock interactions and ultimate solute mobility. An experimental approach also provides a means of obtaining data for shales for which no groundwater data are available as well as data on chemical species which are not usually determined or reported

Geochemistry of shale groundwaters: Results of preliminary laboratory leaching experiments

Energy Technology Data Exchange (ETDEWEB)

Von Damm, K.L.; Johnson, K.O.

1987-09-01

Twelve shales were reacted with distilled water at 20/sup 0/C and 100/sup 0/C; the composition of the waters and the mineralogy were determined before and after reaction. The experiments were conducted in a batch mode over a period of approximately 40 days. Major changes occurred in the solution chemistry; in most cases sulfate became the dominant anion while either sodium or calcium was the major cation. The high sulfate is most likely a result of the oxidation of pyrite in the samples. In the 100/sup 0/C experiments some of the solutions became quite acidic. Examination of the observed mineralogy and comparison to the mineral assemblage calculated to be in equilibrium with the experimentally determined waters, suggests that the acidic waters are generated when no carbonate minerals remain to buffer the groundwaters to a more neutral pH. The pH of shale waters will be determined by the balance between the oxidation of pyrite and organic matter and the dissolution of carbonate minerals. The experimental data are helping to elucidate the chemical reactions that control the pH of shale groundwaters, a critical parameter in determining other water-rock and waste-water-rock interactions and ultimate solute mobility. An experimental approach also provides a means of obtaining data for shales for which no groundwater data are available as well as data on chemical species which are not usually determined or reported.

Kinetics of carbonate dissolution in CO2-saturated aqueous system at reservoir conditions

Science.gov (United States)

Peng, Cheng; Crawshaw, John P.; Maitland, Geoffrey; Trusler, J. P. Martin

2014-05-01

In recent years, carbon capture and storage (CCS) has emerged as a key technology for limiting anthropogenic CO2 emissions while allowing the continued utilisation of fossil fuels. The most promising geological storage sites are deep saline aquifers because the capacity, integrity and injection economics are most favourable, and the environmental impact can be minimal. Many rock-fluid chemical reactions are known to occur both during and after CO2 injection in saline aquifers. The importance of rock-fluid reactions in the (CO2 + H2O) system can be understood in terms of their impact on the integrity and stability of both the formation rocks and cap rocks. The chemical interactions between CO2-acidified brines and the reservoir minerals can influence the porosity and permeability of the formations, resulting in changes in the transport processes occurring during CO2 storage. Since carbonate minerals are abundant in sedimentary rocks, one of the requirements to safely implement CO2 storage in saline aquifers is to characterise the reactivity of carbonate minerals in aqueous solutions at reservoir conditions. In this work, we reported measurements of the intrinsic rate of carbonate dissolution in CO2-saturated water under high-temperature high-pressure reservoir conditions extending up to 373 K and 14 MPa. The rate of carbonate dissolution in CO2-free HCl(aq) was also measured at ambient pressure at temperatures up to 353 K. Various pure minerals and reservoir rocks were investigated in this study, including single-crystals of calcite and magnesite, and samples of dolomite, chalks and sandstones. A specially-designed batch reactor system, implementing the rotating disc technique, was used to obtain the intrinsic reaction rate at the solid/liquid interface, free of mass transfer effects. The effective area and mineralogy of the exposed surface was determined by a combination of surface characterisation techniques including XRD, SEM, EDX and optical microscopy. The

Geochemical processes controlling groundwater quality under semi arid environment: A case study in central Morocco.

Science.gov (United States)

Karroum, Morad; Elgettafi, Mohammed; Elmandour, Abdenabi; Wilske, Cornelia; Himi, Mahjoub; Casas, Albert

2017-12-31

Bahira plain is an important area for Morocco due to its agriculture and mining activities. Situated in a sub-arid to arid climate, this plain hosts an aquifer system that represents sequences of carbonates, phosphates, evaporates and alluvial deposits. Groundwater flows from Ganntour plateau (recharge area) to the basin-fill deposits and Zima Lake and Sed Elmejnoun where water evaporates. The objective of this study was to characterize the chemical properties of the groundwater and to assess the processes controlling the groundwater's chemistry. We can divide water samples into three hydrochemical water groups: recharge waters (Ca/Mg-HCO 3 ), transition zone waters (Ca-HCO 3 -SO 4 /Cl) and discharge waters (Na-Cl/SO 4 ). Accordingly, compositions of waters are determined by the availability of easily soluble minerals like calcite (Ca-HCO 3 dominant), halite (Na-Cl dominant) and gypsum (Ca-SO 4 dominant). Cl/Br ratios show that Cl concentration increases from dissolution of natural halite. When groundwater is affected by extreme evaporation Cl/Br ratios may increase up to 1900. High fluoride concentrations are associated with low Ca 2+ concentrations (<100mg/L). That means when recharge waters enter the aquifer, it starts dissolving fluorite since the Ca 2+ concentration is low. Once groundwater becomes saturated with Ca 2+ , the immobilization of fluoride is occurring by precipitation of fluoride-rich minerals like fluoro-apatite. According to the environmental isotope ( 18 O and 2 H) analyses, they are three potential processes affecting groundwater: 1. Evaporation as verified by low slope value, 2. Water-rock interaction, 3. admixture of waters showed different stable isotope compositions and salinities. Copyright © 2017 Elsevier B.V. All rights reserved.

Mathematical methods for quantification and comparison of dissolution testing data

Directory of Open Access Journals (Sweden)

Edina Vranić

2002-02-01

Full Text Available In recent years, drug release/dissolution from solid dosage forms has been the subject of intense and profitable scientific developments. Whenever a new solid dosage form is developed or produced, it is necessary to ensure that drug dissolutionoccurs in an appropriate manner. The pharmaceutical industry and the registration authorities do focus, nowadays, on drug dissolution studies. The quantitative analysis of the values obtained in dissolution/release tests is easier when mathematicalformulas that express the dissolution results as a function of some of the dosage forms characteristics are used. This work discusses the analysis of data obtained for dissolution profiles under different media pH conditions using mathematical methodsof analysis described by Moore and Flanner. These authors have described difference factor (f1 and similarity factor (f2, which can be used to characterise drug dissolution/release profiles. In this work we have used these formulas for evaluation of dissolution profiles of the conventional tablets in different pH of dissolution medium (range of physiological variations.

Groundwater Dynamics in Fossil Fractured Carbonate Aquifers in Eastern Arabian Peninsula

Science.gov (United States)

Farag, A. Z. A.; Heggy, E.; Helal, M.; Thirunavukkarasu, D.; Scabbia, G.; Palmer, E. M.

2017-12-01

analysis and geologic setting suggest a common genesis from elevated groundwater along faults during wet climatic periods. The present study suggests that ascending gaseous-rich deep waters along faults in Qatar is degrading the water quality and causing dissolution of carbonates and evaporites leading to strong karstification with abundant collapse features.

Dissolution of covalent adaptable network polymers in organic solvent

Science.gov (United States)

Yu, Kai; Yang, Hua; Dao, Binh H.; Shi, Qian; Yakacki, Christopher M.

2017-12-01

It was recently reported that thermosetting polymers can be fully dissolved in a proper organic solvent utilizing a bond-exchange reaction (BER), where small molecules diffuse into the polymer, break the long polymer chains into short segments, and eventually dissolve the network when sufficient solvent is provided. The solvent-assisted dissolution approach was applied to fully recycle thermosets and their fiber composites. This paper presents the first multi-scale modeling framework to predict the dissolution kinetics and mechanics of thermosets in organic solvent. The model connects the micro-scale network dynamics with macro-scale material properties: in the micro-scale, a model is developed based on the kinetics of BERs to describe the cleavage rate of polymer chains and evolution of chain segment length during the dissolution. The micro-scale model is then fed into a continuum-level model with considerations of the transportation of solvent molecules and chain segments in the system. The model shows good prediction on conversion rate of functional groups, degradation of network mechanical properties, and dissolution rate of thermosets during the dissolution. It identifies the underlying kinetic factors governing the dissolution process, and reveals the influence of different material and processing variables on the dissolution process, such as time, temperature, catalyst concentration, and chain length between cross-links.

Status report on dissolution model development

International Nuclear Information System (INIS)

Jackson, D.D.

1983-07-01

The computer program PROTOCOL models the dissolution reactions of chemical species in water. It is being developed particularly to study the dissolution of proposed nuclear waste forms and related phases. Experimentally derived leaching rate functions are coupled to thermochemical equilibrium calculations and water flow rates. The program has been developed over a period of years. This report describes improvements that have been done in the past year

An optimized groundwater extraction system for the toxic burning pits area of J-Field, Aberdeen Proving Ground, Maryland

Energy Technology Data Exchange (ETDEWEB)

Quinn, J.J.; Johnson, R.L.; Patton, T.L.; Martino, L.E.

1996-06-01

Testing and disposal of chemical warfare agents, munitions, and industrial chemicals at the J-Field area of the Aberdeen Proving Ground (APG) have resulted in contamination of soil and groundwater. The discharge of contaminated groundwater to on-site marshes and adjacent estuaries poses a potential risk to ecological receptors. The Toxic Burning Pits (TBP) area is of special concern because of its disposal history. This report describes a groundwater modeling study conducted at J-Field that focused on the TBP area. The goal of this modeling effort was optimization of the groundwater extraction system at the TBP area by applying linear programming techniques. Initially, the flow field in the J-Field vicinity was characterized with a three-dimensional model that uses existing data and several numerical techniques. A user-specified border was set near the marsh and used as a constraint boundary in two modeled remediation scenarios: containment of the groundwater and containment of groundwater with an impermeable cap installed over the TBP area. In both cases, the objective was to extract the minimum amount of water necessary while satisfying the constraints. The smallest number of wells necessary was then determined for each case. This optimization approach provided two benefits: cost savings, in that the water to be treated and the well installation costs were minimized, and minimization of remediation impacts on the ecology of the marsh.

A cost-effective system for in-situ geological arsenic adsorption from groundwater.

Science.gov (United States)

Shan, Huimei; Ma, Teng; Wang, Yanxin; Zhao, Jie; Han, Hongyin; Deng, Yamin; He, Xin; Dong, Yihui

2013-11-01

An effective and low-cost in-situ geological filtration system was developed to treat arsenic-contaminated groundwater in remote rural areas. Hangjinhouqi in western Hetao Plain of Inner Mongolia, China, where groundwater contains a high arsenic concentration, was selected as the study area. Fe-mineral and limestone widely distributed in the study area were used as filter materials. Batch and column experiments as well as field tests were performed to determine optimal filtration parameters and to evaluate the effectiveness of the technology for arsenic removal under different hydrogeochemical conditions. A mixture containing natural Fe-mineral (hematite and goethite) and limestone at a mass ratio of 2:1 was found to be the most effective for arsenic removal. The results indicated that Fe-mineral in the mixture played a major role for arsenic removal. Meanwhile, limestone buffered groundwater pH to be conducive for the optimal arsenic removal. As(III) adsorption and oxidation by iron mineral, and the formation of Ca-As(V) precipitation with Ca contributed from limestone dissolution were likely mechanisms leading to the As removal. Field demonstrations revealed that a geological filter bed filled with the proposed mineral mixture reduced groundwater arsenic concentration from 400 μg/L to below 10 μg/L. The filtration system was continuously operated for a total volume of 365,000L, which is sufficient for drinking water supplying a rural household of 5 persons for 5 years at a rate of 40 L per person per day. © 2013.

Assess arsenic distribution in groundwater applying GIS in capital of Punjab, Pakistan

Science.gov (United States)

Akhtar, M. M.; Zhonghua, T.; Sissou, Z.; Mohamadi, B.

2015-03-01

Arsenic contamination of groundwater resources threatens the health of millions of people worldwide, particularly in the densely populated river deltas of Southeast Asia. Arsenic causes health concerns due to its significant toxicity and worldwide presence in portable water. The major sources of arsenic pollution may be natural process such as dissolution of arsenic containing minerals and anthropogenic activities. Lahore is groundwater dependent city, arsenic contamination is a major issue of portable water and has recently been most environmental health management issue especially in the plain region, where population density is very high. GIS was used in this study for visualizing distribution of arsenic groundwater concentration through geostatistics analysis technique, and exposure risk zones for two years (2010 and 2012). Town's data was compared and concentration variation evaluated. ANOVA test was also applied to compare concentration between cities and years. Arsenic concentrations widely range 7.3-67.8 and 5.2-69.3 μg L-1 in 2010 and 2012, respectively. Over 71% area is represented arsenic concentration range from 20 to 30 μg L-1 in both analyzed years. However, in 2012 arsenic concentration over 40 μg L-1 has covered 7.6% area of Data Gunjbuksh and 8.1% of Ravi Town, while over 90% area of Allama Iqbal, Aziz Bhatti and Samanabad Town contain arsenic concentration between 20-30 μg L-1. ANOVA test depicts concentration probability less than 0.05, while differences were detected among towns. In light of current results, it needs urgent step to ensure groundwater protection and preservation for future.

8 Dissolution Kinetics

African Journals Online (AJOL)

user

Experiments measuring the dissolution rates of stilbite (NaCa [Al Si O ].14H O) in pH-buffered ... The rate law was established as R = k (a ) , where k is ... crystalline hydrated aluminosilicate minerals ..... from the crushing process, thin edges or.

Groundwater resources of Ribeira Fajã basin, island of São Nicolau, Cape Verde, West Africa

Science.gov (United States)

Heilweil, Victor M.; Gingerich, Stephen B.; Plummer, Niel; Verstraeten, Ingrid M.

2010-01-01

Groundwater resources in Cape Verde provide water for agriculture, industry, and human consumption. These resources are limited and susceptible to contamination. Additional groundwater resources are needed for continued agricultural development, particularly during times of drought, but increased use and (or) climatic change may have adverse effects on the quantity and quality of freshwater available. In volcanic island aquifers such as those of Cape Verde, a lens of fresh groundwater typically ?floats? upon a layer of brackish water at the freshwater/saltwater boundary, and increased pumping may cause salt water intrusion or other contamination. A recent U.S. Geological Survey study assessed baseline groundwater conditions in watersheds on three islands of Cape Verde to provide the scientific basis for sustainably developing water resources and minimizing future groundwater depletion and contamination.

Dissolution studies of synthetic soddyite and uranophane

International Nuclear Information System (INIS)

Casas, I.; Perez, I.; Torrero, E.; Bruno, J.; Cera, E.; Duro, L.

1997-09-01

The dissolution of synthetically obtained soddyite and uranophane has been studied in solutions of low ionic strength. These are the likely final phases of the oxidative alternation pathway of uranium dioxide. The thermodynamic and kinetic dissolution properties of these phases have been determined at different bicarbonate concentrations. The solubilities determined in the experiments with soddyite correspond fairly well to the theoretical model calculated with a log K 0 s0 =3.9±0.7. For uranophane, the best fitting was obtained for a log K 0 s0 =11.7±0.6. The dissolution rate in the presence of bicarbonate gave for soddyite an average value of 6.8(±4.4) 10 -10 mol m -2 s -1 . For uranophane, under the same experimental conditions, the following dissolution rate equation has been derived: r 0 (mol m -2 s -1 )=10 -9±2. [HCO 3 - ] 0.69±0.09 2

Comparative Analysis of Fluoride Concentrations in Groundwaters in Northern and Southern Ghana: Implications for the Contaminant Sources

Science.gov (United States)

Sunkari, Emmanuel Daanoba; Zango, Musah Saeed; Korboe, Harriet Mateko

2018-04-01

Bongo and Sekyere South districts, both in the northern and southern parts of Ghana, respectively, have high populations living in rural areas and most of them use groundwater for drinking purposes. The groundwater in these areas is prone to contamination from natural and/or artificial sources. Therefore this study aims; (1) to present a comparative analysis of the fluoride concentration in groundwater samples from Bongo and Sekyere South districts and the associated groundwater-rock interaction that may be the cause for the varied fluoride concentrations, (2) to determine the leaching potential of fluoride from the host rocks as the possible mechanism for groundwater contamination. Sixty (60) groundwater samples from active pumping wells and twelve (12) rock samples from outcrops were collected from various communities in the two districts for fluoride concentration and mineralogical analysis. Based on the variations in fluoride concentration, fluoride spatial distribution maps were prepared using empirical Bayesian kriging interpolation method and analysed by means of hierarchical cluster analysis. The fluoride concentration in Bongo district varies between 1.71 and 4.0 mg/L, whereas that in Sekyere South district changes from 0.3 to 0.8 mg/L. From the mineralogical studies, biotite has the highest percentage in the Bongo district and has positive correlation with fluoride concentration in the analysed water samples than in the Sekyere South district. The elevated fluoride concentration in the Bongo district relative to the Sekyere South district is due to the dissolution of biotite in the groundwater and the sufficient groundwater-rock interaction since the water samples are mainly sourced from deeper boreholes. This high fluoride concentration has resulted in a plethora of reported cases of dental fluorosis and other health-related issues in Bongo.

Does the dose-solubility ratio affect the mean dissolution time of drugs?

Science.gov (United States)

Lánský, P; Weiss, M

1999-09-01

To present a new model for describing drug dissolution. On the basis of the new model to characterize the dissolution profile by the distribution function of the random dissolution time of a drug molecule, which generalizes the classical first order model. Instead of assuming a constant fractional dissolution rate, as in the classical model, it is considered that the fractional dissolution rate is a decreasing function of the dissolved amount controlled by the dose-solubility ratio. The differential equation derived from this assumption is solved and the distribution measures (half-dissolution time, mean dissolution time, relative dispersion of the dissolution time, dissolution time density, and fractional dissolution rate) are calculated. Finally, instead of monotonically decreasing the fractional dissolution rate, a generalization resulting in zero dissolution rate at time origin is introduced. The behavior of the model is divided into two regions defined by q, the ratio of the dose to the solubility level: q 1 (saturation of the solution, saturation time). The singular case q = 1 is also treated and in this situation the mean as well as the relative dispersion of the dissolution time increase to infinity. The model was successfully fitted to data (1). This empirical model is descriptive without detailed physical reasoning behind its derivation. According to the model, the mean dissolution time is affected by the dose-solubility ratio. Although this prediction appears to be in accordance with preliminary application, further validation based on more suitable experimental data is required.

Kinetics of Inorganic Calcite Dissolution in Seawater under Pressure

Science.gov (United States)

Dong, S.; Subhas, A.; Rollins, N.; Berelson, W.; Adkins, J. F.

2016-02-01

While understanding calcium carbonate dissolution is vital in constructing global carbon cycles and predicting the effect of seawater acidification as a result of increasing atmospheric CO2, there is still a major debate over the basic formulation of a dissolution rate law. The kinetics of calcium carbonate dissolution are typically described by the equation: Rate=k(1-Ω)n, while Ω=[Ca2+][CO32-]/Ksp. In this study, 13C-labeled calcite is dissolved in unlabeled seawater and the evolving d13C composition of the fluid is traced over time to establish dissolution rate. Instead of changing ion concentration to obtain varying Ω (as in our previous study; Subhas et al. 2015), we changed Ksp by conducting experiments under different pressures (described in theory as ∂lnKsp/∂P=-ΔV/RT, where ΔV is partial molal volume). This involved the construction of a pressure vessel that could hold our sample bag and provide aliquots while remaining pressurized. Pressure experiments were conducted between 0-2000PSI. Results support the conclusion in our previous study that near-equilibrium dissolution rates are highly nonlinear, but give a disparate relationship between undersaturation and dissolution rate if Ω is calculated assuming the specific ΔV embedded in CO2SYS. A revised ΔV from -37cm3 to -65cm3 would make the dissolution formulation equation agree, but clearly appears unreasonable. Our results are explained by a pressure effect on carbonate dissolution kinetics over and above the influence of pressure on Ω. If this is a phenomenon that occurs in nature, then we would predict that dissolution should be occurring shallower in the water column (as sometimes observed) than indicated by standard Ω calculations.

Mechanisms and kinetics laws of inactive R7T7 reference glass dissolution in water at 90 deg C: initial dissolution rate measurements

International Nuclear Information System (INIS)

Advocat, T.; Ghaleb, D.; Vernaz, E.

1993-02-01

The initial dissolution rate of inactive R7T7 reference glass was measured at 90 deg C in dilute aqueous solutions first at unspecified pH, then with imposed pH values. In distilled water, R7T7 glass corrosion initially involved preferential extraction of boron and network modifier elements (Li, Na, Ca) as long as the solution pH remained acid. When the solution pH became alkaline, glass dissolution was stoichiometric. These two mechanisms were confirmed by dissolution tests in aqueous solutions at imposed pH values under acid and alkaline conditions. The initial dissolution rate r 0 in mole.cm -3 .s -1 also increased significantly in alkaline media when the pH of the aqueous phase increased: in slightly acid media, selective glass dissolution formed a residual, de-alkalinized, hydrated glass that was characterized by transmission electron microscopy and secondary ion mass spectrometry. Under steady-state dissolution conditions, the initial glass corrosion rate (in mole.cm -3 .s -1 ) was: in acid and alkaline media, amorphous and crystallized alteration products formed after complete dissolution of the silicated glass network. The first products formed consisted mainly of Zr, Rare Earths, Fe and Al. (author). 67 refs., 29 figs., 26 tabs., 21 plates

Actor bonds after relationship dissolution

DEFF Research Database (Denmark)

Skaates, Maria Anne

2000-01-01

Most of the presented papers at the 1st NoRD Workshop can be classified as belonging to the business marketing approach to relationship dissolution. Two papers were conceptual, and the remaining six were empirical studies. The first conceptual study by Skaates (2000) focuses on the nature...... of the actor bonds that remain after a business relationship has ended. The study suggests that an interdisciplinary approach would provide a richer understanding of the phenomenon; this could be achieved by using e.g. Bourdieu's sociological concepts in dissolution research....

Controls on groundwater flow in the Bengal Basin of India and Bangladesh: regional modeling analysis

Science.gov (United States)

Michael, Holly A.; Voss, Clifford I.

2009-11-01

Groundwater for domestic and irrigation purposes is produced primarily from shallow parts of the Bengal Basin aquifer system (India and Bangladesh), which contains high concentrations of dissolved arsenic (exceeding worldwide drinking water standards), though deeper groundwater is generally low in arsenic. An essential first step for determining sustainable management of the deep groundwater resource is identification of hydrogeologic controls on flow and quantification of basin-scale groundwater flow patterns. Results from groundwater modeling, in which the Bengal Basin aquifer system is represented as a single aquifer with higher horizontal than vertical hydraulic conductivity, indicate that this anisotropy is the primary hydrogeologic control on the natural flowpath lengths. Despite extremely low hydraulic gradients due to minimal topographic relief, anisotropy implies large-scale (tens to hundreds of kilometers) flow at depth. Other hydrogeologic factors, including lateral and vertical changes in hydraulic conductivity, have minor effects on overall flow patterns. However, because natural hydraulic gradients are low, the impact of pumping on groundwater flow is overwhelming; modeling indicates that pumping has substantially changed the shallow groundwater budget and flowpaths from predevelopment conditions.

Controls on groundwater flow in the Bengal Basin of India and Bangladesh: Regional modeling analysis

Science.gov (United States)

Michael, H.A.; Voss, C.I.

2009-01-01

Groundwater for domestic and irrigation purposes is produced primarily from shallow parts of the Bengal Basin aquifer system (India and Bangladesh), which contains high concentrations of dissolved arsenic (exceeding worldwide drinking water standards), though deeper groundwater is generally low in arsenic. An essential first step for determining sustainable management of the deep groundwater resource is identification of hydrogeologic controls on flow and quantification of basin-scale groundwater flow patterns. Results from groundwater modeling, in which the Bengal Basin aquifer system is represented as a single aquifer with higher horizontal than vertical hydraulic conductivity, indicate that this anisotropy is the primary hydrogeologic control on the natural flowpath lengths. Despite extremely low hydraulic gradients due to minimal topographic relief, anisotropy implies large-scale (tens to hundreds of kilometers) flow at depth. Other hydrogeologic factors, including lateral and vertical changes in hydraulic conductivity, have minor effects on overall flow patterns. However, because natural hydraulic gradients are low, the impact of pumping on groundwater flow is overwhelming; modeling indicates that pumping has substantially changed the shallow groundwater budget and flowpaths from predevelopment conditions. ?? Springer-Verlag 2009.

Laboratory simulation of salt dissolution during waste removal

International Nuclear Information System (INIS)

Wiersma, B.J.; Parish, W.R.

1997-01-01

Laboratory experiments were performed to support the field demonstration of improved techniques for salt dissolution in waste tanks at the Savannah River Site. The tests were designed to investigate three density driven techniques for salt dissolution: (1) Drain-Add-Sit-Remove, (2) Modified Density Gradient, and (3) Continuous Salt Mining. Salt dissolution was observed to be a very rapid process as salt solutions with densities between 1.38-1.4 were frequently removed. Slower addition and removal rates and locating the outlet line at deeper levels below the top of the saltcake provided the best contact between the dissolution water and the saltcake. It was observed that dissolution with 1 M sodium hydroxide solution resulted in salt solutions that were within the current inhibitor requirements for the prevention of stress corrosion cracking. This result was independent of the density driven technique. However, if inhibited water (0.01 M sodium hydroxide and 0.011 M sodium nitrite) was utilized, the salt solutions were frequently outside the inhibitor requirements. Corrosion testing at conditions similar to the environments expected during waste removal was recommended

Investigation of dissolution kinetics of a Nigerian columbite in ...

African Journals Online (AJOL)

Investigation of dissolution kinetics of a Nigerian columbite in hydrofluoric acid using the shrinking core model. ... Experimental results indicate that the dissolution rate is chemical reaction controlled, with reaction order of 0.57. Dissolution of over 90 % of the columbite was achieved in 5 h, using 20 M HF at 90 oC with 100 ...

Study of variation in groundwater quality in a coastal aquifer in north-eastern Tunisia using multivariate factor analysis

KAUST Repository

Charfi, Sihem; Zouari, Kamel; Feki, Saber; Mami, Ezeddine

2013-01-01

This work focuses on the Grombalia aquifer which constitutes the main water resource in Northeast Tunisia, Cap Bon Peninsula. The recharge of this aquifer is ensured mainly by direct infiltration of rainwater through permeable layers. Under semi-arid climatic conditions and increasing water demand for irrigation, about 80% of the Grombalia aquifer system shows different vulnerabilities to anthropogenic activities. The total dissolved solids values range from 0.75 to 5.6g/l.Isotopic characterization with stable isotopes (δ2H and δ18O) of Grombalia aquifer system identified geochemistry processes that control water chemistry. In addition, the multivariate statistical technique (Principal Component Analysis) was used to identify the origin, the recharge mode and geochemical processes controlling groundwater quality. The principal reactions responsible for the hydrochemical evolution in the Grombalia groundwater fall into three categories: (1) denitrification process; (2) dissolution of salts; and (3) irrigation return flow process. Tritium data in groundwater from the study area suggest the existence of pre1950 and post1960 recharge. © 2012 Elsevier Ltd and INQUA.

Study of variation in groundwater quality in a coastal aquifer in north-eastern Tunisia using multivariate factor analysis

KAUST Repository

Charfi, Sihem

2013-07-01

This work focuses on the Grombalia aquifer which constitutes the main water resource in Northeast Tunisia, Cap Bon Peninsula. The recharge of this aquifer is ensured mainly by direct infiltration of rainwater through permeable layers. Under semi-arid climatic conditions and increasing water demand for irrigation, about 80% of the Grombalia aquifer system shows different vulnerabilities to anthropogenic activities. The total dissolved solids values range from 0.75 to 5.6g/l.Isotopic characterization with stable isotopes (δ2H and δ18O) of Grombalia aquifer system identified geochemistry processes that control water chemistry. In addition, the multivariate statistical technique (Principal Component Analysis) was used to identify the origin, the recharge mode and geochemical processes controlling groundwater quality. The principal reactions responsible for the hydrochemical evolution in the Grombalia groundwater fall into three categories: (1) denitrification process; (2) dissolution of salts; and (3) irrigation return flow process. Tritium data in groundwater from the study area suggest the existence of pre1950 and post1960 recharge. © 2012 Elsevier Ltd and INQUA.

Fingerprinting groundwater salinity sources in the Gulf Coast Aquifer System, USA

Science.gov (United States)

Chowdhury, Ali H.; Scanlon, Bridget R.; Reedy, Robert C.; Young, Steve

2018-02-01

Understanding groundwater salinity sources in the Gulf Coast Aquifer System (GCAS) is a critical issue due to depletion of fresh groundwater and concerns for potential seawater intrusion. The study objective was to assess sources of groundwater salinity in the GCAS using ˜1,400 chemical analyses and ˜90 isotopic analyses along nine well transects in the Texas Gulf Coast, USA. Salinity increases from northeast (median total dissolved solids (TDS) 340 mg/L) to southwest (median TDS 1,160 mg/L), which inversely correlates with the precipitation distribution pattern (1,370- 600 mm/yr, respectively). Molar Cl/Br ratios (median 540-600), depleted δ2H and δ18O (-24.7‰, -4.5‰) relative to seawater (Cl/Br ˜655 and δ2H, δ18O 0‰, 0‰, respectively), and elevated 36Cl/Cl ratios (˜100), suggest precipitation enriched with marine aerosols as the dominant salinity source. Mass balance estimates suggest that marine aerosols could adequately explain salt loading over the large expanse of the GCAS. Evapotranspiration enrichment to the southwest is supported by elevated chloride concentrations in soil profiles and higher δ18O. Secondary salinity sources include dissolution of salt domes or upwelling brines from geopressured zones along growth faults, mainly near the coast in the northeast. The regional extent and large quantities of brackish water have the potential to support moderate-sized desalination plants in this location. These results have important implications for groundwater management, suggesting a current lack of regional seawater intrusion and a suitable source of relatively low TDS water for desalination.

Dissolution of Simulated and Radioactive Savannah River Site High-Level Waste Sludges with Oxalic Acid & Citric Acid Solutions

International Nuclear Information System (INIS)

STALLINGS, MARY

2004-01-01

sludge solids. We recommend that these results be evaluated further to determine if these solutions contain sufficient neutron poisons. We observed low general corrosion rates in tests in which carbon steel coupons were contacted with solutions of oxalic acid, citric acid and mixtures of oxalic and citric acids. Wall thinning can be minimized by maintaining short contact times with these acid solutions. We recommend additional testing with oxalic and oxalic/citric acid mixtures to measure dissolution performance of sludges that have not been previously dried. This testing should include tests to clearly ascertain the effects of total acid strength and metal complexation on dissolution performance. Further work should also evaluate the downstream impacts of citric acid on the SRS High-Level Waste System (e.g., radiochemical separations in the Salt Waste Processing Facility and addition of organic carbon in the Saltstone and Defense Waste Processing facilities)

Hydrogeochemical and isotopic investigation and water quality assessment of groundwater in the Sisseb El Alem Nadhour Saouaf aquifer (SANS), northeastern Tunisia

Science.gov (United States)

Hamdi, Mohamed; Zagrarni, Mohamed Faouzi; Jerbi, Hamza; Tarhouni, Jamila

2018-05-01

In the Sisseb El Alem Nadhour Saouaf basin (SANS), as in all other arid regions, surface water is scarce and groundwater is the greatest most important source of water for all uses. This study aims to identify the processes governing groundwater mineralization in order to assess the suitability of the groundwater for drinking and agriculture purposes. This research used a geodatabase which includes information on hydrogeology, geochemistry, land cover, and geology. We identified the most important factors involved in the deterioration of water quality, including anhydrite and gypsum dissolution, silicate weathering, downward leakage between aquifers, evaporation, groundwater over-exploitation, and the overuse of fertilizers. Furthermore, the two following important factors were identified: the intrusion of Sebkhat El Kelbia and the vertical flow from the deep aquifer. Results were used to develop a conceptual geochemical model, wherein three geochemical regions were differentiated. Statistical techniques, such as Principal Component Analysis (PCA) and Hierarchical Cluster Analysis (HCA) were used to confirm the water affinities and the presence of three different geochemical regions. The water quality index (WQI), Wilcox and Richards's diagrams were performed to assess the suitability of groundwater to drinking and irrigation purposes. These indexes confirm the fact that the groundwater of this aquifer is not suitable for irrigation, neither for drinking. Furthermore, 18O and deuterium isotope data indicate the importance of evaporation in the basin, and the recharge with modern rainfall.

Dissolution behavior of PFBR MOX fuel in nitric acid

International Nuclear Information System (INIS)

Kelkar, Anoop; Kapoor, Y.S.; Singh, Mamta; Meena, D.L.; Pandey, Ashish; Bhatt, R.B.; Behere, P.G.

2017-01-01

Present paper describes the dissolution characteristics of PFBR MOX fuel (U,Pu)O 2 in nitric acid. An overview of batch dissolution experiments, studying the percentage dissolution of uranium and plutonium in (U, Pu)O 2 MOX sintered pellets with different percentage of PuO 2 with reference to time and nitric acid concentration are described. 90% of uranium and plutonium of PFBR MOX gets dissolves in 2 hrs and amount of residue increases with the decrease in nitric acid concentration. Overall variation in percentage residue in PFBR MOX fuel after dissolution test also described. (author)

Do Workplace Sex Ratios Affect Partnership Formation and Dissolution?

DEFF Research Database (Denmark)

Svarer, Michael

In this paper, I analyse the association between workplace sex ratios and partnership formation and dissolution. I find that the risk of dissolution increases with the fraction of coworkers of the opposite sex at both the female and male workplace. On the other hand, workplace sex ratios are not ......In this paper, I analyse the association between workplace sex ratios and partnership formation and dissolution. I find that the risk of dissolution increases with the fraction of coworkers of the opposite sex at both the female and male workplace. On the other hand, workplace sex ratios...

Identification of the Hydrogeochemical Processes in Groundwater Using Classic Integrated Geochemical Methods and Geostatistical Techniques, in Amol-Babol Plain, Iran

Science.gov (United States)

Sheikhy Narany, Tahoora; Ramli, Mohammad Firuz; Aris, Ahmad Zaharin; Sulaiman, Wan Nor Azmin; Juahir, Hafizan; Fakharian, Kazem

2014-01-01

Hydrogeochemical investigations had been carried out at the Amol-Babol Plain in the north of Iran. Geochemical processes and factors controlling the groundwater chemistry are identified based on the combination of classic geochemical methods with geographic information system (GIS) and geostatistical techniques. The results of the ionic ratios and Gibbs plots show that water rock interaction mechanisms, followed by cation exchange, and dissolution of carbonate and silicate minerals have influenced the groundwater chemistry in the study area. The hydrogeochemical characteristics of groundwater show a shift from low mineralized Ca-HCO3, Ca-Na-HCO3, and Ca-Cl water types to high mineralized Na-Cl water type. Three classes, namely, C1, C2, and C3, have been classified using cluster analysis. The spatial distribution maps of Na+/Cl−, Mg2+/Ca2+, and Cl−/HCO3 − ratios and electrical conductivity values indicate that the carbonate and weathering of silicate minerals played a significant role in the groundwater chemistry on the southern and western sides of the plain. However, salinization process had increased due to the influence of the evaporation-precipitation process towards the north-eastern side of the study area. PMID:24523640

The complexity of nanoparticle dissolution and its importance in nanotoxicological studies

International Nuclear Information System (INIS)

Misra, Superb K.; Dybowska, Agnieszka; Berhanu, Deborah; Luoma, Samuel N.; Valsami-Jones, Eugenia

2012-01-01

Dissolution of nanoparticles (NPs) is an important property that alters their abundance and is often a critical step in determining safety of nanoparticles. The dissolution status of the NPs in exposure media (i.e. whether they remain in particulate form or dissolve — and to what extent), strongly affects the uptake pathway, toxicity mechanisms and the environmental compartment in which NPs will have the highest potential impact. A review of available dissolution data on NPs demonstrates there is a range of potential outcomes depending on the NPs and the exposure media. For example two nominally identical nanoparticles, in terms of size and composition, could have totally different dissolution behaviours, subject to different surface modifications. Therefore, it is imperative that toxicological studies are conducted in conjunction with dissolution of NPs to establish the true biological effect of NPs and hence, assist in their regulation. -- Graphical abstract: Various physicochemical factors affecting dissolution of nanoparticles. Highlights: ► In this study we discuss dissolution of nanoparticles. ► Physicochemical properties of nanoparticles influence dissolution. ► Measuring dissolution of nanoparticles can help to understand their biological response.

Hydro-geochemical paths of multi-layer groundwater system in coal mining regions - Using multivariate statistics and geochemical modeling approaches.

Science.gov (United States)

Liu, Pu; Hoth, Nils; Drebenstedt, Carsten; Sun, Yajun; Xu, Zhimin

2017-12-01

Groundwater is an important drinking water resource that requires protection in North China. Coal mining industry in the area may influence the water quality evolution. To provide primary characterization of the hydrogeochemical processes and paths that control the water quality evolution, a complex multi-layer groundwater system in a coal mining area is investigated. Multivariate statistical methods involving hierarchical cluster analysis (HCA) and principal component analysis (PCA) are applied, 6 zones and 3 new principal components are classified as major reaction zones and reaction factors. By integrating HCA and PCA with hydrogeochemical correlations analysis, potential phases, reactions and connections between various zones are presented. Carbonates minerals, gypsum, clay minerals as well as atmosphere gases - CO 2 , H 2 O and NH 3 are recognized as major reactants. Mixtures, evaporation, dissolution/precipitation of minerals and cation exchange are potential reactions. Inverse modeling is finally used, and it verifies the detailed processes and diverse paths. Consequently, 4 major paths are found controlling the variations of groundwater chemical properties. Shallow and deep groundwater is connected primarily by the flow of deep groundwater up through fractures and faults into the shallow aquifers. Mining does not impact the underlying aquifers that represent the most critical groundwater resource. But controls should be taken to block the mixing processes from highly polluted mine water. The paper highlights the complex hydrogeochemical evolution of a multi-layer groundwater system under mining impact, which could be applied to further groundwater quality management in the study area, as well as most of the other coalfields in North China. Copyright © 2017 Elsevier B.V. All rights reserved.

Dissolution Flowsheet for High Flux Isotope Reactor Fuel

Energy Technology Data Exchange (ETDEWEB)

Daniel, W. E. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Rudisill, T. S. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); O' Rourke, P. E. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Karay, N. S [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL)

2016-09-27

As part of the Spent Nuclear Fuel (SNF) processing campaign, H-Canyon is planning to begin dissolving High Flux Isotope Reactor (HFIR) fuel in late FY17 or early FY18. Each HFIR fuel core contains inner and outer fuel elements which were fabricated from uranium oxide (U₃O₈) dispersed in a continuous Al phase using traditional powder metallurgy techniques. Fuels fabricated in this manner, like other SNF’s processed in H-Canyon, dissolve by the same general mechanisms with similar gas generation rates and the production of H₂. The HFIR fuel cores will be dissolved and the recovered U will be down-blended into low-enriched U. HFIR fuel was previously processed in H-Canyon using a unique insert in both the 6.1D and 6.4D dissolvers. Multiple cores will be charged to the same dissolver solution maximizing the concentration of dissolved Al. The objective of this study was to identify flowsheet conditions through literature review and laboratory experimentation to safely and efficiently dissolve the HFIR fuel in H-Canyon. Laboratory-scale experiments were performed to evaluate the dissolution of HFIR fuel using both Al 1100 and Al 6061 T6 alloy coupons. The Al 1100 alloy was considered a representative surrogate which provided an upper bound on the generation of flammable (i.e., H₂) gas during the dissolution process. The dissolution of the Al 6061 T6 alloy proceeded at a slower rate than the Al 1100 alloy, and was used to verify that the target Al concentration in solution could be achieved for the selected Hg concentration. Mass spectrometry and Raman spectroscopy were used to provide continuous monitoring of the concentration of H₂ and other permanent gases in the dissolution offgas, allowing the development of H₂ generation rate profiles. The H₂ generation rates were subsequently used to evaluate if a full HFIR core could be dissolved in an H-Canyon dissolver without exceeding 60% of the

Stable isotopes (2H, 18O and 13C) in groundwaters from the northwestern portion of the Guarani Aquifer System (Brazil)

Science.gov (United States)

Gastmans, Didier; Chang, Hung Kiang; Hutcheon, Ian

2010-09-01

The groundwater flow pattern of the western part of the Guarani Aquifer System (GAS), Brazil, is characterized by three regional recharge areas in the north, and a potentiometric divide in the south, which trends north-south approximately. Groundwater flow is radial from these regional recharge areas toward the center of Paraná Sedimentary Basin and toward the western outcrop areas at the border of the Pantanal Matogrossense, because of the potentiometric divide. The isotopic composition of GAS groundwater leads to understanding the paleoclimatic conditions in the regional recharge areas. The δ18O and δ2H isotopic ratios of GAS groundwaters vary, respectively, from -9.1 to -4.8‰ V-SMOW and -58.4 to -21.7‰ V-SMOW. In the recharge zones, enriched δ18O values are observed, while in the confined zone lighter δ18O values are observed. These suggest that climatic conditions were 10°C cooler than the present during the recharge of these waters. The δ13C ratios in groundwater of GAS, in the study area, vary from -19.5 to -6.5‰ VPDB, increasing along the regional flow lines toward the confined zone. This variation is related to dissolution of carbonate cement in the sandstones.

Groundwater residence time : tell me who you are and I will tell which information you may provide

Science.gov (United States)

Aquilina, Luc; Labasque, Thierry; Kolbe, Tamara; Marçais, Jean; Leray, Sarah; Abbott, Ben; de Dreuzy, Jean-Raynald

2016-04-01

Groundwater residence-time or ages have been widely used in hydrogeology during the last decades. Following tritium measurements, anthropogenic gases (CFC, SF6, 35Kr) have been developed. They provide information at the aquifer scale on long residence times. They complement the more localized data obtained from sparse boreholes with hydraulic and geophysical methods. Anthropogenic tracer concentrations are most generally considered as "Groundwater ages" using a piston flow model providing an order of magnitude for the residence time. More advanced information can however be derived from the combined analysis of the tracer concentrations. For example, the residence time distribution over the last 50 years can be well approached by the concentration of two sufficient different anthropogenic tracers in the group (CFC, SF6, 35Kr), i.e. tracers whose anthropogenic chronicles are sufficiently different. And, with additional constrains on geological and hydraulic properties, groundwater ages contribute to characterize the aquifer structures and the groundwater resources. Complex geological environments also include old groundwater bodies in extremely confined aquifer sections. In such cases, various tracers are related to highly different processes. CFCs can be taken as a marker of modern contamination to track exchanges between shallower and deeper aquifers, leakage processes, and modification of circulations linked to recent anthropogenic changes. 14C or 36Cl can be used to evidence much older processes but have to be related to the history of the chemical element itself. Numerous field studies in fact demonstrate the broad-range extent of the residence time distribution spanning in some cases several orders of magnitude. Flow and transport models in heterogeneous structures confirm such wide residence times and help to characterize their distribution. Residence times also serve as a privileged interface to the fate of some contaminants in aquifers or to trace

Carbon mineralization and pyrite oxidation in groundwater: Importance for silicate weathering in boreal forest soils and stream base-flow chemistry

International Nuclear Information System (INIS)

Klaminder, J.; Grip, H.; Moerth, C.-M.; Laudon, H.

2011-01-01

Research highlights: → Organic compounds is mineralized during later transport in deep groundwater aquifers. → Carbonic acid generated by this process stimulates dissolution of silicate minerals. → Protons derived from pyrite oxidation also affects weathering in deep groundwater. → The identified weathering mechanisms affect base-flow chemistry in boreal streams. - Abstract: What role does mineralized organic C and sulfide oxidation play in weathering of silicate minerals in deep groundwater aquifers? In this study, how H 2 CO 3 , produced as a result of mineralization of organic matter during groundwater transport, affects silicate weathering in the saturated zone of the mineral soil along a 70 m-long boreal hillslope is demonstrated. Stream water measurements of base cations and δ 18 O are included to determine the importance of the deep groundwater system for downstream surface water. The results suggest that H 2 CO 3 generated from organic compounds being mineralized during the lateral transport stimulates weathering at depths between 0.5 and 3 m in the soil. This finding is indicated by progressively increasing concentrations of base cations-, silica- and inorganic C (IC) in the groundwater along the hillslope that co-occur with decreasing organic C (OC) concentrations. Protons derived from sulfide oxidation appear to be an additional driver of the weathering process as indicated by a build-up of SO 4 2- in the groundwater during lateral transport and a δ 34 S per mille value of +0.26-3.76 per mille in the deep groundwater indicating S inputs from pyrite. The two identified active acids in the deep groundwater are likely to control the base-flow chemistry of streams draining larger catchments (>1 km 2 ) as evident by δ 18 O signatures and base cation concentrations that overlap with that of the groundwater.

Carbon mineralization and pyrite oxidation in groundwater: Importance for silicate weathering in boreal forest soils and stream base-flow chemistry

Energy Technology Data Exchange (ETDEWEB)

Klaminder, J., E-mail: jonatan.klaminder@emg.umu.se [Department of Forest Ecology and Management, SLU, SE-901 83 Umea (Sweden)] [Department of Ecology and Environmental Science, Umea University, SE-901 87 (Sweden); Grip, H. [Department of Forest Ecology and Management, SLU, SE-901 83 Umea (Sweden); Moerth, C.-M. [Department of Geological Sciences, Stockholm University, 106 91 Stockholm (Sweden); Laudon, H. [Department of Forest Ecology and Management, SLU, SE-901 83 Umea (Sweden)

2011-03-15

Research highlights: {yields} Organic compounds is mineralized during later transport in deep groundwater aquifers. {yields} Carbonic acid generated by this process stimulates dissolution of silicate minerals. {yields} Protons derived from pyrite oxidation also affects weathering in deep groundwater. {yields} The identified weathering mechanisms affect base-flow chemistry in boreal streams. - Abstract: What role does mineralized organic C and sulfide oxidation play in weathering of silicate minerals in deep groundwater aquifers? In this study, how H{sub 2}CO{sub 3}, produced as a result of mineralization of organic matter during groundwater transport, affects silicate weathering in the saturated zone of the mineral soil along a 70 m-long boreal hillslope is demonstrated. Stream water measurements of base cations and {delta}{sup 18}O are included to determine the importance of the deep groundwater system for downstream surface water. The results suggest that H{sub 2}CO{sub 3} generated from organic compounds being mineralized during the lateral transport stimulates weathering at depths between 0.5 and 3 m in the soil. This finding is indicated by progressively increasing concentrations of base cations-, silica- and inorganic C (IC) in the groundwater along the hillslope that co-occur with decreasing organic C (OC) concentrations. Protons derived from sulfide oxidation appear to be an additional driver of the weathering process as indicated by a build-up of SO{sub 4}{sup 2-} in the groundwater during lateral transport and a {delta}{sup 34}S per mille value of +0.26-3.76 per mille in the deep groundwater indicating S inputs from pyrite. The two identified active acids in the deep groundwater are likely to control the base-flow chemistry of streams draining larger catchments (>1 km{sup 2}) as evident by {delta}{sup 18}O signatures and base cation concentrations that overlap with that of the groundwater.

Crystal modifications and dissolution rate of piroxicam.

Science.gov (United States)

Lyn, Lim Yee; Sze, Huan Wen; Rajendran, Adhiyaman; Adinarayana, Gorajana; Dua, Kamal; Garg, Sanjay

2011-12-01

Piroxicam is a nonsteroidal anti-inflammatory drug with low aqueous solubility which exhibits polymorphism. The present study was carried out to develop polymorphs of piroxicam with enhanced solubility and dissolution rate by the crystal modification technique using different solvent mixtures prepared with PEG 4000 and PVP K30. Physicochemical characteristics of the modified crystal forms of piroxicam were investigated by X-ray powder diffractometry, FT-IR spectrophotometry and differential scanning calorimetry. Dissolution and solubility profiles of each modified crystal form were studied and compared with pure piroxicam. Solvent evaporation method (method I) produced both needle and cubic shaped crystals. Slow crystallization from ethanol with addition of PEG 4000 or PVP K30 at room temperature (method II) produced cubic crystal forms. Needle forms produced by method I improved dissolution but not solubility. Cubic crystals produced by method I had a dissolution profile similar to that of untreated piroxicam but showed better solubility than untreated piroxicam. Cubic shaped crystals produced by method II showed improved dissolution, without a significant change in solubility. Based on the XRPD results, modified piroxicam crystals obtained by method I from acetone/benzene were cube shaped, which correlates well with the FTIR spectrum; modified needle forms obtained from ethanol/methanol and ethanol/acetone showed a slight shift of FTIR peak that may be attributed to differences in the internal structure or conformation.

Dissolution of cellulose in ionic liquid: A review

Science.gov (United States)

Mohd, N.; Draman, S. F. S.; Salleh, M. S. N.; Yusof, N. B.

2017-02-01

Dissolution of cellulose with ionic liquids (IL) and deep eutectic solvent (DES) lets the comprehensive dissolution of cellulose. Basically, cellulose can be dissolved, in some hydrophilic ionic liquids, such as 1-butyl-3-methylimidazolium chloride (BMIMCl) and 1-allyl-3-methylimidazolium chloride (AMIMCl). Chloride based ionic liquids are suitable solvents for cellulose dissolution. Although the ILs is very useful in fine chemical industry, its application in the pharmaceutical and food industry have been very limited due to issues with toxicity, purity, and high cost. Seeing to these limitations, new green alternative solvent which is DES was used. This green solvents, may be definitely treated as the next-generation reagents for more sustainable industrial development. Thus, this review aims to discuss the dissolution of cellulose either with ionic liquids or DES and its application.

The anodic dissolution of zinc and zinc alloys in alkaline solution. II. Al and Zn partial dissolution from 5% Al–Zn coatings

International Nuclear Information System (INIS)

Vu, T.N.; Mokaddem, M.; Volovitch, P.; Ogle, K.

2012-01-01

Graphical abstract: - Abstract: The polarization behavior of a 5 wt% Al–Zn steel coating (Galfan™) has been investigated in alkaline solution using atomic emission spectroelectrochemistry (AESEC). The instantaneous Zn and Al dissolution rates were measured as a function of time during a linear scan and potential step transients. The formation rate of insoluble oxides was determined from the difference between the convoluted total current and the sum of the elemental dissolution currents. It was found that, over a wide potential range, the zinc and aluminum partial currents behaved in a similar way to pure zinc and pure aluminum independently. However, during the period in which zinc was active, aluminum dissolution was inhibited. This is attributed to the inhibitive effect of the first and/or the second states of zinc oxide that are formed during the active potential domain. The third form of zinc oxide, observed at higher potential and responsible for the passivation of zinc dissolution, does not have a measurable effect on the Al dissolution rate.

Dilution physics modeling: Dissolution/precipitation chemistry

International Nuclear Information System (INIS)

Onishi, Y.; Reid, H.C.; Trent, D.S.

1995-09-01

This report documents progress made to date on integrating dilution/precipitation chemistry and new physical models into the TEMPEST thermal-hydraulics computer code. Implementation of dissolution/precipitation chemistry models is necessary for predicting nonhomogeneous, time-dependent, physical/chemical behavior of tank wastes with and without a variety of possible engineered remediation and mitigation activities. Such behavior includes chemical reactions, gas retention, solids resuspension, solids dissolution and generation, solids settling/rising, and convective motion of physical and chemical species. Thus this model development is important from the standpoint of predicting the consequences of various engineered activities, such as mitigation by dilution, retrieval, or pretreatment, that can affect safe operations. The integration of a dissolution/precipitation chemistry module allows the various phase species concentrations to enter into the physical calculations that affect the TEMPEST hydrodynamic flow calculations. The yield strength model of non-Newtonian sludge correlates yield to a power function of solids concentration. Likewise, shear stress is concentration-dependent, and the dissolution/precipitation chemistry calculations develop the species concentration evolution that produces fluid flow resistance changes. Dilution of waste with pure water, molar concentrations of sodium hydroxide, and other chemical streams can be analyzed for the reactive species changes and hydrodynamic flow characteristics

Determination of the dissolution slowness surface by study of etched shapes I. Morphology of the dissolution slowness surface and theoretical etched shapes

Science.gov (United States)

Leblois, T.; Tellier, C. R.

1992-07-01

We propose a theoretical model for the anisotropic etching of crystals, in order to be applied in the micromachining. The originality of the model is due to the introduction of dissolution tensors to express the representative surface of the dissolution slowness. The knowledge of the equation of the slowness surface allows us to determine the trajectories of all the elements which compose the starting surface. It is then possible to construct the final etched shape by numerical simulation. Several examples are given in this paper which show that the final etched shapes are correlated to the extrema of the dissolution slowness. Since the slowness surface must be determined from experiments, emphasis is placed on difficulties encountered when we correlate theory to experiments. Nous avons modélisé le processus de dissolution anisotrope des cristaux en vue d'une application à la simulation des formes obtenues par photolithogravure chimique. La principale originalité de ce modèle tient à l'introduction de tenseurs de dissolution pour exprimer la surface représentative de la lenteur de dissolution. La connaissance de l'équation de la lenteur de dissolution permet de calculer les trajectoires des différents éléments constituant la surface de départ puis de reconstituer par simulation la forme dissoute. Les simulations démontrent que les formes limites des cristaux dissous sont corrélées aux extrema de la lenteur de dissolution. La détermination de la surface de la lenteur se faisant à partir de mesures expérimetales, nous nous sommes efforcés de montrer toutes les difficultés attachées à cette analyse.

Dissolution of synthetic uranium dibutyl phosphate deposits in oxidizing and reducing chemical formulations

International Nuclear Information System (INIS)

Rufus, A.L.; Sathyaseelan, V.S.; Narasimhan, S.V.; Velmurugan, S.

2013-01-01

Graphical abstract: SEM of the U-DBP coated stainless steel coupon before and after exposure to chemical formulation containing acid permanganate at 80 °C. -- Highlights: •Combination of oxidation and reduction processes efficiently dissolves U-DBP deposits. •NP and NAC formulations are compatible with SS-304. •Dissolved uranium and added chemicals are effectively removed via ion exchangers. -- Abstract: Permanganate and nitrilotriacetic acid (NTA) based dilute chemical formulations were evaluated for the dissolution of uranium dibutyl phosphate (U-DBP), a compound that deposits over the surfaces of nuclear reprocessing plants and waste storage tanks. A combination of an acidic, oxidizing treatment (nitric acid with permanganate) followed by reducing treatment (NTA based formulation) efficiently dissolved the U-DBP deposits. The dissolution isotherm of U-DBP in its as precipitated form followed a logarithmic fit. The same chemical treatment was also effective in dissolving U-DBP coated on the surface of 304-stainless steel, while resulting in minimal corrosion of the stainless steel substrate material. Investigation of uranium recovery from the resulting decontamination solutions by ion exchange with a bed of mixed anion and cation resins showed quantitative removal of uranium

Dissolution of synthetic uranium dibutyl phosphate deposits in oxidizing and reducing chemical formulations

Energy Technology Data Exchange (ETDEWEB)

Rufus, A.L.; Sathyaseelan, V.S.; Narasimhan, S.V.; Velmurugan, S., E-mail: svelu@igcar.gov.in

2013-06-15

Graphical abstract: SEM of the U-DBP coated stainless steel coupon before and after exposure to chemical formulation containing acid permanganate at 80 °C. -- Highlights: •Combination of oxidation and reduction processes efficiently dissolves U-DBP deposits. •NP and NAC formulations are compatible with SS-304. •Dissolved uranium and added chemicals are effectively removed via ion exchangers. -- Abstract: Permanganate and nitrilotriacetic acid (NTA) based dilute chemical formulations were evaluated for the dissolution of uranium dibutyl phosphate (U-DBP), a compound that deposits over the surfaces of nuclear reprocessing plants and waste storage tanks. A combination of an acidic, oxidizing treatment (nitric acid with permanganate) followed by reducing treatment (NTA based formulation) efficiently dissolved the U-DBP deposits. The dissolution isotherm of U-DBP in its as precipitated form followed a logarithmic fit. The same chemical treatment was also effective in dissolving U-DBP coated on the surface of 304-stainless steel, while resulting in minimal corrosion of the stainless steel substrate material. Investigation of uranium recovery from the resulting decontamination solutions by ion exchange with a bed of mixed anion and cation resins showed quantitative removal of uranium.

Magnetic resonance imaging of tablet dissolution.

Science.gov (United States)

Nott, Kevin P

2010-01-01

Magnetic resonance imaging (MRI) is the technique of choice for measuring hydration, and its effects, during dissolution of tablets since it non-invasively maps (1)H nuclei associated with 'mobile' water. Although most studies have used MRI systems with high-field superconducting magnets, low-field laboratory-based instruments based on permanent magnet technology are being developed that provide key data for the formulation scientist. Incorporation of dissolution hardware, in particular the United States Pharmacopeia (USP) apparatus 4 flow-through cell, allows measurements under controlled conditions for comparison against other dissolution methods. Furthermore, simultaneous image acquisition and measurement of drug concentration allow direct comparison of the drug release throughout the hydration process. The combination of low-field MRI with USP-4 apparatus provides another tool to aid tablet formulation. Copyright 2009 Elsevier B.V. All rights reserved.

Dissolution kinetics of lead telluride in alkali solutions of hydrogen peroxide

International Nuclear Information System (INIS)

Danilova, M.G.; Sveshnikova, L.L.; Stavitskaya, T.A.; Repinskij, S.M.

1991-01-01

Dissolution kinetics of lead telluride in alkali solutions of hydrogen peroxide was investigated. Dependences of change of PbTe dissolution rate on concentration of hydrogen peroxide and alkali in the solution were obtained. It is shown that dissolution rate of lead telluride is affected by dissolution rate of lead oxide, representing the product of ReTe dissolution. The obtained regularities can be explained by change of solution structure with increase of KOH concentration and by the state of hydrogen peroxide in the solution

Effect of dissolution on the load–settlement behavior of shallow foundations

KAUST Repository

Cha, Minsu

2016-03-10

Mineral dissolution and solid-liquid phase change may cause settlement or affect the bearing capacity of shallow foundations. The effect of gradual grain dissolution on small-scale shallow foundation behavior is investigated using the discrete element method. Results show that dissolution is most detrimental during early stages, as initially contacting particles shrink and force chains must reform throughout the medium. Porosity tends to increase during dissolution and force chains evolve into strong localized forces with a honeycomb topology. Higher settlements are required to mobilize bearing resistance in postdissolution sediments than in pre-dissolution ones. Subsurface mineral dissolution beneath a footing under load is the worst condition; in fact, settlements in such cases are higher than when a foundation load is applied on a sediment that has already experienced dissolution. © the author(s) or their institution(s).

Effect of dissolution on the load–settlement behavior of shallow foundations

KAUST Repository

Cha, Minsu; Santamarina, Carlos

2016-01-01

Mineral dissolution and solid-liquid phase change may cause settlement or affect the bearing capacity of shallow foundations. The effect of gradual grain dissolution on small-scale shallow foundation behavior is investigated using the discrete element method. Results show that dissolution is most detrimental during early stages, as initially contacting particles shrink and force chains must reform throughout the medium. Porosity tends to increase during dissolution and force chains evolve into strong localized forces with a honeycomb topology. Higher settlements are required to mobilize bearing resistance in postdissolution sediments than in pre-dissolution ones. Subsurface mineral dissolution beneath a footing under load is the worst condition; in fact, settlements in such cases are higher than when a foundation load is applied on a sediment that has already experienced dissolution. © the author(s) or their institution(s).

Simulating Salt Movement using a Coupled Salinity Transport Model in a Variably Saturated Agricultural Groundwater System

Science.gov (United States)

Tavakoli Kivi, S.; Bailey, R. T.; Gates, T. K.

2017-12-01

Salinization is one of the major concerns in irrigated agricultural fields. Increasing salinity concentrations are due principally to a high water table that results from excessive irrigation, canal seepage, and a lack of efficient drainage systems, and lead to decreasing crop yield. High groundwater salinity loading to nearby river systems also impacts downstream areas, with saline river water diverted for application on irrigated fields. To assess the different strategies for salt remediation, we present a reactive transport model (UZF-RT3D) coupled with a salinity equilibrium chemistry module for simulating the fate and transport of salt ions in a variably-saturated agricultural groundwater system. The developed model accounts not for advection, dispersion, nitrogen and sulfur cycling, oxidation-reduction, sorption, complexation, ion exchange, and precipitation/dissolution of salt minerals. The model is applied to a 500 km2 region within the Lower Arkansas River Valley (LARV) in southeastern Colorado, an area acutely affected by salinization in the past few decades. The model is tested against salt ion concentrations in the saturated zone, total dissolved solid concentrations in the unsaturated zone, and salt groundwater loading to the Arkansas River. The model now can be used to investigate salinity remediation strategies.

The distribution and hydrogeological controls of fluoride in the groundwater of central Ethiopian rift and adjacent highlands

Science.gov (United States)

Ayenew, Tenalem

2008-05-01

Occurrence of fluoride (F) in groundwater has drawn worldwide attention, since it has considerable impact on human health. In Ethiopia high concentrations of F in groundwaters used for community water supply have resulted in extensive dental and skeletal fluorosis. As a part of a broader study, the distribution of F in groundwater has been investigated, and compared with bedrock geology and pertinent hydrochemical variables. The result indicates extreme spatial variations. High F concentration is often associated with active and sub-active regional thermal fields and acidic volcanics within high temperature rift floor. Variations in F can also be related to changes in calcium concentration resulting from dissolution of calcium minerals and mixing with waters of different chemical composition originated from variable hydrogeological environment across the rift valley. The concentration of F dramatically declines from the rift towards the highlands with the exception of scattered points associated with thermal springs confined in local volcanic centers. There are also interactions of F-rich alkaline lakes and the surrounding groundwater. Meteoric waters recharging volcanic aquifers become enriched with respect to F along the groundwater flow path from highland recharge areas to rift discharge areas. Locally wells drilled along large rift faults acting as conduits of fresh highland waters show relatively lower F. These areas are likely to be possible sources of better quality waters within the rift. The result of this study has important implications on site selection for water well drilling.

Dissolution characteristics of mixed UO2 powders in J-13 water under saturated conditions

International Nuclear Information System (INIS)

Veleckis, E.; Hoh, J.C.

1991-03-01

The Yucca Mountain Project/Spent Fuel program at Argonne National Laboratory is designed to determine radionuclide release rates by exposing high-level waste to repository-relevant groundwater. To gain experience for the tests with spent fuel, a scoping experiment was conducted at room temperature to determine the uranium release rate from an unirradiated UO 2 powder mixture (14.3 wt % enrichment in 235 U) to J-13 water under saturated conditions. Another goal set for the experiment was to develop a method for utilizing isotope dilution techniques to determine whether the dissolution rate of UO 2 matrix is in accordance with an existing kinetic model. Results of these analyses revealed unequal uranium dissolution rates from the enriched and depleted portions of the powder mixture because of undisclosed differences between them. Although the presence of this inhomogeneity has precluded the application of the kinetic model, it also provided an opportunity to elaborate on the utilization of isotope dilution data in recognizing and quantifying such conditions. Detailed listings of uranium release and solution chemistry data are presented. Other problems commonly associated with spent fuel, such as the effectiveness of filtering media, the existence of uranium concentration peaks during early stages of the leach tests, the need for concentration corrections due to water replenishments of sample volumes, and experience derived from isotope dilution data are discussed in the context of the present results. 10 refs., 5 figs., 7 tabs

Investigation of the gas formation in dissolution process of nuclear reactor fuel

International Nuclear Information System (INIS)

Zhang Qinfen; Liao Yuanzhong; Chen Yongqing; Sun Shuyun; Fan Yincheng

1987-12-01

The gas formation in dissolution process of two kinds of nuclear fuels was studied. The results shows that the maximum volume flow released from dissolution system is composed of two parts. One of them is air remained in dissolver and pushed out by acid vapor. The other is produced in dissolution reaction. The procedure of calculating the gas amount produced in dissolution process has been given. It is based on variation of components of dissolution solution. The gas amount produced in dissolution process of spent UO 2 fuel elements was calculated. The condenser system and loading volume of disposal system of tail gas of dissolution of spent fuel were discussed

Chemical dissolution of spent fuel and cladding using complexed fluoride species

International Nuclear Information System (INIS)

Rance, P.J.W.; Freeman, G.A.; Mishin, V.; Issoupov, V.

2001-01-01

The dissolution of LWR fuel cladding using two fluoride ion donors, HBF 4 and K 2 ZrF 6 , in combination with nitric acid has been investigated as a potential reprocessing head-end process suitable for chemical decladding and fuel dissolution in a single process step. Maximum zirconium concentrations in the order of 0,75 to 1 molar have been achieved and dissolution found to continue to low F:Zr ratios albeit at ever decreasing rates. Dissolution rates of un-oxidised zirconium based fuel claddings are fast, whereas oxidised materials exhibit an induction period prior to dissolution. Data is presented relating to the rates of dissolution of cladding and UO 2 fuels under various conditions. (author)

Evaluation of groundwater quality and suitability for irrigation and drinking purposes in southwest Punjab, India using hydrochemical approach

Science.gov (United States)

Sharma, Diana Anoubam; Rishi, Madhuri S.; Keesari, Tirumalesh

2017-10-01

Groundwater samples from alluvial aquifers of Bathinda district, southwest Punjab were measured for physicochemical parameters as well as major ion chemistry to evaluate the groundwater suitability for drinking and irrigation purposes and to present the current hydrochemical status of groundwater of this district. Temporal variations were analyzed by comparing the pre- and post-monsoon groundwater chemistry. Most of the samples showed contamination: F- (72 %), Mg2+ (22 %), SO4 2- (28 %), TH (25 %), NO3 - (22 %), HCO3 - (22 %) and TDS (11 %) during pre-monsoon and F- (50 %), Mg2+ (39 %), SO4 2- (22 %), TH (28 %), NO3 - (22 %) and TDS (28 %) during post-monsoon above permissible limits for drinking, while rest of the parameters fall within the limits. Irrigation suitability was checked using sodium absorption ratio (SAR), residual sodium carbonate (RSC), percent sodium (Na%) and permeability index (PI). Most of the samples fall under good to suitable category during pre-monsoon period, but fall under doubtful to unsuitable category during post-monsoon period. Presence of high salt content in groundwater during post-monsoon season reflects leaching of salts present in the unsaturated zone by infiltrating precipitation. Hydrochemical data was interpreted using Piper's trilinear plot and Chadha's plot to understand the various geochemical processes affecting the groundwater quality. The results indicate that the order of cation dominance is Na+ > Mg2+ > Ca2+, while anion dominance is in the order Cl- > HCO3 - > SO4 2-. The geochemistry of groundwater of this district is mainly controlled by the carbonate and silicate mineral dissolution and ion exchange during pre-monsoon and leaching from the salts deposited in vadose zone during post-monsoon. The main sources of contamination are soluble fertilizers and livestock wastes. This study is significant as the surface water resources are limited and the quality and quantity of groundwater are deteriorating with time due to