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At least 91 records · Page 5

Percolation in Salt Rocks - 18652

We present laboratory investigations of fluid percolation in salt rocks, performed on drilled core samples, which show that natural rock salt does not become permeable at high pressures and temperatures, as had been claimed in the literature. Rather, we confirm the existence of a percolation threshold: Fluid migration is only possible when the fluid pressure equals or exceeds the lowest confining stress. The lab tests corroborate in-situ-determinations of the percolation threshold in salt formations: The threshold is given by the minimal stress in the rock mass (minimal stress criterion), and fluid pressure-driven percolation starts once it is exceeded. The hypothesis that the percolation threshold vanishes at high pressure and temperature is thus refuted by experiments on natural rock salt. These experimental tests, performed in the framework of the KOSINA project, are an important prerequisite for the proof of integrity of saliferous barriers in the disposal of radioactive waste in salt rocks. (authors)

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A Decision-Based Iterative Modeling Framework for Probabilistic Performance Assessments - 18441

Radiological probabilistic performance assessments (PPAs) employ highly complex computer models to simulate the release of radionuclides from wastes in an engineered disposal facility, migration of these radionuclides over time, and resulting radiological dose to potentially exposed individuals. An iterative approach to PPA modeling is described to help define the appropriate complexity of the computer model. An initial model is developed that addresses all relevant processes and media, but that employs preliminary statistical parameter distributions to minimize the initial effort expended. Where appropriate, transport and exposure submodels with simplifying assumptions are also used in the initial model. Different assumptions and boundaries may be explored with the initial model to assess their importance in constraining model results. Exploration of the results of the initial model are used to determine the benefits of model refinements, and to guide such refinements to focus on specific areas of the model that most influence the model outputs of interest. This approach promotes efficiency and model parsimony, but does not compromise defensibility when performed in a transparent manner. Key model boundaries for a PPA include the time frame of the modeling (temporal boundaries), where future human receptors may be located (spatial boundaries), and what types of land uses and activities may exist in the future (exposure scenarios). Simplified transport and exposure models can be useful in helping decision makers and stakeholders establish such boundaries by analyzing the consequences of selecting different bounds and understanding which assumptions and boundaries have the greatest influence on the magnitude and distribution of model results. Pathway analysis and parameter sensitivity analysis performed on PPA model results are key components of the iterative modeling approach. The objective of pathway analysis is to identify the critical radionuclides and pathways contributing to radiation dose during the modeling performance period. An environmental 'pathway' is described by the connections from a waste package or cell in the disposal facility to a future human exposure event. These connections are commonly visualized using graphical means. A simple example of a potentially complete pathway for radon-222 is: radium-containing waste → radon emanation → upwards diffusion in cap material → diffusion/advection into a future building → inhalation exposure to a building occupant Parameter sensitivity analysis is conducted on the results of a PPA to identify those specific model input parameters whose distribution of values contributes the most to the distribution of target model output, such as annual radiation dose. Pathway and sensitivity analyses on initial modeling results provide information for guiding subsequent model development, and possibly interim decisions, by informing questions tied to the modeling objectives and performance criteria. For example, questions related to radiological doses from existing disposals may include: 1. Is radiation dose from radiological exposures either obviously negligible or obviously unacceptable based on initial modeling results? 2. If dose is not obviously negligible or unacceptable relative to applicable performance criteria, what model refinements would reduce uncertainty in the results to better inform decisions? (authors)

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Sorption of Cationic Radionuclides on Chlorite and Sericite formed by the Hydrothermal Alteration - 18180

Chlorite and sericite formed by the hydrothermal alteration of granite distribute predominantly around the geological repository in deep underground. These minerals often cover the surface of a solid phase and fill the fracture of granite considered as the natural barrier to the migration of radionuclides leaching from radioactive waste. Therefore, to assess the practical performance of the natural barrier, it is necessary to clarify the interaction between radionuclides and these minerals. This study examined the sorption of cationic radionuclides by chlorite and sericite through batch experiments, whereby Cs{sup +}, Sr{sup 2+}, and Eu{sup 3+} were used as tracer ions. In these experiments, powder-form chlorite or sericite was mixed with the solutions of the tracer ions to a liquid/solid ratio of 10 ml/g, and the resulting mixture was allowed to incubate for 2-7 days. The concentration of tracer ions was set to 1 mM and that of NaCl to a specific value in the 0-0.6 M range. The solution pH was 3, 5, or 8. As a result, tracer ions were significantly adsorbed by chlorite and sericite, regardless of pH or NaCl concentration, except when NaCl concentration reached the high value of 0.6 M. The distribution coefficient for europium ions at pH 5 was estimated to be 2-7 mL/g in chlorite and 10{sup 3}-10{sup 4} mL/g in sericite. These values significantly exceeded that measured for feldspar (2-4 mL/g), the predominant component of granite before it undergoes any hydrothermal alteration. These results suggest that cationic radionuclides will be immobilized through sorption in chlorite and sericite filling granite fractures, even if these thermal-fluid-formed minerals cover the surface of granite. (authors)

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Regulatory Technology Development Plan - Sodium Fast Reactor. Mechanistic Source Term - Metal Fuel Radionuclide Release

The development of an accurate and defensible mechanistic source term will be vital for the future licensing efforts of metal fuel, pool-type sodium fast reactors. To assist in the creation of a comprehensive mechanistic source term, the current effort sought to estimate the release fraction of radionuclides from metal fuel pins to the primary sodium coolant during fuel pin failures at a variety of temperature conditions. These release estimates were based on the findings of an extensive literature search, which reviewed past experimentation and reactor fuel damage accidents. Data sources for each radionuclide of interest were reviewed to establish release fractions, along with possible release dependencies, and the corresponding uncertainty levels. Although the current knowledge base is substantial, and radionuclide release fractions were established for the elements deemed important for the determination of offsite consequences following a reactor accident, gaps were found pertaining to several radionuclides. First, there is uncertainty regarding the transport behavior of several radionuclides (iodine, barium, strontium, tellurium, and europium) during metal fuel irradiation to high burnup levels. The migration of these radionuclides within the fuel matrix and bond sodium region can greatly affect their release during pin failure incidents. Post-irradiation examination of existing high burnup metal fuel can likely resolve this knowledge gap. Second, data regarding the radionuclide release from molten high burnup metal fuel in sodium is sparse, which makes the assessment of radionuclide release from fuel melting accidents at high fuel burnup levels difficult. This gap could be addressed through fuel melting experimentation with samples from the existing high burnup metal fuel inventory.

21 SPECIFIC NUCLEAR REACTORS AND ASSOCIATED PLANTS↗

Phosphate-Mediated Remediation of Metals and Radionuclides

Worldwide industrialization activities create vast amounts of organic and inorganic waste streams that frequently result in significant soil and groundwater contamination. Metals and radionuclides are of particular concern due to their mobility and long-term persistence in aquatic and terrestrial environments. As the global population increases, the demand for safe, contaminant-free soil and groundwater will increase as will the need for effective and inexpensive remediation strategies. Remediation strategies that include physical and chemical methods (i.e., abiotic) or biological activities have been shown to impede the migration of radionuclide and metal contaminants within soil and groundwater. However, abiotic remediation methods are often too costly owing to the quantities and volumes of soils and/or groundwater requiring treatment. The in situ sequestration of metals and radionuclides mediated by biological activities associated with microbial phosphorus metabolism is a promising and less costly addition to our existing remediation methods. This review highlights the current strategies for abiotic and microbial phosphate-mediated techniques for uranium and metal remediation.

Martinez, Robert J.↗

Development of Upscaling Techniques and Construction of Calibrated Models for Fractured Rocks Using Discrete Fracture Network Approaches

The Pahute Mesa Corrective Action Unit on the Nevada National Security Site (NNSS) contains several fractured aquifers that can potentially provide high-permeability pathways for radionuclides to migrate away from underground nuclear testing locations. Although the geometric properties of fractures, such as length and orientation, can be found using geophysical methods and borehole image analyses, the hydraulic property of fractures (which are primarily influenced by apertures) are often unknown or have a high degree of uncertainty attached to their values. The aperture values have a profound impact on groundwater velocity and are critical to understanding transport scales at Pahute Mesa. Fracture aperture values and their distributions also have dominant control over radionuclide transport with potential for long-range correlations or scale-invariant dynamics. Understanding of the small-scale transport variability in fractures could lead to identification of distinct characteristics on larger scales. Furthermore, upscaling techniques need to be developed to adequately predict transport behavior at field scales by capturing the transport trends of smaller scale networks. This report explores these vital modeling needs to understand the role of fractures in Pahute Mesa. Discrete fracture network (DFN) models are the basis for constructing a well-calibrated model to ascertain aperture values of fractures in lava-flow aquifers. These models are also used to develop and compare the usefulness of several random-walk-based models to perform transport upscaling.

54 ENVIRONMENTAL SCIENCES↗

Analysis of the Human Biohazard of Long-Lived Fission Products and Actinides for BREST-OD-300 Spent Fuel

The aim of this work is to perform a comparative analysis of the biohazard for the population of long-lived fission products and actinides from BREST-OD-300 reactor spent fuel taking account of the time required for different radionuclides to reach Earth’s surface by migrating from a deep disposal site. It was found that the biohazard of fission products is significantly greater than that of actinides for a long time (20000 years according to the accepted scenario of radionuclide migration). The radiological impact on the population is predicted after {sup 99}Tc – radionuclide with high migration capability – reaches the soil surface. {sup 137}Cs and {sup 90}Sr will not appreciably affect the dose load because of their relatively short half-life. In order to maintain radio-ecological balance between long-lived wastes and native uranium during the entire possible time period, it is sufficient to extract from the BREST-OD-300 spent fuel 90% of the technetium and 75% of the americium with 99.9% of the fissile materials extracted.

11 NUCLEAR FUEL CYCLE AND FUEL MATERIALS↗

NANOFLUIDICS REVOLUTION: PROTECTING THE WORLD ONE DROP AT A TIME

Nanofluidics is a technology that involves the transport of very small liquid samples, on the order of micro- or pico-liters, confined to nanoscale structures. Scientists at the Savannah River National Laboratory (SRNL) in collaboration with the University of South Carolina are investigating a new measurement technique using nanofluidics for fast and easy verification of the presence of special nuclear material (SNM) in aqueous solutions. Research is specifically geared toward developing small-footprint high sensitivity lab-on-a-chip devices for the detection and separation of plutonium. It also laid the groundwork for developing ultra-sensitive sensors using in structural health monitoring system for in situ, noninterrupted detection of the leaching and migration of radionuclides outside the cementitious barriers for nuclear waste storage facilities. This innovative method has promise for the nuclear industry's processing technologies, environmental protection, and safeguards.

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Interactions of cesium and barium ions with calcium silicate hydrate under the condition saturated with saline water - 15247

The interaction of cesium (Cs) and barium (Ba) ions with calcium silicate hydrate (CSH gel) without drying processes was examined under the condition saturated with saline water, by monitoring the concentrations of Cs and Ba and using the Raman spectroscopy and the zeta potential. In the experiments, Ca/Si molar ratios of CSH gel were set to 0.4, 0.8, 1.2 and 1.6. Each sample was synthesized with CaO powder, SiO{sub 2} powder and NaCl solution in given combinations. The concentration of NaCl solution was set to 0.006, 0.06 and 0.6 M. At the same time, CsCl or BaCl{sub 2} solution was added to the sample in order to adjust its concentration to 1.0 mM. The curing period was set to 7, 14, 30 days. As a results, the sorption of Cs and Ba ions on CSH gel became stronger with lower Ca/Si molar ratio. On the other hand, even though the zeta potential showed the surface charge of higher Ca/Si ratio samples was positive charge which inhibits the sorption of cations, Cs and Ba ions significantly sorbed on CSH gel. In addition, Raman spectra of higher Ca/Si ratio samples showed that the degree of depolymerization of silicate chain increased with the sorption of Cs and Ba ions on CSH gel. In other words, even in higher Ca/Si ratio samples, Cs and Ba ions can sorb on CSH gel through the structural deformation of CSH gel. These results suggest that CSH gel might be able to contribute the migration retardation of Cs and/or Ba ions through the interaction with CSH gel, even if the near-field of the geological repository are saturated by saline groundwater. (authors)

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Status of Triso fuel irradiations in the advanced test reactor supporting high-temperature gas-cooled reactor designs - 18468

The Advanced Gas Reactor (AGR) Fuel Development and Qualification Program is irradiating up to seven experiments on low-enriched uranium tri-structural isotropic (TRISO) particle fuel. Irradiations and fuel development are being accomplished at Idaho National Laboratory s Advanced Test Reactor to support development of the next generation of reactors in the United States. The experiments are being irradiated over several years to demonstrate and qualify new TRISO-coated particle fuel for use in high-temperature gas reactors, with goals of providing irradiation performance data to support fuel process development, qualifying fuel for normal operating conditions, supporting development and validation of fuel performance and fission product transport models and codes, and providing irradiated fuel and materials for post-irradiation examination and safety testing. The experiments are irradiated in an inert sweep gas atmosphere, with individual online temperature monitoring and control of each capsule and online fission product monitoring of effluent to track individual capsule fuel performance. The first experiment (AGR-1) started irradiation in December 2006 and was completed in November 2009. The second experiment (AGR-2) started irradiation in June 2010 and completed in October 2013. The third and fourth experiments have been combined into a single experiment (AGR-3/4), which started its irradiation in December 2011 and completed in April 2014. Because the purpose of this experiment was to provide data on fission product migration and retention in the next generation reactor, the design of this experiment was significantly different from the first two experiments. The final experiment (AGR-5/6/7) is scheduled to begin irradiation in early summer 2017. (authors)

21 SPECIFIC NUCLEAR REACTORS AND ASSOCIATED PLANTS↗

Progress of the Enhanced Hanford Single Shell Tank (SST) Integrity Project

To improve the understanding of the single-shell tanks (SSTs) integrity, Washington River Protection Solutions, LLC (WRPS), the USDOE Hanford Site tank contractor, developed an enhanced Single-Shell Tank Integrity Project (SSTIP) in 2009. An expert panel on SST integrity, consisting of various subject matters experts in industry and academia, was created to provide recommendations supporting the development of the project. This panel developed 33 recommendations in four main areas of interest: structural integrity, liner degradation, leak integrity and prevention, and mitigation of contamination migration. In late 2010, seventeen of these recommendations were used to develop the basis for the M-45-10-1 Change Package for the Hanford Federal Agreement and Compliance Order, which is also known as the Tri-Party Agreement.

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Comparing modelling approaches for a generic nuclear waste repository in salt

This paper contains a comparison of five modelling approaches for a simplified nuclear waste repository in a domal salt formation. It is the result of a four-year collaboration between five international teams on Task F of the DECOVALEX-2023 project on performance assessment modelling. The primary objectives of Task F are to build confidence in the models, methods, and software used for performance assessment (PA) of deep geologic nuclear waste repositories, and/or to bring to the fore additional research and development needed to improve PA methodologies. This work demonstrates how these objectives are accomplished through staged development and comparison of the models and methods used by participating teams in their PA frameworks. Participating teams made a wide range of model assumptions, ranging from compartmentalized networks to full 3D models of the salt formation and repository. Despite differences in the modelling strategies, all models indicate that salt compaction and diffusion of radionuclides in brine are key processes in the repository. For the isothermal spent nuclear fuel and vitrified waste scenario with multiple early failures considered, all models indicate little of the disposed radionuclides will migrate beyond the repository seal over the 100,000-year simulations. In general, the model output quantities have the largest differences over the short term and near the waste. Disparities between the models are believed to be due to differing simplifications from the conceptual model.

DECOVALEX↗

Report on simulation of fission gas and fission product diffusion in UO 2

In UO 2 nuclear fuel, the retention and release of fission gas atoms such as xenon (Xe) are important for nuclear fuel performance by, for example, reducing the fuel thermal conductivity, causing fuel swelling that leads to mechanical interaction with the clad, increasing the plenum pressure and reducing the fuel–clad gap thermal conductivity. We use multi-­scale simulations to determine fission gas diffusion mechanisms as well as the corresponding rates in UO 2 under both intrinsic and irradiation conditions. In addition to Xe and Kr, the fission products Zr, Ru, Ce, Y, La, Sr and Ba have been investigated. Density functional theory (DFT) calculations are used to study formation, binding and migration energies of small clusters of Xe atoms and vacancies. Empirical potential calculations enable us to determine the corresponding entropies and attempt frequencies for migration as well as investigate the properties of large clusters or small fission gas bubbles. A continuum reaction-­diffusion model is developed for Xe and point defects based on the mechanisms and rates obtained from atomistic simulations. Effective fission gas diffusivities are then obtained by solving this set of equations for different chemical and irradiation conditions using the MARMOT phase field code. The predictions are compared to available experimental data. The importance of the large Xe U3O cluster (a Xe atom in a uranium + oxygen vacancy trap site with two bound uranium vacancies) is emphasized, which is a consequence of its high mobility and high binding energy. We find that the Xe U3O cluster gives Xe diffusion coefficients that are higher for intrinsic conditions than under irradiation over a wide range of temperatures. Under irradiation the fast-­moving Xe U3O cluster recombines quickly with irradiation-induced interstitial U ions, while this mechanism is less important for intrinsic conditions. The net result is higher concentration of the Xe U3O cluster for intrinsic conditions than under irradiation. We speculate that differences in the irradiation conditions and their impact on the Xe U3O cluster can explain the wide range of diffusivities reported in experimental studies. However, all vacancy-­mediated mechanisms underestimate the Xe diffusivity compared to the empirical radiation-­enhanced rate used in most fission gas release models. We investigate the possibility that diffusion of small fission gas bubbles or extended Xe-­vacancy clusters may give rise to the observed radiation-­enhanced diffusion coefficient. These studies highlight the importance of U divacancies and an octahedron coordination of uranium vacancies encompassing a Xe fission gas atom. The latter cluster can migrate via a multistep mechanism with a rather low effective barrier, which together with irradiation-induced clusters of uranium vacancies, gives rise to the irradiation-enhanced diffusion coefficient observed in experiments.

11 NUCLEAR FUEL CYCLE AND FUEL MATERIALS↗

Contaminant Migration Modeling to Support the In Situ Decommissioning of Hardened Nuclear Facilities - 20215

The decommissioning of hardened nuclear facilities provides a unique challenge in balancing current worker dose with exposure to future receptors and media. In situ decommissioning (ISD) is a cost-effective and safe option for the closure of such facilities but requires a detailed understanding of the threat that radioactive and hazardous constituents remaining in the facilities pose to groundwater and surrounding surface water. The Savannah River Site (SRS) extensively employs contaminant migration models within the decommissioning process to develop site-specific removal, grouting, and monitoring strategies in support of safe and effective final end states of nuclear facilities. This work discusses the use of contaminant migration modeling in the ISD process at SRS, including specific examples from the closure of P-Reactor and R-Reactor, Building 235-F, F-Canyon and F/H Laboratory Complex. Migration models developed during the closure of P-Reactor and R-Reactor were divided into four source areas: the reactor vessel, the process area, the disassembly basin, and the purification wing. Each source area was assigned a specific inventory and migration pathway and was then subject to varying hypothetical removal, capping, and grouting schemes. Modeling indicated that groundwater Maximum Concentration Limits (MCLs) might be exceeded if no action was taken for eleven and ten constituents of concern (COCs) at P-Reactor and R-Reactor, respectively. These exceedances could occur in as few as 200 to 500 years. Alternatively, the migration modeling demonstrated that the selected ISD actions reduced contaminant mobility which allowed for significant radioactive decay and resulted in fewer predicted exceedances of groundwater MCLs (five COCs for P-Reactor; eight COCs for R-Reactor). In response to the modeling results for P-Reactor and R-Reactor, effectiveness monitoring programs were developed to target contaminants, specific to each reactor, that may migrate to groundwater. Contaminant migration modeling also revealed that roof collapse was a large factor in the release of COCs to the environment, giving rise to roof improvements, and an inspection and vegetation control program to ensure roof stability over time. Contaminant migration modeling is also aiding in the closure planning for hardened facilities in F Area. Building 235-F housed the Actinide Billet Line, which produced Np-237 billets for irradiation in SRS reactors, and the Plutonium Fuel Form (PuFF) facility that produced Pu-238 heat sources for the space program. As a result of these missions, areas within Building 235-F contain considerable residual amounts of both Pu-238 and Np-237. Contaminant migration modeling of Building 235-F was originally performed in 2012 to identify the feasibility of ISD and the amount of radioactive material removal required to prevent the exceedance of groundwater MCLs. The original model indicated that a 60% reduction in the PuFF facility Pu-238 inventory could keep groundwater concentrations below standards, while Np-237 did not pose a threat to groundwater. However, updates to the model with an emphasis on source impact pathways revealed that, due to the orientation of the source areas relative to groundwater flow, no amount of reasonable removal of Pu-238 would keep groundwater concentrations below MCLs and that Np-237 could be a large contributor to localized MCL exceedances. With this insight, the refined 2019 model is being used to assist in the development of grouting plans specific to each facility source area, where bentonite may be utilized to slow the migration of Pu-238 and its daughter products from the PuFF facility and a reducing grout may decrease Np-237 transport by ensuring the nuclide remains in the less mobile +IV oxidation state. The beginning phases of contaminant migration modeling are underway for F-Canyon and associated facilities using lessons learned from the Reactors and Building 235-F. A contaminant migration pathway, similar to the pathway used for the reactor vessels, is being developed for the hot and warm canyons. The F-Canyon inventories are being spatially refined to identify specific and localized source zones, comparable to Building 235-F, that may impact groundwater. Contaminant migration modeling provides vital input within the ISD process, from facility investigation to post closure effectiveness monitoring, making it a valuable tool in the development of safe and effective end states for hardened nuclear facilities at SRS. (authors)

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Water Infiltration and Solute Transport in An Unsaturated Underground Porous Environment - 18442

Water flow and contaminant transport in an unsaturated porous medium are studied by solving the Richards equation for the moisture movement and the convective-dispersive transport of contaminant by using the software HYDRUS 1D for prescribed head condition at the top boundary of a soil layer: a single peak and two peaks of finite duration. While the moisture migration is solved separately, the contaminant transport is coupled to moisture movement. Due to unsaturated nature of the medium the downward water flux in the soil shows vertical variation. The movement of contaminant concentration disturbance is slowed down as it moves downwards. For two separated head peaks in time, the two concentration peaks merge into one and this tendency takes place faster for larger sorption coefficient. (authors)

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Using ASCEM Modeling and Visualization to Inform Stakeholders of Contaminant Plume Evolution and Remediation Efficacy at F-Basin Savannah River, SC – 15156

Communication with stakeholders, regulatory agencies, and the public is an essential part of implementing different remediation and monitoring activities, and developing site closure strategies at contaminated sites. Modeling of contaminant plume evolution plays a critical role in estimating the benefit, cost, and risk of particular options. At the same time, effective visualization of monitoring data and modeling results are particularly important for conveying the significance of the results and observations. In this paper, we present the results of the Advanced Simulation Capability for Environmental Management (ASCEM) project, including the discussion of the capabilities of newly developed ASCEM software package, along with its application to the F-Area Seepage Basins located in the U.S. Department of Energy Savannah River Site (SRS). ASCEM software includes state-of-the-art numerical methods for simulating complex flow and reactive transport, as well as various toolsets such as a graphical user interface (GUI), visualization, data management, uncertainty quantification, and parameter estimation. Using this software, we have developed an advanced visualization of tritium plume migration coupled with a data management system, and simulated a three-dimensional model of flow and plume evolution on a high-performance computing platform. We evaluated the effect of engineered flow barriers on a nonreactive tritium plume, through advanced plume visualization and modeling of tritium plume migration. In addition, we developed a geochemical reaction network to describe complex geochemical processes at the site, and evaluated the impact of coupled hydrological and geochemical heterogeneity. These results are expected to support SRS’s monitoring activities and operational decisions.

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Diffusive parameters of tritiated water and uranium in chalk

The Cretaceous Chalk of North-western Europe exhibits a double porosity (matrix and fracture) providing pathways for both slow and rapid flow of water. The present study aims at understanding and predicting the contaminant transfer properties through a significant section of this formation, with a particular emphasis on diffusion. This requires to study the nature of porosity and to perform diffusion experiments in representative samples using uranium and tritiated water (HTO), respectively taken as a reactive tracer and an inert one. The diffusive parameters, i.e. the accessible porosity and the effective diffusion coefficient were determined. Additional information was obtained with mercury porosimetry, gravimetric water content, textural and mineralogical characterization. The diffusion tests performed with HTO appear to be the best method to measure the total accessible porosity in any type of porous media, especially those having large pore size distributions. Our study demonstrates that classical gravimetric water content measurements are not sensitive to the reduction in pore size as opposed to HTO diffusion tests because capillary water is not extracted by conventional gravimetric method but can still be probed by diffusion experiments. We found effective diffusion coefficients D{sub e}(U(VI)) near 4 x 10{sup -10} m{sup 2}s{sup -1}). The slower migration of U(VI) compared to HTO indicates sorption, with R{sub d}(U(VI)) from 100 to 360 mL g{sup -1}. These values are one order of magnitude larger than other determinations of the U(VI) sorption coefficient because only the matrix porosity is concerned here. The migration of U(VI) in chalk is only limited by sorption on ancillary Fe-Pb-bearing minerals. Transport of HTO and U(VI) is independent of the porosity distribution. Uranium diffusion in the chalk matrix porosity is fast enough to allow the total invasion of the pore space within characteristic time scales of the order of 1000 years. This results in a partitioning of uranium velocities in fracture flow and matrix flow proportionally to the respective fracture and matrix porosities. (authors)

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Floodplain statement of findings for corrective actions in Potrillo Canyon technical area-36, Los Alamos National Laboratory, Los Alamos, New Mexico

In 2014, baseline storm water monitoring samples for Potrillo Canyon Sample Management Area at Los Alamos National Laboratory (LANL) exceeded the National Pollutant Discharge Elimination System Individual Permit No. NM0030759 target action level (TAL) of 15 picocuries per liter (pCi/L) for gross-alpha radioactivity (393 pCi/L) and a TAL of 30 pCi/L for radium-226 and radium-228 (95.9 pCi/L). Consequently, erosion control measures within the management area are proposed to minimize sediment migration, a corrective action under the permit that is a requirement of the New Mexico Environment Department consent decree and a good management practice to limit off-site sediment migration. The area proposed for erosion controls consists of portions of Technical Area 36 that were used as firing sites primarily involving high explosives (HE) and metal (e.g., depleted uranium, lead, copper, aluminum, and steel), small-explosives experiments and burn pits (burn pits were used for burning and disposal of test debris). In addition, underground explosive tests at an approximate depth of 100 feet were also conducted. These watershed-based storm water controls will focus on addressing erosion occurring within the floodplain through mitigating and reducing both current and future channelization and head cutting.

54 ENVIRONMENTAL SCIENCES↗