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In Rifle, Colorado, Berkeley Lab earth scientist, Kenneth Hurst Williams, highlights the role subsurface microbial communities can play in controlling the flow of contaminants in groundwater. The DOE Joint Genome Institute is a key collaborator in the research. Williams is Component Lead of Watershed Structure and Controls within Berkeley Lab's Genomes-to-Watershed Scientific Focus Area.
A new method for in situ formation of a calcium apatite permeable reactive barrier that is a groundbreaking technology for containing radioactive/heavy metal contaminants threatening groundwater supplies.
This presentation, part of the JISEA 10th Annual (Virtual) Meeting, explores the next generation of low-carbon technologies for deployment on contaminated lands.
Per- and Polyfluoroalkyl Substances (PFAS) are a manufactured group of chemicals that have been used since the 1940s. PFAS break down very slowly and studies show that exposure to these chemicals may cause negative reproductive effects, developmental delays in children, increased risk of some cancers, and interference with the body’s natural hormones. On June 15, 2022, EPA issued interim updated drinking water health advisories for the two most widely studied PFAS, perfluorooctanoic acid (PFOA) and perfluorooctane sulfonic acid (PFOS). The concentrations for the health advisory limits are 0.004 parts per trillion (ppt) and 0.02 ppt respectively. Because data is often reported in combined PFOA and PFOS concentrations, and for ease of data visualization, concentrations of the two chemicals will be discussed as a single, summed value and will be compared to the combined health advisory limits of 0.024 ppt. Due to the recently published near-zero health advisory limits and the known negative health effects, a map of estimated PFAS groundwater contamination was created using ArcGIS Pro and geostatistical tools to inform the public and determine which regions are most at-risk.
This presentation describes fiscal year 2022 status and accomplishments for NREL's Hydrogen Contaminant Detector project.
Hexavalent chromium (Cr{sup 6+}) is a contaminant of concern at multiple Department of Energy (DOE) and industrial sites across the United States. It is used in stainless steel production, textile dyes, tanning, wood preservation, and in conversion coatings. It was used at DOE sites, such as the Hanford Nuclear Reservation in Washington state, in the form sodium dichromate (Na{sub 2}Cr{sub 2}O{sub 7}) to inhibit corrosion. This has resulted in the release of chromate (CrO{sub 4}{sup 2-}) to groundwater. Chromate is anionic and is readily transported with ground water through the subsurface to receptors such as river biota at Hanford, and in some regions to potable water wells. To improve Cr{sup 6+} groundwater plume monitoring while reducing monitoring cost, a cable-deployed, submersible sensor was developed for direct measurements of Cr{sup 6+} in natural groundwater. With a diameter of 3.8 cm (1.5 inch) the sensor could be deployed in 5 cm (2 inch) diameter screened wells. The sensor uses ultra violet (UV) photo-spectroscopy to measure Cr{sup 6+} at concentrations as low as 5 to 10 μg L{sup -1} (as hexavalent chromium, Cr{sup +6}) in natural water. Turbidity, caused by colloidal material suspended in natural water, can interfere with the chromate measurement but was automatically compensated within the instrument. Because the instrument had some temperature sensitivity, a correction was also applied based on in situ temperature measurements in the sensor. The sensor has been tested in the laboratory and was deployed to the field with encouraging results. Laboratory calibrations consistently yielded concentration measurements that correlate well with standard analytical methods (r{sup 2} = 0.99). (authors)
The former Wolff-Alport Chemical Company operated at the location in densely populated urban area in Queens, New York, between 1920 to about 1954. The company imported, stored on-site and processed monazite sand ores from the Belgium Congo. The extracted refined products enriched in rare-earth metals were sold on the commercial market. The process residues, rich in thorium and its progeny, were originally disposed of directly to the city sewer line and probably on-site also. The site's buildings are currently occupied by the auto shops, corner delicatessen store, light construction company, ice maker/distributor, and two residential apartments. Preliminary site investigations found multiple areas with elevated levels of direct gamma radiation with the maximum reported rates of 22 micro-sievert/hour (2.2 milli-rem/hour) at surface level and 40 micro-sievert/hour (4 milli-rem/hour) inside sewer manhole access. The thoron (Rn-220) gas air concentration in outdoor areas was reported reaching 13.5 kBq/m{sup 3} (366 pCi/L) and the radon (Rn-222) gas air concentrations was reported exceeding 148 Bq/ m{sup 3} (4 pCi/L) in some buildings. The dose assessments indicated that, under realistic scenarios, some members of the public were likely to receive the radiation exposure from this contamination in excess of the New York City and Nuclear Regulatory Commission general public radiation dose limit of 1 milli-sievert /yr (100 milli-rem/yr). The interim remedial action was planned and conducted by the U.S. Environmental Protection Agency (U.S. EPA) Region 2 in close cooperation with the New York City and New York State in 2012-13. The purpose of the action was to take necessary interim measures to reduce annual public dose below limit of 1 milli-sievert/yr (100 milli-rem/yr) and reduce radon gas concentration levels in impacted indoor spaces below U.S. EPA Action Level for residencies of 148 Bq/ m{sup 3} (4 pCi/L). In order to achieve these goals, the following actions were taken: detailed radiological and occupancy surveys; development of realistic exposure scenarios; dose assessments; installation of the fence and gates around the 'backyard' portion of the site; vegetation removal; development and detailed assessment of the radiation shielding options; application of the multilayer radiation shielding in some buildings, portions of the sidewalk and unpaved areas; mitigation of radon/thoron gas entry point; and installation of the radon mitigation system in one of the buildings. The preliminary post-action analyses indicated that the action goal would likely be achieved. The interim remedial action was conducted in a tight urban setting; it has significantly reduced public health risk from radiation without closure of businesses that continued operating within the site perimeter. (authors)
There is limited understanding of the scientific interaction of the chemical contaminants to DOE facility materials which can alter the stability of the materials, and in turn, affecting the general safety. In addition, the materials themselves can be considered secondary waste and decontamination is necessary. Therefore, the overall goal of this project is to determine the physiochemical interactions of Hg and Cs to steel and concrete using spectroscopic, adsorption and computational studies. To achieve the overall goal, this proposal has the following objectives: 1) Evaluate the physicochemical interactions of Hg and Cs to steel and concrete using spectroscopic techniques under standard conditions and 2) Evaluate the impact of environmental conditions (temp., salt content, pH, and time) on the physicochemical interactions of Hg and Cs to steel and concrete using spectroscopic techniques. Less labor intensive than traditional wet chemical analyses, spectroscopic methods have the advantage of elucidating both structural and chemical changes at the micro to nano-scale. The potential impacts of the proposed work could lead to cost effective decontamination methods, minimize secondary waste, and reduce worker exposure. (authors)
This work describes the development of mathematical models for radionuclides distribution and transport in the environment. The applicability of the models involves an integrated approach to assess the quantitative dispersion of the radionuclides in different environmental compartments when released from uranium tailings or from other low-activity mining wastes storages. For every compartment the important pathways of contamination and the radionuclides of major concern are identified and selected, based on their chemical, physical, radiological and toxic properties. Each compartment represents an environmental media: air, soil, water, vegetation and biota. Depending on the characteristics of the sources different types of possible releases are evaluated using phenomenological models. Models of environmental release, dispersion, transport and fate within each environmental compartment, as well as models of transfer between them, are applied to a specific site. The model outputs are the radionuclides activities for each one of the environmental compartments, where relevant exposure end-points are previously identified. The methodology was applied to a specific Uranium Mill Site, referred here as the 'Mill'. The site comprises approximately 3.2 km and includes two inactive mills, former ore stockpiles areas, a partially reclaimed tailings pond disposal area and a current tailings pond disposal area. The Mill site began operations in the late 1950's extracting uranium ore by alkaline leaching. Later on, a new facility using acid leaching for extracting uranium begun to operate in 1980. The mill operated first continuously and after intermittently until its closure, in March 2006. The data required for the model input was acquired from different sources: direct measurements from this particular site and available from multiple site investigation reports (in particular, environmental data for groundwater, soil, surface water, sediments and biota); other, were selected from published data. For the unknown data, assumptions were made. (authors)
Using traditional high-flow purge methods for long-term water quality monitoring of deep groundwater wells can be expensive, affect contaminant migration, and produce excessive volumes of discharge water that can be difficult to manage. The use of low-flow pumping methods and depth discrete bailers (DDBs) can reduce the cost of sampling deep groundwater wells. In general, using different pumping methods to obtain reproducible and representative groundwater can be challenging. Passive diffusion samplers (PDSs) have successfully been used in long-term monitoring for volatile organic compounds, major ions, and trace-elements, but application has been limited for stable and radioactive isotopes. Beginning in 2018, the United States Geological Survey (USGS) conducted three sampling events to test the ability of PDSs and DDBs to obtain reproducible and representative groundwater samples. The sampled well is completed in a regional, permeable carbonate aquifer and is one in a set of wells that have historically been used for tritium tracer testing. All samples were obtained at 180 m (590 ft) below land surface (bls) in a 13.97 cm (5.5 inch) uncased well that has a total depth of 202 m (662 ft) bls. The first sampling event deployed a regenerated cellulose dialysis membrane (RCDM) PDS for 14 days with deionized water as the blank. The second sampling event deployed a RCDM for 27 days also with deionized water as the blank. The third sampling event deployed a Dual Membrane (DM) PDS for 65 days using a blank of tritium-dead carbonate water. The DM PDS was used to assess the effect of longer term deployment on tritium concentrations and address whether or not the PDSs reached equilibrium with ambient groundwater. The day after each of the three passive samplers were retrieved a DDB was used to obtain discrete non-integrated groundwater samples. For each DDB sampling day, the bailer was lowered into the well 10 consecutive times to determine if the water chemistry changed from the first to the last bailed sample. Quality assurance samples including blanks and duplicates were obtained during all three sampling events. All blank waters had tritium concentrations less than 21±33 pCi/L. Major ion (e.g. calcium, chloride, sodium, and sulfate) results were compared between all samples obtained with RCDM and DDB. Major ion concentrations showed a coefficient of variation of less than 6% between all RCDM and DDB samples; however, the coefficient of variation between the different deployment times and the two different methods for trace-element concentrations was much larger, particularly for manganese (82%), lead (41%), and zinc (33%). Stable isotope values were compared between the RCDM and DDB samples. The DDB sample results all fell within analytical uncertainty and were considered representative of the formation groundwater. The stable isotope values from the RCDM samples indicated that a longer deployment time was necessary to gain equilibrium and to obtain representative groundwater samples. Tritium results from groundwater samples obtained from the RCDM, DM, and DDB indicate that groundwaters obtained with PDSs produced tritium concentrations 2 to 3 times higher (between 1,426 and 3,060±87 pCi/L) than groundwaters obtained with a DDB (479 to 1,219±51 pCi/L). The longer the passive diffusion samplers were deployed, the higher the tritium concentration, suggesting that equilibrium with tritium was not reached within a 27-day deployment. DDB samples showed tritium results declining from the first to the last bailed sample for all three sampling events. This research suggests that tritium results from groundwater samples obtained from PDSs are more reproducible than samples obtained from DDBs. Also, PDSs likely do not accumulate isotopes of water but rather equilibrate with the ambient groundwater. On the other hand, both PDSs and DDBs were able to provide representative groundwater samples for major ions and have the potential to produce representative groundwater samples for stable isotopes of water (δD and δ{sup 18}O). Utilizing the most effective method for sampling groundwater is important for long-term groundwater monitoring. Quantifying the ability of passive diffusion groundwater samplers to obtain representative radioactive chemistry samples will help determine if these methods can be a useful alternative to pumping and purging wells for long-term monitoring. (authors)
Researchers from Los Alamos National Laboratory (LANL) performed measurements during a series of Godiva IV bursts to determine the effectiveness of engineering controls to reduce contamination. (authors)
Surrogate models are commonly used in Bayesian approaches such as Markov Chain Monte Carlo (MCMC) to avoid repetitive CPU-demanding model evaluations. However, the approximation error of a surrogate may lead to biased estimations of the posterior distribution. This bias can be corrected by constructing a very accurate surrogate or implementing MCMC in a two-stage manner. Since the two-stage MCMC requires extra original model evaluations, the computational cost is still high. If the information of measurement is incorporated, a locally accurate approximation of the original model can be adaptively constructed with low computational cost. Based on this idea, we propose a Gaussian process (GP) surrogate-based Bayesian experimental design and parameter estimation approach for groundwater contaminant source identification problems. A major advantage of the GP surrogate is that it provides a convenient estimation of the approximation error, which can be incorporated in the Bayesian formula to avoid over-confident estimation of the posterior distribution. The proposed approach is tested with a numerical case study. Without sacrificing the estimation accuracy, the new approach achieves about 200 times of speed-up compared to our previous work using two-stage MCMC.
Protonic ceramic fuel cells (PCFCs) are one of the most efficient energy conversion devices. However, the performance of current PCFCs is greatly limited by the sluggish oxygen reduction reaction (ORR) kinetics and the fast degradation of cathode due to contaminants poisoning (such as Cr species and steam). In this work, we report a surface regulating of a double perovskite PrBa 0.5 Sr 0.5 Co 1.5 Fe 0.5 O 5+δ (PBSCF) cathode by a Pr 0.9 Fe 0.7 Co 0.3 O 3 (PFC) catalyst coating to enhance the ORR activity and stability. When tested in direct contact with Cr in the air with 3% H 2 O at 650 °C, the polarization resistance (Rp) of the PFC-PBSCF electrode increases from $\approx$0.39 to 0.45 Ω cm 2 after 100 h operation; in contrast, the R p of a PBSCF electrode increases from 0.63 to 0.82 Ω cm 2 . Further, a PCFC with the PFC-PBSCF cathode demonstrates an excellent peak power density ($\approx$1.08 W cm -2 at 650 °C) and significantly enhanced durability (degradation rate of 0.03 % h -1 ), much better than those of the cells with a PBSCF cathode ($\approx$0.75 W cm -2 and degradation rate of 0.12 % h -1 ). Raman spectroscopy and density functional theory calculations indicate that the PFC catalyst coating diminishes the formation of Cr species, such as (Ba 1-x Sr x )CrO 4 , on the cathode surface.
Neutron-induced swelling in austenitic and ferritic steels is sensitive to the carbon level in the steel, as well as its distribution in matrix or precipitates. It has recently become known that ion-irradiation to high dpa levels leads to a progressive ion-beam-induced increase in carbon concentration and precipitation within the ion range, with concurrent reductions in void swelling. This neutron-atypical phenomenon imperils the credibility of ion simulation for light water reactor applications. A series of experiments involving pure iron and a structural alloy HT9, was conducted to identify the source and distribution of injected carbon. It was found that negatively-charged carbon atoms are entrained in the self-ion beam by a Coulomb drag effect, and thereby delivered at low drift energy to the irradiated surface, followed by ion-beam-mixing and diffusion. A technique for filtering out contaminants, especially carbon, oxygen and nitrogen, was developed and resulted in higher, more neutron-relevant swelling levels than achieved without filtering.
The discovery of the stop — the Supersymmetric partner of the top quark — is a key goal of the physics program enabled by the Large Hadron Collider. Although much of the accessible parameter space has already been probed, all current searches assume the top mass is known. This is relevant for the “stealth stop” regime, which is characterized by decay kinematics that force the final state top quark off its mass shell; such decays would contaminate the top mass measurements. We investigate the resulting bias imparted to the template method based ATLAS approach. A careful recasting of these results shows that effect can be as large as 2.0 GeV, comparable to the current quoted uncertainty on the top mass. Thus, a robust exploration of the stealth stop splinter requires the simultaneous consideration of the impact on the top mass. Additionally, we explore the robustness of the template technique, and point out a simple strategy for improving the methodology implemented for the semi-leptonic channel.
The in-situ immobilization effect of sepiolite and biochar on the compound pollution of cadmium (Cd) and atrazine in acid red soil of south China was studied. Results showed that in a certain concentration range, sepiolite and biochar can improve the germination rate, ensure normal growth and increase biomass of pakchoi, reduce the content of Cd in edible parts of pakchoi in different degrees and meet international standards, and restrain absorption of atrazine in pakchoi completely. Sepiolite was more effective than biochar for the immobilization of Cd, while biochar was more effective than sepiolite for the immobilization of atrazine. Combined application of sepiolite and biochar in soil contaminated by Cd and atrazine was better than individual applications of sepiolite or biochar. The remediation method applied in this research can effectively repair the acid red soil with combined pollution of Cd and atrazine in south China, while also providing ideas for in-situ remediation of farmland soil with combined pollution of pesticides and metals.
This research has been carried out for assessing phytoremediation of contaminated soils with 4 concentrations of arsenic by three plants, namely Vetiver grass (Vetiveria zizanioides), Chara algae (Chara vulgaris) and Water hyacinth (Hyacintus orientalis). The experimental results showed that at least two sampling times were significantly different. In addition, at least two plants were also significantly different in terms of percentages of total arsenic that were removed from the soil of the pots, as well as significant interactions between plant and arsenic concentrations. The results obtained from the thermodynamic studies show that, obtained by zero Gibbs free-energy, the process reached an equilibrium on the 60th day of the experiment, and, in fact, the adsorption of arsenic after the 60th day would be negligible.
A pot experiment was conducted to investigate the effect of three additives – citric acid (CA), polyaspartic acid (PASP), and FeCl{sub 3} – on the phytoextraction efficiency of cadmium (Cd) and lead (Pb) by ryegrass (Lolium perenneL.) from artificially contaminated soils with different heavy metal concentrations. The results showed that as the concentration of pollutants increased, the TI (tolerance index) and BCF (bio-concentration factor) of ryegrass gradually increased only when FeCl{sub 3} was applied. FeCl{sub 3} also exhibited the most significant biomass enhancement and heavy metal accumulation of ryegrass, as well as the highest phytoextraction efficiency in heavily-polluted soils. The overall orders of the optimal phytoextraction efficiency for the three additives in terms of their MER (metal extraction ratio) were: FeCl{sub 3} > PASP > CA. Therefore, FeCl{sub 3} can be used to improve the Cd and Pb phytoextraction efficiency of ryegrass in heavily-polluted soils.