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At least 739 records · Page 41

Observational Study Reveals Inverse Relationship: Rising PM2.5 Concentrations Linked to Decreasing Muon Flux

Muon flux, the rate of muons reaching Earth from the atmosphere, is impacted by various factors such as air pressure, temperature, and humidity. However, the influence of concentrations of PM2.5 (particulate matter with diameters 2.5 mm or smaller) on muon detection rates remains unexplored. During the summer of 2023, smoke from Canadian wildfires (containing significant amounts of particulate matter) blew over regions in the Northern US, introducing huge fluctuations in PM2.5 concentrations, thus inspiring this experiment to investigate the correlation of PM2.5 concentrations and muon rates. To investigate the correlation, muon collision rates were measured and analyzed alongside PM2.5 concentration data over the periods of both light and heavy smoke. Other confounding variables, including temperature, humidity, and atmospheric pressure, were also considered. The results reveal a statistically significant inverse correlation between muon flux and PM2.5 concentrations, indicating that particulate matter has an impact on the rate of muons reaching the earth’s surface.

72 PHYSICS OF ELEMENTARY PARTICLES AND FIELDS↗

Observational Study Reveals Inverse Relationship: Rising PM2.5 Concentrations Linked to Decreasing Muon Flux

Muon flux, the rate of muons reaching Earth from the atmosphere, is impacted by various factors such as air pressure, temperature, and humidity. However, the influence of concentrations of PM2.5 (particulate matter with diameters 2.5 mm or smaller) on muon detection rates remains unexplored. During the summer of 2023, smoke from Canadian wildfires (containing significant amounts of particulate matter) blew over regions in the Northern US, introducing huge fluctuations in PM2.5 concentrations, thus inspiring this experiment to investigate the correlation of PM2.5 concentrations and muon rates. To investigate the correlation, muon collision rates were measured and analyzed alongside PM2.5 concentration data over the periods of both light and heavy smoke. Other confounding variables, including temperature, humidity, and atmospheric pressure, were also considered. The results reveal a statistically significant inverse correlation between muon flux and PM2.5 concentrations, indicating that particulate matter has an impact on the rate of muons reaching the earth’s surface.

72 PHYSICS OF ELEMENTARY PARTICLES AND FIELDS↗

Use of Groundwater Flow, Solute Transport, and Geochemical Modeling To Evaluate Long-Term Nitrate Plume Concentrations Following Phreatophyte Source Control - 17262

The Monument Valley, Arizona, Processing Site is a former uranium mill site within the Navajo Nation in northeastern Arizona. Milling activities between 1955 and 1968 resulted in contamination of groundwater in the shallow alluvium at the site. Remedial action was completed under Title I of the Uranium Mill Tailings Radiation Control Act of 1978. Site remediation activities between 1992 and 1994 removed surficial source material and other site-related contamination, but contamination of deeper soil, primarily by nitrate, remained between the excavation depth and the water table. Residual nitrate in these soils, from uranium ore processing at the mill, has continued to be a source of groundwater contamination. To evaluate the potential for native phreatophytes to control remaining source material, four-wing salt-bush and black grease-wood were planted in 2000 and 2005 within the footprints of the former tailings piles. The objectives of the plantings were to increase nitrate removal from soil water through root uptake and, because phreatophyte water usage is expected to equal or exceed annual precipitation, to halt nitrate loading to groundwater. Recent evaluation showed more than an 80% decrease in soil nitrate concentrations and no effective groundwater recharge in the planting area. Numerical groundwater flow, solute transport, and geochemical modeling were performed to evaluate the long-term response of the existing nitrate plume to the phreatophyte source control measures. This modeling will help determine if 100-year natural flushing is a viable compliance strategy for the nitrate plume. Results showed that nitrate concentrations in the alluvial aquifer are expected to drop below the standard of 10 mg/L as N in approximately 70 years as a result of the phreatophyte planting. Companion sensitivity analysis was also performed to better understand how uncertainty in groundwater flow model and solute transport model inputs would impact cleanup times. Even considering input uncertainty, nitrate concentrations are expected to reach the standard in the alluvial aquifer within 100 years. Recognizing that model predictions are not absolute, but represent the general potential for an event to occur, the model was used to identify key sampling locations to verify that the nitrate plume will attenuate as predicted. This evaluation identified locations that can be used to assess the viability of the modeling predictions within the next 50 years. If the source diminishes or no longer exists, modeling predicts that concentrations of nitrate and ammonium in these wells should show significant declines over the next 10-55 years. If downward concentration trends do not occur as predicted, other remedial strategies may need to be evaluated to meet groundwater standards within the specified 100-year duration. (authors)

12 MANAGEMENT OF RADIOACTIVE AND NON-RADIOACTIVE W↗

Spatial analysis of concentrations of multiple air pollutants using NASA DISCOVER-AQ aircraft measurements: Implications for exposure assessment

Highlights: • Aircraft measurements showed spatially varying relations of multiple air pollutants. • NO{sub x}, toluene, and xylenes/ethylbenzene were reasonable proxies of traffic and urban air pollution. • Between-pollutant concentration correlations and ratios varied by space. • Multiple pollutant relations provided insights for exposure assessment and multipollutant epidemiology. In recent years, multipollutant approaches have been employed to investigate the association with health outcomes to better represent real-world conditions than more traditional analysis that considers a single pollutant. With regard to the exposure assessment of a mixture of air pollutants, it is critical to understand the spatial variability in multipollutant relations in order to assess their potential health implications. In this study, we investigated the spatial relations of multiple pollutant concentrations (i.e., NO{sub x}, NO{sub y}, black carbon, carbon monoxide, acetaldehyde, formaldehyde, toluene, xylenes/ethylbenzene, ozone, water-soluble organic carbon, and aerosol extinction) observed from the P-3B aircraft in the 2011 NASA field campaign in Baltimore/Washington D.C. areas during July 2011. The between-pollutant Pearson correlations and Z-scores (calculated from log-transformed concentrations) between near-highways and non-highways and between near-urban centers and non-urban centers varied by pollutant pair and space. We found generally lower correlations between NO{sub x} and other pollutants for near-highways (average r = 0.36) than for non-highways (average r = 0.41) and also for non-urban centers (average r = 0.37) than for near-urban centers (average r = 0.41). This indicated that the temporal associations between NO{sub x} and health outcomes might be less affected by other pollutants, which were also related to same health outcomes, for near-highways and non-urban centers. The analysis of between-pollutant Z-scores showed varying spatial relations for popular traffic-related pollutants with the Z-score differences of 0.43 (NO{sub x}-carbon monoxide), 0.29 (NO{sub x}-black carbon), and 0.17 (black carbon-carbon monoxide) between near-highways and non-highways. This result exhibited heterogeneous traffic-related pollutant mixtures with the proximity to highways, potentially leading to the diverse extent of health associations. Furthermore, a mixed effects model presented pollutant-specific associations between the concentrations and the proximity to highways and urban centers, showing larger declines for NO{sub x}, xylenes/ethylbenzene, toluene, and NO{sub y} than those for the pollutants related to secondary pollutant formation. The model also demonstrated the different sensitivity of each pollutant to meteorological parameters, which may modify the spatial and temporal variability in the relations between the pollutants. Our findings provide insights for exposure assessment studies to better understand the cumulative health consequences associated with multiple air pollutants simultaneously.

54 ENVIRONMENTAL SCIENCES↗

Optical and heat transfer performance of a novel non-imaging concentrator

In this study, the Crossed Compound Parabolic Concentrator CCPC is modified to demonstrate for the first time a new generation of solar concentrators working simultaneously as an electricity generator and thermal collector. It is designed to have two complementary surfaces, one reflective and one absorptive, and is called an absorptive/reflective CCPC (AR-CCPC). Usually, the height of the CCPC is truncated with a minor sacrifice of the geometric concentration. These truncated surfaces rather than being eliminated are instead replaced with absorbent surfaces to collect heat from solar radiation. The optical, thermal and total efficiency of the AR-CCPC was simulated and compared for different geometric concentration ratios varying from 3.6x to 4x. It was found that the combined electrical and thermal efficiency of the AR-CCPC 3.6x/4x remains constant and high all day long and the overall efficiency reach up to 94%. In addition, the temperature distributions of AR-CCPC surfaces and the assembled solar cell were simulated based on those heat flux boundary conditions. It shows that the adding of thermal absorbent surface can apparently increase the wall temperature.

14 SOLAR ENERGY↗

Determination of indoor radon concentrations at the elementary schools of Fatih district in Istanbul

Radon is an odorless, tasteless, colorless noble radioactive gas which is produced within the radioactive decay chain of Uranium. The Radon forms in rocks, diffuses into soil and then escapes into atmosphere. When human exposure to high concentration of radon gas from inside, risk of developing lung cancer is increased. There are many methods to determine {sup 222}Rn concentration in the air. In this study, radon concentration of confined air spaces were measured by using LR-115 solid state nuclear track detectors. 509 LR-115 nuclear trace detectors were placed to 25 schools in Fatih District and they effective dose values were calculated. The results of measurements showed that the radon concentration varies between 40-395 Bq/m{sup 3}. This results compared with Turkey’s limits (400 Bq/m{sup 3}) are low, conversely higher compared with WHO’s limits (100 Bq/m{sup 3}).

07 ISOTOPE AND RADIATION SOURCES↗

Measurements of radon concentrations in Spa waters in Amasya, Turkey

The aim of this study is to determine the radon concentrations in thermal waters in the Amasya basin in Turkey and to explore the relationship between radon anomalies and active geological faults. The radon concentration measurements were performed in four thermal Spas around Amasya basin. The water samples were collected from tap waters in thermal water sources. The obtained radon concentrations ranged from 0.15 ± 0.12 to 0.71 ± 0.32 BqL{sup −1} for Spa waters. The relationship between the radon concentration anomalies and earthquakes that occurred in the sampling period are discussed.

07 ISOTOPE AND RADIATION SOURCES↗

Optimization of SHINE Process: Design and Verification of Plant-Scale AG 1 Anion-Exchange Concentration Column and Titania Sorbent Pretreatment

Argonne National Laboratory has developed a Mo-recovery and -purification system for the SHINE medical technologies process, which uses a uranyl sulfate solution for the accelerator-driven production of Mo-99. The objective of this effort is to reduce the processing time for the acidification of the Mo-99 product prior to loading onto a concentration column and concentration of the Mo-99 product solution. Two methods were investigated: (1) the replacement of the titania concentration column by an anion-exchange column to decrease processing time and increase the radioiodine-decontamination efficiency and (2) pretreatment of the titania sorbent to improve its effectiveness for the Mo-recovery and -concentration columns. Promising results are reported for both methods.

38 RADIATION CHEMISTRY, RADIOCHEMISTRY, AND NUCLEA↗

SCILLA Secondary Aerosol Volume Concentration Airborne Data

This data set contains secondary aerosol volume concentration in cubic micrometers per cubic centimeter (um^3/cm^3). The aerosol was generated in an oxidation flow reactor (OFR) and its volume concentration measured with a scanning mobility particle sizer (SMPS). Both components were designed and built at the University of California Riverside. Ambient particles were removed with a Teflon filter upstream of the OFR and then pure ammonium sulfate particles were added to create a stable aerosol surface area on which low-volatility oxidation products condense. High concentrations of hydroxyl radical (OH) formed inside the OFR accelerate the oxidative chemistry that would typically occur over a period of several days in the atmosphere, resulting in the production of secondary aerosol from precursor gases present in the ambient air. Concentrations of added ozone and water vapor were controlled to produce the desired and approximately constant level of photochemical aging. The reactor temperature was controlled, while the pressure was not, and was always slightly lower than that of the sampled outside air. Sampled air was pulled from above the Naval Postgraduate School’s (NPS) Twin Otter aircraft through a rear-facing, ¼” OD PFA Teflon tube. The sample stream was split between the OFR and several gas analyzers (NOx, CO, O3, and H2O). Though not contained in these files, data from an aerosol mass spectrometer intermittently operated downstream of the OFR are also available.

{"secondary aerosol concentration",aerosol_concent↗

Radiological Modeling for Determination of Derived Concentration Levels of an Area with Uranium Residual Material - 13533

As a result of a pilot project developed at the old Spanish 'Junta de Energia Nuclear' to extract uranium from ores, tailings materials were generated. Most of these residual materials were sent back to different uranium mines, but a small amount of it was mixed with conventional building materials and deposited near the old plant until the surrounding ground was flattened. The affected land is included in an area under institutional control and used as recreational area. At the time of processing, uranium isotopes were separated but other radionuclides of the uranium decay series as Th-230, Ra-226 and daughters remain in the residue. Recently, the analyses of samples taken at different ground's depths confirmed their presence. This paper presents the methodology used to calculate the derived concentration level to ensure that the reference dose level of 0.1 mSv y-1 used as radiological criteria. In this study, a radiological impact assessment was performed modeling the area as recreational scenario. The modelization study was carried out with the code RESRAD considering as exposure pathways, external irradiation, inadvertent ingestion of soil, inhalation of resuspended particles, and inhalation of radon (Rn-222). As result was concluded that, if the concentration of Ra-226 in the first 15 cm of soil is lower than, 0.34 Bq g{sup -1}, the dose would not exceed the reference dose. Applying this value as a derived concentration level and comparing with the results of measurements on the ground, some areas with a concentration of activity slightly higher than latter were found. In these zones the remediation proposal has been to cover with a layer of 15 cm of clean material. This action represents a reduction of 85% of the dose and ensures compliance with the reference dose. (authors)

54 ENVIRONMENTAL SCIENCES↗

Enhanced Cycling Stability of Rechargeable Li-O2 Batteries Using High Concentration Electrolytes

The electrolyte stability against reactive reduced-oxygen species is crucial for the development of rechargeable Li-O2 batteries. In this work, we systematically investigated the effect of lithium salt concentration in 1,2-dimethoxyethane (DME)-based electrolytes on the cycling stability of Li-O2 batteries. Cells with high concentration electrolyte illustrate largely enhanced cycling stability under both the full discharge/charge (2.0-4.5 V vs. Li/Li+) and the capacity limited (at 1,000 mAh g-1) conditions. These cells also exhibit much less reaction-residual on the charged air electrode surface, and much less corrosion to the Li metal anode. The density functional theory calculations are conducted on the molecular orbital energies of the electrolyte components and the Gibbs activation barriers for superoxide radical anion to attack DME solvent and Li+-(DME)n solvates. In a highly concentrated electrolyte, all DME molecules have been coordinated with salt and the C-H bond scission of a DME molecule becomes more difficult. Therefore, the decomposition of highly concentrated electrolyte in a Li-O2 battery can be mitigated and both air-cathodes and Li-metal anodes exhibits much better reversibility. As a results, the cyclability of Li-O2 can be largely improved.

Environmental Molecular Sciences Laboratory↗

Current–Induced Ion Concentration Polarization at a Perfect Ion–Exchange Patch in an Infinite Insulating Wall

This research examines theoretically the ion concentration polarization, ion fluxes, and electrostatic fields near an ion exchange patch in the wall of an electrified fluidic channel. These phenomena are important in related microfluidic ion-preconcentration systems. Under an electric field, counterions enter the ion-exchange patch at one side and leave at the other, with salt depletion occurring near the entrance and accumulation near the exit. Furthermore, the high patch conductivity and the concentration profiles lead to local electric field perturbations that may facilitate preconcentration. This study includes analytical expressions of ion concentrations and electrochemical potentials at small to moderate electric fields, as well as numerical simulations. Additionally, a simple matrix of polynomial coefficients (obtained via fitting of numerical data) enables analytical calculation of the 2-dimensional concentration profiles at all electric fields within the range investigated in the numerical simulations. This is possible because a single dimensionless parameter controls this problem.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Concentrations, Sources, and Risk Assessment of Organohalogen Compounds in Soils from Kiambu to Mombasa, Kenya

Concentrations, sources, and risk assessment of 16 organochlorinated pesticides (OCPs), seven polychlorinated biphenyls (PCBs) and seven polybrominated diphenyl ethers (PBDEs) were determined in soils from Kiambu to Mombasa in Kenya. The total concentrations of OCPs ranged between 7.62 and 76.09 ng/g, dominated by HCHs. Source identification displayed recent inputs and historical use of DDTs and lindane. The total concentrations of PCBs ranged from 9.90 to 20.8 ng/g with an average of 14.40 ng/g dominated by penta-PCBs from old transformers leakages. The total PBDEs concentrations were in the range of 1.89–38.36 ng/g and with a mean of 11.38 ng/g. Electric and electronic equipment waste and PBDE containing materials as sources of PBDE. The risk assessment of OCPs and PCBs showed low potential human health risk from OCPs, while PCBs indicated to pose a high risk.

54 ENVIRONMENTAL SCIENCES↗

Exploration of the Effect of Chitosan and Crosslinking Agent Concentration on the Properties of Dual Responsive Chitosan-g-Poly (N-Isopropylacrylamide) Co-polymeric Particles

The objective of the present study was to synthesize and evaluate the effect of change in concentration of chitosan (CS) and N,N-methylenebisacrylamide (MBA)- a cross linking agent, on various properties such as lower critical solution temperature (LCST), zeta potential, particle size and poly dispersity index (PDI) of the synthesized co-polymer. Nine different formulations of chitosan-g-poly (N-isopropylacrylamide) (CS-g-PNIPAAm) co-polymer with varying CS and MBA concentrations were synthesized by a surfactant free dispersion copolymerization method. The synthesized co-polymer was further characterized and confirmed for its structure, morphology, particle size, zeta-potential, thermo and pH responsive properties, in-vitro cyto-compatability and stability studies using various analytical tools. The data confirms the successful synthesis of co-polymer. The increase in the concentrations of CS and MBA during the polymerization of co-polymer, resulted in proportional increase of LCST and zeta potential with decrease in particle size of co-polymeric nanoparticles. pH responsive studies showed that as the pH of the medium increases particle size and zeta potential decreases with increase in LCST of co-polymeric nanoparticles. From the results, it can be inferred that the synthesized co-polymeric nanoparticles exerted thermo and pH responsive properties with biocompatibility. By varying the CS and MBA concentrations in the co-polymer, desired LCST, particle size and zeta potential for co-polymeric nanoparticles can be obtained and thus the synthesized co-polymer may have great potential to be used as a drug carrier (nanoform) with both thermo and pH responsiveness.

36 MATERIALS SCIENCE↗

Effect of NaOH Concentration and Adding Sequences on Structural and Magnetic Properties of Ni{sub 0.4}Co{sub 0.6}Fe{sub 2}O{sub 4} Nanopowders Prepared Via Co-precipitation Route

Ni{sub 0.4}Co{sub 0.6}Fe{sub 2}O{sub 4} nanopowders were prepared via the co-precipitation route followed by annealing treatment. The structural and magnetic properties of the as-synthesized samples were determined by XRD, FT-IR, TG-DSC, and PPMS measurements, respectively. The XRD patterns indicated a single-phase cubic spinel structure for all the Ni-Co ferrite samples, regardless of adding sequences of the reactants or NaOH concentration. The analysis of the XRD patterns revealed that the enhancement in lattice constant with increasing NaOH concentration is related to the prevention of oxidization of Co{sup 2+} ions in the Ni-Co ferrite lattice. The FT-IR spectra indicated that samples prepared in the B process have fewer impurities than those prepared in the A process. The enhancement in saturation magnetization with the increase in sodium hydroxide concentration could be attributed to the strengthening of super-exchange interaction between A and B sublattices, due to replacements of Co{sup 3+} ions (magnetic moment of 0 μ{sub B}) by Co{sup 2+} ions (magnetic moment of 3 μ{sub B}) at B sublattices. The obvious increase in the coercivity field with the increase in concentration of NaOH solutions can be interpreted in terms of enhancement of magneto-crystalline anisotropy that originated from gradual substitutions of Co{sup 3+} ions with Co{sup 2+} ions at the octahedral sites.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗

Quantifying uncertainty in uranium concentration measurements via K-edge densitometry

This study quantifies the uncertainty in uranium concentration predictions of fluoride and chloride-based salts within a steel pipe using K-edge densitometry. Modeling and simulation was conducted with the Monte Carlo N-Particle Transport (MCNP) code. The quality of of this technique’s prediction in a pipe requires proper characterization of the pipe’s thickness, which is dependent on the source size and axial offset from the pipe centerline. The thickness was determined as either the center-line thickness seen by the X-ray source or an average value determined through random sampling. Generally, the predicted concentrations were slightly better at lower offset with the random sampling thickness and using the center-line thickness for the highest offsets. For a line-beam source and varying axial offsets, the relative error of concentration was within 1% of the true value but uncertainty increased by 2 orders of magnitude. Similarly, for no axial offset, the relative error was significantly less than 1% while no trend for uncertainty was found. However, at the largest possible offset for a given source size, the concentrations become erroneous and greater than the allowable 1% relative error. Furthermore, high offsets tended to increase the variance of the transmission spectra by 3 orders of magnitude.

Characterization and Analytical Technique↗

The Influence of Lactic Acid Concentration on the Separation of Light Rare Earth Elements by Continuous Liquid–Liquid Extraction with 2-Ethylhexyl Phosphonic Acid Mono-2-ethylhexyl Ester

The separation of rare earth elements (REEs) using solvent extraction adding complexing agents appears to be an alternative to saponification of the extractant. We evaluated the effect of lactic acid concentration on didymium (praseodymium and neodymium) and lanthanum extraction with 2-ethylhexyl phosphonic acid mono-2-ethyl hexyl ester [HEH(EHP)] as extractant. First, we investigated in batch experiments the separation of lanthanum (La) and didymium (Pr and Nd) using McCabe–Thiele diagrams to estimate the number of extraction stages when the feed solution was or was not conditioned with lactic acid. Additionally, we conducted continuous liquid–liquid extraction experiments and evaluated the influence of lactic acid concentration on the REE extraction and separation. The tests showed that the extraction percentage of REEs and the separation factor Pr/La increased when the lactic acid concentration increased, but the didymium purity decreased. Lanthanum, praseodymium, and neodymium extraction rate were 23.0, 89.7, and 99.2 pct, respectively, with 1:1 aqueous/organic volume flow rate and feed solution doped with 0.52 mol L{sup −1} lactic acid. The highest didymium purity reached was 92.0 pct with 0.26 mol L{sup −1} lactic acid concentration.

36 MATERIALS SCIENCE↗

Global and regional trends in mercury emissions and concentrations, 2010–2015

Mercury (Hg) is a naturally occurring element in the Earth's crust. It can be harmful to human health when released in large quantities and/or converted to the neurotoxicant methyl mercury in aquatic ecosystems. This study analyzes here global and regional trends in anthropogenic Hg releases to the atmosphere between 2010 and 2015, as well as the associated trends in modeled and measured Hg concentrations at sites around the world. In general, we find that global Hg emissions and concentrations have grown slightly in this period, as declines from the phase-out of commercial Hg use in the developed world have been more than matched by increases in Hg-related activities in the industrializing countries of the world. We estimate that global Hg emissions between 2010 and 2015 have grown at a rate of 1.8%/yr, from 2188 Mg (+44%/-20%, 80% C.I.) in 2010 to 2390 Mg (+42%/-19%, 80% C.I.) in 2015. Regionally, emissions declined over this period in the U.S. (-10%), OECD Europe (-5.8%), and Canada (-3.2%), while they increased in Central America (+5.4%), South Asia (+4.6%), and Eastern Africa (+4.0%). East Asia remained the largest emitting region at 1012 Mg in 2015, though growth there has slowed significantly in recent years. The production of Hg (+7.9%), caustic soda (+6.3%), and cement (+6.3%) showed the highest increases by source type, though artisanal and small-scale gold mining (ASGM) was the single largest source of emissions in 2015 (775 Mg). The commercial use of Hg in dental applications (-5.6%) and electrical equipment (-5.2%) continued to decline. These emission trends show a continuation of the regional and sectoral shifts that began in the 1970s, but with a resulting reversal in global trends, because the benefits from Hg phase-out in North America and Europe have been largely realized and industrial growth in developing countries has begun to dominate. The emission trends are in agreement with trends in modeled and measured concentrations, which show small declines in surface air total gaseous Hg concentrations in eastern North America and Western Europe between 2010 and 2015, but slight increases for much of the rest of the world, driven by the continued increases in emissions from Asia and from ASGM. Our results suggest that reductions of Hg in the North Atlantic region have been largely successful, and focus now needs to shift to Asia and to the continued practice of ASGM worldwide.

54 ENVIRONMENTAL SCIENCES↗