SEARCH · Search NASA
Results for “quantification”
Search indexed NASA NTRS and DOE OSTI research on propulsion, heat transfer, battery materials and energy systems. Follow report and document links to the original sources.
Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.
X‐Ray Spectroscopic Quantification of Struvite and Dittmarite Recovered from Wastewater
Phosphorus recovery from wastewater as struvite (MgNH 4 PO 4 ⋅6H 2 O) or dittmarite (MgNH 4 PO 4 ⋅H 2 O) can decrease water pollution risk, as well as produce a P‐rich material suitable as fertilizer. However, most studies to date have focused on the removal of P from wastewater, rather than on characterization of the recovered P materials. The objective of this work was to apply microfocused X‐ray fluorescence (XRF) spectroscopy, and both bulk and microfused X‐ray absorption near edge structure (XANES) spectroscopy, to provide insight into the speciation of recovered P in various struvite‐containing and struvite‐like materials. Three materials were investigated: homogeneous crystalline struvite on apatite seed, homogeneous dittmarite, and heterogeneous struvite with sand contamination (referred to as the “sandy” material). The struvite materials were recovered from dairy wastewater, whereas the dittmarite was from a cheese processing plant. Phosphorus speciation in the crystalline struvite on apatite seed material was ∼17% apatite and 83% struvite; in the “sandy” material, P was ∼24% apatite and ∼76% struvite, with an uncertainty of approximately ±15%. The P K ‐edge XANES spectra of recovered dittmarite appeared pure. These findings highlight the heterogeneity of recovered P materials and underscore the importance of P speciation to understand P release behavior and bioavailability from recovered phosphates. Core Ideas Multiple methods should be used to corroborate spectroscopic estimates of P speciation. Dittmarite P K ‐edge XANES spectra are distinct from spectra of chemically similar struvite. Phosphorus K ‐edge XANES spectroscopy can quantify Mg‐associated P >15 atom% P.
Normalization of Soil DNA Extraction for Accurate Quantification of Target Genes by Real-Time PCR and DGGE
Not Available
Phenomena-based Uncertainty Quantification in Predictive Coupled- Physics Reactor Simulations
This project has sought to develop methodologies, tailored to phenomena that govern nuclearreactor behavior, to produce predictions (including uncertainties) for quantities of interest (QOIs) in the simulation of steady-state and transient reactor behavior. Examples of such predictions include, for each QOI, an expected value as well as a distribution around this value and an assessment of how much of the distribution stems from each major source of uncertainty. The project has sought to test its methodologies by comparing against measured experimental outcomes. The main experimental platform has been a 1-MW TRIGA reactor. This is a flexible platform for a wide range of experiments, including steady state with and without temperature feedback, slow transients with and without feedback, and rapid transients with strong feedback. The original plan was for the primary experimental data to come from in-core neutron detectors. We made considerable progress toward this goal but did not get as far along as we had planned. We have designed, developed, installed, and tested vertical guide tubes, each able to accept a detector or stack of detectors that can be moved axially inside the tube, and we have tested several new detector designs. One of these shows considerable promise.
Quantification of uncertainty in photon source spot size inference during laser-driven radiography experiments at TRIDENT
Images of the R2DTO resolution target were obtained during laser-driven-radiography experiments performed at the TRIDENT laser facility, and analysis of these images using the Bayesian Inference Engine (BIE) determines a most probable full-width half maximum (FWHM) spot size of 78 μm. However, significant uncertainty prevails due to variation in the measured detector blur. Propagating this uncertainty in detector blur through the forward model results in an interval of probabilistic ambiguity spanning approximately 35-195 μm when the laser energy impinges on a thick (1 mm) tantalum target. In other phases of the experiment, laser energy is deposited on a thin (~100 nm) aluminum target placed 250 μm ahead of the tantalum converter. When the energetic electron beam is generated in this manner, upstream from the bremsstrahlung converter, the inferred spot size shifts to a range of much larger values, approximately 270-600 μm FWHM. This report discusses methods applied to obtain these intervals as well as concepts necessary for interpreting the result within a context of probabilistic quantitative inference.
Uncertainty Quantification of Multi-Phase Closures
In the ensemble-averaged dispersed phase formulation used for CFD of multiphase ows in nuclear reactor thermohydraulics, closures of interphase transfer of mass, momentum, and energy constitute, by far, the biggest source of error and uncertainty. Reliable estimators of this source of error and uncertainty are currently non-existent. Here, we report on how modern Validation and Uncertainty Quanti cation (VUQ) techniques can be leveraged to not only quantify such errors and uncertainties, but also to uncover (unintended) interactions between closures of di erent phenomena. As such this approach serves as a valuable aide in the research and development of multiphase closures. The joint modeling of lift, drag, wall lubrication, and turbulent dispersion|forces that lead to tranfer of momentum between the liquid and gas phases|is examined in the frame- work of validation of the adiabatic but turbulent experiments of Liu and Banko , 1993. An extensive calibration study is undertaken with a popular combination of closure relations and the popular k-ϵ turbulence model in a Bayesian framework. When a wide range of super cial liquid and gas velocities and void fractions is considered, it is found that this set of closures can be validated against the experimental data only by allowing large variations in the coe cients associated with the closures. We argue that such an extent of variation is a measure of uncertainty induced by the chosen set of closures. We also nd that while mean uid velocity and void fraction pro les are properly t, uctuating uid velocity may or may not be properly t. This aspect needs to be investigated further. The popular set of closures considered contains ad-hoc components and are undesirable from a predictive modeling point of view. Consequently, we next consider improvements that are being developed by the MIT group under CASL and which remove the ad-hoc elements. We use non-intrusive methodologies for sensitivity analysis and calibration (using Dakota) to study sensitivities of the CFD representation (STARCCM+) of uid velocity pro les and void fraction pro les in the context of Shaver and Podowski, 2015 correction to lift, and the Lubchenko et al., 2017 formulation of wall lubrication.
Wireless Chemical Sensor Systems (Optimization of Field-Structured Chemiresistors for in situ Quantification of Propellant Stabilizer Concentration)
This project is a Cooperative Research and Development Agreement (CRADA) with International Electronic Machines Corp. (IEM, Troy, NY), who is contracted through the U.S. Naval Air Systems Command (NAVAIR) (under SBIR N111-010) to develop an in situ wireless chemical sensor system called the Stabilizer Level Accurate Measurement System (SLAMS). The SLAMS device is specified to include a miniature, very thin, self-contained chemical-sensor node to detect and track the level of stabilizer present in various PADs and CADs. IEM is focused on the wireless sensor platform, node communication, and electronics; whereas Sandia National Laboratories’ (SNL’s) efforts are focused on the chemical sensor development and integration. The sensor technology being employed is known as field-structured chemiresistors (FSCRs), which was invented by James Martin, et al. (SNL) and refined by Martin and Read. These sensors are small, require very little power, and have tunable sensitivity and selectivity. In the following, we discuss SNL’s efforts to optimize the FSCRs for the demanding chemical and environmental conditions that will be encountered in this application.
Predictive Modeling, Inverse Problems, and Uncertainty Quantification with Application to Emergency Response
No abstract provided.
Mechanical Behavior of UO 2 at Sub-grain Length Scales: Quantification of Elastic, Plastic and Creep Properties via Microscale Testing
Techniques were developed to measure properties at sub-grain scales using depleted Uranium Oxide (d-UO2) samples heat-treated to obtain different grain sizes and oxygen stoichiometries, through three main tasks: 1) sample processing and characterization, 2) microscale and conventional testing and 3) modeling. Grain size and crystallography were characterized using Scanning Electron Microscopy (SEM), in conjunction with Electron Backscattering Diffraction (EBSD) and Electron Channeling Contrast Imaging (ECCI). Grains were then carefully selected based on their crystallographic orientations to perform ex-situ micromechanical tests with samples machined via Focused Ion Beam (FIB), with emphasis on micro-cantilever bending. These experiments were performed under controlled atmospheres, to insure stoichiometry control, at temperatures up to 700 °C and allowed measurements involving elastic (effective Young’s modulus), plastic (critical resolved shear stresses) and creep (creep strain rates) behavior. Conventional compression experiments were performed simultaneously to compare with the ex-situ measurements and study potential size effects. Modeling was implemented using anisotropic elasticity and inelastic constitutive relations for plasticity and creep based on kinematics and kinetics of dislocation glide that account for the effects of crystal orientation, and stress. The models will be calibrated and validated using the experimental data. This project provided insight on correlations among stoichiometry, crystallography and mechanical behavior in advanced oxide fuels, provided valuable experimental data to validate and calibrate mesoscale fuel performance codes and also a framework to measure sub-grain scale mechanical properties that should be suitable for use with irradiated samples due to small volumes required. The goals and metrics of the ongoing study of thermo-mechanical behavior in depleted uranium dioxide (d-UO 2 ) outlined in this project have been concluded successfully, resulting in: 1) the successful fabrication, processing, and characterization of large-grained samples with various orientations (up to and including single crystals) having stoichiometric and hyper-stoichiometric O/U ratios; 2) formulation, calibration, and validation of a crystal plasticity constitutive model to describe the creep deformation of UO 2 at the sub-grain length scale (single crystal level) at intermediate temperatures; 3) the successful calibration of a crystal plasticity constitutive model to describe the elasto-plastic deformation of microcantilever beams, also at moderate temperatures. Samples were prepared from natural uranium oxide powder of production-quality provided by Areva. The powder was pressed in a die to a pressure of 100 MPa to produce green pellets with no sintering aids, lubricants, or any other additives. The green pellets were then heated up to 1700 °C under ultra-high purity argon atmosphere (~1 ppm O2). The atmosphere was then changed to 79% Argon, 21% O 2 and the temperature was held at 1700 °C for 2 hours to sinter the pellets under oxidative conditions [1] that are known to increase grain growth kinetics in UO 2 [2]. Samples were then cooled down under Ar-4%H2 atmosphere to reduce the samples back to stoichiometric UO 2 . For macro-scale procedures, testing of UO 2 samples with large grains was performed at 1200 °C using a modified load frame capable of applying dead-weight loads to ensure constant stress conditions, while displacement of the sample produced by the applied load was measured with high precision micrometers to obtain strains. Stress steps were used during testing and the strains were monitored to measured creep strain rates under steady state for each level of stress used, so that stress exponents could be obtained. The results of the mechanical testing, along with sample geometry and crystal orientation of the grains in the samples, as well as post-test sample characterization were used to formulate a viscoplastic model to account for steady state (stage II) creep behavior, along with basic assumptions from crystal plasticity and kinematic constraints due to testing fixtures. In the micro-scale, testing of microcantilever beams at temperatures ranging from 25 to 570 °C was performed in-situ with a scanning electron microscope with a special attachment to apply load and measure displacement while the samples were at temperature. The load-displacement curves obtained showed linear behavior before fracture for all temperatures attempted except 570 °C, where clear deviations from non-linearity were observed before fracture. These deviations were consistently observed for all samples tested for a given orientation. A viscoplastic model was used to account for the presence of inelastic strain, along with basic assumptions from crystal plasticity and beam theory. These models were kept as simple as possible, and results from tests performed in a set of samples with a given crystal orientation were used to calibrate the material constants for the model, while results from a different sample set were then used for validation, thus satisfying the conditions of all main tasks within the parameters of this project. Details of these efforts are outlined in this report.
Enhanced Analytical Simulation Tool (EASiTool) for CO 2 Storage Capacity Estimation and Uncertainty Quantification
An enhanced analytical simulation tool (EASiTool) was developed to estimate CO 2 storage capacity in saline aquifers. The tool provides a quantitative estimate of storage capacity for multi-well injection/extraction systems by applying novel analytical models for both closed- and open-boundary saline aquifers and analyzes the potential of enhancing storage efficiency by integrating active brine management (brine extraction technology). Brine extraction would enhance the storage capacity and partially control the pressure buildup. EASiTool includes a user-friendly interface and can be used to provide reservoir and basin-scale storage capacity estimates.
Detection and Quantification of Ground Surface Changes from an Underground Explosion
No abstract provided.
Sensitivity Analysis and Uncertainty Quantification of the Feynman Y and Sm 2
Neutron multiplicity counting (NMC) experiments are frequently used to perform non-destructive assay (NDA) of special nuclear material (SNM) [2]. While the behavior of a critical or nearly critical system is well described by the mean count rate, which is the mean of the NMC distribution, the behavior of a highly subcritical system exhibits large fluctuation in time. Fission chains do not last long enough to overlap and thus the neutron population is relatively small with a large dispersion. The system behavior must therefore be described in terms of higher-order NMC distribution moments.
Sensitivity Analysis and Uncertainty Quantification of the Feynman Y and Sm 2
No abstract provided.
Adjoint-Based Sensitivity Analysis and Uncertainty Quantification for keff: Using the MCNP KSEN Card
No abstract provided.
An Extended Study on the Uncertainty Quantification of a Photodiode's Spectral Responsivity
An extended study was done on the analysis procedure for spectral responsivity of a silicon detector from the range of 200 nm to 1100 nm for the Optical Component Calibration laboratory at Livermore Operations in Livermore California. As a result, the uncertainty of the procedure was quantified to account for variables that contribute to uncertainty; such as the reproducibility and repeatability of the working standards, quantifying Type A and B uncertainties, validating laboratory equipment and associated software, and looking at environmental variables. The findings lead to a revised analysis reporting procedure that reports uncertainties depending on three spectral ranges, 300 nm to 400 nm, 400 nm to 700 nm, and 700 nm to 1100 nm. A proficiency test was done to compare the difference between both methods and a noticeable difference was found. The results showed that the previous reporting method over estimated uncertainty as much as 3.5% for the 300 nm to 400 nm range, 4% in the >400 nm to 700 nm range, and 2% in the >700 nm to 1100 nm range. The findings lead to the use of the revised procedure when producing calibration certificates, better quantified measurement uncertainties, and will be used for the process of updating the scope of accreditation from the National Voluntary Laboratory Accreditation Program.
Mathematical Foundations for Uncertainty Quantification in Materials Design. Final Report
Final report DE-SC0010723. Our key accomplishment in the first year of the grant is that we started developing pathwise information theory-based and goal-oriented sensitivity analysis and parameter identification methods for complex high-dimensional dynamics and in particular of nonequilibrium extended systems. The combination of these novel methodologies provide the first methods in the literature which are capable to handle UQ questions for stochastic complex systems with some or all of the following features: (a) multi-scale models with a very large number of parameters, (b) spatially distributed systems such as Kinetic Monte Carlo or Langevin Dynamics, (c) non-equilibrium processes typically associated with coupled physico-chemical mechanisms, driven boundary conditions, etc. The first two such publications sponsored by the grant, have just been published.
Developing an Automated Uncertainty Quantification Tool to Improve Watershed-Scale Predictions of Water and Nutrient Cycling
Explore the source record for details and available documents.