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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.

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At least 73 records · Page 4

A size-invariant bud-duration timer enables robustness in yeast cell size control

Cell populations across nearly all forms of life generally maintain a characteristic cell type-dependent size, but how size control is achieved has been a long-standing question. The G1/S boundary of the cell cycle serves as a major point of size control, and mechanisms operating here restrict passage of cells to Start if they are too small. In contrast, it is less clear how size is regulated post-Start, during S/G2/M. To gain further insight into post-Start size control, we prepared budding yeast that can be reversibly blocked from bud initiation. While blocked, cells continue to grow isotropically, increasing their volume by more than an order of magnitude over unperturbed cells. Upon release from their block, giant mothers reenter the cell cycle and their progeny rapidly return to the original unperturbed size. We found this behavior to be consistent with a size-invariant 'timer' specifying the duration of S/G2/M. These results indicate that yeast use at least two distinct mechanisms at different cell cycle phases to ensure size homeostasis.

59 BASIC BIOLOGICAL SCIENCES↗

Introducing the GeoRePORT Resource Size Tool: Reporting on Geothermal Resource Size Estimations Using the Geothermal Resource Portfolio Optimization and Reporting Technique (GeoRePORT): Preprint

The Geothermal Resource Portfolio Optimization and Reporting Technique (GeoRePORT) was developed with funding from the U.S. Department of Energy Geothermal Technologies Office to assist in identifying and pursuing long-term investment strategies through the development of a resource reporting protocol. The assessment protocols used in GeoRePORT allow for comparison of project attributes across locations and geological settings to understand the feasibility of geothermal development. This work introduces the Resource Size Tool, a new feature within the GeoRePORT package that compiles two independent methods for estimating geothermal resource size in terms of energy capacity in MW. Energy production potential for twenty-three case studies was estimated with the Resource Size Tool in order to 1) generate a reasonable range of resource size estimates for a particular geothermal field; 2) illustrate the advantages and limitations of each methodology (such as data input requirements, estimate accuracy and precision, and the appropriate circumstances of use); and 3) test the ability of the resource size tool to provide useful and accurate information for geothermal stakeholders. The tool employs two methods widely used in the geothermal industry: (1) USGS Volumetric and (2) Power Density. Results from our case studies show general overlap between these two methods in terms of resource size estimates; however, they also reveal key differences between the two approaches that should be considered when using such estimates to drive development. First, the two methods rely on different input parameters and therefore one method may be more appropriate and/or accurate for a given project than the other. Second, the Power Density method was found to generate wider ranges of resource size predictions, more consistently aligning with actual power production of the field but with larger scales of error; whereas the USGS Volumetric method predicts narrower ranges but tends to overestimate when compared to current MW production. Future work will refine variables used in the methods with input data from other sections of GeoRePORT and modify uncertainty levels based on the particular datasets used for a given project.

geological↗

Oligogermanes as molecular precursors for germanium(0) nanoparticles: Size control and size-dependent fluorescence

Graphical abstract: Catenated germanium compounds are employed as molecular precursors for germanium(0) nanoparticles. The size of the nanoparticles, and their fluorescence spectra, depend on the number of catenated germanium atoms present in the precursor. - Highlights: • We have used oligogermanes for the size-specific synthesis of germanium(0) nanoparticles. • The size of the nanomaterials obtained depends directly on the degree of catenation present in the oligogermane precursor. • The nanoparticles are shown to exhibit size-dependent fluorescence. • Oligogermanes will function as useful precursors for the synthesis of a variety of nanomaterials. - Abstract: Germanium nanoparticles were synthesized in solution from novel oligogermane molecular precursors. The size of the nanoparticles obtained is directly related to the number of catenated germanium atoms present in the oligogermane precursor and the nanoparticles exhibit size-dependent fluorescence. The germanium nanoparticles were also characterized by TEM, powder XRD, FTIR, EDS and XPS methods. This method appears to be a promising new route for the synthesis of germanium nanoparticles since the size of the materials obtained can be controlled by the choice of the oligogermane used as the precursor.

36 MATERIALS SCIENCE↗

Size Effects on Gamma Radiation Response of Magnetic Properties of Barium Hexaferrite Powders

Little is currently known about the effects of gamma-ray irradiation on oxide magnet materials. In particular, the effect of particle size on radiation susceptibility was investigated. Two commercial powders of BaFe12O19 were thoroughly characterized, then exposed to 1 MGy of gamma radiation from a 60Co source. AC susceptibility and DC magnetometry and Mössbauer spectroscopy were performed after irradiation and compared to pre-irradiated measurements. DC magnetization and AC susceptibility decreased for both samples with the relative change of DC magnetization being larger for the micrometer-sized particles and the relative change of the AC susceptibility being larger for the nanometer-sized particles. Mössbauer spectroscopy indicated a decrease in both the hyperfine fieldsand in the distribution of hyperfine fields for each Fe site, particularly in the larger particle sample. Decreases in susceptibility are believed to be due to recrystallization of the particles and redistribution of an amorphous component, in the bulk or on the surface, and consequent reduction in the particle magnetic moment. This radiation damage mechanism is different than that seen in previous studies of neutron and heavy ion irradiation of BaFe12O19.

72 PHYSICS OF ELEMENTARY PARTICLES AND FIELDS↗

A Novel Approach to Synthesize Micrometer-Sized Porous Silicon as a High Performance Anode for Lithium-Ion Batteries

Porous structured silicon (p-Si) has been recognized as one of the most promising anodes for Li-ion batteries. However, many available methods to synthesize p-Si are difficult to scale up due to their high production cost. Here we introduce a new scalable approach to obtain spherical micrometer-sized silicon with unique porous structure by using a microemulsion and magnesiothermic reduction method. The spherical micron-sized p-Si particles prepared by this approach consist of highly aligned nano-sized silicon and exhibit a tap density close to that of bulk Si particles. They have demonstrated significantly improved electrochemical stability compared to nano-Si. Well controlled void space and a highly graphitic carbon coating on the p-Si particles enable good stability of the structure and low overall resistance, thus resulting in a Si-based anode with high capacity (~1467 mAh g-1 at 1C), enhanced cycle life (200 cycles with 90% capacity retention), and high rate capability (~650 mAh g-1 at 5C). This scalable approach may also be generalized to prepare other hierarchical structured high capacity anode materials for constructing high energy density lithium ion batteries.

Jia, Haiping↗

Design of a Particle Shadow-graph Velocimetry and Size (PSVS) System to Determine Particle Size and Density Distributions in Hanford Nuclear Tank Wastes - 12280

Accurate particle size and density distributions for nuclear tank waste materials are essential information that helps determine the engineering requirements for a host of waste management unit operations (e.g., tank mixing, pipeline transport, and filtration). The most prevalent approach for determining particle size and density distribution is highly laborious and involves identifying individual particles using scanning electron microscope/x-ray diffraction and then acquiring the density of the materials from the technical literature. Other methods simply approximate individual particle densities by assuming chemical composition, rather than obtaining actual measurements of particle density. To overcome these limitations, a Particle Shadow-graph Velocimetry and Size (PSVS) system has been designed to simultaneously obtain particle size and density distributions for a broad range of Hanford tank waste materials existing as both individual particles and agglomerates. The PSVS system uses optical hardware, a temperature-controlled settling column, and particle introduction chamber to accurately and reproducibly obtain images of settling particles. Image analysis software provides a highly accurate determination of both particle terminal velocity and equivalent spherical particle diameter. The particle density is then calculated from Newton's terminal settling theory. The PSVS system was designed to accurately image particle/agglomerate sizes between 10 and 1000 μm and particle/agglomerate densities ranging from 1.4 to 11.5 g/cm{sup 3}, where the maximum terminal velocity does not exceed 10 cm/s. Preliminary testing was completed with standard materials and results were in good agreement with terminal settling theory. Recent results of this method development are presented, as well as experimental design. The primary goal of these PSVS system tests was to obtain accurate and reproducible particle size and velocity measurements to estimate particle densities within 20 percent of direct measured density values. The average percent error observed in particle densities was 4.8, 8.2, and 25.8 percent for S1D3 (high-density soda-lime glass), S3D4 (zirconia), and S1D2 (soda-lime glass) beads, respectively. The maximum measured particle density error observed was 14.5, 21.0, and 58.4, for S1D3, S3D4, and S1D2 beads, respectively. Multiple sources of error can exist that contribute to inaccurate estimates of particle density using the PSVS approach. Two significant influences observed were thermal convective currents in the settling column fluid and non-spherical (irregular) particle shapes in the standard test materials. Experimental results using buoyant beads suggest thermal convective currents can influence the movement of settling particles as much as 4 mm/s. These thermal convective currents are clearly a significant concern for smaller and less-dense particles/agglomerates which have terminal velocities of the same magnitude. Significant effort went into the design and fabrication of a thermal control system for the PSVS settling column. However, small temperature variations (<0.3 deg. C) are difficult to prevent and measure accurately. Therefore, although designing the thermal control system was necessary, it is not considered the only solution to minimize error due to thermal convective currents. The use of small diameter (10 to 27 μm) polyethylene buoyant beads (in low concentrations) during actual settling experiments may be necessary to provide insight into particle-particle interactions and fluid velocity correction factors to account for potential influences from thermal convective currents. Future testing will incorporate the buoyant beads into the analysis technique when the suspension fluid is chemically compatible. The use of the Newton's law to calculate particle/agglomerate densities assumes spherical particle shapes. As the actual particle/agglomerates diverge from spherical, the margin of error increases. The selection of high quality (in density and shape) monodispersed particle standards was a direct attempt to reduce the uncertainties associated with non-spherical or irregular particles and to only observe the PSVS method and analysis error. While investigating the source of data scatter for the S1D3 bead (nominal 700 μm) standard, significant irregular particles where discovered. Yet, a subsequent investigation into the S3D4 bead standard was also conducted and it was determined that 60 percent of the particles had a 0.9 to 0.8 centricity, 32 percent were between 0.8 and 0.7, only 7 percent were between 1.0 and 0.9, and the remaining 1 percent of the particles had centricities between 0.7 and 0.6. Contrast this with the S1D3 bead standard, where 100 percent of particles had centricities between 0.95 and 0.98, upon applying the centricity filter. The influence of the non-spherical shape of the S3D4 bead standard is evident when comparing a 3.9 percent average density error for S1D3 glass bead standard with an 8.3 percent average density error for the S3D4 bead standard. Model corrections for non-spherical shape must be implemented to account for these measurement errors during future method validation and system performance assessments. In addition, further work is needed to resolve the higher than expected velocities for the smaller S1D2 particles. Initial measurements conducted with buoyant beads as fluid velocity tracers indicate that fluid velocities can be subtracted from the increased particle velocities to determine the particle terminal velocity, regardless of the surrounding fluid velocity. However, this approach is in its infancy and will need to be carefully and methodically validated. (authors)

12 MANAGEMENT OF RADIOACTIVE AND NON-RADIOACTIVE W↗

Uncovering the Size-dependent Thermal Solid Transformation of Akaganéite

Investigating the structural evolution and phase transformation of iron oxides is crucial for gaining a deeper understanding of geological changes on diverse planets and preparing oxide materials suitable for industrial applications. In this study, we employed in-situ heating techniques in conjunction with transmission electron microscopy (TEM) observations and ex-situ characterization to thoroughly analyze the thermal solid-phase transformation of akaganéite one-dimensional (1D) nanostructures with varying diameters. Our findings offer compelling evidence for a size-dependent morphology evolution in akaganéite 1D nanostructures, which can be attributed to the transformation from akaganéite to maghemite (?-Fe2O3) and subsequent crystal growth. Specifically, we observed that akaganéite nanorods with a diameter of around 50 nm transformed into hollow polycrystalline maghemite nanorods, which demonstrated remarkable stability without arresting crystal growth under continuous heating. In contrast, smaller akaganéite nanoneedles or nanowires with a diameter ranging from 20 to 8 nm displayed a propensity for forming single-crystal nanoneedles or nanowires through phase transformation and densification. By manipulating the size of the precursors, we have developed a straightforward method for the synthesis of single-crystal and polycrystalline maghemite nanowires through solid-phase transformation. These significant findings provide new insights into the size-dependent structural evolution and phase transformation of iron oxides at the nanoscale.

Wang, Xiang↗

Quantifying structural errors in cloud condensation nuclei activity from reduced representation of aerosol size distributions

Aerosol effects on clouds and radiation are the dominant contribution to uncertainty in radiative forcing relative to the pre-industrial atmosphere. While previous studies have assessed the impact of parametric uncertainty on modeled forcing, structural errors from the numerical representation of particle distributions have not been well quantified. Here we present a framework for quantifying error in aerosol size distributions and cloud condensation nuclei activity, which we apply to the widely used 4-mode version of the Modal Aerosol Module (MAM4). Box model predictions from the MAM4 are evaluated against the Particle Monte Carlo Model for Simulating Aerosol Interactions and Chemistry (PartMC-MOSAIC), a benchmark model that tracks the evolution of individual particles. We show that size distributions simulated by MAM4 diverge from those simulated by PartMC-MOSAIC after only a few hours of aging by condensation and coagulation in polluted conditions, which leads to large errors in modeled cloud condensation nuclei concentrations. We find that differences between MAM4 and PartMC-MOSAIC are largest under polluted conditions, where the size distribution evolves rapidly though aging by condensation of semi-volatile substances and coagulation among particles. These findings suggest that structural error in modeled aerosol properties contributes to the large inter-model variability in aerosol radiative forcing.

Fierce, Laura M.↗

Ab-Initio Investigation of Finite Size Effects in Rutile Titania Nanoparticles with Semilocal and Nonlocal Density Functionals

In this work, we employ hybrid and generalized gradient approximation (GGA) level density functional theory (DFT) calculations to investigate the convergence of surface properties and electronic gap of rutile titania nanoparticles with particle size. The surface energies and electronic gaps are calculated for cuboidal particles with minimum dimension ranging from 3.7 Angstrom (24 atoms) to 10.3 Angstrom (384 atoms) using a highly-parallel real-space DFT code to enable hybrid level DFT calculations of larger nanoparticles than are typically practical. We deconvolute the geometric and electronic finite size effects in surface energy, and evaluate the influence of defects on electronic gap and density of states (DOS). The electronic finite size effects in surface energy vanish when the minimum length scale of the nanoparticles becomes greater than 10 Angstrom. We show that this length scale is consistent with a computationally efficient numerical analysis of the characteristic length scale of electronic interactions. The surface energy of nanoparticles having minimum dimension beyond this characteristic length can be approximated using slab calculations that account for the geometric defects. In contrast, the finite size effects on the electronic gap and DOS is highly dependent on the shape and size of these particles. Furthermore, the DOS for cuboidal particles and more realistic particles constructed using the Wulff algorithm reveal that defect states within the electronic gap play a key role in determining the eigen value distribution of nanoparticles and the electronic gap does not converge to the bulk limit for the particle sizes investigated.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

3D Morphology of Bimodal Porous Copper with Nano-Sized and Micron-Sized Pores to Enhance Transport Properties for Functional Applications

Multiscale porous metals with multiscale porosity from nanometer to micrometer have a high specific surface area and high effective diffusivity for ion transport, thereby enhancing functionalities and extending the applications of porous metals. Herein, the Cu–Fe–Al ternary system was selected as the precursor alloy to construct multiscale, bimodal porous copper by the chemical dealloying method. The effect of the phase composition and initial microstructure of precursor alloys (Al x Fe 75– x Cu 25 , x = 10–60) on the three-dimensional (3D) morphology of multiscale porous metals was systematically investigated, with a goal to precisely control the multiscale porous structure. The four crystal structure phases (body-centered cubic (BCC), face-centered cubic (FCC), CsCl type (B2), and monoclinic) in precursor alloys were analyzed by synchrotron X-ray diffraction refinement. The 3D morphology, feature size distribution, and tortuosity of four representative porous Cu after dealloying Al x Fe 75– x Cu 25 ( x = 10, 30, 50, and 60) precursor alloys were directly visualized and quantified via advanced synchrotron X-ray nanotomography. The relationship between the phases/crystal structures of precursor alloys and their corresponding porous morphology was established: the micron-sized pores in bimodal porous Cu are formed by dissolving the CuFeAl phase with BCC and monoclinic crystal structures, and the nano-sized pores are formed by dealloying the CuFeAl phase with FCC and B2 crystal structures. The size of the nanoporous structure depends on the ratio between the more noble and more active components in the precursor alloy, while the size of the microporous structure depends on the corresponding phase size in the precursor alloy. The tortuosity results showed that the multiscale porous structure with both nanoporosity and microporosity exhibits lower tortuosity, which will enhance transport properties for functional applications.

25 ENERGY STORAGE↗

Simple size-controlled synthesis of Au nanoparticles and their size-dependent catalytic activity

The controlled preparation of Au nanoparticles (NPs) in the size range of 6 to 22 nm is explored in this study. The Au NPs were prepared by the reduction of tetrachloroauric acid using maltose in the presence of nonionic surfactant Tween 80 at various concentrations to control the size of the resulting Au NPs. With increasing concentration of Tween 80 a decrease in the size of produced Au NPs was observed, along with a significant decrease in their size distribution. The size-dependent catalytic activity of the synthesized Au NPs was tested in the reduction of 4-nitrophenol with sodium borohydride, resulting in increasing catalytic activity with decreasing size of the prepared nanoparticles. Eley-Rideal catalytic mechanism emerges as the more probable, in contrary to the Langmuir-Hinshelwood mechanism reported for other noble metal nanocatalysts.

36 MATERIALS SCIENCE↗