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At least 973 records · Page 54

A universal density structure for circumgalactic gas

We develop a new method to constrain the physical conditions in the cool (∼10{sup 4} K) circumgalactic medium (CGM) from measurements of ionic column densities by assuming that the cool CGM spans a large range of gas densities and that small high-density clouds are hierarchically embedded in large low-density clouds. The new method combines the information available from different sightlines during the photoionization modeling, thus yielding tighter constraints on CGM properties compared to traditional methods that model each sightline individually. Applying this new technique to the COS Halos survey of low-redshift ∼L* galaxies, we find that we can reproduce all observed ion columns in all 44 galaxies in the sample, from the low ions to O VI, with a single universal density structure for the cool CGM. The gas densities span the range 50≲ρ/ ρ-bar {sub b}≲5×10{sup 5} ( ρ-bar {sub b} is the cosmic mean), while the physical size of individual clouds scales as ∼ρ {sup −1}, from ≈35 kpc for the low-density O VI clouds to ≈6 pc for the highest-density low-ion clouds. The deduced cloud sizes are too small for this density structure to be driven by self-gravity; thus, its physical origin is unclear. The implied cool CGM mass within the virial radius is (1.3 ± 0.4) × 10{sup 10} M{sub ⊙} (∼1% of the halo mass), distributed rather uniformly over the 4 decades in density. The mean cool gas density profile scales as R{sup −1.0±0.3}, where R is the distance from the galaxy center. We construct a 3D model of the cool CGM based on our results, which we argue provides a benchmark for the CGM structure in hydrodynamic simulations. Our results can be tested by measuring the coherence scales of different ions.

79 ASTRONOMY AND ASTROPHYSICS↗

Synthesis and characterization of anatase TiO{sub 2} nanotubes with controllable crystal size by a simple MWCNT template method

Highly crystalline phase-pure anatase TiO{sub 2} nanotubes were produced by performing a simple calcinations process in air of the TiO{sub 2} coated MWCNTs composite material prepared by an in situ sol-gel method. A homogeneous thin coating layer of TiO{sub 2} on the surface of MWCNTs is firstly obtained. Calcination in ambient air at appropriate temperatures is performed to transform phase of TiO{sub 2} into anatase and remove MWCNTs simultaneously, resulting in pure anatase TiO{sub 2} nanotubes. Both end tips of the nanotubes are observed to be closed, probably due to covering up MWCNTs with TiO{sub 2} particles. The crystallization of anatase phase was formed upon 350 Degree-Sign C, and MWCNTs are completely oxidized between 500 and 650 Degree-Sign C, leaving anatase TiO{sub 2} nanotubes with an average crystal size increasing from about 8 to 24 nm as the temperature rises. Moreover, the tubular structure was found to collapse after calcinations at 700 Degree-Sign C. - Graphical abstract: TGA analysis and TEM images of the samples after calcinations in air at different temperatures: (a) before calcinations, (b) 350 Degree-Sign C, (c) 500 Degree-Sign C, and (d) 650 Degree-Sign C. Highlights: Black-Right-Pointing-Pointer Highly crystalline and stable phase-pure anatase TiO{sub 2} nanotubes were produced by a simply MWCNT template method. Black-Right-Pointing-Pointer A homogeneous thin coating layer of TiO{sub 2} on the surface of MWCNTs could be obtained. Black-Right-Pointing-Pointer Small crystal size of anatase is formed at lower temperatures and higher temperatures cause significant increase of crystal size from 8 to 24 nm. Black-Right-Pointing-Pointer Convex closed tip structure of TiO{sub 2} nanotubes is formed owing to the good coating of TiO{sub 2}.

36 MATERIALS SCIENCE↗

Microphysical Properties of Tropical Tropopause Layer Cirrus

Pervasive cirrus clouds in the tropical tropopause layer (TTL) play an important role in determining the composition of stratospheric air through dehydration of tropospheric air entering the stratosphere. This dehydration affects Earth's energy budget and climate, yet uncertainties remain regarding the microphysical processes that govern TTL cirrus. TTL cirrus were sampled with the NASA Global Hawk UAV for over 30 hr in the Western Pacific in 2014 during the Airborne Tropical TRopopause EXperiment. In situ measurements by a Fast Cloud Droplet Probe and Hawkeye probe (combination Fast Cloud Droplet Probe, Two‐Dimensional Stereo optical array probe, and Cloud Particle Imager) provided particle concentrations and sizing between 1‐ and 1,280‐μm diameter and high resolution images for habit identification. We present the variability in ice concentrations, size distributions, and habits as functions of temperature, altitude, and time since convective influence. Observed ice particles were predominantly small and quasi‐spheroidal in shape, with the percentage of quasi‐spheroids increasing with decreasing temperature. In comparison to the large fraction of the population consisting of quasi‐spheroids, faceted habits (columns, plates, rosettes, and budding rosettes) constituted a smaller percentage of the overall population and exhibited the opposite correlation with temperature. The trend of higher percentages of faceted crystals occurring at warmer temperatures may be due to diffusional growth or aggregation as particles descend through cloud, and/or the more rapid diffusional growth rate at warmer temperatures. Sampling was typically well away from deep convection, however, and very few aggregates were observed, so the trend of higher percentages of faceted habits is likely attributable to diffusional growth.

Woods, Sarah↗

A Mo-anode-based in-house source for small-angle X-ray scattering measurements of biological macromolecules

We demonstrate the use of a molybdenum-anode-based in-house small-angle X-ray scattering (SAXS) setup to study biological macromolecules in solution. Our system consists of a microfocus X-ray tube delivering a highly collimated flux of 2.5 × 10{sup 6} photons/s at a beam size of 1.2 × 1.2 mm{sup 2} at the collimation path exit and a maximum beam divergence of 0.16 mrad. The resulting observable scattering vectors q are in the range of 0.38 Å{sup −1} down to 0.009 Å{sup −1} in SAXS configuration and of 0.26 Å{sup −1} up to 5.7 Å{sup −1} in wide-angle X-ray scattering (WAXS) mode. To determine the capabilities of the instrument, we collected SAXS data on weakly scattering biological macromolecules including proteins and a nucleic acid sample with molecular weights varying from ∼12 to 69 kDa and concentrations of 1.5–24 mg/ml. The measured scattering data display a high signal-to-noise ratio up to q-values of ∼0.2 Å{sup −1} allowing for an accurate structural characterization of the samples. Moreover, the in-house source data are of sufficient quality to perform ab initio 3D structure reconstructions that are in excellent agreement with the available crystallographic structures. In addition, measurements for the detergent decyl-maltoside show that the setup can be used to determine the size, shape, and interactions (as characterized by the second virial coefficient) of detergent micelles. This demonstrates that the use of a Mo-anode based in-house source is sufficient to determine basic geometric parameters and 3D shapes of biomolecules and presents a viable alternative to valuable beam time at third generation synchrotron sources.

46 INSTRUMENTATION RELATED TO NUCLEAR SCIENCE AND ↗

Develop Accurate Techniques for Passive SiC Temperature Monitoring of Miniature Samples for Cross-Cutting Applications

Passive thermometry is critically important because most fuels and materials irradiation experiments are not instrumented, and it is necessary to understand the irradiation temperature to properly interpret any post-irradiation examination data, including evolving properties and/or microstructures. The standard passive thermometry approach uses continuous dilatometry to evaluate changes in the instantaneous coefficient of thermal expansion during post-irradiation thermal annealing. This approach has limitations in terms of sample size (minimum length requirements) and the maximum irradiation temperature that can be accurately determined, which is limited by the reduced swelling (and therefore recovery) following higher temperature irradiation and limitations on the furnaces used with push-rod dilatometers. This work evaluates two new proposed techniques for post-irradiation evaluation of passive SiC temperature monitors: differential scanning calorimetry (DSC) and Raman spectroscopy. DSC is an extremely sensitive technique that can be used for any specimen geometry and is capable of higher temperature operation. Raman spectroscopy is similar in that it is a surface technique capable of examining extremely small samples (submillimeter), can be used with a heated stage up to 1,500°C (planned for future work), and is capable of mapping local irradiation temperatures throughout a sample. Existing SiC samples that were previously irradiated over a wide range of temperatures were cut into multiple pieces to allow for annealing studies using multiple different techniques: dilatometry, DSC, and Raman spectroscopy. This approach mitigates the concern that samples analyzed using one technique may have a slightly different irradiation history than those analyzed using a different technique. Recovery was clearly observed during annealing using both DSC and dilatometry. In some cases, a direct comparison could not be made due to some of the DSC runs accidentally including material from multiple specimens and issues with using an alternative DSC sample holder for the highest temperature annealing studies. Nevertheless, one trend was clear: the DSC runs resulted in higher irradiation temperatures compared to those of the dilatometry runs. Part of this could be attributed to the higher temperature ramp rates used during the DSC runs, which are often preferred to reduce noise in the measurements. By comparison, dilatometry has previously been shown to produce better data at lower ramp rates. Future work should further investigate the ideal ramp rate for both techniques to produce consistent results. Additional work should evaluate the best holder material to use for DSC runs exceeding 1,000°C to provide reliable data while preventing interactions between SiC and the holder.

11 NUCLEAR FUEL CYCLE AND FUEL MATERIALS↗

Develop Accurate Techniques for Passive SiC Temperature Monitoring of Miniature Samples for Cross-Cutting Applications

Passive thermometry is critically important because most fuels and materials irradiation experiments are not instrumented, and it is necessary to understand the irradiation temperature to properly interpret any post-irradiation examination data, including evolving properties and/or microstructures. The standard passive thermometry approach uses continuous dilatometry to evaluate changes in the instantaneous coefficient of thermal expansion during post-irradiation thermal annealing. This approach has limitations in terms of sample size (minimum length requirements) and the maximum irradiation temperature that can be accurately determined, which is limited by the reduced swelling (and therefore recovery) following higher temperature irradiation and limitations on the furnaces used with push-rod dilatometers. This work evaluates two new proposed techniques for post-irradiation evaluation of passive SiC temperature monitors: differential scanning calorimetry (DSC) and Raman spectroscopy. DSC is an extremely sensitive technique that can be used for any specimen geometry and is capable of higher temperature operation. Raman spectroscopy is similar in that it is a surface technique capable of examining extremely small samples (submillimeter), can be used with a heated stage up to 1,500°C (planned for future work), and is capable of mapping local irradiation temperatures throughout a sample. Existing SiC samples that were previously irradiated over a wide range of temperatures were cut into multiple pieces to allow for annealing studies using multiple different techniques: dilatometry, DSC, and Raman spectroscopy. This approach mitigates the concern that samples analyzed using one technique may have a slightly different irradiation history than those analyzed using a different technique. Recovery was clearly observed during annealing using both DSC and dilatometry. In some cases, a direct comparison could not be made due to some of the DSC runs accidentally including material from multiple specimens and issues with using an alternative DSC sample holder for the highest temperature annealing studies. Nevertheless, one trend was clear: the DSC runs resulted in higher irradiation temperatures compared to those of the dilatometry runs. Part of this could be attributed to the higher temperature ramp rates used during the DSC runs, which are often preferred to reduce noise in the measurements. By comparison, dilatometry has previously been shown to produce better data at lower ramp rates. Future work should further investigate the ideal ramp rate for both techniques to produce consistent results. Additional work should evaluate the best holder material to use for DSC runs exceeding 1,000°C to provide reliable data while preventing interactions between SiC and the holder.

11 NUCLEAR FUEL CYCLE AND FUEL MATERIALS↗

Albedos and size distribution of meteoroids from 0.3 to 4.8 AU

Observational data are compared on the distribution of very small micrometeoroids (1 billionth to 1 hundred-millionth g), the scattering source function of the zodiacal light, the distribution of larger micrometeoroids (at least 1 hundred-thousandth g) as observed from Helios A and Pioneer 10, and the distribution of meteoroids from the sample seen from earth. The experiments, analyses, and simulations involved in obtaining these data are described in detail. It is shown that the various groups of data can be reconciled only by small albedos that decrease outward from 0.1 to at least about 3.3 AU for the particles which produce both the zodiacal light and the observed meteors. The results also indicate that there must be a maximum in the distribution of the larger particles somewhere between the orbits of earth and Jupiter. It is suggested that a search for fireballs in Jupiter's atmosphere by the television cameras of the MJS 77 mission should aid in locating this maximum.

Cook, A. F.↗

The impact of environment on size: Galaxies are 50% smaller in the Fornax Cluster compared to the field

Size is a fundamental parameter for measuring the growth of galaxies and the role of the environment on their evolution. However, the conventional size definitions used for this purpose are often biased and miss the diffuse, outermost signatures of galaxy growth, including star formation and gas accretion. We address this issue by examining low surface brightness truncations or galaxy ‘edges’ as a physically motivated tracer of size based on star formation thresholds. Our total sample consists of ∼900 galaxies with stellar masses ranging from 10 5 M ⊙ < M ⋆ < 10 11 M ⊙ . This sample of nearby cluster, group satellite, and nearly isolated field galaxies was compiled using multi-band imaging from the Fornax Deep Survey, deep IAC Stripe 82, and Dark Energy Camera Legacy Surveys. We find that the edge radii scale as R edge ∝ M ⋆ 0.42 , with a very small intrinsic scatter (∼0.07 dex). The scatter is driven by the morphology and environment of galaxies. In both the cluster and field, early-type dwarfs are systematically smaller by approximately 20% compared to late-type dwarfs. However, galaxies in the Fornax cluster are the most impacted. At a fixed stellar mass, edges in the cluster can be found at about 50% smaller radii, and the average stellar surface density at the edges is a factor of two higher, ∼1 M ⊙ /pc 2 . Our findings support the rapid removal of loosely bound neutral hydrogen (H I ) in hot, crowded environments, which truncates galaxies outside-in earlier, preventing the formation of more extended sizes and lower density edges. Our results highlight the importance of deep imaging surveys to the study of low surface brightness imprints of the large-scale structure and environment on galaxy evolution.

Astronomy & Astrophysics↗

Identifying Spectral Descriptors for Protonation in BaZr 0.8 Y 0.2 O 3-x with Electron Energy Loss Spectroscopy

Hydrogen economy is of paramount importance in the global transition to a sustainable, clean energy source that contributes to decarbonization efforts. In particular, the proton conducting proton ceramic fuel cells (PCFCs) play a crucial role in promoting hydrogen energy technology [1-5]. In a PCFC, the electrolyte is typically a solid oxide material that enables proton transport and can operate at temperatures lower than those of traditional oxygen ion conducting fuel cells [6]. The reduced operating temperature of PCFCs contributes to their durability, scalability, and efficiency [7,8]. BaZr 0.8 Y 0.2 O 3-x (BZY) is a promising proton conducting solid oxide electrolyte [9,10]. The emphasis on proton conductivity entails the importance of understanding proton content in the system. However, previous studies have largely relied on bulk techniques such as electrochemical impedance spectroscopy [7,11], Karl-Fischer titration [12,13], and thermogravimetric analysis [14] to obtain proton concentration. This is due to the small atomic size and light mass of hydrogen species making direct detection challenging. Bulk methods may be useful in estimating the proton content; however, it overlooks possible proton concentration gradient or segregation that may occur across or within a nanoparticle, especially when proton incorporation occurs nonuniformly through steam exposure on powder samples. In this paper, BZY is protonated at an estimated 0.15 mol of protons via steam exposure. Electron energy loss spectroscopy (EELS) with nanoscale spatial resolution is explored to identify proxy signals for proton detection using a JEOL ARM300 microscope operated at 300 kV with a Gatan GIF Continuum detector.

08 HYDROGEN↗

RELICS: High-resolution Constraints on the Inner Mass Distribution of the z = 0.83 Merging Cluster RXJ0152.7-1357 from Strong Lensing

Strong gravitational lensing (SL) is a powerful means of mapping the distribution of dark matter. Here, we perform an SL analysis of the prominent X-ray cluster RXJ0152.7-1357 ( z = 0.83, also known as CL0152.7-1357) in Hubble Space Telescope images, taken in the framework of the Reionization Lensing Cluster Survey (RELICS). On top of a previously known z = 3.93 galaxy multiply imaged by RXJ0152.7-1357, for which we observe an additional multiple image, guided by a light-traces-mass approach, we identify seven new sets of multiply imaged background sources lensed by this cluster, spanning the redshift range [1.79–3.93]. A total of 25 multiple images are seen over a small area of ~0.4 arcmin 2 , enabling us to put relatively high-resolution constraints on the inner matter distribution. Although modestly massive, the high degree of substructure, together with its very elongated shape, makes RXJ0152.7-1357 a very efficient lens for its size. This cluster also comprises the third-largest sample of z ~ 6–7 candidates in the RELICS survey. Lastly, we present a comparison of our resulting mass distribution and magnification estimates with those from a Lenstool model. These models are made publicly available through the Mikulski Archive for Space Telescopes.

79 ASTRONOMY AND ASTROPHYSICS↗

Chemical consequences of the initial diffusional growth of cloud droplets - A clean marine case

A simple microphysical cloud parcel model and a simple representation of the background marine aerosol are used to predict the concentrations and compositions of droplets of various sizes near cloud base. The aerosol consists of an externally-mixed ammonium bisulfate accumulation mode and a sea-salt coarse particle mode. The difference in diffusional growth rates between the small and large droplets as well as the differences in composition between the two aerosol modes result in substantial differences in solute concentration and composition with size of droplets in the parcel. The chemistry of individual droplets is not, in general, representative of the bulk (volume-weighted mean) cloud water sample. These differences, calculated to occur early in the parcel's lifetime, should have important consequences for chemical reactions such as aqueous phase sulfate production.

Twohy, C. H.↗

Plasma Interactions With a Negative Biased Electrodynamic Tether

The ProSEDS conductive tether design incorporates two distinct types of tethers from a plasma interaction viewpoint. The 200 m closest to the Delta II spacecraft is insulated from the plasma, and the remaining 4800 m is semi-bare. This latter portion is considered semi-bare because a conductive coating, which is designed to collect electrons from the plasma, was applied to the wires to regulate the overall tether temperature. Because the tether has both insulating and conductive tether sections, a transition point exists between the two that forms a triple point with the space plasma. Also, insulated tethers can arc to the space plasma if the insulation is weakened or breached by pinholes caused by either improper handling or small meteoroid and orbital debris strikes. Because electrodynamic tethers are typically long, they have a high probability of these impacts. The particles, which strike the tether, may not have sufficient size to severe the tether, but they can easily penetrate the tether insulation producing a plasma discharge to the ambient plasma. Samples of both the ProSEDS tether transition region and the insulated tether section with various size of pinholes were placed into the MSFC plasma chamber and biased to typical ProSEDS open circuit tether potentials (-500 V to -1600 V). The results of the testing showed that the transition region of the tether (i.e. the triple point) arced to the ambient plasma at -900 V, and the tethers damaged by a pinhole or simulated debris strike arced to the plasma between -700 V and -900 V. Specific design steps were taken to eliminate the triple point issue in the ProSEDS tether design and make it ready for flight. To reduce the pinhole arcing risk, ProSEDS mission operations were changed to eliminate the high negative potential on the insulated tether. The results of the testing campaign and the design changes implemented to ensure a successful flight are described.

Vaughn, Jason A.↗

Phase changes in fluoropolymer binders

Motivation: Understanding fluoropolymer binder structure and aging response continues to be an important goal for the prediction and assessment of polymer bonded explosive compositions within the stockpile. As part of ongoing efforts within NNM, we are developing new methods to quantify crystallization and chemical degradation within aged Fluoropolymer materials. Significance: Time, temperature and radiation are known to alter the mechanical properties of fluoropolymers as crystalline domains nucleate and grow within the material. However, current methods do not accurately quantify and assess the degree or rapidity of these physical aging processes. For this reason, we are developing methods that directly measure crystalline domain, composition, size and shape and cross-correlating them with traditional techniques. Progress: Most recently, we thermally aged fluoropolymer binder, FK800, for various durations up to 23 days at several temperatures including: 25C (red), 35C (green), and 60C (blue). We used wide angle X-ray scattering (WAXS) to observe when crystalline peaks emerged, signaling a phase transition from amorphous to partially crystalline. Some of these data are summarized in Figure 1. As expected, samples held at 25C (red), which is below the glass transition temperature at 28C, remain amorphous – the WAXS data (Figure 1b) lacks sharp peaks indicative of crystallinity and the ultra-small angle X-ray scattering (USAXS) also has a smooth background without peaks indicative of structure (Figure 1a). By contrast, samples held at 35C and 60C have new peaks in both the USAXS and WAXS data. The structure is clearer after subtracting off the amorphous background from the WAXS data (Figure 1c). These data show that samples aged at 60C are more crystalline as determined by the more defined peaks and also have a larger lattice constant as seen by the shift in peak position as compared to the 35C samples. The corresponding USAXS data (Figure 1a) indicate that the size of the crystals was larger at 60C than at 35C as seen by the shift in the knee position to lower q-values. Interestingly, the shape of the scatter curve also changed, which indicates a change in morphology. Atomic force microscopy (AFM) was used to image the fluoropolymer (Figure 1c-e). At 35C, ~50nm long stacked crystal plates are observed. High resolution imaging shows that the stacks consist of 2-6 lamellae that are spaced approximately 3nm apart. At 60C, the individual lamella appear both thicker and longer and are intertwined to fill the surface. Morphological data such as these images help to interpret & model volume averaging techniques like X-ray scattering and NMR. We also expect the shift from isolated islands to intertwined clusters to impact mechanical properties.

36 MATERIALS SCIENCE↗

A methodology for small scale rural land use mapping in semi-arid developing countries using orbital imagery. Part 6: A low-cost method for land use mapping using simple visual techniques of interpretation

The author has identified the following significant results. It was found that color composite transparencies and monocular magnification provided the best base for land use interpretation. New methods for determining optimum sample sizes and analyzing interpretation accuracy levels were developed. All stages of the methodology were assessed, in the operational sense, during the production of a 1:250,000 rural land use map of Murcia Province, Southeast Spain.

Vangenderen, J. L.↗

Microfocus x-ray imaging of traceable pointlike {sup 22}Na sources for quality control

Purpose: The purpose of this study is to propose a microfocus x-ray imaging technique for observing the internal structure of small radioactive sources and evaluating geometrical errors quantitatively, and to apply this technique to traceable pointlike {sup 22}Na sources, which were designed for positron emission tomography calibration, for the purpose of quality control of the pointlike sources. Methods: A microfocus x-ray imaging system with a focus size of 0.001 mm was used to obtain projection x-ray images and x-ray CT images of five pointlike source samples, which were manufactured during 2009-2012. The obtained projection and tomographic images were used to observe the internal structure and evaluate geometrical errors quantitatively. Monte Carlo simulation was used to evaluate the effect of possible geometrical errors on the intensity and uniformity of 0.511 MeV annihilation photon pairs emitted from the sources. Results: Geometrical errors were evaluated with sufficient precision using projection x-ray images. CT images were used for observing the internal structure intuitively. As a result, four of the five examined samples were within the tolerance to maintain the total uncertainty below {+-}0.5%, given the source radioactivity; however, one sample was found to be defective. Conclusions: This quality control procedure is crucial and offers an important basis for using the pointlike {sup 22}Na source as a basic calibration tool. The microfocus x-ray imaging approach is a promising technique for visual and quantitative evaluation of the internal geometry of small radioactive sources.

07 ISOTOPE AND RADIATION SOURCES↗

Tuning transition metal nanoparticles on a non-traditional support via experimental design

The ability to control metal nanoparticle size and morphology on supported catalysts is crucial for optimizing catalytic performance in targeted applications. Here, this work presents a systematic approach for tuning Ni particle and crystallite size on an unconventional, low-porosity silica fume support through select thermal treatments. The catalyst was synthesized via the deposition of nickelocene onto silica fume, resulting in well-dispersed Ni nanoparticles. A face-centered central composite design was employed to systematically assess the effects of time, temperature, and sintering gas environment on metal particle growth. The results demonstrate that the sintering gas environment is the primary factor governing particle and crystallite evolution, with temperature as the next most significant influence. Nickel nanoparticles sintered at temperatures of 650 °C and above under inert conditions exhibited substantial growth and polycrystalline structures, whereas samples treated in oxidative environments formed NiO, restricting particle mobility. Minimally oxidative (500 ppm O₂) environments facilitated rapid sintering while effectively removing residual ligands from the one-step nickelocene deposition process. Extensive structural characterization via a combination of scanning transmission electron microscopy, X-ray diffraction, hydrogen temperature programmed reduction, and small-angle X-ray scattering revealed that oxidative treatments enhanced metal-support interactions, as evidenced by increased reduction temperatures and narrower particle size distributions. These findings establish quantitative relationships between sintering parameters and Ni nanoparticle characteristics, providing a framework for rational catalyst design through controlled thermal treatments. This methodology is broadly applicable to other catalytic systems and provides a quantitative foundation for catalyst design.

CVD↗

Grain-Refined Microstructure and Hard Surface Layer Produced by SMRGT Process for Improved Corrosion Behavior of Mg-3Al-1Zn Alloy

To improve the surface properties and performance, a grain-refined surface layer was produced on AZ31B Mg alloy by a newly developed surface nano-crystallization and hardening process called surface mechanical rolling grinding treatment (SMRGT). The grain size refinement and minimal surface hardening were confirmed by the microstructure observations, XRD results and microhardness tests and were attributed to the multipass small strain-induced plastic deformation of the material during the SMRGT process. A nano-grain surface layer (average grain size of ~ 100 nm) and a graded microhardness variation (average ~ 113 HV adjacent to surface) along the thickness direction were generated. The E{sub corr} values of the as-SMRGTed samples were − 1.43 ± 0.03 and − 1.42 ± 0.02 V, increasing by ~ 30-40 mV compared with the values of the as-received (AR) sample (− 1.46 ± 0.02 V), corresponding to i{sub corr} ranging from 3.0 × 10{sup −5} to 1.0 × 10{sup −5} and 5.0 × 10{sup −6} A/cm{sup 2}, respectively. Charge transfer resistance (R{sub ct}) increased from 93.4 to 292.4 and 578.3 Ω (~ 3-6 times) with the increasing number of SMRGT passes. The corrosion resistance improvement was attributed mainly to the dramatic strain-induced surface grain refinement and minimal surface hardening that give rise to a more smooth and densely packed surface state.

36 MATERIALS SCIENCE↗

Disorder-to-Order Transition Mediated by Size Refocusing: A Route toward Monodisperse Intermetallic Nanoparticles

Intermetallic nanoparticles are remarkable because of their often enhanced catalytic, magnetic, and optical properties, which arise from their ordered crystal structures and high structural stability. Typical syntheses of intermetallic nanoparticles include thermal annealing of the disordered counterpart in atmosphere (or vacuum) or colloidal syntheses, where the phase transformation is achieved in solution. Although both methods can produce intermetallic nanoparticles, there is difficulty in achieving monodisperse nanoparticles, which is critical to exploiting their properties for various applications. In this work, we demonstrate that overgrowth on random alloy AuCu nanoparticles mediated by size refocusing yields monodisperse intermetallic AuCu nanoparticles. Size refocusing has been used in syntheses of semiconductor and upconverting nanocrystals to achieve monodisperse samples, but now we demonstrate size refocusing as a mechanism to achieve the disorder-to-order phase transformation in multimetallic nanoparticles. The phase transformation was monitored by time evolution experiments, where analysis of reaction aliquots with transmission electron microscopy and powder X-ray diffraction revealed the generation and dissolution of small nanoparticles coupled with an increase in the average size of the nanoparticles and conversion to the ordered phase. This demonstration advances the understanding of intermetallic nanoparticle formation in colloidal syntheses, which can expedite the development of electrocatalysts and magnetic storage materials.

77 NANOSCIENCE AND NANOTECHNOLOGY↗