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All sourcesNASA NTRSDOE OSTI
DOE OSTI2019

Nuclear Data Sheets for A=50

The experimental nuclear structure and decay data are evaluated for all the known nuclides of mass 50 (Cl, Ar, K, Ca, Sc, Ti, V, Cr, Mn, Fe, Co, Ni). Here, detailed evaluated nuclear structure information are presented in individual decay and reaction datasets and the best values are recommended in the Adopted dataset for level properties, γ and β radiations, and other spectroscopic information. No excited states are known in 50Cl and 50Ni, and limited information is available for 50 Ar, 50 K, 50 Fe and 50 Co. This work supersedes earlier evaluations of A=50 by 2011El01, 1995Bu09, 1990Bu18, 1984Al29, and 1976Au07.

73 NUCLEAR PHYSICS AND RADIATION PHYSICS↗
DOE OSTI2011

Nuclear Data Sheets for A = 50

The experimental nuclear spectroscopic data for known nuclides of mass number 50 (Cl,Ar,K,Ca,Sc,Ti,V, Cr,Mn,Fe,Co,Ni) have been evaluated and presented together with Adopted properties for levels and {gamma} rays. This evaluation has been carried out about 15 years after the previous one by Thomas Burrows (1995Bu29). Except for {sup 50}Sc and {sup 50}V, extensive new data have become available for all the other nuclides in the intervening years. The data for {sup 50}Sc and {sup 50}V have also been checked again in detail and several changes made. No data are yet available for excited states in {sup 50}Cl, {sup 50}Ar and {sup 50}Ni. This work supersedes earlier evaluations (1995Bu29, 1990Bu18, 1984Al29, 1976Au07) of A=50 nuclides.

73 NUCLEAR PHYSICS AND RADIATION PHYSICS↗
DOE OSTI2018

Thermal Conductivity of Single-Crystal ZrO{sub 2}-Based Solid Solutions Stabilized with Scandium and Yttrium Oxides in the Temperature Range 50–300 K

The thermal conductivity of single-crystal (ZrO{sub 2}){sub 1 –} {sub x}(Sc{sub 2}O{sub 3}){sub x} (x = 0.09, 0.10) and (ZrO{sub 2}){sub 1 ‒} {sub x} {sub ‒} {sub y}(Sc{sub 2}O{sub 3}){sub x}(Y{sub 2}O{sub 3}){sub y} (x = 0.003–0.10; y = 0.01–0.025) solid solutions has been experimentally determined in the temperature range 50–300 K. The results are analyzed with allowance made for the phase compositions and features of imperfect crystal structures.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗
DOE OSTI2018

Investigation of the Thermal Conductivity Terbium Gallium and Terbium Scandium Aluminum Garnet Crystals

The thermal conductivity of terbium gallium and terbium scandium aluminum garnet crystals has been studied by the method of steady-state longitudinal heat flow in the temperature range of 50‒300 K. The effect of the impurity composition of terbium gallium garnet crystals and the formula composition of terbium scandium aluminum garnet crystals on their thermal conductivity is shown.

36 MATERIALS SCIENCE↗
DOE OSTI2021

Precision Mass Measurements of Neutron-Rich Scandium Isotopes Refine the Evolution of N = 32 and N = 34 Shell Closures

In this work, we report high-precision mass measurements of 50–55 Sc isotopes performed at the LEBIT facility at NSCL and at the TITAN facility at TRIUMF. Our results provide a substantial reduction of their uncertainties and indicate significant deviations, up to 0.7 MeV, from the previously recommended mass values for 53–55 Sc. The results of this work provide an important update to the description of emerging closed-shell phenomena at neutron numbers N = 32 and N = 34 above proton-magic Z = 20. In particular, they finally enable a complete and precise characterization of the trends in ground state binding energies along the N = 32 isotone, confirming that the empirical neutron shell gap energies peak at the doubly magic 52 Ca. Moreover, our data, combined with other recent measurements, do not support the existence of a closed neutron shell in 55 Sc at N = 34. The results were compared to predictions from both ab initio and phenomenological nuclear theories, which all had success describing N = 32 neutron shell gap energies but were highly disparate in the description of the N = 34 isotone.

73 NUCLEAR PHYSICS AND RADIATION PHYSICS↗
DOE OSTI2023

Evaluation of two extraction chromatography resins for scandium and titanium separation for medical isotope production

Scandium-47 ( 47 Sc) can be used in nuclear medicine as a therapeutic-diagnostic, or "theragnostic," radioactive medical isotope for cancer detection and treatment. The 47 Sc isotope can be produced through the photonuclear reaction 48 Ti(γ,p) 47 Sc by irradiating enriched 48 Ti target material. The enriched target material necessary for production is costly; 48 TiO 2 costs ~ $\$$1550/g, and targets can be > 50 g ($\$$77,500) to produce medically relevant amounts of 47 Sc. In order to keep costs low, a highly efficient separation of scandium from bulk titanium is desired, along with efficient methods for recycling the target material. Here this research is focused on evaluating efficient methods for the separation of scandium from bulk quantities of titanium using commercially available diglycolamide-based and hydroxamate-based extraction chromatography resins (DGA resin and ZR resin, respectively). The sorption of 47 Sc and Ti on these resins were investigated at varying concentrations of HNO 3 , HCl, H 2 SO 4 , and HF to explore how they might be used in a large-scale production/processing setting.

38 RADIATION CHEMISTRY, RADIOCHEMISTRY, AND NUCLEA↗
DOE OSTI2013

The influence of pairing correlations on the isospin symmetry breaking corrections of superallowed Fermi beta decays

Within the framework of quasi-particle random phase approximation, the isospin breaking correction of superallowed 0{sup +} {yields} 0{sup +} beta decay and unitarity of Cabibbo-Kobayashi-Maskawa mixing matrix have been investigated. The broken isotopic symmetry of nuclear part of Hamiltonian has been restored by Pyatov's method. The isospin symmetry breaking correction with pairing correlations has been compared with the previous results without pairing. The effect of pairing interactions has been examined for nine superallowed Fermi beta decays; their parent nuclei are {sup 26}Al, {sup 34}Cl, {sup 38}K, {sup 42}Sc, {sup 46}V, {sup 50}Mn, {sup 54}Co, {sup 62}Ga, {sup 74}Rb.

73 NUCLEAR PHYSICS AND RADIATION PHYSICS↗
DOE OSTI2023

Production of Radioisotopes of Scandium for Imaging and Therapy (Final Report)

The theranostic approach is a powerful technique that enables scientists and physicians to diagnose and treat diseases using the same targeting moiety labeled with radionuclides for imaging and therapy. A challenge behind synthesizing and evaluating these theranostic radiopharmaceuticals lies in the production of suitable radionuclides. This study aimed to investigate the production of high radionuclidic purity 43 Sc from enriched [ 46 Ti]TiO 2 for Positron Emission Tomography (PET) and 47 Sc from enriched [ 50 Ti]TiO 2 for targeted radiotherapy, as well as establish a target recycling technique for continued production of these radionuclides. Methods: Targets were prepared with 100 mg of either enriched [ 46 Ti]TiO 2 or [ 50 Ti]TiO 2 , pressed into pellets, and placed into Ta target holders with a 0.127 mm natTi cover foil. The 46 Ti targets were bombarded with 18 MeV protons at 20 µA for 1.5 h, while 50Ti targets were bombarded with 24 MeV protons at 20 µA for 4 or 8 h. The radioscandium nuclides were purified using branched N, N, N’, N’ -tetra-2-ethylhexyldiglycolamide (DGA) resin. The titanium targets were recycled by precipitating the dissolved Ti collected from the column effluent and wash streams, pH adjustment, vacuum filtration, and then drying the solid at 250 °C prior to reforming the target for the subsequent bombardment. The apparent molar activity of the isolated radioscandiums was analyzed by titration with 1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid (DOTA). The relative imaging performance of 18 F, 43 Sc, and 68 Ga were analyzed with PET images acquired with 30-min static scans. Results: The average radioscandium recovery for 43Sc was 91.7 ± 7.4 %, with a radionuclidic purity of 98.8 %. The average recovery of 47Sc was 89.9 ± 3.9 %, with a radionuclidic purity of 90.8%. The average recovery of enriched TiO2 was 96 ± 4.0 %. The highest apparent molar activity for [43Sc]Sc-DOTA was 23.2 GBq/µmol and 3.39 GBq/µmol for [ 47 Sc]Sc-DOTA. The order of PET resolution from highest to lowest was 18 F > 43 Sc > 68 Ga. Conclusions: This work demonstrates the feasibility of using enriched recycled [ 46 Ti]TiO 2 and [ 50 Ti]TiO 2 targets for the production of the 43 Sc and 47 Sc theranostic isotope pair in high purity.

38 RADIATION CHEMISTRY, RADIOCHEMISTRY, AND NUCLEA↗
DOE OSTI2015

Production and characterization of thin film group IIIB, IVB and rare earth hydrides by reactive evaporation

A recent short history of reactive evaporation by D. M. Mattox [History Corner—A Short History of Reactive Evaporation, SVC Bulletin (Society of Vacuum Coaters, Spring 2014), p. 50–51] describes various methods for producing oxides, nitrides, carbides, and some compounds, but hydrides were not mentioned. A study was performed in the mid-1970s at the General Electric Company Neutron Devices Department in Largo, FL, by the author to study preparation of thin film hydrides using reactive evaporation and to determine their unique characteristics and properties. Films were produced of scandium (Sc), yttrium (Y), titanium (Ti), zirconium (Zr), and the rare earth praseodymium (Pr), neodymium (Nd), gadolinium (Gd), dysprosium (Dy), and erbium (Er) hydrides by hot crucible filament and electron beam evaporation in atmospheres of deuterium and tritium gases. All-metal vacuum systems were used and those used with tritium were dedicated for this processing. Thin film test samples 1000 nm thick were prepared on 1.27 cm diameter molybdenum disk substrates for each occluder (i.e., an element that can react with hydrogen to form a hydride) material. Loading characteristics as determined by gas-to-metal atomic ratios, oxidation characteristics as determined by argon–sputter Auger analysis, film structure as determined by scanning electron microscope analysis, and film stress properties as determined by a double resonator technique were used to define properties of interest. Results showed hydrogen-to-metal atomic ratios varied from 1.5 to 2.0 with near maximum loading for all but Pr and Nd occluders which correlated with the oxidation levels observed, with all occluder oxidation levels being variable due to vacuum system internal processing conditions and the materials used. Surface oxide levels varied from ∼80 Å to over 1000 Å. For most films studied, results showed that a maximum loading ratio of near 2.0 and a minimum surface oxide level of ∼80 Å could be obtained with a bulk film oxygen level of ∼0.54 oxygen as determined by microprobe analysis when an evaporation rate of ∼0.313 mg/cm{sup 2} min was used in an atmosphere of D{sub 2} or T{sub 2} gas at a system deposition pressure of 1 × 10{sup −3 }Torr (1.33 × 10{sup −1 }Pa) in an evaporation time of ∼2 min. Platelet type (i.e., a film microstructure showing an overlay of flat plates with large grain sizes) film structures were observed for most films with some film mechanical properties determined (i.e., grain size and Vickers μ-hardness), and reduced stress levels were seen with initial normalized differential (tensile) stress levels being (1.0–4.0) × 10{sup 8 }dyne/cm{sup 2} for tritium loaded samples and (1.5 ± 0.5) × 10{sup 9 }dyne/cm{sup 2} for deuterium loaded samples. Also, stress aging characteristics were determined for some hydride films prepared in a radioactive tritium gas atmosphere. Tritium loading, however, had the undesirable characteristic of having to dispose of the internal processing system fixtures, which can be minimized, but the reactive evaporation technique produced desirable thin films.

36 MATERIALS SCIENCE↗
DOE OSTI2013

Electrical properties of scandium nitride epitaxial films grown on (100) magnesium oxide substrates by molecular beam epitaxy

Scandium nitride (ScN) films were grown on (100) MgO single crystals by a molecular beam epitaxy method. The effects of growth conditions, including [Sc]/[N] ratio, growth temperature, and nitrogen radical state, on the electrical properties of the ScN films were studied. The ScN films comprised many small columnar grains. Hall coefficient measurements confirmed that the ScN films were highly degenerate n-type semiconductors and that the carrier concentration of the ScN films was sensitive to the growth temperature and the nitrogen radical states during the film growth. The carrier concentrations of the ScN films ranged from 10{sup 19}–10{sup 21} cm{sup −3} while the Hall mobilities ranged from 50–130 cm{sup 2}·V{sup −1}·s{sup −1} for undoped films. The temperature-dependent Hall coefficient measurements showed that the carrier concentration is nearly independent of temperature, indicating that the change in resistivity with temperature is explained by a change in the Hall mobility. The temperature-dependence of the Hall mobility was strongly affected by the growth conditions.

36 MATERIALS SCIENCE↗
DOE OSTI2022

High Yield, Economical and Environmentally Benign Production of Rare Earth Elements from Coal Ash (Phase II Final Summary Report)

Fly ash stored in landfills and ponds across the United States is an attractive, abundant domestic resource for the cost-effective recovery of rare earth elements (REE) and other critical minerals (CM). Physical Sciences Inc. (PSI) and its team members, Winner Water Services (WWS) and University of Kentucky/Center for Applied Energy Research (UK/CAER) successfully executed a multiphase program that developed technologies and their implementation in a pilot plant. We demonstrated plant operations for cost-effective and environmentally-friendly production of rare earth element oxide (REO) concentrates, and the critical minerals scandium and aluminum (in the forms of salts or oxide products), from coal ash. We also constructed and demonstrated a research-scale (0.5 kg/day) micropilot facility to validate the key physical and chemical processing operations, predict yields, and troubleshoot process bottlenecks. The project team then designed, constructed and operated two decoupled pilot plants: (1) an operational pilot plant for physical separation processes with capacity of 0.4 metric tons per day (tpd), where we optimized processes to produce selected ash fractions as the feedstock for chemical processing and as valuable byproducts such as cenospheres, magnetic ash, and secondary fuel carbon, and (2) an operational pilot plant for chemical ash processing with a capacity of 0.5 tpd that developed optimized processes for the production of: (a) REO concentrates, (b) critical minerals (Sc, Al), and (c) beneficiated ash as a valuable byproduct suitable for cement applications. In Phase I, the project team (with Equinox Chemicals in place of WWS) developed and demonstrated the feasibility of the physical and chemical separation processes, developed the design of a pilot plant, and began the development of a preliminary techno-economic model. In the baseline (initial) Phase II program, the project team developed and demonstrated the above pilot scale plant, producing salable REE concentrates, including Y and Sc (REYSc), plus commercially viable byproducts, using environmentally safe and high-yield physical and chemical enrichment processes. The team successfully demonstrated chemical pilot design, construction, shakedown, and operations of the plant. We produced the Phase II deliverable REYSc concentrate ((50 g of >60 wt.% purity REYSc salts on elemental basis), generated the feed for the Phase II follow-on program, identified processing challenges for future optimizations, and refined the techno-economic model. In the Phase II follow-on program, the project team: (1) developed and demonstrated processes to increase the REE amount by 3X (content basis) and convert the Phase II REE salt mixture to an oxide mixture, (2) produced/delivered >38 g of REO mixture with >85 wt.% purity (elemental basis); (3) developed processes to recover critical minerals scandium and aluminum from intermediate streams; (4) produced/delivered > 1 g of scandium salt mixture with >85 wt. % purity (elemental basis); (5) produced/delivered > 100 g of aluminum oxide type material with >70% wt. purity (elemental basis); and (6) updated the techno-economic model from the baseline Phase II program to assess CAPEX and OPEX of a commercial operation. This program has developed extensive databases on process chemistry, unit operations, plant engineering, and techno-economics that will enable further scale-up toward commercial plant design. Specific future developments will be focused on achieving dramatic savings in energy, reagent usage, and operating costs. The combined results will contribute significantly for maturing the technologies of REE recovery from coal byproducts and promote the establishment of domestic REE and CM supply chains.

01 COAL, LIGNITE, AND PEAT↗
DOE OSTI2018

Proceedings 43rd Stanford Geothermal Workshop

Herein we summarize the results of an investigation dealing with the concentrations and inventories of strategic, critical and valuable materials (SCVM) in produced fluids from geothermal and hydrocarbon reservoirs (50-250° C) in Nevada and Utah. Water samples were collected from thirty-four production wells across eight geothermal fields, the Uinta Basin oil/gas province in northeast Utah, and the Covenant oil field in southwestern Utah; additional water samples were collected from six hot springs in the Sevier Thermal Belt in southwestern Utah. Most SCVM concentrations in produced waters range from <0.1 to 100 µg/kg; the main exception is lithium, which has concentrations that range from <1000 to 25,000 ug/kg. Relatively high concentrations of gallium, germanium, scandium, selenium, and tellurium are measured too. Geothermal waters contain very low concentrations of REEs, below analytical detections limits (0.01 µg/kg), but the concentrations of lanthanum, cerium, and europium range from 0.05 to 5 µg/kg in Uinta basin waters. Among the geothermal fields, the Roosevelt Hot Spring reservoir appears to have the largest inventories of germanium and lithium, and Patua appears to have the largest inventories of gallium, scandium, selenium, and tellurium. By comparison, the Uinta basin has larger inventories of gallium. The concentrations of gallium, germanium, lithium, scandium, selenium, and tellurium in produced waters appear to be partly related to reservoir temperature and concentrations of total dissolved salts. The relatively high concentration and large inventory of lithium occurring at Roosevelt Hot Springs may be related to granitic-gneissic crystalline rocks, which host the reservoir. Analyses of calcite scales from Dixie Valley indicate enrichments in cobalt, gallium, gold, palladium, selenium and tellurium, and these metals appear to be depositing at deep levels in production wells due to boiling. Comparisons with SCVM mineral deposits suggest that brines in sedimentary basins, or derived from lacustrine evaporites, enable aqueous transport of gallium, germanium, and lithium.

Simmons, Stuart↗
DOE OSTI2010

Investigation of terahertz sheet beam traveling wave tube amplifier with nanocomposite cathode

Particle-in-cell simulations of a staggered double grating array traveling wave tube intended as a wideband amplifier for terahertz communications, sensing, and imaging applications showed that, for an electron beam power of 5 kW, it produces 150-275 W, corresponding to 3%-5.5% electronic efficiency, at 0.22 THz with over {approx}30% bandwidth and with greater than 12 dB/cm growth rate. The circuit has been fabricated by both UV lithography and high precision computer-numerical-control machining with {approx}2-3 {mu}m dimensional tolerance and {approx}50 nm surface roughness. A scandate nanocomposite (Sc{sub 2}O{sub 3}-W) cathode for the electron beam source has successfully emitted 120 A/cm{sup 2} (space charge limited) at 1150 deg. C and 50 A/cm{sup 2} at 1050 deg. C for 8000 h as required to produce the requisite high current density electron beam.

46 INSTRUMENTATION RELATED TO NUCLEAR SCIENCE AND ↗
DOE OSTI2019

Western USA Assessment of High Value Materials in Geothermal Fluids and Produced Fluids

This report documents the results of investigations dealing with the concentrations and availabilities of strategic, critical and valuable materials (SCVM) in produced waters from geothermal and hydrocarbon reservoirs (50-250° C) in Idaho, Nevada, New Mexico, Oregon, and Utah. Analytical results were obtained for water samples from 47 production wells in 12 geothermal fields. Results were also obtained for samples from 25 oil/gas production wells in the Uinta and Paradox Basins and Covenant oil field, from 14 groundwater wells in the Tularosa play fairway (New Mexico), and from 20 groundwater wells and hot springs in the Sevier Thermal Belt (southwestern Utah). Most SCVM concentrations in produced waters range from <0.1 to 100 ug/kg. Lithium is the only element, which has much higher concentrations and which ranges from 10 to 26,000 ug/kg. Relatively high concentrations of gallium (10-80 ug/kg geothermal; 10-10,000 ug/kg Uinta Basin), germanium (1-70 ug/kg geothermal; 10-500 ug/kg Uinta and Paradox Basins), scandium (0.1-2.0 ug/kg geothermal; 5-10 ug/kg Paradox Basin), selenium (1-100 ug/kg geothermal; 10-20,000 ug/kg Uinta and Paradox Basins), and tellurium (0.1-10 ug/kg geothermal; 1-500 ug/kg Uinta and Paradox Basins) are measured too. Geothermal production waters contain very low concentrations of REEs, below analytical detections limits of 0.01 ug/kg, but the concentrations of some REEs (lanthanum, cerium, and europium) range from 0.05 to 5 ug/kg in Uinta Basin waters. Among the geothermal fields, the Roosevelt Hot Spring reservoir appears to have the largest endowments of germanium (20,000 kg) and lithium (7 million kg), the Patua reservoir appears to have the largest endowments of gallium (25,000 kg), selenium (47,000 kg), and tellurium (2500 kg), and the Raft River reservoir appears to have the large endowment of scandium (700 kg). By comparison, the Uinta Basin has larger inventories of gallium (>100,000 kg). These estimates are provisional, and they were calculated using geologically reasonable values for reservoir volumes and porosities. The concentrations of gallium, germanium, lithium, scandium, selenium, and tellurium in produced waters appear to be partly controlled by reservoir temperature and concentrations of total dissolved salts. The relatively high concentration and large endowment of lithium occurring at Roosevelt Hot Springs appears to be related to hot water interaction with crystalline granitic rocks, which host the reservoir and the hydrothermal system, and elevated concentrations of TDS. Analyses of calcite scales from Dixie Valley show that cobalt, gallium, gold, palladium, selenium and tellurium are depositing at deep levels in production wells due to boiling. Comparisons with SCVM mineral deposits suggest that brines in sedimentary basins or derived from lacustrine evaporites enable aqueous transport of gallium, germanium, and lithium.

15 GEOTHERMAL ENERGY↗
DOE OSTI2021

Microbe-Encapsulated Silica Gel Biosorbents for Selective Extraction of Scandium from Coal Byproducts

Establishing an inexpensive and environmentally friendly scandium (Sc) supply is critical for the development of clean energy technologies. However, refining Sc from Sc-bearing sources using current technologies poses economic and environmental challenges due to its low concentration relative to base metals and chemically similar lanthanides. In this work, we developed a biosorption-based flow-through process for extraction of Sc from low-grade feedstocks. A novel biosorbent material was synthesized by encapsulating Arthrobacter nicotianae, a bacterium that selectively adsorbs Sc, within a porous silica matrix. Through the use of several complementary microscopy techniques, we demonstrated a highly porous biosorbent structure with a high cell-loading density and a homogenous cell distribution. Batch adsorption assays revealed selective Sc adsorption over lanthanides and common based metals, with the exception of Fe(III), as evidenced by separation factors greater than 50. The MESG particles were packed into fixed-bed columns to enable adsorption under flow-through conditions, which demonstrated effective Sc extraction at flow rates up to 0.08 cm/s and high stability for reuse; greater than 95% of the adsorption capacity was maintained after 10 consecutive adsorption/desorption cycles. When applied to a lignite coal leachate, whose Fe content was depleted through pH-mediated precipitation, the MESG particles yielded Sc breakthrough at 30 bed volumes, whereas all other metals broke through after only a few bed volumes. Following desorption, an eluate with a 124-fold increase in Sc purity was achieved relative to the lignite leachate with Sc constituting 96.4% of the total REEs. This study established a rapid, facile, and scalable cell immobilization approach that enables the use of microbial biomass for Sc recovery from low-grade sources.

Dong, Ziye↗
DOE OSTI2017

Chemical/Optical Properties of Oliktok Aerosols Field Campaign Report

The arctic environment is changing at an alarming rate. During this time of escalation, it is important to understand the impacts of aerosols, both natural and anthropogenic. To support this effort, an aerosol sampling campaign was conducted at the U.S. Department of Energy (DOE) Atmospheric Radiation Measurement (ARM) Climate Research Facility third Mobile Facility (AMF3) at Oliktok Point on the North Slope of Alaska (NSA). The specific objectives of the campaign were to collect aerosol particles as a function of aerodynamic particle size in order to better understand the varying chemical and optical properties of the aerosols in the different particle size modes. A DRUM-style cascading impactor (Davis Rotating-Unit for Monitoring) was deployed at the beginning of March 2017 through the end of May 2017, collecting samples in eight size bins for each 12-hour period, thereby obtaining a diurnal signature. On March 6, a fire burned down the power generation shed at the sampling site. No samples were collected again until March 10. Due to DRUM sampler rotation issues, samples were collected intermittently until March 13. From March 14 through the end of the study, samples were collected with little interference. The size bins of the instrument range from approximately 10 to 0.09 μm; however, deployment at the Oliktok Point facility required an inlet configuration that effectively filtered out the coarsest size bin. Therefore, the reported size bins are 5.0 to 2.5, 2.5 to 1.15, 1.15 to 0.75, 0.75 to 0.56, 0.56 to 0.34, 0.34 to 0.26, and 0.26 to 0.09 μm. It is also possible that ultrafine particles were removed by electrostatic charging of the high-density polyethylene inlet tubing; however, confirmation of this would require further testing. The collected samples were returned to the University of California (UC), Davis for offline analysis. Particle mass concentrations were measured by soft-beta ray attenuation while optical attenuation was determined by broadband transmission spectrometry (10 wavelengths from 349 to 849 nm in 50 nm increments, minus 649 nm). The samples were then taken to the Advanced Light Source facility at Lawrence Berkeley National Laboratory for synchrotron-induced X-ray fluorescence spectrometry (SXRF). Thirty elements were detected, from sodium to molybdenum plus lead. The polarized nature of the synchrotron beam eliminates 97.5% of the primary Compton background, providing approximately a factor of 10 greater sensitivity than unpolarized X-ray instruments (Barberie et al. 2013). The data were reduced using custom software packages and analyzed for any sources of contamination, sample damage, or other potential causes of data invalidation. The interpretation of the final data set is ongoing and only early results will be described in this report. In spite of power and instrumental issues at the start, the field campaign was largely successful. Excluding the first stage that did not receive sample and power/rotational issues, the remaining stages were 99.7% complete (number of valid measurements/total number of measurements made). The percent of measurements below detection were < 30% for all species with the exception of sodium, magnesium, arsenic, and scandium. Sodium and magnesium were expected to be difficult to measure using SXRF due to low sensitivity at that energy range. Scandium is very rare in ambient samples unless near a very strong source. Arsenic is fairly common in urban settings but is not expected in the arctic environment.

54 ENVIRONMENTAL SCIENCES↗
DOE OSTI2015

Microstructure and transformation behavior of Ni{sub 24.7}Ti{sub 50.3}Pd{sub 25} high temperature shape-memory alloy with Sc micro-addition

NiTiPd shape-memory alloys (SMAs) are potential functional materials for use as solid-state actuators in the temperature range 100–250 °C. The present study investigates the effect of 1.0 at.% Sc micro-addition to Ni{sub 24.7}Ti{sub 50.3}Pd{sub 25} alloy, Sc replacing either Ti or Ni. Results show that all the three alloys studied have stable transformation behavior on stress-free thermal cycling and hence, are suitable for cyclic actuation applications. However, the addition of Sc to NiTiPd alloy leads to decrease of transformation temperatures, the magnitude of decrease being greater for the alloy with Sc replacing Ni. The martensite finish (M{sub f}) temperature of 181 °C for the NiTiPd alloy decreased to 139 °C for Sc replacing Ti and 83 °C for Sc replacing Ni. Also, the indentation modulus of NiTiPdSc (Sc replacing Ni) alloy is found to be significantly low compared to the other alloys. Analysis indicates that the observed differences in the alloy properties are related to the solubility of Sc in the NiTiPd matrix. While the quaternary NiTiPdSc alloy, Sc replacing Ti, has a single phase microstructure, the alloy with Sc replacing Ni shows the presence of Sc-rich and TiPd-type second phases in the microstructure. TEM examination revealed that the TiPd-type phase has a distinct rod-like morphology (30–50 nm) arranged in a grid-like structure. The transformation and indentation behavior of the alloys is elucidated using thermodynamic calculations of frictional energy and an electronic structure based analysis. - Highlights: • TEM of Ni{sub 23.7}Ti{sub 50.3}Pd{sub 25}Sc{sub 1} showed distinct grid of TiPd-type phase nanorods < 50 nm. • Stress-free thermal cycling of all the three alloys showed stable transformation behavior. • Ni{sub 24.7}Ti{sub 49.3}Pd{sub 25}Sc{sub 1} and Ni{sub 23.7}Ti{sub 50.3}Pd{sub 25}Sc{sub 1} showed single and multiphase structures. • Sc micro-addition (1 at.%) to Ni{sub 24.7}Ti{sub 50.3}Pd{sub 25} alloy decreased TTs significantly. • Ni{sub 23.7}Ti{sub 50.3}Pd{sub 25}Sc{sub 1} exhibited lower modulus of 67 GPa to 85 GPa of Ni{sub 24.7}Ti{sub 50.3}Pd{sub 25}.

36 MATERIALS SCIENCE↗
DOE OSTI2018

Microstructural development of electron beam processed Al-3Ti-1Sc alloy under different electron beam scanning speeds

A systematic study has been made of the microstructural development in as-cast 30 mm thick Al-3Ti-1Sc (wt%) plate samples that were processed by electron beam (EB) melting at different scanning speeds of 3, 5, 8, 12, 15 and 20 mm/s. The composition of the alloy is designed to capitalize on the potential for significantly extended solubility values of both Sc and Ti in Al when cooled at high cooling rates. The resulting microstructures are characterised using transmission electron microscopy (TEM) and other analytical means, assisted with Thermo-Calc predictions and Vicker's microhardness measurements. EB scanning speed plays a key role in determining the phase formation and microstructural development in the Al-3Ti-1Sc alloy when the beam is applied an accelerating voltage of 50 kV and a current of 30 μA. The major microstructural features in the re-solidified zone include (i) the formation of the primary tetragonal Al{sub 3}(Ti,Sc) phases and their retention or subsequent transformation to stable cubic Al{sub 3}(Ti,Sc) phases; (ii) the complete suppression of the primary tetragonal Al{sub 3}(Ti,Sc) phases at the scanning speed of 20 mm/s; and (iii) the formation of cubic Al{sub 3}(Ti,Sc) precipitates in the α(Al) matrix supersaturated with both Sc and Ti. These experimental findings are informative for both EB processing of Al-Ti-Sc alloys and the design of new Al alloys for additive manufacturing processes.

36 MATERIALS SCIENCE↗