The nucleation and growth of Al on 7 × 7 and $\sqrt 3 \times \sqrt 3$R30 Al reconstructed Si(111) that result in strain-free Al overgrown films grown with an atomically abrupt metamorphic interface are compared. The reconstructed surfaces and abrupt strain relaxations are verified using reflection high-energy electron diffraction. The topography of evolution is examined with atomic force microscopy. The growth of Al on both the surfaces exhibits 3D island growth, but the island evolution of growth is dramatically different. On the 7 × 7 surface, mounds formed are uniformly distributed across the substrate, and growth appears to proceed uniformly. Alternatively, on the $\sqrt 3 \times \sqrt 3$R30 surface, Al atoms exhibit a clear preference to form mounds near the step edges. During Al growth, mounds increase in size and number, expanding out from step edges until they cover the whole substrate. Consistent expression of a mounded nucleation and growth mode imparts a physical limitation to the achievable surface roughness that may impact the ultimate performance of layered devices such as Josephson junctions that are critical components of superconducting quantum circuits.

This study examines the nature of highly fragile reaction products that form in low water content supercritical carbon dioxide (scCO2) using a combination of focus ion beam/scanning electron microscopy, confocal Raman spectroscopy, helium ion microscopy (HeIM), and transmission electron microscopy (TEM). HeIM images show these precipitates are fragile rosettes. Using the TEM revealed details on the interfacial structure between the newly formed surface precipitates and the underlying initial solid phases. Detailed microscopy analysis revealed that growth of the precipitates either followed a tip growth mechanism, with precipitates forming directly on the forsterite surface if the initial solid was nonporous (natural forsterite) or growth from the surface of the precipitates, where fluid was conducted through the porous (nanoforsterite) agglomerates to the growth center. Identification of the mechanism of formation of hydrated/hydroxylated magnesium carbonate compound phases is a key factor in unraveling the impact of water recycling on mineral reactivity in low water content scCO2 solutions, which has received a great deal of attention as a result of the potential for CO2 to act as an atmospheric greenhouse gas. Techniques used here to examine these fragile structures are also used to examine a wide range of fragile material surfaces.

Although the last decade in electron microscopy has seen tremendous gains in image resolution, new challenges in the field have come to the forefront. First, new ultra-sensitive instruments bring about unprecedented environmental specifications and facility needs for their optimal use. Second, in the quest for higher spatial resolutions, the importance of developing and sharing crucial expertise—from sample preparation to scientific vision—has perhaps been deemphasized. Finally, for imaging to accelerate discoveries related to large scientific and societal problems, in situ capabilities that replicate real-world process conditions are often required to deliver necessary information. This decade, these are among the hurdles leaders in the field are striving to overcome.

Previous in situ examination of U(VI) spiked concrete indicated that uranyl-oxyhydroxide phases that were initially formed, later led to the formation of mixed uranyl-oxyhydroxide/silicates, which subsequently transformed into uranyl-silicates, and finally altered into mixed uranyl-silicate/phosphate and uranyl-phosphate phases. We conducted solubility studies of the identified final uranyl-phosphate phase (calcium meta-autunite) in phosphate solutions ranging in concentration from 0.001 – 0.1M as a function of pH. These studies indicated a secondary phosphate phase that formed during the solubility of meta-autunite regulated the uranium concentrations at relatively low levels under high pH conditions (>12) typically encountered in cement pore waters. The importance of uranyl-phosphate minerals in concrete waste forms has, to date, been neglected because of the minimal amount of phosphorus present in most concrete compositions. However, because concrete is a continuously reacting solid, the thermodynamic stability of uranyl minerals that form at the later stages of reaction may have a substantial impact on the long-term fate of uranium in the waste forms. This study suggests that any future investigations should consider the potential benefit of including phosphorus in concrete waste forms.

Individual magnetostrictive nanobars and arrays comprised of magnetostrictive nanobars were recently introduced as a high performance biosensor platform. In this paper, we report the fabrication and characterization of magnetostrictive nanobars based on Fe-B alloy. The nanobars were synthesized using a template-based electrochemical deposition method. The composition and microstructure of the Fe-B nanobars are directly related to their performance as a biosensor platform. The Fe-B nanobar arrays and individual nanobar were characterized using scanning electron microscopy (SEM), transmission electron microscopy (TEM), as well as Auger electron spectroscopy (AES). Morphologically, nanobars have a very flat top and a smooth cylindrical surface, which are critical factors for obtaining high performance as sensor platforms. Structurally, electron diffraction reveals that the Fe-B nanobars are amorphous. AES analysis indicates that Fe-B nanobars show no significant compositional variation along the length direction. It is found that the nanobars were covered by an oxidation layer of a typical thickness of ∼ 10 nm. It is believed that this oxidation layer is related to the passivation of nanobars in air. High temperature annealing and subsequent structural analysis indicate that the Fe-B nanobars possess a good thermal stability.

Solid phase physical and chemical characterization methods have been used in an ongoing study of residual wastes from several single-shell underground waste tanks at the U.S. Department of Energy's Hanford Site in southeastern Washington State. Because these wastes are highly-radioactive dispersible powders and are chemically-complex assemblages of crystalline and amorphous solids that contain contaminants as discrete phases and/or co-precipitated within oxide phases, their detailed characterization offers an extraordinary technical challenge. X-ray diffraction (XRD) and scanning electron microscopy/energy dispersive x-ray spectroscopy (SEM/EDS) are the two principal methods used, along with a limited series of analyses by synchrotron-based methods, to characterize solid phases and their contaminant associations in these wastes. Depending on the specific tank, numerous solids (e.g., èejkaite; Na2U2O7; clarkeite; gibbsite; böhmite; dawsonite; cancrinite; Fe oxides such as hematite, goethite, and maghemite; rhodochrosite; lindbergite; whewellite; nitratine; and several amorphous phases) have been identified in residual wastes studied to date. Because many contaminants of concern are heavy elements, SEM analysis using the backscattered electron (BSE) signal has proved invaluable in distinguishing phases containing elements, such as U and Hg, within the complex assemblage of particles that make up each waste. XRD, SEM/EDS, and synchrotron-based methods provide different, but complimentary characterization data about the morphologies, crystallinity, particle sizes, surface coatings, and compositions of phases in these wastes. The impact of these techniques is magnified when each is used in an iterative fashion to help interpret the results from the other analysis methods and identify additional, more focused analyses.

Straw-Flow is a novel housing system for growing pigs which simplifies the handling of bedding and manure by allowing pigs to take unchopped straw from dispensers. Three groups of 50, 50 and 60 Large-White × Landrace pigs were housed in Straw-Flow pens from 5 to 90 kg. They were supplied daily with 50 to 100 g unchopped straw per pig and given food ad libitum. From 30 to 90 kg, mean growth rate was 863 g/day and food conversion ratio was 2·56 kg food per kg growth. The pigs' behaviour was divided approximately into: 0·820 lying, 0·100 active, 0·075 feeding and 0·005 drinking (on a proportional basis). There were no differences (P > 0·05) between groups or different weights for any of the behaviour categories. The pigs were less active before noon than after noon (P < 0·05). The daily number of visits to the drinker between weights 5 and 25 kg fell from 23·7 to 11·0 (P < 0·05). A single drinker, of new design, appeared to be adequate for a group of 50 to 60 pigs.

Bend strength, compression strength, and fracture toughness of niobium beryllide intermetallic compounds have been assessed at temperatures from ambient to 1200°C. Hot-isostatically-pressed (HIP) Be12Nb showed significantly improved lowand high-temperature mechanical properties over vacuum-hot-pressed (VHP) material. Strengths at 20°C were 250 MPa in bending and 2750 MPa in compression with a fracture toughness of ∼4 Mpa√m, much higher than previously measured for this compound. High-temperature (≥ 1000°C) mechanical properties were also improved with bend strengths of 250 MPa at 1200°C as compared to only 70 to 100 MPa for the VHP material. However, severe pest embrittlement was detected in the HIP material at temperatures between 650 and 1000°C.