Scanning Acoustic Microscopy of SCS-6 Silicon Carbide Fiber

Scanning acoustic microscopy of SCS-6 silicon carbide fiber reveals large radial variations in acoustic reflectivity associated with the chemical composition and microstructure of a given fiber region. Rayleigh wave fringe patterns observed in each of five subregions are used to calculate the average Young modulus of that subregion. The Young modulus is found to increase monotonically from 40 GPa in the carbon core to a value of 413 GPa in the stoichiometric SiC region. The effective Young modulus of the fiber as a whole is estimated from the moduli of the individual regions and it is compared with mechanical measurements reported in the literature.     

On the stability preserving property of the double bilinear transformation on a class of 2-D transfer functions

This paper addresses the BIBO (bounded-input bounded-output) stability of a class of discrete 2-D quarter-plane filters in the presence of nonessential singularities of the second kind (NSSK's) on the unit bidisk. Conditions under which the double bilinear transformation (DBT) preserves stability are derived. The results presented here also extend the class of systems whose stability can be predicted. Use of the inverse DBT to produce a continuous equivalent of the discrete 2-D transfer function allows easy application of a continuous-domain equivalent of a criterion developed by Dautov. The necessary and sufficient condition for stability derived in this work provides a simple check for the class of systems under consideration. From this class of systems, it is also possible to construct stable pairs of mutually inverse transfer functions.     

Cytokine responses of human lung cells (BEAS-2B) treated with micron-sized and nanoparticles of metal oxides compared to soil dusts

Background  

The induction of cytokines by airway cells in vitro has been widely used to assess the effects of ambient and occupational particles. This study measured cytotoxicity and the release of the proinflammatory cytokines IL-6 and IL-8 by human bronchial epithelial cells treated with manufactured nano- and micron-sized particles of Al₂O₃, CeO₂, Fe₂O₃, NiO, SiO₂, and TiO₂, with soil-derived particles from fugitive dust sources, and with the positive controls LPS, TNF-α, and VOSO₄.     

High-temperature crystallization behaviour of amorphous Fe80B20

Samples of 0.003 in. round Fe₈₀B₂₀ amorphous wires were annealed in vacuo for 1 sec to 8 h periods at 780° C and the crystallinity induced in these wires from this heat treatment was studied through X-ray diffraction and field-ion microscopy. X-ray diffraction studies indicate that complete crystallinity is produced following 1 sec anneal at 780° C. However, the initial product is a primitive-tetragonal Fe₃B phase unlike the body-centred tetragonal Fe₃B observed in low-temperature isothermal transformation studies with this alloy. The Fe₃B phase is seen to persist in the diffraction patterns for annealing durations of up to 15 min. Upon annealing for periods of up to 1 h, an intermediate three-phase structure consisting of -Fe, Fe₃B, and Fe₂B is seen to result with a gradual decrease in the Fe₃B phase corresponding to longer annealing durations. Anneals of more than 1 h at 780° C are seen to result in the disappearance of the Fe₃B phase producing a two-phase microstructure consisting of -Fe(b c c) and Fe₂B (b c t). Field-ion-microscopy with a pure neon imaging gas at 78 K likewise indicates that existence of a three-stage phase structural change during the isothermal anneals, and the atomic arrangement of the various species are quite readily discernible because of the different symmetries contained in the three distinct phases.     

Annealing behaviour of amorphous Fe80B20 on continuous heating

Resistance measurements during direct heating of Fe₈₀B₂₀ amorphous alloys indicate phase changes occur at 395, 500, 720 and 840° C. Samples heated to these temperatures, and maintained for five minutes in a neutral atmosphere, show that a hardness maximum occurs at the crystallization temperature of 395° C and that annealing at 500° C produces a material with the same hardness. Above 500° C the microhardness is seen to drop below that of the amorphous alloy. Saturation magnetization measurements show a steady increase following each anneal, up to a temperature of 720° C, and the rate of increase is seen to drop in the range of 720 to 840° C. X-ray diffraction studies show that only a small fraction of the matrix is crystallized following the anneal at 395° C and the transformed phases are -Fe and Fe₃B. Following annealing at 500° C, an increased proportion of -Fe and Fe₃B are observed with complete crystallinity while samples heattreated at 720° C are seen to consist of a three-phase mixture of -Fe, Fe₂₃B₆ and Fe₂B. Annealing at 840° C is seen to produce an equilibrium phase mixture of -Fe and Fe₂B phases. Only in the sample annealed at 395° C is a fraction of the amorphous phase seen to persist, indicating that a 5 min anneal is not sufficient, at this temperature, to induce complete crystallization. These structural features are corroborated by field ion microscope analyses, made at liquid nitrogen temperature in a medium of pure neon, and scanning electron microscopy, and are also consistent with our earlier study involving the isothermal annealing, for various times, of Fe₈₀B₂₀ alloy at 780° C.     

Numerical Modeling of Multimaterial Thermoelectric Devices Under Static and Cyclic Thermal Loading

Selection of materials for thermoelectric devices is generally based on a figure of merit that is a function of the Seebeck coefficient, electrical conductivity, and thermal conductivity. While this figure of merit is a useful metric for comparing materials, the relative importance of the constituent properties depends on the particular application and conditions. In addition, multiple materials can be used together to improve the performance or extend the operating range, and determining the performance of such multimaterial combinations requires analysis beyond simply averaging the properties of the constituent materials. In this paper, finite-element numerical simulations under static and cyclic thermal loadings are used to investigate how device performance can be improved by judicious location of the different materials within the device. The results show that the performance of a device with two different materials can be better than that of either of the individual materials. The greatest improvement in performance occurs with cyclic heating, where the overall performance is strongly influenced by the behavior under transient conditions during heating and cooling.     

Discrimination of aerial deposition sources of polychlorinated dibenzo-p-dioxin and polychlorinated dibenzofuran downwind from a pulp mill near Ketchikan, Alaska

Drinking water is supplied by individual roof-catchment systems for homes and businesses near a dissolving sulfite pulp mill (now closed) located just north of Ketchikan in southeast Alaska. This study was conducted to determine if polychlorinated dibenzo-p-dioxins and polychlorinated dibenzofurans (PCDDs/Fs) found in the sediments of the roof-catchment cisterns resulted from historical deposition of stack emissions from the pulp mill's multi-fuel power boilers. Fly ash from the power boilers had maximum total PCDD/F concentrations of 3.08 x 10(5)-3.10 x 10(6) ng/kg, which resulted from combustion of bleach plant wastewater sludge and saltwater-soaked wood waste. Cistern sediments had maximum total PCDD/F concentrations of 7.71 x 10(4) ng/kg. Potential sources of PCDDs/Fs in the cistern sediments were considered to be automobile exhaust, heating oil combustion, and private trash burning as well as pulp mill boiler emissions. Discriminant analysis was used to analyze differences between profiles of tetra through octa homologue classes of PCDDs/ Fs (defined as proportional contributions to total concentration) from different source terms. Homologue profiles of potential sources from Ketchikan included in this analysis were fly ash collected from the mill's power boilers and soils collected from background areas (areas with similar PCDD/F sources as the residences [e.g., auto exhaust and burn barrels] near the mill but beyond the zone of aerial deposition of emissions from the mill). Profiles for emissions from automobile exhaust, fertilizers, oil heating, residential trash burning, and residential wood heating were also included in the source "training" data set (for the discriminant analysis) using data from published literature. The classification rules developed from the discriminant analysis were applied to the following test media sampled at Ketchikan: roof-catchment cistern sediments and soils collected from areas in the vicinity of the mill's power boilers (i.e., nearby residential or commercial [developed] areas, on the mill property, and nearby forestlands). The homologue profiles of cistern sediment and nearby developed area soil samples were similar to background soils, whereas the profiles for the forestland soil samples (influenced by emissions from the mill but not other anthropogenic sources) closely matched the fly ash pattern. The homologue profiles of the emission sources from published data were more similar to one another than either background soils or fly ash. Soil samples from the mill property were classified as members of all source groups. On the basis of these analyses, the composition of PCDDs/Fs detected in the cistern sediments is typical of Ketchikan background conditions and not reflective of mill emissions.     

Crown ether-doped sol-gel materials for strontium(II) separation

Hybrid organic/inorganic sol-gel materials containing an encapsulated crown ether ligand were found to selectively remove 91.4 +/- 1.3% of Sr2+ from a solution containing excess of competing ions such as Ca2+. The crown ether ligand, 1,4,10,13-tetraoxa-7,16-diazacyclooctadecane-7,16-bis(malonate) ligand (Na4oddm), with known high affinity for Sr2+ was encapsulated in hydrophilic SiO2 through a simple sol-gel process. Washing the Sr(2+)-loaded gel with acid or ethylenediaminetetraacetic acid disodium salt recovered the Sr2+ from the sol-gel sorbent and regenerated the doped gel for subsequent Sr2+ intake. The approach reported here is a new alternative to the use of crown ethers in metal ion separation through, for example, solvent extraction or the use of sorbents containing chemically grafted crown ether ligands.     

Thioether adducts of a new imine reactive intermediate of the pneumotoxin 3-methylindole

Cytochrome P450 enzymes can potentially oxygenate 3-methylindole to form 2,3-epoxy-3-methylindoline which could rearrange to the stable metabolite 3-methyloxindole or open to form 3-hydroxy-3-methylindolenine, a putative electrophilic imine. The purpose of the current work was to determine if the imine was formed, and to characterize it via its adducts with thiol nucleophiles. Thiols were added to incubations of goat lung microsomes with 3-methylindole and deuterated analogues of 3-methylindole to trap the imine intermediate as its thioether conjugates. The N-acetylcysteine conjugate of 3-hydroxy-3-methylindolenine was detectable by LC/MS, but a molecular ion was not observed because the adduct rapidly dehydrated to form the 2-substituted indole. However, the imine was S-alkylated, and the intermediate carbinol was intramolecularly trapped using thioglycolic acid as a trapping agent that induced cyclocondensation to a lactone. The retention of one atom of deuterium from [2-2H]-3-methylindole and three from 3-[2H3-methyl]indole substantiated the mechanism in which the lactone adduct was produced by sulfur addition to either 3-hydroxy-3-methylindolenine or the epoxide. Tandem mass spectrometry of the lactone adduct produced a daughter ion spectrum consistent with this adduct. These studies demonstrated the existence of a new reactive intermediate of 3-methylindole, 3-hydroxy-3-methylindolenine, which may play a role in the pneumotoxicity of this chemical.     

Expression of constitutively active Notch arrests follicle cells at a precursor stage during Drosophila oogenesis and disrupts the anterior-posterior axis of the oocyte

During early development, there are numerous instances where a bipotent progenitor divides to give rise to two progeny cells with different fates. The Notch gene of Drosophila and its homologues in other metazoans have been implicated in many of these cell fate decisions. It has been argued that the role of Notch in such instances may be to maintain cells in a precursor state susceptible to specific differentiating signals. This has been difficult to prove, however, due to a lack of definitive markers for precursor identity. We here perform molecular and morphological analyses of the roles of Notch in ovarian follicle cells during Drosophila oogenesis. These studies show directly that constitutively active Notch arrests cells at a precursor stage, while the loss of Notch function eliminates this stage. Expression of moderate levels of activated Notch leads to partial transformation of cell fates, as found in other systems, and we show that this milder phenotype correlates with a prolonged, but still transient, precursor stage. We also find that expression of constitutively active Notch in follicle cells at later stages leads to a defect in the anterior-posterior axis of the oocyte.