4,003 research outputs found
Biomechanical Tolerance of Whole Lumbar Spines in Straightened Posture Subjected to Axial Acceleration
Quantification of biomechanical tolerance is necessary for injury prediction and protection of vehicular occupants. This study experimentally quantified lumbar spine axial tolerance during accelerative environments simulating a variety of military and civilian scenarios. Intact human lumbar spines (T12âL5) were dynamically loaded using a customâbuilt drop tower. Twentyâthree specimens were tested at subâfailure and failure levels consisting of peak axial forces between 2.6 and 7.9âkN and corresponding peak accelerations between 7 and 57âg. Military aircraft ejection and helicopter crashes fall within these high axial acceleration ranges. Testing was stopped following injury detection. Both peak force and acceleration were significant (pâ\u3câ0.0001) injury predictors. Injury probability curves using parametric survival analysis were created for peak acceleration and peak force. Fiftyâpercent probability of injury (95%CI) for force and acceleration were 4.5 (3.9â5.2âkN), and 16 (13â19âg). A majority of injuries affected the L1 spinal level. Peak axial forces and accelerations were greater for specimens that sustained multiple injuries or injuries at L2âL5 spinal levels. In general, forceâbased tolerance was consistent with previous shorterâsegment lumbar spine testing (3â5 vertebrae), although studies incorporating isolated vertebral bodies reported higher tolerance attributable to a different injury mechanism involving structural failure of the cortical shell. This study identified novel outcomes with regard to injury patterns, wherein more violent exposures produced more injuries in the caudal lumbar spine. This caudal migration was likely attributable to increased injury tolerance at lower lumbar spinal levels and a faster inertial mass recruitment process for high rate load application. Published 2017. This article is a U.S. Government work and is in the public domain in the USA
The Critical Role of Water at the Gold-titania Interface in Catalytic CO Oxidation
We provide direct evidence of a water-mediated reaction mechanism for room-temperature CO oxidation over Au/TiO2 catalysts. A hydrogen/deuterium kinetic isotope effect of nearly 2 implicates O-H(D) bond breaking in the rate-determining step. Kinetics and in situ infrared spectroscopy experiments showed that the coverage of weakly adsorbed water on TiO2 largely determines catalyst activity by changing the number of active sites. Density functional theory calculations indicated that proton transfer at the metal-support interface facilitates O2 binding and activation; the resulting Au-OOH species readily reacts with adsorbed Au-CO, yielding Au-COOH. Au-COOH decomposition involves proton transfer to water and was suggested to be rate determining. These results provide a unified explanation to disparate literature results, clearly defining the mechanistic roles of water, support OH groups, and the metal-support interface
Theory for the electromigration wind force in dilute alloys
A multiple scattering formulation for the electromigration wind force on
atoms in dilute alloys is developed. The theory describes electromigration via
a vacancy mechanism. The method is used to calculate the wind valence for
electromigration in various host metals having a close-packed lattice
structure, namely aluminum, the noble metals copper, silver and gold and the
transition metals. The self-electromigration results for aluminum and the
noble metals compare well with experimental data. For the metals small
wind valences are found, which make these metals attractive candidates for the
experimental study of the direct valence.Comment: 18 pages LaTeX, epsfig, 8 figures. to appear in Phys. Rev. B 56 of
15/11/199
NaBr Poisoning of Au/TiO\u3csub\u3e2\u3c/sub\u3e Catalysts: Effects on Kinetics, Poisoning Mechanism, and Estimation of the Number of Catalytic Active Sites
Sodium bromide was used to intentionally poison a commercial Au/TiO2 catalyst with the goals of understanding the nature of halide poisoning and evaluating the number and nature of the catalytic active sites. A series of eight poisoned catalysts were prepared by impregnating the parent catalyst with methanolic solutions of NaBr. Each catalyst was tested with CO oxidation catalysis under differential reactor conditions; O2 reaction orders and Arrhenius activation energies were determined for each material. All of the kinetic data, including a MichaelisâMenten analysis, indicated that the primary effect of adding NaBr was to reduce the number of catalytically active sites. Density functional theory calculations, employed to evaluate likely binding sites for NaBr, showed that NaBr binds more strongly to Au corner and edge atoms than it does to the titania support or to exposed Au face atoms. Infrared spectroscopy of adsorbed CO, along with a Temkin analysis of the data, was also used to evaluate changes to the catalyst upon NaBr deposition. These studies suggested that NaBr addition induces some subtle changes in the coverage dependent properties of CO adsorption, but that these did not substantially impact the CO coverage of the CO binding sites. The experimental and computational results are discussed in terms of possible poisoning mechanisms (siteblocking vs off-site binding and modification); the nature and number of active sites are also discussed in the context of the results
LNK (SH2B3): paradoxical effects in ovarian cancer.
LNK (SH2B3) is an adaptor protein studied extensively in normal and malignant hematopoietic cells. In these cells, it downregulates activated tyrosine kinases at the cell surface resulting in an antiproliferative effect. To date, no studies have examined activities of LNK in solid tumors. In this study, we found by in silico analysis and staining tissue arrays that the levels of LNK expression were elevated in high-grade ovarian cancer. To test the functional importance of this observation, LNK was either overexpressed or silenced in several ovarian cancer cell lines. Remarkably, overexpression of LNK rendered the cells resistant to death induced by either serum starvation or nutrient deprivation, and generated larger tumors using a murine xenograft model. In contrast, silencing of LNK decreased ovarian cancer cell growth in vitro and in vivo. Western blot studies indicated that overexpression of LNK upregulated and extended the transduction of the mitogenic signal, whereas silencing of LNK produced the opposite effects. Furthermore, forced expression of LNK reduced cell size, inhibited cell migration and markedly enhanced cell adhesion. Liquid chromatography-mass spectroscopy identified 14-3-3 as one of the LNK-binding partners. Our results suggest that in contrast to the findings in hematologic malignancies, the adaptor protein LNK acts as a positive signal transduction modulator in ovarian cancers
Keldysh Green's function approach to coherence in a non-equilibrium steady state: connecting Bose-Einstein condensation and lasing
Solid state quantum condensates often differ from previous examples of
condensates (such as Helium, ultra-cold atomic gases, and superconductors) in
that the quasiparticles condensing have relatively short lifetimes, and so as
for lasers, external pumping is required to maintain a steady state. On the
other hand, compared to lasers, the quasiparticles are generally more strongly
interacting, and therefore better able to thermalise. This leads to questions
of how to describe such non-equilibrium condensates, and their relation to
equilibrium condensates and lasers. This chapter discusses in detail how the
non-equilibrium Green's function approach can be applied to the description of
such a non-equilibrium condensate, in particular, a system of microcavity
polaritons, driven out of equilibrium by coupling to multiple baths. By
considering the steady states, and fluctuations about them, it is possible to
provide a description that relates both to equilibrium condensation and to
lasing, while at the same time, making clear the differences from simple
lasers
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