A study of the factors affecting boundary layer two-dimensionality in wind tunnels

The effect of screens, honeycombs, and centrifugal blowers on the two-dimensionality of a boundary layer on the test section floors of low-speed blower tunnels is studied. Surveys of the spanwise variation in surface shear stress in three blower tunnels revealed that the main component responsible for altering the spanwise properties of the test section boundary layer was the last screen, thus confirming previous findings. It was further confirmed that a screen with varying open-area ratio, produced an unstable flow. However, contrary to popular belief, it was also found that for given incoming conditions and a screen free of imperfections, its open-area ratio alone was not enough to describe its performance. The effect of other geometric parameters such as the type of screen, honeycomb, and blower were investigated. In addition, the effect of the order of components in the settling chamber, and of wire Reynolds number were also studied

Scanning probe microscopy imaging of metallic nanocontacts

We show scanning probe microscopy measurements of metallic nanocontacts between controlled electromigration cycles. The nanowires used for the thinning process are fabricated by shadow evaporation. The highest resolution obtained using scanning force microscopy is about 3 nm. During the first few electromigration cycles the overall slit structure of the nanocontact is formed. The slit first passes along grain boundaries and then at a later stage vertically splits grains in the course of consuming them. We find that first the whole wire is heated and later during the thinning process as the slit forms the current runs over several smaller contacts which needs less power.Comment: 4 pages, 4 figure

Detection mechanism for ferroelectric domain boundaries with lateral force microscopy

The contrast mechanism for the visualization of ferroelectric domain boundaries with lateral force microscopy is generally assumed to be caused by mechanical deformation of the sample due to the converse piezoelectric effect. We show, however, that electrostatic interactions between the charged tip and the electric fields arising from the surface polarization charges dominate the contrast mechanism. This explanation is sustained by quantitative analysis of the measured forces as well as by comparative measurements on different materials

Sorption of Perfluorochemicals to Granular Activated Carbon in the Presence of Ultrasound

Perfluorochemicals (PFCs) are emerging pollutants of increasing public health and environmental concern due to their worldwide distribution, environmental persistence, and bioaccumulation potential. Activated carbon adsorption is an effective method to remove PFCs from water. Herein, we report on the sorption of four PFCs: perfluorooctane sulfonate (PFOS), perfluorooctanoate (PFOA), perfluorobutane sulfonate (PFBS), and perfluorobutanoate (PFBA), from deionized water (MQ) and landfill groundwater (GW) by granular activated carbon (GAC) in the absence and presence of 20 kHz ultrasound. In all cases, the adsorption kinetics were found to be well-represented by a pseudosecond-order model, with maximum monolayer sorption capacity and initial sorption rate values following the orders q_(e)^(PFOS) > q_(e)^(PFOA) > q_(e)^(PFBS) > q_(e)^(PFBA) and v_(0)^(PFOS) > v_(0)^(PFBS) > v_(0)^(PFOA) > v_(0)^(PFBA), respectively. The equilibrium adsorption was quantified by the BET multilayer absorption isotherm, and the monolayer sorption capacity increased with increasing PFC chain length: q_(m)^(PFOS) > q_(m)^(PFOA) > q_(m)^(PFBS) > q_(m)^(PFBA). The equilibrium PFC sorption constants, q_e and q_m, and the sorption kinetic constants, v_0 and k_2, were greater in Milli-Q water than in landfill groundwater with or without pretreatment, indicating competition for sorption sites by natural and cocontaminant groundwater organics. Ultrasonic irradiation significantly increased the PFC−GAC sorption kinetics, 250−900%, and slightly increased the extent of PFC equilibrium adsorption, 5−50%. The ultrasonic PFC−GAC sorption kinetics enhancement increased with increasing PFC chain length, suggesting ultrasound acts to increase the PFC diffusion rate into GAC nanopores

Flow direction measurement criteria and techniques planned for the 40- by 80-/80- x 120-foot wind tunnel integrated systems tests

A study was performed in order to develop the criteria for the selection of flow direction indicators for use in the Integrated Systems Tests (ISTs) of the 40 by 80/80 by 120 Foot Wind Tunnel System. The problems, requirements, and limitations of flow direction measurement in the wind tunnel were investigated. The locations and types of flow direction measurements planned in the facility were discussed. A review of current methods of flow direction measurement was made and the most suitable technique for each location was chosen. A flow direction vane for each location was chosen. A flow direction vane that employs a Hall Effect Transducer was then developed and evaluated for application during the ISTs

Can only flavor-nonsinglet H dibaryons be stable against strong decays?

Using the QCD sum rule approach, we show that the flavor-nonsinglet $H$ dibaryon states with J$^{\pi} = 1^+$, J$^{\pi} = 0^+$, I=1 (27plet) are nearly degenerate with the J$^{\pi} = 0^+$, I=0 singlet $H_0$ dibaryon, which has been predicted to be stable against strong decay, but has not been observed. Our calculation, which does not require an instanton correction, suggests that the $H_0$ is slightly heavier than these flavor-nonsinglet $H$s over a wide range of the parameter space. If the singlet $H_0$ mass lies above the $\Lambda \Lambda$ threshold (2231~MeV), then the strong interaction breakup to $\Lambda \Lambda$ would produce a very broad resonance in the $\Lambda \Lambda$ invariant mass spectrum which would be very difficult to observe. On the other hand, if these flavor-nonsinglet J=0 and 1 $H$ dibaryons are also above the $\Lambda \Lambda$ threshold, but below the $\Xi^0n$ breakup threshold (2254 MeV), then because the direct, strong interaction decay to the $\Lambda \Lambda$ channel is forbidden, these flavor-nonsinglet states might be more amenable to experimental observation. The present results allow a possible reconciliation between the reported observation of $\Lambda \Lambda$ hypernuclei, which argue against a stable $H_0$, and the possible existence of $H$ dibaryons in general.Comment: 10 pages, 2 figure

Sonolytic Decomposition of Aqueous Bioxalate in the Presence of Ozone

Ultrasonic irradiation in the presence of ozone is demonstrated to be effective for the rapid oxidation of oxalic acid, bioxalate, and oxalate (H_(2)C_(2)O_(4)/HC_(2)O_(4)−/C_(2)O_(4)^2−) in aqueous solution to CO_2 and H_(2)O. The degradation rate of bioxalate exposed to “sonozone” (i.e., simultaneous ultrasonication and ozonolysis) was found to be 16-times faster than predicted by the linear addition of ozonolysis and ultrasonic irradiation rates. The hydroxyl radical (•OH) is the only oxy-radical produced that can oxidize oxalate on a relevant time-scale. Thus, plausible •OH production mechanisms are evaluated to explain the observed kinetic synergism of ultrasonication and ozonolysis toward bioxalate decomposition. •OH production via decomposition of O_3 in the cavitating bubble vapor and via the reaction of O_3 and H_(2)O_2 are considered, but kinetic estimations and experimental evidence indicate neither to be a sufficient source of •OH. A free-radical chain mechanism is proposed in which the HC_(2)O_(4)− + •OH reaction functions as a primary propagation step, while the termination occurs through the O_3 + CO_(2)•− reaction via an O-atom transfer mechanism. Kinetic simulations confirm that ozone reacts efficiently with the superoxide (O_(2)•−) ion that is produced by the reaction of O_2 and CO_(2)•− to form •OH radical, and that the reaction of O_3 + CO_(2)•− must be chain terminating. Oxalate is also readily oxidized by “peroxone” treatment (i.e., H_(2)O_2 and O_3). However, the addition of H_(2)O_2 during the course of the sonolytic ozonation of oxalic acid does not appear to increase the observed degradation rate and decreases rates at millimolar levels

Quantification of antithrombin isoform proportions in plasma samples of healthy subjects, sepsis patients, and in antithrombin concentrates

Antithrombin (AT) circulates in plasma in two isoforms, AT-alpha (90-95%) and AT-beta (5-10%). AT isoform proportions were measured in plasma samples of 17 healthy subjects and 26 posttraumatic or postoperative septic patients, as well as in 4 commercially available AT concentrates. Total AT was immune-purified from plasma and concentrates. Micellar electrokinetic chromatography was used to analytically separate and quantify the isoforms. Compared with plasma samples of healthy donors, septic plasmas revealed significantly reduced AT activity (p < 0.001) and beta-isoform content (p < 0.05). AT-beta correlated inversely with urea and creatinine serum concentrations (p < 0.01), indicating a relationship between better renal function and higher beta-isoform content. beta-Isoform neither correlated with age, gender, and 28-day mortality, nor with plasma concentrations of various inflammatory and organ function parameters. The commercial AT concentrate, which is equivalent to the current WHO standard, had an AT-beta content close to that found in plasma of healthy subjects. The availability of this novel quantitative AT isoform assay allows, for the first time, a closer look at the role of AT isoforms in hemostasis and sepsis pathophysiology. Copyright (C) 2002 S. Karger AG, Basel

Sonochemical Degradation of Perfluorooctane Sulfonate (PFOS) and Perfluorooctanoate (PFOA) in Landfill Groundwater: Environmental Matrix Effects

Perfluorinated chemicals such as perfluorooctane sulfonate (PFOS) and perfluorooctanoic acid (PFOA) are environmentally persistent and recalcitrant to most conventional chemical and microbial treatment technologies. In this paper, we show that sonolysis is able to decompose PFOS and PFOA present in groundwater beneath a landfill. However, the pseudo first-order rate constant for the sonochemical degradation in the landfill groundwater is reduced by 61 and 56% relative to MilliQ water for PFOS and PFOA, respectively, primarily due to the presence of other organic constituents. In this study, we evaluate the effect of various organic compounds on the sonochemical decomposition rates of PFOS and PFOA. Organic components in environmental matrices may reduce the sonochemical degradation rates of PFOS and PFOA by competitive adsorption onto the bubble−water interface or by lowering the average interfacial temperatures during transient bubble collapse events. The effect of individual organic compounds depends on the Langmuir adsorption constant, the Henry’s law constant, the specific heat capacity, and the overall endothermic heat of dissociation. Volatile organic compounds (VOCs) are identified as the primary cause of the sonochemical rate reduction for PFOS and PFOA in landfill groundwater, whereas the effect of dissolved natural organic matter (DOM) is not significant. Finally, a combined process of ozonation and sonolysis is shown to substantially recover the rate loss for PFOS and PFOA in landfill groundwater