282 research outputs found

    Airborne next: rethinking airborne organization and applying new concepts

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    The airborne concept has had a lasting impact on military force structures since its employment on a large scale during World War II. It is puzzling to consider how little airborne organizational structures and employment concepts have changed in the intervening seven decades, considering the great amount of change occurring in warfare. This thesis examines the future potential of airborne concepts by rethinking traditional airborne organizational structures and employment concepts. Using a holistic approach in the areas of organization, doctrine, technology, and strategy as guiding frames of reference, this thesis recommends updating the organizational structures of airborne forces to model a small and many approach over a large and few approach, while incorporating a swarming concept. Utilizing historical and contemporary vignettes to demonstrate airborne utility, this research reveals how a parachute capability displays the unique attributes to complement a swarming concept. Under an updated organizational structure and new employment concept, airborne forces can offer renewed relevancy to the U.S. Department of Defense against modern adversaries in crises and conflict.http://archive.org/details/airbornenextreth1094545878Major, United States ArmyApproved for public release; distribution is unlimited

    Nanocrystalline materials studied by powder diffraction line profile analysis

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    X-ray powder diffraction is a powerful tool for characterising the microstructure of crystalline materials in terms of size and strain. It is widely applied for nanocrystalline materials, especially since other methods, in particular electron microscopy is, on the one hand tedious and time consuming, on the other hand, due to the often metastable states of nanomaterials it might change their microstructures. It is attempted to overview the applications of microstructure characterization by powder diffraction on nanocrystalline metals, alloys, ceramics and carbon base materials. Whenever opportunity is given, the data provided by the X-ray method are compared and discussed together with results of electron microscopy. Since the topic is vast we do not try to cover the entire field

    Quasi-free Compton Scattering and the Polarizabilities of the Neutron

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    Differential cross sections for quasi-free Compton scattering from the proton and neutron bound in the deuteron have been measured using the Glasgow/Mainz tagging spectrometer at the Mainz MAMI accelerator together with the Mainz 48 cm ⊘\oslash ×\times 64 cm NaI(Tl) photon detector and the G\"ottingen SENECA recoil detector. The data cover photon energies ranging from 200 MeV to 400 MeV at θγLAB=136.2∘\theta^{LAB}_\gamma=136.2^\circ. Liquid deuterium and hydrogen targets allowed direct comparison of free and quasi-free scattering from the proton. The neutron detection efficiency of the SENECA detector was measured via the reaction p(γ,π+n)p(\gamma,\pi^+ n). The "free" proton Compton scattering cross sections extracted from the bound proton data are in reasonable agreement with those for the free proton which gives confidence in the method to extract the differential cross section for free scattering from quasi-free data. Differential cross sections on the free neutron have been extracted and the difference of the electromagnetic polarizabilities of the neutron have been obtained to be α−β=9.8±3.6(stat)12.1.1(syst)±2.2(model)\alpha-\beta= 9.8\pm 3.6(stat){}^{2.1}_1.1(syst)\pm 2.2(model) in units 10−4fm310^{-4}fm^3. In combination with the polarizability sum α+β=15.2±0.5\alpha +\beta=15.2\pm 0.5 deduced from photoabsorption data, the neutron electric and magnetic polarizabilities, αn=12.5±1.8(stat)−0.6+1.1±1.1(model)\alpha_n=12.5\pm 1.8(stat){}^{+1.1}_{-0.6}\pm 1.1(model) and βn=2.7∓1.8(stat)−1.1+0.6(syst)∓1.1(model)\beta_n=2.7\mp 1.8(stat){}^{+0.6}_{-1.1}(syst)\mp 1.1(model) are obtained. The backward spin polarizability of the neutron was determined to be γπ(n)=(58.6±4.0)×10−4fm4\gamma^{(n)}_\pi=(58.6\pm 4.0)\times 10^{-4}fm^4

    Upgrade of the Glasgow photon tagging spectrometer for Mainz MAMI-C

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    The Glasgow photon tagging spectrometer at Mainz has been upgraded so that it can be used with the 1500 MeV electron beam now available from the Mainz microtron MAMI-C. The changes made and the resulting properties of the spectrometer are discussed.Comment: 20 pages, 12 figure

    Quasi-free π0\pi^0 Photoproduction from the Bound Nucleon

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    Differential cross-sections for quasi-free π0\pi^0 photoproduction from the proton and neutron bound in the deuteron have been measured for Eγ=200−400E_\gamma= 200 - 400 MeV at θγlab=136.2∘\theta^{\rm lab}_\gamma = 136.2^\circ usind the Glasgow photon tagger at MAMI, the Mainz 48 cm ∅\varnothing ×\times 64 cm NaI(Tl) photon detector and the G\"ottingen SENECA recoil detector. For the proton measurements made with both liquid deuterium and liquid hydrogen targets allow direct comparison of "free" π0\pi^0 photoproduction cross-sections as extracted from the bound proton data with experimental free cross sections which are found to be in reasonable agreement below 320 MeV. At higher energies the "free" cross sections extracted from quasifree data are significantly smaller than the experimental free cross sections and theoretical predictions based on multipole analysis. For the first time, "free" neutron cross sections have been extracted in the Δ\Delta-region. They are also in agreement with the predictions from multipole analysis up to 320 MeV and significantly smaller at higher photon energies

    Neutron polarizabilities investigated by quasi-free Compton scattering from the deuteron

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    Measuring Compton scattered photons and recoil neutrons in coincidence, quasi-free Compton scattering by the neutron has been investigated at MAMI (Mainz) at thetaγlab=136otheta^{lab}_\gamma=136^o in an energy range from 200 to 400 MeV. From the data a polarizability difference of αn−βn=9.8±3.6(stat)−1.1+2.1(syst)±2.2(model)\alpha_n - \beta_n = 9.8 \pm 3.6(stat)^{+2.1}_{-1.1}(syst)\pm 2.2(model) in units of 10−4fm310^{-4}fm^3 has been determined. In combination with the polarizability sum αn+βn=15.2±0.5\alpha_n+\beta_n= 15.2\pm 0.5 deduced from photo absorption data, the neutron electric and magnetic polarizabilities, αn=12.5±1.8(stat)−0.6+1.1(syst)±1.1(model)\alpha_n=12.5\pm 1.8(stat)^{+1.1}_{-0.6}(syst)\pm 1.1(model) and βn=2.7∓1.8(stat)−1.1+0.6(syst)∓1.1(model)\beta_n = 2.7\mp 1.8(stat)^{+0.6}_{-1.1}(syst)\mp 1.1(model), are obtained

    Fabrication and characterization of dual function nanoscale pH-scanning ion conductance microscopy (SICM) probes for high resolution pH mapping

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    The easy fabrication and use of nanoscale dual function pH-scanning ion conductance microscopy (SICM) probes is reported. These probes incorporate an iridium oxide coated carbon electrode for pH measurement and an SICM barrel for distance control, enabling simultaneous pH and topography mapping. These pH-SICM probes were fabricated rapidly from laser pulled theta quartz pipets, with the pH electrode prepared by in situ carbon filling of one of the barrels by the pyrolytic decomposition of butane, followed by electrodeposition of a thin layer of hydrous iridium oxide. The other barrel was filled with an electrolyte solution and Ag/AgCl electrode as part of a conductance cell for SICM. The fabricated probes, with pH and SICM sensing elements typically on the 100 nm scale, were characterized by scanning electron microscopy, energy-dispersive X-ray spectroscopy, and various electrochemical measurements. They showed a linear super-Nernstian pH response over a range of pH (pH 2–10). The capability of the pH-SICM probe was demonstrated by detecting both pH and topographical changes during the dissolution of a calcite microcrystal in aqueous solution. This system illustrates the quantitative nature of pH-SICM imaging, because the dissolution process changes the crystal height and interfacial pH (compared to bulk), and each is sensitive to the rate. Both measurements reveal similar dissolution rates, which are in agreement with previously reported literature values measured by classical bulk methods

    Ongoing outbreak of hepatitis A in Italy: preliminary report as of 31 May 2013

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    Since January 2013, an unusual increase in hepatitis A cases has been detected in northern Italy. A total number of 352 cases were reported to the integrated surveillance system between January and the end of May 2013 and this represents a 70% increase compared to the same period of the previous year. The outbreak is ongoing and the public health authorities are continuing their investigations to establish the transmission vehicle and to control the outbreak

    Atomic-scale modeling of the deformation of nanocrystalline metals

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    Nanocrystalline metals, i.e. metals with grain sizes from 5 to 50 nm, display technologically interesting properties, such as dramatically increased hardness, increasing with decreasing grain size. Due to the small grain size, direct atomic-scale simulations of plastic deformation of these materials are possible, as such a polycrystalline system can be modeled with the computational resources available today. We present molecular dynamics simulations of nanocrystalline copper with grain sizes up to 13 nm. Two different deformation mechanisms are active, one is deformation through the motion of dislocations, the other is sliding in the grain boundaries. At the grain sizes studied here the latter dominates, leading to a softening as the grain size is reduced. This implies that there is an ``optimal'' grain size, where the hardness is maximal. Since the grain boundaries participate actively in the deformation, it is interesting to study the effects of introducing impurity atoms in the grain boundaries. We study how silver atoms in the grain boundaries influence the mechanical properties of nanocrystalline copper.Comment: 10 pages, LaTeX2e, PS figures and sty files included. To appear in Mater. Res. Soc. Symp. Proc. vol 538 (invited paper). For related papers, see http://www.fysik.dtu.dk/~schiotz/publist.htm
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