1,295 research outputs found

    Thermodynamics of Constituent Quarks

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    We investigate the thermal behavior of quarks and antiquarks interacting via a temperature-dependent linear potential. The quarks are constituent quarks with dynamically generated masses from the background linear σ\sigma-model.We find a transition from a system of bound mesons to a correlated quark gas at the same temperature as the chiral transition temperature.Comment: 24 pages, 5 Postscript figures, uses article.sty, epsf.sty, epsfig.st

    Real-Time Hand Shape Classification

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    The problem of hand shape classification is challenging since a hand is characterized by a large number of degrees of freedom. Numerous shape descriptors have been proposed and applied over the years to estimate and classify hand poses in reasonable time. In this paper we discuss our parallel framework for real-time hand shape classification applicable in real-time applications. We show how the number of gallery images influences the classification accuracy and execution time of the parallel algorithm. We present the speedup and efficiency analyses that prove the efficacy of the parallel implementation. Noteworthy, different methods can be used at each step of our parallel framework. Here, we combine the shape contexts with the appearance-based techniques to enhance the robustness of the algorithm and to increase the classification score. An extensive experimental study proves the superiority of the proposed approach over existing state-of-the-art methods.Comment: 11 page

    Dynamics of CrO3–Fe2O3 catalysts during the high-temperature water-gas shift reaction: molecular structures and reactivity

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    A series of supported CrO3/Fe2O3 catalysts were investigated for the high-temperature water-gas shift (WGS) and reverse-WGS reactions and extensively characterized using in situ and operando IR, Raman, and XAS spectroscopy during the high-temperature WGS/RWGS reactions. The in situ spectroscopy examinations reveal that the initial oxidized catalysts contain surface dioxo (O═)2Cr6+O2 species and a bulk Fe2O3 phase containing some Cr3+ substituted into the iron oxide bulk lattice. Operando spectroscopy studies during the high-temperature WGS/RWGS reactions show that the catalyst transforms during the reaction. The crystalline Fe2O3 bulk phase becomes Fe3O4 ,and surface dioxo (O═)2Cr6+O2 species are reduced and mostly dissolve into the iron oxide bulk lattice. Consequently, the chromium–iron oxide catalyst surface is dominated by FeOx sites, but some minor reduced surface chromia sites are also retained. The Fe3–-xCrxO4 solid solution stabilizes the iron oxide phase from reducing to metallic Fe0 and imparts an enhanced surface area to the catalyst. Isotopic exchange studies with C16O2/H2 → C18O2/H2 isotopic switch directly show that the RWGS reaction proceeds via the redox mechanism and only O* sites from the surface region of the chromium–iron oxide catalysts are involved in the RWGS reaction. The number of redox O* sites was quantitatively determined with the isotope exchange measurements under appropriate WGS conditions and demonstrated that previous methods have undercounted the number of sites by nearly 1 order of magnitude. The TOF values suggest that only the redox O* sites affiliated with iron oxide are catalytic active sites for WGS/RWGS, though a carbonate oxygen exchange mechanism was demonstrated to exist, and that chromia is only a textural promoter that increases the number of catalytic active sites without any chemical promotion effect

    Designing and Operating Safe and Secure Transit Systems: Assessing Current Practices in the United States and Abroad, MTI Report 04-05

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    Public transit systems around the world have for decades served as a principal venue for terrorist acts. Today, transit security is widely viewed as an important public policy issue and is a high priority at most large transit systems and at smaller systems operating in large metropolitan areas. Research on transit security in the United States has mushroomed since 9/11; this study is part of that new wave of research. This study contributes to our understanding of transit security by (1) reviewing and synthesizing nearly all previously published research on transit terrorism; (2) conducting detailed case studies of transit systems in London, Madrid, New York, Paris, Tokyo, and Washington, D.C.; (3) interviewing federal officials here in the United States responsible for overseeing transit security and transit industry representatives both here and abroad to learn about efforts to coordinate and finance transit security planning; and (4) surveying 113 of the largest transit operators in the United States. Our major findings include: (1) the threat of transit terrorism is probably not universal—most major attacks in the developed world have been on the largest systems in the largest cities; (2) this asymmetry of risk does not square with fiscal politics that seek to spread security funding among many jurisdictions; (3) transit managers are struggling to balance the costs and (uncertain) benefits of increased security against the costs and (certain) benefits of attracting passengers; (4) coordination and cooperation between security and transit agencies is improving, but far from complete; (5) enlisting passengers in surveillance has benefits, but fearful passengers may stop using public transit; (6) the role of crime prevention through environmental design in security planning is waxing; and (7) given the uncertain effectiveness of antitransit terrorism efforts, the most tangible benefits of increased attention to and spending on transit security may be a reduction in transit-related person and property crimes

    Five-Torsion in the Homology of the Matching Complex on 14 Vertices

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    J. L. Andersen proved that there is 5-torsion in the bottom nonvanishing homology group of the simplicial complex of graphs of degree at most two on seven vertices. We use this result to demonstrate that there is 5-torsion also in the bottom nonvanishing homology group of the matching complex M14M_{14} on 14 vertices. Combining our observation with results due to Bouc and to Shareshian and Wachs, we conclude that the case n=14n=14 is exceptional; for all other nn, the torsion subgroup of the bottom nonvanishing homology group has exponent three or is zero. The possibility remains that there is other torsion than 3-torsion in higher-degree homology groups of MnM_n when n≄13n \ge 13 and n≠14n \neq 14.Comment: 11 page

    Anomalous reactivity of supported V2O5 nanoparticles for propane oxidative dehydrogenation: influence of the vanadium oxide precursor

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    Dieser Beitrag ist mit Zustimmung des Rechteinhabers aufgrund einer (DFG geförderten) Allianz- bzw. Nationallizenz frei zugĂ€nglich.This publication is with permission of the rights owner freely accessible due to an Alliance licence and a national licence (funded by the DFG, German Research Foundation) respectively.The oxidative dehydrogenation (ODH) of propane to propylene by supported vanadia catalysts has received much attention in recent years, but different reactivity trends have been reported for this catalytic reaction system. In the present investigation, the origin of these differing trends are investigated with synthesis of supported V/SiO2, V/TiO2, and V/Al2O3 catalysts prepared with three different vanadium oxide precursors (2-propanol/vanadyl triisopropoxide [VO(O-Pri)3] (VTI), oxalic acid/ammonium metavanadate [NH4VO3] (AMV), and toluene/vanadyl acetylacetonate [VO(C5H7O2)2] (VAA)) in order to elucidate the influence of the precursor on supported vanadia phase and propane ODH activity. In situ Raman spectroscopy revealed that the choice of vanadium precursor does not affect the dispersion of the supported vanadium oxide phase below 4 V nm−2 (0.5 monolayer coverage), where only isolated and oligomeric surface VO4 species are present, and only the AMV precursor favors crystalline V2O5 nanoparticle (NP) formation below monolayer coverage (8 V nm−2). The propane ODH specific reactivity trend demonstrated that there is no significant difference in TOF for the isolated and oligomeric surface VO4 sites. Surprisingly, V2O5 NPs in the ∌1–2 nm range exhibit anomalously high propane ODH TOF values for the supported vanadia catalysts. This was found for all supported vanadium oxide catalysts examined. This comparative study with different V-precursors and synthesis methods and oxide supports finally resolves the debate in the catalysis literature about the dependence of TOF on the surface vanadium density that is related to the unusually high reactivity of small V2O5 NPs.DFG, SFB 546, Struktur, Dynamik und ReaktivitĂ€t von Übergangsmetalloxid-Aggregate

    Chronic Disease Self-Management and Behavior Change Attitudes in Older Adults: A Mixed-Method Feasibility Study

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    The population of older adults with chronic disease is increasing, yet little is known about their perception of chronic disease and self-management. To develop successful and sustainable chronic disease self-management interventions in the older adult population, health care providers must first understand older adults’ attitudes toward health status and behavior change. This pilot study was conducted to determine the feasibility of the study design. The purpose of this pilot study was to assess the appropriateness of using a mixed-methods research design to investigate Appalachian older adult’s attitude toward the chronic disease experience and health behavior change. A convergent, parallel mixed-method design included a quantitative questionnaire and qualitative focus groups in churches in northeast Tennessee. The aim of the study was met, and the methodology of the study was found to be feasible for larger studies. Divergence of data was found when evaluating qualitative and quantitative data. The study instrument was found to be reliable for future use. The implications of the results suggest that the study design is appropriate for the purpose of the study

    Normal Ordering for Deformed Boson Operators and Operator-valued Deformed Stirling Numbers

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    The normal ordering formulae for powers of the boson number operator n^\hat{n} are extended to deformed bosons. It is found that for the `M-type' deformed bosons, which satisfy aa†−qa†a=1a a^{\dagger} - q a^{\dagger} a = 1, the extension involves a set of deformed Stirling numbers which replace the Stirling numbers occurring in the conventional case. On the other hand, the deformed Stirling numbers which have to be introduced in the case of the `P-type' deformed bosons, which satisfy aa†−qa†a=q−n^a a^{\dagger} - q a^{\dagger} a = q^{-\hat{n}}, are found to depend on the operator n^\hat{n}. This distinction between the two types of deformed bosons is in harmony with earlier observations made in the context of a study of the extended Campbell-Baker-Hausdorff formula.Comment: 14 pages, Latex fil

    Some identities on derangement and degenerate derangement polynomials

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    In combinatorics, a derangement is a permutation that has no fixed points. The number of derangements of an n-element set is called the n-th derangement number. In this paper, as natural companions to derangement numbers and degenerate versions of the companions we introduce derangement polynomials and degenerate derangement polynomials. We give some of their properties, recurrence relations and identities for those polynomials which are related to some special numbers and polynomials.Comment: 12 page

    Nature of catalytically active sites in the supported WO3/ZrO2 solid acid system: a current perspective

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    Tungstated zirconia (WO3/ZrO2) is one of the most well-studied solid acid catalyst systems and continues to attract the attention of both academia and industry. Understanding and controlling the properties of WO3/ZrO2 catalysts has been a topic of considerable interest over almost the past three decades, with a particular focus on discovering the relationship between catalytic activity and the molecular structure of the surface acid site. Amorphous tungsten oxide (WOx) species on ZrO2 surfaces were previously proposed to be very active for different acidic reactions such as alcohol dehydration and alkane isomerization. Recent developments in electron optical characterization and in situ spectroscopy techniques have allowed researchers to isolate the size, structure, and composition of the most active catalytic species, which are shown to be three-dimensional distorted Zr-WOx clusters (0.8–1.0 nm). Complementary theoretical calculations of the Brþnsted acidity of these Zr-WOx clusters have confirmed that they possess the lowest deprotonation energy values. This new insight provides a foundation for the future characterization and theory of acidic supported metal oxide catalytic materials that will, hopefully, lead to the design of more active and selective catalysts. This perspective presents an up-to-date, comprehensive summary of the leading models of WO3/ZrO2 solid acid catalysts
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