3,140 research outputs found

    Impeller blade design method for centrifugal compressors

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    The design of a centrifugal impeller with blades that are aerodynamically efficient, easy to manufacture, and mechanically sound is discussed. The blade design method described here satisfies the first two criteria and with a judicious choice of certain variables will also satisfy stress considerations. The blade shape is generated by specifying surface velocity distributions and consists of straight-line elements that connect points at hub and shroud. The method may be used to design radially elemented and backward-swept blades. The background, a brief account of the theory, and a sample design are described

    High Energy Quark-Antiquark Elastic scattering with Mesonic Exchange

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    We studies the high energy elastic scattering of quark anti-quark with an exchange of a mesonic state in the tt channel with −t/Λ2≫1-t/\Lambda^{2} \gg 1. Both the normalization factor and the Regge trajectory can be calculated in PQCD in cases of fixed (non-running) and running coupling constant. The dependence of the Regge trajectory on the coupling constant is highly non-linear and the trajectory is of order of 0.20.2 in the interesting physical range.Comment: 29 page

    Use of an oocyte expression assay to reconstitute inductive signaling.

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    Dynamic approach for micromagnetics close to the Curie temperature

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    In conventional micromagnetism magnetic domain configurations are calculated based on a continuum theory for the magnetization which is assumed to be of constant length in time and space. Dynamics is usually described with the Landau-Lifshitz-Gilbert (LLG) equation the stochastic variant of which includes finite temperatures. Using simulation techniques with atomistic resolution we show that this conventional micromagnetic approach fails for higher temperatures since we find two effects which cannot be described in terms of the LLG equation: i) an enhanced damping when approaching the Curie temperature and, ii) a magnetization magnitude that is not constant in time. We show, however, that both of these effects are naturally described by the Landau-Lifshitz-Bloch equation which links the LLG equation with the theory of critical phenomena and turns out to be a more realistic equation for magnetization dynamics at elevated temperatures

    Dynamics of magnetic domain wall motion after nucleation: Dependence on the wall energy

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    The dynamics of magnetic domain wall motion in the FeNi layer of a FeNi/Al2O3/Co trilayer has been investigated by a combination of x-ray magnetic circular dichroism, photoelectron emission microscopy, and a stroboscopic pump-probe technique. The nucleation of domains and subsequent expansion by domain wall motion in the FeNi layer during nanosecond-long magnetic field pulses was observed in the viscous regime up to the Walker limit field. We attribute an observed delay of domain expansion to the influence of the domain wall energy that acts against the domain expansion and that plays an important role when domains are small.Comment: Accepted for publication in Physical Review Letter

    Shaping Robust System through Evolution

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    Biological functions are generated as a result of developmental dynamics that form phenotypes governed by genotypes. The dynamical system for development is shaped through genetic evolution following natural selection based on the fitness of the phenotype. Here we study how this dynamical system is robust to noise during development and to genetic change by mutation. We adopt a simplified transcription regulation network model to govern gene expression, which gives a fitness function. Through simulations of the network that undergoes mutation and selection, we show that a certain level of noise in gene expression is required for the network to acquire both types of robustness. The results reveal how the noise that cells encounter during development shapes any network's robustness, not only to noise but also to mutations. We also establish a relationship between developmental and mutational robustness through phenotypic variances caused by genetic variation and epigenetic noise. A universal relationship between the two variances is derived, akin to the fluctuation-dissipation relationship known in physics

    Double logarithms, ln2(1/x)ln^2(1/x), and the NLO DGLAP evolution for the non-singlet component of the nucleon spin structure function, g1g_1

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    Theoretical predictions show that at low values of Bjorken xx the spin structure function, g1g_1 is influenced by large logarithmic corrections, ln2(1/x)ln^2(1/x), which may be predominant in this region. These corrections are also partially contained in the NLO part of the standard DGLAP evolution. Here we calculate the non-singlet component of the nucleon structure function, g1NS=g1p−g1ng_1^{NS}=g_1^p-g_1^n, and its first moment, using a unified evolution equation. This equation incorporates the terms describing the NLO DGLAP evolution and the terms contributing to the ln2(1/x)ln^2(1/x) resummation. In order to avoid double counting in the overlapping regions of the phase-space, a unique way of including the NLO terms into the unified evolution equation is proposed. The scheme-independent results obtained from this unified evolution are compared to the NLO fit to experimental data, GRSV'2000. Analysis of the first moments of g1NSg_1^{NS} shows that the unified evolution including the ln2(1/x)ln^2(1/x) resummation goes beyond the NLO DGLAP analysis. Corrections generated by double logarithms at low xx influence the Q2Q^2-dependence of the first moments strongly.Comment: 13 pages, latex, 2 figures; Appendix adde

    Formative peer assessment in a CSCL environment

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    In this case study our aim was to gain more insight in the possibilities of qualitative formative peer assessment in a computer supported collaborative learning (CSCL) environment. An approach was chosen in which peer assessment was operationalised in assessment assignments and assessment tools that were embedded in the course material. The course concerned a higher education case-based virtual seminar, in which students were asked to conduct research and write a report in small multidisciplinary teams. The assessment assignments contained the discussion of assessment criteria, the assessment of a group report of a fellow group, and writing an assessment report. A list of feedback rules was one of the assessment tools. A qualitative oriented study was conducted, focussing on the attitude of students towards peer assessment and practical use of peer assessment assignments and tools. Results showed that students’ attitude towards peer assessment was positive and that assessment assignments had added value. However, not all students fulfilled all assessment assignments. Recommendations for implementation of peer assessment in CSCL environments as well as suggestions for future research are discussed

    Interplay between magnetic anisotropy and interlayer coupling in nanosecond magnetization reversal of spin-valve trilayers

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    The influence of magnetic anisotropy on nanosecond magnetization reversal in coupled FeNi/Cu/Co trilayers was studied using a photoelectron emission microscope combined with x-ray magnetic circular dicroism. In quasi-isotropic samples the reversal of the soft FeNi layer is determined by domain wall pinning that leads to the formation of small and irregular domains. In samples with uniaxial magnetic anisotropy, the domains are larger and the influence of local interlayer coupling dominates the domain structure and the reversal of the FeNi layer

    Biochemical Suppression of Small-Molecule Inhibitors: A Strategy to Identify Inhibitor Targets and Signaling Pathway Components

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    SummaryIdentification of small-molecule targets remains an important challenge for chemical genetics. We report an approach for target identification and protein discovery based on functional suppression of chemical inhibition in vitro. We discovered pirl1, an inhibitor of actin assembly, in a screen conducted with cytoplasmic extracts. Pirl1 was used to partially inhibit actin assembly in the same assay, and concentrated biochemical fractions of cytoplasmic extracts were added to find activities that suppressed pirl1 inhibition. Two activities were detected, separately purified, and identified as Arp2/3 complex and Cdc42/RhoGDI complex, both known regulators of actin assembly. We show that pirl1 directly inhibits activation of Cdc42/RhoGDI, but that Arp2/3 complex represents a downstream suppressor. This work introduces a general method for using low-micromolar chemical inhibitors to identify both inhibitor targets and other components of a signaling pathway
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