310 research outputs found

    Dataset concerning the analytical approximation of the Ae3 temperature.

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    In this paper we present a new polynomial function for calculating the local phase transformation temperature (Ae3 ) between the austenite+ferrite and the fully austenitic phase fields during heating and cooling of steel:[Formula: see text] The dataset includes the terms of the function and the values for the polynomial coefficients for major alloying elements in steel. A short description of the approximation method used to derive and validate the coefficients has also been included. For discussion and application of this model, please refer to the full length article entitled "The role of aluminium in chemical and phase segregation in a TRIP-assisted dual phase steel" 10.1016/j.actamat.2016.05.046 (Ennis et al., 2016) [1]

    Metastable austenite driven work-hardening behaviour in a TRIP-assisted dual phase steel

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    The mechanically-induced transformation behaviour of the metastable austenite phase in a high-strength industrial TRIP-assisted Dual Phase steel was monitored in situ using high-energy synchrotron diffraction under uniaxial loading. This allowed direct quantification of the impact of the transformation of the metastable austenite phase (16 vol %), embedded in a ferrite-bainite-martensite matrix, on the work hardening behaviour of this steel. Our results show that the mechanically induced transformation of austenite does not begin until the onset of matrix yielding. We provide experimental evidence which demonstrates for the first time that the austenite transformation increases the work-hardening contribution, σw thereby supporting a driving force approach to transformation induced plasticity. The transformation work required leads to an increase in the macroscopic work-hardening rate after matrix yielding and continues to offset the decrease in the work-hardening rate in the ferrite and martensite phases up to the UTS. Further we show conclusively that martensite yielding does not occur until the completion of the mechanically induced transformation of austenite. Plastic deformation of martensite is immediately followed by local plastic instability leading to necking and ultimate failure of this material

    MYSTIC: Michigan Young STar Imager at CHARA

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    This is the final version of the article. Available from SPIE via the DOI in this record.We present the design for MYSTIC, the Michigan Young STar Imager at CHARA. MYSTIC will be a K-band, cryogenic, 6-beam combiner for the Georgia State University CHARA telescope array. The design follows the image-plane combination scheme of the MIRC instrument where single-mode fibers bring starlight into a non-redundant fringe pattern to feed a spectrograph. Beams will be injected in polarization-maintaining fibers outside the cryogenic dewar and then be transported through a vacuum feedthrough into the ~220K cold volume where combination is achieved and the light is dispersed. We will use a C-RED One camera (First Light Imaging) based on the eAPD SAPHIRA detector to allow for near-photon-counting performance. We also intend to support a 4-telescope mode using a leftover integrated optics component designed for the VLTI-GRAVITY experiment, allowing better sensitivity for the faintest targets. Our primary science driver motivation is to image disks around young stars in order to better understand planet formation and how forming planets might influence disk structures.MYSTIC is funded by the USA National Science Foundation (PI: Monnier, NSF-ATI 1506540) while the MIRC-X project is funded by the European Research Council (PI: Kraus, ERC, Grant # 639889)

    The MIRC-X 6-telescope imager: Key science drivers, instrument design and operation

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    This is the final version of the article. Available from SPIE via the DOI in this recordMIRC-X is a new beam combination instrument at the CHARA array that enables 6-telescope interferometric imaging on object classes that until now have been out of reach for milliarcsecond-resolution imaging. As part of an instrumentation effort lead by the University of Exeter and University of Michigan, we equipped the MIRC instrument with an ultra-low read-noise detector system and extended the wavelength range to the J and H-band. The first phase of the MIRC-X commissioning was successfully completed in June 2017. In 2018 we will commission polarisation control to improve the visibility calibration and implement a 'cross-talk resiliant' mode that will minimise visibility cross-talk and enable exoplanet searches using precision closure phases. Here we outline our key science drivers and give an overview about our commissioning timeline. We comment on operational aspects, such as remote observing, and the prospects of co-phased parallel operations with the upcoming MYSTIC combiner.MIRC-X is funded by a Starting Grant from the European Research Council (ERC; grant agreement No. 639889, PI: Kraus) and funds from the University of Exeter. The project builds on earlier investments from the University of Michigan and the National Science Foundation (NSF, PI: Monnier)

    MIRC-X/CHARA: sensitivity improvements with an ultra-low noise SAPHIRA detector

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    This is the final version of the article. Available from Society of Photo Optical Instrumentation Engineers (SPIE) via the DOI in this record.MIRC-X is an upgrade of the six-telescope infrared beam combiner at the CHARA telescope array, the world's largest baseline interferometer in the optical/infrared, located at the Mount Wilson Observatory in Los Angeles. The upgraded instrument features an ultra-low noise and fast frame rate infrared camera (SAPHIRA detector) based on e-APD technology. We report the MIRC-X sensitivity upgrade work and first light results in detail focusing on the detector characteristics and software architecture.MIRC-X is funded, in parts, by a Starting Grant from the European Research Council (ERC; grant agreement No. 639889, PI: Kraus) and builds on earlier investments from the University of Michigan and the National Science Foundation (NSF, PI: Monnier). This research has made use of the Jean-Marie Mariotti Center OIFits Explorer service (http://www.jmmc.fr/oifitsexplorer)

    A Comparative Study of Leptospirosis and Dengue in Thai Children

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    Two of the most common causes of acute febrile illnesses among children in the tropics are leptospirosis and dengue. Early in illness, these two conditions are often indistinguishable and rapid laboratory confirmation of the infecting pathogen is generally not available. An enhanced ability to distinguish leptospirosis from dengue in children would guide clinicians and public health personnel in the appropriate use of limited healthcare resources

    Regulation of the High Affinity IgE Receptor (FcεRI) in Human Neutrophils: Role of Seasonal Allergen Exposure and Th-2 Cytokines

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    The high affinity IgE receptor, FcεRI, plays a key role in the immunological pathways involved in allergic asthma. Previously we have demonstrated that human neutrophils isolated from allergic asthmatics express a functional FcεRI, and therefore it was of importance to examine the factors regulating its expression. In this study, we found that neutrophils from allergic asthmatics showed increased expression of FcεRI-α chain surface protein, total protein and mRNA compared with those from allergic non asthmatics and healthy donors (p<0.001). Interestingly, in neutrophils isolated from allergic asthmatics, FcεRI-α chain surface protein and mRNA expression were significantly greater during the pollen season than outside the pollen season (n = 9, P = 0.001), an effect which was not observed either in the allergic non asthmatic group or the healthy donors (p>0.05). Allergen exposure did not affect other surface markers of neutrophils such as CD16/FcγRIII or IL-17R. In contrast to stimulation with IgE, neutrophils incubated with TH2 cytokines IL-9, GM-CSF, and IL-4, showed enhanced FcεRI-α chain surface expression. In conclusion, these results suggest that enhanced FcεRI expression in human neutrophils from allergic asthmatics during the pollen season can make them more susceptible to the biological effects of IgE, providing a possible new mechanism by which neutrophils contribute to allergic asthma

    A human ribonuclease induces apoptosis associated with p21WAF1/CIP1 induction and JNK inactivation

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    <p>Abstract</p> <p>Background</p> <p>Ribonucleases are promising agents for use in anticancer therapy. Among the different ribonucleases described to be cytotoxic, a paradigmatic example is onconase which manifests cytotoxic and cytostatic effects, presents synergism with several kinds of anticancer drugs and is currently in phase II/III of its clinical trial as an anticancer drug against different types of cancer. The mechanism of cytotoxicity of PE5, a variant of human pancreatic ribonuclease carrying a nuclear localization signal, has been investigated and compared to that of onconase.</p> <p>Methods</p> <p>Cytotoxicity was measured by the MTT method and by the tripan blue exclusion assay. Apoptosis was assessed by flow cytometry, caspase enzymatic detection and confocal microscopy. Cell cycle phase analysis was performed by flow cytometry. The expression of different proteins was analyzed by western blot.</p> <p>Results</p> <p>We show that the cytotoxicity of PE5 is produced through apoptosis, that it does not require the proapoptotic activity of p53 and is not prevented by the multiple drug resistance phenotype. We also show that PE5 and onconase induce cell death at the same extent although the latter is also able to arrest the cell growth. We have compared the cytotoxic effects of both ribonucleases in the NCI/ADR-RES cell line by measuring their effects on the cell cycle, on the activation of different caspases and on the expression of different apoptosis- and cell cycle-related proteins. PE5 increases the number of cells in S and G<sub>2</sub>/M cell cycle phases, which is accompanied by the increased expression of cyclin E and p21<sup>WAF1/CIP1 </sup>together with the underphosphorylation of p46 forms of JNK. Citotoxicity of onconase in this cell line does not alter the cell cycle phase distribution and it is accompanied by a decreased expression of XIAP</p> <p>Conclusions</p> <p>We conclude that PE5 kills the cells through apoptosis associated with the p21<sup>WAF1/CIP1 </sup>induction and the inactivation of JNK. This mechanism is significantly different from that found for onconase.</p
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