7 research outputs found

    On the suitability of single-edge notch tension (SENT) testing for assessing hydrogen-assisted cracking susceptibility

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    Combined experiments and computational modelling are used to increase understanding of the suitability of the Single-Edge Notch Tension (SENT) test for assessing hydrogen embrittlement susceptibility. The SENT tests were designed to provide the mode I threshold stress intensity factor (Kth) for hydrogen-assisted cracking of a C110 steel in two corrosive environments. These were accompanied by hydrogen permeation experiments to relate the environments to the absorbed hydrogen concentrations. A coupled phase-field-based deformation–diffusion-fracture model is then employed to simulate the SENT tests, predicting Kth in good agreement with the experimental results and providing insights into the hydrogen absorption–diffusion–cracking interactions. The suitability of SENT testing and its optimal characteristics (e.g., test duration) are discussed in terms of the various simultaneous active time-dependent phenomena, triaxiality dependencies, and regimes of hydrogen embrittlement susceptibility

    NanoMagSat, a 16U nanosatellite constellation high-precision magnetic project to initiate permanent low-cost monitoring of the Earth’s magnetic field and ionospheric environment

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    International audienceThe geomagnetic field has been continuously monitored from low-Earth orbit (LEO) since 1999, complementing ground-based observatory data by providing calibrated scalar and vector measurements with global coverage. The successful three-satellite ESA Swarm constellation is expected to remain in operation up to at least 2025. Further monitoring the field from space with high-precision absolute magnetometry beyond that date is of critical importance for improving our understanding of dynamics of the multiple components of this field, as well as that of the ionospheric environment. Here, we will report on the latest status of the NanoMagSat project, which aims to deploy and operate a new constellation concept of three identical 16U nanosatellites, using two inclined (approximately 60°) and one polar LEO, as well as an innovative payload including an advanced Miniaturized Absolute scalar and self-calibrated vector Magnetometer (MAM) combined with a set of precise star trackers (STR), a compact High-frequency Field Magnetometer (HFM, sharing subsystems with the MAM), a multi-needle Langmuir Probe (m-NLP) and dual frequency GNSS receivers. The data to be produced will at least include 1 Hz absolutely calibrated and oriented magnetic vector field (using the MAM and STR), 2 kHz very low noise magnetic scalar (using the MAM) and vector (using the HFM) field, 2 kHz local electron density (using the m-NLP) as well as precise timing, location and TEC products. In addition to briefly presenting the nanosatellite and constellation concepts, as well as the evolving programmatic status of the mission (which already underwent a consolidation study funded by the ESA Scout programme), this presentation will illustrate through a number of E2E simulations the ability of NanoMagSat to complement and improve on many of the science goals of the Swarm mission at a much lower cost, and to bring innovative science capabilities for ionospheric investigations. NanoMagSat could form the basis of a permanent collaborative constellation of nanosatellites for low-cost long-term monitoring of the geomagnetic field and ionospheric environment from space

    Structural basis for the killing of human beta cells by CD8(+) T cells in type 1 diabetes

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    The structural characteristics of the engagement of major histocompatibility complex (MHC) class II–restricted self antigens by autoreactive T cell antigen receptors (TCRs) is established, but how autoimmune TCRs interact with complexes of self peptide and MHC class I has been unclear. Here we examined how CD8+ T cells kill human islet beta cells in type 1 diabetes via recognition of a human leukocyte antigen HLA-A*0201–restricted glucose-sensitive preproinsulin peptide by the autoreactive TCR 1E6. Rigid 'lock-and-key' binding underpinned the 1E6–HLA-A*0201–peptide interaction, whereby 1E6 docked similarly to most MHC class I–restricted TCRs. However, this interaction was extraordinarily weak because of limited contacts with MHC class I. TCR binding was highly peptide centric, dominated by two residues of the complementarity-determining region 3 (CDR3) loops that acted as an 'aromatic-cap' over the complex of peptide and MHC class I (pMHCI). Thus, highly focused peptide-centric interactions associated with suboptimal TCR-pMHCI binding affinities might lead to thymic escape and potential CD8+ T cell–mediated autoreactivity

    An Introduction to Data Assimilation and Predictability in Geomagnetism

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