245 research outputs found
Design and characterisation of metallic glassy alloys of high neutron shielding capability
This paper reports the design, making and characterisation of a series of Fe-based bulk metallic glass alloys with the aim of achieving the combined properties of high neutron absorption capability and sufficient glass forming ability. Synchrotron X-ray diffraction and pair distribution function methods were used to characterise the crystalline or amorphous states of the samples. Neutron transmission and macroscopic attenuation coefficients of the designed alloys were measured using energy resolved neutron imaging method and the very recently developed microchannel plate detector. The study found that the newly designed alloy (Fe48Cr15Mo14C15B6Gd2 with a glass forming ability of Ø5.8 mm) has the highest neutron absorption capability among all Fe-based bulk metallic glasses so far reported. It is a promising material for neutron shielding applications
Recovering the second moment of the strain distribution from neutron Bragg edge data
Point by point strain scanning is often used to map the residual stress (strain) in engineering materials and components. However, the gauge volume and hence spatial resolution is limited by the beam defining apertures and can be anisotropic for very low and high diffraction (scattering) angles. Alternatively, wavelength resolved neutron transmission imaging has a potential to retrieve information tomographically about residual strain induced within materials through measurement in transmission of Bragg edges - crystallographic fingerprints whose locations and shapes depend on microstructure and strain distribution. In such a case the spatial resolution is determined by the geometrical blurring of the measurement setup and the detector point spread function. Mathematically, reconstruction of strain tensor field is described by the longitudinal ray transform; this transform has a non-trivial null-space, making direct inversion impossible. A combination of the longitudinal ray transform with physical constraints was used to reconstruct strain tensor fields in convex objects. To relax physical constraints and generalise reconstruction, a recently introduced concept of histogram tomography can be employed. Histogram tomography relies on our ability to resolve the distribution of strain in the beam direction, as we discuss in the paper. More specifically, Bragg edge strain tomography requires extraction of the second moment (variance about zero) of the strain distribution which has not yet been demonstrated in practice. In this paper we verify experimentally that the second moment can be reliably measured for a previously well characterised aluminium ring and plug sample. We compare experimental measurements against numerical calculation and further support our conclusions by rigorous uncertainty quantification of the estimated mean and variance of the strain distribution
Recovering the second moment of the strain distribution from neutron Bragg edge data
Point by point strain scanning is often used to map the residual stress
(strain) in engineering materials and components. However, the gauge volume and
hence spatial resolution is limited by the beam defining apertures and can be
anisotropic for very low and high diffraction (scattering) angles.
Alternatively, wavelength resolved neutron transmission imaging has a potential
to retrieve information tomographically about residual strain induced within
materials through measurement in transmission of Bragg edges - crystallographic
fingerprints whose locations and shapes depend on microstructure and strain
distribution. In such a case the spatial resolution is determined by the
geometrical blurring of the measurement setup and the detector point spread
function. Mathematically, reconstruction of strain tensor field is described by
the longitudinal ray transform; this transform has a non-trivial null-space,
making direct inversion impossible. A combination of the longitudinal ray
transform with physical constraints was used to reconstruct strain tensor
fields in convex objects. To relax physical constraints and generalise
reconstruction, a recently introduced concept of histogram tomography can be
employed. Histogram tomography relies on our ability to resolve the
distribution of strain in the beam direction, as we discuss in the paper. More
specifically, Bragg edge strain tomography requires extraction of the second
moment (variance about zero) of the strain distribution which has not yet been
demonstrated in practice. In this paper we verify experimentally that the
second moment can be reliably measured for a previously well characterised
aluminium ring and plug sample. We compare experimental measurements against
numerical calculation and further support our conclusions by rigorous
uncertainty quantification of the estimated mean and variance of the strain
distribution
Exploring the potential of neutron imaging for life sciences on IMAT
ABSTRACT Neutron imaging has been employed in life sciences in recent years and has proven to be a viable technique for studying internal features without compromising integrity and internal structure of samples in addition to being complementary to other methods such as X-ray or magnetic resonance imaging. Within the last decade, a neutron imaging beamline, IMAT, was designed and built at the ISIS Neutron and Muon Source, UK, to meet the increasing demand for neutron imaging applications in various fields spanning from materials engineering to biology. In this paper, we present the first neutron imaging experiments on different biological samples during the scientific commissioning of the IMAT beamline mainly intended to explore the beamline’s capabilities and its potential as a non-invasive investigation tool in fields such as agriculture (soil-plants systems), palaeontology and dentistry
The 100,000 genomes pilot on rare disease diagnosis in healthcare – a preliminary report: The 100,000 Genomes Project Pilot Investigators
BACKGROUND: The UK 100,000 Genomes Project is in the process of investigating the role of genome sequencing of patients with undiagnosed rare disease following usual care, and the alignment of research with healthcare implementation in the UK’s national health service. (Other parts of this Project focus on patients with cancer and infection.)
METHODS: We enrolled participants, collected clinical features with human phenotype ontology terms, undertook genome sequencing and applied automated variant prioritization based on virtual gene panels (PanelApp) and phenotypes (Exomiser), alongside identification of novel pathogenic variants through research analysis. We report results on a pilot study of 4660 participants from 2183 families with 161 disorders covering a broad spectrum of rare disease.
RESULTS: Diagnostic yields varied by family structure and were highest in trios and larger pedigrees. Likely monogenic disorders had much higher diagnostic yields (35%) with intellectual disability, hearing and vision disorders, achieving yields between 40 and 55%. Those with more complex etiologies had an overall 25% yield. Combining research and automated approaches was critical to 14% of diagnoses in which we found etiologic non-coding, structural and mitochondrial genome variants and coding variants poorly covered by exome sequencing. Cohort-wide burden testing across 57,000 genomes enabled discovery of 3 new disease genes and 19 novel associations. Of the genetic diagnoses that we made, 24% had immediate ramifications for the clinical decision-making for the patient or their relatives.
CONCLUSION: Our pilot study of genome sequencing in a national health care system demonstrates diagnostic uplift across a range of rare diseases
Deflecting lithium dendritic cracks in multi-layered solid electrolytes
Charging current densities of solid-state batteries with lithium metal
anodes and ceramic electrolytes are severely limited due to lithium
dendrites that penetrate the electrolyte leading to a short circuit.
We show that dendrite growth can be inhibited by different crack
deflection mechanisms when multi-layered solid electrolytes, such
as Li6PS5Cl/Li3ScCl6/Li6PS5Cl and Li6PS5Cl/Li10GeP2S12/Li6PS5Cl,
are employed but not when the inner layer is Li3PS4. X-ray tomographic imaging shows crack deflection along mechanically weak interfaces between solid electrolytes as a result of local mismatches in
elastic moduli. Cracks are also deflected laterally within Li3ScCl6,
which contains preferentially oriented particles. Deflection occurs
without lithium being present. In cases where the inner layers react
with lithium, the resulting decomposition products can fill and block
crack propagation. All three mechanisms are effective at low stack
pressures. Operating at 2.5 MPa, multi-layered solid electrolytes
Li6PS5Cl/Li3ScCl6/Li6PS5Cl and Li6PS5Cl/Li10GeP2S12/Li6PS5Cl can
achieve lithium plating at current densities exceeding 15 mA cm–2
Correlative tomography of an exceptionally preserved Jurassic ammonite implies hyponome-propelled swimming
The extreme rarity of soft-tissue preservation in ammonoids has meant there are open questions regarding fundamental aspects of their biology. We report an exceptionally preserved Middle Jurassic ammonite with unrivaled information on soft-body organization interpreted through correlative neutron and X-ray tomography. Three-dimensional imaging of muscles and organs of the body mass for the first time in this iconic fossil group provides key insights into functional morphology. We show that paired dorsal muscles withdrew the body into the shell, rather than acting with the funnel controlling propulsion as in Nautilus. This suggests a mobile, retractable body as a defense strategy and necessitates a distinct swimming mechanism of hyponome propulsion, a trait that we infer evolved early in the ammonoid-coleoid lineage.Copyright © 2021, The Authors. This document is the author’s final accepted version of the journal article. You are advised to consult the published version if you wish to cite from it
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Author Correction: Nuclear-mitochondrial DNA segments resemble paternally inherited mitochondrial DNA in humans
An amendment to this paper has been published and can be accessed via a link at the top of the paper
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