23 research outputs found

    Thermodynamic Assessment of the Cu-Pt System

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    A CALPHAD assessment of the Cu-Pt system has been carried out. Two and four sublattice models were applied to describe the Gibbs free energies of ordered phases where the contribution of SRO is taken explicitly into account through the reciprocal parameters. The disordered fcc A1 and liquid phases were treated as substitutional solutions. A consistent set of parameters for the phases in the Cu-Pt system as obtained, and those parameters can satisfactorily reproduce the experimental phase equilibria and thermodynamic properties, such as enthalpies, activity of Cu, and long-range order parameters

    Para-infectious brain injury in COVID-19 persists at follow-up despite attenuated cytokine and autoantibody responses

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    To understand neurological complications of COVID-19 better both acutely and for recovery, we measured markers of brain injury, inflammatory mediators, and autoantibodies in 203 hospitalised participants; 111 with acute sera (1–11 days post-admission) and 92 convalescent sera (56 with COVID-19-associated neurological diagnoses). Here we show that compared to 60 uninfected controls, tTau, GFAP, NfL, and UCH-L1 are increased with COVID-19 infection at acute timepoints and NfL and GFAP are significantly higher in participants with neurological complications. Inflammatory mediators (IL-6, IL-12p40, HGF, M-CSF, CCL2, and IL-1RA) are associated with both altered consciousness and markers of brain injury. Autoantibodies are more common in COVID-19 than controls and some (including against MYL7, UCH-L1, and GRIN3B) are more frequent with altered consciousness. Additionally, convalescent participants with neurological complications show elevated GFAP and NfL, unrelated to attenuated systemic inflammatory mediators and to autoantibody responses. Overall, neurological complications of COVID-19 are associated with evidence of neuroglial injury in both acute and late disease and these correlate with dysregulated innate and adaptive immune responses acutely
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