1,137 research outputs found

    Using the incremental Hole-drilling technique for measuring residual stresses in fibre-reinforce polymer composites

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    The Incremental hole-drilling technique (IHD) seems to be a promising technique, among the destructive (relaxation) techniques, to determine in-depth non-uniform residual stresses in fibre-reinforced polymer composites. Hence, valid theoretical approaches for IHD residual stress determination in composite laminates, based on a set of strain-depth relaxation curves, are needed. Nevertheless, the influence of the drilling process itself on the initial residual stress state, i.e. existing prior to hole drilling, must be verified first. In this work, the IHD residual stress evaluation procedures in composite laminates will be reviewed and an original hybrid experimental-numerical methodology will be used to quantify the residual strain induced by the drilling process. Thus, residual strains induced by ultra-high speed drilling processes on carbon-epoxy laminates (CFRPs) have been quantified. The results seem to show that IHD technique can be improved to be successfully applied for measuring residual stresses in CFRPs

    Molybdenite as a rhenium carrier : first results of a spectroscopic approach using synchrotron radiation

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    The chemical and physical properties of rhenium render it a highly demanded metal for advanced applications in important industrial fields. This very scarce element occurs mainly in ores of porphyry copper-molybdenum deposits associated with the mineral molybdenite, MoS2, but it has also been found in granite pegmatites and quartz veins as well as in volcanic gases. Molybdenite is a typical polytype mineral which crystal structure is based on the stacking of [S-Mo-S] with molybdenum in prismatic coordination by sulphide anions; however, it is not yet clearly established if rhenium ions replace Mo4+ cations in a disordered way or else, if such replacement gives rise to dispersed nanodomains of a rhenium-rich phase. As a contribution to clarify this question, an X-ray absorption spectroscopy (XANES) study using synchrotron radiation was performed at the Re L3-edge of rhenium-containing molybdenite samples. Obtained results are described and discussed supporting the generally accepted structural perspective that rhenium is mainly carried by molybdenite through the isomorphous replacement of Mo, rather than by the formation of dispersed Re-specific nanophase(s)

    Selenium speciation in waste materials from an exhausted Iberian Pyrite Belt mine

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    Selenium is an essential nutrient for humans, animals and microorganisms, but it becomes toxic at concentrations slightly above the nutritional levels. This naturally occurring trace element can be released to the environment from various anthropogenic sources such as mining, agricultural, petrochemical and industrial processes and its toxicity is developed along a complex cycle involving adsorption by soil components and subsequent accumulation by plants. In the environment, selenium can occur in several oxidation states ranging from selenide (Se=) to elemental selenium (Se0), selenite (Se4+) and selenate (Se6+). Selenium contents above 900 ppm were recently assigned in mine wastes from the sulphur factory at the São Domingos exhausted pyrite mine exploited in the Iberian Pyrite Belt (south Portugal) since Roman times until 1966. Aiming at a sustainable remediation of this mining site, an X-ray absorption spectroscopy study using synchrotron radiation, combined with X-ray diffraction, was undertaken to clarify the speciation state of selenium and the nature of Se-carrier phase(s). The results show that selenium does not significantly replace sulphur under the form of selenate in the dominant sulphate phases and occasionally remains as a substituting selenide anion in debris of the original sulphides present in the mine waste materials

    Measuring co-authorship and networking-adjusted scientific impact

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    Appraisal of the scientific impact of researchers, teams and institutions with productivity and citation metrics has major repercussions. Funding and promotion of individuals and survival of teams and institutions depend on publications and citations. In this competitive environment, the number of authors per paper is increasing and apparently some co-authors don't satisfy authorship criteria. Listing of individual contributions is still sporadic and also open to manipulation. Metrics are needed to measure the networking intensity for a single scientist or group of scientists accounting for patterns of co-authorship. Here, I define I1 for a single scientist as the number of authors who appear in at least I1 papers of the specific scientist. For a group of scientists or institution, In is defined as the number of authors who appear in at least In papers that bear the affiliation of the group or institution. I1 depends on the number of papers authored Np. The power exponent R of the relationship between I1 and Np categorizes scientists as solitary (R>2.5), nuclear (R=2.25-2.5), networked (R=2-2.25), extensively networked (R=1.75-2) or collaborators (R<1.75). R may be used to adjust for co-authorship networking the citation impact of a scientist. In similarly provides a simple measure of the effective networking size to adjust the citation impact of groups or institutions. Empirical data are provided for single scientists and institutions for the proposed metrics. Cautious adoption of adjustments for co-authorship and networking in scientific appraisals may offer incentives for more accountable co-authorship behaviour in published articles.Comment: 25 pages, 5 figure

    Towards the recovery of by-product metals from mine wastes : an X-Ray absorption spectroscopy study on the binding state of rhenium in debris from a centennial Iberian Pyrite Belt mine

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    Rhenium is a very scarce element, occurring in the Earth's crust mainly carried by molybdenite (MoS2). Due to a very low availability comparative to actual industrial demand, rhenium is nowadays one of the most expensive mineral commodities and an increased interest is focused on exploring residues resulting from a long-term mining, particularly of sulphide ore deposits. It is therefore noteworthy to assign the presence of rhenium (in a concentration up to 3 ppm) in the waste materials from the old sulphur factory at the abandoned mine of São Domingos (Iberian Pyrite Belt, Southeast Portugal), exploited since the Roman occupation of Iberia. Aiming at a potential sustainable recovery of rhenium as a by-product, X-ray near-edge absorption spectroscopy (XANES) was applied to clarify the Re-binding and mode of occurrence by comparing Re L3-edge XANES spectra obtained from mine waste samples (previously fully characterized by X-ray laboratory techniques) with similar spectra collected from Re-rich molybdenites (Mo1-xRexS2) and from Re-O model compounds configuring various valences and coordination environments of rhenium ions. Obtained results are commented, ruling out a possible Re-S binding and rather conforming with the binding of rhenium to oxygen in the analysed mine waste materials
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