154 research outputs found

    Probing O-enrichment in C-rich dust planetary nebulae

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    The abundance of O in planetary nebulae (PNe) has been historically used as a metallicity indicator of the interstellar medium (ISM) where they originated; e.g., it has been widely used to study metallicity gradients in our Galaxy and beyond. However, clear observational evidence for O self enrichment in low-metallicity Galactic PNe with C-rich dust has been recently reported. Here we report asymptotic giant branch (AGB) nucleosynthesis predictions for the abundances of the CNO elements and helium in the metallicity range Zsun/4 < Z < 2Zsun. Our AGB models, with diffusive overshooting from all the convective borders, predict that O is overproduced in low-Z low-mass (~1-3 Msun) AGB stars and nicely reproduce the recent O overabundances observed in C-rich dust PNe. This confirms that O is not always a good proxy of the original ISM metallicity and another chemical elements such as Cl or Ar should be used instead. The production of oxygen by low-mass stars should be thus considered in galactic-evolution models.Comment: Accepted for publication in MNRAS Letters (5 pages, 1 figure, and 1 table

    Galactic planetary nebulae with precise nebular abundances as a tool to understand the evolution of asymptotic giant branch stars

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    We present nucleosynthesis predictions (HeCNOCl) from asymptotic giant branch (AGB) models, with diffusive overshooting from all the convective borders, in the metallicity range Z/4 < Z < 2Zsun. They are compared to recent precise nebular abundances in a sample of Galactic planetary nebulae (PNe) that is divided among double-dust chemistry (DC) and oxygen-dust chemistry (OC) according to the infrared dust features. Unlike the similar subsample of Galactic carbon-dust chemistry PNe recently analysed by us, here the individual abundance errors, the higher metallicity spread, and the uncertain dust types/subtypes in some PNe do not allow a clear determination of the AGB progenitor masses (and formation epochs) for both PNe samples; the comparison is thus more focussed on a object-by-object basis. The lowest metallicity OC PNe evolve from low-mass (~1 Msun) O-rich AGBs, while the higher metallicity ones (all with uncertain dust classifications) display a chemical pattern similar to the DC PNe. In agreement with recent literature, the DC PNe mostly descend from high-mass (M > 3.5 Msun) solar/supersolar metallicity AGBs that experience hot bottom burning (HBB), but other formation channels in low-mass AGBs like extra mixing, stellar rotation, binary interaction, or He pre-enrichment cannot be disregarded until more accurate C/O ratios would be obtained. Two objects among the DC PNe show the imprint of advanced CNO processing and deep second dredge-up, suggesting progenitors masses close to the limit to evolve as core collapse supernovae (above 6 Msun). Their actual C/O ratio, if confirmed, indicate contamination from the third dredge-up, rejecting the hypothesis that the chemical composition of such high-metallicity massive AGBs is modified exclusively by HBB.Comment: Accepted for publication in MNRAS (11 pages, 3 figures, and 2 tables

    Synthesis of easily sinterable ceramic electrolytes based on Bi-doped 8YSZ for IT-SOFC applications

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    Ceramic electrolytes formed by Bi (4 mol%)-doped 8YSZ, i.e., Y2O3 (8 mol%)-doped ZrO2, were synthesized by a simple co-precipitation route, using ammonia solution as precipitating agent. The amorphous as-synthesized powders convert into zirconia-based single phase with fluorite structure through a mild calcination step at 500 \ub0C. The calcined powders were sintered at very low temperatures (i.e., 900-1100 \ub0C) achieving in both cases very high values of relative densities (i.e., &gt; 95%); the corresponding microstructures were highly homogeneous and characterized by micrometric grains or sub-micrometric grains for sintering at 1100 \ub0C and 900 \ub0C, respectively. Very interesting electrochemical properties were determined by Electrochemical Impedance Spectroscopy (EIS) in the best samples. In particular, their total ionic conductivity, recorded at 650 \ub0C, are 6.06 7 10-2S/cm and 4.44 7 10-2S/cm for Bi (4 mol%)-doped 8YSZ sintered at 1100 \ub0C and 900 \ub0C, respectively. Therefore, Bi was proved to be an excellent sintering aid dopant for YSZ, highly improving its densification at lower temperatures while increasing its total ionic conductivity

    Studying the evolution of AGB stars in the Gaia epoch

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    We present asymptotic giant branch (AGB) models of solar metallicity, to allow the interpretation of observations of Galactic AGB stars, whose distances should be soon available after the first release of the Gaia catalogue. We find an abrupt change in the AGB physical and chemical properties, occurring at the threshold mass to ignite hot bottom burning,i.e. 3.5M3.5M_{\odot}. Stars with mass below 3.5M3.5 M_{\odot} reach the C-star stage and eject into the interstellar medium gas enriched in carbon , nitrogen and 17O^{17}O. The higher mass counterparts evolve at large luminosities, between 3×104L3\times 10^4 L_{\odot} and 105L10^5 L_{\odot}. The mass expelled from the massive AGB stars shows the imprinting of proton-capture nucleosynthesis, with considerable production of nitrogen and sodium and destruction of 12C^{12}C and 18O^{18}O. The comparison with the most recent results from other research groups are discussed, to evaluate the robustness of the present findings. Finally, we compare the models with recent observations of galactic AGB stars, outlining the possibility offered by Gaia to shed new light on the evolution properties of this class of objects.Comment: 21 pages, 11 figure, 3 tables, accepted for publication in MNRAS (2016 July 11

    Parameters Expediting the Thermal Conversion of Ba-Exchanged Zeolite A to Monoclinic Celsian

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    Four samples of Ba-exchanged zeolite A, bearing small residual amounts of Na (0.27, 0.43, 0.58, and 0.74 meq/g), were thermally treated in the temperature range 200–1500∘C for times up to 28 hours. The same samples were pressed at 30 and 60 MPa to form cylindrical pellets which were thermally treated at 1300∘C for 5 hours. All materials were characterized by room temperature XRD. The sequence of thermal transformations that Ba-exchanged zeolite A undergoes (zeolite → amorphous phase → hexacelsian → monoclinic celsian) and the strong mineralizing action developed by Na are confirmed. Pressing the Ba-exchanged zeolite A powder-like samples to obtain cylindrical pellets is found to expedite the sluggish final phase transition hexacelsian → monoclinic celsian. The optimum residual Na content of Ba-exchanged zeolite A for transformation into monoclinic celsian is assessed to be between 0.27 and 0.43 meq/g

    Separation of biological entities from human blood by using magnetic nanocomposites obtained from zeolite precursors

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    In this work, three novel magnetic metal-ceramic nanocomposites were obtained by thermally treating Fe-exchanged zeolites (either A or X) under reducing atmosphere at relatively mild temperatures (750-800 ◦C). The so-obtained materials were thoroughly characterized from the point of view of their physico-chemical properties and, then, used as magnetic adsorbents in the separation of the target gene factors V and RNASE and of the Staphylococcus aureus bacteria DNA from human blood. Such results were compared with those obtained by using a top ranking commercial separation system (namely, SiMAG-N-DNA by Chemicell). The results obtained by using the novel magnetic adsorbents were similar to (or even better than) those obtained by using the commercial system, both during manual and automated separations, provided that a proper protocol was adopted. Particularly, the novel magnetic adsorbents showed high sensitivity during tests performed with small volumes of blood. Finally, the feasible production of such magnetic adsorbents by an industrial process was envisaged as well

    On the role of dust and mass loss in the extended main sequence turnoff of star clusters: the case of NGC 1783

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    The Color Magnitude Diagram (CMD) morphology of the "extended" main sequence turnoff (eMSTO) and upper main sequence (MS) of the intermediate age (2\lesssim 2 Gyr) Large Magellanic Cloud Cluster NGC 1783 shows the presence of a small group of UV-dim stars, that, in the ultraviolet Hubble Space Telescope filters, are located at colors on the red side of the typical "fan" shape displayed by the eMSTO. We model the UV-dim stars by assuming that some of the stars which would intrinsically be located on the left side of the eMSTO are obscured by a ring of dust due to grain condensation at the periphery of the excretion disc expelled when they spin at the high rotation rates typical of stars in the Be stage. A reasonably low optical depth at 10μ\mu is necessary to model the UV-dim group. Introduction of dust in the interpretation of the eMSTO may require a substantial re-evaluation of previous conclusions concerning the role of age and/or rotation spreads in the MC clusters: the entire eMSTO can be populated by dusty stars, and the reddest UV-dim stars simply represents the tail of the distribution with both maximum obscuration and the dust ring seen along the line of sight. The model stars having higher rotational projected velocity (vsinv \sin i) are predicted to be preferentially redder than the slowly-rotating stars. The mass loss responsible for the dust may also cause the non-monotonic distribution of stars in the upper main sequence, with two peaks and gaps showing up in the UV CMD.Comment: 11 pages, 13 figures. This is a pre-copyedited, author-produced PDF of an article (stad851) accepted for publication in MNRAS following peer revie

    Reverse Micelle Strategy for the Synthesis of MnOx-TiO2Active Catalysts for NH3-Selective Catalytic Reduction of NOxat Both Low Temperature and Low Mn Content

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    MnOx-TiO2catalysts (0, 1, 5, and 10 wt % Mn nominal content) for NH3-SCR (selective catalytic reduction) of NOxhave been synthesized by the reverse micelle-assisted sol-gel procedure, with the aim of improving the dispersion of the active phase, usually poor when obtained by other synthesis methods (e.g., impregnation) and thereby lowering its amount. For comparison, a sample at nominal 10 wt % Mn was obtained by impregnation of the (undoped) TiO2sample. The catalysts were characterized by using an integrated multitechnique approach, encompassing X-ray diffraction followed by Rietveld refinement, micro-Raman spectroscopy, N2isotherm measurement at −196 °C, energy-dispersive X-ray analysis, diffuse reflectance UV-vis spectroscopy, temperature-programmed reduction technique, and X-ray photoelectron spectroscopy. The obtained results prove that the reverse micelle sol-gel approach allowed for enhancing the catalytic activity, in that the catalysts were active in a broad temperature range at a substantially low Mn loading, as compared to the impregnated catalyst. Particularly, the 5 wt % Mn catalyst showed the best NH3-SCR activity in terms of both NOxconversion (ca. 90%) and the amount of produced N2O (ca. 50 ppm) in the 200-250 °C temperature range
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