1,206 research outputs found

    Initial mass function of intermediate mass black hole seeds

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    We study the Initial Mass Function (IMF) and host halo properties of Intermediate Mass Black Holes (IMBH, 10^{4-6} Msun) formed inside metal-free, UV illuminated atomic cooling haloes (virial temperature T_vir > 10^4 K) either via the direct collapse of the gas or via an intermediate Super Massive Star (SMS) stage. We achieve this goal in three steps: (a) we derive the gas accretion rate for a proto-SMS to undergo General Relativity instability and produce a direct collapse black hole (DCBH) or to enter the ZAMS and later collapse into a IMBH; (b) we use merger-tree simulations to select atomic cooling halos in which either a DCBH or SMS can form and grow, accounting for metal enrichment and major mergers that halt the growth of the proto-SMS by gas fragmentation. We derive the properties of the host halos and the mass distribution of black holes at this stage, and dub it the "Birth Mass Function"; (c) we follow the further growth of the DCBH due to accretion of leftover gas in the parent halo and compute the final IMBH mass.We consider two extreme cases in which minihalos (T_vir < 10^4 K) can (fertile) or cannot (sterile) form stars and pollute their gas leading to a different IMBH IMF. In the (fiducial) fertile case the IMF is bimodal extending over a broad range of masses, M= (0.5-20)x10^5 Msun, and the DCBH accretion phase lasts from 10 to 100 Myr. If minihalos are sterile, the IMF spans the narrower mass range M= (1-2.8)x10^6 Msun, and the DCBH accretion phase is more extended (70-120 Myr). We conclude that a good seeding prescription is to populate halos (a) of mass 7.5 < log (M_h/Msun) < 8, (b) in the redshift range 8 < z < 17, (c) with IMBH in the mass range 4.75 < log (M_BH/Msun) < 6.25.Comment: MNRAS, in press. Comments welcom

    Pragas ocasionais em lavouras de soja no Rio Grande do Sul.

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    bitstream/CNPT-2010/40709/1/p-do91.pd

    Dissecting the Pharmacodynamics and Pharmacokinetics of MSCs to Overcome Limitations in Their Clinical Translation

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    Recently, mesenchymal stromal stem cells (MSCs) have been proposed as therapeutic agents because of their promising preclinical features and good safety profile. However, their introduction into clinical practice has been associated with a suboptimal therapeutic profile. In this review, we address the biodistribution of MSCs in preclinical studies with a focus on the current understanding of the pharmacodynamics (PD) and pharmacokinetics (PK) of MSCs as key aspects to overcome unsatisfactory clinical benefits of MSC application. Beginning with evidence of MSC biodistribution and highlighting PK and PD factors, a new PK-PD model is also proposed. According to this theory, MSCs and their released factors are key players in PK, and the efficacy biomarkers are considered relevant for PD in more predictive preclinical investigations. Accounting for the PK-PD relationship in MSC translational research and proposing new models combined with better biodistribution studies could allow realization of the promise of more robust MSC clinical translation. The number of clinical trials based on MSCs that are publicly available exceeds 800; however, data regarding MSC pharmacodynamics (PD), pharmacokinetics (PK), and biodistribution are still scarce. For this reason, we dissected the PD and PK properties of MSCs, presenting factors that may influence MSC-based PK studies to then conceive a new PK-PD model that would support better and more robust MSC clinical translation

    Improvement in the sustainability and stability of acrylic protective coatings for outdoor bronze artworks

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    Outdoor bronze artworks are an entrenched part of our urban landscape. They are usually covered by a patina resulting from their exposition to the environment. This patina plays an important aesthetic role and may provide some passivation on the surface, nonetheless it does not prevent the degradation processes promoted by external factors such as pollution, light and humidity. One of the strategies to slow down these unwanted processes is the application of protective coatings. The products currently available have some limitations due to the loss of effectiveness over time and poor environmental sustainability. With the aim of proposing more performing alternatives, coatings based on Paraloid (R) B44 modified with corrosion inhibitors and light stabilizers were prepared and characterized. Two non-toxic corrosion inhibitors were studied, 5-mercapto-1-pheniltetrazole (MPT) and 5-ethyl-1,3,4-thiadiazol-2-amine (AEDTA), comparing them with the traditional benzotriazole (BTA). The approach used aimed to identify the blend providing the most stable coatings. The chemical and physical properties of the coatings, such as colour, solubility, glass transition and composition, were studied and monitored over time. All coatings have shown adequate visual properties; however, corrosion inhibitors degrade some other properties of the coatings and need to be used in conjunction with light stabilizers. The permanence of corrosion inhibitors in the coatings over time was also studied by investigating the role of the support. The establishment of specific interactions between inhibitors and the bronze surface lengthens their permanence in the coatings compared to what happens with inert supports. Especially for AEDTA, the inhibitor retention within the coating and at the coating-bronze interface is better than for BTA and MPT. The effect of each of the additives on the photooxidation stability of the coating was evaluated and the most promising inhibitor and stabilizer combination was identified

    Distorted Copulas: Constructions and Tail Dependence

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    Given a copula C, we examine under which conditions on an order isomorphism ψ of [0, 1] the distortion C ψ: [0, 1]2 → [0, 1], C ψ(x, y) = ψ{C[ψ−1(x), ψ−1(y)]} is again a copula. In particular, when the copula C is totally positive of order 2, we give a sufficient condition on ψ that ensures that any distortion of C by means of ψ is again a copula. The presented results allow us to introduce in a more flexible way families of copulas exhibiting different behavior in the tails

    Colour and chemical stability of bismuth oxide in dental materials with solutions used in routine clinical practice

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    Bismuth(III) oxide is included as a radio-opacifier in dental materials, including hydraulic silicate cements, the material of choice for several endodontic procedures. It has been implicated in tooth discoloration after contact with endodontic irrigants, in particular NaOCl solution, To date, there has been no work on the chemistry: all reports have been of clinical findings only. The purpose now was to report the reactions leading to colour change from Bi2O3 in contact with solutions used in routine endodontic practice. Ten-gram portions of Bi2O3 were immersed in either water, NaOH, NaCl, NaOCl or HCl solution, either in the dark or exposed to visible light, and samples retrieved at 1, 4, 12 and 24 weeks. After washing, these were exposed to either added CO2 or not, for 1 week while drying, and under the same dark or light conditions. Changes in appearance were monitored by photography and colour measurement, and chemically by X-ray diffraction and Fourier-transform infrared spectroscopy. 24-week material was studied using electron paramagnetic resonance and Raman spectroscopy; NaOCl-treated material was also examined by scanning electron microscopy. With water, NaCl and NaOH, bismuth subcarbonate was formed. With or without added carbon dioxide, discoloration occurred from pale yellow to light brown when exposed to light, and to a lesser extent in the dark, intensifying with time. In contrast, exposure to NaOCl rapidly formed a dark brown-black sodium bismuthate. With HCl, white BiOCl was formed. Bi2O3 is not at all inert in this context as is commonly believed, denying its principle of use. Previously unreported solution-mediated reaction occurs readily even in water and NaCl solution, forming new compounds that discolour. In contact with NaOCl sodium bismuthate is formed; severe darkening occurs rapidly. The reactivity is such that Bi2O3 is not indicated for dental materials and should be withdrawn from use
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