Nonmonotonic Evolution of the Blocking Temperature in Dispersions of Superparamagnetic Nanoparticles

We use a Monte Carlo approach to simulate the influence of the dipolar interaction on assemblies of monodisperse superparamagnetic ${\gamma}-Fe_{2}O_{3}$ nanoparticles. We have identified a critical concentration c*, that marks the transition between two different regimes in the evolution of the blocking temperature ($T_{B}$) with interparticle interactions. At low concentrations (c < c*) magnetic particles behave as an ideal non-interacting system with a constant $T_{B}$. At concentrations c > c* the dipolar energy enhances the anisotropic energy barrier and $T_{B}$ increases with increasing c, so that a larger temperature is required to reach the superparamagnetic state. The fitting of our results with classical particle models and experiments supports the existence of two differentiated regimes. Our data could help to understand apparently contradictory results from the literature.Comment: 13 pages, 7 figure

Conference report: The 13th Congress of the International Society of Developmental and Comparative Immunology

9 páginas.-- L. Courtney Smith ... et al.The 13th Congress of the International Society of Developmental and Comparative Immunology took place in Murcia Spain from June 28 to July 3, 2015 at the Victor Villegas Auditorium and Convention Center. There were two or three parallel sessions during the Congress that covered a wide range of immunological topics and brought researchers together from around the world who work in different areas of immunology. The Congress included three plenary presentations, 12 oral sessions, two poster sessions, and a special symposium. Here we report on some of the talks and a few of the posters that were presented at the meetingFunding from the US National Science Foundation (IOS-1461716) awarded to LCS and Louise Rollins-Smith (Vanderbilt University, USA) supported students and postdocs from laboratories in the US to attend the 13th Congress of ISDCIPeer reviewe

Understanding the Absorption of Fluorinated Gases in Fluorinated Ionic Liquids for Recovering Purposes Using Soft-SAFT

2020.00835.CEEIND 2021.01432.CEECIND RC2-2019-007It is proven that fluorinated gases (F-gases) have a vast impact on climate change due to their high global warming potential. Hence, it is imperative to search for new molecules to replace them in current applications, as well as technologies to capture, recover, and recycle F-gases to avoid their emissions to the atmosphere. One of the attractive technologies for this purpose is to absorb them in fluorinated ionic liquids (FILs), given their solubilization power. However, the complexity of FILs and the time-consuming experimental methodologies to fully characterize them hinder their prompt usage in this urgent field. In this work, the soft-Statistical Associating Fluid Theory (soft-SAFT) Equation of State is used as a tool to investigate the solubility of six different F-gases (R-32, R-125, R-134a, R-14, R-116, R-218) in five FILs ([C2C1Im][C4F9SO3], [C2C1Im][C4F9CO2], [C2C1py][C4F9SO3], [C2(C6F13)C1Im][N(CF3SO2)2], and [C2(C6F13)C1Im][N(C2F5SO2)2]). The robustness of the soft-SAFT approach allowed the establishment of new FIL models in a simple and fast way, and the calculation of F-gases solubility in them, in excellent agreement with existing experimental data. Once the models were assessed, a systematic study was performed regarding the structural features of FILs favoring their performance to absorb F-gases by using the soft-SAFT approach as a screening tool. It has been obtained that the solubility is favored by the presence of a perfluoroalkyl chain in the imidazolium cation, together with a bulkier anion. In all cases, [C2(C6F13)C1Im][N(C2F5SO2)2] shows a superior solubility of F-gases than the [C2(C6F13)C1Im][N(CF3SO2)2], also indicating that the addition of one carbon to the two anionic symmetric fluorinated chains contributes to the gas-philicity of the FILs. This work proves the relevance of using the soft-SAFT framework to obtain insights into the behavior of such complex systems and key trends, even when experimental data are scarce, as a step forward in assessing systems for separating and recovering F-gases.publishersversioninpres

Berezinskii-Kosterlitz-Thouless Transition in Heavy Fermion Superlattices

We propose an explanation of the superconducting transitions discovered in the heavy fermion superlattices by Mizukami et al. (Nature Physics 7, 849 (2011)) in terms of Berezinskii-Kosterlitz-Thouless transition. We observe that the effective mass mismatch between the heavy fermion superconductor and the normal metal regions provides an effective barrier that enables quasi 2D superconductivity in such systems. We show that the resistivity data, both with and without magnetic field, are consistent with BKT transition. Furthermore, we study the influence of a nearby magnetic quantum critical point on the vortex system, and find that the vortex core energy can be significantly reduced due to magnetic fluctuations. Further reduction of the gap with decreasing number of layers is understood as a result of pair breaking effect of Yb ions at the interface.Comment: 7 pages, 6 figure

Calculations of giant magnetoresistance in Fe/Cr trilayers using layer potentials determined from {\it ab-initio} methods

The ab initio full-potential linearized augmented plane-wave method explicitly designed for the slab geometry was employed to elucidate the physical origin of the layer potentials for the trilayers nFe/3Cr/nFe(001), where n is the number of Fe monolayers. The thickness of the transition-metal ferromagnet has been ranged from $n=1$ up to n=8 while the spacer thickness was fixed to 3 monolayers. The calculated potentials were inserted in the Fuchs-Sondheimer formalism in order to calculate the giant magnetoresistance (GMR) ratio. The predicted GMR ratio was compared with the experiment and the oscillatory behavior of the GMR as a function of the ferromagnetic layer thickness was discussed in the context of the layer potentials. The reported results confirm that the interface monolayers play a dominant role in the intrinsic GMR.Comment: 17 pages, 7 figures, 3 tables. accepted in J. Phys.: Cond. Matte

Unveiling the Influence of Non-Toxic Fluorinated Ionic Liquids Aqueous Solutions in the Encapsulation and Stability of Lysozyme

Proteins are bioactive compounds with high potential to be applied in the biopharmaceutical industry, food science and as biocatalysts. However, protein stability is very difficult to maintain outside of the native environment, which hinders their applications. Fluorinated ionic liquids (FILs) are a promising family of surface-active ionic liquids (SAILs) that have an amphiphilic behavior and the ability to self-aggregate in aqueous solutions by the formation of colloidal systems. In this work, the protein lysozyme was selected to infer on the influence of FILs in its stability and activity. Then, the cytotoxicity of FILs was determined to evaluate their biocompatibility, concluding that the selected compounds have neglected cytotoxicity. Therefore, UV–visible spectroscopy was used to infer the FIL-lysozyme interactions, concluding that the predominant interaction is the encapsulation of the lysozyme by FILs. The encapsulation efficiency was also tested, which highly depends on the concentration and anion of FIL. Finally, the bioactivity and thermal stability of lysozyme were evaluated, and the encapsulated lysozyme keeps its activity and thermal stability, concluding that FILs can be a potential stabilizer to be used in protein-based delivery systems.publishersversionpublishe

Functionalization of fluorinated ionic liquids: A combined experimental-theoretical study

FCT/MCTES (Portugal), through: grant SFRH/BD/130965/2017 (M.LF.); Investigador FCT 2014 (IF/00190/2014 to A.B.P. and IF/00210/2014 to J.M.M.A.); projects PTDC/EQU-EQU/29737/2017, PTDC/QEQ-FTT/3289/2014 and IF/00210/2014/CP1244/CT0003. Associate Laboratory for Green Chemistry-LAQV, financed by national funds from FCT/MCTES (UID/QUI/50006/2019). projects 2018-LC-01 and 2019-URL-IR1rQ-011, from Obra Social "la Caixa" and by Khalifa University through project RCII-2018-0024.We present new experimental and modelling data concerning imidazolium based-FILs synthesized with a hydroxyl group in the end of the cationic hydrogenated side chain and compared them with the analogous non-functionalized FILs in order to verify their suitability in the biomedical field. The thermophysical and thermodynamic properties of the neat compounds and the self-aggregation behaviour of FILs in aqueous solutions were measured and compared with theoretical results from the soft-SAFT equation of state, in good agreement with each other. Results showed that the presence of the hydroxyl group increases the density and viscosity of pure compounds and aqueous mixtures, whereas the thermal stability, melting, free volume, ionicity and self-aggregation behaviour decrease. These properties are improved with respect to the conventional perfluorosurfactants for the desired application, due to the full miscibility in water and the promising improved biocompatibility.authorsversionpublishe

Human mesenchymal stem cells response to multi-doped silicon-strontium calcium phosphate coatings

The search for apatitic calcium phosphate coatings to improve implants osteointegration is, nowadays, preferentially focused in the obtaining of compositions closer to that of the inorganic phase of bone. Silicon and strontium are both present in trace concentrations in natural bone and have been demonstrated, by separate, to significantly improve osteoblastic response on calcium phosphate bioceramics. This work aims the controlled and simultaneous multidoping of carbonated calcium phosphate coatings with both elements, Si and Sr, by pulsed laser deposition technique and the biological response of human mesenchymal stem cells to them. A complete physicochemical characterization has been also performed to analyze the coatings and significant positive effect was obtained at the osteogenic differentiation of cells, confirming the enormous potential of this multi-doping coating approach.Technical staff of CACTI (University of Vigo) is gratefully acknowledged. This work was partially supported by the UE-POCTEP 0330IBEROMARE1P project, UE-INTERREG 2011-1/164MARMED and Ministerio de Ciencia e Innovacion (Project MAT2010-18281). M Lopez-Alvarez thanks funding support from FP7/REGPOT-2012-2013.1 (no 316265, BIOCAPS)