Nuclear microprobe: the tool to characterize new materials for energy conversion [Poster]

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On the reuse of SLS Polyamide 12 powder

In the Selective Laser Sintering (SLS) technique, the great majority of the powder involved is not included in the final printed parts, being just used as a support material. However, the quality of this powder is negatively affected during the process since it is subjected to high temperatures (close to its melting temperature) during a long time, i.e., the printing cycle time, especially in the neighborhood of the printed part contour. This type of powder is relatively expensive and large amounts of used powder result after each printing cycle. The present paper focuses on the reuse of Polyamide 12 (PA 12) powder. For this sake, the same PA 12 powder was used in consecutive printing cycles. After each cycle, the remaining non-used powder was milled and filtered before subsequent use. Properties of the powder and corresponding prints were characterized in each cycle, using differential scanning calorimetry (DSC), scanning electron microscopy (SEM), computed tomography (CT), and tensile tests. It was concluded that subjecting the same powder to multiple SLS printing cycles affects the properties of the printed parts essentially regarding their morphology (voids content), mechanical properties reproducibility, and aesthetical aspect. However, post-processing treatment of the powder enabled to maintain the mechanical performance of the prints during the first six printing cycles without the need to add virgin powder.O.S.C. acknowledges funding by National Funds through the FCT—Portuguese Foundation for Science and Technology, References UIDB/05256/2020 and UIDP/05256/2020. A.C.A. acknowledges the partial support of the Portuguese Foundation for Science and Technology (FCT), Portugal, under the UIDB/04436/2020 project

Catastrophizing and Risk-Taking

Background: Catastrophizing, when an individual overestimates the probability of a severe negative outcome, is related to various aspects of mental ill-health. Here, we further characterize catastrophizing by investigating the extent to which self-reported catastrophizing is associated with risk-taking, using an online behavioural task and computational modelling. Methods: We performed two online studies: a pilot study (n = 69) and a main study (n = 263). In the pilot study, participants performed the Balloon Analogue Risk Task (BART), alongside two other tasks (reported in the Supplement), and completed mental health questionnaires. Based on the findings from the pilot, we explored risk-taking in more detail in the main study using two versions of the Balloon Analogue Risk task (BART), with either a high or low cost for bursting the balloon. Results: In the main study, there was a significant negative relationship between self-report catastrophizing scores and risk-taking in the low (but not high) cost version of the BART. Computational modelling of the BART task revealed no relationship between any parameter and Catastrophizing scores in either version of the task. Conclusions: We show that increased self-reported catastrophizing may be associated with reduced behavioural measures of risk-taking, but were unable to identify a computational correlate of this effect

Electrochemical response of Ti joints vacuum brazed with TiCuNi, AgCu, and Ag fillers

The properties of the joints are dictated by the nature, distribution, and morphology of the phases formed at the interface. The mechanical properties of brazed joints are well documented in the literature, contrarily to their electrochemical behaviour. Thus, the main objective of this study was to understand the influence of the phases formed at the interface on the corrosion behaviour of commercially pure Ti brazed joints, produced by using TiCuNi, eutectic AgCu, and Ag filler foils. The electrochemical behaviour of the Ti joints was accessed by open circuit potential and potentiodynamic polarization tests in phosphate buffer saline solution electrolyte at body temperature. Results showed that Ag-based fillers induced susceptibility to micro-galvanic corrosion between the Ag-rich and Ti phases formed at the interface and commercially pure Ti base metal. However, no significant differences were observed between the joint system and the base material when brazing with TiCuNi filler.This work was supported by Portuguese FCT, under the reference project UIDB/04436/2020 and M-ERA-NET/0001/2015 project. The authors would also like to acknowledge A. I. COSTA for her help on the experimental studies

Microscopy techniques for dye distribution in DSCs nanocrystalline TiO2 films

Capture of sunlight has attracted an increasing interest in the scientific community and triggered the development of efficient and cheap photovoltaic devices. Amongst recent generation technologies for solar energy conversion, dye-sensitized solar cells (DSCs) show an optimal trade-off between high-conversion efficiency and low-cost manufacturing. For the last two decades, significant progress has been made and best energy conversion efficiency of the DSC at the laboratory scale has surpassed 12% [1]. A lot of work has focused on the enlargement of surface areas to enhance the amount of adsorbed dyes by reduction of nanoparticle sizes or utilization of novel structures. Nevertheless there remain some crucial details of DSC operation for which limited information is available, namely dye diffusion and adsorption, surface coverage and dye distribution throughout the nc-TiO2 film. Microprobe techniques can be powerful tools to evaluate the dye load, the dye distribution and dye depth profile in sensitized films. Electron Probe Microanalysis (EPMA) and Ion Beam Analytical (IBA) techniques using a micro-ion beam, namely micro-Particle Induced X-ray Emission ( PIXE) and Rutherford Backscattering Spectrometry (RBS), were used to quantify and to study the distribution of the ruthenium organometallic (N719) dye in TiO2 films, profiting from the different penetration depth and beam sizes of each technique. Two different types of films were prepared and sensitized, mesoporous nanoparticles and 1D nanostructured TiO2 films (figure 1). Despite the low concentration of Ru, the high sensitive analytical techniques used allowed to assess the Ru surface distribution and depth profile. Fig. 2 shows the PIXE maps of Ru and Ti indicating an homogeneous surface distribution. The same figure presents the RBS spectra obtained with a 2 MeV proton beam of the same sample showing that a good spectra fit is obtained considering only two sample layers: the first one with a 1.7 ìm thickness; the second one being the SiO2 substrate. The Ru RBS signal also shows that the dye has an homogeneous depth distribution. Due to the fine spatial resolution of the EPMA/WDS (Wavelength Dispersive Spectroscopy) technique it was possible to visualise the dye distribution in sample cross-section (with micrometer or submicrometer dimensions) as presented in Fig. 3 for the elemental mapping of a mesoporous nanoparticle TiO2 film. Dye load evaluation by two different techniques (ìPIXE and EPMA/WDS) provided similar results (Ru/Ti values around 0.5 %). The distribution analysis of the organometallic dye (N719) was done through ruthenium distribution via X-ray mapping. RBS was used to assess the ruthenium depth profile. This assessment can lead to a better understanding of the device performance

Dye assessment in nanostructured TiO2 sensitized films by microprobe techniques

Dye sensitized solar cells (DSCs) have received considerable attention once this technology offers economic and environmental advantages over conventional photovoltaic (PV) devices. The PV performance of a DSC relies on the characteristics of its photoanode, which typically consists of a nanocrystalline porous TiO2 film, enabled with a large adsorptive surface area. Dye molecules that capture photons from light during device operation are attached to the film nanoparticles. The effective loading of the dye in the TiO2 electrode is of utmost importance for controlling and optimizing solar cell parameters. Relatively few methods are known today for quantitative evaluation of the total dye adsorbed on the film. In this work, a new approach combining microprobe techniques namely, Ion Beam Analytical (IBA) techniques using a micro-ion beam (Rutherford Backscattering Spectrometry (RBS) and Particle Induced X-ray Emission (PIXE)) and Electron Probe Micro-Analysis (EPMA) was carried out to assess dye distribution and depth profile in TiO2 films and the dye load based on Ru/Ti mass ratio. Different 1D nanostructured TiO2 films were prepared, morphologically characterised by SEM, sensitized and analysed by the referred techniques. Dye load evaluation in different TiO2 films by three different techniques (PIXE, RBS and EPMA/ wavelength dispersive spectrometry (WDS)) provided similar results of Ru/Ti mass fraction ratio. Moreover, it was possible to assess dye surface distribution and its depth profile, by means of Ru signal, and to visualise the dye distribution in sample cross-section through X-ray mapping by EPMA/ energy dispersive spectrometry (EDS). PIXE maps of Ru and Ti indicated an homogeneous surface distribution. The assessment of ruthenium depth profile by RBS showed that some films have homogeneous Ru depth distribution while others present different Ru concentration in the top layer (2 ìm thickness). These results are consistent with the EPMA/EDS maps obtained. EPMA (WDS and EDS) together with IBA techniques proved to be powerful tools for functional materials characterisation and provided very promising results in the study of nanostructured TiO2 sensitized films

Assessment of dye distribution in sensitized solar cells by microprobe techniques

Dye sensitized solar cells (DSCs) have received considerable attention once this technology offers economic and environmental advantages over conventional photovoltaic (PV) devices. The PV performance of a DSC relies on the characteristics of its photoanode, which typically consists of a nanocrystalline porous TiO2 film, enabled with a large adsorptive surface area. Dye molecules that capture photons from light during device operation are attached to the film nanoparticles. The effective loading of the dye in the TiO2 electrode is of paramount relevance for controlling and optimizing solar cell parameters. Relatively few methods are known today for quantitative evaluation of the total dye adsorbed on the film. In this context, microprobe techniques come out as suitable tools to evaluate the dye surface distribution and depth profile in sensitized films. Electron Probe Microanalysis (EPMA) and Ion Beam Analytical (IBA) techniques using a micro-ion beam were used to quantify and to study the distribution of the Ru organometallic dye in TiO2 films, making use of the different penetration depth and beam sizes of each technique. Different 1D nanostructured TiO2 films were prepared, morphologically characterized by SEM, sensitized and analyzed by the referred techniques. Dye load evaluation in different TiO2 films by three different techniques (PIXE, RBS and EPMA/WDS) provided similar results of Ru/Ti mass fraction ratio. Moreover, it was possible to assess dye surface distribution and its depth profile, by means of Ru signal, and to visualize the dye distribution in sample cross-section through X-ray mapping by EPMA/EDS. PIXE maps of Ru and Ti indicated an homogeneous surface distribution. The assessment of Ru depth profile by RBS showed that some films have homogeneous Ru depth distribution while others present different Ru concentration in the top layer (2 lm thickness). These results are consistent with the EPMA/EDS maps obtained

Molecular epidemiology of Clostridioides difficile in companion animals: Genetic overlap with human strains and public health concerns

Research Areas: Public, Environmental & Occupational HealthIntroduction: The changing epidemiology of Clostridioides difficile reflects a well-established and intricate community transmission network. With rising numbers of reported community-acquired infections, recent studies tried to identify the role played by non-human reservoirs in the pathogen's transmission chain. This study aimed at describing the C. difficile strains circulating in canine and feline populations, and to evaluate their genetic overlap with human strains to assess the possibility of interspecies transmission. Methods: Fecal samples from dogs (n = 335) and cats (n = 140) were collected from two populations (group A and group B) in Portugal. C. difficile isolates were characterized for toxigenic profile and PCR-ribotyping. The presence of genetic determinants of antimicrobial resistance was assessed in all phenotypically resistant isolates. To evaluate the genetic overlap between companion animals and human isolates from Portugal, RT106 (n = 42) and RT014/020 (n = 41) strains from both sources were subjected to whole genome sequencing and integrated with previously sequenced RT106 (n = 43) and RT014/020 (n = 142) genomes from different countries. The genetic overlap was assessed based on core-single nucleotide polymorphism (SNP) using a threshold of 2 SNP. ResultsThe overall positivity rate for C. difficile was 26% (76/292) in group A and 18.6% (34/183) in group B. Toxigenic strains accounted for 50% (38/76) and 52.9% (18/34) of animal carriage rates, respectively. The most prevalent ribotypes (RT) were the toxigenic RT106 and RT014/020, and the non-toxigenic RT010 and RT009. Antimicrobial resistance was found for clindamycin (27.9%), metronidazole (17.1%) and moxifloxacin (12.4%), associated with the presence of the ermB gene, the pCD-METRO plasmid and point mutations in the gyrA gene, respectively. Both RT106 and RT014/020 genetic analysis revealed several clusters integrating isolates from animal and human sources, supporting the possibility of clonal interspecies transmission or a shared environmental contamination source. Discussion: This study shows that companion animals may constitute a source of infection of toxigenic and antimicrobial resistant human associated C. difficile isolates. Additionally, it contributes with important data on the genetic proximity between C. difficile isolates from both sources, adding new information to guide future work on the role of animal reservoirs in the establishment of community associated transmission networks and alerting for potential public health risk.info:eu-repo/semantics/publishedVersio

Antimicrobial activities of highly bioavailable organic salts and ionic liquids from fluoroquinolones

As the development of novel antibiotics has been at a halt for several decades, chemically enhancing existing drugs is a very promising approach to drug development. Herein, we report the preparation of twelve organic salts and ionic liquids (OSILs) from ciprofloxacin and norfloxacin as anions with enhanced antimicrobial activity. Each one of the fluoroquinolones (FQs) was combined with six di erent organic hydroxide cations in 93–100% yield through a bu er-assisted neutralization methodology. Six of those were isomorphous salts while the remaining six were ionic liquids, with four of them being room temperature ionic liquids. The prepared compounds were not toxic to healthy cell lines and displayed between 47- and 1416-fold more solubility in water at 25 and 37 C than the original drugs, with the exception of the ones containing the cetylpyridinium cation. In general, the antimicrobial activity against Klebsiella pneumoniae was particularly enhanced for the ciprofloxacin-based OSILs, with up to ca. 20-fold decreases of the inhibitory concentrations in relation to the parent drug, while activity against Staphylococcus aureus and the commensal Bacillus subtilis strain was often reduced. Depending on the cation–drug combination, broad-spectrum or strain-specific antibiotic salts were achieved, potentially leading to the future development of highly bioavailable and safe antimicrobial ionic formulations.info:eu-repo/semantics/publishedVersio

Effect of bio-functional MAO layers on the electrochemical behaviour of highly porous Ti

Ti foams are attractive for orthopaedic applications due to reduced Young's modulus and ability of bone ingrowth. However, poor corrosion behaviour and lack of bioactivity are yet to be overcome. In the present work, highly porous Ti samples were processed by powder metallurgy with space holder technique and bio-functionalized by micro-arc oxidation, resulting in nano/micro structured TiO2 surfaces containing bioactive elements. The electrochemical behaviour of these bio-functionalized highly porous Ti surfaces was evaluated through potentiodynamic polarization and EIS in physiological solution at body temperature. Results showed that bio-functionalization improved the corrosion behaviour of highly porous Ti. However, increased macro-porosity led to an increased corrosion rate.This work is supported by FCT with the reference project UID/EEA/04436/2019, M-ERA NET/0001/2015 project, and Programa de Accoes Universitarias Integradas Luso-Francesas' (PAUILF TC-12_14). CQE is financed by FCT under Pluriannual contract 2020-2023. The authors also gratefully acknowledge the "Investissements d'avenir" programs (nos. ANR-11-IDEX-0003-02 and ANR-10-EQPX-37 MATMECA Grant) for financial support on Micro-CT analysis