Phase equilibria in the binary rare-earth alloys: The erbium-magnesium system

The Er-Mg system was examined using differential thermal analysis (DTA), X-ray examination, metallography, and microprobe analysis. Four intermediate phases are found to exist, and their crystal structures have been confirmed or determined as the following:β phase (≈Er₂Mg) (cubic, cI2-W type, peritectic formation 1255 °C); ErMg (cubic, cP2-CsCl type, peritectic formation 830 °C); ErMg₂ (hexagonal, hP12-MgZn₂ type, peritectic formation 670 °C); and Er₅Mg₂₄ (cubic, cI58-α-Mn type, peritectic formation 600 °C). Theβ phase undergoes a eutectoidal decomposition at 680 °C and 30.5 at. pct Mg. A eutectic reaction was observed to occur at 570 °C and 89.5 at. pct Mg. Comparisons of the general properties between the ErMg phases and with those of the other R-Mg compounds (R = rare earth) are briefly discussed. Properties and structures of the R-Mg, R-rich alloys are specially considered and compared with those of a few groups of rare-earth alloys. The alloying behavior of R-rich R-Me alloys (R = Ho, Er, Tm, Lu; Me = Mg, Cd, In, Tl) is systematically presented and/or predicted.     

On the applicability of the load separation criterion in determining the fracture resistance (<Emphasis Type="Italic">J</Emphasis><Subscript>Ic</Subscript>) of ductile polymers at low and high loading rates

In this work, the applicability of a procedure based on the load separation criterion in determining the fracture resistance (J _Ic) of a rubber modified polyamide 66 (PA66) was analyzed and discussed. In particular, the effects of the testing conditions, with particular reference to geometry and loading rate, on the applicability of the method were investigated. The tests were performed both at low (from 0.5 to 50 mm/min) and moderately high (0.6 m/s) loading rates, on single edge notched in bending specimens with different initial crack length to width ratios (a ₀/W), which ranged between 0.3 and 0.7. Among the various findings it is worthwhile to point out that this analysis revealed that the plastic displacement at the end of the blunting process (at fracture initiation) resulted geometry independent. A clear dependence of such a parameter on the loading rate was observed. Further, it was shown that load separation is maintained beyond the blunting phase, as observed in the experiments carried out at low rate.     

Fabric evolution and strain localisation in inherently anisotropic specimens of anisometric particles (lentils) under triaxial compression

Granular Matter - Engineered granular materials have gained considerable interest in recent years. For this substance, the primary design variable is grain shape. Optimizing grain form to achieve a...     

Nanographene-Based Decoration as a Panchromatic Antenna for Metalloporphyrin Conjugates

Porphyrins, a type of heterocyclic aromatic compounds consisting of tetrapyrroles connected by four substituted methine groups, are appealing building blocks for solar energy applications. However, their photosensitization capability is limited by their large optical energy gap, which results in a mismatch in absorption toward efficient harvesting of the solar spectrum. Porphyrin π-extension by edge-fusing with nanographenes can be employed for narrowing their optical energy gap from 2.35 to 1.08 eV, enabling the development of porphyrin-based panchromatic dyes with an optimized energy onset for solar energy conversion in dye-sensitized solar fuel and solar cell configurations. By combining time-dependent density functional theory with fs transient absorption spectroscopy, it is found that the primary singlets, which are delocalized across the entire aromatic part, are transferred into metal centred triplets in only 1.2 ps; and subsequently, relax toward ligand-delocalized triplets. This observation implies that the decoration of the porphyrin moiety with nanographenes, while having a large impact on the absorption onset of the novel dye, promotes the formation of a ligand-centred lowest triplet state of large spatial extension, potentially interesting for boosting interactions with electron scavengers. These results reveal a design strategy for broadening the applicability of porphyrin-based dyes in optoelectronics.     

Immersive virtual reality and passive haptic interfaces to improve procedural learning in a formal training course for first responders

Virtual Reality - One key aspect for the safety and success of first responders’ operations is the compliance, during the intervention, with all the safety procedures and prescribed...     

On the Role of Temperature in the Depolymerization of PET by FAST-PETase: An Atomistic Point of View on Possible Active Site Pre-Organization and Substrate-Destabilization Effects

Enzyme FAST-PETase, recently obtained by a machine learning approach, can depolymerize poly(ethylene terephthalate) (PET), a synthetic resin employed in plastics and in clothing fibers. Therefore it represents a promising solution for the recycling of PET-based materials. In this study, a model of PET was adopted to describe the substrate, and all-atoms classical molecular dynamics (MD) simulations on apo- and substrate-bound FAST-PETase were carried out at 30 and 50 °C to provide atomistic details on the binding step of the catalytic cycle. Comparative analysis shed light on the interactions occurring between the FAST-PETase and 4PET at 50 °C, the optimal working conditions of the enzyme. Pre-organization of the enzyme active and binding sites has been highlighted, while MD simulations of FAST-PETase:4PET pointed out the occurrence of solvent-inaccessible conformations of the substrate promoted by the enzyme. Indeed, neither of these conformations was observed during MD simulations of the substrate alone in solution performed at 30, 50 and 150 °C. The analysis led us to propose that, at 50 °C, the FAST-PETase is pre-organized to bind the PET and that the interactions occurring in the binding site can promote a more reactive conformation of PET substrate, thus enhancing the catalytic activity of the enzyme.