Vertical (La,Sr)MnO3 Nanorods from Track‐Etched Polymers Directly Buffering Substrates

A novel and general methodology for preparing vertical, complex‐oxide nanostructures from a sol–gel‐based polymer‐precursor solutions is developed using track‐etched polymers directly buffering substrates. This method is able to develop a nanostructure over the entire substrate, the dimensions and localization of the vertical nanostructures being preset by the polymeric nanotemplate. Thereby, nanostructures with lateral sizes in the range of 100 to 300 nm and up to 500 nm in height have been grown. Two examples are presented herein, the latter being the evolution of the initial, metastable nanostructure. Specifically, La_0.7Sr_0.3MnO₃ polycrystalline rods are grown at mild temperatures (800 °C); upon strong thermal activation (1000 °C) they suffer a profound transformation into vertical, single‐crystalline (La,Sr)_xO_y nanopyramids sitting on a La_0.7Sr_0.3MnO₃ epitaxial wetting layer. The driving force for this outstanding nanostructural evolution is the minimization of the total energy of the system, which is reached by reducing the grain‐boundary, total‐surface, and strain‐relaxation energies. Finally, advanced electron‐microscopy techniques are used to highlight the complex phase separation and structural transformations occurring when the metastable state is overcome.     

Calcium–Alginate–Inulin Microbeads as Carriers for Aqueous Carqueja Extract

Carqueja (Pterospartum tridentatum) is an endemic species and various bioactive compounds have been identified in its aqueous extract. The aim of this study was to protect the natural antioxidants from the aqueous extract of carqueja by encapsulation in Ca–alginate microbeads and Ca–alginate microbeads containing 10% and 20% (w/v) of inulin. The microbeads produced by electrostatic extrusion technique had an average diameter from 625 μm to 830 μm depending on the portion of inulin. The sphericity factor of the hydrogel microbeads had values between 0.014 and 0.026, while freeze dried microbeads had irregular shape, especially those with no excipient. The reduction in microbeads size after freeze drying process (expressed as shrinkage factor) ranged from 0.338 (alginate microbeads with 20% (w/v) of inulin) to 0.523 (plain alginate microbeads). The expressed radical scavenging activity against ABTS and DPPH radicals was found to be between 30% and 40% for encapsulated extract, while the fresh extract showed around 47% and 57% of radical scavenging activity for ABTS and DPPH radicals, respectively. The correlation between antioxidant activity and the total phenolic content were found to be positive (in both assay methods, DPPH and ABTS), which indicate that the addition of inulin didn't have influence on antioxidant activity. The presence of inulin reduced stiffness of the hydrogel, and protected bead structure from collapse upon freeze‐drying. Alginate–inulin beads are envisaged to be used for delivery of aqueous P. tridentatum extract in functional food products.     

Ultrasound as a probe of dislocation density in aluminum

Dislocations are at the heart of the plastic behavior of crystalline materials yet it is notoriously difficult to perform quantitative, non-intrusive measurements of their single or collective properties. Dislocation density is a critical variable that determines dislocation mobility, strength and ductility. On the one hand, individual dislocations can be probed in detail with transmission electron microscopy. On the other hand, their collective properties must be simulated numerically. Here we show that ultrasound technology can be used to measure dislocation density. This development rests on theory—a generalization of the Granato–Lücke theory for the interaction of elastic waves with dislocations—and resonant ultrasound spectroscopy (RUS) measurements. The chosen material is aluminum, to which different dislocation contents were induced through annealing and cold-rolling processes. The dislocation densities obtained with RUS compare favorably with those inferred from X-ray diffraction, using the modified Williamson–Hall method.     

Copper manganite as a catalyst for the PROX reaction. Deactivation studies

CuMn₂O₄ nanocatalysts synthesised by silica aquagel confined co-precipitation were analysed for the preferential oxidation of CO at different temperatures and concentration conditions. The catalysts show a higher activity than copper–ceria catalysts synthesised by the same method but, like these, they suffer from slow deactivation during the reaction. Surface analysis (FTIR and XPS) was used to unravel the deactivation mechanisms. Gradual reduction of the catalysts by the carbon monoxide present in the PROX stream was concluded to be the main cause of deactivation.     

Diffusion bonding of TiAl using Ni/Al multilayers

With the stimulus of temperature and pressure Ni and Al can quickly react and produce the intermetallic compound NiAl. This reaction is highly exothermic and high temperatures can be attained in the surroundings. These characteristics make Ni/Al multilayers very attractive to technological applications as localised heat sources. In this study, Ni/Al multilayer thin films are used to promote bonding between TiAl intermetallic alloys. Ni and Al alternated nanolayers were deposited by d.c. magnetron sputtering onto TiAl samples, with periods of 5, 14 and 30 nm. Joining experiments were performed at 900 °C for 60 or 30 min, in a vertical furnace with a vacuum level better than 10⁻² Pa. Applied pressures of 5 MPa were tested. The microstructure of the cross-sections of the bond interface was analysed by energy dispersive X-ray spectroscopy and characterised by scanning electron microscopy. The observation of the microstructure for 14 and 30 nm period multilayers revealed sound bonding, while for 5 nm period porosity and cracks within the interlayer thin film were observed. The interface is divided into three distinct zones: one with columnar grains, another with very small equiaxed grains and the third with larger equiaxed grains. The joining process appears to depend on the diffusion of Ni and Ti across the interface and is assisted by the nucleation of nanometric grains at the interface. The mechanical strength of the joints was evaluated by shear tests. The bonds produced at 900 °C/5 MPa/60 min/14 nm exhibited the highest shear strength of 314 MPa.     

Characteristics of a refuge for native freshwater mussels (Bivalvia: Unionidae) in Lake St. Clair

The Lake St. Clair delta (∼ 100 km²) provides an important refuge for native freshwater mussels (Unionidae) wherein 22 of the ∼ 35 historical species co-occur with invasive dreissenids. A total of 1875 live unionids representing 22 species were found during snorkeling surveys of 32 shallow (∼ 1 m) sites throughout the delta. Richness and density of unionids and zebra mussel infestation rates varied among sites from 3 to 13 unionid species, 0.02 to 0.12 unionids/m², and < 1 to 35 zebra mussels/unionid, respectively. Zebra mussel infestation of unionids in the delta appears to be mitigated by dominant offshore currents, which limit densities of zebra mussel veligers in nearshore compared to offshore waters (13,600 vs. 28,000/m³, respectively). Glycogen concentrations in the tissues of a common and widespread species in the delta (Lampsilis siliquoidea) suggest that zebra mussels may be adversely affecting physiological condition of unionids in a portion of the Lake St. Clair delta. Physiological condition and community structure of unionids within the delta may also be influenced by differences in food quantity and quality resulting from the uneven distribution of water flowing from the St. Clair River. The delta likely supports the largest living unionid community in the lower Great Lakes and includes several species that have been listed as Endangered or Threatened in Canada and/or the state of Michigan, making it an important refuge for the conservation of native unionids.     

Cognitive Deficit in Schizophrenia: From Etiology to Novel Treatments

Schizophrenia is a major mental illness characterized by positive and negative symptoms, and by cognitive deficit. Although cognitive impairment is disabling for patients, it has been largely neglected in the treatment of schizophrenia. There are several reasons for this lack of treatments for cognitive deficit, but the complexity of its etiology—in which neuroanatomic, biochemical and genetic factors concur—has contributed to the lack of effective treatments. In the last few years, there have been several attempts to develop novel drugs for the treatment of cognitive impairment in schizophrenia. Despite these efforts, little progress has been made. The latest findings point to the importance of developing personalized treatments for schizophrenia which enhance neuroplasticity, and of combining pharmacological treatments with non-pharmacological measures.     

Ammonia chemistry in oxy-fuel combustion of methane

The oxidation of NH₃ during oxy-fuel combustion of methane, i.e., at high [CO₂], has been studied in a flow reactor. The experiments covered stoichiometries ranging from fuel rich to very fuel lean and temperatures from 973 to 1773 K. The results have been interpreted in terms of an updated detailed chemical kinetic model. A high CO₂ level enhanced formation of NO under reducing conditions while it inhibited NO under stoichiometric and lean conditions. The detailed chemical kinetic model captured fairly well all the experimental trends. According to the present study, the enhanced CO concentrations and alteration in the amount and partitioning of O/H radicals, rather than direct reactions between N-radicals and CO₂, are responsible for the effect of a high CO₂ concentration on ammonia conversion. When CO₂ is present as a bulk gas, formation of NO is facilitated by the increased OH/H ratio. Besides, the high CO levels enhance HNCO formation through NH₂+CO. However, reactions NH₂+O to form HNO and NH₂+H to form NH are inhibited due to the reduced concentration of O and H radicals. Instead reactions of NH₂ with species from the hydrocarbon/methylamine pool preserve reactive nitrogen as reduced species. These reactions reduce the NH₂ availability to form NO by other pathways like via HNO or NH and increase the probability of forming N₂ instead of NO.