The mechanical behaviour of aluminium foam structures in different loading conditions

The use of foam has the potential for energy absorption enhancement. Many types of materials can be produced in the form of foams, including metals and polymers. Of the metallic based foams, aluminium based are among the most advanced. Aluminium foams couple good specific mechanical properties with high thermal stability. Among the various aspects still to be investigated regarding their mechanical behaviour is the influence of a hydrostatic state of stress on yield strength. Unlike metals, the hydrostatic component affects yields. Therefore, different loading conditions have to be considered to fully identify the material behaviour. Another important issue in foam structure design is the analysis of composite structures. The mechanical behaviour of an aluminium foam has been examined. The foam was subjected to uniaxial, hydrostatic stress, pure deviatoric stress, and combinations thereof. Results obtained will be presented as quasi-static and dynamic uniaxial compression and quasi-static bending and shear loading. Moreover, composite structures were made by assembling the foam into aluminium cold extruded closed section 6060 aluminium tubes. The results show that the energy absorption capability of the composite structures is much greater than the sum of the energy absorbed by the two components, the foam and the tube.     

Magnetic Imaging of Cyanide‐Bridged Co‐ordination Nanoparticles Grafted on FIB‐Patterned Si Substrates

Prussian blue CsNiCr nanoparticles are used to decorate selected portions of a Si substrate. For successful grafting to take place, the Si surface needs first to be chemically functionalized. Low‐dose focused ion beam patterning on uniformly functionalized surfaces selects those portions that will not participate in the grafting process. Step‐by‐step control is assured by atomic force and high‐resolution scanning electron microscopy, revealing a submonolayer distribution of the grafted nanoparticles. By novel scanning Hall‐probe microscopy, an in‐depth investigation of the magnetic response of the nanoparticles to varying temperature and applied magnetic field is provided. The magnetic images acquired suggest that low‐temperature canted ferromagnetism is found in the grafted nanoparticles, similar to what is observed in the equivalent bulk material.     

Sensing Pollution on Online Social Networks: A Transportation Perspective

Transportation policy and planning strategies, as well as Intelligent Transportation Systems (ITS), can all play important roles in decreasing pollution levels and their negative effects. Interestingly, limited effort has been devoted to exploring the potential of social network analysis in such context. Social networks provide direct feedback from people and, hence, potentially valuable information. A post telling how a person feels about pollution at a given time at a given location, could be useful to policy-makers, planners or environmentally-aware ITS designers. This work verifies the feasibility of sensing air pollution from social networks and of integrating such information with real sensors feeds, unveiling how people advertise such phenomenon, acting themselves as smart objects, and how online posts relate to true pollution levels. This work explores a new dimension in pollution sensing for the benefit of environmental and transportation research in future smart cities, confronting over 1,500,000 posts and pollution readings obtained from governmental on-the-field sensors over a one-year span.     

Kinetic modulation of pulsed chronopotentiometric polymeric membrane ion sensors by polyelectrolyte multilayers

Polymeric membrane ion-selective electrodes are normally interrogated by zero current potentiometry, and their selectivity is understood to be primarily dependent on an extraction/ion-exchange equilibrium between the aqueous sample and polymeric membrane. If concentration gradients in the contacting diffusion layers are insubstantial, the membrane response is thought to be rather independent of kinetic processes such as surface blocking effects. In this work, the surface of calcium-selective polymeric ion-selective electrodes is coated with polyelectrolyte multilayers as evidenced by zeta potential measurements, atomic force microscopy, and electrochemical impedance spectroscopy. Indeed, such multilayers have no effect on their potentiometric response if the membranes are formulated in a traditional manner, containing a lipophilic ion exchanger and a calcium-selective ionophore. However, drastic changes in the potential response are observed if the membranes are operated in a recently introduced kinetic mode using pulsed chronopotentiometry. The results suggest that the assembled nanostructured multilayers drastically alter the kinetics of ion transport to the sensing membrane, making use of the effect that polyelectrolyte multilayers have different permeabilities toward ions with different valences. The results have implications to the design of chemically selective ion sensors since surface-localized kinetic limitations can now be used as an additional dimension to tune the operational ion selectivity.     

An improved method for Organic Bound Tritium (OBT) determination in urine samples

The Organic Bound Tritium (OBT) amount in the body may induce changes in the evaluation of the internal exposure to tritium, due to its different retention time relative to HTO. OBT measurements for urine are not performed routinely, mainly because of the lengthy work needed in preparation of the samples, when using the standard oxygen combustion method. A simpler and more rapid method based on liquid scintillation counting (LSC) was employed, and an evaluation was performed to check its suitability for urine samples. The principle of the proposed method is based on subtracting the LSC counts of the water phase sample (HTO) from the total activity of the urine sample (OBT+HTO). A good correlation was found between the results obtained when applying the proposed direct method and the Gold standard method. The minimum detectable activity when using this method was determined.     

Ab initio correlation effects on the electronic and transport properties of metal(II)-phthalocyanine-based devices

Using first-principles calculations in the framework of density functional theory, we investigated the electronic and transport properties of metal(II)-phthalocyanine (M(II)Pc) systems, both in a single-molecule configuration and in a model device geometry. In particular, using copper(II)-Pc and manganese(II)-Pc as prototypical examples, we studied how electronic correlations on the central metal ion influence the analysis of the electronic structure of the system and we demonstrated that the choice of the exchange-correlation functional, also beyond the standard local or gradient corrected level, is of crucial importance for a correct interpretation of the data. Finally, our electronic transport simulations have shown that M(II)Pc-based devices can act selectively as molecular conductors, as in the case of copper, or as spin valves, as in the case of manganese, demonstrating once more the great potential of these systems for molecular nanoelectronics applications.     

Prediction of the Candida antarctica lipase A protein structure by comparative modeling and site-directed mutagenesis

A number of model structures of the CalA suggested by comparative modeling were tested by site-directed mutagenesis. Enzyme variants were created where amino acids predicted to play key roles for the lipase activity in the different models were replaced by an inert amino acid (alanine). The results from activity measurements of the overproduced and purified mutant enzymes indicate a structure where the active site consists of amino acid residues Ser184, His366, and Asp334 and in which there is no lid. This model can be used for future targeted modifications of the enzyme to obtain new substrate acceptance, better thermostability, and higher enantioselectivity.