Experimental and theoretical analysis of the operation of a natural gas cogeneration system using a polymer exchange membrane fuel cell

This paper reports experimental and numerical results of an investigation of five identical cogeneration systems using PEM (Polymer Exchange Membrane) fuel cells and running on natural gas. The natural gas is reformed locally to produce hydrogen. The accuracy of numerical results is validated by comparison with experimental data and the system performances are analysed in terms of electrical, thermal and total efficiencies. It appears that the energetic performances are low, particularly at low current. Simple solutions for enhancing the system electrical performances by modifying control laws are proposed.     

Electronic transfer through Langmuir-Blodgett layers of capped platinum nanoparticles: An electrochemical approach

Amine functionalized platinum nanoparticles have been modified by over-grafting two different molecules, 2-thiophenecarbonyl chloride (Pt-1) and 1-hexyl-4-(4-isothiocyanatophenyl)-bicyclo (2, 2, 2) octane (Pt-2). Cyclic voltammetry was performed at gold electrodes coated with Langmuir-Blodgett (LB) mixed films of Pt-1 and Pt-2 nanoparticles, and behenic acid. From five layers the electrochemical response was essentially provided by the last LB component. The electrochemical responses towards the [Fe(CN)₆]^3−/4− couple were strongly influenced by the nature of the over-grafted molecules: films of Pt-2 presented an almost complete blocking effect, while films of Pt-1 allowed the redox reaction to occur on Pt nanoparticles. In order to understand the reasons for such different behaviors we built up hetero-nanostructures by superposing Pt-1 and Pt-2 LB layers in different ways, yielding different kinds of “sandwich” structures. The electrochemical response depended on the electrode ending. When Pt-1 nanoparticles were in the outer layer, in contact with the electrolyte solution, the electrode was electroactive toward the redox probe, while when Pt-2 layers were in the outer layer no electroactivity was detected. For sandwiches made of Pt-1, with a variable thickness of an intercalated film of Pt-2, the electrode response to [Fe(CN)₆]^3−/4− was modulated by the thickness of the inter-layer: the thicker the layer, the lower the response.     

In situ visualization of drop deformation,erosion, and breakup in high viscosity ratio polymeric systems under high shearing stress conditions

In this paper, deformation and breakup under simple shear of single molten polymer drops in a polymer matrix were investigated. Flow visualization was carried out in a Couette‐Flow apparatus under relatively high shear rates and temperatures up to 230°C. Drop/Matrix combinations were composed of polystyrene drops of 0.5–0.6 mm in diameter in polyethylene matrix, and ethylene–propylene copolymer drops of approximately the same size in polypropylene matrix. The deformation and breakup processes were studied under steady state and time‐dependent shearing conditions. Either for steady state or time‐dependant shearing conditions, drop elasticity generated at relatively high shear rates helped the drops to align perpendicular to the flow direction, i.e., parallel to vorticity axis. Also, the most striking non‐Newtonian effects for the high viscosity ratio systems were the surface erosion and the drop splitting mechanisms. The particles eroded off the main droplet surface were very fine, in the range of 10–50 μm, and led to a significant reduction in main drop size before its final breakup. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 2582–2591, 2006     

Low Breakdown Voltage Varistors by Grain Boundary Diffusion of Molten Bi2O3 in ZnO

Diffusion of molten Bi₂O₃ into the grain boundaries of sintered, alumina-doped (0.23 and 0.7 mol%) ZnO pellets resulted in varistors with breakdown voltages in the 3–5 V range and nonlinearity coefficients of 10–24. The varistors were fabricated by spreading a thin layer of Bi₂O₃ powder on the surface of ZnO pellets and heating the combination to various temperatures (860–1155°C) and different times. The highest nonlinearity coefficients (20–24) and lowest breakdown voltages (3–5 V) were recorded in samples annealed at 860°C for 35 min. Longer annealing times and/or higher temperatures resulted in progressively higher breakdown voltages. Eventually the devices became insulating, which was attributed to the formation of an insulating Bi₂O₃ layer between the grains. Separate wetting experiments have shown that the penetration of Bi₂O₃ into ZnO grain boundaries was a strong function of alumina doping —the penetration rate was decreased by a factor of 5–7 as the ZnO was doped with as little as 0.2 mol% alumina. It is this slowing down of the penetration of the ZnO grain boundaries that is believed to be critical in the development of the low breakdown voltages observed.     

Dispersive mixing efficiency of an elongational flow mixer on PP/EPDM blends: Morphological analysis and correlation with viscoelastic properties

Polypropylene and ethylene‐propylene‐diene terpolymer (PP/EPDM) blends were melt compounded in a new mixing device, designed in our laboratory under the trademark of RMX®, which predominantly generates elongational flows. Dispersion of the EPDM minor phase in PP was carried out in both RMX® and in an internal mixer (Haake Rheomix 600) at equivalent specific mixing energies and the resultant morphologies obtained by SEM were analyzed and compared. A better dispersive mixing efficiency of the RMX® mixer, i.e., lower D_n and D_v of the dispersed EPDM phase was observed. The impact of elongational flow was more pronounced for blends having a high viscosity ratio p, indicating an enhanced droplet break‐up mechanism, which was attributed to the combination of high shear rates inside the mixing element and important elongational flows in the convergent/divergent zones. The morphology of the blends was correlated with their linear viscoelastic properties by using the Palierne model. Very good agreement was found for the PP/EPDM 80/20 blends but for higher EPDM content, the Palierne model failed to describe the rheological behavior, which was attributed to percolation of the minor phase with increasing the concentration. Higher elasticity at low frequencies was observed for blends processed in the RMX®, which was attributed to a higher generated interfacial area. POLYM. ENG. SCI., 54:1444–1457, 2014. © 2013 Society of Plastics Engineers     

Discovery of Heterocyclic Nonacetamide Synaptic Vesicle Protein 2A (SV2A) Ligands with Single‐Digit Nanomolar Potency: Opening Avenues towards the First SV2A Positron Emission Tomography (PET) Ligands

The role of the synaptic vesicle protein 2A (SV2A) protein, target of the antiepileptic drug levetiracetam, is still mostly unknown. Considering its potential to provide in vivo functional insights into the role of SV2A in epileptic patients, the development of an SV2A positron emission tomography (PET) tracer has been undertaken. Using a 3D pharmacophore model based on close analogues of levetiracetam, we report the rationale design of three heterocyclic non‐acetamide lead compounds, UCB‐A, UCB‐H and UCB‐J, the first single‐digit nanomolar SV2A ligands with suitable properties for development as PET tracers.     

Novel Heterobimetallic Radiotheranostic: Preparation,Activity, and Biodistribution

A novel Ru^II(arene) theranostic complex is presented. It is based on a 1,4,7,10‐tetraazacyclododecane‐1,4,7,10‐tetraacetic acid macrocycle bearing a triarylphosphine and can be tracked in vivo by using the γ emission of ¹⁵³Sm atoms. Notably, the heteroditopic ligand can be selectively metalated with ruthenium at the phosphorus atom despite the presence of other functionalities that are prone to metal coordination. Subsequent labeling with radionuclides such as ¹⁵³Sm can then be performed easily. The resulting heterobimetallic complex exhibits favorable solubility and stability properties in biologically relevant media. It also shows in vitro cytotoxicity in line with that expected for this type of metallodrug, and is nontoxic to the organism as a whole. As a proof of concept, initial studies in healthy mice were performed to obtain information about the uptake, biodistribution, and excretion of the radiolabeled complex.     

Slip Length Measurements Using µPIV and TIRF-Based Velocimetry

The goal of this paper is to review progress (mostly recent) made in micro and nanovelocimetry, focusing on two techniques: µPIV (microparticle image velocimetry) and nanoPTV (nanoparticle tracking velocimetry). The paper focuses on the measurement of slippage (taken as a benchmark for these techniques), concentrating on work done in our group. We review the developments of µPIV that led, in the last ten years, to the achievement of 100 nm accuracy in the measurement of slip lengths. Later, this approach was complemented by nanoPTV, which recently obtained ±5 nm precision. Here, we also mention recent application of these techniques toward better characterization of microgel and polymer flows. As a whole, the two techniques have conveyed valuable information on flow behavior within and close to the boundaries of microchannels, on the importance of wetting, and on the role of surface heterogeneities. µPIV is commercially available but nanoPTV is not mature. Interesting instrumental developments are expected in the future for the latter technique.