The photophysical determination of the minimum hydrotrope concentration of aromatic hydrotropes

A method based on the aggregate to monomol emission ratio, I(aggr)/I(monomol), was used to determine the minimal hydrotropic concentration (MHC) of aromatic hydrotropes. The main advantage of this method is that it does not require the use of probes or other additives, which might disrupt the aggregation process. Also, it relies on spectrophotometric measurements, which are more sensitive and less arduous than others, like conductivity, light scattering and surface tension.     

Effect of surfactant structure on the residual fluorescence of micelle-based fluorescent probes

In the present paper we have investigated some photo-physical characteristics of different micellar-based fluorescent probes containing a fluorophore (pyrene) and a quencher unit (dodecyl-dioxo 2,3,2). The fluorescent response of the probe in the presence of Cu(II) ions was studied using different micellar substrates, and it was found that the pH at which the On-Off jump occurs is not influenced by the chemical structure of surfactant. In addition, the experimental residual fluorescence is not proportionally affected by microviscosity or by the size of the micellar aggregates. The signal of the native fluorescence of pyrene was observed even when the quencher's occupancy number was greater than one. Moreover, we observed discrepancies between experimental values and calculated residual fluorescence using Laplace data. These results were interpreted suggesting that the residual fluorescence has two main components, one that seems to be independent on micellar properties, while the other is directly related to location of molecules inside the surfactant aggregates that serve as substrate.     

A video-optical system for time-resolved whole-body measurement on vascular segments

This paper presents a novel experimental setup to get the three-dimensional (3-D) whole-body deformation of arterial segments under finite inflation and extension. A simple one camera/one shot arrangement allows non-contacting, full-field, real-time measurements to be performed. A concave conical mirror mounted coaxially to the camera provides the whole 360° field view of a large number of closely spaced micro-spheres affixed to the sample surface. Then, on the basis of radial metrology concepts, each single frame of the loading sequence is automatically processed to track 3-D marker positions and, thus, to obtain sample deformation at the camera frame acquisition rate.Preliminary tests are run to evaluate measurement accuracy and to calibrate the system for in-vitro testing in physiological solution. Then, pressure–diameter tests at various levels of axial extension are performed on an excised porcine arterial segment using a specially designed in-vitro rig.Experimental data demonstrate that the present method can provide either global parameters to be used within standard constitutive frameworks and important full-field information on the eventual in-homogeneity of deformation. To better illustrate the latter achievement, results related to the ‘bend buckling’ of a straight porcine vascular vessel tested at low axial stretch are reported. Remarkably, the experimental apparatus can be adapted to a large variety of test protocols and sample geometries.     

Oxygen reduction reaction features in neutral media on glassy carbon electrode functionalized by chemically prepared gold nanoparticles

Gold nanoparticles (AuNPs) were prepared by chemical route using four different protocols by varying reducer, stabilizing agent, and solvent mixture. The obtained AuNPs were characterized by transmission electronic microscopy (TEM), UV-visible, and zeta potential measurements. From these latter, surface charge densities σ were calculated to evidence the effect of the solvent mixture on AuNP stability. The AuNPs were then deposited onto glassy carbon (GC) electrodes by drop casting, and the resulting deposits were characterized by cyclic voltammetry (CV) in H₂SO₄ and field emission gun scanning electron microscopy (FEG-SEM). The electrochemical kinetic parameters of the four different modified electrodes toward oxygen reduction reaction (ORR) in neutral NaCl-NaHCO₃ media (0.15 M/0.028 M, pH 7.4) were evaluated by rotating disk electrode voltammetry and subsequent Koutecky-Levich treatment. Contrary to what we previously obtained with electrodeposited AuNPs [Gotti et al., Electrochim. Acta 2014], the highest cathodic transfer coefficients β were not obtained on the smallest particles, highlighting the influence of the stabilizing ligand together with the deposit morphology on the ORR kinetics.     

A photosynthetic biosensor with enhanced electron transfer generation realized by laser printing technology

One of the limits of current electrochemical biosensors is a lack of methods providing stable and highly efficient junctions between biomaterial and solid-state devices. This paper shows how laser-induced forward transfer (LIFT) can enable efficient electron transfer from photosynthetic biomaterial immobilized on screen-printed electrodes (SPE). The ideal pattern, in terms of photocurrent signal of thylakoid droplets giving a stable response signal with a current intensity of approximately 335 ± 13 nA for a thylakoid mass of 28 ± 4 ng, was selected. It is shown that the efficiency of energy production of a photosynthetic system can be strongly enhanced by the LIFT process, as demonstrated by use of the technique to construct an efficient and sensitive photosynthesis-based biosensor for detecting herbicides at nanomolar concentrations.     

Superhydrophobic behaviour of plasma modified electrospun cellulose nanofiber-coated microfibers

In this work, a method is presented for production of a textile cellulose fiber with non-wetting properties suitable for applications ranging from wound care and tissue engineering to clothing and other textile applications. Non-wettability is achieved by coating a textile cellulose microfiber with electrospun cellulose nanofibers, creating a large and rough surface area that is further plasma treated with fluorine plasma. High surface roughness and efficient deposition of covalently bound fluorine groups results in the fiber exhibiting non-wetting properties with contact angle measurements indicating superhydrophobicity (>150° water contact angle). It is an environmentally friendly method and the flexibility of the electrospinning process allows for careful design of material properties regarding everything from material choice and surface chemistry to fiber morphology and fiber assembly, pointing to the potential of the method and the developed fibers within a wide range of applications.     

Influence of Catalyses on the Preparation of YVO<Subscript>4</Subscript>:Eu<Superscript>3+</Superscript> Phosphors by the Sol–gel Methodology

YVO(4):Eu(3+) phosphors have been prepared by the hydrolytic sol-gel methodology, with and without alkaline catalyst. The solid powder was obtained by reaction between yttrium III chloride and vanadium alkoxides; the europium III chloride was used as structural probe. The powder was treated at 100, 400, 600, or 800 °C for 4 h. The samples were characterized by X-ray diffraction, thermal analysis, and photoluminescence. The XRD patterns revealed YVO(4) crystalline phase formation for the sample prepared without the catalyst and heat-treated at 600 °C and for the sample prepared in the presence of ammonium as catalyst and heat-treated at 100 °C. The average nanosized crystallites were estimated by the Scherrer equation. The sample which was produced via alkaline catalysis underwent weight loss in two stages, at 100 and 400 °C, whereas the sample obtained without catalyst presented four stages of weight loss, at 150, 250, 400, and 650 °C. The excitation spectra of the samples treated at different temperatures displayed the charge transfer band (CTB) at 320 nm. PL data of all the samples revealed the characteristic transition bands arising from the (5)D(0) → (5)F(J) (J = 0, 1, 2, 3, and 4) manifolds under maximum excitation at 320, 394, and 466 nm in all cases. The (5)D(0) → (7)F(2) transition often dominates the emission spectra, indicating that the Eu(3+) ion occupies a site without inversion center. The long lifetime suggests that the matrix can be applied as phosphors. In conclusion, the sol-gel methodology is a very efficient approach for the production of phosphors at low temperature.     

Two‐dimensional non‐close‐packed arrays of nanoparticles via core‐shell nanospheres and reactive ion etching

Nanosized PTFE/polystyrene core‐shell particles were prepared by seed emulsion polymerization technique starting from PTFE seeds of 20 nm. At the end of the reaction, no residual PTFE nor secondary nucleation was observed and by appropriately choosing the ratio between the monomer and the PTFE seed it was possible to obtain particles, with predetermined size in the range 60–100 nm, featuring an extremely narrow size distribution. These particles were successfully employed as building blocks for the preparation of large scale nanosized monolayers through the floating technique. Reactive ion etching was further applied to modulate the size characteristics of the resulting 2D ordered nanostructure. Although for relatively short RIE times a peculiar continuous morphology was observed in which the particles are interconnected through thin arms, on further increasing the RIE time a well‐organized 2D arrangement of particles with size of about 30 nm was obtained. Considering the shell as an expendable ordering and spacing tool, the use of core‐shell nanospheres allows a wide variety of controlled morphologies to be designed and prepared thus opening new perspectives for nanostructure fabrication processes through nanosphere lithography (NSL). Copyright © 2011 John Wiley & Sons, Ltd.