Mean field homogenization and experimental investigation of short and long fiber reinforced polymers

The effective elastic material properties of short fiber reinforced polypropylen are determined by means of the self-consistent (SC) method and the interaction direct derivative (IDD) method. In order to account for thermoelastic effective material properties, a Hashin-Shtrikman (HS) based two-step homogenization method with variable reference stiffness is used. The influence of the reference stiffness, dependent on a scalar parameter is investigated. Information on the microstructure are derived by computed tomography scans (µCT) and considered within the homogenization schemes. Thermomechanical properties of a long fiber reinforced polymer (LFRP) and a short fiber reinforced polymer (SFRP) are obtained by means of dynamic mechanical analysis (DMA). Simulation results for SFRP are compared to experimental results. (© 2016 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim)     

Spectroscopic, morphological, and mechanistic investigation of the solvent-promoted aggregation of porphyrins modified in meso-positions by glucosylated steroids

Solvent-driven aggregation of a series of porphyrin derivatives was studied by UV/Vis and circular dichroism spectroscopy. The porphyrins are characterised by the presence in the meso positions of steroidal moieties further conjugated with glucosyl groups. The presence of these groups makes the investigated macrocycles amphiphilic and soluble in aqueous solvent, namely, dimethyl acetamide/water. Aggregation of the macrocycles is triggered by a change in bulk solvent composition leading to formation of large architectures that express supramolecular chirality, steered by the presence of the stereogenic centres on the periphery of the macrocycles. The aggregation behaviour and chiroptical features of the aggregates are strongly dependent on the number of moieties decorating the periphery of the porphyrin framework. In particular, experimental evidence indicates that the structure of the steroid linker dictates the overall chirality of the supramolecular architectures. Moreover, the porphyrin concentration strongly affects the aggregation mechanism and the CD intensities of the spectra. Notably, AFM investigations reveal strong differences in aggregate morphology that are dependent on the nature of the appended functional groups, and closely in line with the changes in aggregation mechanism. The suprastructures formed at lower concentration show a network of long fibrous structures spanning over tens of micrometres, whereas the aggregates formed at higher concentration have smaller rod-shaped structures that can be recognised as the result of coalescence of smaller globular structures. The fully steroid substituted derivative forms globular structures over the whole concentration range explored. Finally, a rationale for the aggregation phenomena was given by semiempirical calculations at the PM6 level.     

Selective transfer of energy through an alamethicin-doped artificial lipid membrane studied at discrete molecular level

In this study we present novel evidence that strengthens the paradigm of selective transfer of energy mediated by a random gating of ion channels. Specifically, we investigated the spectral response of a noisy artificial biomembrane whose electrical properties were largely dictated by embedded alamethicin oligomers. In this respect, we first evaluated experimentally the linear transfer function of the system via the white-noise analysis method. We prove that such a system displays specific ranges of frequency over which input signals pass preferentially, depending on their spectral content and the holding potential across the artificial bilayer which contains alamethicin. By employing voltage-driven periodic stimulation of alamethicin oligomers, we demonstrate that overall response of the system obeys qualitatively the predictions inferred from the transfer function analysis of it. These results emphasize the exquisite ability of excitable membranes to behave as band-limited filters and allow for maximal transfer of energy from an external stimulus over well-defined frequency ranges.     

A time discretization scheme of a characteristics method for a fluid–rigid system with discontinuous density

We propose a new characteristics method for the time discretization of a fluid–rigid system in the case when the densities of the fluid and the solid are different. This method is based on a global weak formulation involving only terms defined on the whole fluid–rigid domain. The main idea is to construct a characteristic function which preserves the rigidity of the solid at the discrete time levels. A convergence result for this semi-discrete scheme is then given.     

Modifications Induced by UV-Vis Irradiation on DNA Extract of Kiwifruit Investigated by Spectroscopic and Statistic Methods

ABSTRACT

Revealing molecular alterations induced on kiwifruit under UV-Vis irradiation requires a discussion of biochemical-cell infrared (IR) fingerprint (900 cm^?1–1800 cm^?1) bands characteristic of nucleic acids. FTIR-ATR spectroscopy and statistics and nondestructive methods for screening exposure effects induced by irradiation were used. There the irradiation influence on the main molecular bonds (i.e., ν(C-C), ν_s(PO₂?) and ν_as(PO₂?)) can be observed. Regression methods were used for statistical investigations. Two categories of variables were used: the absorbance measured at fixed wavenumber variables and the exposure dose. The bivariate correlations, partial correlations, and polynomial regression methods from SPSS were used for statistical investigations. The obtained results show that FTIR-ATR, in correlation with statistics techniques, might be useful to assess immediate radiation and oxidative-induced damage to nucleic acids. In this case IR spectroscopy can be used successfully to study conformational changes during DNA reversible denaturation especially on the sugar-phosphate vibrations domain.     

Simultaneous thermal and contraction/expansion analyses of cast iron solidification process

Journal of Thermal Analysis and Calorimetry - Simultaneous thermal and contraction/expansion analysis of hypoeutectic grey (lamellar graphite) and ductile (nodular graphite) cast irons...     

Long-living BLOCH oscillations of matter waves in periodic potentials

The dynamics of matter waves in linear and nonlinear optical lattices subject to a spatially uniform linear force is studied both analytically and numerically. It is shown that by properly designing the spatial dependence of the scattering length it is possible to induce long-living Bloch oscillations of gap-soliton matter waves in optical lattices. This occurs when the effective nonlinearity and the effective mass of the soliton have opposite signs for all values of the crystal momentum in the Brillouin zone. The results apply to all systems modeled by the periodic nonlinear Schr?dinger equation, including propagation of light in photonic and photorefractive crystals with tilted band structures.     

Open-pore biodegradable foams prepared via gas foaming and microparticulate templating

Open-pore biodegradable foams with controlled porous architectures were prepared by combining gas foaming and microparticulate templating. Microparticulate composites of poly(epsilon-caprolactone) (PCL) and micrometric sodium chloride particles (NaCl), in concentrations ranging from 70/30 to 20/80 wt.-% of PCL/NaCl were melt-mixed and gas-foamed using carbon dioxide as physical blowing agent. The effects of microparticle concentration, foaming temperature, and pressure drop rate on foam microstructure were surveyed and related to the viscoelastic properties of the polymer/microparticle composite melt. Results showed that foams with open-pore networks can be obtained and that porosity, pore size, and interconnectivity may be finely modulated by optimizing the processing parameters. Furthermore, the ability to obtain a spatial gradient of porosity embossed within the three-dimensional polymer structure was exploited by using a heterogeneous microparticle filling. Results indicated that by foaming composites with microparticle concentration gradients, it was also possible to control the porosity and pore-size spatial distribution of the open-pore PCL foams.     

Atomic force microscopy measurement of heterogeneity in bacterial surface hydrophobicity

The structure and physicochemical properties of microbial surfaces at the molecular level determine their adhesion to surfaces and interfaces. Here, we report the use of atomic force microscopy (AFM) to explore the morphology of soft, living cells in aqueous buffer, to map bacterial surface heterogeneities, and to directly correlate the results in the AFM force-distance curves to the macroscopic properties of the microbial surfaces. The surfaces of two bacterial species, Acinetobacter venetianus RAG-1 and Rhodococcus erythropolis 20S-E1-c, showing different macroscopic surface hydrophobicity were probed with chemically functionalized AFM tips, terminating in hydrophobic and hydrophilic groups. All force measurements were obtained in contact mode and made on a location of the bacterium selected from the alternating current mode image. AFM imaging revealed morphological details of the microbial-surface ultrastructures with about 20 nm resolution. The heterogeneous surface morphology was directly correlated with differences in adhesion forces as revealed by retraction force curves and also with the presence of external structures, either pili or capsules, as confirmed by transmission electron microscopy. The AFM force curves for both bacterial species showed differences in the interactions of extracellular structures with hydrophilic and hydrophobic tips. A. venetianus RAG-1 showed an irregular pattern with multiple adhesion peaks suggesting the presence of biopolymers with different lengths on its surface. R. erythropolis 20S-E1-c exhibited long-range attraction forces and single rupture events suggesting a more hydrophobic and smoother surface. The adhesion force measurements indicated a patchy surface distribution of interaction forces for both bacterial species, with the highest forces grouped at one pole of the cell for R. erythropolis 20S-E1-c and a random distribution of adhesion forces in the case of A. venetianus RAG-1. The magnitude of the adhesion forces was proportional to the three-phase contact angle between hexadecane and water on the bacterial surfaces.