Some optical and electrical properties of the As2Se3−xTex system

Some optical and electrical properties of the As₂Se_3?xTe_x system (0 ≤ x ≤ 0.15) have been studied. The value of the optical gap decreases from 1.74 eV to 1.59 eV. The slope of the absorption edge changes, so that value of E_o from the relation α ～ exp ($\text{h}\text{?}\text{ω}\text{E}{}_{\mathrm{o}}$) exhibits a maximum value in neighbourhood of composition As₂Se_2.9Te_0.1. The d.c. and a.c. conductivities have been studied. The value of the activation energy E_el ～ 1.8 eV is almost unchanged up to x = 0.15. The a.c. conductivity fulfils the relation $\text{б(ω) ～ ω}{}^{\mathrm{<mtext>s</mtext>}}$ where s ? 1 and 1.1. at frequencies f < 1 kHz and f > 1 kHz respectively.     

Enzymatic degradation of the hydrogels based on synthetic poly(α-amino acid)s

Biodegradable hydrogels are studied as potential scaffolds for soft tissue regeneration. In this work biodegradable hydrogels were prepared from synthetic poly(α-amino acid)s, poly(AA)s. The covalently crosslinked gels were formed by radical copolymerization of methacryloylated poly(AA)s, e.g. poly[N ⁵-(2-hydroxy-ethyl)-l-glutamine-ran-l-alanine-ran-N ⁶-methacryloyl-l-lysine], as a multifunctional macro-monomer with a low-molecular-weight methacrylic monofunctional monomer, e.g. 2-hydroxyethyl methacrylate (HEMA). Methacryloylated copolypeptides were synthesized by polymerization of N-carboxyanhydrides of respective amino acids and subsequent side-chain modification. Due to their polypeptide backbone, synthetic poly(AA)s are cleavable in biological environment by enzyme-catalyzed hydrolysis. The feasibility of enzymatic degradation of poly(AA)s alone and the hydrogels made from them was studied using elastase, a matrix proteinase involved in tissue healing processes, as a model enzyme. Specificity of elastase for cleavage of polypeptide chains behind the l-alanine residues was reflected in faster degradation of l-alanine-containing copolymers as well as of hydrogels composed of them.     

Comparative triplex tandem mass spectrometry assays of lysosomal enzyme activities in dried blood spots using fast liquid chromatography: application to newborn screening of Pompe, Fabry, and Hurler diseases

We report a comparative study of triplex tandem mass spectrometry (MS/MS) based assays of lysosomal enzymes in dried blood spots for the early detection of Pompe, Fabry, and Hurler diseases in newborns. Four methods have been evaluated that differed in sample handling and the equipment used. A newly developed method uses assay quenching with acetonitrile to precipitate blood proteins followed by analysis on an LC-electrospray/MS/MS system capable of multiple consecutive sample injections on two parallel chromatographic columns. This method requires 1.5 min per a triplex analysis of enzyme products and internal standards, which matches the throughput of the previously reported flow injection method. LC separation reduces matrix effects and allows for more facile sample workup. The new LC-based method showed figures of merit that were superior to those of the currently used method based on liquid-liquid extraction into ethyl acetate and flow injection into the mass spectrometer. The other methods we investigated for comprehensive comparison involved liquid-liquid extraction into ethyl acetate followed by LC-ESI-MS/MS and acetonitrile quenching followed by direct flow injection. Both methods using acetonitrile quenching were found to be robust and provide good quality data while requiring fewer liquid transfer steps and less disposable material and labor than did the extraction methods. The individual merits of the new methods are discussed to present an evaluated alternative approach to high-throughput analysis in newborn screening laboratories.     

Graphene fluoride: a stable stoichiometric graphene derivative and its chemical conversion to graphene

Stoichoimetric graphene fluoride monolayers are obtained in a single step by the liquid-phase exfoliation of graphite fluoride with sulfolane. Comparative quantum-mechanical calculations reveal that graphene fluoride is the most thermodynamically stable of five studied hypothetical graphene derivatives; graphane, graphene fluoride, bromide, chloride, and iodide. The graphene fluoride is transformed into graphene via graphene iodide, a spontaneously decomposing intermediate. The calculated bandgaps of graphene halides vary from zero for graphene bromide to 3.1 eV for graphene fluoride. It is possible to design the electronic properties of such two-dimensional crystals.     

Texture evolution in Fe–3% Si steel treated under unconventional annealing conditions

The present work investigates texture evolution stages in grain-oriented steel heat-treated using unconventional conditions. The Fe–3%Si steel taken after final cold rolling reduction from an industrial line was subjected to a laboratory isothermal annealing at different temperatures. The annealing temperatures were varied in a range of 850–1150 °C. During the annealing each specimen was heated at 10 °C/s and kept at the stated temperature for 5 min. Development of microstructure and texture in the annealed specimens were followed by the DC measurements of magnetic properties. The grain oriented steel, taken from the same industrial line after final box annealing was also analyzed and compared with the laboratory annealed specimens. It was shown that there is an optimal temperature region that, with combination of a fast heating rate, led to the best conditions of a drastically reduced development time of the {110} < 001 > crystallographic texture in the cold rolled grain-oriented steel. Materials heat treated below the optimum temperature region account for a primary recrystallization, while applying heat above this region leads to a secondary recrystallization without abnormal grain growth. Moreover, in the optimum temperature range, there was a particular temperature leading to the most optimal microstructure and texture. The magnetic properties, measured after the optimal heat treatment, were close to that measured on specimens taken after the final box annealing. The electron back scattered diffraction measurement technique revealed that sharpness of the {110} < 001 > crystallographic texture, developed at the optimum temperature is comparable to the steel taken after the industrial final box annealing. This fact is evidence that there is a temperature where the abnormal grain growth proceeds optimally.     

Preparation of TiAl15Si15 intermetallic alloy by mechanical alloying and the spark plasma sintering method

This work is devoted to the preparation of alloys based on intermetallic compounds in the Ti–Al–Si system by powder metallurgy using mechanical alloying and the spark plasma sintering (SPS) method. The aim was to describe the formation of intermetallic phases during mechanical alloying of TiAl15Si15 (wt-%) alloy and to consolidate the powder prepared by optimised conditions. Phase composition, microstructure and hardness of compacted alloy were determined. Four hours of mechanical alloying is sufficient time for preparation of pure elements free material composed only of intermetallic phases. After consolidation, the TiAl15Si15 alloy has a homogeneous structure composed of silicide (Ti₅Si₃) in aluminide (TiAl) matrix. The hardness of the material reaches 865?±?42 HV 5.     

An anchoring element for prestressed FRP reinforcement: simplified design of the anchoring area

Today, fibre-reinforced polymers (FRP) are widely used construction materials. The use of non-metallic reinforcement as inner reinforcement has many advantages, as is well known, but there are some areas of application that need to be resolved in order to improve the usage of FRP reinforcement in real-world conditions. One of these is the design of a suitable anchorage for prestressed FRP applications. It is difficult to design a safe anchorage using conventional methods of anchoring (systems for the anchorage of steel tendons) due to the well-known low compressive strength perpendicular to the fibres, this being due to the anisotropy of composite materials. Most of the anchoring systems commonly used worldwide are based on the use of metal parts (steel tubes, wedges, etc.) in a system which is primarily designed to be non-metallic. It is in contradiction with the initial intention to use non-metallic reinforcement. The presented text describes the basic physical and mechanical properties of a developed non-metallic anchor element. The essential principles of an analytical solution of the developed anchoring element based on the stiffness parameters of the system’s individual components are also presented. The behaviour of each material used is described in terms of simplify form. The functionality of the anchoring system was verified by a number of load tests and the obtained results were compared with theoretically and numerically calculated values. The presented results show the high efficiency of the anchoring system as well as the suitability of the derived analytical solution for simplified design and evaluation of the anchoring area.     

Magnetic Properties of ZnFe<Subscript>2</Subscript>O<Subscript>4</Subscript> Nanoparticles Synthesized by Starch-Assisted Sol–Gel Auto-combustion Method

In this paper, ZnFe₂O₄ spinel ferrite nanoparticles with different grain sizes at different annealing temperatures have been synthesized using the starch-assisted sol–gel auto-combustion method. The synthesized nanoparticles were characterized by conventional powder X-ray diffraction, Raman spectroscopy, Fourier transform infrared spectroscopy, field emission scanning electron microscopy, and vibrating sample magnetometer. The X-ray diffraction (XRD) patterns demonstrated that the ZnFe₂O₄ nanoparticles consist of single-phase spinel structure with crystallite sizes 4.81, 8.72, 12.06, 29.32, and 72.60 nm annealed at 400, 600, 800, 1000, and 1200 °C, respectively. Field emission scanning electron microscopy reveals that particles are of spherical morphology at lower annealing temperature and hexagonal-like morphology at higher temperature. An infrared spectroscopy study shows the presence of two principal absorption bands in the frequency range around 525 cm^?1 (ν ₁) and around 350 cm^?1 (ν ₂), which indicate the presence of tetrahedral and octahedral group complexes, respectively, within the spinel ferrite nanoparticles. Raman spectroscopy study also indicated the change in octahedral and tetrahedral site-related Raman modes in zinc ferrite nanoparticles with change of particle size. The nanocrystalline ZnFe₂O₄ samples (4.81, 8.72, 12.06, 29.32 nm) show ferrimagnetic behavior, and bulk sample (72.60 nm) shows paramagnetic behavior. This change in magnetic behavior is due to change of cation distribution in ZnFe₂O₄ nanoparticles with decrease of particle size.