Enhancement of magnetic losses in hybrid polymer composites with MnZn-ferrite and conductive fillers

Polymer composites (PCs) with a polyurethane (PU) matrix filled with magnetic filler (MnZn ferrite) and hybrid polymer composites (HPCs) consisting of this magnetic filler and various types of conductive fillers (carbon black, carbon fibers, aluminum powder, polypyrrole) are prepared. The matrix structure of a HPC is formed (i) by a polymer filled with conductive filler, which forms the skeleton of an infinite cluster, and (ii) by ferrite particles that are larger than conductive particles. Thus, an HPC represents an ensemble of ferrite particles each of which is surrounded by a conductive medium and can be considered as a “core–shell” structure. The development of a core–shell structure is evidenced by the lower electric percolation threshold in an HPC compared with that in PU filled with conductive filler. Magnetic and dielectric spectra of PCs and HPCs are studied in the frequency range from 1 MHz to 10 GHz. Hybrid systems exhibit a considerable enhancement of magnetic losses compared with PCs. The enhancement of magnetic losses in HPCs is due to the conduction currents that are induced in the conductive shell by a microwave magnetic field.     

Low complexity adaptive power and subcarrier allocation for OFDMA

The problem of low complexity sub-optimal power and subcarrier allocation for OFDMA systems is addressed in the paper. We propose a heuristic non-iterative method that is an extension of the ordered subcarrier selection algorithm recently proposed for a single user case to the OFDMA systems. The suggested method improves the average BER-performance of the system and it also provides fairness between the users in terms of the bit rates. Both the theoretical analysis and simulation results confirm efficiency of the proposed technique. Based on the proven lemma about inversion of power gains, we strengthen the suggested method by low complexity power loading that consists in equalization of the received signal-to-noise ratios of each user     

Polarizability,Susceptibility, and Dielectric Constant of Nanometer‐Scale Molecular Films: A Microscopic View

The size‐dependence of the polarizability, susceptibility, and dielectric constant of nanometer‐scale molecular layers is explored theoretically. First‐principles calculations based on density functional theory are compared to phenomenological modeling based on polarizable dipolar arrays for a model system of organized monolayers composed of oligophenyl chains. Size trends for all three quantities are primarily governed by a competition between out‐of‐plane polarization enhancement and in‐plane polarization suppression. Molecular packing density is the single most important factor controlling this competition and it strongly affects the bulk limit of the dielectric constant as well as the rate at which it is approached. Finally, the polarization does not reach its “bulk” limit, as determined from the Clausius–Mossotti model, but the susceptibility and dielectric constant do converge to the correct bulk limit. However, whereas the Clausius–Mossotti model describes the dielectric constant well at low lateral densities, finite size effects of the monomer units cause it to be increasingly inaccurate at high lateral densities.     

Effect of metal purity and testing procedure on surface tension measurements of liquid tin

The surface tension of liquid tin of three different grades of purity (99.85, 99.96, and 99.999%) was measured by the classical sessile drop method over the temperature range 523–1023 K, in heating and cooling regimes. The results obtained show that the metal purity affects the values of surface tension and its temperature dependence. The highest values of surface tension and smooth linear temperature dependence were obtained in cooling regime for tin of the highest purity. With increasing content of impurities, both surface tension and its temperature coefficient decrease while the scatter of the data increases. The surface tension values measured on heating regime show higher scatter, compared to those obtained in cooling regime, and the temperature dependence of the surface tension is curvilinear rather than linear.     

Structure and phase behavior of a disk-necklace polymer: Cyclolinear polymethylsiloxane

The structure and phase transitions of cyclolinear polyorganosiloxane copolymer containing 12-member polysiloxane rings have been studied using synchrotron WAXS, DSC, TEM, variable-temperature AFM and polarized optical microscopy. The primary structure of this polymer can be viewed as a necklace of disk-shaped entities (cyclic groups) connected via flexible linkers.In the mesomorphic state, the presence of two different LC phases has been derived from the analysis of WAXS fiber diffractograms. The morphology of one of the phases shows a conventional hexagonal packing of LC chains where the chain axes are perpendicular to the plane of the 2D hexagonal lattice. The other one, so-called R-phase, has a vertically oriented rectangular 2D lattice formed by inter-chain correlations between the bulky polysiloxane cycles (disks). To our knowledge, such a disk-necklace mesophase in which the LC lattice is parallel to the backbone direction has not been reported in the literature so far.     

Hydrocarbon-ammonia moulding-a new technology for production of combustion catalysts

Fluidized bed catalytic combustion has proved to be very promising for industrial application. The milestone problem is development of support and catalyst with high mechanical and thermal stability. We have developed a new technology for production of alumina supports with desired spherical shape, texture and structure. Properties of spherical granules depend on the method of granulation and most attention has been paid to development and optimization of hydrocarbon-ammonia moulding to produce uniform alumina spheres. Optimization of high quality spheres production focused on study of effect of initial hydroxide properties and molding conditions on properties of final product. Modification of spherical alumina with oxides of Mg, La, Ce, and Si proved to be effective to substantially improve the mechanical and thermal stability. This effect is most pronounced when, pairs of these dopes are introduced simultaneously.     

Control of polyaniline conductivity and contact angles by partial protonation

Many studies require a specific value of conductivity when investigating conducting polymers. The conductivity of polyaniline can efficiently be controlled by partial protonation of the polyaniline base. Although this is a simple task in principle, practical guidelines are missing. In the present study, the changes in the conductivity of polyaniline base after immersion in aqueous solutions of various acids are reported. Polyaniline base has been reprotonated in aqueous solutions of picric, camphorsulfonic and phosphoric acids. The conductivity of partially reprotonated polyaniline varied between 10⁻⁹ and 10⁰ S cm⁻¹. The relation between the pH of a phosphoric acid solution, which was in equilibrium with polyaniline, and the conductivity σ is pH = 0.77 − 0.64 log(σ [S cm⁻¹]). The wettability, i.e. water contact angles, can similarly be set by partial protonation to between 78° for polyaniline base and 44° for polyaniline reprotonated in 1 mol L⁻¹ phosphoric acid. In solutions of picric acid, the transition from the non‐conducting to the conducting state occurs over a narrow range of acid concentrations, and the tuning of conductivity is consequently difficult. Phosphoric acid is well suited for the control of conductivity of polyaniline because of the moderate dependence of the conductivity on the acid concentration or pH. Copyright © 2007 Society of Chemical Industry     

Wetting Behavior and Reactivity of Molten Silicon with h-BN Substrate at Ultrahigh Temperatures up to 1750 °C

For a successful implementation of newly proposed silicon-based latent heat thermal energy storage systems, proper ceramic materials that could withstand a contact heating with molten silicon at temperatures much higher than its melting point need to be developed. In this regard, a non-wetting behavior and low reactivity are the main criteria determining the applicability of ceramic as a potential crucible material for long-term ultrahigh temperature contact with molten silicon. In this work, the wetting of hexagonal boron nitride (h-BN) by molten silicon was examined for the first time at temperatures up to 1750 °C. For this purpose, the sessile drop technique combined with contact heating procedure under static argon was used. The reactivity in Si/h-BN system under proposed conditions was evaluated by SEM/EDS examinations of the solidified couple. It was demonstrated that increase in temperature improves wetting, and consequently, non-wetting-to-wetting transition takes place at around 1650 °C. The contact angle of 90° ± 5° is maintained at temperatures up to 1750 °C. The results of structural characterization supported by a thermodynamic modeling indicate that the wetting behavior of the Si/h-BN couple during heating to and cooling from ultrahigh temperature of 1750 °C is mainly controlled by the substrate dissolution/reprecipitation mechanism.     

Investigation of Serine‐Proteinase‐Catalyzed Peptide Splicing in Analogues of Sunflower Trypsin Inhibitor 1 (SFTI‐1)

Serine‐proteinase‐catalyzed peptide splicing was demonstrated in analogues of the trypsin inhibitor SFTI‐1: both single peptides and two‐peptide chains (C‐ and N‐terminal peptide chains linked by a disulfide bridge). In the second series, peptide splicing with catalytic amount of proteinase was observed only when formation of acyl–enzyme intermediate was preceded by hydrolysis of the substrate Lys–Ser peptide bond. Here we demonstrate that with an equimolar amount of the proteinase, splicing occurs in all the two‐peptide‐chain analogues. This conclusion was supported by high resolution crystal structures of selected analogues in complex with trypsin. We showed that the process followed a direct transpeptidation mechanism. Thus, the acyl–enzyme intermediate was formed and was immediately used for a new peptide bond formation; products associated with the hydrolysis of the acyl–enzyme were not observed. The peptide splicing was sequence‐ not structure‐specific.     

Transformation of CH4 and liquid fuels into syngas on monolithic catalysts

Active components comprised of fluorite-like Ln_x(Ce_0.5Zr_0.5)_1−xO_2−y (Ln = La, Pr, Sm) and perovskite-like La_0.8Pr_0.2Mn_0.2Cr_0.8O₃ mixed oxides and their composites with yttria-doped zirconia (YSZ) promoted by precious metals (Pt, Ru) and/or Ni were supported on several types of heat-conducting substrates (compressed Ni-Al foam, Fecralloy foil or gauze protected by corundum layer, Cr-Al-O microchannel cermets, titanium platelets protected by oxidic layer) as well as on honeycomb corundum monolithic substrate. These structured catalysts were tested in pilot-scale reactors in the reactions of steam reforming of methane, selective oxidation of decane and gasoline and steam/autothermal reforming of biofuels (ethanol, acetone, anisole, sunflower oil). Applied procedures of supporting nanocomposite active components on monolithic/structured substrates did not deteriorate their coking stability in real feeds with a small excess of oxidants, which was reflected in good middle-term (up to 200 h) performance stability promising for further up-scaling and long-term tests. Equilibrium yield of syngas at short contact times was achieved by partial oxidation of decane and gasoline without addition of steam usually required to prevent coking. For the first time possibility of successive transformation of biofuels (ethanol, acetone, anisole, sunflower oil) into syngas at short contact times on monolithic catalysts was demonstrated. This was provided by a proper combination of active component, thermal conducting monolithic substrates and unique evaporation/mixing unit used in this research.