Characterization of CVD Bonded Tyranno® Fibers Oxidized at High Temperatures

The oxidation of highly porous ceramic matrix composites (PCMCs) based on different Tyranno^® fibers has been analyzed by means of thermogravimetry and electron microscopy. Both uncoated fibers and PCMC materials exhibit parabolic kinetics between 900°C and 1250°C, these being faster for Ti‐doped than for Zr‐doped Tyranno fibers. Oxide layers in Ti‐doped fibers are porous and partially crystalline, whereas in Zr‐doped materials a significant fraction of relatively coarse β‐SiC grains is still found embedded in the amorphous silica matrix. On the other hand, the CVD‐SiC coatings exhibit higher oxidation rates from the outer surface than from the inner one, a phenomenon that has been associated not only with the more difficult access of oxygen to the inner face but also with the highly <111>  textured structure of these coatings, for which very different oxidation rates have been published for the inward and outward directions. Cracking phenomena observed above 1100°C for long dwelling times do not lead to an acceleration of the oxidation process, which could be due to the simultaneous crystallization of the amorphous silica layers.     

Physical and Functional Properties of Blackberry Freeze- and Spray-Dried Powders

The aim of the present work was to develop two products from blackberry juice by freeze and spray drying with potential use as food colorants or healthy ingredients. A characterization of the physical and functional properties of the powdered juices was done. Maltodextrin or a mixture of trehalose and maltodextrin were assessed as carrier matrices. Freeze-dried, maltodextrin-containing powders presented the best retention of bioactive compounds and antiradical activity; however, they showed a narrow relative humidity range for storage in the glassy state. Spray-dried powders showed better physical properties, bearing higher glass transition temperature and lower molecular mobility than freeze-dried formulations.     

Development and Applications of Coarse-Grained Models for RNA

In contrast to proteins, much less attention has been focused on the development of computational models for describing RNA molecules, which are being recognized as playing key roles in many cellular functions. Current atomically detailed force fields are not accurate enough to capture the properties of even simple nucleic acid constructs. In this article, we review our efforts to develop coarse-grained (CG) models that capture the underlying physics for the particular length scale of interest. Two models are discussed. One of them is the three interaction site (TIS) model, in which each nucleotide is represented by three beads corresponding to sugar, phosphate, and base. The other is the self-organized polymer (SOP) model, in which each nucleotide is represented as a single interaction center. Applications of the TIS model to study the complexity of hairpin formation and the effects of crowding in a shifting equilibrium between two conformations in human telomerase pseudoknot are described. The work on crowding illustrates a direct link to the activity of telomerase. We use the SOP model to describe the response of the Tetrahymena ribozyme to force. The simulated unfolding pathways agree well with single molecule pulling experiments. We also review predictions for the unfolding pathways for the Azoarcus ribozyme. The success of the CG applications to describe dynamics in RNA gives hope that more complex processes involving RNA-protein interactions can be tackled using variants of the proposed models.     

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.     

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.     

On the modeling of phase and chemical equilibria by equations of state for systems containing supercritical components and ionic species

A technique of modeling of phase and chemical equilibria by equations of state for systems containing supercritical components and ionic species is considered. Attention is focused on the structure of equation of states with inclusion of non-electrolyte and electrostatic contributions. A hole quasichemical model was applied to illustrate the technique and to show how an EOS can be modified for systems with chemical reactions and electrostatic interactions in the liquid phase. The concentration dependency of the density and dielectric permittivity was taken into account in describing the electrostatic contribution that is required for thermodynamic consistency of the results of modeling. A method of assessing the appropriate relationships for mixtures containing supercritical components is suggested, alongside with the way to estimate the “true” composition of mixtures where ionic species are formed due to chemical reactions. The raised questions are discussed with respect to the following systems: solutions of acid gases in water-alkanolamine mixtures and water-ammonia-carbon dioxide system in a broad interval of temperatures and pressures.     

Tunable Dielectric Function in Electric‐Responsive Glass with Tree‐Like Percolating Pathways of Chargeable Conductive Nanoparticles

The design of nanostructured materials with specific physical properties is generally pursued by tuning nanoparticle size, concentration, or surface passivation. An important step forward is to realize “active” systems where nanoparticles are vehicles for controlling, in situ, some specific, tuneable features of a responsive functional material. In this perspective, this work focuses on the rational design of a nanostructured glass with electrically tuneable dielectric function obtained by injection and accumulation of charge on embedded conductive nanocrystals. This enables electrically controlled switching of semiconducting nanophases to charged polarisable states to be achieved, which could lead to smart, field‐enhancement applications in nanophotonics and plasmonics. Here, it is shown that such response switching can be obtained if a percolating charge‐transport mechanism is activated through a disordered tree‐like network, as is demonstrated to be possible in SiO₂ films where suitable dispersions of SnO₂ nanocrystals, with conductive interfaces, are obtained as a result of a new synthesis strategy.     

Characterization of Edible Active Coating Based on Alginate–Thyme Oil–Propionic Acid for the Preservation of Fresh Chicken Breast Fillets

Chicken meat presents serious problems of processing and storage. Edible coatings are used commercially to improve the shelf life of fresh foods. The aim of this study is to develop an effective antimicrobial edible coating to improve the shelf life and safety of fresh chicken meat. The effect of propionic acid and thyme essential oils as antimicrobial and antioxidant compounds incorporated into alginate‐based edible coating was evaluated. Physical, antimicrobial and sensorial analyses were performed in coated and uncoated samples. Sensorial analysis showed no significant differences between coated and uncoated samples, which do not influence the buying decisions of consumers. The pH of the meat surface, color and sensorial analysis changed during storage time, showing similar behavior between coatings, the principal parameters to determine the shelf life of this product were weight loss and microbiological deterioration, where coatings had different behaviors. The selected coating increased the shelf life by about 33% with the lowest dehydration.