Dielectric,ferroelectric, and energy storage properties in dysprosium doped sodium bismuth titanate ceramics

In this work, Na_0.5(Bi_1-xDy_x)_0.5TiO₃ (0?≤?x?≤?15%) ceramics were prepared via solid state reaction method and were characterized. A stable and pure perovskite phase was revealed by X-ray diffraction analysis for all compositions and a symmetry change from rhombohedral to orthorhombic phase was detected beyond 10% of Dy substitution. The incorporation of Dy³⁺ into Sodium Bismuth Titanate (Na_0.5Bi_0.5TiO₃) matrix allows a substantial decrease of the coercive field, an increase in the resistivity, and leads to a high stability of the dielectric permittivity (??/?_(150?°C) ≤?±?15%) over a wide temperature range. Furthermore, this system was found to exhibit improved energy storage properties at high temperatures with a maximum energy density of 1.2?J/cm³ obtained for 2%Dy composition at 200?°C. The obtained results are very promising for energy storage capacitors operating at high temperatures.     

A non-parametric method for estimating enthalpy-temperature functions of shape-stabilized phase change materials

A method for thermodynamic characterization of shape-stabilized phase change materials (PCM) based on one-single sample and one-single experiment has been proposed. The simplicity of the experimental device is comparable to that of the T-History method. However, instead of simple energy balances as in T-History method, a numerical heat transfer model is used to retrieve the whole set of parameters/functions characterizing the PCM from temperature measurements at one-single point within the PCM. An efficient inversion technique has been proposed for that. Its most striking feature is that it allows non-parametric identification of the enthalpy-temperature function in an easy way. Such a function is retrieved by solving a problem of nonhomogeneous heat source term estimation by inversion of a linear heat conduction model.     

Binding of ²³⁹Pu and ⁹⁰Sr to organic colloids in soil solutions: evidence from a field experiment

Colloidal transport has been shown to enhance the migration of plutonium in groundwater downstream from contaminated sites, but little is known about the adsorption of ??Sr and plutonium onto colloids in the soil solution of natural soils. We sampled soil solutions using suction cups, and separated colloids using ultrafiltration to determine the distribution of 23?Pu and ??Sr between the truly dissolved fraction and the colloidal fraction of the solutions of three Alpine soils contaminated only by global fallout from the nuclear weapon tests. Plutonium was essentially found in the colloidal fraction (>80%) and probably associated with organic matter. A significant amount of colloidal ??Sr was detected in organic-rich soil solutions. Our results suggest that binding to organic colloids in the soil solutions plays a key role with respect to the mobility of plutonium in natural alpine soils and, to a lesser extent, to the mobility of ??Sr.     

Coumarins from Seseli devenyense Simonk.: Isolation by Liquid–Liquid Chromatography and Potential Anxiolytic Activity Using an In Vivo Zebrafish Larvae Model

Different types of anxiety disorders have become the number one mental health issue in developed countries. The search for new, safer and effective drug-like molecules among naturally derived substances faces two difficulties: an efficient method of isolation compounds with a high-purity and high-throughput animal model for activity assay. Thus, the aim of the present study was to isolate by liquid–liquid chromatography high-purity rare coumarins from the fruits of Seseli devenyense Simonk. and evaluate their anxiolytic effect (defined as reversed thimotaxis) using a 5-days post-fertilization (dpf) Danio rerio larvae model. Liquid–liquid chromatography enabled the isolation of one simple hydroxycoumarin (devenyol) and four pyranocoumarins (cis-khellactone, d-laserpitin, isolaserpitin and octanoyllomatin). The anxiolytic effect was defined as a decrease in the time spent in the boundaries of the living space (also described as reversed thigmotaxis). Our results show that all isolated courmarins exerted a significant influence on the anxiety behavior (anxiolytic activity) in the zebrafish larvae model. According to our knowledge, this is the first report of anxiolytic activity of pyranocoumarins and devenyol.     

Solid-Phase Synthesis of Substrate-Based Dipeptides and Heterocyclic Pseudo-dipeptides as Potential NO Synthase Inhibitors

More than 160 arginine analogues modified on the C-terminus via either an amide bond or a heterocyclic moiety (1,2,4-oxadiazole, 1,3,4-oxadiazole and 1,2,4-triazole) were prepared as potential inhibitors of NO synthases (NOS). A methodology involving formation of a thiocitrulline intermediate linked through its side-chain on a solid support followed by modification of its carboxylate group was developed. Finally, the side-chain thiourea group was either let unchanged, S-alkylated (Me, Et) or guanidinylated (Me, Et) to yield respectively after TFA treatment the corresponding thiocitrulline, S-Me/Et-isothiocitrulline and N-Me/Et-arginine substrate analogues. They all were tested against three recombinant NOS isoforms. Several compounds containing a S-Et- or a S-Me-Itc moiety and mainly belonging to both the dipeptide-like and 1,2,4-oxadiazole series were shown to inhibit nNOS and iNOS with IC₅₀ in the 1–50 μM range. Spectral studies confirmed that these new compounds interacted at the heme active site. The more active compounds were found to inhibit intra-cellular iNOS expressed in RAW264.7 and INS-1 cells with similar efficiency than the reference compounds L-NIL and SEIT.     

Phototransformation of water-soluble polymers. Part II: photooxidation of poly(ethylene oxide) in aqueous solution

Poly(ethylene oxide) (PEO) was irradiated in aqueous solution under long wavelengths (λ>300 nm, 20 °C) and in presence of oxygen. The photooxidation of PEO was studied by IR spectrophotometry, viscometry and size exclusion chromatography. The formation of the oxidation photoproducts was studied by infrared analysis of films obtained by evaporation of aliquots of irradiated aqueous solutions. The photoproducts were identified by chemical derivatization treatments coupled with infrared measurements. Viscosimetry and SEC analysis showed that photooxidation was leading to a dramatic decrease of the molecular weights. The influence of the pH of the aqueous solutions was also examined. Unexpected results were obtained for the pH 12 solutions, indicating a strong inhibition of the oxidation.

Comparison with the results obtained in the case of PEO irradiated in the solid state showed that no direct transposition of the knowledge concerning the behavior of the solid polymer could be made.     

Yeast sequencing reports. CAN1, a gene encoding a permease for basic amino acids in Candida albicans

The first gene coding for an amino-acid permease of Candida albicans was sequenced. The DNA fragment complementing the lysine-permease deficiency was 3385 bp long. An open reading frame of 1713 nucleotides was found encoding a protein of 571 amino acids, with a calculated molecular weight of 63 343. Analysis of the deduced primary structure revealed ten membrane spanning regions and three potential N-glycosylation sites. The protein sequence is strongly homologous to both permeases for basic amino acids (Can1 and Lyp1) of Saccharomyces cerevisiae. C-terminal part of another ORF (105 aa), highly homologous to the gene HAL2 of S. cerevisiae, was found 133 bp downstream, and in tail-to-tail orientation to the permease gene. The sequence data will appear in the EMBL/GenBank/DDBJ Nucleotide Sequence Data Libraries under the accession number X76689.     

Kinetic study of acrylic monomer grafting in the presence of a polyfunctional monomer onto radioperoxided poly(ethylene–tetrafluoroethylene) copolymer

Acrylic acid (AA), methacrylic acid (MA) and diethyleneglycol dimethacrylate (DEGDM) are grafted onto 100 μm radioperoxided poly(ethylene–tetrafluroethylene) copolymer (ETFE). The influences of the homopolymerization inhibitor, the solvent, the grafting temperature, and the monomer content on the grafting kinetics are studied. For the grafting of acrylic monomers, the limitation of the grafting yield is more important for AA grafting whatever the nature of the metallic salt; the difference between the two homopolymerization inhibitors is their respective concentration to obtain a given grafting yield. For the AA + DEGDM cografting, the grafting yield increases with the DEGDM content of the grafting solution. In both cases, the overall activation energy has been calculated, and its variation as a function of the composition of the grafting solution is discussed. © 1994 John Wiley & Sons, Inc.