A feasibility study of using CeO2 as a surrogate material during the investigation of UO2 thermal conductivity enhancement

A possible substitution of UO₂ for research purposes is the cerium dioxide (CeO₂) owing to its chemical and physical properties. Neutronic properties are different and fission is absent in the case of CeO₂; however, similarities were studied recently to have a possibility to compare the neutronic influence of secondary additives into the matrix. This paper deals with increasing the thermal conductivity of UO₂ nuclear fuel on surrogate material (CeO₂); the main focus of the research is given on the sintering behaviour of CeO₂. The incorporation of highly thermally conductive material (SiC) is the investigated concept of thermal conductivity enhancement. Conventional sintering and spark plasma sintering (SPS) were applied to compare the behaviour of CeO₂ and UO₂ reported in the literature. High temperature thermal conductivity measurements did not confirm the positive influence of SiC additive inside the CeO₂ matrix mainly due to grain boundary disruptions. Similar behaviour was also previously reported for UO₂ pellets with SiC.     

Uncertainties in determination of 131I activity in thyroid gland

The values of the iodine (131)I uptake determined from the measurements with a NaI scintillation counter might be significantly influenced by the thyroid position in the human neck. It is shown that the ratio of the counting rate in the energy peak of 364 keV to the counting rate in the Compton scattering band can be used for the determination of the effective depth of the thyroid. The uncertainties of the standard method are discussed basing on results of calibration measurements. The investigations of 95 patients with different thyroid diseases showed that the measured iodine spectrum was considerably different from the standard for about 20% of them, indicating possible high uncertainties of the standard measurements, which assume a fixed thyroid depth of 20 mm.     

Gene Expression Data Mining Reveals the Involvement of GPR55 and Its Endogenous Ligands in Immune Response,Cancer, and Differentiation

G protein-coupled receptor 55 (GPR55) is a recently deorphanized lipid- and peptide-sensing receptor. Its lipidic endogenous agonists belong to lysoglycerophospholipids, with lysophosphatidylinositol (LPI) being the most studied. Peptide agonists derive from fragmentation of pituitary adenylate cyclase-activating polypeptide (PACAP). Although GPR55 and its ligands were implicated in several physiological and pathological conditions, their biological function remains unclear. Thus, the aim of the study was to conduct a large-scale re-analysis of publicly available gene expression datasets to identify physiological and pathological conditions affecting the expression of GPR55 and the production of its ligands. The study revealed that regulation of GPR55 occurs predominantly in the context of immune activation pointing towards the role of the receptor in response to pathogens and in immune cell lineage determination. Additionally, it was revealed that there is almost no overlap between the experimental conditions affecting the expression of GPR55 and those modulating agonist production. The capacity to synthesize LPI was enhanced in various types of tumors, indicating that cancer cells can hijack the motility-related activity of GPR55 to increase aggressiveness. Conditions favoring accumulation of PACAP-derived peptides were different than those for LPI and were mainly related to differentiation. This indicates a different function of the two agonist classes and possibly the existence of a signaling bias.     

Werkstoffe für SCWO-Prozesse zur Oxidation von chlorhaltigen Schadstoffen in überkritischem Wasser

Materials for SCWO processes for the oxidation of chlorine containing residues in supercritical water The oxidation of harmful residues in supercritical water (SCWO – Supercritical Water Oxidation) is an efficient procedure for converting hazardous substances into environmentally friendly products. Due to the usually high chlorine concentrations, however, the reactor material is subjected to a highly corrosive medium at high pressures and temperatures. For the corrosion studies an experimental set-up was used, that allows to subject the materials to these conditions. The nickel base materials Alloy 625 and Alloy 686 were studied at 500°C and 46.5 MPa up to 320 hours. The model fluid consisted of HCl+H₂O+NaCl+methanol with H₂O₂ as oxidant. Alloy 625 forms complex scales consisting of alternating Cr-Mo-Nb-O mixed oxide layers and chloride layers, mostly NiCl₂. Alloy 686 forms similar corrosion scales and shows after 320 h additionally stress corrosion cracking. The ICP-AES analysis of the fluid in function of time shows time intervals with high Ni concentrations alternating with time intervals with high Mo and Cr concentrations, which indicates that alternating mechanisms control the corrosion process.     

Torsion classes of <Emphasis Type="Italic">MV</Emphasis>-algebras

 Torsion classes of MV-algebras are defined as radical classes which are closed with respect to homomorphisms; in this paper we investigate their relations to radical classes of lattice ordered groups and to varieties of MV-algebras. Supported by Grant VEGA 1/9056/02.