Periods of stable and unstable ERP topography for target and nontarget visual stimuli

Topographic analysis of event-related potentials (ERPs) has been used for segmentation of brain activity into microstates for a long time. But little is known about dynamics of topographic changes. This work shows that this dynamics is rather complex: ERPs consist of relatively long periods of stable topography (about 50 ms long) and relatively short unstable periods interspersed with them (about 20 ms long). A mathematical algorithm used for estimation of a degree of ERP topography instability is given. It is based on calculation of successive difference between normalized topographical vectors.     

Fibrous carbon materials having a protective oxidation resistant coating

Conclusions -- A gas-phase method of depositing one- or multiple-component carbide coatings on CFM of various textile structures has been developed. With preservation of the strength and elastic characteristics of the CFM, the thermo-oxidative resistance of the material is increased, plus the temperature range for the decomposition is shifted into the higher temperature region — by 150–250°C as compared with the starting material.-- CFM with protective coatings are finding ever greater use in making filters for cleaning up high-temperature gas-air mixtures.VNIIPV. Translated from Khimicheskie Volokna, No. 3, pp. 47–48, May–June, 1991.     

High-modulus,high-strength carbon fibre based on polyacrylonitrile

Conclusions -- The effect of the method of preliminary heat treatment and of the structure of fibre being subjected to boronation on the strength of high-modulus carbon fibres has been shown.-- A moreoriented structure of the fibre subjected to boronation and stress relaxation during the heat-treatment process aid in bringing about an increase in strength of high-modulus carbon fibre up to 3.0–3.5 GPa at an elastic modulus greater than 700 GPa.All-Union Scientific Research and Project-Technological Institute of Electrical Carbon Articles, Élektrougli. Translated from Khimicheskie Volokna, No. 3, pp. 29–30, May–June, 1991.     

Modification of the surface of polyacrylonitrile fibres before oxidation with a dispersion of technical carbon

Conclusions -- The possibility of using dispersions of technical carbon in a medium of ethylene glycol, an aqueous solution of a binder of the Sokrat-binder type, or an alcoholic solution of polyvinyl butyral for the modification of polyacrylonitrile fibres before thermo-oxidation, which ensure obtaining a stable and uniform carbon-containing film on the fibre surface has been established.-- The use of ethylene glycol as the dispersion medium leads to retention of the strength of fibres after heat treatment at the level of the starting fibres and reduces the specific bulk electrical resistance.-- Application of aqueous solutions of the Sokrat-binder aids in preserving fibre strength during thermo-oxidation. The linear density of the fibre and its ability to be oxidized are increased, but the specific bulk electrical resistance and elongation are reduced.-- The use of alcoholic solutions of polyvinyl butyral makes it possible not only to preserve fibre strength but also to considerably increase it during the thermo-oxidation process. Thereupon, the linear density of the fibres is significantly reduced, and at a dispersion content of 10% by wt. technical carbon, one can obtain electrically-conducting oxidized fibres.Translated from Khimicheskie Volokna, No. 4, pp. 36–37, July–August, 1991.     

Versuchsplanerische Untersuchung der Umesterung von Sojaöl mit Ethanol im Mikroreaktor

Base‐catalyzed transesterification of fats and oils with primary alcohols in discontinuous operation is an established batch process for the biodiesel production. However, the application of microreaction technology and continuous flow process lead to an increase of process intensification. The ethanol/soy bean oil ratio at low flow rates as well as the reactor geometry have the most evident effects on the fatty acid ethyl ester yield of KOH‐catalyzed ethanolysis of soy bean oil in microreactors. The influence of the catalyst concentration is of a lower importance.     

Complex of HIV-1 Integrase with Cellular Ku Protein: Interaction Interface and Search for Inhibitors

The interaction of HIV-1 integrase and the cellular Ku70 protein is necessary for HIV replication due to its positive effect on post-integration DNA repair. We have previously described in detail the Ku70 binding site within integrase. However, the integrase binding site in Ku70 remained poorly characterized. Here, using a peptide fishing assay and site-directed mutagenesis, we have identified residues I72, S73, and I76 of Ku70 as key for integrase binding. The molecular dynamics studies have revealed a possible way for IN to bind to Ku70, which is consistent with experimental data. According to this model, residues I72 and I76 of Ku70 form a “leucine zipper” with integrase residues, and, therefore, their concealment by low-molecular-weight compounds should impede the Ku70 interaction with integrase. We have identified such compounds by molecular docking and have confirmed their capacity to inhibit the formation of the integrase complex with Ku70. Our data demonstrate that the site of IN binding within Ku70 identified in the present work may be used for further search for inhibitors of the integrase binding to Ku70.     

Comparative Effects of Deferiprone and Salinomycin on Lead-Induced Disturbance in the Homeostasis of Intrarenal Essential Elements in Mice

Lead (Pb) exposure induces severe nephrotoxic effects in humans and animals. Herein, we compare the effects of two chelating agents, salinomycin and deferiprone, on Pb-induced renal alterations in mice and in the homeostasis of essential elements. Adult male mice (Institute of Cancer Research (ICR)) were randomized into four groups: control (Ctrl)—untreated mice administered distilled water for 28 days; Pb-exposed group (Pb)—mice administered orally an average daily dose of 80 mg/kg body weight (BW) lead (II) nitrate (Pb(NO₃)₂) during the first two weeks of the experimental protocol followed by the administration of distilled water for another two weeks; salinomycin-treated (Pb + Sal) group—Pb-exposed mice, administered an average daily dose of 16 mg/kg BW salinomycin for two weeks; deferiprone-treated (Pb + Def) group—Pb-exposed mice, administered an average daily dose of 20 mg/kg BW deferiprone for 14 days. The exposure of mice to Pb induced significant accumulation of the toxic metal in the kidneys and elicited inflammation with leukocyte infiltrations near the glomerulus. Biochemical analysis of the sera revealed that Pb significantly altered the renal function markers. Pb-induced renal toxicity was accompanied by a significant decrease in the endogenous renal concentrations of phosphorous (P), calcium (Ca), copper (Cu) and selenium (Se). In contrast to deferiprone, salinomycin significantly improved renal morphology in Pb-treated mice and decreased the Pb content by 13.62% compared to the Pb-exposed group. There was also a mild decrease in the renal endogenous concentration of magnesium (Mg) and elevation of the renal concentration of iron (Fe) in the salinomycin-treated group compared to controls. Overall, the results demonstrated that salinomycin is a more effective chelating agent for the treatment of Pb-induced alterations in renal morphology compared to deferiprone.     

Peculiar electric properties of polarized layer in alkaline silicate glasses

Broadband dielectric spectroscopy (BDS) was applied to study polarization phenomena in alkaline silicate glasses, in particular, properties and structure of subsurface (anodic) polarized layers forming in poling with deposited film electrodes of different structures. A model of poled glasses which does not contradict experimental data is proposed. In accordance with the model, a poled glass is presented as two resistor-capacitor circuits in a series connection, one of which is the polarized layer and another is the rest of the sample. It is found that the electric properties of the layers essentially depend on the structure of the anodic electrode used in glass poling. It is also shown that the dielectric response of poled glass samples is mainly determined by the electric properties of the submicron polarized layers and this gives an opportunity to reveal specific properties of the layers rather than ones of the glass sample bulk. Revealed temperature dependence of DC conductivity of the polarized layers obeys Arrhenius's law, and determining activation energy does not depend on the electrode. Finally, it is noted that today above-mentioned information about polarized layers can be obtained only by BDS.     

Regeneration of Pd/TiO2 catalyst deactivated in reductive CCl4 transformations by the treatment with supercritical CO2, ozone in supercritical CO2 or oxygen plasma

Carbonaceous deposits formation was established as the primary reason of Pd/TiO₂ catalyst deactivation during reductive processing of CCl₄ to form hydrodechlorination and oligomerization products. Three methods of carbonaceous deposits elimination were tested: (1) extraction by supercritical CO₂, (2) oxidation by ozone in supercritical CO₂, and (3) low-temperature glow-discharge oxygen plasma treatment. Synchronic thermal analysis confirms effective carbonaceous deposits removal during regeneration by ozone or low temperature glow-discharge oxygen plasma; by XPS deep oxidation of surface Pd after oxidative treatment (by ozone or oxygen plasma) was found. Thus H₂ reduction was proposed as the second step making possible full regeneration of initial catalytic activity of Pd/TiO₂.     

Effect of the nature of the support of a cobalt catalyst on the synthesis of hydrocarbons from CO,H<Subscript>2</Subscript>, and C<Subscript>2</Subscript>H<Subscript>4</Subscript>

The effect of the nature of the support of a Co catalyst on the synthesis of hydrocarbons from CO, H₂, and C₂H₄ was studied in this work. It was found that the introduction of ethylene into synthesis gas resulted in an increase in the yield of liquid hydrocarbons. In this case, the conversion of C₂H₄ was complete and the degree of its involvement into the synthesis of C₅₊ hydrocarbons depended on the concentration of this component in the starting mixture and the nature of the support. Specific features of the adsorption of CO and C₂H₄ on the used Co catalysts were determined using a temperature-programmed desorption method.