Значение традиционных нравственно-эстетических ценностей в формировании духовного мира ребенка в произведениях Эмиля Амита

Предлагаемый вниманию материал посвящён значению традиционных нравственно-эстетических ценностей в формировании духовного мира подрастающего поколения. Обращение к испокон веков ценимым ценностям под пером автора обретает особое звучание.Пропонований увазі матеріал присвячений проблемі еволюції морального ідеалу в творчості Е.Аміт. Традиційні споконвічні ціності під пером автора набувають особливого звучання.The material which is proposed to you dedicated to a problem of the evolution of the moral ideal in the creation of A Rmit

Деградация человеческого потенциала как фактор латентной составляющей деятельности высшей школы Украины

Рассмотрены проблемы тенизации и коррупционности функционирования украин-ской высшей школы на фоне вектора развития показателей потенциала населения страны.Розглянуті проблеми тінізації і коррупційності функціонування української вищої школи на тлі вектору розвитку показників потенціалу населення країни

All-solid-state lithium-sulfur battery based on a nanoconfined LiBH₄ electrolyte

In this work we characterize all-solid-state lithium-sulfur batteries based on nano-confined LiBH4in mesoporous silica as solid electrolytes. The nano-confined LiBH4has fast ionic lithium conductivity at room temperature, 0.1 mScm-1, negligible electronic conductivity and its cationic transport number (t+= 0.96), close to unity, demonstrates a purely cationic conductor. The electrolyte has an excellent stability against lithium metal. The behavior of the batteries is studied by cyclic voltammetry and repeated charge/discharge cycles in galvanostatic conditions. The batteries show very good performance, delivering high capacities versus sulfur mass, typically 1220 mAhg-1after 40 cycles at moderate temperature (55°C), 0.03 C rates and working voltage of 2 V. © The Author(s) 2016

Стратегия хирургического лечения местнораспространенных опухолей малого таза с применением эвисцераций. Сообщение1. Синдромы кишечной непроходимости, кровотечения и сдавления мочевых путей

Представлен обзор и анализ методов хирургической коррекции синдромов кишечной непроходимости, кровотечения и сдавления мочевых путей при местнораспространенных опухолях малого таза. Обобщен 10−летний опыт хирургического лечения данной патологии в Институте общей и неотложной хирургии. Приведена классификация основных методов оперативных пособий, направленных на достижение гемостаза и деривации мочи и кала.The methods of surgical correction of syndromes of intestinal obstruction, hemorrhage and urinary tract compression at local tumors of the small pelvis are reviewed and analyzed. The 10−year experience of surgical treatment for this pathology at Institute for General and Urgent Surgery is generalized. Main methods of operative treatment aimed at achievement of hemostasis and urine and feces derivation are presented

In Situ Transmission Electron Microscopy to Study the Location and Distribution Effect of Pt on the Reduction of Co3O4–SiO2

The addition of Pt generally promotes the reduction of Co3O4 in supported catalysts, which further improves their activity and selectivity. However, due to the limited spatial resolution, how Pt and its location and distribution affect the reduction of Co3O4 remains unclear. Using ex situ and in situ ambient pressure scanning transmission electron microscopy, combined with temperature-programmed reduction, the reduction of silica-supported Co3O4 without Pt and with different location and distribution of Pt is studied. Shrinkage of Co3O4 nanoparticles is directly observed during their reduction, and Pt greatly lowers the reduction temperature. For the first time, the initial reduction of Co3O4 with and without Pt is studied at the nanoscale. The initial reduction of Co3O4 changes from surface to interface between Co3O4 and SiO2. Small Pt nanoparticles located at the interface between Co3O4 and SiO2 promote the reduction of Co3O4 by the detachment of Co3O4/CoO from SiO2. After reduction, the Pt and part of the Co form an alloy with Pt well dispersed. This study for the first time unravels the effects of Pt location and distribution on the reduction of Co3O4 nanoparticles, and helps to design cobalt-based catalysts with efficient use of Pt as a reduction promoter

Carbon supported lithium hydride nanoparticles: Impact of preparation conditions on particle size and hydrogen sorption

Nanosizing of light metal hydrides has yielded significant improvements to their hydrogen storage properties. We explored for the first time a procedure for preparing supported LiH nanoparticles. Impregnation of a carbon framework with a butyllithium solution, followed by reaction with gaseous hydrogen yielded LiH particles ranging in size from 2 nm to the micrometer scale. Reducing the reaction temperature from 300 C to 100 C, as well as the use of a t-butyllithium precursor instead of an n-butyllithium precursor, gave significant improvements on the degree of confinement of the LiH particles. The particle size of the LiH has a significant impact on the hydrogen release profile, 11 nm crystallites begin to release hydrogen as low as 100 C under argon flow, a reduction of roughly 400 C on the macrocrystalline system. The hydrogen release is reversible, with hydrogen uptake after desorption as high as 7.0 wt% w.r.t. LiH (0.8 wt% w.r.t the sample) under 0.1 bar of hydrogen at 200 C and full uptake takes place within 5 min at 26 bar. This new preparation procedure for supported light metal hydrides is particularly relevant for the field of hydrogen storage

Surface-modified carbon materials for CO2 electroreduction

The electrochemical reduction of CO2 to produce sustainable fuels and chemicals has attracted great attention in recent years. It is shown that surface-modified carbons catalyze the CO2RR. This study reports a strategy to modify the surface of commercially available carbon materials by adding oxygen and nitrogen surface groups without modifying its graphitic structure. Clear differences in CO2RR activity, selectivity and the turnover frequency between the surface-modified carbons were observed, and these differences were ascribed to the nature of the surface groups chemistry and the point of zero charge (PZC). The results show that nitrogen-containing surface groups are highly selective towards the formation of CO from the electroreduction of CO2 in comparison with the oxygen-containing surface groups, and the carbon without surface groups. This demonstrates that the selectivity of carbon for CO2RR can be rationally tuned by simply altering the surface chemistry via surface functionalization

Ionic conductivity in complex metal hydride-based nanocomposite materials: The impact of nanostructuring and nanocomposite formation

Complex metal hydrides have recently gained interest as solid electrolytes for all-solid-state batteries due to their light weight, easy deformability, and fast ion mobility at elevated temperatures. However, increasing their low conductivity at room temperature is a prerequisite for application. In this review, two strategies to enhance room temperature conductivity in complex metal hydrides, nanostructuring and nanocomposite formation, are highlighted. First, the recent achievements in nanostructured complex metal hydride-based ion conductors and complex metal hydride/metal oxide nanocomposite ion conductors are summarized, and the trends and challenges in their preparation are discussed. Then, the reported all-solid-state batteries based on complex metal hydride nanocomposite electrolytes are highlighted. Finally, future research directions and perspectives are proposed, both for the preparation of improved metal hydride ion conductors, as well as metal hydride-based all-solid-state batteries

Improving the Cycle Life of Solid-State Batteries by Addition of Oxide Nanoparticles to a Complex Hydride Solid Electrolyte

We report that the addition of silica nanoparticles to the iodide-substituted LiBH4 (h-Li(BH4)0.8(I)0.2) improves the ion conductivity and, remarkably, the cycle life of the all-solid state batteries. The h-Li(BH4)0.8(I)0.2-SiO2 was synthesized by mechanochemical treatment and possesses a Li+ conductivity of 9.3 × 10-5 S cm-1 at RT. It has an electrochemical stability window of about 2.5 V vs Li+/Li and an improved stability against Li-metal, compared to h-Li(BH4)0.8(I)0.2, owing to the addition of oxide nanoparticles, which we ascribed to a greater mechanical stability of the solid-state electrolyte. The all-solid state battery Li|h-Li(BH4)0.8(I)0.2-SiO2|TiS2 demonstrated a good long-term cyclability, i.e., over 200 cycles at C/20 and even including a C-rate of C/5, demonstrating that the addition of oxide nanoparticles improves the cycling stability of the electrolyte