Effect of Y substitution on the structural and magnetic properties of Dy1-xYxCo5 compounds

Structural and magnetization studies were carried out on Dy1-xYxCo5 [x = 0, 0.2, 0.4, 0.6, 0.8, 1] compounds which crystallize in the hexagonal CaCu5-type structure. Lattice parameters and unit-cell volume increase with Y concentration. Large thermomagnetic irreversibility between the field-cooled and the zero-field cooled magnetization data has been observed in all the compounds, which has been attributed to the domain wall pinning effect. Temperature dependence of magnetization data shows that except DyCo5 and YCo5, all the compounds show spin reorientation transitions in the range of 5-300 K. The spin reorientation temperature decreases from 266 K for x=0.2 to 100 K for x=0.8. Powder x-ray diffractograms of the magnetically aligned samples show that DyCo5 has planar anisotropy at room temperature whereas all the other compounds possess axial anisotropy. The spin reorientation transition has been attributed to a change in the easy magnetization direction from the ab-plane to the c-axis, as the temperature is increased. The anisotropy field and the first order anisotropy constant are found to be quite high in all the compounds except DyCo5. The magnetic properties have been explained by taking into account the variations in contributions arising from the rare earth and transition metal sublattices.Comment: 12 pages, 7 figure

Perspective of interstitial hydrides of high-entropy alloys for vehicular hydrogen storage

The transport sector is an important source of CO2 emissions worldwide, and a transition towards hydrogen-fuelled vehicles is a potential remedy. These vehicles require improvements in storage capacities, which can be realised by forming the interstitial hydrides of High-Entropy Alloys (HEAs) by synthesising single-phase hydrides with a randomised atomic distribution of the metal elements within these alloys. Not only is the randomness of elemental distribution in the hydride essential, so too is the affinity of the individual components towards hydride formation, which drastically improves the prospective storage. By evaluating the composition and properties of the best-performing hydride forming alloys, various parameters strongly influencing hydrogen capacities can be inferred. Herein, the state of literature regarding the parameters with the highest importance for hydrogen sorption in HEAs is discussed for the first time with particular focus on how they may be introduced to storage on-board vehicles

“DARE TO THINK, DARE TO SPEAK, DARE TO ACT”: TRANSLATING POLITICAL SLOGANS IN MO YAN’S FROG FROM CHINESE INTO ROMANIAN, ITALIAN AND SPANISH

Slogans are some of the most typical elements of Chinese politics and a significant part of the important decisions took by the Communist Party are made known to the masses using slogans, such as “It is right to rebel!”, “Destroy the four olds!”, or “The most serious problem is to teach the peasants”. Participation in political life after the founding of the People’s Republic, in 1949, could be done only by employing slogans or formulae derived from the elite political discourse. The major impact of politics upon people’s lives has transformed the slogan from a manifestation of political authority into a manipulation tool used by people to make their counterparts react in a desired way. Mo Yan’s novel Frog (Wa/Broaște/Rana/Le rane) shows to what extent slogans can influence ordinary people’s lives, where the use of real political slogans or even make-believe slogans – discourse modeled to resemble a political slogan –, are either attempts by the characters to make their voices heard and participate into decision making, or small acts of rebellion against the system. Considering the culture specific character of the slogans, the fact that they were created into a very particular socio-political context, the paper analyzes the translations of the slogans in Mo Yan’s novel into three Romance languages, in an attempt to identify not only the techniques and the choices made by the translators, but also the possibility, or impossibility, to recreate the slogan and conserve its original impact into the target culture

Etude cristallographique et magnétique de composés intermétalliques à base d’éléments de terre rare, de cobalt et d’éléments p, dérivant de la structure CaCu5

This study is devoted to the structural and magnetic properties of intermetallic compounds of rare earth elements, cobalt and p elements, deriving from the CaCu5 type structure.The RCo5-xMx (M = Al, Ga and Si) phases preserve the CaCu5 structure, whereas the Rn+1Co3n+5B2n compounds form various superstructures. A preferential occupation of Al, Ga and Si atoms for the 3g site of the CaCu5 structure was established by means of neutron diffraction. The iron for cobalt substitution in the PrCo4Al and PrCo4Ga compounds shows a preferential occupation for the 3g site.The presence of M elements in the RCo5-xMx compounds modifies significantly the magnetic phase diagrams. X-ray absorption spectroscopy measurements performed for CeCo5-xMx and Cen+1Co3n+5B2n demonstrate that cerium shows an intermediate valence state.Hydrogen insertion in Y2Co7 induces an orthorhombic distortion for the Y2Co7H6 hydride. A metamagnetic transition is observed in this hydride.Ce travail est consacré à l’étude des propriétés structurales et magnétiques des composés intermétalliques à base d’éléments de terre rare, de cobalt et d’éléments p dérivant de la structure CaCu5. Les phases RCo5-xMx (M = Al, Ga et Si) conservent la structure CaCu5, tandis que les composés Rn+1Co3n+5B2n présentent des surstructures variées. Une occupation préférentielle des atomes Al, Ga, Si pour le site 3g de la structure CaCu5 a été démontrée par diffraction neutronique. La substitution du fer au cobalt dans les composés PrCo4Al et PrCo4Ga s’effectue préférentiellement dans le site 3g de la structure. La présence d’éléments M dans les phases RCo5-xMx modifie sensiblement les diagrammes de phase magnétiques. Les mesures de spectroscopie d’absorption X réalisées pour les composés CeCo5-xMx et Cen+1Co3n+5B2n ont établit que le cérium est dans un état de valence intermédiaire. L’insertion de l’hydrogène dans Y2Co7 conduit à une distorsion orthorhombique pour Y2Co7H6 et provoque l’apparition d’une transition métamagnétique

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

Ultrasmall MgH_2 Nanoparticles Embedded in an Ordered Microporous Carbon Exhibiting Rapid Hydrogen Sorption Kinetics

MgH_2 nanoparticles with different average sizes have been prepared as ordered microporous carbon by tuning the Mg amount from 15 to 50 wt %. Ultrasmall particles with mean sizes of 1.3 and 3.0 nm have been obtained for 15 and 25 wt % Mg contents, respectively. The hydrogen desorption properties strongly depend on the nanoparticle size, as evidenced by different thermal analysis techniques. The onset temperature of hydrogen desorption for MgH_2 nanoparticles below 3 nm occurs at a temperature about 245 K lower than for microcrystalline material. Two distinct hydrogen desorption peaks are noticed for nanoparticles with mean sizes of 1.3 and 3.0 nm, as confirmed by TDS and HP-DSC. 1H NMR investigations suggest the presence of two MgH_2 populations with enhanced hydrogen mobility, as compared to the microcrystalline hydride. The short hydrogen diffusion path and the enhanced hydrogen mobility may explain the increased desorption kinetics of these ultrasmall nanoparticles

Metal Hydrides and Related Materials - Energy Carriers for Novel Hydrogen and Electrochemical Storage

The seventh edition of the International Renewable and Sustainable Energy Conference (IRSEC) was held in Agadir (Sofitel Royal Bay, November 27–30, Morocco) under the Program Chair of Prof. Ahmed Ennaoui (IRESEN). IRSEC, as one of the biggest conferences in north Africa, aims at creating an international forum to facilitate discussions and exchanges in all aspects of renewable and sustainable energy. This Viewpoint will summarize the scientific presentations and stimulated discussions during the Special Session (November 28–29) on Metal Hydrides’ Energy covering topics of metal hydrides and energy related issues for innovative processes and technologies, with a focus on magnesium-based hydrides, intermetallic hydrides, complex and melt hydrides, porous materials, and thin films

Analysis of high and selective uptake of CO2 in an oxamide-containing {Cu2(OOCR)4}-based metal-organic framework

The porous framework [Cu2(H2O)2L].4H2O.2DMA ((H¬4¬L = oxalylbis(azanediyl)diisophthalic acid; DMA = N,N-dimethylacetamide), denoted NOTT-125, is formed by connection of {Cu2(RCOO)4} paddlewheels with the isophthalate linkers in L4-. A single crystal structure determination reveals that NOTT-125 crystallises in monoclinic cell with a = 27.9161(6) Å, b = 18.6627(4) Å and c = 32.3643(8) Å, space group P2 (1)/c. The structure of this material shows fof topology, which can be viewed as the packing of two types of cages (Cage A and Cage B) in 3-dimensional space. Cage A is constructed by twelve {Cu2(OOCR)4} paddlewheels and six linkers to form an ellipsoid-shaped cavity approximately 24.0 Å along its long axis and 9.6 Å across the central diameter. Cage B consists of six {Cu2(OOCR)4} units and twelve linkers with a spherical diameter of 12.7 Å taking into account the van der Waals radii of the atoms. NOTT-125 incorporates oxamide functionality within the pore walls, and this, combined with high porosity in the desolvated NOTT-125a, is responsible for excellent CO2 uptake (40.1 wt% at 273 K and 1 bar) and selectivity for CO2 over CH4 or N2. Grand canonical Monte Carlo (GCMC) simulations show excellent agreement with the experimental gas isotherm data, and a computational study into the specific interactions and binding energies of both CO2 and CH4 with the linkers in NOTT-125 reveals a set of strong interactions between CO2 and the oxamide motif, which are not possible with a single amide

A new method to position and functionalize metal-organic framework crystals

With controlled nanometre-sized pores and surface areas of thousands of square metres per gram, metal-organic frameworks (MOFs) may have an integral role in future catalysis, filtration and sensing applications. In general, for MOF-based device fabrication, well-organized or patterned MOF growth is required, and thus conventional synthetic routes are not suitable. Moreover, to expand their applicability, the introduction of additional functionality into MOFs is desirable. Here, we explore the use of nanostructured poly-hydrate zinc phosphate (α-hopeite) microparticles as nucleation seeds for MOFs that simultaneously address all these issues. Affording spatial control of nucleation and significantly accelerating MOF growth, these α-hopeite microparticles are found to act as nucleation agents both in solution and on solid surfaces. In addition, the introduction of functional nanoparticles (metallic, semiconducting, polymeric) into these nucleating seeds translates directly to the fabrication of functional MOFs suitable for molecular size-selective applications