Case report: Acute peritonitis from non-traumatic rupture of the bladder

Spontaneous bladder rupture (SBR) is rare. This entity occurs outside of any traumatic context. A 70 years-old man was admitted for acute peritonitis, acute urinary retention and hematuria. Laparotomy and exploration showed acute generalized peritonitis related to a centimeter hole in the bladder dome. Peritoneal lavage was done with biopsy of the perforation edges, a cystostomy and suturing of the bladder. The immediate postoperative course was uneventful. The etiological investigation revealed a locally advanced and metastatic prostate cancer. The evolution was rapidly fatal and the patient’s death occurred two months later due to metastatic disease. The causes, diagnosis and treatment of SBR are reviewed by the authors

Phase boundary between Na–Si clathrates of structures I and II at high pressures and high temperatures

Understanding of the covalent clathrate formation is a crucial point for the design of new superhard materials with intrinsic coupling of superhardness and metallic conductivity. It has been found that silicon clathrates have the archetype structures, which can serve an existent model compounds for superhard clathrate frameworks Si–B, Si–C, B–C and C with intercalated atoms (e.g., alkali metals or even halogens) that can assure the metallic properties. Here we report our in situ and ex situ studies of high-pressure formation and stability of clathrates Na₈Si₄₆ (structure I) and Na₂₄₊xSi₁₃₆ (structure II). Experiments have been performed using standard Paris–Edinburgh cells (opposite anvils) up to 6 GPa and 1500 K. We have established that chemical interactions in the Na–Si system and transition between two structures of clathrates occur at temperatures below silicon melting. The strong sensitivity of crystallization products to the sodium concentration has been observed. A tentative diagram of clathrate transformations has been proposed. At least up to ~ 6 GPa, Na₂₄₊xSi₁₃₆ (structure II) is stable at lower temperatures as compared to Na₈Si₄₆ (structure I).Изучен in situ и ex situ процесс образования при высоких давлениях и стабильности клатратов Na₈Si₄₆ (структура I) и Na₂₄₊xSi₁₃₆ (структура II). Эксперименты были проведены в стандартных Париж-Эдинбургских ячейках (opposite anvils) при давлениях и температурах до 6 ГПа и 1500 K соответственно. Установлено, что химическое взаимодействие в системе Na–Si и переходы между двумя структурами клатратов происходят при температурах ниже температуры плавления кремния. Предложено первое приближение диаграммы превращений клатратов. Отмечена большая чувствительность продуктов кристаллизации к концентрации натрия. Na₂₄₊xSi₁₃₆ (структура II) является стабильной при более низких температурах по сравнению с Na₈Si₄₆ (структура I), по крайней мере до ~ 6 ГПа.Вивчено in situ і ex situ процес утворення при високих тисках і стабільності клатратів Na₈Si₄₆ (структура I) і Na₂₄₊xSi₁₃₆ (структура II). Експерименти було проведено в стандартних Париж-Единбурзький комірках (opposite anvils) при тисках і температурах до 6 ГПа і 1500 K відповідно. Встановлено, що хімічна взаємодія в системі Na–Si і переходи між двома структурами клатратов відбуваються при температурах нижче температури плавлення кремнію. Запропоновано перше наближення діаграми перетворень клатратів. Відзначено велику чутливість продуктів кристалізації до концентрації натрію. Na₂₄₊xSi₁₃₆ (структура II) є стабільною при більш низьких температурах у порівнянні з Na₈Si₄₆ (структура I), принаймні до ~ 6 ГПа

Spherical Polyelectrolyte Brushes Templated Hollow C MnO Nanospheres as Sulfur Host Materials for Li S Batteries

Li amp; 8722;S battery has been considered as the next generation energy storage device, which still suffers from the shuttle effect of lithium polysulfides LiPSs . In this work, mesoporous hollow carbon coated MnO nanospheres C MnO have been designed and synthesized using spherical polyelectrolyte brushes SPB as template, KMnO4 as MnO precursor, and polydopamine as carbon source to improve the electrochemical performance of Li amp; 8722;S battery. The hollow C MnO nanospheres enable the combination of physical confinement and chemical adsorption of the LiPSs. The thin carbon coating layer can provide good electrical conductivity and additional physical confinement to polysulfides. Moreover, the encapsulated MnO inside the carbon shell exhibits strong chemical adsorption to polysulfides. The constructed C MnO S cathode shows the discharge capacity of 1026 amp; 8197;mAh amp; 8201;g amp; 8722;1 at 0.1 amp; 8197;C with 79 capacity retention after 80 cycles. The synthesized hollow C MnO nanoparticles can work as highly efficient sulfur host materials, providing an effective solution to suppress the shuttle effect in Li amp; 8722;S batter

Set optimization - a rather short introduction

Recent developments in set optimization are surveyed and extended including various set relations as well as fundamental constructions of a convex analysis for set- and vector-valued functions, and duality for set optimization problems. Extensive sections with bibliographical comments summarize the state of the art. Applications to vector optimization and financial risk measures are discussed along with algorithmic approaches to set optimization problems

Optimal Reinsurance with One Insurer and Multiple Reinsurers

In this paper, we consider a one-period optimal reinsurance design model with n reinsurers and an insurer. For very general preferences of the insurer, we obtain that there exists a very intuitive pricing formula for all reinsurers that use a distortion premium principle. The insurer determines its optimal risk that it wants to reinsure via this pricing formula. This risk it wants to reinsure is then shared by the reinsurers via tranching. The optimal ceded loss functions among multiple reinsurers are derived explicitly under the additional assumptions that the insurer’s preferences are given by an inverse-S shaped distortion risk measure and that the reinsurer’s premium principles are some functions of the Conditional Value-at-Risk. We also demonstrate that under some prescribed conditions, it is never optimal for the insurer to cede its risk to more than two reinsurers

The Role of Orientation and Temperature on the Mechanical Properties of a 20 Years Old Wind Turbine Blade GFR Composite

This work evaluates the mechanical properties of the glass fiber reinforced polymer (GFRP) material taken from an out of service 100 KW power wind turbine blade which has been in service life of 20 years old. Investigated samples were taken from two positions of undamaged regions at 1.6 m and 5.4 m from the rotor hub, respectively. Microstructure investigation and lay-up analysis were carried out. Fiber weight fraction of the investigated samples was ranging between 0.55–0.60. Tensile and compression tests were carried out at the temperature range from −10 °C to +50 °C on specimens which were machined so as to be loaded in the blade length direction LD, transverse to the blade length TD and off axis; 45° to the blade length. Tensile elastic modulus of the investigated GFRP was determined in the three direction tested. The number of fiber fabric layers found to be decreasing along the blade length away from the root and the density of the fibers along the length is the highest (858 gm/mm2) and in the transverse direction is the lowest (83 gm/mm2). The microstructure of the GFRP composite showed good wetting for the fiber by the polymer with some features of lack of penetration at the high density fiber bundles and some production porosity in the matrix. The tensile Properties at room temperature (RT) and high temperature are almost similar with the highest properties for the samples aligned with the blade length. The compressive strength is highest at the transverse direction samples and lowest at the blade length direction and decreasing with the increase of the test temperature. The bending properties are significantly affected by the fiber orientation with the highest properties for samples aligned with the blade length and the lowest for the samples with the transverse direction