Experimental quantification of natural convective heat transfer within annulus space filled with a H2O-Cu nanofluid saturated porous medium. Application to electronics cooling

This experimental study deals with cooling electronics contained in a hemispherical cavity whose cupola is maintained isothermal, being its base inclined at an angle varying from 0° (horizontal disc with the cupola oriented upwards) to 135°. The active component is a dome centered on this base. The space between the differentially heated elements of the assembly is filled with a porous medium of high porosity saturated by a water–copper nanofluid whose volume fraction varies between 0% (pure water) and 7%. The Rayleigh number based on the radius of the cupola reaches high values up to 7.29 × 10¹⁰ given the important surface heat flux generated by the device during operation. The ratio between the thermal conductivity of the solid matrix and that of the base fluid ranges between 0 (interstitial volume without porous medium) and 41.4 corresponding to the intended applications. This experimental study done with an industrial prototype at scale 1 quantifies the natural convective heat transfer via the Nusselt number determined for many configurations obtained by varying the solid-fluid thermal conductivity ratio, the inclination angle, the Rayleigh number, and the volume fraction. The study clearly shows that the cooling performance of the Cu-H₂O nanofluid degrades with its age and the number of times it has been used. Analysis of the results reproducibility also proves the irreversibility of the performance. The measured values were compared with those obtained in a recent numerical study based on the volume control method. The observed deviations taking into account the experimental uncertainty margins validate the mathematical model implemented in the numerical approach.     

Experimental confirmation of Kelvin's equilibria

We experimentally corroborate the core analytical deductions of Thomson's 124-year-old theorem, vis-à-vis the stability of a ring of N vortices. Observations made in water vortices produced inside a cylinder via a revolving disk confirm that the regular N-gons are stable for Nor=8. The N相似文献   

Design and characterization of new advanced energetic biopolymers based on surface functionalized cellulosic materials

A new class of energetic biopolymers, which contain nitrate ester (O-NO₂) and nitramine (N-NO₂) as explosophoric groups, was successfully synthesized by surface modification of renewable pristine cellulose (PC) and microcrystalline cellulose (MCC) via epichlorohydrin-mediated amination followed by nitration process to produce new promising energetic aminated and nitrated cellulose and microcrystalline cellulose (APCN and AMCCN). Their structural, thermal, crystallinity and morphological features were examined and compared to those of the common cellulose nitrate. Furthermore, their energetic performances were evaluated by EXPLO5 V6.04 software. Experimental results confirm the successful chemical functionalization process to develop insensitive APCN and AMCCN with outstanding features such as nitrogen content of 15.01% and 15.39%, density of 1.692 g/cm³ and 1.708 g/cm³, and detonation velocity of 7526 m/s and 7752 m/s, respectively, which are significantly higher than those of the nitrated unmodified cellulosic biopolymers. The present investigation provides a suitable pathway to design new insensitive and energy-rich dense cellulosic biopolymers for potential application in high-performance solid propellants and composite explosives.

     

Oxidative Addition of Carbon–Carbon Bonds to Gold

The oxidative addition of strained C? C bonds (biphenylene, benzocyclobutenone) to DPCb (diphosphino‐carborane) gold(I) complexes is reported. The resulting cationic organogold(III) complexes have been isolated and fully characterized. Experimental conditions can be adjusted to obtain selectively acyl gold(III) complexes resulting from oxidative addition of either the C(aryl)? C(O) or C(alkyl)? C(O) bond of benzocyclobutenone. DFT calculations provide mechanistic insight into this unprecedented transformation.     

Thermal design of a spherical electronic device naturally cooled by means of water–copper nanofluid saturated porous media

Journal of Thermal Analysis and Calorimetry - The present work deals with thermal regulation of a spherical electronic device used in naval navigation techniques. Cooling is achieved by means of...     

A GENERAL DECAY AND OPTIMAL DECAY RESULT IN A HEAT SYSTEM WITH A VISCOELASTIC TERM

We consider a quasilinear heat system in the presence of an integral term and establish a general and optimal decay result from which improves and generalizes several stability results in the literature.     

On a solvable system of p difference equations of higher order

Periodica Mathematica Hungarica - In this paper we present the well-defined solution of the following system of higher-order rational difference equations: $$\begin{aligned}...     

Thermal and FTIR analysis of the miscibility and phase behaviour of poly (isobutyl methacrylate-co-4-vinylpyridine)/poly (styrene-co-acrylic acid) systems

The miscibility and phase behaviour of poly (isobutyl methacrylate-co-4-vinylpyridine) containing 20 mol% of 4-vinylpyridine (IBM4VP20) and poly (styrene-co-acrylic acid) containing 27 or 32 mol% of acrylic acid (SAA27 or SAA32) mixtures were investigated by DSC, TGA and FTIR spectroscopy in the 25–180 °C temperature range. The results showed that sufficient specific carboxyl–pyridine hydrogen bonding interactions occurred between these copolymers and led to miscible blends as cast from THF and to inter-polymer complexes of significantly improved thermal stability when butan-2-one is the common solvent. The self-association effect on the inter-polymer interactions was evidenced by the decrease of complexation yields, observed when the carboxylic content is increased above 27 mol% as with SAA32.The trend of phase behaviour predicted by a thermodynamic analysis of the specific interactions of hydrogen bonding type that occurred between the two components of the SAA27/IBM4VP20 blends, neglecting the weak carboxyl–ester interactions and the functional group accessibility effect, carried out using the Painter–Coleman association model that considers the screening effects, is in a fair agreement with the experimental results. Moreover an LCST is predicted to occur at relatively high temperature.     

Nigericin and grisorixin methyl ester from the Algerian soil-living Streptomyces youssoufiensis SF10 strain: a computational study on their epimeric structures and evaluation of glioblastoma stem cells growth inhibition

The present work describes the metabolites produced by a strain identified as Streptomyces youssoufiensis, whose secondary metabolites profile has not been studied so far. The crude ethyl acetate extract was analyzed by high performance liquid chromatography-electrospray ionization mass spectrometry, leading to the detection of the ionophoric polyethers nigericin, epinigericin, abierixin and the newly isolated grisorixin methyl ester. The presence of epimeric forms of nigericin/epinigericin and grisorixin/epigrisorixin has spurred density functional theory computational calculations. This analysis was able to provide the relative stability of the most favored epimers, setting the basis for general structural considerations applicable to several other polyethers. Both nigericin sodium salt and grisorixin methyl ester showed to affect glioblastoma stem cells proliferation in a dose-dependent manner, with a higher activity for the more lipophilic grisorixin methyl ester (GI₅₀ values of 3.85 and 3.05 μM for VIPI and COMI human glioblastoma stem cells, respectively).     

Cationic Gold(III) Alkyl Complexes: Generation,Trapping, and Insertion of Norbornene

Migratory insertion of alkenes into gold–carbon bonds, a fundamental yet unprecedented organometallic transformation, has been investigated from a discrete (P,C) cyclometalated gold(III) dimethyl complex. Methide abstraction by B(C₆F₅)₃ is shown to generate a highly reactive cationic Au^III complex that evolves spontaneously by C₆F₅ transfer from boron. In the presence of norbornene, migratory insertion into the Au C bond proceeds readily. The resulting norbornyl complex is efficiently trapped with pyridines or chloride to give stable four‐coordinate adducts.