Almost sure existence of global weak solutions for super-critical Navier-Stokes equations

In this paper we show that after suitable data randomization there exists a large set of super-critical periodic initial data, in $H^{-\alpha}({\mathbb T}^d)$ for some $\alpha(d) > 0$, for both 2d and 3d Navier-Stokes equations for which global energy bounds are proved. As a consequence, we obtain almost sure super-critical global weak solutions. We also show that in 2d these global weak solutions are unique.Comment: 22 pages, a revised argument in Section 5, the $d=3$ cas

Electrodeposition of iron powder particles of different characteristics

Iron deposits obtained at high current densities and overpotentials are very important from a technological point of view. It has been stated that the open and porous structures of copper or iron deposits obtained at high current densities were ideally suited for use as electrodes in electrochemical devices such as fuel cells, batteries and chemical sensors, while the extremely high surface area is relevant for evaluating some electrochemical reactions. Mainly two types of electrolytes were investigated and these were based on sulfate and chloride electrolytes. With increasing duration of electrolysis, dendrites merge, which is unacceptable for the case of further application. These deposits must be grinded in order to obtain powders. However, in the range of lower acidity the deposits become powdery and, in some cases, may be spongy and sticky. Generally, up to now research indicates that electrodeposition of Fe powders have two steps, deposition of fragile film and grinding. It must be emphasized that we tried and succeeded to obtain Fe powders without grinding process. The aim of this work was to investigate electrodeposition processes of Fe powders from sulfate and chloride electrolytes and morphologies of powder as a function of type of electrolyte and current density.Belgrade, Serbia, June 6-10, 201

Electrodeposition of iron powder particles of different characteristics

Iron deposits obtained at high current densities and overpotentials are very important from a technological point of view. It has been stated that the open and porous structures of copper or iron deposits obtained at high current densities were ideally suited for use as electrodes in electrochemical devices such as fuel cells, batteries and chemical sensors, while the extremely high surface area is relevant for evaluating some electrochemical reactions. Mainly two types of electrolytes were investigated and these were based on sulfate and chloride electrolytes. With increasing duration of electrolysis, dendrites merge, which is unacceptable for the case of further application. These deposits must be grinded in order to obtain powders. However, in the range of lower acidity the deposits become powdery and, in some cases, may be spongy and sticky. Generally, up to now research indicates that electrodeposition of Fe powders have two steps, deposition of fragile film and grinding. It must be emphasized that we tried and succeeded to obtain Fe powders without grinding process. The aim of this work was to investigate electrodeposition processes of Fe powders from sulfate and chloride electrolytes and morphologies of powder as a function of type of electrolyte and current density.Belgrade, Serbia, June 6-10, 201

Electrodeposition of Fe Powder from Citrate Containing Electrolytes

Polarization characteristics of the electrodeposition processes of Fe powders from different citrate electrolytes and the morphology of the obtained powders were investigated. The effect of complexing agents on the cathodic polarization, the current efficiency and morphology of electrodeposited Fe powders were investigated. The morphology of obtained powders depends on the kind of supporting electrolyte, but not on the current density in investigated range. A characteristic feature of powders deposited from citrate-chloride supporting electrolyte is cauliflower-like compressed structure. On the other side, Fe powders electrodeposited from citrate-sulfate supporting electrolyte appeared in the form of spongy-like agglomerates. Possibility of Fe powders protection from corrosion in the process of production and during long-term storing has been shown

The Effect of Periodically Changing Regimes on the Electrodeposition of Silver Powder

The effect of different deposition regimes (constant and reversing currents, constant and pulsating overpotential), on the powdered and dendritic silver electrodeposits morphology were investigated. The morphology of electrodeposited silver powder was studied utilizing a scanning electron microscope. The results obtained in constant regimes were compared with those obtained in pulsating and reversing regimes. The size of dendrites decreased strongly with increased overpotential or current. It was also shown that the agglomeration of silver dendrites in spongy-like agglomerates was strongly decreased by pulsating overpotential electrodeposition or reversing current. The possibility of obtaininig powder particles, with different properties, depending on conditions of electrolysis was demonstrated

Analysis of the initial-stage sintering of mechanically activated SrTiO3

The initial-stage of sintering plays a significant role in determining the final microstructure that defines the main characteristics of electroceramics materials such as functional properties. In this article non-isothermal sintering of non-activated and mechanically activated SrTiO3 samples was investigated up to 1300 °C. Dilatometric curves indicate that mechanical activation leads to an earlier onset of sintering, suggesting that it should lead to a more homogenous and denser sintered product. Analysis of the initial stage of sintering reveals that the sintering process of all examinated samples consists of two or three overlapping single-step processes, with a change in the dominant mass transport mechanism. The values of apparent activation energy of the considered single-step process exhibit a significant decrease with an increase in mechanical activation time. The values of the density of samples after isothermal sintering indicate that the final stage of sintering has not been reached by 1300 °C

Synthesis and sintering of high-temperature composites based on mechanically activated fly ash

Amount of fly ash which is and yet to be generated in the coming years highlights the necessity of developing new methods of the recycling where this waste can be reused in significant quantity. A new possibility for fly ash utilization is in high-temperature application (thermal insulators or/and refractory material products). As such, fly ash has to adequately answer the mechanical and thermal stability criteria. One of the ways of achieving it is by applying mechanical activation procedure on fly ash. In present study, fly ashes from two different power plants were mechanically activated in a planetary ball mill. Mechanically treated fly ashes were cemented with two different binders: standard Portland cement and high-aluminates cement. Physico-chemical analysis and investigation of mineralogical components of composites are emphasized, due to the changes occurred in fly ash during mechanical activation and sintering of composites. Macro-performance of the composites was correlated to the microstructure of fly ash studied by means of XRD and SEM analysis. Thermal stability of crystalline phases was investigated with DTA. Highlight was placed on determination of relationship between mechanically activated fly ash and obtained composites microstructure on one side and behavior of sintered composites on the other side. [Projekat Ministarstva nauke Republike Srbije, br. 172057, 45008 and a project F-198, financed by Serbian Academy of Sciences and Arts

Analysis of the Initial-Stage Sintering of Mechanically Activated SrTiO3

The initial-stage of sintering plays a significant role in determining the final microstructure that defines the main characteristics of electroceramics materials such as functional properties. In this article non-isothermal sintering of non-activated and mechanically activated SrTiO3 samples was investigated up to 1300 degrees C. Dilatometric curves indicate that mechanical activation leads to an earlier onset of sintering, suggesting that it should lead to a more homogenous and denser sintered product. Analysis of the initial stage of sintering reveals that the sintering process of all examinated samples consists of two or three overlapping single-step processes, with a change in the dominant mass transport mechanism. The values of apparent activation energy of the considered single-step process exhibit a significant decrease with an increase in mechanical activation time. The values of the density of samples after isothermal sintering indicate that the final stage of sintering has not been reached by 1300 degrees C