Annular Impinging Jet Controlled by Radial Synthetic Jets

This experimental study focuses on generation and control of annular impinging jets. The annular nozzle used in the investigations was designed with an active flow control system using 12 synthetic jets issuing radially from the central nozzle body. Measurements of the control effects were made on the impingement wall. The data acquisition involved wall pressure and wall mass transfer (by the naphthalene sublimation technique) using air as the working fluid. Also measured was time-mean flow velocity (by a Pitot probe) in the jet flow field. Moreover, flow visualization was carried out. Two main flow-field patterns (A and B) were identified. The patterns differ in the size of the separated-flow recirculation regions that develop attached to the nozzle central body: While pattern A is characterized by a quite small recirculation region (bubble) extending not far from the nozzle exit, pattern B exhibits a large recirculation region, reaching up to the impingement wall, on which it forms a stagnation circle. The control action modifies the flow field, resulting in changes of the corresponding heat/mass transfer distributions. The convective transfer rate on the stagnation circle can be demonstrably enhanced by 20% at a moderate nozzle-to-wall distance, equal to 0.6 of the nozzle outer diameter.     

Modelling of pharmaceutical tablet swelling and dissolution using discrete element method

This work presents a novel use of the Discrete Element Method (DEM) combined with inter-particle mass transfer in order to simulate polymer swelling and dissolution. Each particle can absorb water and swell, pushing on its neighbours and causing an overall expansion. Once the disentanglement threshold is reached, the polymer dissolves and the particle reduces in size. This paper applies DEM to simulate the radial swelling and dissolution of cylindrical tablets. The method was validated against exact numerical solution of the same system to assess the accuracy of the DEM simulations for different DEM particle sizes. Parametric studies were done to assess the impact of physical parameters – namely the concentration-dependent diffusion coefficient of water through the polymer, the dissolution rate constant of the polymer and the disentanglement threshold of the polymer – on the radial expansion of the tablet. It was found that different settings of the concentration-dependent water diffusion coefficient function could produce similar radial expansion curves but with different internal concentration profiles. Increasing the dissolution rate constant or decreasing the disentanglement threshold of the polymer caused a reduction in the maximum radius of tablet. Lastly, ATR-FTIR spectroscopic imaging was used to obtain chemical images of a pure hydroxy-propyl methylcellulose (HPMC) tablet swelling and dissolving. The model was optimised to match both the HPMC tablet radius and the concentration profiles over time.     

Impacts of Climate Variables on Residential Water Consumption in the Czech Republic

The paper investigates whether there is a statistically significant impact of short-term climate variables (specifically air temperature and rainfall) on residential water consumption at two selected case sites in the Czech Republic. The analysis is based on a unique time series of daily data from 2004–2009. The statistical methods used are CART methodology and a decomposition of these time series based on a locally weighted regression method. Apart from the data analysis results, the investigation raises several methodological questions regarding the use of daily data and the scope of analysis based on such data sets.     

Electrochemical hydriding as method for hydrogen storage?

Electrochemical hydriding of magnesium alloys in alkaline solutions is proposed as a method of storing hydrogen in a solid phase. In this article, we present a new approach to hydrogen storage for mobile applications. Rapidly solidified ribbons of Mg–14Ni alloy were prepared by melt spinning. Subsequently, they were exposed to electrochemical hydriding at 90 °C/120 min in various alkaline electrolytes. It was found that hydrogen reached up to 1.4 wt.%. Higher hydrogen concentrations might be achieved by proper adjustment of hydriding conditions.     

Refining the Undecidability Border of Weak Bisimilarity

Weak bisimilarity is one of the most studied behavioural equivalences. This equivalence is undecidable for pushdown processes (PDA), process algebras (PA), and multiset automata (MSA, also known as parallel pushdown processes, PPDA). Its decidability is an open question for basic process algebras (BPA) and basic parallel processes (BPP). We move the undecidability border towards these classes by showing that the equivalence remains undecidable for weakly extended versions of BPA and BPP. In fact, we show that the weak bisimulation equivalence problem is undecidable even for normed subclasses of BPA and BPP extended with a finite constraint system.     

Approximating curves and their offsets using biarcs and Pythagorean hodograph quintics

This paper compares two techniques for the approximation of the offsets to a given planar curve. The two methods are based on approximate conversion of the planar curve into circular splines and Pythagorean hodograph (PH) splines, respectively. The circular splines are obtained using a novel variant of biarc interpolation, while the PH splines are constructed via Hermite interpolation of C¹ boundary data.We analyze the approximation order of both conversion procedures. As a new result, the C¹ Hermite interpolation with PH quintics is shown to have approximation order 4 with respect to the original curve, and 3 with respect to its offsets. In addition, we study the resulting data volume, both for the original curve and for its offsets. It is shown that PH splines outperform the circular splines for increasing accuracy, due to the higher approximation order.     

Stabilization of New Phases in Ion-Conducting Nanocomposites

Physical properies of ion-conducting nanocomposites are reviewed. Special attention is paid to the change of the bulk characteristics of ionic salts in the nanocomposites due to the formation of the interface phases. The main thermodynamic reason of the formation of the nanocomposite as well as the stabilization of the interface phases is the adhesion energy _a. At sufficiently high _a values, the ionic salt tends to spread along the oxide surface, which leads to the formation of the nanocomposite on sintering. The adhesion is the result of the interface interaction and incorporates the stage of the specific adsorption of the interface ions. It leads to the formation of the double layer formed by the point defects in the interface region of the ionic salt. In the case of the strong adhesion, the structural reconstruction or the formation of the metastable interface phase takes place. Analysis of the experimental data shows that interface phases exist in composites AgI–Al₂O₃, MeNO₃–Al₂O₃ (Me = Li, Na, K, Rb, and Cs), CsHSO₄–SiO₂, RbNO₃–SiO₂ and CsCl–Al₂O₃. Their structure may be either epitaxial crystalline, or amorphous. The thickness of the interface phase as estimated on the basis of the brick-wall model is about 3–4 nm.     

Spectroscopic characterization of 1,5-diphenyl-3,7-dihydroxy-1,5-diazacyclooctane — (8C ring compound) formed in N,N-diglycidylanaline/aniline curing systems

Summary A NMR and infrared analysis of the cyclic product formed by the reaction of N,N-diglycidylaniline with aniline confirms the structure of an eight-membered ring (I). The conformational structure of this compound is discussed.     

The crystal structure of the processive endocellulase CelF of Clostridium cellulolyticum in complex with a thiooligosaccharide inhibitor at 2.0 A resolution

The mesophilic bacterium Clostridium cellulolyticum exports multienzyme complexes called cellulosomes to digest cellulose. One of the three major components of the cellulosome is the processive endocellulase CelF. The crystal structure of the catalytic domain of CelF in complex with two molecules of a thiooligosaccharide inhibitor was determined at 2.0 A resolution. This is the first three-dimensional structure to be solved of a member of the family 48 glycosyl hydrolases. The structure consists of an (alpha alpha)6-helix barrel with long loops on the N-terminal side of the inner helices, which form a tunnel, and an open cleft region covering one side of the barrel. One inhibitor molecule is enclosed in the tunnel, the other exposed in the open cleft. The active centre is located in a depression at the junction of the cleft and tunnel regions. Glu55 is the proposed proton donor in the cleavage reaction, while the corresponding base is proposed to be either Glu44 or Asp230. The orientation of the reducing ends of the inhibitor molecules together with the chain translation through the tunnel in the direction of the active centre indicates that CelF cleaves processively cellobiose from the reducing to the non-reducing end of the cellulose chain.