Investigations of the distribution of elements in phases present in G-AlMg5Si cast alloy with EDX/WDX spectrometers and AES

The mechanical properties of most aluminium alloys depend heavily on chemical composition, casting methods and heat treatment. Alloys of type G-AlMg₅Si are known for good corrosion resistance and mechanical properties at elevated temperatures. Under the designation Hydronalium (Hy 511) they are used for the production of heads for air cooled Diesel engines. To obtain better mechanical characteristics, titanium is added to the alloy. This paper deals with the results obtained during investigations of the distribution of elements in binary eutectic Mg₂Si and ternary eutectic as well as the distribution of titanium in samples of Hy 511, obtained during casting of cylinder heads. Studies of the distribution of the elements were performed using EDX/ WDX spectrometry, and the distribution of titanium was studied also with Auger electron spectroscopy.Dedicated to Professor Günther Tölg on the occasion of his 60th birthday     

Surface-induced order and diffusion in 5CB liquid crystal confined to porous glass.

Liquid crystals confined into small cavities are known to have a weak orientational order even above the nematic-isotropic transition temperature. The surface-induced order and molecular dynamics in this temperature range are studied with the aid of deuteron NMR spectra, spin relaxation times T(1) and T(2,) proton dipolar-correlation effect, and direct measurements of the effective diffusion coefficient for the liquid crystal 5CB confined to controlled-pore glasses. Our results show that an arrangement of molecules parallel to the wall is induced by local molecular interactions between the liquid crystal and solid, resulting in a weak and temperature independent surface order parameter, S(0) approximately 0.02 +/- 0.01. There is no indication of a significant slowing-down of molecular diffusion at the wall, neither rotational nor translational. In cavities of nanometer size, where the nematic order evolves gradually upon cooling, a broadening of the NMR linewidths due to dynamic effects should be taken into account.     

7th International k0-Users’ Workshop

Journal of Radioanalytical and Nuclear Chemistry -     

Simulation of void fraction profile evolution in subcooled nucleate boiling flow in a vertical annulus using a bubble-tracking approach

A three-dimensional bubble-tracking model of subcooled nucleate boiling flow in a vertical channel at low-pressure conditions is proposed with specific application to the case of boiling in an annulus with a central heating rod. Vapour is distributed in the liquid in the form of individually tracked bubbles. The overall behaviour of the liquid–vapour system results from motion, interaction, coalescence and boiling mechanisms prescribed mostly at the level of bubbles. Bubbles are nucleated at nucleation sites randomly distributed over the heated surface. After nucleation, bubbles slide on the heated wall, detach and then migrate into the lower-temperature region away from the heated surface, where they condense. The proposed model was applied to experiments on subcooled boiling from Purdue University (USA). Experimental and calculated void fraction radial profiles at different axial locations are compared.     

Controlling ion motion in polymer light-emitting diodes containing conjugated polyelectrolyte electron injection layers

The properties and function of an anionic conjugated polyelectrolyte (CPE)-containing ion-conducting polyethylene oxide pendant (PF(PEO)CO(2)Na) as electron injection layers (EILs) in polymer light-emitting diodes (PLEDs) are investigated. A primary goal was to design a CPE structure that would enable acceleration of the device temporal response through facilitation of ion motion. Pristine PLEDs containing PF(PEO)CO(2)Na exhibit luminance response times on the order of tenths of seconds. This delay is attributed to the formation of ordered structures within the CPE film, as observed by atomic force microscopy. Complementary evidence is provided by electron transport measurements. The ordered structures are believed to slow ion migration within the CPE EIL and hence result in a longer temporal response time. It is possible to accelerate the response by a combination of thermal and voltage treatments that "lock" ions within the interfaces adjacent to PF(PEO)CO(2)Na. PLED devices with luminance response times of microseconds, a 10(5) fold enhancement, can therefore be achieved. Faster luminance response time opens up the application of PLEDs with CPE layers in display technologies.     

Determination of caffeine and associated compounds in food, beverages, natural products, pharmaceuticals, and cosmetics by micellar electrokinetic capillary chromatography

A method is described for quantitating caffeine, theobromine, theophylline, paracetamol, propyphenazone, acetylsalicylic acid, salicylic acid, and codeine phosphate in corresponding real samples of food, beverages, natural products, pharmaceuticals, and cosmetic preparations by micellar electrokinetic capillary chromatography. The separation is carried out at 25 degrees C and 25 kV, using a 20mM phosphate buffer (pH 9.0), 80mM sodium dodecyl sulfate, and 7.5% (v/v) acetonitrile. UV detection is at 210 nm. The method is shown to be specific, accurate (recoveries over the range 98.9-101.2%), linear over the tested range (correlation coefficients >/= 0.9993), and precise (relative standard deviation below 2.1%). The method is applied for the quantitative analysis of these compounds in different foods, beverages, natural products, pharmaceuticals, and cosmetic products.     

Thermodynamic characterization of polyanetholesulfonic acid and its alkaline salts

Experimental and theoretical results for the thermodynamic properties of polyanetholesulfonic acid and its lithium, sodium, and cesium salts in aqueous solution at 298 K are presented. The osmotic pressure was measured using membrane and vapor pressure apparatus in the concentration range c(m) = 0.001-0.30 monomoles/dm(3). The osmotic coefficients obtained from these measurements were low, from 0.2 to 0.45 in this concentration range, indicating a strong interaction between counterions and polyions. The osmotic coefficients of the polyacid and its lithium and sodium salts appeared to be equal within experimental error, but the results for the cesium salt were lower. This indicates a somewhat stronger binding of cesium ions to the polyanion. In addition, enthalpies of dilution, DeltaH(D), from a certain concentration, m(m), to m(m) = 0.0044 monomoles/kg were measured. The measured heats of dilution were exothermic, with the acid producing the strongest and the cesium salt the weakest effect. These results were compared with previously published data for polyelectrolytes of similar structure, namely, polystyrenesulfonic acid and its alkaline salts. The osmotic pressure results indicate that polystyrenesulfonates bind the counterions more strongly than polyanetholesulfonic acid and its salts. Consistent with this finding, the enthalpies of dilution reveal that more heat is released upon dilution of polyanetholesulfonates (stronger exothermic effect) in comparison with the corresponding solutions of polystyrenesulfonic acid in its alkaline salts. These findings can be explained in terms of the structural differences between the two polyions. The experimental results were analyzed in relation to popular electrostatic theories such as the Manning condensation theory and the Poisson-Boltzmann cell model approach, where the polyion is pictured as a uniformly charged line or cylinder. In addition, we performed Monte Carlo simulations for a model polyanetholesulfonic anion having discrete charges. In all of the calculations, the solvent was treated as a continuum with the dielectric constant of pure water under the conditions of measurement. The theoretical considerations mentioned above yield results in semiquantitative agreement with the measured quantities.     

A Planar linear arboricity conjecture

The linear arboricity la(G) of a graph G is the minimum number of linear forests (graphs where every connected component is a path) that partition the edges of G. In 1984, Akiyama et al. [Math Slovaca 30 (1980), 405–417] stated the Linear Arboricity Conjecture (LAC) that the linear arboricity of any simple graph of maximum degree Δ is either ?Δ/2? or ?(Δ + 1)/2?. In [J. L. Wu, J Graph Theory 31 (1999), 129–134; J. L. Wu and Y. W. Wu, J Graph Theory 58(3) (2008), 210–220], it was proven that LAC holds for all planar graphs. LAC implies that for Δ odd, la(G) = ?Δ/2?. We conjecture that for planar graphs, this equality is true also for any even Δ?6. In this article we show that it is true for any even Δ?10, leaving open only the cases Δ = 6, 8. We present also an O(n logn) algorithm for partitioning a planar graph into max{la(G), 5} linear forests, which is optimal when Δ?9. © 2010 Wiley Periodicals, Inc. J Graph Theory