Interpretation of noncharacteristic M X-rays in heavy colliding systems by selfconsistent relativistic molecular calculations

The result of the first calculation of a self-consistent relativistic many electron correlation diagram ever done (for the system Au-I) leads to a good agreement of the spectral shape and position of the observed noncharacteristic X-rays within the quasi adiabatic model.     

Biodegradable and bioactive hybrid organic–inorganic PEG-siloxane fibers. Preparation and characterization

A mixture of triethoxysilanefunctionalized poly(ethylene glycol), f-PEG, and tetraethoxysilane, TEOS, was used as precursors in the preparation of continuous hybrid f-PEG-siloxane sol–gel derived fibers. The fibers were spun by extrusion through a spinneret. The thus prepared fibers had a diameter of 20–50 m. ²⁹Si-CPMAS NMR measurements confirmed that the functionalized PEG is incorporated into the siloxane network through covalent bonds. The hybrid fiber elasticity was much higher than that of fibers spun from sols with TEOS as the only source for silica. However, the f-PEG chain length plays a crucial role for the spinnability of the sol, since, as a result of bridging flocculation, macroscopic phase separation occurred readily with increasing chain length of the f-PEG. The fibers were shown to be effective substrates for the nucleation and growth of bone-like hydroxyapatite.     

Constant-factor approximations for Capacitated Arc Routing without triangle inequality

Given an undirected graph with edge costs and edge demands, the Capacitated Arc Routing problem (CARP) asks for minimum-cost routes for equal-capacity vehicles so as to satisfy all demands. Constant-factor polynomial-time approximation algorithms were proposed for CARP with triangle inequality, while CARP was claimed to be NP-hard to approximate within any constant factor in general. Correcting this claim, we show that any factor  α$\alpha$ approximation for CARP with triangle inequality yields a factor  α$\alpha$ approximation for the general CARP.     

Computation of period matrices of real algebraic curves

In this paper we derive a numerical method which allows us to compute periods of differentials on areal algebraic curve with real points. This leads to an algorithm which can be implemented on a computer and can be used to study the Torelli mapping numerically. Dedicated to the memory of Mario Raimondo This work was supported by the EC Science Plan Contract No. SC1^*-CT91-0716 and the Academy of Finland.     

Enhanced stability of symmetrical polymer electrolyte membrane fuel cell single cells based on novel hierarchical microporous-mesoporous carbon supports

Fuel cell electrodes were prepared from Pt nanocluster activated hierarchical microporous-mesoporous carbon powders. The carbon supports were synthesized from molybdenum carbide applying the high-temperature chlorination method. Six different synthesis temperatures within the range from 600 to 1000 °C were used for preparation of carbon supports. Thermogravimetric analysis, X-ray diffraction, low-temperature nitrogen sorption, and high-resolution scanning electron microscopy methods were used to characterize the structure of the electrode materials and symmetrical membrane electrode assemblies (MEAs). The MEAs prepared were used to conduct the proton exchange membrane fuel cell (PEMFC)single-cell measurements. The polarization and power density curves for single cells were calculated to evaluate the activity of the catalyst materials synthesized. The electrochemically active surface area (from 2.4 to 11.9 m² g^?1) was obtained in order to estimate the contact surface areas of platinum and Nafion® electrolyte. The values of the electrolyte resistance, polarization resistance, and cell degradation rate were calculated from electrochemical impedance spectroscopy data. The carbon materials synthesized within temperature range from 600 to 850 °C were found to be the most suitable supports for PEMFCs, having higher maximum power density values and better stability (cell potential degradation 240 μV h^?1) than commercial carbon-based (Vulcan XC72; 670 μV h^?1) single cells.     

Adsorption of PEO-PPO-PEO triblock copolymers with end-capped cationic chains of poly(2-dimethylaminoethyl methacrylate)

We study the adsorption of a symmetric triblock copolymer of ethylene oxide, EO, and propylene oxide, PO, end-capped with quarternized poly(2-dimethylaminoethyl methacrylate), DMAEMA (DMAEMA(24)-EO(132)PO(50)EO(132)-DMAEMA(24)). Light scattering and tensiometry are used to measure the relative size of the associated structures and surface excess at the air-liquid interface. The adsorbed amount, the amount of coupled water, and the viscoelasticity of the adsorbed polymer layer are measured on hydrophobic and hydrophilic surfaces (polypropylene, cellulose, and silica) by using quartz crystal microgravimetry (QCM) and surface plasmon resonance (SPR) at different ionic strengths and temperatures. The results of the experiments are compared with those obtained after adsorption of the uncharged precursor copolymer, without the cationic end-caps (EO(132)PO(50)EO(132)). DMAEMA(24)-EO(132)PO(50)EO(132)-DMAEMA(24) possesses higher affinity with the negatively charged silica and cellulose surfaces while the uncharged copolymer adsorbs to a larger extent on polypropylene surfaces. In this latter case, adsorption increases with increasing solution ionic strength and temperature. Adsorption of EO(132)PO(50)EO(132) on silica surfaces has little effect on the water contact angle (WCA), while adsorption of DMAEMA(24)-EO(132)PO(50)EO(132)-DMAEMA(24) increases the WCA of silica to 32°, indicating a large density of exposed PPO blocks upon adsorption. After adsorption of EO(132)PO(50)EO(132) and DMAEMA(24)-EO(132)PO(50)EO(132)-DMAEMA(24) on PP, the WCA is reduced by ≈14° and ≈28°, respectively, due to the exposed hydrophilic EO and highly water-soluble DMAEMA segments on the surfaces. The extent of surface coverage at saturation at the polypropylene/liquid interfaces (≈31 and 40 nm(2)/molecule obtained by QCM and SPR, respectively) is much lower, as expected, when compared with results obtained at the air/liquid interface, where a tighter packing is observed. The percentage of water coupled to the adsorbed cationic polymer decreases with solution ionic strength. Overall, these observations are ascribed to the effects of electrostatic screening, polymer hydrodynamic size, and solvency.     

Zur Bestimmung der Jodzahl von Monoenfetts?uren mittels Bromsuccinimid

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