Crystallization kinetics of amorphous SiC films: Influence of substrate

The crystallization kinetics of amorphous silicon carbide films was studied by means of X-ray diffractometry (XRD) and transmission electron microscopy (TEM). The films were deposited by radio frequency (r.f.) magnetron sputtering on glassy carbon and single crystalline silicon substrates, respectively. TEM micrographs and XRD patterns show the formation of nano-crystalline β-SiC with crystallite sizes in the order of 50 nm during annealing at temperatures between 1200 and 1600 °C. A modified Johnson-Mehl-Avrami-Kolmogorov (JMAK) formalism was used to describe the isothermal transformation of amorphous SiC into β-SiC as an interface controlled, three-dimensional growth processes from pre-existing small crystallites in the order of 10 nm. These pre-existing crystallites are formed in a transient process in the early stages of crystallization. For films deposited on the silicon substrate, the obtained rate constants of crystallite growth obey an Arrhenius behavior with an activation enthalpy of 4.1 ± 0.5 eV in accordance with literature data. Films deposited on glassy carbon show an increased stability of amorphous SiC films, which is reflected in smaller rate constants of crystallite growth of several orders of magnitude at low temperatures and a higher activation enthalpy of 8.9 ± 0.9 eV. A model is proposed, where the faster crystallization of films on silicon substrates can be explained with the presence of superabundant point defects, which diffuse from the substrate into the film and accelerate the incorporation of atoms from the amorphous into the crystalline phase.     

Crystal growth, structure and electrical properties of thorium phosphorosulfide

Single crystals of thorium phosphorosulfide have been grown by the chemical vapour transport method. The X-ray diffraction examination showed that the unit cell of the crystals belongs to a tetragonal system of the PbFCl-type structure. The basal plane resistivity ρ(300 K)=64 μΩ cm and thermoelectric power S(300 K)=−7.7 μV/K, examined between 0.4 and 315 K, show metallic behaviour.     

Separation methods for the study of collagen and treatment of collagen disorders

Liquid chromatographic and electrophoretic methods applicable to the separation of collagen and its fragments are reviewed. Special attention is paid to the separation of both stabile and labile crosslinking elements. Identification procedures exploiting the mapping of either collagen alpha-chains or of cyanogen bromide fragments are discussed. These methods can be used for diagnosing inborn errors of collagen metabolism using bioptic or necroptic samples. Analysis of urinary hydroxyproline-containing peptides or the determination of peptidically bound pyridinoline is suitable for measuring the intensity of collagen metabolism.     

Exploiting planarity in separation routines for the symmetric traveling salesman problem

At present, the most successful approach for solving large-scale instances of the Symmetric Traveling Salesman Problem to optimality is branch-and-cut. The success of branch-and-cut is due in large part to the availability of effective separation procedures; that is, routines for identifying violated linear constraints.

For two particular classes of constraints, known as comb and domino-parity constraints, it has been shown that separation becomes easier when the underlying graph is planar. We continue this line of research by showing how to exploit planarity in the separation of three other classes of constraints: subtour elimination, 2-matching and simple domino-parity constraints.     

PH-Bestimmungsmethoden

Ohne Zusammenfassung     

β-Nitrostyrenes as electrophiles in Parham cyclization chemistry: reaction with o-lithiobenzonitrile

β-Nitrostyrenes react with o-lithiobenzonitrile, generated from the requisite aryl bromide at −100 °C by bromine-lithium exchange with n-butyllithium in THF, to afford 2-nitro-3-phenyl-3H-inden-1-ylamines resulting from 1,4-addition to the β-nitrostyrene followed by intramolecular capture of the resultant nitronate anion by the ortho-cyano functional group.     

Neuere Methoden zum Nachweis, zur Isolierung und quantitativen Bestimmung des Eiwei?es sowie seiner h?heren und tieferen Abbauprodukte

Ohne Zusammenfassung