Das verhalten von systemen in gleichgewichtslagen innerhalb von gleichgewichtsbereichen

In order to characterize the equilibrium positions of a system inside an equilibrium domain, direction elements are defined. These follow from the response of the autonomous system in such a position to small disturbances by impulses, which effect initial velocities of the system. The direction elements establish for the equilibrium domain a direction field, which gives information about the different behaviour of the system in the equilibrium positions of the domain. Examples are also considered.     

Über die Züchtung von ZnS-, ZnSe- und ZnTe-Einkristallen unter Anwendung der chemischen Transportreaktion

In connection with investigations on the synthesis of ZnS, ZnSe and ZnTe single crystals by chemical transport using iodine as transport agent in sealed tubes the mechanism of mass-transport and the relationship between material-transport and growth process were studied. In this way the optimum conditions for growing single crystals were found. The dependence of the transport rate on the undercooling ΔT, on the diameter of the ampoule and on the pressure in the system is described. Relative large crystals in good quality could be propared by influencing the nucleation and the growth process by help of well defined transport rates. In all cases crystals with sphalerite structure only were obtained. The habit with the most common faces (110), (111) and (211) was found to be predominant. The dominant habit is responsive to variations in the experimental parameters. The crystal perfection have been determined by etch patterns and by X-ray topography.     

Carbon-Based Ternary Nanocomposite: Bullet Type ZnO–SWCNT–CuO for Substantial Solar-Driven Photocatalytic Decomposition of Aqueous Organic Contaminants

A facile two-step synthesis of ternary hetero-composites of ZnO, CuO, and single-walled carbon nanotubes (SWCNTs) was developed through a recrystallization process followed by annealing. A series of nanocomposites were prepared by varying the weight ratio of copper(II) acetate hydrate and zinc(II) acetate dihydrate and keeping the weight ratio of SWCNTs constant. The results revealed the formation of heterojunctions (ZnO–SWCNT–CuO, ZSC) of three crystal structures adjacent to each other, forming a ternary wurtzite-structured nanoparticles along with defects. Enhanced charge separation (electron-hole pairs), reduced band gap, defect-enhanced specific surface area, and promoted oxidation potential were key factors for the enhanced photocatalytic activity of the ternary nanocomposites. OH^• radicals were the main active species during dye degradation, and O₂^−• and h⁺ were also involved to a lesser extent. A type II heterojunction mechanism approach is proposed based on the charge carrier migration pattern. Among the synthesized nanocomposites, the sample prepared using copper(II) acetate hydrate and zinc(II) acetate dihydrate in a 1: 9 ratio (designated a ZSC3) showed the highest photocatalytic activity. ZSC3 achieved 99.2% photodecomposition of methylene blue in 20 min, 94.1% photodecomposition of Congo red in 60 min, and 99.6% photodecomposition of Rhodamine B in 40 min under simulated sunlight. Additionally, ZSC3 showed excellent reusability and stability, maintaining 96.7% of its activity even after five successive uses. Based on overall results, the ZSC sample was proposed as an excellent candidate for water purification applications.     

Perfluororganozink-verbindungen: darstellung und eigenschaften von (Rf)2Zn-komplexen (Rf = CF3, C2F5, C3F7, C6F5) [1]

A new method for the preparation of bis(perfluoroorgano) zinc compounds is described: CF₃I and C₆F₅I react with dialkylzinc in the presence of a Lewis base quantitatively to give (CF₃)₂Zn and (C₆F₅)₂Zn complexes, while the analogous reactions with C₂F₅I and iC₃F₇I do not yield the pure compounds. ¹H, ¹⁹F n.m.r, i.r. and Raman spectra are presented.     

Synthesis and stereochemical assignment of DNA spore photoproduct analogues

Investigation of the DNA repair process performed by the spore photoproduct (SP) lyase repair enzyme is strongly hampered by the lack of defined substrates needed for detailed enzymatic studies. The problem is particularly severe because the repair enzyme belongs to the class of strongly oxygen-sensitive radical (S)-adenosylmethionine (SAM) enzymes, which are notoriously difficult to handle. We report the synthesis of the spore photoproduct analogues 1 a and 1 b, which have open backbones and are diastereoisomers. In order to solve the problem of stereochemical assignment, two further derivatives 2 a and 2 b with closed backbones were prepared. The key step of the synthesis of 2 a/b is a metathesis-based macrocyclization that strongly increases the conformational rigidity of the synthetic spore photoproduct derivatives. NOESY experiments of the cyclic isomers furnished a clear cross-peak pattern that allowed the unequivocal assignment of the stereochemistry. The results were transferred to the data for isomers 1 a and 1 b, which were subsequently used for enzymatic-repair studies. These studies were performed with the novel spore photoproduct lyase repair enzyme from Geobacillus stearothermophilus. The studies showed an accordance with a recent investigation performed by us with the spore photoproduct lyase from Bacillus subtilis, in that only the S isomer 1 a is recognized and repaired. The ability to prepare a defined functioning substrate now paves the way for detailed enzymatic studies of the SP-lyase lesion recognition and repair process.     

WEFTA interlaboratory comparison on total lipid determination in fishery products using the Smedes method

Lipid determination by the Smedes method was tested in an interlaboratory trial performed by nine laboratories from seven countries belonging to the West European Fish Technologists Association Analytical Methods Working Group. Five samples of fish and fishery products with different lipid contents, including two blind duplicates, were distributed among the participants. All laboratories applied a slightly modified Smedes method, which included extraction of lipids by cyclohexane and isopropanol, transfer of lipids to the cyclohexane phase by addition of water, phase separation by centrifugation, and gravimetric lipid determination. The results indicate that the RSD for reproducibility (RSD(R)) was between 4.11 and 6.31% for samples with moderate (7%) and high (14%) lipid content, depending on the sample. Larger SDs among the laboratories were obtained for a cod sample with low lipid content of 0.5%. The method is judged to be suitable as a routine method for lipid determination in fish and fishery products.