Hydrogen microscopy – Distribution of hydrogen in buckled niobium hydrogen thin films

Hydrogen absorption in thin metal films clamped to rigid substrates results in mechanical stress that changes the hydrogen's chemical potential by Δμ_H(σ) = −1.124σ kJ/mol_H for σ measured in [GPa]. In this paper we show that local stress relaxation by the detachment of niobium hydrogen thin films from the substrate affects the chemical potential on the local scale: using coincident proton–proton scattering at a proton microprobe, the hydrogen concentration is determined with μm resolution, revealing that hydrogen is not homogenously distributed in the film. The local hydrogen solubility of the film changes with its local stress state, mapping the buckled film fraction. In niobium hydrogen thin films loaded up to nominal concentrations in the two-phase coexistence region, the clamped film fraction remains in the solid solution phase, while the buckles represent the hydride phase. These results are compared to a simple model taking the stress impact on the chemical potential into account.     

Influence of store dimensions and auxiliary volume configuration on the performance of medium-sized solar combisystems

To increase the fractional energy savings achieved with solar thermal combisystems the store volume may be increased. Installation of large stores in single-family houses is, however, often limited by space constraints. In this article the influence of the store dimensions, as well as internal and external auxiliary volume configurations, are investigated for large solar water stores by annual dynamic TRNSYS simulations. The results show that store sizes up to 4 m³ may be used in solar heating systems with 30 m² collector area. It is further shown that well-insulated stores are rather insensitive to the geometry. Stores deviating from the conventional dimensions still yield high fractional energy savings. Furthermore, the simulations show that the performance of an internal auxiliary volume configuration in most cases exceeds that of a solution with an external auxiliary unit. The practical limitations of very thin auxiliary volumes must, however, be further investigated.     

Unterscheidung von Palmölen und Palmöl-Fraktionen durch HPLC der Triglyceride

Analytical Characterisation of Palm Oil Fractions by HPLC of Triglycerides The increasing importance of palm oils and palm oil fractions in international trade makes it necessary to develop analytical criteria for the characterisation of these products. One problem is the correct identification of palm oleins, which are often difficult to distinguish from palm oils. These products frequently exhibit similar fatty acid by GLC and similar iodine values. The correct identification of palm stearins by GLC is comparatively more easy. Palm oleins and palm oils can be characterized by HPLC using conditions that permit not only the separation of triolein from less unsaturated triglycerides of the same carbon number, but also, at the same time, a separation of tripalmitin from triglycerides containing oleic acid. By establishing the peak area ratios for a number of selected triglycerides a clear differentiation between palm oils and palm oleins, as well as various other palm oil fractions and their mixtures is obtained.     

Donor Atom‐Stabilized Aluminum Alkyls as Cocatalysts for the Ziegler–Natta Polymerization of Propene

A number of organoaluminum compounds, stabilized with intramolecular nitrogen‐ or oxygen‐donor functions, have been used as cocatalysts for the MgCl₂/TiCl₄‐catalyzed homopolymerization of propene as well as for the copolymerization of ethene with propene. The polymerization behavior of these aluminum alkyls was examined at different Al/Ti ratios within the range of 2 to 50 and compared with the reference of triethylaluminum (TEA). Especially the alkyls [2‐(N,N‐dimethylaminomethyl)phenyl]dimethylaluminum ( 1 ) and [2‐(N,N‐dimethylaminomethyl)phenyl]diethylaluminum ( 2 ) show the highest activities at very low Al/Ti ratios in the homopolymerization of propene, whereas TEA is almost inactive. The species [8‐(N,N‐dimethylamino)naphthyl]dimethylaluminum ( 4 ) reaches the highest activity of all examined alkyls and is very close to the highest value obtained with TEA. Bulky iso‐butyl groups at the aluminum center are responsible for the very poor performance of the nitrogen stabilized cocatalysts [8‐(N,N‐dimethylamino)naphthyl]diisobutylaluminum ( 5 ) and [2‐(N,N‐dimethylaminomethyl)phenyl]diisobutylaluminum ( 3 ). The properties of the polypropenes synthesized with the stabilized organoaluminum species are similar to those produced with TEA but with a distinctly higher molar mass. In the case of 1 , it was possible to increase the molar mass by a factor of three. For the copolymerizations, the compounds [2‐(N,N‐diethylaminomethyl)phenyl]diethylaluminum ( 7 ) and (2‐methoxybenzyl)diisobutylaluminum ( 8 ) were found to be most suitable, producing polymers with significantly higher activities than TEA. For all copolymers two fractions were obtained, one crystalline fraction with a low and an amorphous part with a high amount of comonomer. In both fractions, 7 and 8 provide a higher comonomer incorporation than TEA.     

Reactive surfactants in heterophase polymerization. VI. Synthesis and screening of polymerizable surfactants (surfmers) with varying reactivity in high solids styrene—butyl acrylate—acrylic acid emulsion polymerization

Several polymerizable surfactants (surfmers) have been used in the semi-continuous emulsion copolymerization of styrene, butyl acrylate, and acrylic acid. Three of the (anionic) surfmers (sodium 11-crotonoyl undecan-1-yl sulfate, sodium 11-methacryloyl undecan-1-sulfate, and sodium sulfopropyl tetradecyl maleate) were prepared in house with purities between 53 and 82%. Physicochemical properties such as the critical micelle concentration, the adsorption isotherm, and the specific adsorption area were determined. The surfmers were then used with constant addition profiles in semicontinuous reactions, and the instantaneous conversions of the main monomers determined. The particle size, amount of coagulum, surface tension, and stability against electrolyte solutions of the latices were evaluated. Films were cast of some of the latices, and the visual appearance and water adsorption were assessed. © 1997 John Wiley & Sons, Inc. J Appl Polym Sci 66: 183–1820, 1997     

Isothiazol-1,1-dioxide – vom Süßstoff zum chiralen Auxiliar in der stereoselektiven Synthese

Isothiazole 1,1-dioxides – From Sweeter to Chiral Auxiliar in the Stereoselective Synthesis This review gives a report of the last ten years on the new synthetic methods, reactions and biological applications of isothiazole 1,1-dioxide derivatives. the formation of monocyclic and heterocyclic annelated isothiazole 1,1-dioxides by oxidation of isothiazoles, cyclocondensation of sulfonamides and cycloaddition of isothiazol-3(2H)-one 1,1-dioxides are discussed in more detail. Furthermore, the preparation of pharmacologically important N-substituted saccharines is reported. New saccharine-derived chiral N-enoyl-and N-acyl-2,3-dihydro-1,2-benzisothiazole 1,1-dioxides serve as advantageous stereoface-directing dienophile and dipolarophile auxiliaries in Diels-Alder-reactions and 1,3-dipolar cycloadditions. Asymmetric alkylations, acylations and aldolizations are also described.