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91.
Univ. -Prof. Dipl. -Ing. Dr. mont. Helmut Flachberger 《BHM Berg- und Hüttenm?nnische Monatshefte》2012,157(6-7):225-229
On the occasion of his 75th birthday, this publication pursues the goals to approach the personality Hans J?rg Steiner from the perspective of one of his students and to acknowledge his work from his successor’s point of view. The author regretfully, but with composure recognizes that the portrait of this great Austrian mineral processing engineer as drawn by him can only be fragmentary, and invites the gentle reader to do the same. 相似文献
92.
Managing community content in mobile communities is challenging, since informal groups may emerge spontaneously whenever opportunities exist. To deal with group dynamics, encounter based community support systems can be a solution. In encounter networks, peers exchange content whenever they physically meet, i.e., whenever peers are near to each other. To assure content availability within the community network, content needs to be replicated (cached) and continuously updated. A?well known drawback of this scheme is the fact that the resource usage can be quite high. In this paper we present new caching strategies based on sociological knowledge, aiming at improving the overall content quality. We derive mobility and connectivity aware cache policies and simulate their benefit for knowledge building with urban life simulations. Results show that context precision and recall can be greatly improved in comparison to traditional cache strategies applied in the majority of encounter networks. 相似文献
93.
94.
Single‐step synthesis of a radically polymerizable 1,1′‐bi‐2‐naphthol derivative for asymmetric catalysis
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A new polymerizable 1,1′‐bi‐2‐naphthol derivative for polymer‐supported catalytic asymmetric synthesis is presented. The synthesis is conducted within a single reaction step, which is a major advantage over other approaches presented in the literature. The ligand‐bearing polymer is prepared through copolymerization with N‐isopropylacrylamide. Preliminary experiments on the utility in catalytic asymmetric alkylation reactions reveal the accessibility and activity of the polymer‐attached catalysts. The stereoselectivity of the reaction is found to be somewhat lower than for reactions performed in the presence of free 1,1′‐bi‐2‐naphthol, and thus requires further optimization. The enantiomeric excess of the reaction products was determined via 1H NMR spectroscopy after chiral derivatization with (R)‐α‐methylbenzyl isocyanate. © 2015 Society of Chemical Industry 相似文献
95.
In recent years, finite element analyses have increasingly been utilized for slope stability problems. In comparison to limit equilibrium methods, numerical analyses do not require any definition of the failure mechanism a priori and enable the determination of the safety level more accurately. The paper compares the performances of strength reduction finite element analysis (SRFEA) with finite element limit analysis (FELA), whereby the focus is related to non-associated plasticity. Displacement-based finite element analyses using a strength reduction technique suffer from numerical instabilities when using non-associated plasticity, especially when dealing with high friction angles but moderate dilatancy angles. The FELA on the other hand provides rigorous upper and lower bounds of the factor of safety (FoS) but is restricted to associated flow rules. Suggestions to overcome this problem, proposed by Davis (1968), lead to conservative FoSs; therefore, an enhanced procedure has been investigated. When using the modified approach, both the SRFEA and the FELA provide very similar results. Further studies highlight the advantages of using an adaptive mesh refinement to determine FoSs. Additionally, it is shown that the initial stress field does not affect the FoS when using a Mohr-Coulomb failure criterion. 相似文献
96.
Picking processes have gained importance in recent years because of increasing online trade, increasing pressure on lead times in production, procurement and distribution of goods, and the introduction of just-in-time concepts. Typically, there is a trade-off between throughput times, quality, and cost. The article examines the contribution of alternative manual picking systems to achieve these objectives, and in particular looks at the role of humans in the process. 相似文献
97.
Dr. Aline Telzerow Dr. Juraj Paris Dr. Maria Håkansson Dr. Javier González-Sabín Dr. Nicolas Ríos-Lombardía Prof. Dr. Harald Gröger Dr. Francisco Morís Dr. Martin Schürmann Prof. Dr. Helmut Schwab Dr. Kerstin Steiner 《Chembiochem : a European journal of chemical biology》2021,22(7):1232-1242
Amine transaminases (ATAs) are used to synthesize enantiomerically pure amines, which are building blocks for pharmaceuticals and agrochemicals. R-selective ATAs belong to the fold type IV PLP-dependent enzymes, and different sequence-, structure- and substrate scope-based features have been identified in the past decade. However, our knowledge is still restricted due to the limited number of characterized (R)-ATAs, with additional bias towards fungal origin. We aimed to expand the toolbox of (R)-ATAs and contribute to the understanding of this enzyme subfamily. We identified and characterized four new (R)-ATAs. The ATA from Exophiala sideris contains a motif characteristic for d -ATAs, which was previously believed to be a disqualifying factor for (R)-ATA activity. The crystal structure of the ATA from Shinella is the first from a Gram-negative bacterium. The ATAs from Pseudonocardia acaciae and Tetrasphaera japonica are the first characterized (R)-ATAs with a shortened/missing N-terminal helix. The active-site charges vary significantly between the new and known ATAs, correlating with their diverging substrate scope. 相似文献
98.
Catalytic performance of methacrylate‐based poly‐4‐(dialkylamino)‐pyridines: activity prediction via NMR shifts
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The synthesis of the 4‐(dialkylamino)pyridine derivative 3‐(4‐(pyridin‐4‐yl)piperazin‐1‐yl)propyl methacrylate and its copolymerization with n‐butyl methacrylate are presented. The catalytic activity was evaluated in the acylation of tert‐butanol with acetic anhydride yielding tert‐butyl acetate. It is observed that the activity of polymer‐attached 4‐(dimethylamino)pyridine analogues correlates remarkably well with the chemical shift of the β‐pyridyl protons. Differences in catalytic efficiency result from distinct electronic densities of the pyridine ring, while embedding the catalytically active moiety into a polymeric structure has nearly no deleterious effect on the performance. © 2015 Society of Chemical Industry 相似文献
99.
This mini review gives an overview of the synthesis of polyurethanes and polyesters with pendant hydroxyl groups performed mainly in our group. Significant for the synthesis of most of these polymers with hydroxyl‐functional side groups is that no protection groups are needed. This is realised either by generating the OH group during polymer synthesis—demonstrated by the preparation of hydroxyl‐functional polyurethanes from dicarbonate monomers and diamines—or by using catalysts which discriminate between primary and secondary OH groups—demonstrated by the synthesis of hydroxyl‐functional polyesters based on malic acid using scandium triflate as catalyst. In addition, the potential of carbonate couplers for the synthesis of multifunctional polyurethane is presented. The application of such multifunctional polyurethanes as antimicrobial polymers and coatings is briefly discussed. Copyright © 2012 Society of Chemical Industry 相似文献
100.
Bernd Garska Monir Tabatabai Urs Fischer Norbert Moszner Andreas Utterodt Helmut Ritter 《Polymer International》2012,61(7):1061-1066
We describe the synthesis of 5,11,17,23‐tetra‐tert‐butyl‐25,27‐dioxypropylphosphonic acid‐26,28‐dimethacryloyloxy‐calix [4]arene and 5,11,17,23‐tetra‐tert‐butyl‐25‐oxypropylphosphonic acid‐27‐hydroxy‐26,28‐dimethacryloyloxy‐calix[4]arene starting from para‐tert‐butyl‐calix[4]arene. The complete reaction was proved by matrix‐assisted laser desorption ionization time of flight mass spectrometry and nuclear magnetic resonance spectroscopy. The influence of these compounds on the kinetics of the radical polymerization of methyl methacrylate was shown by dilatometry. Furthermore, the adhesive properties of dental adhesives containing these calix[4]arene derivatives were investigated. Copyright © 2012 Society of Chemical Industry 相似文献