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31.
Dr. Richard Kudernatsch 《Monatshefte für Chemie / Chemical Monthly》1901,23(2):119-122
Ohne Zusammenfassung 相似文献
32.
Richard Brown 《Geometriae Dedicata》2003,97(1):129-150
In this note, we show that given a closed, orientable genus-g surface S
g
, any hyperbolic toral automorphism has a positive power which induces a quadratic, orientable pseudo-Anosov homeomorphism on S
g
. To show this, we lift Anosov toral automorphisms through a ramified topological covering and present the lifted homeomorphism via a standard set of Lickorish twists. This construction provides a general method of producing pseudo-Anosov maps of closed surfaces with predetermined orientable foliations and quadratic dilatation. Since these lifted automorphisms have orientable foliations, this construction is a sort of converse to that of Franks and Rykken [Trans. Amer. Math. Soc. 1999], who established that one can associate to a quadratic pseudo-Anosov homeomorphism with oriented unstable foliation a hyperbolic toral automorphism. 相似文献
33.
Richard Baldus 《Mathematische Annalen》1928,100(1):321-333
Ohne ZusammenfassungBis auf Nr. 8 und 9 im wesentlichen, mit Ausnahme der Anmerkungen, vorgetragen auf der Kissinger Mathematikertagung, September 1927, vgl. Jahresber. d. Deutsch. Mathem. Vergg.37 (1928), 2. Abt., S. 3 Auf Anregung von Herrn P. Bernays hin oder veranlaßt durch die neuesten Arbeiten der Herren P. Finsler und B. Baer sind zur ursprünglichen Fassung der vorliegenden Arbeit aus dem September 1927 Nr. 8 und 9, sowie die Anmerkungen23),24),26) hinzugekommen. 相似文献
34.
35.
Philippe Jean 《Applied Acoustics》2004,65(9):861-882
A numerical model of sound transmission inside dwellings has been developed. It is based on a decoupled method mixing integral, modal and geometric approaches. Kropp's formulation has been adapted to take balconies into account. Architectural effects such as projected roofs or nearby buildings have been analysed. Sound transmission is strongly affected by the angle of incidence of incoming waves. The proposed approach makes use of velocity fields on windows either computed or measured with a laser vibrometer. Comparisons between computations and measurements are reported. 相似文献
36.
Eitan Altman Konstantin Avrachenkov Richard Marquez Gregory Miller 《Mathematical Methods of Operations Research》2005,62(3):375-386
We consider a zero-sum stochastic game with side constraints for both players with a special structure. There are two independent
controlled Markov chains, one for each player. The transition probabilities of the chain associated with a player as well
as the related side constraints depend only on the actions of the corresponding player; the side constraints also depend on
the player’s controlled chain. The global cost that player 1 wishes to minimize and that player 2 wishes to maximize, depend
however on the actions and Markov chains of both players. We obtain a linear programming formulations that allows to compute
the value and saddle point policies for this problem. We illustrate the theoretical results through a zero-sum stochastic
game in wireless networks in which each player has power constraints 相似文献
37.
G. Richard Geier III 《Tetrahedron》2004,60(50):11435-11444
To better understand the effects of diverse substituents on reactions leading to porphyrins, pyrrole+aldehyde condensations and related reactions of dipyrromethanes were examined. The course of pyrrole+aldehyde condensations was investigated by monitoring the yield of porphyrin (by UV-Vis spectroscopy), reaction of aldehyde (by TLC), and changes in the composition of oligomers (by laser desorption mass spectrometry). Reaction reversibility was examined via exchange experiments. Reversibility of reactions leading to porphyrin was further probed with studies of dipyrromethanes. The reaction course was found to depend on the nature of the substituent and the acid catalyst. Alkyl or electron-donating substituents displayed levels of reversibility (exchange/scrambling) on par or greater than that of the phenyl substituent, whereas electron-withdrawing or sterically bulky substituents exhibited little to no reversibility. The results obtained provide insight into the electronic and steric effects of different substituents and should facilitate the design of synthetic plans for preparing porphyrinic macrocycles. 相似文献
38.
Ccile Nouvel Philippe Dubois Edith Dellacherie Jean‐Luc Six 《Journal of polymer science. Part A, Polymer chemistry》2004,42(11):2577-2588
The whole controlled synthesis of novel amphiphilic polylactide (PLA)‐grafted dextran copolymers was achieved. The control of the architecture of such biodegradable and potentially biocompatible copolymers has required a three‐step synthesis based on the “grafting from” concept. The first step consisted of the partial silylation of the dextran hydroxyl groups. This protection step was followed by the ring‐opening polymerization of D ,L ‐lactide initiated from the remaining OH functions of the partially silylated polysaccharide. The third step involved the silylether group deprotection under very mild conditions. Based on previous studies, in which the control of the first step was achieved, this study is focused on the last two steps. Experimental conditions were investigated to ensure a controlled polymerization of D ,L ‐lactide, in terms of grafting efficiency, graft length, and transesterification limitation. After polymerization, the final step was studied in order to avoid degradation of both polysaccharide backbone and polyester grafts. The chemical stability of dextran backbone was checked throughout each step of the synthesis. PLA‐grafted dextrans and PLA‐grafted (silylated dextrans) were proved to adopt a core‐shell conformation in various solvents. Furthermore, preliminary experiments on the potential use of these amphiphilic grafted copolymers as liquid/liquid interface stabilizers were performed. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 2577–2588, 2004 相似文献
39.
Arunee Tabtiang Noree Phochalam Richard Venables 《Journal of Polymer Science.Polymer Physics》2004,42(6):965-973
The effects of the copolymer microstructure on the morphology evolution in polyethylene/poly(ethylene‐co‐α‐olefin) blends were investigated. Microscopy revealed that the melt‐phase morphology, inferred from the solid‐state morphologies of annealed and quenched samples, was strongly affected by the copolymer structure, that is, the branch content and branch length. Higher molecular weight α‐olefin comonomer residues and residue contents in the copolymers led to faster coarsening of the morphology. The molecular weight of the polyethylene and the copolymers affected the coarsening rates of the morphology, principally through its influence on the melt viscosity. The effects of the molecular weight were largely explained by the normalization of the coarsening rate data with respect to the thermal energy and zero‐shear‐rate viscosity. Thus, the effect of the molecular weight on the compatibility of the blends was much smaller than the effects of the branch length and branch number. © 2004 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 42: 965–973, 2004 相似文献
40.
Richard Kotek Kyeong Pang Ben Schmidt Alan Tonelli 《Journal of Polymer Science.Polymer Physics》2004,42(23):4247-4254
Poly(ethylene isophthalate) (PEI) was synthesized for this research with essentially a condensation polymerization of isophthalic acid and ethylene glycol catalyzed by zinc acetate and antimony trioxide. Several samples were obtained, and their characteristics were observed and compared with poly(ethylene terephthalate) (PET). The synthesized PEI samples were chemically identified by 1H NMR. Thermal analysis with differential scanning calorimetry (DSC) yielded results that indicate the samples were primarily amorphous, with a glass‐transition temperature of 55–60 °C. Molecular weights of these PEI samples were also obtained through intrinsic viscosity measurements (Mark–Houwink equation). Molecular weights varied with conditions of the polymerization, and the highest molecular weight achieved was 21,000 g/mol. Finally, the diffusion coefficient, solubility, and permeability of CO2 gas in PEI were measured and found to be substantially lower than in PET, as anticipated from their isomeric chemical structures. This is because in PET the phenyl rings are substituted in the para (1,4) positions, which allows for their facile flipping, effectively permitting gases to pass through. However, the meta‐substituted phenyl rings in PEI do not permit such ring flipping, and thus PEI may be more suitable for barrier applications. © 2004 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 42: 4247–4254, 2004 相似文献