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11.
Daniele Andreucci Paolo Bisegna Emmanuele DiBenedetto 《Comptes Rendus Mathematique》2002,335(4):329-332
We compute the homogenized-concentrated limit for a pair of non-linearly coupled diffusion equations in a perforated cylindric domain with coaxial cylindric holes periodically distributed along its axis. This problem arises from visual transduction. To cite this article: D. Andreucci et al., C. R. Acad. Sci. Paris, Ser. I 335 (2002) 329–332. 相似文献
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In this article, we solve in closed form a system of nonlinear differential equations modelling the elastica in space of a thin, flexible, straight rod, loaded by a constant thrust at its free end. Common linearizations of strength of materials are of course not applicable any way, because we analyze great deformations, even if not so large to go off the linear elasticity range. By passing to cylindrical coordinates ρ, θ, z, we earn a more tractable differential system evaluating ρ as elliptic function of polar anomaly θ and also providing z through elliptic integrals of I and III kind. Deformed rod’s centerline is then completely described under both tensile or compressive load. Finally, the planar case comes out as a degeneracy, where the Bernoulli lemniscatic integral appears. 相似文献
14.
A calibration technique for the constant-temperature hot-wire anemometer is presented, which is based on traversing the probe
through the boundary layer of a flat plate while simultaneously performing fluctuation measurements. The free stream Mach
number was M = 2.54, and the Reynolds number Red, based on wire diameter, ranged from 9 to 23. A comparison of the sensitivity values obtained with the aid of such a calibration
procedure — under the condition of neglecting low temperature loadings (t<0.6) — agrees well with sensitivities determined with free-stream data-The use of a modified transfer function for correcting
the power spectra of flow perturbations revealed a conformity of wide parts of the corrected spectra with the Kolmogorov decay.
The fluctuation levels of total temperature and mass flux were computed for the boundary layer of a flat plate.
This work was presented at the International Conference on the Methods of Aerophysical Research ICMAR 2007, which was held
in Novosibirsk on 5–10 February 2007. 相似文献
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16.
Luigi Angiolini Daniele Caretti Elisabetta Salatelli Monique Biesemans 《Journal of organometallic chemistry》2006,691(9):1965-1972
Starting from 4-isopropylbenzoic acid, three new triorganotin carboxylates bearing methyl, butyl and phenyl substituents at tin, respectively, were prepared and fully characterized by spectroscopic and thermal techniques, with particular regard to the coordination number of tin atom, in solution as well as in the solid state. The triorganotin compounds, tested as transesterification catalysts in the reaction between ethyl acetate and primary, secondary or tertiary alcohol, respectively, displayed, as expected, a strong decrease of activity on passing from the primary to the tertiary alcohol reactant. Different activities by the tin carboxylates were also observed in the reaction between primary alcohol and ethyl acetate. The reaction mechanism, as elucidated by Sn NMR, involves coordination of both ester substrate and alcohol reactant to the triorganotin compound, the reaction conversion appearing related not only to the Lewis acidity of the tin atom, but also to the nature of the reactants. Preliminary catalytic tests were also carried out in the reaction between glyceryl tridodecanoate (as a model of natural triglyceride) and ethanol, mimicking the preparation of biodiesel fuel. Although in this case lower conversions were obtained with respect to the reactions on ethyl acetate, the catalytic activity of organotin derivatives appears considerable. 相似文献
17.
Benati L Bencivenni G Leardini R Minozzi M Nanni D Scialpi R Spagnolo P Zanardi G 《The Journal of organic chemistry》2005,70(8):3046-3053
Thermal reaction of various alpha-azido esters with Bu(3)SnH in refluxing benzene results in smooth production of 3-(tributylstannyl)-1-triazene adducts affording cyclized 1,2,3-triazol-4-ones in preference to reduced amines and thence provides a new useful method for the preparation of these triazole derivatives. In the presence of AIBN the occurrence of triazene products still remains important or even exclusive and, consequently, generation of the expected stannylaminyl radicals is seriously limited. With 2-azidomalonates and alpha-azido-beta-keto esters stannyltriazenes can similarly occur in the absence of the radical initiator, but in the latter cases the ensuing triazenes undergo preferential cyclization onto the ketone moiety to give reactive hydroxytriazolines. Contrary to alpha-azido esters, in the presence of AIBN alpha-azido-beta-keto esters as well as azidomalonates give rise only to the usual stannylaminyl radicals. A possible explanation for the different behavior of the mono- and dicarbonyl azides in the presence of AIBN is put forward. 相似文献
18.
Benati L Leardini R Minozzi M Nanni D Spagnolo P Strazzari S Zanardi G 《Organic letters》2002,4(18):3079-3081
[reaction: see text] Aryl- and alkyl-derived azidoacyl radicals, generated from thiolesters by intramolecular homolytic substitution at the sulfur, can undergo five- and six-membered cyclization onto the azido moiety to give cyclized lactams. 相似文献
19.
Hans-Rudolf Dicke Robert W. Lenz 《Journal of polymer science. Part A, Polymer chemistry》1983,21(8):2581-2588
A series of terephthalate polyesters was prepared from substituted hydroquinone monomers that contained a single cyclic or branched alkyl group. All the polymers were crystalline with melting points well below 400°C that decreased as the size of the cycloalkyl substituent increased. Most of the polymers had clearing temperatures below 400°C and all formed nematic melts. Copolyesters that contained equimolar amounts of two different substituted hydroquinone monomers, which were crystalline and had broad temperature ranges for nematic phase formation, were also prepared. 相似文献
20.
The cyclic voltammetric technique is used to study hydrogen-bond formation in some polar organic solvents (S) of electroanalytical interest (1,2-dimethoxy, tetrahydrofuran, dimethylformamide, dimethyl sulphoxide and pyridine). The cathodic shift of the proton reduction caused by stepwise addition of the solvent investigated to a solution of anhydrous perchloric acid in acetonitrile is utilized. The theoretical treatment applied produced evidence that HS+ and HS+2 are the only acidic species involved, so that the relevant formation constants can be evaluated. The data obtained mostly compare well with those available in the literature. The features that condition the tendency to hydrogen-bonding and the effect of hydrogen bonding on solvent basicity are discussed. 相似文献