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101.
Antonio Vera López 《Israel Journal of Mathematics》1986,56(2):179-187
We get new properties of the numbersr G(xN) = |{Cl G (g)|Cl G (g)∩xN ≠ Ø} (whereG is a finite group andN is a normal subgroup ofG) that are useful in the analysis of the classification of the finite groups according to the number of conjugacy classes. 相似文献
102.
We report an analysis of two different clays from the region of Umbria (Italy): 1. potteries found one inside and the other
outside the town of Todi, dating from the end of the IV century B. C., 2. bond clays of Bagnara (Nocera Umbra) and Colfiorito
(Foligno) dating V century B.C. 相似文献
103.
Nenad Mladenović Milan Dražić Vera Kovačevic-Vujčić Mirjana Čangalović 《European Journal of Operational Research》2008
We suggest a new heuristic for solving unconstrained continuous optimization problems. It is based on a generalized version of the variable neighborhood search metaheuristic. Different neighborhoods and distributions, induced from different metrics are ranked and used to get random points in the shaking step. We also propose VNS for solving constrained optimization problems. The constraints are handled using exterior point penalty functions within an algorithm that combines sequential and exact penalty transformations. The extensive computer analysis that includes the comparison with genetic algorithm and some other approaches on standard test functions are given. With our approach we obtain encouraging results. 相似文献
104.
105.
106.
Two composite supports with a mixed inorganic–organic structure were synthesized: BTAl and UTAl. Hydrophilic–hydrophobic dual properties of the supports were suitable for preparing egg-shell-supported metal catalysts for selective hydrogenation reactions. The catalysts were characterized by ICP, XRD, OM, TEM, EPMA, XPS and TGA. Their mechanical resistance was assessed. Activity and selectivity were tested with the hydrogenation of 2,3-butanedione (diacetyl) to 3-hydroxy-2-butanoneacetoin (acetoin). The same order of increasing metal particle size was found for the two tested supports: Pt < Ru < Pd. The XPS analysis showed that the metal/composite catalysts reduced in H2 at 503 K had two kinds of active sites: reduced (Me°) and electron-deficient (Me+). It was rationalized that the hydrogen bond cleavage was performed on the Me° active sites, while reactant adsorption occurred on the Me+ sites. The differences in activity and selectivity between the composite catalysts were attributed to electronic effects on the different metals and to different adsorptive properties of the different polymers. The high selectivity to acetoin was attributed to the preferential adsorption of diacetyl as compared to the adsorption of acetoin. The BTAl catalysts were slightly more active and selective than the UTAl ones. This was attributed to electronic effects caused by remnant organic groups on the composite supports (urethane or biphenyl on UTAl or BTAl, respectively). Pd-BTAl was the most active and selective catalyst, a fact related to electronic effects of both palladium and the support. 相似文献
107.
Evgeny Yu. Taran Yury V. Pridatchenko Vera A. Gryaznova 《Comptes Rendus Mecanique》2004,332(4):279-284
The problem of rotary motion of rigid axially symmetric elongated particles in the Couette flow of dilute suspension with anisotropic carrier fluid is solved. It is shown that the stable stationary solutions of the dynamical set of ordinary differential equations describing the particles rotary motion are possible in the case of forming the stationary anisotropy in the carrier fluid of the suspension. It allows us to detect the stationary orientation of suspended particles and formation of stable anisotropic liquid-crystalline structures in the considered suspension under the action of hydrodynamic forces. The study of rheological properties of such a structured suspension shows that it behaves as a viscoelastic quasi-Newtonian anisotropic liquid medium. To cite this article: E.Yu. Taran et al., C. R. Mecanique 332 (2004). 相似文献
108.
109.
Daiane P. Torres Ingrid M. Dittert Vera L.A. Frescura Adilson J. Curtius 《Microchemical Journal》2010,96(1):32-699
A simple method for the determination of mercury in gasoline samples diluted with ethanol by graphite furnace atomic absorption spectrometry (GF AAS) after cold vapor (CV) generation, pre-concentration in a gold column and trapping on a graphite tube is proposed. The methodology is based upon conventional analytical processes that can be performed by any laboratory with a chemical generation and gold amalgamation systems coupled to the atomic absorption spectrometer. The GF AAS temperature was optimized, being the retention, pyrolysis and atomization temperatures, respectively, 100 °C, 150 °C and 800 °C. Gasoline samples were prepared simply by forming a 2-fold diluted solution in ethanol. The mercury formed vapors by reacting the sample with the reducing agent were pre-concentrated in a gold column and further retained on a graphite tube, coated with gold as permanent modifier. Five samples from different gas stations around the UFSC Campus (Florianópolis, Brazil) were analyzed and the Hg concentrations were found to be in the range from 0.40 µg L− 1 to 0.90 µg L− 1. Calibration against aqueous standard solutions in acidic medium was carried out. The standard solutions had about the same viscosity as the gasoline diluted in ethanol. The relative standard deviations were lower than 2.4% for the samples. The limits of detection in the samples were 0.08 and 0.14 µg L− 1, with and without pre-concentration in the gold column, respectively. The accuracy of the method was estimated by applying the recovery test and recovery values between 92 and 100% were obtained. A sample throughput of 4 h− 1 was achieved. Simplicity and high detection capability are some of the qualities of the method. 相似文献
110.
Vera Vasylyeva 《Journal of fluorine chemistry》2010,131(3):446-4255
The influence of fluorine substituents on the crystallisation behaviour of pyridine was investigated by crystal structure determinations. The low melting compounds 2-fluoropyridine, 2,6-difluoropyridine and 2,4,6-trifluoropyridine were crystallised by in situ crystallisation directly on the single crystal X-ray diffractometer. 相似文献