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The flow structure behind wire grids is studied for flows with a low subsonic velocity, and the effect of grids on the boundarylayer flow structure is considered. It is shown that the meanvelocity inhomogeneity induced by the grid does not disappear until a distance of 925 calibers downstream of the grid is reached. Liquidcrystal thermography combined with hotwire measurements made it possible to find the source of steady largescale streamwise vortex structures in the boundary layer on a wedge and on an airfoil and to determine the parameters of these structures.  相似文献   
2.
Flow visualization tests have been performed to examine the structure of the near-wall flow over a low-aspect ratio straight wing installed at various angles of attack a and chord Reynolds numberRe c=Uc=1.76×105. The experiments were carried out at two free-stream turbulence levels, ε=0.1% and ε=1%, the latter one having been achieved using a baffling grid. To visualize the flow, termochromic cholesteric liquid crystals and digital processing of video images were used. At the low turbulence level and α=27°, a flow stall on the lee side of the wing was observed, with a pair of largescale vortices rotating in the wing plane. Simultaneously, no vortex structures were observed on the windward wing surface. It was found the flow patterns on either side of the wing significantly changed with increasing free-stream turbulence level. A separation bubble appeared near the leading edge on the lee side of the airfoil at ε=1%, and large-scale stationary longitudinal vortices originated over the wing windward surface. The number and sizes of the longitudinal structures were found to be dependent on the angle of attack.  相似文献   
3.
The catalytic systems [(BPMEN)FeII(CH3CN)2](ClO4)2/H2O2/CH3OOH and [(TPA)FeII(CH3CN)2](ClO4)2/H2O2/CH3OOH, where BPMEN = N,N′-dimethyl-N,N′-bis(2-pyridylmethyl)-1,2-diaminoethane and TPA = tris(2-pyridylmethyl)amine, provide selective olefin epoxidation. Proton NMR studies showed that the mononuclear iron(IV) oxo complexes [(L)FeIV=O]2+, with L = BPMEN or TPA, are present in the cited catalytic systems. These intermediates are the decomposition products of the acylperoxo complexes [(L)FeIII-O3CCH3]2+. Such a complex was observed by the 2H NMR technique at low temperatures. The [(L)FeIV=O]2+ and [(L)FeV=O]3+ oxo complexes are possible active species in the studied catalytic systems.  相似文献   
4.
Oxidation of cycloolefins (cyclohexene, cyclooctene, and cyclododecene) with a 30% solution of hydrogen peroxide at 65 °C in the presence of heteropoly acids (HPA) H3PW12–x Mo x O40 (x = 0—12), which are precursors of active peroxo complexes, and phase transfer catalysts Q+Cl, where Q+ is the quaternary ammonium cation containing C4—C18 alkyl groups or [C5H5NC16H33]+, was studied. The catalytic activity decreases in the HPA series: H3PW12O40 > H3PW9Mo3O40 > H3PW6Mo6O40 > H3PW3Mo9O40 > H3PMo12O40. The state of the H3PW12O40—I2I2 system was studied using UV, IR, and 31P NMR spectroscopies with variation of the [H2O2] : [HPA] ratio from 2 to 200 during cyclohexene epoxidation. Despite different catalytic precursors, the reaction proceeds through the same peroxo complex.  相似文献   
5.
Results for a turbulized flow past the windward side of a swept wing model are presented. Origination of steady disturbances in the form of streamwise structures is found. The greatest effect on the formation of these disturbances is exerted by the curvature of the external flow streamlines. The secondary flow in the boundary layer leads to an increase in the characteristic scale of disturbances in the transverse direction, as compared to the flow around the model at a zero yaw angle.  相似文献   
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