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111.
以LCD为目标的自动定焦判据选择   总被引:2,自引:0,他引:2  
在光学综合自动测量中 ,使用液晶显示屏作为分划板可以大大简化结构 ,提高效率 ,真正地实现自动测量。由于液晶显示具有对比度低、噪声大等特点 ,所以根据液晶的这些特点以及图像处理和CCD信号接收的特点选择两种适用的判据进行了分析和试验比较 ,并给出了结果。结果表明 ,这两种判别函数都适用于以液晶显示屏为目标和用图像处理方法进行光学参数测量的系统 ,其中锐度判别函数更优于信息熵判别函数 ,前者具有更好的抗干扰性和稳定性 ,而且其判定结果更接近目视清晰度判别  相似文献   
112.
We establish that the kinematic constraints on the steady planar motion of an ideal fiber-reinforced fluid can be consolidated in a single third-order nonlinear equation. Remarkably, this equation admits a solitonic reduction related to the classical sine-Gordon equation. The kinematic conditions in this case admit a novel duality property and a Bäcklund transformation.  相似文献   
113.
This article discusses an immersed finite element (IFE) space introduced for solving a second‐order elliptic boundary value problem with discontinuous coefficients (interface problem). The IFE space is nonconforming and its partition can be independent of the interface. The error estimates for the interpolation of a function in the usual Sobolev space indicate that this IFE space has an approximation capability similar to that of the standard conforming linear finite element space based on body‐fit partitions. Numerical examples of the related finite element method based on this IFE space are provided. © 2004 Wiley Periodicals, Inc. Numer Methods Partial Differential Eq 20: 338–367, 2004  相似文献   
114.
We find necessary and sufficient conditions for the connected Julia set of a polynomial of degree d?2 to be an indecomposable continuum. One necessary and sufficient condition is that the impression of some prime end (external ray) of the unbounded complementary domain of the Julia set J has nonempty interior in J. Another is that every prime end has as its impression the entire Julia set. The latter answers a question posed in 1993 by the second two authors.We show by example that, contrary to the case for a polynomial Julia set, the image of an indecomposable subcontinuum of the Julia set of a rational function need not be indecomposable.  相似文献   
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116.
Let R be a discrete complete valuation ring, with algebraically closedresidue field. Let X be a semi-stable R-curve, with smooth generic fibre. In this paper we study tame coverings of X.  相似文献   
117.
New mesoporous covalent frameworks, based on hybrid fluorinated organosilicas, were prepared to realize a periodic architecture of fast molecular rotors containing dynamic dipoles in their structure. The mobile elements, designed on the basis of fluorinated p‐divinylbenzene moieties, were integrated into the robust covalent structure through siloxane bonds, and showed not only the rapid dynamics of the aromatic rings (ca. 108 Hz at 325 K), as detected by solid‐state NMR spectroscopy, but also a dielectric response typical of a fast dipole reorientation under the stimuli of an applied electric field. Furthermore, the mesochannels are open and accessible to diffusing in gas molecules, and rotor mobility could be individually regulated by I2 vapors. The iodine enters the channels of the periodic structure and reacts with the pivotal double bonds of the divinyl‐fluoro‐phenylene rotors, affecting their motion and the dielectric properties.  相似文献   
118.
Here we demonstrate that neat reactions of amphoteric azoles with more basic azoles give a family of finely tunable, nonstoichiometric liquids which are useful for N‐donor coordination chemistry. Reacting 4,5‐dicyanoimidazole (4,5‐DCNIm) with 1‐methylimidazole (1‐mim) gives new compounds with composition‐dependent speciation. Two crystalline compounds, a 1:1 protic salt, [H(1‐mim)][4,5‐DCNIm], and a 1:2 salt co‐crystal, [H(1‐mim)][4,5‐DCNIm]?4,5‐DCNIm, were isolated and structurally characterized, while differential scanning calorimetry revealed both suppression of crystallization and the presence of neutral and anionic species in the melt. Reactions of Cu(NO3)2?2.5 H2O, CuO, and ZnO with the neat 2:1 1‐mim/4,5‐DCNIm melt resulted in the isolation of entirely N‐donor ligated complexes of the formula M(4,5‐DCNIm)2(1‐mim)4 (M=Cu, Zn).  相似文献   
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120.
Small-angle neutron scattering and surface tension have been used to characterize a class of surfactants (SURFs), including surfactant ionic liquids (SAILs). These SURFs and SAILs are based on organic surfactant anions (single-tail dodecyl sulfate, DS, double-chain aerosol-OT, AOT, and the trichain, TC) with substituted quaternary ammonium cations. This class of surfactants can be obtained by straightforward chemistry, being cheaper and more environmentally benign than standard cationic SAILs. A surprising aspect of the results is that, broadly speaking, the physicochemical properties of these SURFs and SAILs are dominated by the nature of the surfactant anion and that the chemical structure of the added cation plays only a secondary role.  相似文献   
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