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101.
We will prove a result concerning the inclusion of non-trivial invariant ideals inside non-trivial ideals of a twisted crossed
product. We will also give results concerning the primeness and simplicity of crossed products of twisted actions of locally
compact groups on -algebras.
Received: 25 January 2002; in final form: 22 May 2002/Published online: 2 December 2002
This work is partially supported by Hong Kong RGC Direct Grant. 相似文献
102.
The influence of the sample orientation on the effective value of the hydrostatic piezoelectric coefficients d
h
(i)
of Sn2P2S6 crystals has been studied. The hydrostatic piezoelectric coefficients d
h
(1)
and d′
h
(3)
, were measured, d
h
(1)
=(244±3) pC/N and d′
h
(3)
=(92±1) pC/N. The hydrostatic piezoelectric coefficient d
h
(3)
for orthogonal axis system was calculated to be d
h
(3)
=(87±2) pC/N. The, optimal orientation of the sample has been found as (Xy l)−20°-cut. Maximal value of the effective hydrostatic piezoelectric coefficient d
h
(1)
equals 260 pC/N. Double rotated samples were also studied. The orientation of the samples insensitive to the pressure has
been found. The theoretical mean value of hydrostatic piezoelectric coefficient (d
h
)
mean
corresponding to randomly oriented Sn2P2S6 grains in a poled composite has been calculated to be (d
h
)
mean
=136 pC/N. 相似文献
103.
Vincent Maurice 《Surface science》2005,581(1):88-104
STM, STS, LEED and XPS data for crystalline θ-Al2O3 and non-crystalline Al2O3 ultra-thin films grown on NiAl(0 0 1) at 1025 K and exposed to water vapour at low pressure (1 × 10−7-1 × 10−5 mbar) and room temperature are reported. Water dissociation is observed at low pressure. This reactivity is assigned to the presence of a high density of coordinatively unsaturated cationic sites at the surface of the oxide film. The hydroxyl/hydroxide groups cannot be directly identify by their XPS binding energy, which is interpreted as resulting from the high BE positions of the oxide anions (O1s signal at 532.5-532.8 eV). However the XPS intensities give evidence of an uptake of oxygen accompanied by an increase of the surface coverage by Al3+ cations, and a decrease of the concentration in metallic Al at the alloy interface. A value of ∼2 for the oxygen to aluminium ions surface concentration ratio indicates the formation of an oxy-hydroxide (AlOxOHy with x + y ∼ 2) hydroxylation product. STM and LEED show the amorphisation and roughening of the oxide film. At P(H2O) = 1 × 10−7 mbar, only the surface of the oxide film is modified, with formation of nodules of ∼2 nm lateral size covering homogeneously the surface. STS shows that essentially the valence band is modified with an increase of the density of states at the band edge. With increasing pressure, hydroxylation is amplified, leading to an increased coverage of the alloy by oxy-hydroxide products and to the formation of larger nodules (∼7 nm) of amorphous oxy-hydroxide. Roughening and loss of the nanostructure indicate a propagation of the reaction that modifies the bulk structure of the oxide film. Amorphisation can be reverted to crystallization by annealing under UHV at 1025 K when the surface of the oxide film has been modified, but not when the bulk structure has been modified. 相似文献
104.
105.
Luminescence properties of anodic aluminum oxide films with organic luminophores embedded into pores
V. V. Gruzinskii A. V. Kukhto A. M. Mozalev V. F. Surganov 《Journal of Applied Spectroscopy》1997,64(4):497-502
Luminescence properties of porous anodic aluminum oxide films formed in a 0.6 M solution of citric acid and luminescence of
paraterphenyl, perylene, coumarin 7, and rhodamine 6G dyes adsorbed by the films are investigated. The nature of emitting
centers in anodic aluminum oxide is revealed. Intense photoluminescence of all tested dyes embedded into pores of anodic aluminum
oxide has been found. A redshift of fluorescence spectra of dyes adsorbed by the matrix and emergence of an additional longwave
band have been detected. Data obtained can be used in developing new thin-film luminescent coatings for future applications
in optoelectronics and molecular electronics.
Translated from Zhurnal Prikladnoi Spektroskopii, Vol. 64, No 4, pp. 483–488, July–August, 1997. 相似文献
106.
107.
Mass distributions of fragments in the low-energy fission of nuclei from 187Ir to 213At have been analysed. This analysis has shown that shell effects in symmetric-mode fragment mass yields from the fission of pre-actinide nuclei could be described if one assumes the existence of two strongly deformed neutron shells in the arising fragments with neutron numbers N1 ≈ 52 and N2 ≈ 68. A new method has been proposed for quantitatively describing the mass distributions of the symmetric fission mode for pre-actinides with A ≈ 180–220. 相似文献
108.
We investigate several versions of a cardinal characteristic defined by Frankiewicz. Vojtáš showed , and Blass showed . We show that all the versions coincide and that is greater than or equal to the splitting number. We prove the consistency of and of .
Received: 2 October 1996 / Revised version: 22 May 1997 相似文献
109.
本文首先提出逆(反)对策这一新问题,给出了数学模型;探讨了“奇门遁甲”预测理论(术)中的数学问题;通过系统分析“专门遁甲”预测过程,可知它的预测过程隐含着一个特殊的逆(反)对策问题;最后指出逆(反)对策问题的广泛存在并给出案例分析. 相似文献
110.
Summary. We study a diffusion model of an interacting particles system with general drift and diffusion coefficients, and electrostatic
inter-particles repulsion. More precisely, the finite particle system is shown to be well defined thanks to recent results
on multivalued stochastic differential equations (see [2]), and then we consider the behaviour of this system when the number
of particles goes to infinity (through the empirical measure process). In the particular case of affine drift and constant diffusion coefficient,
we prove that a limiting measure-valued process exists and is the unique solution of a deterministic PDE. Our treatment of
the convergence problem (as ) is partly similar to that of T. Chan [3] and L.C.G. Rogers - Z. Shi [5], except we consider here a more general case allowing
collisions between particles, which leads to a second-order limiting PDE.
Received: 5 August 1996 / In revised form: 17 October 1996 相似文献