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41.
U.R.Mikael Kjellin Per M. Claesson Roland Audebert 《Journal of colloid and interface science》1997,190(2):476
Interactions between two negatively charged mica surfaces across aqueous solutions containing various amounts of a 10% charged cationic polyelectrolyte have been studied. It is found that the mica surface charge is neutralized when the polyelectrolyte is adsorbed from a 10–50 ppm aqueous solution. Consequently no electrostatic double-layer force is observed. Instead an attractive force acts between the surfaces in the distance regime 250–100 Å. We suggest that this attraction is caused by bridging. Additional adsorption takes place when the polyelectrolyte concentration is increased to 100 and 300 ppm, and a long-range repulsion develops. This repulsive force is both of electrostatic and steric origin. The polyelectrolyte layer adsorbed from a 50 ppm solution does not desorb when the polyelectrolyte solution is replaced with an aqueous polyelectrolyte-free solution. Injection of sodium dodecyl sulfate (SDS) into the measuring chamber to a concentration of about 0.01 CMC (8.3 × 10−5M) does not affect the adsorbed layers or the interaction forces. However, when the SDS concentration is increased to 0.02 CMC (0.166 mM) the adsorbed layer expands dramatically due to adsorption of SDS to the polyelectrolyte chains. The sudden swelling suggests a cooperative adsorption of SDS to the preadsorbed polyelectrolyte layer and that the critical aggregation concentration between the polyelectrolyte and SDS at the surface is about 0.02 CMC. The flocculation behavior of the polyelectrolyte in solution upon addition of SDS was also examined. It was found that 0.16–0.32 mol SDS/mol charged segments on the polyelectrolyte is enough to make the solution slightly turbid. 相似文献
42.
We study perturbations of the quantized version
0 of integrable Hamiltonian systems by point interactions. We relate the eigenvalues of to the zeros of a certain meromorphic function . Assuming the eigenvalues of
0 are Poisson distributed, we get detailed information on the joint distribution of the zeros of and give bounds on the probability density for the spacings of eigenvalues of . Our results confirm the wave chaos phenomenon, as different from the quantum chaos phenomenon predicted by random matrix theory.SFB 237 Essen-Bochum-Düsseldorf 相似文献
43.
The phonon dispersion curves, phonon frequency distribution function as well as the lattice specific heat of body-centred
tetragonal indium have been deduced using a lattice dynamical model which includes central, angular and volume forces. Six
elastic constants, four zone boundary frequencies and an equilibrium condition were used in the evaluation of the force constants.
It is shown that this model is elastically consistent and satisfies the symmetry requirements of the lattice, the phonon frequencies
of indium deduced from it are in very good agreement with the experimental values of Reichardt and Smith and the theoretical
values of Garrett and Swihart, and theθ
D values compare well with the experimental values over a wide temperature range. The apparent discrepancies in the phonon
dispersion curves and theθ
D-T curves obtained from deficient models, importance of umklapp processes and the significance of angular forces in the lattice
dynamical models are discussed. 相似文献
44.
The system containing six benzylideneanilines (BA) has been studied: Group 1:
The crystal structures of Group 1 are isostructural. They crystallize in a monoclinic cell, space groupP21. They are rare examples of planar benzylideneanilines in a nondisordered crystal structure. The crystal structures exhibit an intermolecular ring containing five atoms and hal- - - hal. C-H- - - hal interactions, which may contribute to the planarity of the molecule. The structures in Group 2 crystallize in a monoclinic cell, space groupP21/c. The conformation is nonplanar and there are no intermolecular halogen- - -halogen interactions. The abovementioned five atom pattern ring does not occur in these structures. These two groups of structures show that the type and mode of molecular substitution can lead to specific intermolecular interactions which in turn stabilize an otherwise unfavorable molecular conformation. 相似文献
I: | N-(p-Chlorobenzylideneaniline)m-chloroaniline (BA, X=4-Cl, Y=3-Cl) |
II: | N-(p-Bromobenzylideneaniline)m-bromoaniline (BA, X=4-Br, Y=3-Br) |
III: | N-(p-Bromobenzylideneaniline)m-chloroaniline (BA, X=4-Br, Y=3-Cl) |
IV: | N-(p-Chlorobenzylideneaniline)m-bromoaniline (BA, X=4-Cl, Y=3-Br) Group 2: |
V: | N-(m-Chlorobenzylideneaniline)p-bromoaniline (BA, X=3-Cl, Y=4-Br) |
VI: | N-(m-Bromobenzylidencaniline)p-chloroaniline (BA, X=3-Br, Y=4-Br) |
45.
Surface forces in wetting films 总被引:4,自引:0,他引:4
Churaev NV 《Advances in colloid and interface science》2003,103(3):197-218
A short review of various components of surface forces acting in a non-symmetrical system such as wetting films is presented here. Experimental results are compared with modified DLVO theory, which includes, besides dispersion and electrostatic, structural (solvation) forces caused by a change in liquid structure in conditions of confined geometry. The peculiarities of disjoining pressure isotherms and conditions of the film stability of non-polar and polar simple liquids, as well as of aqueous solutions of electrolytes and surfactants, are systematically considered from a historical perspective. 相似文献
46.
The deformation, drainage, and rupture of an axisymmetrical film between colliding drops in the presence of insoluble surfactants under the influence of van der Waals forces is studied numerically at small capillary and Reynolds numbers and small surfactant concentrations. Constant-force collisions of Newtonian drops in another Newtonian fluid are considered. The mathematical model is based on the lubrication equations in the gap between drops and the creeping flow approximation of Navier–Stokes equations in the drops, coupled with velocity and stress boundary conditions at the interfaces. A nonuniform surfactant concentration on the interfaces, governed by a convection–diffusion equation, leads to a gradient of the interfacial tension which in turn leads to additional tangential stress on the interfaces (Marangoni effects). The mathematical problem is solved by a finite-difference method on a nonuniform mesh at the interfaces and a boundary-integral method in the drops. The whole range of the dispersed to continuous-phase viscosity ratios is investigated for a range of values of the dimensionless surfactant concentration, Peclét number, and dimensionless Hamaker constant (covering both “nose” and “rim” rupture). In the limit of the large Peclét number and the small dimensionless Hamaker constant (characteristic of drops in the millimeter size range) a fair approximation to the results is provided by a simple expression for the critical surfactant concentration, drainage being virtually uninfluenced by the surfactant for concentrations below the critical surfactant concentration and corresponding to that for immobile interfaces for concentrations above it. 相似文献
47.
《Wave Motion》2017
The traveling wave ultrasonic stator is normally fabricated with teeth. The tooth geometry improves the driving speed, but it creates natural frequency splitting and mode contamination, especially a distorted traveling wave. A dynamic model of a stepped-plate periodic stator is developed to examine the distortion. The stator is treated as an annular supported by a thin mid plate, and the support stiffness is formulated by using equivalent energy principle. The effects of the tooth and mid plate on the natural frequency and vibration mode are examined by using the perturbation method. The rules governing the frequency splitting, frequency perturbation as well as mode contamination are also identified. The traveling wave response and elliptical trace on stator surface are obtained by using the mode superposition method and they are proved to be distorted due to the tooth geometry. The response at the repeated doublets becomes coupled forward and backward traveling waves, but that at the split doublets becomes coupled forward traveling, standing and backward traveling waves. The results indicate that the tooth mass instead of the stiffness decreases the vibration amplitude and driving speed of the dominant wave, but their effects are different at the repeated and split doublets. Inspection of the model implies that the distortion can be suppressed by using a suitable combination of the wavenumber, tooth count, tooth height and occupying fraction. Numerical calculations are carried out to demonstrate the tooth geometry effect on the transient waveform, driving speed and elliptical trace. The optimization of the tooth geometry that can help achieve a purer traveling wave is discussed. 相似文献
48.
We study the average energy – or particle – density of waves inside disordered 1D multiply-scattering media. We extend the transfer-matrix technique that was used in the past for the calculation of the intensity beyond the sample to study the intensity in the interior of the sample by considering the transfer matrices of the two segments that form the entire waveguide. The statistical properties of the two disordered segments are found using a maximum-entropy ansatz subject to appropriate constraints. The theoretical expressions are shown to be in excellent agreement with 1D transfer-matrix simulations. 相似文献
49.
Uniform spreading of oil on solid surfaces is important in many processes where proper lubrication is required and this can be controlled using surfactants. The role of oil–solid interfacial self-assembled surfactant structure (SASS) in oil spreading is examined in this study for the case of hexadecane-surfactant droplet spreading on a flat horizontal copper surface, with triphenyl phosphorothionate surfactants having varying chain lengths (0 to 9). It is shown that the frictional forces (FSASS) as determined by the SASS regulate droplet spreading rate according to surfactant chain length; surfactants with longer chains led to higher reduction in the spreading rate. The extent of such forces, FSASS, depends on the surfactant density of the evolving SASS, and specific configuration the evolving SASS exhibit as per the orientations of the surfactant chains therein. Thus, FSASS = [k1 + k2(t)] Γδ(t), where Γδ(t) is the surfactant adsorption density of SASS at time ‘t’ during evolution, and, k1 and k2(t) are the force coefficients for Γδ(t) and orientations (as a function of spreading time) of the surfactant chains respectively. As a SASS evolves/grows along with adsorption of surfactants at the spreading induced fresh interface, the k1Γδ(t) component of FSASS increases and contributes to reduction in the net spreading force (S). With a decrease in the net spreading force, the existence of a cross-over period, during which the transition of the spatial dynamics of the chains from disordered to realignment/packing induced ordered orientation occurs, has been inferred from the FSASS vs. chain length relationships. Such relationships also suggested that the rate of realignment/packing is increased progressively particularly due the realignment/packing induced decrease in the net spreading force. Therefore, the realignment process is a self-induced process, which spans a measurable period of time (several minutes), the cross-over period, during which the net spreading force decreases essentially due to such self-induced process. 相似文献
50.