Electric field light scattering by flexible linear polyelectrolytes in aqueous solution

Electric field light scattering results on aqueous solutions of linear, flexible NaPSS at minimal ionic strength are reported. Samples of molecular weights between 356 kg/mol and 2870 kg/mol were investigated. With increasing field strength the intensity as a function of wavenumber develops a pronounced oscillating behaviour. Besides the well-known first peak a second maximum is observed at the position at which a weak maximum for some samples already occurs at zero field. The overall intensity strongly depends on the frequency of the electric field. The electro-optical effect shows a maximum at 300 kHz. Increasing the particle concentration gives a large increase of the peak maximum, normalized to concentration. If plotted versus scattering angle the relative intensity increase is maximum for samples of medium molecular weight. The results strongly indicate a stretching and alignment of the chains, thus leading to or enlarging the short range order of the chains. Received 9 April 1999 and Received in final form 18 August 1999     

Solubility of highly charged anionic polyelectrolytes in presence of multivalent cations: Specific interaction effect

Studies performed on strong polyelectrolytes and on a weak polyelectrolyte, sodium poly(acrylate), show that their stability in presence of multivalent cations depends on the chemical nature of the charged side groups of the polymer. For sulfonate groups (SO₃ ^-) or sulfate groups (OSO₃ ^-) phase separation generally occurs in presence of inorganic cations of valency 3 (as La³⁺) or larger and a resolubilization takes place at high salt concentration. The interactions of the polyelectrolyte with multivalent cations are of electrostatic origin and the phase diagrams are weakly dependent on the chemical nature of the polymer backbone and on the specificity of the counterions. For acrylate groups, (COO^-), the phase separation was observed with inorganic cations of valency 2 (as Ca²⁺) or larger without resolubilization at high salt concentration. The phase separation is due to a chemical association between cations and acrylate groups of two neighboring monomers of the same chain. This chemical association creates a hydrophobic complex by dehydrating both monomer and cation. With organic trivalent cation, as spermidine ⁺H₃N(CH₂)₄NH₂ ⁺(CH₂)₃NH₃ ⁺, where no chemical association occurs with the charged side groups COO^- or SO₃ ^- of the polyelectrolyte, similar phase diagrams were observed whatever was the polyelectrolyte with a resolubilization at high trivalent cation concentration. Received 3 March 1999 and Received in final form 2 September 1999     

稀土掺杂聚苯撑ER流体的研究

选用CeCl4和FeCl3等对自制的对苯撑进行掺杂,将制得的高介电聚苯撑粉末加入到硅油中得到电流变体流体,测量了在电场作用下粘度和漏电流密度,以及相关的物理常数。讨论了电场强度、粒子浓度与粘度和漏电流密度的关系,粘度变化的响应速度和恢复时间,并探讨了其相关机制。     

Lattice-Boltzmann study of spontaneous emulsification

We study the dynamics of spontaneous emulsification of an initially planar oil-water interface when surfactants are added. The thermodynamic properties of the ternary oil-water-surfactant system are modeled by a Ginzburg-Landau-type free energy. The lattice Boltzmann method is used to solve the dynamic equations. The dynamics is found to be governed by a complicated interplay of convection and diffusion as the two relevant transport mechanisms. As long as the interface is almost flat, we find the interfacial area to grow first exponentially and then linearly in time. Later finger-like structures form which grow with a constant velocity. The tip velocity is found to increase roughly linearly with the mobility of the amphiphile, and to decrease as with the solvent viscosity . Received 5 January 1999     

Water droplets in a spherically confined nematic solvent: A numerical investigation

Recently, it was observed that water droplets suspended in a nematic liquid crystal form linear chains [Poulin et al., Science 275, 1770 (1997)]. The chaining occurs, e.g., in a large nematic drop with homeotropic boundary conditions at all the surfaces. Between each pair of water droplets a point defect in the liquid crystalline order was found in accordance with topological constraints. This point defect causes a repulsion between the water droplets. In our numerical investigation we limit ourselves to a chain of two droplets. For such a complex geometry we use the method of finite elements to minimize the Frank free energy. We confirm an experimental observation that the distance d of the point defect from the surface of a water droplet scales with the radius r of the droplet like .When the water droplets are moved apart, we find that the point defect does not stay in the middle between the droplets, but rather forms a dipole with one of them. This confirms a theoretical model for the chaining. Analogies to a second order phase transition are drawn. We also find the dipole when one water droplet is suspended in a bipolar nematic drop with two boojums, i.e., surface defects at the outer boundary. Finally, we present a configuration where two droplets repel each other without a defect between them. Received 11 December 1998     

Non-linear viscoelastic behavior of fumed silica suspensions

Suspensions of fumed silica exhibit a wide range of rheological properties depending on the nature and magnitude of the interparticle forces. In a non-polar fluid, the particles interact through hydrogen bonding and can form a three-dimensional network. The microstructure formation is responsible for the non-linear viscoelastic behavior of fumed silica suspensions, even at very small strain. These non-linear rheological properties have been studied in small amplitude oscillatory experiments as a function of particle size, surface treatment of particles, suspending medium polarity and solids concentration. The non-linear viscoelastic behavior is characterized by a non-sinusoidal waveform of the signal response. For suspensions in a non-polar fluid, both the elastic and the loss moduli are shown to be sensitive to the strain amplitude: the elastic modulus is decreasing with increasing strain whereas the loss moduli is initially increasing with strain. We have chosen to examine the dissipated energy which is clearly related to the breakup of the suspension structure. A comparison of model predictions and the experimental data shows the limitations of these models, recently proposed in the literature to describe the behavior of colloidal suspensions. Received: 9 March 1998 Accepted: 17 November 1998     

The basic character of five two‐phase flow model equation sets

Three test problems were simulated using five different two‐phase flow model equation sets from the open literature. The test problems chosen were a fluidized bed, a batch settling, and a horizontal jet impingement on a vertical wall. These three problems demonstrate an important cross‐section of physical phenomena, such as fluidized bed voidage oscillations, phase separation, countercurrent flow, and jet formation. The dispersed flow regime is selected for all three problems. The study was performed to assess the basic character of the five‐field equation sets responding to the same initial and boundary conditions and using the same finite difference numerical scheme. The general performance of the five equation sets was found to be similar, even though one of them was ill posed as an initial‐value problem. Broad trends are the same and quantitative differences could be assessed by examining the fine structure of the results. None of the equation sets could be entirely rejected on the basis of producing physically impossible or unacceptable results. Copyright © 2000 John Wiley & Sons, Ltd.     

Peculiar features in the rheological behavior of electrorheological suspensions

Studies have been made of concentrated (up to 60%) diatomite suspensions in transformer oil, the structure and theological properties of which depend on an applied electric field. Studies have been conducted of steady-state and transient regimes of straining involving continuous and periodic shear. The structure in such suspensions is formed in the presence of an electric field of 10^–3 –10² duration. The suspensions under continuous stationary strain behave as non-Newtonian fluids with a yield stress dependent on electric intensity. Under periodic deformation conditions the test suspensions exhibit elasticity which abruptly diminishes with increasing deformation amplitude.     

On the non-linear instability of fiber suspensions in a Poiseuille flow

The non-linear instability characteristics of fiber suspensions in a plane Poiseuille flow are investigated. The evolution equation of the perturbation amplitude analogous to Landau equation is formulated and solved numerically for different fiber parameters. It is found that the equilibrium amplitude decreases with the increase of the fiber aspect ratio and volume fraction, i.e. the addition of the fibers reduces the amplitude of the perturbation, and leads to the reduction of the flow instability. This phenomenon becomes significant for large volume concentration and aspect ratio. The mechanism of the reduction of the flow instability is also analyzed by taking into account of the modification of the mean flow and the energy transfer from the mean flow to the perturbation flow.     

粉煤灰微珠的气力分级原理与实验研究

按气固两相流理论,分析了粉煤灰颗粒在气流中的运动规律,按沉降和平移的原理,利用流幕式气力分级系统对沈阳热电厂粗飞灰进行了多次分级实验,得到了分级效果及分级产量随气速变化的初步规律。