Identification of flow mechanisms for a soft crystal

We study the behavior under flow of soft spherical micelles forming a fcc phase at high volume fraction. Due to the size (300 ?) of the elementary objects, the structure can be investigated through X-rays and neutron scattering, at rest and under flow in a Couette cell. Using scattering in two perpendicular directions, different mechanisms of flow are identified. At intermediate shear (around 100 s^-1) the system exhibits the so called layer sliding mechanism where two dimensional hexagonal compact planes of spheres align themselves with the Couette cell walls. At lower shear rate, the fcc structure is locally preserved, and the flow is mediated by defects between crystallites. At high shear rate, we observe the melting of the structure and a liquid-like structure factor. Moreover, we were able to use the existence of the layer sliding regime to generate a fcc monocrystal by annealing the satcking faults between the decorrelated planes created by the layer sliding. Received: 7 July 1997 / Received in final form: 16 January 1998 / Accepted: 5 March 1998     

Bending of charged flexible membranes due to the presence of macroions

We investigate the bending of flexible charged membranes due to the presence of rigid rodlike macroions in the framework of the Debye-Hückel approximation. When the macroions are fixed in space at some distance from the bilayer the membrane bends towards them; we calculate the exact deformation profile. On the other hand a macroion which is adsorbed on the membrane causes a deflection of the bilayer. Finally, we consider swollen lamellar polyanion/charged-lipid complexes where the macroions are intercalated between charged lipid bilayers. We predict the occurrence of a double adsorption (pinching effect) of the macroion for sufficiently flexible membranes. Received: 9 February 1998 / Revised: 9 June 1998 / Accepted: 2 July 1998     

大麦花药培养及其胚性悬浮细胞系的高频快速建立

研究了（1）在低温预处理过程中，不同相对湿度对大麦花药出愈率的影响；（2）低温处理愈伤组织对植株分化的影响；（3）高频快速建立大麦胚性悬浮细胞系，结果表明，低温预处理的较大相对湿度能明显促进花药的出愈率，低温处理愈伤组织能提高绿苗率，以7周龄的花药胚性愈伤组织为起始材料高频快速建立了均质，分散性好的胚性悬浮细胞系，建立频率约为25%～50%，已8～9周龄的花药胚性愈伤组织作为起始材料，难以建立胚性悬浮细胞系。     

Corner flow of a suspension of rigid rods

Stress singularities in the neighbourhood of sharp corners can be a source of severe problems in the numerical simulation of non-Newtonian flows leading to loss of convergence with grid refinement (G.G. Lipscombe, R. Kennings and M.M. Denn, J. Non-Newtonian Fluid Mech., 24 (1987) 85 [1]). For Newtonian flows the nature of this singularity is given by the analysis of Dean and Montagnon (W.R. Dean and P.E. Montagnon, Phil. Trans. R. Soc. London, Ser. A., 308 (1949) 199 [2]) in terms of similarity solutions. In this paper we extend this similarity analysis to a suspension of rigid rods. In the limit of nearly full extension the FENE constitutive model has the same behaviour as such a suspension. Our analysis predicts the possibility of lip vortices but their behaviour is somewhat inconsistent with those observed experimentally.     

DC conductivity of a suspension of insulating particles with internal rotation

We analyse the consequences of Quincke rotation on the conductivity of a suspension. Quincke rotation refers to the spontaneous rotation of insulating particles dispersed in a slightly conducting liquid and subject to a high DC electric field: above a critical field, each particle rotates continuously around itself with an axis pointing in any direction perpendicular to the DC field. When the suspension is subject to an electric field lower than the threshold one, the presence of insulating particles in the host liquid decreases the bulk conductivity since the particles form obstacles to ion migration. But for electric fields higher than the critical one, the particles rotate and facilitate ion migration: the effective conductivity of the suspension is increased. We provide a theoretical analysis of the impact of Quincke rotation on the apparent conductivity of a suspension and we present experimental results obtained with a suspension of PMMA particles dispersed in weakly conducting liquids.     

ELECTROSTATICALLY SUPPORTED MIXING OF FINE GRAINED PARTICLES

The processing of fine-grained particles with diameters between 1 and 10 microns is difficult due to strong van-der-Waals attraction forces. In order to improve the handling properties, the fine-grained particles, i.e. host-particles,are coated with various nanoparticles, i.e. guest-particles. The mixing of fine-grained powders is influenced by particle-particle interactions. If these forces are distinctively used, both interactive and ordered mixtures can be produced.These particle mixtures consist of composite-particles that have new physical properties. These modified properties d epend strongly on the coating process, the diameter- and mass-relationship of the guest- and the host-particles. The properties of the composite-particles can systematically be adjusted to the requirements of industrial applications. For example, a laboratory bubbling fluidized bed can be used to describe the conveying behavior of the functionalized host-particles. Applications for the functionalized particles are in the pharmaceutical and the powder coating industries,e.g. enhanced dry powder inhalers and thin lacquer films. The present research compares three different mixing/coating processes. The composite-particles are characterized by TEM, SEM and with their fluidization characteristics. The coating process itself is monitored by the electrostatic charge of the particles.     

A chiral axial next nearest neighbour xy-model for antiferroelectric liquid crystals

We describe a chiral axial next nearest neighbour xy-model to account for the various subphases exhibited by antiferroelectric liquid crystals made of chiral rod-like molecules. The assumed form of the interlayer interactions is based on physical processes which are discussed. Using a discrete model, the predicted sequence of transitions is SmA-SmC-SmC-FI_H-FI_I-FI_L-SmC ^* A, where FI stands for a ferriphase, as seen in many compounds. The ferri and SmC phases are characterized by relatively large angles between the c-vectors of successive layers and occur only when the compounds have high optical purity. The calculated field induced structures exhibit a plateau of the apparent tilt angle at , where is the tilt angle of the molecules in the ferriphase. The conoscopic figures in the presence of a field and ellipsometric parameters in the absence of a field have also been generated, which agree extremely well with the experimental results. Recent anomalous X-ray scattering studies prove the xy-character of the configurations, though the commensurate structures that are found in the ferriphase require an extension of the model to include lock-in terms. Received 23 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     

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