Apparent slip at a polymer-polymer interface

We consider a planar interface between strongly-segregated homopolymers subjected to steady shear in the plane of the interface. We develop a constitutive equation for stress relaxation in an inhomogeneous system for chains obeying Rouse dynamics. Using this equation, the interfacial viscosity for a symmetric blend is found to be in agreement with a scaling prediction due to de Gennes, where is the bead friction coefficient, b is the segment length, is the segment volume and is the Flory-Huggins interaction parameter driving the phase separation. We generalize our results to asymmetric blends and describe a phenomenological extension to entangled melts. Received: 18 August 1997 / Received in final form: 1 December 1997 / Accepted: 2 December 1997     

Spiky phases of smooth membranes. Implications for smooth strings

We point out a possible mechanism by which smooth surfaces can become spiky as the constant of curvature stiffness falls below a certain critical value. This happens either in a single first-order transition, or in a sequence of two Kosterlitz-Thouless-like transitions. There may also be additional phases in which the spikes form a hexagonal solid-like array or a disordered liquid-like structure. Our discussion suggests that there exist smooth strings between quarks. Received 2 September 1998     

Shear viscosity of polymer and surfactant monolayers

The surface shear viscosity of monolayers formed at the surface of water by adsorbed polyethyl- eneoxyde and by stearic acid is measured as a function of the surface pressure of the monolayer using a new surface viscometer. The principle of the viscometer is the measurement of the drag force on a circular disk undergoing a uniform translation at the water surface: a hydrodynamic model based on the lubrication approximation allows a calculation of the surface viscosities from the absolute measurement of the drag forces. Received: 26 August 1999     

Ascending air bubbles in protein solutions

We report measurements of the ascending velocity of air bubbles in protein (bovine serum albumin) solutions. We show that, because of the protein molecules adsorbed on their surface, the terminal ascending velocity of bubbles is strongly reduced compared to the terminal velocity in pure water: protein- covered bubbles behave hydrodynamically as solid spheres. From the evolution of the ascending velocity with time, we can derive the amount of protein needed to immobilize the bubble interface which is 0.5 mg m^-2, i.e. only one fifth of the amount adsorbed at equilibrium in the range of used bulk concentrations. Received: 6 March 1998 / Revised and accepted: 6 May 1998     

Stability of thin polymer films on a corrugated substrate

We study the wetting behaviour of thin polystyrene (PS) films on regularly corrugated silicon substrates. Below a critical film thickness the PS films are unstable and dewet the substrates. The dewetting process leads to the formation of nanoscopic PS channels filling the grooves of the corrugated substrates. Films thicker than the critical thickness appear stable and follow the underlying corrugation pattern. The critical thickness is found to scale with the radius of gyration of the unperturbed polymer chains. Received 6 April 2000 and Received in final form 24 August 2000     

Effects of finite thickness on interfacial widths in confined thin films of coexisting phases

The capillary broadening of a 2-phase interface is investigated both experimentally and theoretically. When a binary mixture in a thin film with thickness D segregates into two coexisting phases the interface between the two phases may form parallel to the substrate due to preferential surface attraction of one of the components. We show that the interfacial profile (of intrinsic width w₀) is broadened due to capillary waves, which lead to fluctuations, of correlation length of the local interface positions in the directions parallel to the confining walls. We postulate that acts as an upper cutoff for the spectrum of capillary waves on the interface, so that the effective mean square interfacial width w varies as . In the limit of large D this yields or respectively for the case of short- or long-range forces between walls and the interface. We used the Nuclear Reaction Analysis depth profiling technique, to investigate this broadening effect directly in two binary polymer mixtures. Our results reveal that the interfacial width indeed increases with film thickness D, though the observed interfacial width is lower than the predicted w. This is probably due to surface tension effects imposed by the confining surfaces which are not taken into account in our model. Received: 19 February 1998 / Received in final form: 2 September 1998 / Accepted: 8 September 1998     

Polymer thin films and surfaces: Possible effects of capillary waves

It is discussed how the proximity of a free surface or mobile interface may affect the strain relaxation behavior in a viscoelastic material, such as a polymer melt. The eigenmodes of a viscoelastic film are thus derived, and applied in an attempt to explain the experimentally observed substantial shift of the glass transition temperature of sufficiently thin polymer films with respect to the bulk. Based on the idea that the polymer freezes due to memory effects in the material, and exploiting results from mode-coupling theory, the experimental findings of several independent groups can be accounted for quantitatively, with the elastic modulus at the glass transition temperature as the only fitting parameter. The model is finally applied discussing the possibility of polymer surface melting. A surface molten layer is predicted to exist, with a thickness diverging as the inverse of the reduced temperature. A simple model of thin polymer film freezing emerges which accounts for all features observed experimentally so far. Received 8 August 2001     

Gels at interfaces

We discuss the adsorption of polymer gels on flat surfaces. Even in cases of complete wetting where the spreading power S is positive and where an equivalent liquid would spread, the elastic stresses due to the gel deformation upon adsorption oppose the spreading. The competition between elasticity characterized by the bulk shear modulus G and capillarity characterized by the spreading power S defines a typical length scale ℓ = S/G for the deformation in the gel. For loose gels ℓ can be of the order of 1 μm. Macroscopic gels larger than ℓ deform only at their edges over a region of size ℓ. Microscopic gels smaller than ℓ show a finite deformation despite the elastic stresses. The elastic stresses limit the spreading of the polymer, but solvent can be sucked out of a swollen gel by wetting the surface. The thin solvent film can extend rather far from the gel edge and carry solvent. We calculate the kinetics of the solvent film formation and of the solvent transfer from a more swollen gel to a less swollen gel. Received 16 July 2001     

Non-equilibrium wetting transition in a magnetic Eden model

Magnetic Eden clusters (Ausloos et al., Europhys. Lett. 24, 629 (1993)) with ferromagnetic interaction between nearest-neighbor spins are grown in a confined 2d-geometry with short range magnetic fields acting on the surfaces. The change of the growing interface curvature driven by the field and the temperature is identified as a non-equilibrium wetting transition and the corresponding phase diagram is evaluated. Received 27 March 2000     

Limiting phenomena for the spreading of water on polymer films by electrowetting

This paper is about fundamental limitations in electrowetting, used as a tool for spreading water solutions on hydrophobic surfaces, like the surface of a polymer film. Up to which point can an electric voltage decrease the contact angle? The first limitation comes when using pure water, above a threshold voltage, little droplets are emitted at the perimeter of the mother drop. We present an analysis of the drop contour line stability, involving competition between electrostatic and capillary forces, which is compatible with observations. The use of salted water solutions suppresses this instability, then one faces a second limitation: the evolution of the contact angle saturates before complete wetting. We show that this saturation is caused by ionisation of the air in the vicinity of the drop edge. We analyse the luminescence induced by gas ionization and measure the related electrical discharges. We explain how air ionization suppresses the driving force for electrowetting and how it induces the formation of an hydrophillic ring around the drop.     

Super lattice formation of an array of volatile wetting droplets

For an ordered array of critical volatile wetting droplets the formation of a super lattice by an Ostwald-ripening-like competition process is considered. The underlying diffusion problem is treated within a quasistatic approximation and to first order in the inverse droplets distance. The approach is rather general but a square lattice and a triangular lattice are studied explicitly. Dispersion relations for the super lattice growth of these arrays are calculated. Received 29 November 1999 and Received in final form 15 February 2000     

Humidity effects on the stability of a sandpile

Humidity is well-known to significantly affect the mechanical properties, static as well as dynamic, of granular materials. We present the method of humidification of granular media from an under-saturated vapor that we designed in order to experimentally quantify such moisture-induced effects under accurately-controlled humidity conditions. We report the quantitative measurements of the maximum angle of stability of a pile made of small glass beads, as a function of the relative vapor pressure, up to close to saturation. The results obtained with liquids differing in their wetting properties on glass, namely water and heptane, are presented. It is shown that the wetting properties of the liquid on the grains have a strong influence on the cohesion of the non-saturated granular medium. Received 26 October 1998 and Received in final form 30 March 1999     

Wetting of phospholipid membranes on hydrophilic surfaces - Concepts towards self-healing membranes

We report on the wetting behavior of phospholipid membranes on solid surfaces immersed in aqueous solution. Using fluorescence microscopy, the spreading velocity of fluid bilayers advancing from a lipid source is investigated. The kinetic spreading coefficient was measured as a function of temperature for pure DMPC membranes and as a function of charge density and cholesterol content for binary membranes. A theoretical model for the membrane flow is presented, which takes into account the liquid crystalline bilayer architecture of the lipid membrane. The spreading power results from the membrane-solid VdW interaction and is dissipated in hydrodynamic shear flow as well as by inter-monolayer friction within the bilayer. The frictional drag causes a dynamic tension gradient in the spreading membrane, which is manifested by a single exponential decay of the fluorescence intensity profile along the spreading direction. Obstacles are shown to act as pinning centers deforming the advancing line interface. However, no depinning was observed, since the centers are circumflown without abrupt relaxation. Received 6 November 1998     

Azimuthal anchoring of liquid crystals at the surface of photo-induced anisotropic films

Received: 13 November 1996/Accepted: 22 January 1997     

Tetragonal structure of thin nickel films on Cu(001)

The crystallographic structure of thin Ni films deposited on Cu(001) has been studied using Surface Extended X-ray Absorption Fine Structure (SEXAFS). Taking advantage of the linear polarization of the synchrotron radiation, we have shown that Ni adopts the Cu lattice parameter parallel to the interface. This lateral expansion induces a longitudinal compression of the unit cell, leading to a face centered tetragonal structure of the Ni films from 3 to 10 monolayers. The temperature dependence of the EXAFS oscillations has allowed to measure strain inside the Ni layers. Received 22 December 1998     

Elastic interaction between defects in thin and 2D films

Elastic interactions between defects is investigated at the surface of thin layers, a question on which we have given a brief account [P. Peyla et al. Phys. Rev. Lett. 82, 787 (1999)]. Two isotropic defects do not interact in an unlimited medium, regardless of the spatial dimension, a result which can be shown on the basis of the Gauss theorem in electrostatics. Within isotropic elasticity theory, defects interact only (i) if they are, for example, at a surface (or at least if they feel a boundary), or if their action on the material is anisotropic (e.g. they create a non central force distribution, though the material elasticity is isotropic). It is known that two identical isotropic defects on the surface of a semi-infinite material repel each other. The repulsion law behaves as 1/r ³(r = defects separation). We first revisit the Lau-Kohn theory and extend it to anisotropic defects. Anisotropy is found to lead to attraction. We show that in thin films defects may either attract or repel each other depending on the local geometric force distribution caused by the defect. It is shown that the force distribution (or more precisely the forces configuration symmetry) fixes the exponent in the power law 1/r ⁿ (e.g. for a four-fold symmetry n = 4). We discuss the implication of this behaviour in various situations. We treat the interactions in terms of the symmetries associated with the defect. We argue that if the defects are isotropic, then their effective interaction in an unlimited 2D (or a thin film) medium arises from the induced interaction, which behaves as 1/r ⁴ for any defect symmetry. We shall also comment on the contribution to the interaction which arises from flexion of thin films. Received 7 October 2002 Published online 4 June 2003 RID="a" ID="a"e-mail: chaouqi.misbah@ujf-grenoble.fr