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Biomedical subjects

P Richetti

Publications and source records attributed to P Richetti.

8 recordsLinked to original sources

Surfactant boundary lubricant film modified by an amphiphilic diblock copolymer.

The effect of the uptake of a low-molecular-weight amphiphilic diblock copolymer on the morphology of didodecyldimethylammonium bromide (DDAB) adsorbed layers on mica, the interactions between two coated surfaces, and the frictional properties of the boundary film have been studied using an atomic force microscope and a dynamic surface forces apparatus nanotribometer. When DDAB-coated surfaces in aqueous solution were compressed, hemifusion or removal of the adsorbed surfactant bilayers could not be induced, and no frictional force could be measured between the surfaces, which display superior lateral cohesion and lubricant properties. Coadsorbing octadecyl end modified poly(ethylene oxide) chains at low density facilitates hemifusion, generating significant shear stress and leading to stick-slip instabilities. The mixed films regain their lateral cohesion at higher adsorbed copolymer densities, but an extra short-range attraction brings the adsorbed layers into adhesive contact without causing bilayer hemifusion. Here, noticeable frictional forces are also measured.

Journal Article↗

Behavior of adhesive boundary lubricated surfaces under shear: effect of grafted diblock copolymers.

The shear behavior and the normal interaction between mica surfaces covered by surfactant or surfactant-polymer mixtures were studied with a Surface Forces Apparatus (SFA) nanotribometer. If the surfaces are compressed while fully immersed in an aqueous surfactant solution that adsorbs in the form of flat bilayers, hemifusion can be induced. When the hemifused surfaces are subject to shear, at least five different dynamic regimes can be recognized. The general behavior may be described by a model based on the kinetics of formation and rupture of adhesive bonds between the shearing surfaces, with an additional viscous term. Once the adsorbed surfactant layer is decorated with physigrafted copolymers, the number of sliding regimes may be reduced to only one, in which the shear stress increases sublinearly with the driving velocity. The adhesion energy and the resistance to hemifusion of the adsorbed surfactant-polymer layers are also strongly modified as the grafting density increases.

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Friction between two weakly adhering boundary lubricated surfaces in water.

The sliding of adhesive surfactant-bearing surfaces was studied with a surface forces apparatus nanotribometer. When the surfaces are fully immersed in an aqueous solution, the dynamic behavior is drastically different and more varied than under dry conditions. In solution, the shear stress exhibits at least five different velocity regimes. In particular, the sliding may proceed by an "inverted" stick-slip over a large range of driving velocities, this regime being bounded by smooth (kinetic) sliding at both lower and higher driving velocities. The general behavior of the system was studied in detail, i.e., over a large range of experimental conditions, and theoretically accounted for in terms of a general model based on the kinetics of formation and rupture of adhesive links (bonds) between the two shearing surfaces with an additional viscous term.

Journal Article↗