ABSTRACT
We studied the influence of post-treatment rinsing after the formation of self-assembled polyelectrolyte films made with the weak base poly(allylamine hydrochloride) (PAH) and the strong acid poly(styrene sulfonate) (PSS). The stability of the film was studied using optical fixed-angle laser reflectometry to measure the release of polymeric material and AFM experiments to reveal the change of morphology and thickness. We found that the polymer films were stable upon rinsing when the pH was the same in the solution as that used in the buildup (pH 9). The films released most of the polymeric material when rinsed at higher pH values, but a layer remained that corresponded to a PAH monolayer directly bound with the silica surface. Films containing at least four bilayers were stable upon rinsing at lower pH values, but the stability of thinner films depended on the type of the last polymer deposited. They were stable in the case of PSS as an outermost deposit, but they released a large part of their material in the case of PAH. The stability results were determined using a simple model of the step-by-step assembly of the polymer film described formerly.
Subject(s)
Allylamine/chemistry , Polymers/chemistry , Scattering, Radiation , Hydrogen-Ion Concentration , Lasers , PolystyrenesABSTRACT
We report a simple method for generating microaxicons at the extremity of commercial optical fibers. The proposed solution, based on a polishing technique, can readily produce any desired microaxicon cone angle and is independent of the nature of the fiber. An optical study of microaxicon performance, in terms of confinement ability and length of the generated Bessel-like beams, is presented as a function of the microaxicon angle. This study, made possible by the experimental acquisition of the 3D light distribution of the Bessel-like beams, reveals the relationship between the Bessel-like beam confinement zone and the beam length. Finally, the effect of diffraction of the Bessel-like beams, induced by the limited lateral extent of the incident fiber mode, is studied and discussed.
ABSTRACT
We present experimental and theoretical results on the electrorheological response and microstructure of colloidal suspensions composed of silica nanoparticles dispersed in a silicon oil, as a function of electric field strength and silica water content. Using small-angle neutrons scattering experiments, we determined the evolution of the static structure factor of the suspensions when an electric field is applied. Experimental data were fitted with model calculations using the Percus-Yevick solution for Baxter's hard-sphere adhesive potential. The obtained stickiness parameter is directly related to the polarization interactions that depend on the water content of silica particles. The influence of the polarization interparticle potential on the rheology of the silica dispersions was investigated in a second time. A microscopic theory for the shear viscosity of adhesive hard-sphere suspensions was successfully used which describes the steady shear viscosity of suspension in terms of the fractal concept.