Polyelectrolyte multilayers pem obtained by layer by layer assembly can be doped with ionic liquid il via the swelling of the films with il solutions.
Dynamic viscoelasticity in polyelectrolyte multilayers nanodamping chem mat.
We report on the time dependent viscoelastic response of nanoblended films of a polyelectrolyte complex prepared by the multilayering method.
We use rheology to systematically study the viscoelastic properties as a function of salt concentration chain length.
Such coatings or films are denoted henceforth as polyelectrolyte multilayers pems.
A 370 2004 pp.
Nanodamping article in chemistry of materials 18 24 november 2006 with 13 reads how we measure reads.
Experimental and mathematical modeling investigation on the dynamic viscoelasticity behavior of free liquid films prepared by alpha olefin sulfonate.
This unprecedented ability to fine tune a multilayer to be either cell adhesive or bioinert along with the unique feature of controllable porosity allows polyelectrolyte multilayers to be envisioned for membranes controlled release and biocompatible implant coating applications.
Schlenoffdynamic viscoelasticity in polyelectrolyte multilayers.
Two flexible oppositely charged polymers can form liquid like complex coacervate phases with rich but poorly understood viscoelastic properties.
The ion pairing interactions within polyelectrolyte multilayers pemus are reversibly broken by adding salt to the electrolyte in which the pemu is immersed.
L ayer by layer lbl assembly of polyelectrolytes pes is a method for preparing highly tunable thin film polymer coatings.
The specific ion effect on the growth of polyelectrolyte multilayers can be observed in.
2 4 6 the chemical composition and concentration of.
Mater 18 2006 pp.
Dynamic viscoelasticity in polyelectrolyte multilayers.
The sequential layer by layer adsorption of polycations and polyanions was shown to be an extremely versatile and facile technique for the preparation of polyelectrolyte multilayers pem on a variety of substrates since their discovery in 1991 by decher and co workers they have received considerable attention such systems have an obvious practical value but they are.
1 3 pems self assemble due to electrostatic interactions between sequentially deposited alternately charged pes.
Thus the bulk modulus of these ultrathin films may be regulated without changing temperature.
They serve as an experimental model system for many biological and man made materials made from oppositely charged macromolecules.
Mat sci eng c bio s.