Lyotropic behavior of polyelectrolyte complex micelles
ORAL
Abstract
Upon pH stimulus, double hydrophilic block copolymers form polyion complexes (PIC) in the micellar form. We used PIC micelles as ecofriendly templates for the synthesis of ordered mesoporous materials. The porosity of the final material is revealed by simple inversion of the pH stimulus. Various mesoporous silica materials have been obtained from cubic to lamellar.
The control over the structure of the final material is expected to relate to the lyotropic behavior just as observed when micelles of amphiphilic molecules are used as template. However such lyotropic behavior has never been reported for PIC micelles. Moreover the same PIC leads to different structured silica materials depending on the physico-chemical conditions.
Using X-rays and light scattering, optical microscopy and osmometry, we establish the equation of state of a PEO-b-PAA/oligoamine electrostatic complex. Its lyotropic behavior is characterized by a transition of shape at 0.16 w/w and a transition to a lamellar phase at 0.30w/w. The water content of the core of the micelles is addressed from the complete phase diagram of the polyelectrolyte complex in its coacervate form and explains why a single complex leads to porous material of different structure.
The control over the structure of the final material is expected to relate to the lyotropic behavior just as observed when micelles of amphiphilic molecules are used as template. However such lyotropic behavior has never been reported for PIC micelles. Moreover the same PIC leads to different structured silica materials depending on the physico-chemical conditions.
Using X-rays and light scattering, optical microscopy and osmometry, we establish the equation of state of a PEO-b-PAA/oligoamine electrostatic complex. Its lyotropic behavior is characterized by a transition of shape at 0.16 w/w and a transition to a lamellar phase at 0.30w/w. The water content of the core of the micelles is addressed from the complete phase diagram of the polyelectrolyte complex in its coacervate form and explains why a single complex leads to porous material of different structure.
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Presenters
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Martin In
Laboratoire Charles Coulomb, Univ Montpellier CNRS
Authors
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Martin In
Laboratoire Charles Coulomb, Univ Montpellier CNRS
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Melody Mathonat
Univ Montpellier ENSCM CNRS
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Anthony Phimphachanh
Univ Montpellier ENSCM CNRS
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Philippe Dieudonné
Univ Montpellier CNRS
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Patrick Lacroix-Desmazes
ENSCM CNRS
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Nathalie Marcotte
ENSCM CNRS
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Corine Gérardin
ENSCM CNRS