APS March Meeting 2011
Volume 56, Number 1
Monday–Friday, March 21–25, 2011;
Dallas, Texas
Session J44: Focus Session: Kinetic Control of Solution Assemblies
11:15 AM–2:15 PM,
Tuesday, March 22, 2011
Room: A309
Sponsoring
Units:
DPOLY DFD
Chair: Margarita Herrera-Alonso, Johns Hopkins University
Abstract ID: BAPS.2011.MAR.J44.7
Abstract: J44.00007 : Multicompartment and multigeometry nanostructures with block copolymers and kinetic control
12:51 PM–1:27 PM
Preview Abstract
Abstract
Author:
Darrin Pochan
(University of Delaware)
The combination of charged block copolymer architecture with the
kinetic control of solvent processing offers great flexibility for the
creation of new assembled morphologies in solution and outstanding ability
to control and manipulate those morphologies. When charged, acidic blocks
are present, assembled structures are tunable in a well-defined way via
co-assembly of organic bases with adjustable chain structure and control of
the solution assembly pathway. A rich variety of polymeric micelles have
been made such as toroids, disks, and helical cylinders from poly(acrylic
acid)-\textit{block}-poly(methyl acrylate)-\textit{block}-polystyrene (PAA-$b$-PMA-$b$-PS) triblock copolymers
in THF/water mixtures with multiamines to complex with the PAA. Both the
type and amount of multiamine were found to be critical for formation of
specific micelles.
Kinetic pathways and temporal stabilities of different micelles and
nanoscale aggregates have also been studied. Due to low chain exchange
dynamics between block copolymeric micelles in solution, global
thermodynamic equilibrium is extremely difficult, if not impossible, to
achieve. In our block copolymer/THF/water/multiamine quaternary systems,
thermodynamics and kinetics of morphological evolution are governed by three
important factors, including chain length of hydrophobic blocks, ratio of
THF to water, and the interaction of multiamine with hydrophilic PAA block
in the corona. Slow kinetics associated with these factors in solution
greatly hinders the system from reaching a global equilibrium. However, by
taking advantage of slow kinetics behavior of polymeric micelles in
solution, one can purposely produce multicompartment micelles and
mulitgeometry micelles by now mixing different PAA-containing block
copolymers together but forcing them to ultimately reside in the same
nanoscale structure through kinetic processing. While kinetically trapped in
common nanostructures, local phase separation can occur producing
compartments. This compartmentalization can be used within common micelle
geometries to make complex spheres and cylinders or can be used to make new
nanostructures such as multigeometry aggregates (e.g. hybrid cylinder-sphere
aggregates). All is possible through the kinetic control of the assembly
process.
To cite this abstract, use the following reference: http://meetings.aps.org/link/BAPS.2011.MAR.J44.7