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Toward anisotropic materials via forced assembly coextrusion.
Tiffani M Burt1, Alex M Jordan, LaShanda T J Korley
1Department of Macromolecular Science and Engineering, and Center for Layered Polymeric Systems, Case Western Reserve University, Cleveland, Ohio 44106-7202, USA.
ACS Applied Materials & Interfaces
|September 21, 2012
Summary
Multilayer coextrusion of block copolymers (BCP) allows tuning mechanical properties. Changing layer thickness and microdomain orientation significantly impacts film toughness and ductility.
Area of Science:
- Materials Science
- Polymer Science
- Nanotechnology
Background:
- Multilayer coextrusion is a versatile method for studying confinement effects on self-assembling nanomaterials.
- Triblock copolymers (BCP) with cylindrical microstructures can be processed using forced assembly techniques.
Purpose of the Study:
- To investigate the influence of microdomain orientation on the mechanical behavior of multilayer BCP films.
- To understand how layer thickness affects mechanical response in different directions.
Main Methods:
- Processing of a triblock copolymer (BCP) with a cylindrical microstructure using multilayer coextrusion and forced assembly.
- Mechanical testing of multilayer films in both extrusion (ED) and transverse (TD) directions.
- Analysis of stress-strain curves to evaluate yielding behavior and extensibility.
Main Results:
- Mechanical response is influenced by cylinder orientation and interface effects, particularly with decreasing layer thickness.
- Stress applied along the cylinder axis results in sharp yielding, while perpendicular stress shows weak yielding.
- Extensibility in the ED increases with reduced layer thickness, but remains constant in the TD.
Conclusions:
- Coextrusion technology enables tunable mechanical toughness in polymers through a continuous process.
- Altering layer thickness allows for control over mechanical properties, ranging from brittle to ductile.
- This platform facilitates the design of composite materials with tailored mechanics by combining polymer properties.

