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Published on: March 1, 2016
Towards nanoporous membranes based on ABC triblock terpolymers.
Alexandra Sperschneider1, Felix Schacher, Marcel Gawenda
1Physikalische Chemie II, Universität Bayreuth, 95440 Bayreuth, Germany.
Small (Weinheim an Der Bergstrasse, Germany)
|April 24, 2007
Summary
Researchers studied nanostructures in polybutadiene-block-poly(2-vinyl pyridine)-block-poly(tert-butyl methacrylate) (BVT) and polystyrene-block-poly(2-vinyl pyridine)-block-poly(tert-butyl methacrylate) (SVT) thin films. Different terpolymer compositions led to distinct nanostructures, with BVT films showing potential for composite membranes.
Area of Science:
- Polymer Science
- Materials Science
- Nanotechnology
Background:
- Block copolymers self-assemble into ordered nanostructures.
- These nanostructures in thin films have applications in lithography and membranes.
- Structurally analogous triblock terpolymers offer tunable properties.
Purpose of the Study:
- To investigate the nanostructures formed in thin films of BVT and SVT terpolymers.
- To compare the morphological behavior of BVT and SVT films.
- To explore the potential of BVT films for composite membrane fabrication.
Main Methods:
- Synthesis of BVT and SVT triblock terpolymers via sequential living anionic polymerization.
- Preparation of thin films from the synthesized terpolymers.
- Morphological characterization using scanning force microscopy and electron microscopy.
- Annealing of the polymer films to induce self-assembly.
Main Results:
- SVT films formed an ordered perforated lamella phase.
- BVT films exhibited hexagonally packed core/shell cylinders.
- The distinct nanostructures are attributed to differences in terpolymer composition.
- BVT films demonstrated potential for creating composite membranes on porous supports.
Conclusions:
- Terpolymer composition critically influences the self-assembled nanostructure in thin films.
- BVT terpolymers are promising for developing advanced composite membranes.
- The study provides insights into structure-property relationships in block copolymers.
