4.7 Article

Relaxation of Thin Films of Polystyrene Floating on Ionic Liquid Surface

Journal

MACROMOLECULES
Volume 42, Issue 22, Pages 9111-9117

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ma901789k

Keywords

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Funding

  1. US Department of Energy Office of Basic Energy Service
  2. NSF [DMR-0213695l]
  3. Division Of Materials Research
  4. Direct For Mathematical & Physical Scien [820506] Funding Source: National Science Foundation

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We have investigated the dynamics of polymer films, free of physical constraints, floating on the surface of an ionic liquid (IL) to minimize substrate-polymer interactions and constraints arising from the adhesion of the polymer to the substrate. ILs, which have a negligible vapor pressure, were used to support polystyrene (PS) thin films to investigate the relaxation behavior and glass transition temperature (T-g) of thin polymer films. Freely floating films relaxed when heated to the temperatures above the bulk T-g resulting in a thickening of the film and a concomitant shrinkage in the lateral dimensions of the film. The relaxation behavior depended oil the temperature, film thickness, and molecular weight of the polymer. Completely relaxed films showed T-g values similar to that in the bulk, independent of the initial thicknesses, molecular weight, and cooling rate.

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