The effect of changing the solvent surface concentration on the initial rate of solvent removal from solvent-coated polymer films is investigated. An analytical perturbation solution is developed for the nonlinear problem, and predictions are made for different surface concentrations and different d
Influence of solvent and molecular weight on thickness and surface topography of spin-coated polymer films
β Scribed by Lora L. Spangler; John M. Torkelson; J. Scot Royal
- Book ID
- 104522717
- Publisher
- Society for Plastic Engineers
- Year
- 1990
- Tongue
- English
- Weight
- 924 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0032-3888
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β¦ Synopsis
Abstract
The influence of polymer molecular weight, molecular weight distribution, and polymerβsolvent interactions on the thickness and topography of spinβcoated polymer films was examined. For films prepared from dilute solutions, highly volatile solvents or fair or βpoorβ solvents for the polymer adversely affect film surfaces causing nonuniformities (waves) to appear. However, if the concentration of these solutions is increased to approximately the concentration at which entanglements are formed, nearly uniform films are produced even if the solvent employed is highly volatile, such as dichloromethane. When toluene is employed as the solvent, which has a relatively low volatility and therefore forms nearly flat film surfaces, films prepared from dilute solution were found to have thicknesses, h, proportional to Ξ· Ξ©^β0.49^ for polystyrene and Ξ· Ξ©^β0.49^ for poly(methylmethacrylate) where Ξ·~o~ is the zeroβshear rate solution viscosity and Ξ© is the rotational speed at which the films were prepared. These results suggest that the exponents associated with Ξ·~o~ and Ξ© may be nearly independent of the type of polymer used as long as flat films are produced. Finally, the molecular weight parameter most important in controlling final film thickness for films made from dilute solutions is M~v~, the viscosityβaverage molecular weight.
π SIMILAR VOLUMES
## Abstract Experimental observations (ellipsometry, scanning force microscopy, and nuclear magnetic recsonance (NMR)) of the freezing behavior of thin supported films as well as the free surface of atactic polystyrene are reported, taken at a particularly small molecular weight of 2 kg/mol. Remark