Low-density polyethylene films strained up to 35% exhibit an initial increase of diffusivity and permeability which soon reach a maximum and subsequently drop to steadily decreasing values below those of the unstrained starting material. The sorption steadily increases and seems to approach a platea
A critical investigation of polyethylene gas permeability
β Scribed by Alter, Harvey
- Publisher
- John Wiley and Sons
- Year
- 1962
- Weight
- 501 KB
- Volume
- 57
- Category
- Article
- ISSN
- 0022-3832
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β¦ Synopsis
Abstract
The effect of polymer density on the gas permeability of polyethylene film has been studied. The experimental data for permeability P are described by the equation P = K(1 β d)^n^, where K is a constant characteristic of each gas and d is the sample density. This equation is similar to previous analytical descriptions of the permeabilityβdensity relation. Values of K and n (n β 2) and confidence limits for P are given for N~2~, O~2~, and CO~2~. Permeabilityβdensity values are reported for approximately 100 film samples for each of the three gases over a density range from 0.899 to 0.975 g./cc. The density was measured for each sample inserted in the permeability apparatus. The above mathematical model chosen to describe the experimental data is interpreted to mean that the effect of the crystalline phase is to decrease both the gas solubility and diffusion. Gas solubility and diffusion are linear functions of the volume fraction of amorphous material. Permeability, the product of diffusion and solubility, is consequently proportional to the square of the volume fraction of amorphous material. Permeability is related to density rather than volume fraction of amorphous material to avoid choosing a single value for the density of the amorphous fraction. The experimental results suggest additional lowering of the permeability due to restraints on the segmental motion of the amorphous chains.
π SIMILAR VOLUMES
Ionic polyurethane ( PU ) membranes of hydroxyl-terminated polybutadiene ( HTPB ) and 4,4 -dicyclohexylmethane diisocyanate ( H 12 MDI ) were polymerized by a two-stage method. The ionic group was introduced by adding N-methyldiethanolamine ( MDEA ) as the chain extender of which the tertiary amines