On the dissolution behaviour of extended chain polyethylene fibres

J. C. M. Torfs*, G. O. R. Alberda van Ekenstein, A. J. Pennings

*Corresponding author for this work

    Research output: Contribution to journalArticleAcademicpeer-review

    7 Citations (Scopus)

    Abstract

    The influence of stress on the dissolution behaviour of extended-chain high molecular weight polyethylene fibres in p-xylene was investigated. Freely suspended in the solvent, the fibres dissolved at 119.5°, a temperature close to the equilibrium solubility temperature of 118.6° for perfect polyethylene crystals. However, when a stress of 0.4 GPa was exerted by straining the fibre 0.7%, it could withstand a temperature as high as 130° for at least three days. At still higher temperatures the induced stress relaxed completely, and dissolution immediately followed. These phenomena indicate that the fibre has a network structure. The cross-links are of a physical nature. Molecules are connected by topological defects such as entanglements, intertwinings and twist disclinations. These defects are trapped in crystallites; therefore the theory of Gee and Flory is applicable predicting that in such a system dissolution temperature of extended chain crystallites increases with stress. The required stress is transduced by tie molecules bridging the amorphous regions between crystallites. A study of dissolution under stress seems to be a direct method for the detection of topological defects such as entanglements.
    Original languageEnglish
    Pages (from-to)157-161
    Number of pages5
    JournalEuropean Polymer Journal
    Volume17
    Issue number2
    DOIs
    Publication statusPublished - 1981

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