Micromechanical characterization of the interphase layer in semi‐crystalline polyethylene. Issue 16 (20th June 2013)

• Record Type: Journal Article
• Authors: Ghazavizadeh, Akbar; Rutledge, Gregory C.; Atai, Ali A.; Ahzi, Saïd; Rémond, Yves; Soltani, Nasser
• Is Part Of: Journal of polymer science. Volume 51:Issue 16(2013:Aug. 15)
• Page Start: 1228
• Page End: 1243
• Publication Date: 2013-06-20
• Subjects: 547
• DOI: 10.1002/polb.23319
• Languages: English
• ISSNs: 0887-6266

Abstract

<abstract abstract-type="main"> <title>ABSTRACT</title> <p>The interphase layer in semi‐crystalline polyethylene is the least known constituent, compared to the amorphous and crystalline phases, in terms of mechanical properties. In this study, the Monte Carlo molecular simulation results for the interlamellar domain (i.e. amorphous+ interphases), reported in (<italic>Macromolecules</italic> 2006, <italic>39</italic>, 439–447) are employed. The amorphous elastic properties are adopted from the literature and then two distinct micromechanical homogenization approaches are utilized to dissociate the interphase stiffness from that of the interlamellar region. The results of the two micromechanical approaches match perfectly. Interestingly, the dissociated interphase stiffness lacks the common feature of positive definiteness, which is attributed to its nature as a transitional domain between two coexisting phases. The sensitivity analyses reveal that this property is insensitive to the non‐orthotropic components of the interlamellar stiffness and the uncertainties existing in the interlamellar and amorphous stiffnesses. Finally, using the dissociated interphase stiffness, its effective Young's modulus is calculated, which compares well with the effective interlamellar Young's modulus for highly crystalline polyethylene, reported in an experimental study. This satisfactory agreement along with the identical results produced by the two micromechanical approaches confirms the validity of the new information about the interphase elastic properties in addition to making the proposed dissociation methodology quite reliable when applied to similar problems. © 2013 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. <bold>2013</bold>, <italic>51</italic>, 1228–1243</p> </abstract>