The effect of comonomer concentration and distribution on the photo-oxidative degradation of linear low density polyethylene films

Publication date: 16 June 2017
Source:Polymer, Volume 119
Author(s): Yu-Chieh Hsu, Rowan W. Truss, Bronwyn Laycock, Michael P. Weir, Timothy M. Nicholson, Christopher J. Garvey, Peter J. Halley
The photo-oxidative degradation of two complementary linear low density polyethylene (LLDPE) films has been studied: a Ziegler-Natta catalysed 1-octene copolymer (ZN-LLDPE) and a 1-octene copolymer produced by a single site constrained catalyst (m-LLDPE). The degradation processes were followed using a range of characterisation techniques including tensile testing, GPC, MAS-NMR, FTIR, WAXS and SAXS. The chemical species formed on degradation were similar for both polymers. Both also showed an increase in crystallinity and modulus with UV ageing time and a decrease in the long spacing of the lamella. However, the m-LLDPE showed a significantly shorter time to embrittlement than the ZN-LLDPE, which correlated in both polymers with the disappearance of the second yield point. The major observed difference in crystalline structure was a significantly higher interfacial thickness between the crystalline lamellae and the amorphous regions for the ZN-LLDPE, which decreased rapidly on UV ageing. This difference in behaviour was attributed to the nature of the branching in the ZN-LLDPE, which was presumed to sit in blocks along the chain and thus to reside in the interfacial regions. Cleavage of the tertiary carbons in these interfacial regions was less damaging to the mechanical properties than for the m-LLDPE, where chain scission broke more of the tie molecules, thus limiting the ability of the polymer to draw. . This work advances our understanding of polymer microstructural evolution during degradation and the implications of initial polymerisation route and molecular structure on the degradation mechanisms.

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