Abstract
Conformational changes occurring during the melting of various polyethylene (PE) materials, including high-density PE (HDPE), linear low-density PE (LLDPE) and low-density polyethylene (LDPE), were investigated using near-infrared spectroscopy. The assignment of PE to the 1650–1900 nm spectral region was suggested, on the basis of computational and experimental data for normal alkanes. The present results suggested that the 1690 and 1710 nm bands should be assigned to the CH3 groups in branched chains and chain ends, respectively. The HDPE and LDPE crystal lattices have very few defects, in contrast to LLDPE, which has more crystal lattice defects. The chain ends and junctions of LDPE are excluded from the crystal lattice and exist in a thick amorphous layer, whereas LLDPE includes comonomers in its crystalline lattice.
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Mizushima, M., Kawamura, T., Takahashi, K. et al. In situ near-infrared spectroscopic studies of the structural changes of polyethylene during melting. Polym J 44, 162–166 (2012). https://doi.org/10.1038/pj.2011.100
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DOI: https://doi.org/10.1038/pj.2011.100
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