Infrared dichroism is employed to study the orientation of chain molecules in linear and ethyl‐branched polyethylene in the crystalline and noncrystalline regions during drawing and subsequent annealing. A crystalline (1894 cm−1) and a noncrystalline (1368 cm−1) band, as well as the bands at 909 cm−1 and 1375 cm−1 resulting from vinyl endgroups and methyl endgroups and sidegroups, are studied. For these bands relative orientation functions are derived and compared as a function of draw ratio and annealing temperature. It is shown that the relative orientation functions as derived from the dichroism of the noncrystalline, vinyl and methyl bands follow the same curve while the orientation function for the crystalline bands does not. These results support a two‐phase model for partially crystalline polyethylene and additionally favor segregation of the endgroups and sidegroups in the noncrystalline component during crystallization. It is further shown that shrinkage occurs at the temperature at which the noncrystalline chain molecules start to disorient. From the dichroism of the methyl groups in ethyl‐branched polyethylene, a value for the mean orientation of the noncrystalline chain molecules is calculated. We obtain for the orientation function of the noncrystalline regions at highest draw ratios (λ = 15–20), f = 0.35–0.57, while the chain molecules in the crystallites are nearly perfectly oriented (f ≈ 1.0). On the assumption that the noncrystalline component consists of folds, tie molecules, and chain ends, the different contributions of these components to the overall orientation are estimated. From these the relative number of CH2 groups incorporated into folds, tie molecules, and cilia can be derived. Further, on the basis of a simple structural model, the relative number of chains on the crystal surface contributing to the different noncrystalline components and their average length are estimated.
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