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Molecular orientation in film extrusion of high‐density polyethylene
Author(s) -
Picot J. J. C.
Publication year - 1984
Publication title -
polymer engineering and science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.503
H-Index - 111
eISSN - 1548-2634
pISSN - 0032-3888
DOI - 10.1002/pen.760240605
Subject(s) - extrusion , materials science , amorphous solid , differential scanning calorimetry , orientation (vector space) , composite material , polyethylene , deformation (meteorology) , atmospheric temperature range , crystallography , thermodynamics , geometry , physics , mathematics , chemistry
Molecular orientation in film extrusion has been studied using an extrusion‐grade commercial polyethylene resin. First quad (take‐up) speed was varied over the range 50 to 120 m/min, Web crystallinities were found to be in the range 0.60 to 0.65 as determined by differential scanning calorimetry. Web crystalline orientation function f c was slightly negative below a takeup speed of 50 m/min and rose to a value of 0.4 at 120 m/min at a quench bath temperature of 37.8°C and a melt temperature of 251°C for one of the resins used. (Perfect orientation along the machine direction implies f c equal to 1.0). Amorphous orientation function f a remained below 0.1 and was almost constant with takeup speed. This behavior was modified in a minor way by changes in quench bath and melt temperature as well as resin lot. A qualitative model was proposed for this without definite proof. The major mechanism at work in the film‐forming process is macromolecular network structure deformation in elongational flow. Die gap variation at uniform extrusion rate has a secondary effect on web orientation. With the present state of knowledge, it is not possible to quantitatively separate the amorphous orientation function into its various conformational contributions. It was also noted that high take up speeds and low air gaps tend to freeze the web at greater widths.