Crystallization of low-density polyethylene- and linear low-density polyethylene-rich blends

✍ Scribed by Kate M. Drummond; Jefferson L. Hopewell; Robert A. Shanks

• Publisher: John Wiley and Sons
• Year: 2000
• Tongue: English
• Weight: 150 KB
• Volume: 78
• Category: Article
• ISSN: 0021-8995
• DOI: 10.1002/1097-4628(20001031)78:5<1009::aid-app100>3.0.co;2-2

✦ Synopsis

The crystallization of a series of low-density polyethylene (LDPE)-and linear low-density polyethylene (LLDPE)-rich blends was examined using differential scanning calorimetry (DSC). DSC analysis after continuous slow cooling showed a broadening of the LLDPE melt peak and subsequent increase in the area of a second lower-temperature peak with increasing concentration of LDPE. Melt endotherms following stepwise crystallization (thermal fractionation) detailed the effect of the addition of LDPE to LLDPE, showing a nonlinear broadening in the melting distribution of lamellae, across the temperature range 80 -140°C, with increasing concentration of LDPE. An increase in the population of crystallites melting in the region between 110 and 120°C, a region where as a pure component LDPE does not melt, was observed. A decrease in the crystallite population over the temperature range where LDPE exhibits its primary melting peaks (90 -110°C) was noted, indicating that a proportion of the lamellae in this temperature range (attributed to either LDPE or LLDPE) were shifted to a higher melt temperature.