Kinetics of nucleation and crystallization of poly(ε-caprolactone) – Multiwalled carbon nanotube composites

• Nucleating agent efficiency for PCL crystallization was tested by calorimetry.
• Temperatures of homogeneous and heterogeneous nucleation were covered.
• Up to two orders of magnitude faster crystallization of the nucleated polymer.
• Crystallization at temperatures of homogeneous nucleation is independent of additives.
• Homogeneous nucleation is significantly more effective than the heterogeneities.

The nucleation efficiency of multiwall carbon nanotubes (MWCNT) in poly(ε-caprolactone) (PCL), as an example, was tested for a wide range of temperatures and cooling rates and compared to the efficiency of homogeneously formed nuclei. The temperature range below the maximum of crystallization rate is generally not accessible for non-isothermal cooling experiments because the sample becomes amorphous at the needed cooling rates. Isothermal experiments after fast quenches extend the temperature range down to and below the glass transition. The employed differential fast scanning calorimeter (DFSC) allows cooling at rates up to 100,000 K/s and precise adjustment and control of isothermal conditions in the time range from 10−4 to 104 s and longer. As shown in previous work, heterogeneous crystal nucleation dominates at low supercooling, revealing a significant dependence of crystallization rate on MWCNT concentration. Nevertheless, no saturation of the nucleation activity at a MWCNT loading of 0.2–0.5 wt% as seen in slow DSC experiments was observed at the much higher cooling rates employed here. At high supercooling, where homogeneous nucleation is prevalent, the addition of MWCNT neither enhances nor reduces the crystallization rate. At the temperature of maximum homogeneous nucleation rate, formation of homogeneous nuclei always dominates crystallization.

Figure optionsDownload as PowerPoint slide