摘要: 20 wt% polyamide 12 (PA1212) pellets were dissolved in molten caprolactam. The caprolactam was then catalyzed at 180°C and polymerized by means of anionic ring-opening polymerization to produce in situ blends of the resultant polyamide 6 (PA6) and PA1212. Mechanical blends with same ingredient were prepared through melt blending on a twin-screw extruder. Scanning electron microscopy (SEM) observation revealed that contrary to the mechanical blends with small spherulites embedded in the matrix, no phase-separation existed in the in situ blends. The results of thermal analysis by differential scanning calorimetry (DSC) showed that single melting peak and crystallization peak existed for the in situ blends, while two melting and crystallization peaks appeared for the mechanical blends. The in situ blend film and the mixed blend film, both cast from a dilute formic acid solution with a concentration of 0.5 g/L, remained similar crystallization and melting behavior as above. It is proved by solution 13C-NMR analysis that transamidation took place during the in situ blending, and it is suggested that the combination of temperature increasing and the basic surrounding derived from NaOH during polymerization resulted in the occurrence of transamidation. Furthermore, it is proposed that the interchange reaction between PA1212 and PA6 also resulted from the degradative reaction during the anionic polymerization.