Yongjun LiuWeihong GuoZhizhong SuBinyao LiChifei Wu
Recycled poly(ethylene terephthalate) (r-PET) was blended with poly(ethylene octene) (POE) and glycidyl methacrylate grafted poly(ethylene octene) (mPOE). The nonisothermal crystallization behavior of r-PET, r-PET/POE, and r-PET/mPOE blends was investigated using differential scanning calorimetry (DSC). The crystallization peak temperatures (T p ) of the r-PET/POE and r-PET/mPOE blends were higher than that of r-PET at various cooling rates. Furthermore, the half-time for crystallization (t 1/2 ) decreased in the r-PET/POE and r-PET/mPOE blends, implying the nucleating role of POE and mPOE. The mPOE had lower nucleation activity than POE because the in situ formed copolymer PET-g-POE in the PET/mPOE blend restricted the movement of PET chains. Non-isothermal crystallization kinetics analysis was carried out based on the modified Avrami equation, the Ozawa equation, and the Mo method. It was found that the Mo method provided a better fit for the experimental data for all samples. The effective energy barriers for nonisothermal crystallization of r-PET and its blends were determined by the Kissinger method.
Jiann‐Wen HuangYa‐Lan WenChiun‐Chia KangMou‐Yung YehShaw‐Bing Wen
Jiann‐Wen HuangYa‐Lan WenChiun‐Chia KangMou‐Yung YehShaw‐Bing Wen
Yongjun LiuZhizhong SuWeihong GuoBinyao LiChifei Wu
Yongjun LiuZhizhong SuWeihong GuoBinyao LiChifei Wu