A significant enhancement in isothermal crystallization kinetics of biodegradable polylactide(PLA) in its immiscible blends can be accomplished through blending it with a comb-like copolymer. PLA was blended with poly(ethylene glycol) methyl ether acrylate(PEGA) and poly[poly(ethylene glycol) methyl ether acrylate](PPEGA, a comb-like copolymer), respectively. The results measured from phase contrast optical microscopy(PCOM) and differential scanning calorimetry(DSC) indicate that PLA and PEGA components are miscible, whereas PLA and PPEGA components are immiscible. The study of crystallization kinetics for PLA/PEGA and PLA/PPEGA blends by means of polarized optical microscopy(POM) and DSC indicates that both PEGA and PPEGA significantly increase the PLA spherulitic growth rates, G, although PLA/PPEGA blends are immiscible and the glass transition temperatures of PLA only have slight decreases. PPEGA component enhances nucleation for PLA crystallization as compared with PEGA component owing to the heterogeneous nucleation effect of PPEGA at the low composition of 20 wt%, while PLA crystallization-induced phase separation for PLA/PEGA blend might cause further nucleation at the high composition of 50 wt%. DSC measurement further demonstrates that isothermal crystallization kinetics can be relatively more enhanced for PLA/PPEGA blends than for PLA/PEGA blends. The "abnormal" enhancement in G for PLA in its immiscible blends can be explained by local interfacial interactions through the densely grafted PEGA side chains in the comb-like PPEGA, even though the whole blend system(PLA/PPEGA blends) represents an immiscible one.
Yin ChenYaqiong ZhangFeng JiangJunyangWangZhaohua XuZhigang Wang
In this work the nucleation and growth of spherulites for the below polylactide （PLA） layer in poly（ε- caprolactone）/polylactide （PCL/PLA） double-layer films during isothermal crystallization at various temperatures above the melting point of PCL have been investigated by using polarized optical microscopy （POM）. It is revealed that two types of spherulitic morphologies are observed in PCL/PLA double-layer films. One is the well defined highly birefringent spherulites, and the other one is the coarse spherulites. It is interesting to find that the spherulitic growth rate of the coarse spherulites is higher than that of the well defined spherulites. It is thought that the coarse spherulites nucleate and grow with the assistance of the interfaces between the PCL and PLA layers, and the well defined highly birefringent spherulites only nucleate and grow in the PLA layer.
Acid-oxidized multiwalled carbon nanotubes (A-MWCNTs) with a range of reduced aspect ratios (from about 11 to 5.8) were obtained by acid oxidization of MWCNTs in the mixture of HNO 3 and H 2 SO 4 for varying periods of 1, 3, 8 and 12 h, respec- tively. The aspect ratios and surface functionalization of A-MWCNTs were well characterized by scanning electron microsco- py (SEM), Fourier transform infrared spectroscopy (FTIR), Raman spectroscopy and thermogravimetric analysis (TGA). Poly(L-lactide)/A-MWCNT composites containing 0.5 wt% A-MWCNTs with a range of reduced aspect ratios were prepared by solution cast. The effects of added A-MWCNTs on the isothermal crystallization kinetics of poly(L-lactide)/A-MWCNT composites were investigated by means of differential scanning calorimetry (DSC), rheology and polarized optical microscopy (POM). It is surprising to find that not only the addition of A-MWCNTs effectively increases the poly(L-lactide) (PLA) crys- tallization kinetics, but also the nucleation ability of A-MWCNTs for PLA crystallization exponentially increases with the re- duced aspect ratio, that is to say, those with lower aspect ratios show much stronger nucleation ability for PLA crystallization than those with higher aspect ratios. The exponentially increased nucleation ability of A-MWCNTs with a range of reduced aspect ratios for PLA crystallization is disclosed.
