

FOLLOWUS
School of Materials Science and Engineering, Southwest Jiaotong University, Key Laboratory of Advanced Technologies of Materials, Ministry of Education of China, Chengdu 610031, China
Yong Wang(王勇), E-mail:yongwang1976@163.com
Received:10 August 2016,
Revised:2016-9-20,
Accepted:20 September 2016,
Published:25 March 2017
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Wang Yang-peng, Wei Xiao, Duan Jin, et al. Greatly Enhanced Hydrolytic Degradation Ability of Poly(L-lactide) Achieved by Adding Poly(ethylene glycol)[J]. Chinese Journal of Polymer Science, 2017, 35(3): 386-399.
Wang Yang-peng, Wei Xiao, Duan Jin, et al. Greatly Enhanced Hydrolytic Degradation Ability of Poly(L-lactide) Achieved by Adding Poly(ethylene glycol)[J]. Chinese Journal of Polymer Science, 2017, 35(3): 386-399. DOI: 10.1007/s10118-017-1904-y.
Plasticized poly(L-lactide) (PLLA) materials have been applied in many fields and the microstructure performance of such materials attracts much attention of researchers. However
few reports declared the hydrolytic degradation ability of the plasticized PLLA materials. In this article
a small quantity of poly(ethylene glycol) (PEG) was introduced into PLLA
which aimed to understand the hydrolytic degradation behavior of the plasticized PLLA materials. The microstructures of the plasticized samples were comparatively investigated using scanning electron microscopy (SEM)
wide angle X-ray diffraction (WAXD)
differential scanning calorimetry (DSC) and Flourier transform infrared spectroscopy (FTIR)
etc
. The results demonstrated that PEG improved the hydrophilicity of sample surface
and the relatively high content of PEG enhanced the crystallization ability of PLLA matrix. The hydrolytic degradation measurement was carried out at 60℃ in an alkaline solution of pH=12. The results demonstrated that the plasticized PLLA samples exhibited accelerated hydrolytic degradation compared with the pure PLLA sample
and the hydrolytic degradation was also dependent on the PEG content. Further results demonstrated that PEG induced the change of hydrolytic degradation mechanism possibly due to the good dissolution ability of PEG in water
which provided more paths for the penetration of water. Furthermore
the microstructure evolution of the plasticized PLLA during the hydrolytic degradation process was also investigated
and the results demonstrated the occurrence of PLLA crystallization
which was possibly contributed to the decreased hydrolytic degradation rate observed at relatively long hydrolytic degradation time. This work is of great significance and may open a new way for promoting the reclamation of PLLA waste material.
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