结晶度
无定形固体
降级(电信)
材料科学
极限抗拉强度
聚合
复合材料
单体
化学工程
形态学(生物学)
高分子化学
聚合物
化学
结晶学
计算机科学
工程类
电信
生物
遗传学
作者
Daokun Shi,Yahong Kang,Guoyi Zhang,Chenguang Gao,Wei Lu,Caihong Yang,Hua Zou,Hongyan Jiang
标识
DOI:10.1016/j.polymdegradstab.2018.11.005
摘要
Abstract Three kinds of high molecular weight polymers were synthesized by ring-opening polymerization with various monomer feeding ratios (named as PLLA, PLCL 95/5 and PLGC 80/15/5, respectively). Then oriented monofilament was produced through melt-extrusion and tensile orientation based on each kind of polymer. In vitro degradation properties of the monofilaments were studied over a range of degradation time from 1 to 21 days at 60 °C by using SEM, GPC, DSC, XRD and tensile test. Degradation results showed that the mass loss, Tg and morphology integrity of the PLLA monofilament basically remained unchanged, and partial degradation in amorphous region emerged with slight increase of crystallinity. For the PLCL 95/5 monofilament, the crystallinity was increased and the monofilament was fractured at 14 days accompanying with obvious decrease of the mass and Tm, indicating that most part of the amorphous region was degraded. Apparently, the PLGC 80/15/5 monofilament showed the fastest degradation rate with considerable mass loss and decrease of Tg. The amorphous region was degraded sharply in the early stage due to its good water absorbability and lower structural regularity, and the initially-formed crystalline region was degraded slowly later evidenced from the change of crystallinity and it was fractured at 3 days. The accelerated effects calculated according to the first-order kinetic model demonstrated that the PLCL 95/5 monofilament was degraded 2.5 times faster than pure PLLA and the PLGC 80/15/5 monofilament was degraded 7.5 times faster than PLLA. These were nearly consistent with those based on [η] (2.5 and 6.9 times respectively). The comparative study of in vitro degradation behavior of PLLA-based copolymer monofilaments would provide useful information for controlling the monomer composition of PLLA-based materials with specific degradation requirements.
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