Enthalpy relaxation of the glass of poly (L-lactic acid) of different D-isomer content and its effect on mechanical properties

被引:22
|
作者
Iqbal, H. M. Naeem [1 ]
Sungkapreecha, Chanita [1 ]
Androsch, Ren [1 ]
机构
[1] Martin Luther Univ Halle Wittenberg, Ctr Engn Sci, D-06099 Halle, Germany
关键词
Poly (L-lactic acid); Random L/D-lactic acid copolymers; Enthalpy relaxation; Microhardness; Young's modulus; CRYSTAL NUCLEATION; STRUCTURAL RELAXATION; POLY(L-LACTIC ACID); POLY(LACTIC ACID); CRYSTALLIZATION; DEGRADATION; TRANSITION; RECOVERY; BEHAVIOR; KINETICS;
D O I
10.1007/s00289-016-1854-5
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The relaxation of the glass of poly (l-lactic acid) (PLLA) and its random copolymers with 2 and 4 mol% d-isomer co-units has been analyzed by conventional differential scanning calorimetry. It was found that the presence of up to 4% d-isomer co-units in the PLLA chain has no measurable effect on the glass relaxation kinetics in fully amorphous samples. At ambient temperature, after rapid cooling of the melt at a rate of 50 K/min, to avoid crystallization, the glass relaxation begins after about 10 min and is not finished within 5000 min. The relaxation of the glass is accompanied by a major change of mechanical properties as it was revealed by time-resolved measurements of the micro-indentation hardness and Young's modulus. During annealing of amorphous PLLA at ambient temperature, the microhardness and Young's modulus increase by more than 40 and 10%, respectively, within a time period of about one month, and with an equilibrium value not yet achieved even after such a long annealing time. As in case of the enthalpy-relaxation kinetics, both, absolute values and the time evolution of the analyzed mechanical properties are independent on the presence of d-isomer co-units in the PLLA chain within the investigated concentration range.
引用
收藏
页码:2565 / 2573
页数:9
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