posted on 2016-01-04, 00:00authored byYongfeng Huang, Ruoxing Chang, Lili Han, Guorong Shan, Yongzhong Bao, Pengju Pan
A series of triblock copolymers consisting
of the poly(ε-caprolactone-co-δ-valerolactone)
(PCVL) soft midblock and poly(lactic
acid) (PLA) hard end blocks were synthesized via the sequential ring-opening
polymerization. PCVL random copolyester was prepared by the copolymerization
of ε-caprolactone (εCL) and δ-valerolactone (δVL).
PCVL has the lower crystallization temperature but comparable crystallizability
with the poly(ε-caprolactone) homopolymer, indicating the isomorphic
crystallization of εCL and δVL. Molecular weight and chemical
composition of PLA–PCVL–PLAs were controlled by the
feed ratio of lactide monomer to PCVL macroinitiator. PLA–PCVL–PLAs
exhibit the typical characteristics of thermoplastic elastomer (TPE).
Crystallization behavior, thermal, and mechanical properties of PLA–PCVL–PLAs
are readily modulated by changing the length, tacticity, and stereostructure
of PLA end blocks. PLA end blocks retard the crystallization of PCVL
midblock in PLA–PCVL–PLAs. Stereocomplex crystallites
of PLA are conclusively formed in the racemic blends of PLA–PCVL–PLAs,
leading to the increased melting temperature and thermal stability.
SAXS data indicates that the microphase-separated domain size of PLA–PCVL–PLAs
enhances with increasing the PLA block length and the stereocomplexation
impedes forming the ordered microphase-separated structure in the
racemic blends. Tensile strength, Young’s modulus, and heat-resistant
temperature of PLA–PCVL–PLA TPEs increase, whereas their
strains at break and transparency decrease with the crystallization
or stereocomplexation of PLA end blocks.