Thermal Properties and Structural Evolution of Poly( l -lactide)/Poly( d -lactide) Blends

作者：Lidong Feng, Xinchao Bian, Gao Li, Xuesi Chen · 发表于：Macromolecules · 年份：2021 · DOI：10.1021/acs.macromol.1c01866 · 被引用次数：62 · 研究领域：biodegradable polymer synthesis and properties、Carbon dioxide utilization in catalysis、Graphene and Nanomaterials Applications

In order to obtain the forming regulation and structural evolution of poly( l -lactide)/poly( d -lactide) (PLLA/PDLA) stereocomplexes (sc-PLA), a commercial high molecular weight PLLA was blended with a series of PDLAs with different weight-average molecular weights ( M w ) in the range of 7.5–290 kg·mol –1 by solution blending. The thermal properties, morphology, and thermal stability of the PLLA/PDLA blends were investigated by differential scanning calorimetry (DSC), field emission scanning electron microscopy (FE-SEM), and thermogravimetric analysis (TGA). The crystallization of sc-PLA and homochiral PLA (homo-PLA) was competitive and controlled by the M w of PDLA. The phase structure of the PLLA/PDLA blends depended on the melting temperature. By quenching sc-PLA from 280 to 290 °C, a bicontinuous phase structure was observed for PLLA and PDLA. When quenching sc-PLA from 230 to 270 °C, a stereoamorphous mesophase of PLA (sam-PLA) was obtained, which originated from the residual strong hydrogen bonding between PLLA and PDLA. sam-PLA was a new discovery different from sc-PLA and homo-PLA. The PLLA/PDLA blends are not fully compatible among sam-PLA, PLLA, and PDLA. During melting, sc-PLA changed into sam-PLA, and the hydrogen bonding in sam-PLA was destroyed and weakened with increasing temperature at <∼270 °C. At higher than ∼270 °C, the hydrogen bonding became extremely weak and even disappeared.