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Plasticization of Polylactide with Myrcene and Limonene as Bio-Based Plasticizers: Conventional vs. Reactive Extrusion

机译:以月桂烯和柠檬烯为生物基增塑剂的聚丙交酯的增塑:常规挤出与反应挤出

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摘要

Polylactide (PLA) was blended by conventional and reactive extrusion with limonene (LM) or myrcene (My) as bio-based plasticizers. As-processed blends were carefully analyzed by a multiscale and multidisciplinary approach to tentatively determine their chemical structure, microstructure, thermal properties, tensile and impact behaviors, and hydrothermal stability. The main results indicated that LM and My were efficient plasticizers for PLA, since compared to neat PLA, the glass transition temperature was reduced, the ultimate tensile strain was increased, and the impact strength was increased, independently of the type of extrusion. The addition of a free radical initiator during the extrusion of PLA/LM was beneficial for the mechanical properties. Indeed, the probable formation of local branched/crosslinked regions in the PLA matrix enhanced the matrix crystallinity, the tensile yield stress, and the tensile ultimate stress compared to the non-reactive blend PLA/LM, while the other properties were retained. For PLA/My blends, reactive extrusion was detrimental for the mechanical properties since My polymerization was accelerated resulting in a drop of the tensile ultimate strain and impact strength, and an increase of the glass transition temperature. Indeed, large inclusions of polymerized My were formed, decreasing the available content of My for the plasticization and enhancing cavitation from inclusion-matrix debonding.
机译:通过常规挤出和反应挤出,将聚丙交酯(PLA)与作为生物基增塑剂的柠檬烯(LM)或月桂烯(My)混合。通过多尺度和多学科方法仔细分析了加工后的混合物,以初步确定其化学结构,微观结构,热性能,拉伸和冲击行为以及水热稳定性。主要结果表明,LM和My是PLA的高效增塑剂,因为与纯PLA相比,其玻璃化转变温度降低,极限拉伸应变增加,冲击强度增加,而与挤出类型无关。在PLA / LM挤出过程中添加自由基引发剂有利于机械性能。确实,与非反应性共混物PLA / LM相比,PLA基质中可能形成局部支链/交联区域增强了基质的结晶度,拉伸屈服应力和拉伸极限应力,同时保留了其他性能。对于PLA / My混合物,反应性挤出对机械性能有害,因为My聚合反应加速,导致拉伸极限应变和冲击强度下降,并且玻璃化转变温度升高。确实,形成了聚合的My的大夹杂物,从而降低了My用于增塑的有效含量,并增强了夹杂物基质脱胶引起的空化作用。

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