首页> 外文期刊>RSC Advances >Crystallization, rheology and mechanical properties of the blends of poly(l-lactide) with supramolecular polymers based on poly(d-lactide)-poly(epsilon-caprolactone-co-delta-valerolactone)-poly(d-lactide) triblock copolymers
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Crystallization, rheology and mechanical properties of the blends of poly(l-lactide) with supramolecular polymers based on poly(d-lactide)-poly(epsilon-caprolactone-co-delta-valerolactone)-poly(d-lactide) triblock copolymers

机译:基于聚(D-丙交酯) - 聚(Epsilon-Caprolacterone-Co-Delta-Valerologers) - poly(D-丙交酯)三嵌段共聚物,具有基于聚(D-丙交酯)的共分子聚合物的聚(L-丙交酯)共混物的结晶,流变学和力学性能

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In this study, we investigated the blending of poly(l-lactide) (PLLA) with supramolecular polymers based on poly(d-lactide)-poly(epsilon-caprolactone-co-delta-valerolactone)-poly(d-lactide) (PDLA-PCVL-PDLA) triblock copolymers as an efficient way to modify PLLA. The supramolecular polymers (SMP) were synthesized by the terminal functionalization of the PDLA-PCVL-PDLA copolymers with 2-ureido-4[1H]-pyrimidinone (UPy). The structure, thermal properties and rheological behavior of the synthesized supramolecular polymers were studied; we found that the formation of the UPy dimers expanded the molecular chain of the polymer and the incorporation of the UPy groups suppressed the crystallization of polymers. In addition, the synthesized supramolecular polymers had a low glass transition temperature of about -50 degrees C, showing the characteristics of elastomers. On this basis, superior properties such as a fast crystallization rate, high melt strength, and toughness of fully bio-based, i.e., PLA-based materials were achieved simultaneously by blending PLLA with the synthesized supramolecular polymers. In the PLLA/SMP blends, PLLA could form a stereocomplex with its enantiomeric PDLA blocks of supramolecular polymers, and the stereocomplex crystals with the cross-linking networks reinforced the melt strength of the PLLA/SMP blends. The influences of the SMP composition and the SMP content in the PLLA matrix on crystallization and mechanical properties were analyzed. The supramolecular polymers SMP0.49 and SMP1.04 showed a reverse effect on the crystallization of PLLA. Tensile tests revealed that the lower content of the synthesized supramolecular polymers could achieve toughening of the PLLA matrix. Therefore, the introduction of supramolecular polymers based on PDLA-PCVL-PDLA is an effective way to control the crystallization, rheology and mechanical properties of PLLA.
机译:在该研究中,我们研究了基于聚(D-丙交酯)-poly(ε-己内酯 - 共Δ-valeroloLodone -poly(D-丙交酯)(D-丙交酯)(ε-丙交酯)( PDLA-PCVL-PDLA)三嵌段共聚物作为修饰PLLA的有效方法。通过PDLA-PCVL-PDLA共聚物的末端官能化与2-UreidO-4 [1H] - 吡啶酮(UPY)的末端官能化合成了超分子聚合物(SMP)。研究了合成的超分子聚合物的结构,热性质和流变行为;我们发现,UPY二聚体的形成膨胀了聚合物的分子链,并且掺入UPY基团抑制了聚合物的结晶。此外,合成的超分子聚合物具有约-50℃的低玻璃化转变温度,显示弹性体的特性。在此基础上,通过将PLLA与合成的超分子聚合物混合,同时实现了优异的性质,例如快速的结晶速率,高熔体强度和完全生物基础的韧性,即PLA基材料。在PLLA / SMP共混物中,PLLA可以与其对映分子聚合物的对映体PDLA块形成立体络合物,并且具有交联网络的立体络合物晶体加强了PLLA / SMP共混物的熔体强度。分析了SMP组成和SMP含量对结晶和机械性能的影响和SMP含量的影响。超分子聚合物SMP0.49和SMP1.04对PLLA的结晶显示出逆向影响。拉伸试验表明,合成的超分子聚合物的较低含量可以实现PLLA基质的增韧。因此,基于PDLA-PCV1-PDLA的超分子聚合物的引入是控制PLLA的结晶,流变和机械性能的有效方法。

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    《RSC Advances》 |2019年第45期|共13页
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