Jun Li , Zhicong Li , Yuan Yan , Danrong Shao , Yao Guo , Rihui Lin
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引用次数: 0
Abstract
To investigate the synergistic effects of flexible aliphatic chains and rigid aromatic rings on the properties of polylactic acid (PLA)-based composites, a series of mono-esterified octanoyl starches (OC) and dual-esterified octanoyl–benzoyl starches (OC-BA) with comparable degrees of substitution (DS) were synthesized. The modified starches were blended with PLA at a 1:1 mass ratio, and composite films were prepared via solution casting. The results indicated that OC with a moderate DS (DS = 1.2) significantly improved the ductility of the films due to the introduction of flexible aliphatic chains. At a similar DS, the benzene rings in the PLA/OC-BA2 structure, in synergy with the fatty acid chains, enabled the composite film to reach a maximum elongation at break of 250.78%. Moreover, OC-BA2 promoted strong interfacial interactions with the PLA matrix through hydrogen bonding and π–π stacking, thereby enhancing both strength and toughness. Molecular docking simulations further elucidated the interfacial configurations and non-covalent interactions under different substitution patterns. In terms of biodegradability, the mono-esterified OC-based composites significantly accelerated the degradation rate of the films, whereas the dual-esterified OC-BA structure further improved the films’ aging resistance, hydrophobicity, and barrier properties. However, its biodegradability was markedly reduced, with the degradation rate of PLA/OC-BA2 being approximately 11.01%. Therefore, incorporating differently modified starches enables targeted regulation of the performance of PLA composite films to meet specific application requirements.
期刊介绍:
Polymer Degradation and Stability deals with the degradation reactions and their control which are a major preoccupation of practitioners of the many and diverse aspects of modern polymer technology.
Deteriorative reactions occur during processing, when polymers are subjected to heat, oxygen and mechanical stress, and during the useful life of the materials when oxygen and sunlight are the most important degradative agencies. In more specialised applications, degradation may be induced by high energy radiation, ozone, atmospheric pollutants, mechanical stress, biological action, hydrolysis and many other influences. The mechanisms of these reactions and stabilisation processes must be understood if the technology and application of polymers are to continue to advance. The reporting of investigations of this kind is therefore a major function of this journal.
However there are also new developments in polymer technology in which degradation processes find positive applications. For example, photodegradable plastics are now available, the recycling of polymeric products will become increasingly important, degradation and combustion studies are involved in the definition of the fire hazards which are associated with polymeric materials and the microelectronics industry is vitally dependent upon polymer degradation in the manufacture of its circuitry. Polymer properties may also be improved by processes like curing and grafting, the chemistry of which can be closely related to that which causes physical deterioration in other circumstances.