Combined effect of glycerol/levulinic acid‐based bioadditive on enzymatic hydrolysis and plasticization of amorphous and semi‐crystalline poly(lactic acid)

增塑剂 乳酸 甘油 生物降解 聚乳酸 水解 无定形固体 酶水解 解聚 化学 聚酯纤维 生物高聚物 玻璃化转变 化学工程 有机化学 材料科学 高分子化学 聚合物 细菌 生物 遗传学 工程类
作者
Chiara Siracusa,Luca Lenzi,Filippo Fabbri,Leon Ploszczanski,Paola Fabbri,Davide Morselli,Felice Quartinello,Georg M. Guebitz
出处
期刊:Journal of Vinyl & Additive Technology [Wiley]
卷期号:31 (4): 869-885 被引量:3
标识
DOI:10.1002/vnl.22213
摘要

Abstract Polylactic acid (PLA) is a widely used biopolymer, but its brittleness and limited biodegradability hinder its application as a standalone material. To enhance its properties, PLA can be compounded with plasticizers, ideally nontoxic and from sustainable sources. While phthalates remain the predominant plasticizers, their known harmful effects have led to the development of bio‐based alternatives like glycerol trilevulinate (GT). This study investigates the plasticizing effect of GT on amorphous (aPLA) and semi‐crystalline (cPLA) PLA, comparing it to the impact that can be achieved with a conventional plasticizer, diisononyl cyclohexane‐1,2‐dicarboxylate (DINCH). Specifically, GT added at 40 phr reduces the glass transition temperature of aPLA by 20°C and the melting temperature of cPLA by 12°C, whereas DINCH exhibited a more limited effect. Compared to DINCH, GT also demonstrated very low migration in terms of both leaching and volatility. Moreover, GT impacts on the enzymatic depolymerization of the prepared compounds. Specifically, enzymatic hydrolysis tests revealed an enhanced biodegradability of the aPLA/GT compounds, achieving complete degradation within 72 h of incubation, as confirmed by high performance liquid chromatography‐based monomer quantification. The cPLA/GT formulations are also susceptible to hydrolysis, showing an increased weight loss from 18% to 31% when 20 phr of GT is added. These outcomes suggest that GT can be used not only to tune the thermal properties but also to significantly promote polyesters biodegradability, envisioning an environmentally friendly management of the PLA‐based formulations. Highlights A bioplasticizer for amorphous and semi‐crystalline PLA is proposed. Bioplasticizer reduces the glass transition and melting temperature of PLAs. Bioplasticizer also enhances the enzymatic degradation of semi‐crystalline PLA. Bioplasticizer performance has been compared with a commercial plasticizer.
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