Mondol Anindita, Wang Jun, Ein-Mozaffari Farhad, Behzadfar Ehsan
Chemical Engineering Department, Toronto Metropolitan University, Toronto, ON M5B 2K3, Canada.
Sustainable Polymers Research Lab (SPRL), The Creative School, Toronto Metropolitan University, Toronto, ON M5B 2K3, Canada.
ACS Polym Au. 2025 Jun 4;5(4):394-405. doi: 10.1021/acspolymersau.5c00026. eCollection 2025 Aug 13.
Polyhydroxyalkanoates (PHAs) are emerging, promising sustainable biobased, biodegradable polymers with strong potential to replace conventional plastics in packaging, agricultural, cosmetics, and biomedical applications. In this study, we investigate the crystallization behavior of two key PHA typespolyhydroxybutyrate (PHB) and poly-(3-hydroxybutyrate--3-hydroxyvalerate) (PHBV)under both isothermal and nonisothermal conditions using controlled hyperthermal cycles. Isothermal analyses were performed following rapid hypercooling at 500 °C/min to isolate crystallization kinetics, effectively minimizing interference from the cooling stage. The isothermal data revealed activation energies of 91 kJ/mol for PHB and 139 kJ/mol for PHBV. Hypercooling cycles were also employed to examine nonisothermal crystallization kinetics at cooling rates up to 500 °C/min, mimicking industrial processing speeds. The nonisothermal analysis of PHB and PHBV showed a pronounced decrease in crystallinity with increasing cooling rates. Specifically, PHB's crystallinity dropped from 48.6 to 10.9%, while that of PHBV fell from 45.9% to near zero, accompanied by the disappearance of exothermic peaks. The isothermal and nonisothermal crystallization behaviors were analyzed using the commonly used modeling, revealing the limited capability of these models in terms of the prediction of the nonisothermal crystallization kinetics from isothermal crystallization data. This study provides novel insights into the thermally driven crystallization mechanisms of PHAs and underscores their sensitivity to processing conditionscritical knowledge for optimizing manufacturing techniques in sustainable polymer applications.
聚羟基脂肪酸酯(PHA)是一种新兴的、有前景的可持续生物基可生物降解聚合物,在包装、农业、化妆品和生物医学应用中具有很强的潜力来替代传统塑料。在本研究中,我们使用受控的超高温循环研究了两种关键PHA类型——聚羟基丁酸酯(PHB)和聚(3-羟基丁酸酯-3-羟基戊酸酯)(PHBV)在等温及非等温条件下的结晶行为。在以500℃/分钟的速度快速过冷后进行等温分析,以分离结晶动力学,有效减少冷却阶段的干扰。等温数据显示,PHB的活化能为91kJ/mol,PHBV的活化能为139kJ/mol。还采用了过冷循环来研究高达500℃/分钟冷却速率下的非等温结晶动力学,模拟工业加工速度。PHB和PHBV的非等温分析表明,随着冷却速率的增加,结晶度显著降低。具体而言,PHB的结晶度从48.6%降至10.9%,而PHBV的结晶度从45.9%降至接近零,同时放热峰消失。使用常用模型对等温及非等温结晶行为进行了分析,结果表明这些模型在根据等温结晶数据预测非等温结晶动力学方面能力有限。本研究为PHA的热驱动结晶机制提供了新的见解,并强调了它们对加工条件的敏感性——这是优化可持续聚合物应用制造技术的关键知识。