聚乳酸水热全量解聚特性研究OA
Study on fully hydrothermal depolymerization characteristics of poly(lactic acid)
研究了聚乳酸(PLA)塑料餐具和纯PLA材料在特定条件下(190℃高温水热环境)的降解行为,通过质量变化、扫描电子显微镜(SEM)、高效液相色谱(HPLC)、傅里叶变换红外光谱(FTIR)等多种表征手段分析了PLA塑料在水热处理前后的物化特性变化,并总结了PLA在水热解聚过程中乳酸的产生和宏观结构演变的规律.结果表明,PLA固体降解达到100%,乳酸溶液能够显著促进PLA的水解过程,且并不影响最终的乳酸转化率(>90%).而滑石粉、纤维素、PLA餐具中的添加剂在一定程度上也会促进PLA的水解过程,但会抑制最终的乳酸转化率.此外,聚乙二醇(PEG)会显著抑制PLA水解.PLA塑料在水解过程中存在酯键断裂现象,生成了—OH和—COOH端基,导致含有—OH基团的降解产物增加,而含有C=O键的降解产物的含量几乎不变.
This study investigates the degradation behavior of polylactic acid(PLA)plastic tableware and pure PLA un-der specific hydrothermal conditions(190℃).The physical and chemical changes in PLA before and after hydrothermal treatment were characterized using multiple analytical techniques,including mass loss measurements,scanning electron microscopy,high-performance liquid chromatography,and Fourier-transform infrared spectroscopy(FTIR).The kinet-ics of lactic acid generation and the evolution of macrostructure during hydrothermal depolymerization were systematically analyzed.Results indicated that solid-phase degradation of PLA reached completion(100%).The presence of lactic ac-id in solution significantly accelerated the hydrolysis of PLA without compromising the final lactic acid conversion yield(>90%).In contrast,common additives in PLA tableware,such as talc,cellulose,and other formulation compo-nents,moderately enhanced the initial hydrolysis rate but ultimately suppressed the lactic acid conversion efficiency.No-tably,polyethylene glycol exhibited a strong inhibitory effect on PLA hydrolysis.FTIR analysis revealed that hydrolysis proceeded primarily through cleavage of ester bonds,generating terminal—OH and—COOH groups.Consequently,the concentration of degradation products containing hydroxyl groups increased markedly,whereas the abundance of car-bonyl-containing species remained largely unchanged.
刘冠宇;胡方圆;王胤翔;李爱民
大连理工大学环境学院,辽宁 大连 116024大连理工大学环境学院,辽宁 大连 116024大连理工大学环境学院,辽宁 大连 116024大连理工大学环境学院,辽宁 大连 116024
化学化工
聚乳酸化学回收水热降解塑料单体
polylactic acidchemical recoveryhydrothermal degradationplastic monomers
《中国塑料》 2026 (1)
7-15,9
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