{"title":"聚乳酸混合塑料中多个聚酯的一步解聚:工艺优化、纯单体提取及动力学评价","authors":"Olivia A. Attallah, Vasilisa Palkova, Ria Vij","doi":"10.1007/s10924-025-03523-6","DOIUrl":null,"url":null,"abstract":"<div><p>Nowadays, most of the chemical recycling approaches for plastic waste aim primarily for the depolymerization of single polymer plastics or the multiple steps depolymerization of a plastic mixture which in both cases is considered time, cost and energy consuming. Herein, we present an optimized, single step approach for non-catalyzed hydrolysis of multiple polyesters in Poly(lactic acid) (PLA) mixed plastics under mild conventional heating. The proposed depolymerization process simultaneously breaks down plastic polyesters (mainly PLA and polyethylene terephthalate (PET)) into their value-added monomers; lactic acid in the form of Ca lactate and terephthalic acid (TPA) which are further separated and purified in a reduced number of steps. Box-Behnken Design was employed to maximize the conversion of plastics and the yields of the produced monomers through optimization of the depolymerization and monomer extraction conditions, all while adhering to the green chemistry principles. Within 30 min, and at 85 ⁰C temperature, the proposed hydrolysis technique facilitated 83–100% conversion of various PLA products (PLA Polymaker fibers (containing PLA, PET and other additives), PLA pellets and postconsumer PLA cups) into 763.8-929.6 mg/g<sub>plastic</sub> Ca lactate and 51.5 mg/g<sub>plastic</sub> TPA if PET was present. The proposed non-catalyzed process followed first order reaction kinetics with a small activation energy of 78.92 kJ/mol, resulting in an acceptable total energy consumption of 176.0 kJ/g<sub>plastic</sub>. The obtained monomers’ identity and purity were confirmed by FTIR analysis. Additionally, the waste reagents produced during the depolymerization and monomer extraction processes were regenerated for reuse in another cycle of depolymerization while maintaining good performance. The developed approach offers an economically attractive and ecologically sustainable solution for energy and cost-efficient recycling and upcycling of post-consumer plastic waste containing PLA combined with other polyesters.</p></div>","PeriodicalId":659,"journal":{"name":"Journal of Polymers and the Environment","volume":"33 4","pages":"1897 - 1915"},"PeriodicalIF":4.7000,"publicationDate":"2025-02-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://link.springer.com/content/pdf/10.1007/s10924-025-03523-6.pdf","citationCount":"0","resultStr":"{\"title\":\"Single Step Depolymerization of Multiple Polyesters in Poly(Lactic Acid) Mixed Plastics: Process Optimization, Pure Monomers Extraction and Kinetics Evaluation\",\"authors\":\"Olivia A. Attallah, Vasilisa Palkova, Ria Vij\",\"doi\":\"10.1007/s10924-025-03523-6\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Nowadays, most of the chemical recycling approaches for plastic waste aim primarily for the depolymerization of single polymer plastics or the multiple steps depolymerization of a plastic mixture which in both cases is considered time, cost and energy consuming. Herein, we present an optimized, single step approach for non-catalyzed hydrolysis of multiple polyesters in Poly(lactic acid) (PLA) mixed plastics under mild conventional heating. The proposed depolymerization process simultaneously breaks down plastic polyesters (mainly PLA and polyethylene terephthalate (PET)) into their value-added monomers; lactic acid in the form of Ca lactate and terephthalic acid (TPA) which are further separated and purified in a reduced number of steps. Box-Behnken Design was employed to maximize the conversion of plastics and the yields of the produced monomers through optimization of the depolymerization and monomer extraction conditions, all while adhering to the green chemistry principles. Within 30 min, and at 85 ⁰C temperature, the proposed hydrolysis technique facilitated 83–100% conversion of various PLA products (PLA Polymaker fibers (containing PLA, PET and other additives), PLA pellets and postconsumer PLA cups) into 763.8-929.6 mg/g<sub>plastic</sub> Ca lactate and 51.5 mg/g<sub>plastic</sub> TPA if PET was present. The proposed non-catalyzed process followed first order reaction kinetics with a small activation energy of 78.92 kJ/mol, resulting in an acceptable total energy consumption of 176.0 kJ/g<sub>plastic</sub>. The obtained monomers’ identity and purity were confirmed by FTIR analysis. Additionally, the waste reagents produced during the depolymerization and monomer extraction processes were regenerated for reuse in another cycle of depolymerization while maintaining good performance. The developed approach offers an economically attractive and ecologically sustainable solution for energy and cost-efficient recycling and upcycling of post-consumer plastic waste containing PLA combined with other polyesters.</p></div>\",\"PeriodicalId\":659,\"journal\":{\"name\":\"Journal of Polymers and the Environment\",\"volume\":\"33 4\",\"pages\":\"1897 - 1915\"},\"PeriodicalIF\":4.7000,\"publicationDate\":\"2025-02-07\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://link.springer.com/content/pdf/10.1007/s10924-025-03523-6.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Polymers and the Environment\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://link.springer.com/article/10.1007/s10924-025-03523-6\",\"RegionNum\":3,\"RegionCategory\":\"工程技术\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"ENGINEERING, ENVIRONMENTAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Polymers and the Environment","FirstCategoryId":"5","ListUrlMain":"https://link.springer.com/article/10.1007/s10924-025-03523-6","RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENGINEERING, ENVIRONMENTAL","Score":null,"Total":0}
Single Step Depolymerization of Multiple Polyesters in Poly(Lactic Acid) Mixed Plastics: Process Optimization, Pure Monomers Extraction and Kinetics Evaluation
Nowadays, most of the chemical recycling approaches for plastic waste aim primarily for the depolymerization of single polymer plastics or the multiple steps depolymerization of a plastic mixture which in both cases is considered time, cost and energy consuming. Herein, we present an optimized, single step approach for non-catalyzed hydrolysis of multiple polyesters in Poly(lactic acid) (PLA) mixed plastics under mild conventional heating. The proposed depolymerization process simultaneously breaks down plastic polyesters (mainly PLA and polyethylene terephthalate (PET)) into their value-added monomers; lactic acid in the form of Ca lactate and terephthalic acid (TPA) which are further separated and purified in a reduced number of steps. Box-Behnken Design was employed to maximize the conversion of plastics and the yields of the produced monomers through optimization of the depolymerization and monomer extraction conditions, all while adhering to the green chemistry principles. Within 30 min, and at 85 ⁰C temperature, the proposed hydrolysis technique facilitated 83–100% conversion of various PLA products (PLA Polymaker fibers (containing PLA, PET and other additives), PLA pellets and postconsumer PLA cups) into 763.8-929.6 mg/gplastic Ca lactate and 51.5 mg/gplastic TPA if PET was present. The proposed non-catalyzed process followed first order reaction kinetics with a small activation energy of 78.92 kJ/mol, resulting in an acceptable total energy consumption of 176.0 kJ/gplastic. The obtained monomers’ identity and purity were confirmed by FTIR analysis. Additionally, the waste reagents produced during the depolymerization and monomer extraction processes were regenerated for reuse in another cycle of depolymerization while maintaining good performance. The developed approach offers an economically attractive and ecologically sustainable solution for energy and cost-efficient recycling and upcycling of post-consumer plastic waste containing PLA combined with other polyesters.
期刊介绍:
The Journal of Polymers and the Environment fills the need for an international forum in this diverse and rapidly expanding field. The journal serves a crucial role for the publication of information from a wide range of disciplines and is a central outlet for the publication of high-quality peer-reviewed original papers, review articles and short communications. The journal is intentionally interdisciplinary in regard to contributions and covers the following subjects - polymers, environmentally degradable polymers, and degradation pathways: biological, photochemical, oxidative and hydrolytic; new environmental materials: derived by chemical and biosynthetic routes; environmental blends and composites; developments in processing and reactive processing of environmental polymers; characterization of environmental materials: mechanical, physical, thermal, rheological, morphological, and others; recyclable polymers and plastics recycling environmental testing: in-laboratory simulations, outdoor exposures, and standardization of methodologies; environmental fate: end products and intermediates of biodegradation; microbiology and enzymology of polymer biodegradation; solid-waste management and public legislation specific to environmental polymers; and other related topics.