Largely toughened poly(lactic acid) fabricated by melt blending with thermoplastic polyurethane through interfacial compatibilization induced by simultaneous addition of hydrophobic silica nanoparticles and in situ cross‐linking reaction
{"title":"Largely toughened poly(lactic acid) fabricated by melt blending with thermoplastic polyurethane through interfacial compatibilization induced by simultaneous addition of hydrophobic silica nanoparticles and in situ cross‐linking reaction","authors":"Salar Haghjoo, Jafar Khademzadeh Yeganeh, Ismail Ghasemi","doi":"10.1002/pat.6514","DOIUrl":null,"url":null,"abstract":"Polylactic acid (PLA) has gained significant attention as a commercially available biodegradable and biocompatible polymer. However, the brittleness of PLA greatly limits its application. Blending PLA with another rubbery polymer such as thermoplastic polyurethane (TPU) is a simple strategy to toughen PLA. In this study, a largely toughened PLA has been successfully prepared by melt blending with TPU through interfacial compatibilization induced by the simultaneous addition of hydrophobic silica nanoparticles (NPs) and in situ cross‐linking reaction. The torque evolution during melt mixing and rheological analysis confirm a successful dynamic vulcanization process. Scanning electron microscopy images indicate that, dynamic vulcanization and adding NPs synergistically compatibilize the TPU and PLA phases leading to a considerable interfacial adhesion between the phases. Simultaneous addition of NPs at an optimum amount of 5 wt% and in situ cross‐linking reaction significantly improve the elongation at break, and tensile toughness of the PLA/TPU blend as they are achieved 311%, and 91 MJ/m<jats:sup>3</jats:sup>, respectively. Both dynamic vulcanization and NPs play their role independently in the compatibilization of PLA and TPU phases inducing substantial shear yielding of the matrix phase under stress resulting in a highly toughened blend. The microstructural properties of the blends are studied by rheological analysis.","PeriodicalId":20382,"journal":{"name":"Polymers for Advanced Technologies","volume":null,"pages":null},"PeriodicalIF":3.1000,"publicationDate":"2024-07-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Polymers for Advanced Technologies","FirstCategoryId":"5","ListUrlMain":"https://doi.org/10.1002/pat.6514","RegionNum":4,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"POLYMER SCIENCE","Score":null,"Total":0}
引用次数: 0
Abstract
Polylactic acid (PLA) has gained significant attention as a commercially available biodegradable and biocompatible polymer. However, the brittleness of PLA greatly limits its application. Blending PLA with another rubbery polymer such as thermoplastic polyurethane (TPU) is a simple strategy to toughen PLA. In this study, a largely toughened PLA has been successfully prepared by melt blending with TPU through interfacial compatibilization induced by the simultaneous addition of hydrophobic silica nanoparticles (NPs) and in situ cross‐linking reaction. The torque evolution during melt mixing and rheological analysis confirm a successful dynamic vulcanization process. Scanning electron microscopy images indicate that, dynamic vulcanization and adding NPs synergistically compatibilize the TPU and PLA phases leading to a considerable interfacial adhesion between the phases. Simultaneous addition of NPs at an optimum amount of 5 wt% and in situ cross‐linking reaction significantly improve the elongation at break, and tensile toughness of the PLA/TPU blend as they are achieved 311%, and 91 MJ/m3, respectively. Both dynamic vulcanization and NPs play their role independently in the compatibilization of PLA and TPU phases inducing substantial shear yielding of the matrix phase under stress resulting in a highly toughened blend. The microstructural properties of the blends are studied by rheological analysis.
期刊介绍:
Polymers for Advanced Technologies is published in response to recent significant changes in the patterns of materials research and development. Worldwide attention has been focused on the critical importance of materials in the creation of new devices and systems. It is now recognized that materials are often the limiting factor in bringing a new technical concept to fruition and that polymers are often the materials of choice in these demanding applications. A significant portion of the polymer research ongoing in the world is directly or indirectly related to the solution of complex, interdisciplinary problems whose successful resolution is necessary for achievement of broad system objectives.
Polymers for Advanced Technologies is focused to the interest of scientists and engineers from academia and industry who are participating in these new areas of polymer research and development. It is the intent of this journal to impact the polymer related advanced technologies to meet the challenge of the twenty-first century.
Polymers for Advanced Technologies aims at encouraging innovation, invention, imagination and creativity by providing a broad interdisciplinary platform for the presentation of new research and development concepts, theories and results which reflect the changing image and pace of modern polymer science and technology.
Polymers for Advanced Technologies aims at becoming the central organ of the new multi-disciplinary polymer oriented materials science of the highest scientific standards. It will publish original research papers on finished studies; communications limited to five typewritten pages plus three illustrations, containing experimental details; review articles of up to 40 pages; letters to the editor and book reviews. Review articles will normally be published by invitation. The Editor-in-Chief welcomes suggestions for reviews.