Can Jiang , Peng Chen , Jianguo Mi , Xiangdong Wang
{"title":"高刚度高延性PET复合泡沫:E-EA-GMA与LCP/PTFE同步原位颤动的协同效应","authors":"Can Jiang , Peng Chen , Jianguo Mi , Xiangdong Wang","doi":"10.1016/j.polymer.2025.128646","DOIUrl":null,"url":null,"abstract":"<div><div>In polyethylene terephthalate (PET) matrix, the simultaneous in situ formation of elliptical ethylene–ethyl acrylate–glycidyl methacrylate (E-EA-GMA), liquid crystalline polymer (LCP) fibrils, and polytetrafluoroethylene (PTFE) fibrils enables the fabrication of PET composites with both high rigidity and high toughness. At an E-EA-GMA content of 10 wt%, the composite exhibits a tenfold increase in impact strength while maintaining rigidity. E–EA–GMA significantly promotes toughness, while LCP/PTFE fibrils effectively maintain rigidity.</div><div>This PET composite is further processed into PET foams with densities of 240 kg/m<sup>3</sup> (high density), 150 kg/m<sup>3</sup> (medium density), and 100 kg/m<sup>3</sup> (low density). Reducing foam density improves ductility, as evidenced by increased shear elongation at break. More importantly, the enhanced matrix toughness is closely linked to improved foam ductility, particularly in high-density foams, where this correlation becomes more pronounced. Within the PET foam structure, the E-EA-GMA component absorbs energy and undergoes plastic deformation, significantly increasing shear elongation at break. Meanwhile, the rigid rod-like LCP fibrils and flexible PTFE fibrils entangled networks, dispersed within the foam cell walls, provide structural support under external loads, effectively maintaining stiffness. This synergy results in simultaneous improvements in both stiffness and ductility, as evidenced by a 136 % increase in shear strength, a 39 % increase in compressive strength, and a 66 % increase in compressive modulus.</div><div>Although reducing foam density typically improves ductility at the expense of stiffness, the synergistic use of E-EA-GMA with in-situ fibrillation of LCP/PTFE successfully overcomes this trade-off, achieving PET foams with both high ductility and high stiffness.</div></div>","PeriodicalId":405,"journal":{"name":"Polymer","volume":"333 ","pages":"Article 128646"},"PeriodicalIF":4.5000,"publicationDate":"2025-06-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"PET composite foam with high stiffness and high ductility: Synergistic effect of Toughener combined with simultaneous in-situ fibrillation of LCP/PTFE\",\"authors\":\"Can Jiang , Peng Chen , Jianguo Mi , Xiangdong Wang\",\"doi\":\"10.1016/j.polymer.2025.128646\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>In polyethylene terephthalate (PET) matrix, the simultaneous in situ formation of elliptical ethylene–ethyl acrylate–glycidyl methacrylate (E-EA-GMA), liquid crystalline polymer (LCP) fibrils, and polytetrafluoroethylene (PTFE) fibrils enables the fabrication of PET composites with both high rigidity and high toughness. At an E-EA-GMA content of 10 wt%, the composite exhibits a tenfold increase in impact strength while maintaining rigidity. E–EA–GMA significantly promotes toughness, while LCP/PTFE fibrils effectively maintain rigidity.</div><div>This PET composite is further processed into PET foams with densities of 240 kg/m<sup>3</sup> (high density), 150 kg/m<sup>3</sup> (medium density), and 100 kg/m<sup>3</sup> (low density). Reducing foam density improves ductility, as evidenced by increased shear elongation at break. More importantly, the enhanced matrix toughness is closely linked to improved foam ductility, particularly in high-density foams, where this correlation becomes more pronounced. Within the PET foam structure, the E-EA-GMA component absorbs energy and undergoes plastic deformation, significantly increasing shear elongation at break. Meanwhile, the rigid rod-like LCP fibrils and flexible PTFE fibrils entangled networks, dispersed within the foam cell walls, provide structural support under external loads, effectively maintaining stiffness. This synergy results in simultaneous improvements in both stiffness and ductility, as evidenced by a 136 % increase in shear strength, a 39 % increase in compressive strength, and a 66 % increase in compressive modulus.</div><div>Although reducing foam density typically improves ductility at the expense of stiffness, the synergistic use of E-EA-GMA with in-situ fibrillation of LCP/PTFE successfully overcomes this trade-off, achieving PET foams with both high ductility and high stiffness.</div></div>\",\"PeriodicalId\":405,\"journal\":{\"name\":\"Polymer\",\"volume\":\"333 \",\"pages\":\"Article 128646\"},\"PeriodicalIF\":4.5000,\"publicationDate\":\"2025-06-03\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Polymer\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0032386125006329\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"POLYMER SCIENCE\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Polymer","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0032386125006329","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"POLYMER SCIENCE","Score":null,"Total":0}
PET composite foam with high stiffness and high ductility: Synergistic effect of Toughener combined with simultaneous in-situ fibrillation of LCP/PTFE
In polyethylene terephthalate (PET) matrix, the simultaneous in situ formation of elliptical ethylene–ethyl acrylate–glycidyl methacrylate (E-EA-GMA), liquid crystalline polymer (LCP) fibrils, and polytetrafluoroethylene (PTFE) fibrils enables the fabrication of PET composites with both high rigidity and high toughness. At an E-EA-GMA content of 10 wt%, the composite exhibits a tenfold increase in impact strength while maintaining rigidity. E–EA–GMA significantly promotes toughness, while LCP/PTFE fibrils effectively maintain rigidity.
This PET composite is further processed into PET foams with densities of 240 kg/m3 (high density), 150 kg/m3 (medium density), and 100 kg/m3 (low density). Reducing foam density improves ductility, as evidenced by increased shear elongation at break. More importantly, the enhanced matrix toughness is closely linked to improved foam ductility, particularly in high-density foams, where this correlation becomes more pronounced. Within the PET foam structure, the E-EA-GMA component absorbs energy and undergoes plastic deformation, significantly increasing shear elongation at break. Meanwhile, the rigid rod-like LCP fibrils and flexible PTFE fibrils entangled networks, dispersed within the foam cell walls, provide structural support under external loads, effectively maintaining stiffness. This synergy results in simultaneous improvements in both stiffness and ductility, as evidenced by a 136 % increase in shear strength, a 39 % increase in compressive strength, and a 66 % increase in compressive modulus.
Although reducing foam density typically improves ductility at the expense of stiffness, the synergistic use of E-EA-GMA with in-situ fibrillation of LCP/PTFE successfully overcomes this trade-off, achieving PET foams with both high ductility and high stiffness.
期刊介绍:
Polymer is an interdisciplinary journal dedicated to publishing innovative and significant advances in Polymer Physics, Chemistry and Technology. We welcome submissions on polymer hybrids, nanocomposites, characterisation and self-assembly. Polymer also publishes work on the technological application of polymers in energy and optoelectronics.
The main scope is covered but not limited to the following core areas:
Polymer Materials
Nanocomposites and hybrid nanomaterials
Polymer blends, films, fibres, networks and porous materials
Physical Characterization
Characterisation, modelling and simulation* of molecular and materials properties in bulk, solution, and thin films
Polymer Engineering
Advanced multiscale processing methods
Polymer Synthesis, Modification and Self-assembly
Including designer polymer architectures, mechanisms and kinetics, and supramolecular polymerization
Technological Applications
Polymers for energy generation and storage
Polymer membranes for separation technology
Polymers for opto- and microelectronics.