{"title":"解缠超高分子量聚乙烯的结构形成和意外的超快再纠缠动力学","authors":"Zefan Wang, Biying Li, Fotis Christakopoulos, Kefeng Xie, Caizhen Zhu, Jian Xu, Alejandro J. Müller","doi":"10.1021/acs.macromol.4c01733","DOIUrl":null,"url":null,"abstract":"Because of the lack of constraints for crystallization, disentangled ultrahigh molecular weight polyethylene (UHMWPE) materials prepared by solution crystallization or low-temperature polymerization can exhibit ultrahigh drawability, making them ideal materials for producing fibers or tapes with ultrahigh modulus and strength. However, their ultrahigh drawability could vanish after a short annealing time applied above their melting temperature (<i>T</i><sub>m</sub>), hampering the aspiration of obtaining high-performance fibers using melt-spinning methods. The mechanism behind this loss of drawability has yet to be fully understood, and the time scale for reconstructing the entanglement networks is a controversial problem. In this work, we present a detailed comparison study of the structure formation of disentangled UHMWPE samples via solution-cast and low-temperature polymerization methods. All disentangled UHMWPE samples exhibit a relatively high crystallinity (above 70%) and similar lamellar stack morphologies. Constraints for forming UHMWPE crystals could be generated within a short time of melting, leading to lamellar stack structures made of widely distributed crystalline and amorphous layers. We revisit the high-temperature annealing effect (using thermal protocols proposed by Rastogi et al. <i>Macromolecules</i> <b>2016</b>, 49 (19), 7497–7509) on disentangled UHMWPE crystals via differential scanning calorimetry (DSC). The melting enthalpies in the final heating runs remain constant and are independent of the annealing time. Combining self-nucleation and flash DSC measurements, we found that the regeneration of entanglement networks occurs in an ultrashort time scale simultaneously accompanied by partial melting. The associated times are so small that they cannot be accurately determined. Our results reveal that the recovery time of entanglements does not follow the scaling law of τ ∼ <i>M</i><sup>3</sup> proposed by the classical reptation model.","PeriodicalId":51,"journal":{"name":"Macromolecules","volume":"28 1","pages":""},"PeriodicalIF":5.1000,"publicationDate":"2024-10-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Structure Formation and Unexpected Ultrafast Re-entanglement Dynamics of Disentangled Ultrahigh Molecular Weight Polyethylene\",\"authors\":\"Zefan Wang, Biying Li, Fotis Christakopoulos, Kefeng Xie, Caizhen Zhu, Jian Xu, Alejandro J. Müller\",\"doi\":\"10.1021/acs.macromol.4c01733\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Because of the lack of constraints for crystallization, disentangled ultrahigh molecular weight polyethylene (UHMWPE) materials prepared by solution crystallization or low-temperature polymerization can exhibit ultrahigh drawability, making them ideal materials for producing fibers or tapes with ultrahigh modulus and strength. However, their ultrahigh drawability could vanish after a short annealing time applied above their melting temperature (<i>T</i><sub>m</sub>), hampering the aspiration of obtaining high-performance fibers using melt-spinning methods. The mechanism behind this loss of drawability has yet to be fully understood, and the time scale for reconstructing the entanglement networks is a controversial problem. In this work, we present a detailed comparison study of the structure formation of disentangled UHMWPE samples via solution-cast and low-temperature polymerization methods. All disentangled UHMWPE samples exhibit a relatively high crystallinity (above 70%) and similar lamellar stack morphologies. Constraints for forming UHMWPE crystals could be generated within a short time of melting, leading to lamellar stack structures made of widely distributed crystalline and amorphous layers. We revisit the high-temperature annealing effect (using thermal protocols proposed by Rastogi et al. <i>Macromolecules</i> <b>2016</b>, 49 (19), 7497–7509) on disentangled UHMWPE crystals via differential scanning calorimetry (DSC). The melting enthalpies in the final heating runs remain constant and are independent of the annealing time. Combining self-nucleation and flash DSC measurements, we found that the regeneration of entanglement networks occurs in an ultrashort time scale simultaneously accompanied by partial melting. The associated times are so small that they cannot be accurately determined. Our results reveal that the recovery time of entanglements does not follow the scaling law of τ ∼ <i>M</i><sup>3</sup> proposed by the classical reptation model.\",\"PeriodicalId\":51,\"journal\":{\"name\":\"Macromolecules\",\"volume\":\"28 1\",\"pages\":\"\"},\"PeriodicalIF\":5.1000,\"publicationDate\":\"2024-10-23\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Macromolecules\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1021/acs.macromol.4c01733\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"POLYMER SCIENCE\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Macromolecules","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1021/acs.macromol.4c01733","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"POLYMER SCIENCE","Score":null,"Total":0}
Structure Formation and Unexpected Ultrafast Re-entanglement Dynamics of Disentangled Ultrahigh Molecular Weight Polyethylene
Because of the lack of constraints for crystallization, disentangled ultrahigh molecular weight polyethylene (UHMWPE) materials prepared by solution crystallization or low-temperature polymerization can exhibit ultrahigh drawability, making them ideal materials for producing fibers or tapes with ultrahigh modulus and strength. However, their ultrahigh drawability could vanish after a short annealing time applied above their melting temperature (Tm), hampering the aspiration of obtaining high-performance fibers using melt-spinning methods. The mechanism behind this loss of drawability has yet to be fully understood, and the time scale for reconstructing the entanglement networks is a controversial problem. In this work, we present a detailed comparison study of the structure formation of disentangled UHMWPE samples via solution-cast and low-temperature polymerization methods. All disentangled UHMWPE samples exhibit a relatively high crystallinity (above 70%) and similar lamellar stack morphologies. Constraints for forming UHMWPE crystals could be generated within a short time of melting, leading to lamellar stack structures made of widely distributed crystalline and amorphous layers. We revisit the high-temperature annealing effect (using thermal protocols proposed by Rastogi et al. Macromolecules2016, 49 (19), 7497–7509) on disentangled UHMWPE crystals via differential scanning calorimetry (DSC). The melting enthalpies in the final heating runs remain constant and are independent of the annealing time. Combining self-nucleation and flash DSC measurements, we found that the regeneration of entanglement networks occurs in an ultrashort time scale simultaneously accompanied by partial melting. The associated times are so small that they cannot be accurately determined. Our results reveal that the recovery time of entanglements does not follow the scaling law of τ ∼ M3 proposed by the classical reptation model.
期刊介绍:
Macromolecules publishes original, fundamental, and impactful research on all aspects of polymer science. Topics of interest include synthesis (e.g., controlled polymerizations, polymerization catalysis, post polymerization modification, new monomer structures and polymer architectures, and polymerization mechanisms/kinetics analysis); phase behavior, thermodynamics, dynamic, and ordering/disordering phenomena (e.g., self-assembly, gelation, crystallization, solution/melt/solid-state characteristics); structure and properties (e.g., mechanical and rheological properties, surface/interfacial characteristics, electronic and transport properties); new state of the art characterization (e.g., spectroscopy, scattering, microscopy, rheology), simulation (e.g., Monte Carlo, molecular dynamics, multi-scale/coarse-grained modeling), and theoretical methods. Renewable/sustainable polymers, polymer networks, responsive polymers, electro-, magneto- and opto-active macromolecules, inorganic polymers, charge-transporting polymers (ion-containing, semiconducting, and conducting), nanostructured polymers, and polymer composites are also of interest. Typical papers published in Macromolecules showcase important and innovative concepts, experimental methods/observations, and theoretical/computational approaches that demonstrate a fundamental advance in the understanding of polymers.