{"title":"聚氨酯微相载荷传递能力的分子尺度研究","authors":"Hongdeok Kim, Joonmyung Choi","doi":"10.1021/acs.macromol.4c01773","DOIUrl":null,"url":null,"abstract":"In this study, we investigated the mechanism by which the microphase structure of polyurethane (PU), manipulated by the chemical composition, determines its macroscopic mechanical properties. Increasing the hard segment content induced a microphase transition from globular to elongated to bicontinuous. This transition significantly altered the mechanical behavior of PU from hyperelastic to elasto-plastic. This enhancement in the mechanical properties was related to the load-transfer capacity of the hard domains in each microphase. In the globular phase, most of the strain energy was absorbed by the soft matrix, limiting the contribution of the hard phase to the mechanical properties. Conversely, elongated discontinuous structures facilitated a homogeneous strain distribution during tension, promoting an immediate load transfer to the hard domain. To quantitatively evaluate the load-transfer efficiency, a mechanical model in which one soft hyperelastic spring was coupled to two rigid elasto-plastic springs was considered. The effects of the microphase morphology and hard domain dissociation on the load-transfer capability were identified. This study contributes to a molecular-level understanding of the deformation behavior and mechanical response of microphase-separated PU.","PeriodicalId":51,"journal":{"name":"Macromolecules","volume":"6 1","pages":""},"PeriodicalIF":5.1000,"publicationDate":"2024-11-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Molecular-Scale Investigation of the Microphase-Dependent Load Transfer Capability of Polyurethane\",\"authors\":\"Hongdeok Kim, Joonmyung Choi\",\"doi\":\"10.1021/acs.macromol.4c01773\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"In this study, we investigated the mechanism by which the microphase structure of polyurethane (PU), manipulated by the chemical composition, determines its macroscopic mechanical properties. Increasing the hard segment content induced a microphase transition from globular to elongated to bicontinuous. This transition significantly altered the mechanical behavior of PU from hyperelastic to elasto-plastic. This enhancement in the mechanical properties was related to the load-transfer capacity of the hard domains in each microphase. In the globular phase, most of the strain energy was absorbed by the soft matrix, limiting the contribution of the hard phase to the mechanical properties. Conversely, elongated discontinuous structures facilitated a homogeneous strain distribution during tension, promoting an immediate load transfer to the hard domain. To quantitatively evaluate the load-transfer efficiency, a mechanical model in which one soft hyperelastic spring was coupled to two rigid elasto-plastic springs was considered. The effects of the microphase morphology and hard domain dissociation on the load-transfer capability were identified. This study contributes to a molecular-level understanding of the deformation behavior and mechanical response of microphase-separated PU.\",\"PeriodicalId\":51,\"journal\":{\"name\":\"Macromolecules\",\"volume\":\"6 1\",\"pages\":\"\"},\"PeriodicalIF\":5.1000,\"publicationDate\":\"2024-11-13\",\"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.4c01773\",\"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.4c01773","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"POLYMER SCIENCE","Score":null,"Total":0}
Molecular-Scale Investigation of the Microphase-Dependent Load Transfer Capability of Polyurethane
In this study, we investigated the mechanism by which the microphase structure of polyurethane (PU), manipulated by the chemical composition, determines its macroscopic mechanical properties. Increasing the hard segment content induced a microphase transition from globular to elongated to bicontinuous. This transition significantly altered the mechanical behavior of PU from hyperelastic to elasto-plastic. This enhancement in the mechanical properties was related to the load-transfer capacity of the hard domains in each microphase. In the globular phase, most of the strain energy was absorbed by the soft matrix, limiting the contribution of the hard phase to the mechanical properties. Conversely, elongated discontinuous structures facilitated a homogeneous strain distribution during tension, promoting an immediate load transfer to the hard domain. To quantitatively evaluate the load-transfer efficiency, a mechanical model in which one soft hyperelastic spring was coupled to two rigid elasto-plastic springs was considered. The effects of the microphase morphology and hard domain dissociation on the load-transfer capability were identified. This study contributes to a molecular-level understanding of the deformation behavior and mechanical response of microphase-separated PU.
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.