{"title":"Central Role of Filler–Polymer Interplay in Nonlinear Reinforcement of Elastomeric Nanocomposites","authors":"Pierre Kawak, Harshad Bhapkar, David S. Simmons","doi":"10.1021/acs.macromol.4c00489","DOIUrl":null,"url":null,"abstract":"Nanoparticles can greatly enhance the mechanical response of elastomeric polymers essential to a wide range of applications, yet their precise molecular mechanisms of high-strain reinforcement remain largely unresolved. In particular, long-standing questions endure over the extent to which glassy bridges or tie chains between particles are needed to facilitate reinforcement. Here we show, based on molecular dynamics simulations, that high-strain reinforcement emerges from an interplay between granular nanoparticulate compressive behavior in the normal direction and polymer incompressibility. This feedback loop, which is initiated by a mismatch in the Poisson ratios of the nanofiller and the polymer, invokes a contribution from the polymer’s bulk modulus to the elongational stress, while the tendency of the polymer to contract in the normal direction maintains a near-jammed filler state. This effect persists even once the direct filler elongational contribution becomes dissipative after the Payne effect yield, as a consequence of enduring filler normal stresses mediated by direct particle–particle contacts. These results indicate that direct particle–particle contact effects, even in the absence of potential augmenting mechanisms such as glassy polymer bridges, can drive the mechanical reinforcement effects typical of experimental systems.","PeriodicalId":51,"journal":{"name":"Macromolecules","volume":null,"pages":null},"PeriodicalIF":5.1000,"publicationDate":"2024-09-18","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.4c00489","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"POLYMER SCIENCE","Score":null,"Total":0}
引用次数: 0
Abstract
Nanoparticles can greatly enhance the mechanical response of elastomeric polymers essential to a wide range of applications, yet their precise molecular mechanisms of high-strain reinforcement remain largely unresolved. In particular, long-standing questions endure over the extent to which glassy bridges or tie chains between particles are needed to facilitate reinforcement. Here we show, based on molecular dynamics simulations, that high-strain reinforcement emerges from an interplay between granular nanoparticulate compressive behavior in the normal direction and polymer incompressibility. This feedback loop, which is initiated by a mismatch in the Poisson ratios of the nanofiller and the polymer, invokes a contribution from the polymer’s bulk modulus to the elongational stress, while the tendency of the polymer to contract in the normal direction maintains a near-jammed filler state. This effect persists even once the direct filler elongational contribution becomes dissipative after the Payne effect yield, as a consequence of enduring filler normal stresses mediated by direct particle–particle contacts. These results indicate that direct particle–particle contact effects, even in the absence of potential augmenting mechanisms such as glassy polymer bridges, can drive the mechanical reinforcement effects typical of experimental systems.
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.