{"title":"用SAXS, WAXD和拉曼光谱评价聚乙烯固体应变硬化行为的温度依赖性","authors":"Sanshiro Kimura, Takumitsu Kida, Hiroki Takeshita, Katsuhisa Tokumitsu","doi":"10.1021/acs.macromol.5c00095","DOIUrl":null,"url":null,"abstract":"We investigated the effect of temperature on the strain-hardening behavior using Raman spectroscopy and small- and wide-angle X-ray scattering during uniaxial tensile tests. To accurately measure strain hardening, predrawn specimens elongated until the onset of the strain-hardening region were prepared. The temperature dependence of the strain-hardening modulus showed a maximum value at the crystalline-relaxation temperature (∼50 °C). For low-temperature stretching, the crystalline structure was disordered because of the strong stretching load applied to the crystalline chains. Moreover, the formation of a large number of highly loaded molecular chains, which we attributed to taut-tie chains, was revealed by Raman spectroscopy. However, for high-temperature stretching, the crystalline structure was stable in the strain-hardening region, and the stretching load was applied to the crystalline chains more homogeneously than under low-temperature stretching. Moreover, the contribution of plastic deformation was much greater for high-temperature than low-temperature stretching. This suggests that crystalline fragmentation occurred above the crystalline-relaxation temperature. Our results demonstrate that strain hardening proceeds with an increase in the entropy elasticity of taut-tie chains below the crystalline-relaxation temperature, resulting in a negative temperature dependence of the strain-hardening modulus. However, above the crystalline-relaxation temperature, plastic flow due to crystal fragmentation dominates strain hardening, resulting in a decrease in the strain-hardening modulus with increasing temperature.","PeriodicalId":51,"journal":{"name":"Macromolecules","volume":"127 1","pages":""},"PeriodicalIF":5.2000,"publicationDate":"2025-03-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Temperature Dependence of Strain-Hardening Behavior of Polyethylene Solids Evaluated by SAXS, WAXD, and Raman Spectroscopy\",\"authors\":\"Sanshiro Kimura, Takumitsu Kida, Hiroki Takeshita, Katsuhisa Tokumitsu\",\"doi\":\"10.1021/acs.macromol.5c00095\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"We investigated the effect of temperature on the strain-hardening behavior using Raman spectroscopy and small- and wide-angle X-ray scattering during uniaxial tensile tests. To accurately measure strain hardening, predrawn specimens elongated until the onset of the strain-hardening region were prepared. The temperature dependence of the strain-hardening modulus showed a maximum value at the crystalline-relaxation temperature (∼50 °C). For low-temperature stretching, the crystalline structure was disordered because of the strong stretching load applied to the crystalline chains. Moreover, the formation of a large number of highly loaded molecular chains, which we attributed to taut-tie chains, was revealed by Raman spectroscopy. However, for high-temperature stretching, the crystalline structure was stable in the strain-hardening region, and the stretching load was applied to the crystalline chains more homogeneously than under low-temperature stretching. Moreover, the contribution of plastic deformation was much greater for high-temperature than low-temperature stretching. This suggests that crystalline fragmentation occurred above the crystalline-relaxation temperature. Our results demonstrate that strain hardening proceeds with an increase in the entropy elasticity of taut-tie chains below the crystalline-relaxation temperature, resulting in a negative temperature dependence of the strain-hardening modulus. However, above the crystalline-relaxation temperature, plastic flow due to crystal fragmentation dominates strain hardening, resulting in a decrease in the strain-hardening modulus with increasing temperature.\",\"PeriodicalId\":51,\"journal\":{\"name\":\"Macromolecules\",\"volume\":\"127 1\",\"pages\":\"\"},\"PeriodicalIF\":5.2000,\"publicationDate\":\"2025-03-07\",\"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.5c00095\",\"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.5c00095","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"POLYMER SCIENCE","Score":null,"Total":0}
Temperature Dependence of Strain-Hardening Behavior of Polyethylene Solids Evaluated by SAXS, WAXD, and Raman Spectroscopy
We investigated the effect of temperature on the strain-hardening behavior using Raman spectroscopy and small- and wide-angle X-ray scattering during uniaxial tensile tests. To accurately measure strain hardening, predrawn specimens elongated until the onset of the strain-hardening region were prepared. The temperature dependence of the strain-hardening modulus showed a maximum value at the crystalline-relaxation temperature (∼50 °C). For low-temperature stretching, the crystalline structure was disordered because of the strong stretching load applied to the crystalline chains. Moreover, the formation of a large number of highly loaded molecular chains, which we attributed to taut-tie chains, was revealed by Raman spectroscopy. However, for high-temperature stretching, the crystalline structure was stable in the strain-hardening region, and the stretching load was applied to the crystalline chains more homogeneously than under low-temperature stretching. Moreover, the contribution of plastic deformation was much greater for high-temperature than low-temperature stretching. This suggests that crystalline fragmentation occurred above the crystalline-relaxation temperature. Our results demonstrate that strain hardening proceeds with an increase in the entropy elasticity of taut-tie chains below the crystalline-relaxation temperature, resulting in a negative temperature dependence of the strain-hardening modulus. However, above the crystalline-relaxation temperature, plastic flow due to crystal fragmentation dominates strain hardening, resulting in a decrease in the strain-hardening modulus with increasing temperature.
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.