{"title":"Dielectric anomalies in the β-relaxation of glassy 1,4-polybutadiene","authors":"C. Hansen, R. Richert","doi":"10.1002/actp.1997.010481104","DOIUrl":null,"url":null,"abstract":"<p>We have measured the dielectric relaxation of the polymeric glass-former 1,4-polybutadiene in the glassy and supercooled liquid state. The loss spectra ϵ″ of the β-relaxation are measured between the lower detection limit at <i>T</i> = 125 K and <i>T</i> = 225 K > <i>T</i><sub>β</sub>, with <i>T</i><sub>β</sub> ≈ 210 K being the α-β-merging temperature. The related storage data ϵ′(ω) indicates that the β-process is a signature of supressing the higher frequency polarization with increasing temperature, rather than giving rise to additional polarizability at frequencies below the average relaxation frequency of the β-process. This observation, as confirmed by data obtained for <i>o</i>-terphenyl and salol, contradicts the previous understandings of the mechanism underlying the Johari—Goldstein-type β-process in glasses. A tentative link between the β-process and high frequency vibrational modes is established.</p>","PeriodicalId":7162,"journal":{"name":"Acta Polymerica","volume":"48 11","pages":"484-489"},"PeriodicalIF":0.0000,"publicationDate":"2003-03-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/actp.1997.010481104","citationCount":"18","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Acta Polymerica","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/actp.1997.010481104","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 18
Abstract
We have measured the dielectric relaxation of the polymeric glass-former 1,4-polybutadiene in the glassy and supercooled liquid state. The loss spectra ϵ″ of the β-relaxation are measured between the lower detection limit at T = 125 K and T = 225 K > Tβ, with Tβ ≈ 210 K being the α-β-merging temperature. The related storage data ϵ′(ω) indicates that the β-process is a signature of supressing the higher frequency polarization with increasing temperature, rather than giving rise to additional polarizability at frequencies below the average relaxation frequency of the β-process. This observation, as confirmed by data obtained for o-terphenyl and salol, contradicts the previous understandings of the mechanism underlying the Johari—Goldstein-type β-process in glasses. A tentative link between the β-process and high frequency vibrational modes is established.