The Role of Chain Length in Nonergodicity Factor and Fragility of Polymers

Cecile Dalle-Ferrie, Kristine Niss, Alexei Sokolov, Bernhard Frick, Jorge Serrano, Christiane Alba-Simionesco

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

Resumé

The mechanism that leads to different fragility values upon approaching the glass transition remains a topic of active discussion. Many researchers are trying to find an answer in the properties of the frozen glassy state. Following this approach, we focus here on a previously proposed relationship between the fragility of glass-formers and their nonergodicity factor, determined by inelastic X-ray scattering (IXS) in the glass. We extend this molecular liquid study to two model polymers— polystyrene (PS) and polyisobutylene (PIB)—for which we change the molecular weight. Polymers offer the opportunity to change the fragility without altering the chemical structure, just by changing the chain length. Thus, we specifically chose PS and PIB because they exhibit opposite dependences of fragility with molecular weight. Our analysis for these two polymers reveals no unique correlation between the fragility and the nonergodicity parameter. Even after a recently suggested correction for a possible contribution of the β relaxation, the correlation is not restored. We discuss possible causes for the failure of the “fragility−nonergodicity factor” correlation, emphasizing the features that are specific to polymers. We speculate that polymers might have specific contributions to fragility related to the chain connectivity that are absent in nonpolymeric systems.
OriginalsprogEngelsk
TidsskriftMacromolecules
Vol/bind43
Udgave nummer21
Sider (fra-til)8977–8984
ISSN0024-9297
DOI
StatusUdgivet - 9 nov. 2010

Citer dette

Dalle-Ferrie, C., Niss, K., Sokolov, A., Frick, B., Serrano, J., & Alba-Simionesco, C. (2010). The Role of Chain Length in Nonergodicity Factor and Fragility of Polymers. Macromolecules, 43(21), 8977–8984. https://doi.org/10.1021/ma101622f
Dalle-Ferrie, Cecile ; Niss, Kristine ; Sokolov, Alexei ; Frick, Bernhard ; Serrano, Jorge ; Alba-Simionesco, Christiane. / The Role of Chain Length in Nonergodicity Factor and Fragility of Polymers. I: Macromolecules. 2010 ; Bind 43, Nr. 21. s. 8977–8984.
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Dalle-Ferrie, C, Niss, K, Sokolov, A, Frick, B, Serrano, J & Alba-Simionesco, C 2010, 'The Role of Chain Length in Nonergodicity Factor and Fragility of Polymers', Macromolecules, bind 43, nr. 21, s. 8977–8984. https://doi.org/10.1021/ma101622f

The Role of Chain Length in Nonergodicity Factor and Fragility of Polymers. / Dalle-Ferrie, Cecile; Niss, Kristine; Sokolov, Alexei; Frick, Bernhard; Serrano, Jorge; Alba-Simionesco, Christiane.

I: Macromolecules, Bind 43, Nr. 21, 09.11.2010, s. 8977–8984.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

TY - JOUR

T1 - The Role of Chain Length in Nonergodicity Factor and Fragility of Polymers

AU - Dalle-Ferrie, Cecile

AU - Niss, Kristine

AU - Sokolov, Alexei

AU - Frick, Bernhard

AU - Serrano, Jorge

AU - Alba-Simionesco, Christiane

PY - 2010/11/9

Y1 - 2010/11/9

N2 - The mechanism that leads to different fragility values upon approaching the glass transition remains a topic of active discussion. Many researchers are trying to find an answer in the properties of the frozen glassy state. Following this approach, we focus here on a previously proposed relationship between the fragility of glass-formers and their nonergodicity factor, determined by inelastic X-ray scattering (IXS) in the glass. We extend this molecular liquid study to two model polymers— polystyrene (PS) and polyisobutylene (PIB)—for which we change the molecular weight. Polymers offer the opportunity to change the fragility without altering the chemical structure, just by changing the chain length. Thus, we specifically chose PS and PIB because they exhibit opposite dependences of fragility with molecular weight. Our analysis for these two polymers reveals no unique correlation between the fragility and the nonergodicity parameter. Even after a recently suggested correction for a possible contribution of the β relaxation, the correlation is not restored. We discuss possible causes for the failure of the “fragility−nonergodicity factor” correlation, emphasizing the features that are specific to polymers. We speculate that polymers might have specific contributions to fragility related to the chain connectivity that are absent in nonpolymeric systems.

AB - The mechanism that leads to different fragility values upon approaching the glass transition remains a topic of active discussion. Many researchers are trying to find an answer in the properties of the frozen glassy state. Following this approach, we focus here on a previously proposed relationship between the fragility of glass-formers and their nonergodicity factor, determined by inelastic X-ray scattering (IXS) in the glass. We extend this molecular liquid study to two model polymers— polystyrene (PS) and polyisobutylene (PIB)—for which we change the molecular weight. Polymers offer the opportunity to change the fragility without altering the chemical structure, just by changing the chain length. Thus, we specifically chose PS and PIB because they exhibit opposite dependences of fragility with molecular weight. Our analysis for these two polymers reveals no unique correlation between the fragility and the nonergodicity parameter. Even after a recently suggested correction for a possible contribution of the β relaxation, the correlation is not restored. We discuss possible causes for the failure of the “fragility−nonergodicity factor” correlation, emphasizing the features that are specific to polymers. We speculate that polymers might have specific contributions to fragility related to the chain connectivity that are absent in nonpolymeric systems.

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JO - Macromolecules

JF - Macromolecules

SN - 0024-9297

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Dalle-Ferrie C, Niss K, Sokolov A, Frick B, Serrano J, Alba-Simionesco C. The Role of Chain Length in Nonergodicity Factor and Fragility of Polymers. Macromolecules. 2010 nov 9;43(21):8977–8984. https://doi.org/10.1021/ma101622f