Vitrimer Transition Phenomena from the Perspective of Thermal Volume Expansion and Shape (In)stability

Publikationen: Beitrag in FachzeitschriftArtikelForschung(peer-reviewed)

Standard

Vitrimer Transition Phenomena from the Perspective of Thermal Volume Expansion and Shape (In)stability. / Klingler, Andreas; Reisinger, David; Schlögl, Sandra et al.
in: Macromolecules, Jahrgang 57.2024, Nr. 9, 25.04.2024, S. 4246-4253.

Publikationen: Beitrag in FachzeitschriftArtikelForschung(peer-reviewed)

Harvard

APA

Klingler, A., Reisinger, D., Schlögl, S., Wetzel, B., Breuer, U., & Krüger, J. K. (2024). Vitrimer Transition Phenomena from the Perspective of Thermal Volume Expansion and Shape (In)stability. Macromolecules, 57.2024(9), 4246-4253. Vorzeitige Online-Publikation. https://doi.org/10.1021/acs.macromol.4c00207

Vancouver

Klingler A, Reisinger D, Schlögl S, Wetzel B, Breuer U, Krüger JK. Vitrimer Transition Phenomena from the Perspective of Thermal Volume Expansion and Shape (In)stability. Macromolecules. 2024 Apr 25;57.2024(9):4246-4253. Epub 2024 Apr 25. doi: 10.1021/acs.macromol.4c00207

Author

Klingler, Andreas ; Reisinger, David ; Schlögl, Sandra et al. / Vitrimer Transition Phenomena from the Perspective of Thermal Volume Expansion and Shape (In)stability. in: Macromolecules. 2024 ; Jahrgang 57.2024, Nr. 9. S. 4246-4253.

Bibtex - Download

@article{22c94dc8e94a4a1db876e1dc4d24d52c,
title = "Vitrimer Transition Phenomena from the Perspective of Thermal Volume Expansion and Shape (In)stability",
abstract = "Vitrimers are covalently cross-linked polymers that can be reshaped and recycled, triggered by the temperature. Well above the canonical glass transition temperature Tg, they gain malleable, thermoplastic-like properties; below, they behave as thermosets. The responsible molecular mechanism is enabled by dynamic covalent bond exchange. However, the underlying physics of the transition from thermoplastic to thermoset properties is rather unclear and the subject of current scientific debate. In this work, we address the questions of what extent the temperature-dependent malleability of vitrimers is reflected in the thermal expansion behavior and, conversely, to what extent the thermal expansion behavior is suited to characterize the respective creep behavior of vitrimers. It will be shown that at least in the case of the used model vitrimer, only the canonical glass transition is able to stop the vitrimer to undergo irreversible shape changes and that the often-discussed topology freezing temperature of vitrimers Tv is purely operational.",
author = "Andreas Klingler and David Reisinger and Sandra Schl{\"o}gl and Bernd Wetzel and Ulf Breuer and Kr{\"u}ger, {Jan Kristian}",
note = "Publisher Copyright: {\textcopyright} 2024 The Authors. Published by American Chemical Society.",
year = "2024",
month = apr,
day = "25",
doi = "10.1021/acs.macromol.4c00207",
language = "English",
volume = "57.2024",
pages = "4246--4253",
journal = "Macromolecules",
issn = "0024-9297",
publisher = "American Chemical Society",
number = "9",

}

RIS (suitable for import to EndNote) - Download

TY - JOUR

T1 - Vitrimer Transition Phenomena from the Perspective of Thermal Volume Expansion and Shape (In)stability

AU - Klingler, Andreas

AU - Reisinger, David

AU - Schlögl, Sandra

AU - Wetzel, Bernd

AU - Breuer, Ulf

AU - Krüger, Jan Kristian

N1 - Publisher Copyright: © 2024 The Authors. Published by American Chemical Society.

PY - 2024/4/25

Y1 - 2024/4/25

N2 - Vitrimers are covalently cross-linked polymers that can be reshaped and recycled, triggered by the temperature. Well above the canonical glass transition temperature Tg, they gain malleable, thermoplastic-like properties; below, they behave as thermosets. The responsible molecular mechanism is enabled by dynamic covalent bond exchange. However, the underlying physics of the transition from thermoplastic to thermoset properties is rather unclear and the subject of current scientific debate. In this work, we address the questions of what extent the temperature-dependent malleability of vitrimers is reflected in the thermal expansion behavior and, conversely, to what extent the thermal expansion behavior is suited to characterize the respective creep behavior of vitrimers. It will be shown that at least in the case of the used model vitrimer, only the canonical glass transition is able to stop the vitrimer to undergo irreversible shape changes and that the often-discussed topology freezing temperature of vitrimers Tv is purely operational.

AB - Vitrimers are covalently cross-linked polymers that can be reshaped and recycled, triggered by the temperature. Well above the canonical glass transition temperature Tg, they gain malleable, thermoplastic-like properties; below, they behave as thermosets. The responsible molecular mechanism is enabled by dynamic covalent bond exchange. However, the underlying physics of the transition from thermoplastic to thermoset properties is rather unclear and the subject of current scientific debate. In this work, we address the questions of what extent the temperature-dependent malleability of vitrimers is reflected in the thermal expansion behavior and, conversely, to what extent the thermal expansion behavior is suited to characterize the respective creep behavior of vitrimers. It will be shown that at least in the case of the used model vitrimer, only the canonical glass transition is able to stop the vitrimer to undergo irreversible shape changes and that the often-discussed topology freezing temperature of vitrimers Tv is purely operational.

UR - http://www.scopus.com/inward/record.url?scp=85191806203&partnerID=8YFLogxK

U2 - 10.1021/acs.macromol.4c00207

DO - 10.1021/acs.macromol.4c00207

M3 - Article

AN - SCOPUS:85191806203

VL - 57.2024

SP - 4246

EP - 4253

JO - Macromolecules

JF - Macromolecules

SN - 0024-9297

IS - 9

ER -