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Thermal Properties of Plasticized Cellulose Acetate and Its β-Relaxation Phenomenon

Cellulose acetate (CA), an organic ester, is a biobased polymer which exhibits good mechanical properties (e.g., high Young’s modulus and tensile strength). In recent decades, there has been significant work done to verify the thermal and thermomechanical behaviors of raw and plasticized cellulose a...

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Autores principales: Erdmann, Rafael, Kabasci, Stephan, Heim, Hans-Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8122600/
https://www.ncbi.nlm.nih.gov/pubmed/33919294
http://dx.doi.org/10.3390/polym13091356
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author Erdmann, Rafael
Kabasci, Stephan
Heim, Hans-Peter
author_facet Erdmann, Rafael
Kabasci, Stephan
Heim, Hans-Peter
author_sort Erdmann, Rafael
collection PubMed
description Cellulose acetate (CA), an organic ester, is a biobased polymer which exhibits good mechanical properties (e.g., high Young’s modulus and tensile strength). In recent decades, there has been significant work done to verify the thermal and thermomechanical behaviors of raw and plasticized cellulose acetate. In this study, the thermomechanical properties of plasticized cellulose acetate—especially its [Formula: see text]-relaxation and activation energy—were investigated. The general thermal behavior was analyzed and compared with theoretical models. The study’s findings could be of special interest, due to the known [Formula: see text]-relaxation dependency of some polymers regarding mechanical properties—which could also be the case for cellulose acetate. However, this would require further investigation. The concentration of the plasticizers—glycerol triacetate (GTA) and triethyl citrate (TEC)—used in CA ranged from 15 to 40 wt%. DMTA measurements at varying frequencies were performed, and the activation energies of each relaxation were assessed. Increasing plasticizer content first led to a shift in [Formula: see text]-relaxation temperature to highervalues, then reached a maximum before declining again at higher concentrations. Furthermore, the activation energy of the [Formula: see text]-relaxation constantly rose with increases in plasticizer content. The trend in the [Formula: see text]-relaxation temperature of the plasticized CA could be interpreted as a change in the predominant phase of the overlapping [Formula: see text]-relaxation of the CA itself and the [Formula: see text]-relaxation of the plasticizer—which appears in the same temperature range. The plasticizer used (GTA) demonstrated a higher plasticization efficiency than TEC. The efficiencies of both plasticizers declined with increasing plasticizer content. Additionally, both plasticizers hit the saturation point (in CA) at the lowest studied concentration (15 wt%).
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spelling pubmed-81226002021-05-16 Thermal Properties of Plasticized Cellulose Acetate and Its β-Relaxation Phenomenon Erdmann, Rafael Kabasci, Stephan Heim, Hans-Peter Polymers (Basel) Article Cellulose acetate (CA), an organic ester, is a biobased polymer which exhibits good mechanical properties (e.g., high Young’s modulus and tensile strength). In recent decades, there has been significant work done to verify the thermal and thermomechanical behaviors of raw and plasticized cellulose acetate. In this study, the thermomechanical properties of plasticized cellulose acetate—especially its [Formula: see text]-relaxation and activation energy—were investigated. The general thermal behavior was analyzed and compared with theoretical models. The study’s findings could be of special interest, due to the known [Formula: see text]-relaxation dependency of some polymers regarding mechanical properties—which could also be the case for cellulose acetate. However, this would require further investigation. The concentration of the plasticizers—glycerol triacetate (GTA) and triethyl citrate (TEC)—used in CA ranged from 15 to 40 wt%. DMTA measurements at varying frequencies were performed, and the activation energies of each relaxation were assessed. Increasing plasticizer content first led to a shift in [Formula: see text]-relaxation temperature to highervalues, then reached a maximum before declining again at higher concentrations. Furthermore, the activation energy of the [Formula: see text]-relaxation constantly rose with increases in plasticizer content. The trend in the [Formula: see text]-relaxation temperature of the plasticized CA could be interpreted as a change in the predominant phase of the overlapping [Formula: see text]-relaxation of the CA itself and the [Formula: see text]-relaxation of the plasticizer—which appears in the same temperature range. The plasticizer used (GTA) demonstrated a higher plasticization efficiency than TEC. The efficiencies of both plasticizers declined with increasing plasticizer content. Additionally, both plasticizers hit the saturation point (in CA) at the lowest studied concentration (15 wt%). MDPI 2021-04-21 /pmc/articles/PMC8122600/ /pubmed/33919294 http://dx.doi.org/10.3390/polym13091356 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Erdmann, Rafael
Kabasci, Stephan
Heim, Hans-Peter
Thermal Properties of Plasticized Cellulose Acetate and Its β-Relaxation Phenomenon
title Thermal Properties of Plasticized Cellulose Acetate and Its β-Relaxation Phenomenon
title_full Thermal Properties of Plasticized Cellulose Acetate and Its β-Relaxation Phenomenon
title_fullStr Thermal Properties of Plasticized Cellulose Acetate and Its β-Relaxation Phenomenon
title_full_unstemmed Thermal Properties of Plasticized Cellulose Acetate and Its β-Relaxation Phenomenon
title_short Thermal Properties of Plasticized Cellulose Acetate and Its β-Relaxation Phenomenon
title_sort thermal properties of plasticized cellulose acetate and its β-relaxation phenomenon
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8122600/
https://www.ncbi.nlm.nih.gov/pubmed/33919294
http://dx.doi.org/10.3390/polym13091356
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