Samenvatting
We discuss the connection between high-temperature mechanics, block structure, and composition of a model series of industrially relevant, soft, thermoplastic elastomers (TPEs) containing polydisperse hard blocks (HBs). The high-strain deformation behavior of these materials results from the combination of multiple dynamics in the system, i.e., the HB associations and the mobile and entangled amorphous phase. Many soft-TPEs show a reduction in toughness with increasing temperature. Molecular weight (Mw) has been shown to improve the temperature-dependent mechanics by increasing network connectivity. In this work, we investigate the possibility to increase the network connectivity by tuning block length at constant Mw and composition. The average number of HBs per chain can be used to quantify network connectivity; however, by using block statistics, we show how increasing this value is not enough to increase the high-temperature mechanics, especially in the case of polydisperse HBs. Since temperature affects the HB ability to associate with each other, only the number of associated HBs per chain determines network connectivity. The experimental results are consistent with modeling predictions, revealing how decreasing the average block length influences the crystal stability, which ultimately controls network connectivity, and how this relationship is affected by temperature.
| Originele taal-2 | Engels |
|---|---|
| Pagina's (van-tot) | 177-185 |
| Aantal pagina's | 9 |
| Tijdschrift | Journal of Rheology |
| Volume | 66 |
| Nummer van het tijdschrift | 1 |
| DOI's | |
| Status | Gepubliceerd - 1 jan. 2022 |
Bibliografische nota
Funding Information:This work was financially supported by funding from the H2020 Program (MARIE SKŁODOWSKA-CURIE ACTIONS) of the European Commission’s Innovative Training Networks (No. H2020-MSCA-ITN-2017) under DoDyNet REA Grant Agreement No. 0.765811. The authors thankfully acknowledge Louis Pitet, Olga Goor, and the polyester lab in DSM for the synthesis of the model systems, Jildert Overdijk, Anouk van Graven, Junyu Li, and Carole-Ann Charles for the support with the FTIR, DMTA, x-ray, and tensile tests, respectively.
Publisher Copyright:
© 2021 The Society of Rheology.
Financiering
This work was financially supported by funding from the H2020 Program (MARIE SKŁODOWSKA-CURIE ACTIONS) of the European Commission’s Innovative Training Networks (No. H2020-MSCA-ITN-2017) under DoDyNet REA Grant Agreement No. 0.765811. The authors thankfully acknowledge Louis Pitet, Olga Goor, and the polyester lab in DSM for the synthesis of the model systems, Jildert Overdijk, Anouk van Graven, Junyu Li, and Carole-Ann Charles for the support with the FTIR, DMTA, x-ray, and tensile tests, respectively.
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