Abstract
Application of elastomers in general demands the conversion of their soluble networks into crosslinked structures. This abrupt change causes several modifications, both in the atomic/molecular level and at the macro-scale. In this study, solid silicone rubber (high molecular weight poly(dimethylsiloxane)), was crosslinked with dicumylperoxide (DCP), a widely used crosslinking agent by the rubber industry. The changes caused by different DCP concentrations were investigated, aiming to bring attention to the molecular transformations, usually neglected when processing-oriented studies are conducted. DCP concentration showed a limited contribution to the network's molecular dynamics, which was found to be mainly dominated by entanglements. The dominance of entanglements over other molecular constraints, like crosslink points, justifies the threshold and counter-intuitive behavior of tensile and hardness properties. However, differences were found in the crystallization ability after crosslinking, when the more crosslink points were introduced, the lower the crystallinity was and the less stable the PDMS crystallites were. In addition to providing a deeper understanding of an industrially applied rubber system n terms of the effective concentration of DCP, and the reasoning behind such concentration, the findings of this study add to the state-of-the-art comprehension of elastomeric networks, and how they behave on a molecular level.
Originalsprache | Englisch |
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Aufsatznummer | e54111 |
Seitenumfang | 17 |
Fachzeitschrift | Journal of applied polymer science |
Jahrgang | 140.2023 |
Ausgabenummer | 31 |
DOIs | |
Publikationsstatus | Veröffentlicht - 15 Aug. 2023 |
Bibliographische Notiz
Funding Information:The research work of this paper was performed at the Polymer Competence Center Leoben GmbH (PCCL, Austria) within the framework of the COMET‐program of the Federal Ministry for Climate Action, Environment, Energy, Mobility, Innovation and Technology and the Federal Ministry for Digital and Economic Affairs, with contributions from the Montanuniversitaet Leoben (Department of Polymer Engineering and Science, Polymer Processing and Materials Science and Testing of Polymers), Martin‐Luther Universitaet Halle‐Wittenberg (Institut für Physik ‐ NMR), Anton Paar GmbH, and Politecnico di Milano (Department of Aerospace Science and Technology). The authors kindly acknowledge Bernard Lechner and Gerald Meier for experimental support. PCCL is funded by the Austrian Government and the State Governments of Styria, Lower Austria, and Upper Austria.
Funding Information:
The research work of this paper was performed at the Polymer Competence Center Leoben GmbH (PCCL, Austria) within the framework of the COMET-program of the Federal Ministry for Climate Action, Environment, Energy, Mobility, Innovation and Technology and the Federal Ministry for Digital and Economic Affairs, with contributions from the Montanuniversitaet Leoben (Department of Polymer Engineering and Science, Polymer Processing and Materials Science and Testing of Polymers), Martin-Luther Universitaet Halle-Wittenberg (Institut für Physik - NMR), Anton Paar GmbH, and Politecnico di Milano (Department of Aerospace Science and Technology). The authors kindly acknowledge Bernard Lechner and Gerald Meier for experimental support. PCCL is funded by the Austrian Government and the State Governments of Styria, Lower Austria, and Upper Austria.
Publisher Copyright:
© 2023 The Authors. Journal of Applied Polymer Science published by Wiley Periodicals LLC.