Poly(acrylonitrile-co-butadiene) as polymeric crosslinking accelerator for sulphur network formation

The major controlling factors that determine the various mechanical properties of an elastomer system are type of chemical crosslinking and crosslink density of the polymer network. In this study, a catalytic amount of acrylonitrile butadiene copolymer (NBR) was used as a co-accelerator for the curi...

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Veröffentlicht in:Heliyon 2020-08, Vol.6 (8), p.e04659-e04659, Article e04659
Hauptverfasser: Hait, Sakrit, Valentín, Juan López, Jiménez, Antonio González, Ortega, Pilar Bernal, Ghosh, Anik Kumar, Stöckelhuber, Klaus Werner, Wießner, Sven, Heinrich, Gert, Das, Amit
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Sprache:eng
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Zusammenfassung:The major controlling factors that determine the various mechanical properties of an elastomer system are type of chemical crosslinking and crosslink density of the polymer network. In this study, a catalytic amount of acrylonitrile butadiene copolymer (NBR) was used as a co-accelerator for the curing of polybutadiene (BR) elastomer. After the addition of this copolymer along with other conventional sulphur ingredients in polybutadiene compounds, a clear and distinct effect on the curing and other physical characteristics was noticed. The crosslinking density of BR was increased, as evidenced by rheometric properties, solid-state NMR and swelling studies. The vulcanization kinetics study revealed a substantial lowering of the activation energy of the sulphur crosslinking process when acrylonitrile butadiene copolymer was used in the formulation. The compounds were also prepared in the presence of carbon black and silica, and it was found that in the carbon black filled system the catalytic effect of the NBR was eminent. The effect was not only reflected in the mechanical performance but also the low-temperature crystallization behavior of BR systems was altered. Materials science; Materials chemistry; Crosslinking accelerator; Sulphur network; Solid state NMR; Curing kinetics; Activation energy; Acrylonitrile butadiene; Polybutadiene; Low-temperature; Crystallization.
ISSN:2405-8440
2405-8440
DOI:10.1016/j.heliyon.2020.e04659