Abstract:
Thermal degradation of acrylonitrile-butadiene rubber (NBR)-graphene oxide (GO)/reduced graphene Oxide (G) composites (NBR-GO/G) was studied in air O2(g) and nitrogen N2(g) media at ∼800°C, using Thermal Gravimetric Analysis (TGA/DTG). The char yield of the composites was high the in N2(g) medium. This was associated with lower weight loss (%) and higher maximum degradation temperatures, Tmax(°C). Doyle simple kinetic approach was used for the first time to estimate the degradation kinetics of the NBR-GO/G composites and large amounts of activation energy Ea (KJ/mol) was observed, particularly for the NBR-GO composites. In O2(g) medium, severe degradation of NBR occurred irrespective of the GO/G-filler content. This suggested that insignificant char yield was produced to protect the scission of the NBR backbone, as decomposition of the main chain seemed to have been accelerated by the high oxygenated moieties (C–O–C, –O–C=O and O–H) dec orating GO/G-sheets. For instance, NBR showed ∼89, ∼21 and ∼86 % weight residue, Wr (%) than G0.1, G0.5 and G1 respectively and ∼154, ∼350, ∼92 % higher than the respective GO0.1, GO0.5 and GO1 samples. Although, NBR-G recorded higher Wr(%) than NBR-GO, NBR-GO generally slowed the degradation of NBR than NBR-G composites, possibly due to the presence of high concentration of interactions (NBR—Sx—GO—S—NBR and NBR— O—Hσ +—N σ −—C—NBR) which raised the Ea (KJ/mol) barrier for decomposition. The high thermal stability and compression set (%) properties of NBR-GO/G composites obtained as compared to pure NBR indicated that solution processing techniques used in this current work was very effective than those compounded with melt mixing methods or with GO/G functionalized nanoparticles. Therefore, this present study provides insights on tailoring rubber-graphene based materials for thermally harsh and high pressure applications such as; oil/gas drilling hose, oil/gas seals, gasket and tire tread materials.
