Abstract
AbstractCoagents are vinyl monomers that react with free radicals formed by peroxide dissociation and are either grafted to elastomer chains or homopolymerized within a segregated phase to form a crosslinked network. The initial phase distribution within the elastomer matrix is of great importance for the final user properties of a composite material. In this study, the morphology of blends of each of three different coagents, that is, zinc dimethacrylate (ZDMA), N,N′‐m‐phenylene dimaleimide (HVA‐2), and trimethylolpropane trimethacrylate (TMPTMA) on a reinforcing substrate with dicumyl peroxide and hydrogenated acrylonitrile butadiene elastomer after processing was investigated with scanning electron microscopy. The morphology that evolved during processing was then compared to the results obtained from dynamic mechanical analysis (DMA) of the blends. Dynamic mechanical properties were modeled with a continuous relaxation distribution function, the Williams–Landel–Ferry equation, and the modified Guth–Gold equation. In the case of ZDMA and TMPTMA, a microphase and a nanophase evolved during processing, whereas the HVA‐2 phase in the blends remained well segregated. The volume fraction of the particles under 100 nm in ZDMA and TMPTMA blends ranged from 79 to 89%. The DMA results revealed the reinforcing effect of ZDMA and TMPTMA during the glass‐transition and in the plateau region, whereas HVA‐2 exhibited plasticizer‐like behavior. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008
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