Abstract
NMR relaxometry showed that, in spite of its small proportion in the composition of the macrochain, corresponding to the “small additive” range (≤5 parts), the cyclic component has a considerable effect on the structural and dynamic state of ternary copolymeric ethylene–propylene rubber in a blend with chlorosulphonated polyethylene owing to the topochemical processes occurring during mixing of the polymers. The results obtained also indicate the most probable or stable centres of intermolecular interactions of a non-chemical nature that determine the short-range conformational order in the given blends.
Get full access to this article
View all access options for this article.
