It is generally believed that only intermolecular, elastically-effective crosslinks influence elastomer properties. The role of the intramolecular modifications of the polymer chains is marginalized. The aim of our study was the characterization of the structural parameters of cured elastomers, and determination of their influence on the behavior of the polymer network. For this purpose, styrene-butadiene rubbers (SBR), cured with various curatives, such as DCP, TMTD, TBzTD, Vulcuren^®, DPG/S₈, CBS/S₈, MBTS/S₈ and ZDT/S₈, were investigated. In every series of samples a broad range of crosslink density was obtained, in addition to diverse crosslink structures, as determined by equilibrium swelling and thiol-amine analysis. Differential scanning calorimetry (DSC) and dynamic mechanical analysis (DMA) were used to study the glass transition process, and positron annihilation lifetime spectroscopy (PALS) to investigate the size of the free volumes. For all samples, the values of the glass transition temperature (T_g) increased with a rise in crosslink density. At the same time, the free volume size proportionally decreased. The changes in T_g and free volume size show significant differences between the series crosslinked with various curatives. These variations are explained on the basis of the curatives’ structure effect. Furthermore, basic structure-property relationships are provided. They enable the prediction of the effect of curatives on the structural parameters of the network, and some of the resulting properties. It is proved that the applied techniques—DSC, DMA, and PALS—can serve to provide information about the modifications to the polymer chains. Moreover, on the basis of the obtained results and considering the diversified curatives available nowadays, the usability of “part per hundred rubber” (phr) unit is questioned.

Considerable attention is paid to the influence of crosslink density and crosslink structures on the behavior of polymer chains and properties of elastomers. However, a very important parameter seems to be underestimated: the modifications to the polymer chains by curatives, formed by sulfur and fragments of accelerators. We draw attention to this important contribution to performance of spatial networks. The emulsion styrene–butadiene rubber samples, cured with tetramethylthiuram disulfide and sulfur (TMTD/S₈) and zinc dialkyl dithiophosphate with sulfur (ZDT/S₈), were studied. They were characterized in detail in terms of crosslink density and crosslink structures. Microscale techniques were used to obtain information about the behavior of the polymer chains: positron annihilation lifetime spectroscopy (PALS) to study the free volume structure and differential scanning calorimetry (DSC) and dynamic mechanical analysis (DMA) to monitor the glass transition process. Properties such as static mechanical performance and thermo-oxidative stability were also evaluated. All of the investigated characteristics were influenced by a combination of crosslink density, crosslink structures, and, to a large extent, by the modifications of the polymer chains. The effect of the modifications is dependent on the amount and the structure of the curatives' molecules. On the basis of the obtained results, the usefulness of the “phr” unit used for calculation of the curatives' amount has been queried. Furthermore, it has been demonstrated that DSC, DMA, and PALS techniques can provide evidence for the presence of the modifications on the polymer chain by curatives.