Vulcanization represents a cornerstone of modern rubber technology, transforming raw polymers into durable, high-performance materials essential across automotive, healthcare, and industrial applications. By introducing crosslinks between polymer chains, vulcanization imparts elasticity, resilience, and strength unattainable in natural rubber alone. Various curing methods—including sulfur, peroxide, radiation, metal oxide, and resin systems—offer distinct advantages, with sulfur vulcanization remaining the most widely adopted due to its cost-effectiveness and versatility. Within sulfur systems, conventional (CV), semi-efficient (SEV), and efficient (EV) formulations highlight how subtle changes in sulfur-to-accelerator ratios influence crosslink structure, thermal stability, and resistance to reversion. Reversion, the thermal breakdown of polysulfidic crosslinks, poses a critical challenge, particularly in natural rubber. Anti-reversion agents such as N,N’-dibenzylthiocarbamoyldithio-hexane (BDzTH) and 1,3-Bis(citraconimidomethyl)benzene represent significant innovations, stabilizing rubber networks by converting unstable long sulfur chains into thermally robust hybrid linkages. These agents suppress torque decline, preserve mechanical integrity, and enhance performance under prolonged heat exposure. Their application yields improved compression set, reduced heat build-up, extended tire mileage, and enhanced durability in demanding environments. The evolution from conventional curing systems to advanced anti-reversion chemistry underscores the industry’s pursuit of balancing flexibility, strength, and thermal stability. By leveraging molecular design, modern vulcanization not only mitigates reversion but also expands the performance envelope of rubber, ensuring safety, efficiency, and longevity in critical applications.
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Goswami et al. (2026) studied this question.
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