Chemical Aspects of Vulcanization
Abstract C. O. Weber was the first to give an elaborate theory of vulcanization. It is well known that he considered the hot vulcanization process as an addition of sulfur to polyprene (C10H16)n on account of the fact that no large amounts of hydrogen sulfide were evolved during the process. Wo. Ostwald, starting from quite the opposite point of view to Weber, put forward in 1910 the adsorption theory of vulcanization, considering it from an entirely colloidal standpoint, the sulfur being adsorbed by the rubber. It soon became clear that vulcanization was much more complex, and that neither of the two theories was able to explain the facts. Since then many investigations have been carried out, and many views, hypotheses, and theories on vulcanization put forward. If one tries to classify these, it becomes apparent that at the present time there is still a chemical theory and a colloidal theory of vulcanization. The chemical theory of vulcanization may be divided in two opposing hypotheses, viz.: (a) Polymerization of the rubber molecule, combination with sulfur being incidental. (b) Chemical combination of sulfur with rubber as the principal factor. To support this statement a few references and quotations from various investigators are given below.