Abstract
The work of Farmer and other authors has shown that the oxidation of unsaturated polymers proceeds via primary formed hydroperoxides. The addition of antioxidants, including chiefly compounds of the class of the phenols and secondary aromatic amines, makes it possible to delay to a great extent the chemical changes taking place in unsaturated compounds. The mechanism of the action of phenols in the oxidation has been explained by Bolland. It is difficult to separate from the polymer the reaction products which are formed from the antioxidant by the dehydrogenating action of the polymeric hydroperoxide radical. In view of the fact, however, that the kinetics of oxidation in the presence of added peroxide corresponds to the autoxidation of the unsaturated compound, the reaction between phenols or secondary aromatic amines and organic or inorganic oxidation agents has been studied in detail by several workers. Depending on type, position, and number of the substituents, different reaction products are formed from phenols. Diphenylamine reacts with manganese dioxide to form a mixture of N,N′-diphenylbenzidine and the corresponding quinonedianil. N,N,N′-tri-2-naphthyl-1,2-naphthylenediamine is formed from di-2-naphthylamine with potassium permanganate, whereas under similar conditions phenyl-2-naphthylamine forms N,N′-diphenyl-N-2-naphthyl-1,2-naphthylenediamine. Starting from the deduction that the chemical reaction products of the antioxidants accumulate on the surface of the vulcanized rubber due to decreasing solubility, pure gum stocks of cured natural rubber containing diphenylamine, N-phenyl-1- and 2-naphthylamine have been exposed to atmospheric conditions for 8 months. The dark colored reaction products could be removed mechanically from the surface of the cured goods after wetting with methanol. After evaporation, the residue was taken up in ethylidene chloride and the resulting solution evaporated to dryness. Amorphous mixtures of brown colored compounds were isolated from the vulcanizate containing diphenylamine and N-phenyl-2-naphthylamine, the reaction products of the N-phenyl-2-napthylamine being obtained as a dark colored tar. In addition to other compounds, the presence of the N,N′-diphenyl-N-2-naphthyl-1,2-naphthylenediamine was proved by paper partition chromatography of the resulting azodyestuff obtained from the mixture of the reaction products from phenyl-2-naphthylamine by coupling with diazotized 1-aminonaphthalene trisulfonic acid. The presence of this compound had also been shown by the ultraviolet spectra. In the same manner, small quantities of the N,N′-diphenylbenzidine could be recognized from the corresponding azodyestuff formed from the reaction product of diphenylamine. Due to extensive oxidation, the presence of reaction products could not be proved in any appreciable quantity from the reaction mixture of the phenyl-1-naphthylamine.