Abstract

Relatively little is known about the effect of polyphosphoric acid (PPA) on bitumen chemistry and structure. In an effort to increase this understanding, the reaction of indole with PPA was studied by Fourier transform infrared spectroscopy (FTIR). Indole contains a pyrrole functional group very common in bitumen. The results revealed that both the amine and the double bond of indole can be reactive and that the indole concentration affected the reaction pathway. All reactions began with the protonation of the indole double bond, which provided two reactive carbocation intermediates. When the concentration of indole was high, each carbocation coupled with unprotonated indole and two products were obtained. In one case, two N−H groups produced a N−N bond, and in the other case, two indole double bonds produced a cyclobutane ring. When the concentration of indole was reduced by dilution, N−H coupling proceeded without double bonds coupling and a reaction with the PPA anion was found to occur instead. These ...

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