Isoconversional Analysis of the Catalytic Pyrolysis of ABS, HIPS, PC and Their Blends with PP and PVC

Thermochemical recycling of plastics in the presence of catalysts is often employed to facilitate the degradation of polymers. The choice of the catalyst is polymer-oriented, while its selection becomes more difficult in the case of polymeric blends. The present investigation studies the catalytic pyrolysis of polymers abundant in waste electric and electronic equipment (WEEE), including poly(acrylonitrile-butadiene-styrene) (ABS), high-impact polystyrene (HIPS) and poly(bisphenol-A carbonate) (PC), along with their blends with polypropylene (PP) and poly(vinyl chloride) (PVC). The aim is to study the kinetic mechanism and estimate the catalysts' effect on the activation energy of the degradation. The chosen catalysts were Fe2O3 for ABS, Al-MCM-41 for HIPS, Al2O3 for PC, CaO for Blend A (comprising ABS, HIPS, PC and PP) and silicalite for Blend B (comprising ABS, HIPS, PC, PP and PVC). Thermogravimetric experiments were performed in a N2 atmosphere at several heating rates. Information on the degradation mechanism (degradation steps, initial and final degradation temperature, etc.) was attained. It was found that for pure (co)polymers, the catalytic degradation occurred in one-step, whereas in the case of the blends, two steps were required. For the estimation of the activation energy of those degradations, isoconversional kinetic models (integral and differential) were employed. In all cases, the catalysts used were efficient in reducing the estimated E alpha, compared to the values of E alpha obtained from conventional pyrolysis.