Catalytic degradation of high-density polyethylene over different zeolitic structures

The catalytic degradation of high-density polyethylene to hydrocarbons was studied over different zeolites. The product range was typically between C(3) and C(15) hydrocarbons. Distinctive patterns of product distribution were found with different zeolitic structures. Over large-pore ultrastable Y, Y, and beta zeolites, alkanes were the main products with less alkenes and aromatics and only very small amounts of cycloalkanes and cycloalkenes. Medium-pore mordenite and ZSM-5 gave significantly more olefins. In the medium-pore zeolites secondary bimolecular reactions were sterically hindered, resulting in higher amounts of alkenes as primary products. The hydrocarbons formed with medium-pore zeolites were lighter than those formed with large-pore zeolites. The following order was found regarding the carbon number distribution: (lighter products) ZSM-5 < mordenite < beta < Y < US-Y (heavier products). A similar order was found regarding the bond saturation: (more alkenes) ZSM-5 i mordenite < beta < Y < US-Y (more alkanes). Dependent upon the chosen zeolite, a variety of products was obtained with high values as fuel, confirming catalytic degradation of polymers as a promising method of waste plastic recycling.