Understanding Rapid PET Degradation via Reactive Molecular Dynamics Simulation and Kinetic Modeling.

Abstract

As the demand for PET plastic products continues to grow, developing effective processes to reduce their pollution is of critical importance. Pyrolysis, a promising technology to produce lighter and recyclable components from wasted plastic products, has therefore received considerable attention. In this work, the rapid pyrolysis of PET was studied by using reactive molecular dynamics (MD) simulations. Mechanisms for yielding gas species were unraveled, which involve the generation of ethylene and TPA radicals from ester oxygen-alkyl carbon bond dissociation and condensation reactions to consume TPA radicals with the products of long chains containing a phenyl benzoate structure and CO2. As atomistic simulations are typically conducted at the time scale of a few nanoseconds, a high temperature (i.e., >1000 K) is adopted for accelerated reaction events. To apply the results from MD simulations to practical pyrolysis processes, a kinetic model based on a set of ordinary differential equations was established, which is capable of describing the key products of PET pyrolysis as a function of time and temperature. It was further exploited to determine the optimal reaction conditions for low environmental impact. Overall, this study conducted a detailed mechanism study of PET pyrolysis and established an effective kinetic model for the main species. The approach presented herein to extract kinetic information such as detailed kinetic constants and activation energies from atomistic MD simulations can also be applied to related systems such as the pyrolysis of other polymers.