(521o) Understanding the Adsorptive Behavior of Polymeric Materials to Catalyst Surfaces Using Various X-Ray Methods | AIChE

(521o) Understanding the Adsorptive Behavior of Polymeric Materials to Catalyst Surfaces Using Various X-Ray Methods

Authors 

Toney, M. F., SLAC National Accelerator Laboratory
Medlin, J. W., University of Colorado
Hydrogenolysis is an extremely effective method for plastic upcycling. Specifically, Ru-based catalysts supported on metal oxides have shown high reactivity for polyethylene upcycling. Polyethylene hydrogenolysis is an extremely structure-sensitive reaction, where product distribution depends on the size of the adsorbing alkyl chain and the hydrogen availability at the metal oxide support interface. However, surface science studies are required to characterize the structural impact of these dependencies directly.

To study the arrangement of hydrocarbons to the catalyst support, we utilize X-Ray Reflectivity (XRR) and Molecular Dynamics (MD) simulations, and to study the local chemical environment changes of the Ru active site, we utilize Extended X-Ray Adsorption Fine Edge Structure (EXAFS). By utilizing hydrocarbons of various lengths (methane, hexane, dodecane, triacontane, and low-density polyethylene), we will understand preferential adsorption arrangements for undesirable and desirable product species.

We theorize that as hydrocarbon chain length increases, the polymer will adsorb to the support with increased structural order, resulting in increased adsorption potential to the Ru active site. MD simulations of n-dodecane at various temperatures indicates that the preferential adsorption of species parallel to an alumina interface changes, and the application of the distorted crystal model confirms the viability of XRR as an experimental technique, as seen in the attached image. EXAFS data is currently being processed and will yield information about the local relaxation of Ru nanoparticles during species adsorption.

This work aims to understand the structure and arrangement of hydrocarbons to the active metal site and the support, thus allowing for fundamental concepts to be unified and expanded upon. We anticipate our results to inspire future surface science studies to explore how different polymers adsorb to the catalyst surface—ultimately allowing for the creation of catalysts capable of mixed-polymer hydrogenolysis and reduction of energy requirements for polymer upcycling.

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