posted on 2021-10-14, 18:08authored byBernard Whajah, Natalia da Silva Moura, Justin Blanchard, Scott Wicker, Karleigh Gandar, James A. Dorman, Kerry M. Dooley
Low-
and high-density polyethylene (LDPE/HDPE) have been selectively
depolymerized, without added H2, to C2–C20 + alkanes/alkenes
via energy-efficient radio frequency induction heating, coupled with
dual-functional heterogeneous Fe3O4 and Ni-
or Pt-based catalysts. Fe3O4 was used to locally
generate heat when exposed to magnetic fields. Initial results indicate
that zeolite-based Ni catalysts are more selective to light olefins,
while Ni supported on ceria catalysts are more selective to C7–C14
alkanes/alkenes. LDPE conversions up to 94% were obtained with minimal
aromatic, coke, or methane formation which are typically observed
with thermal heating. Two depolymerization mechanisms, a reverse Cossee–Arlman
mechanism or a random cleavage process, were proposed to account for
the different selectivities. The depolymerization process was also
tested on commercial LDPE (grocery bags), polystyrene, and virgin
HDPE using the Ni on Fe3O4 catalyst, with the
LDPE resulting in similar product conversion (∼48%) and selectivity
as for virgin LDPE.