posted on 2025-03-27, 17:46authored byHyejin Yu, Younghoon Oh, Yu Lim Kim, Cong Liu, Kyobin Park, Hyun Gil Cha, Massimiliano Delferro, Donghyeon Kang
Polyethylene terephthalate (PET) depolymerization in
base/alcohol
hybrid systems represents a promising low-energy approach for chemically
recycling PET waste into valuable monomers. This study investigates
the mechanistic pathways of PET depolymerization in NaOH/alcohol solutions,
emphasizing the competing roles of hydroxide and alkoxide species.
Utilizing a combination of experimental techniques, density functional
theory (DFT) calculations, and molecular dynamics (MD) simulations,
we explore how factors such as base concentration, alcohol chain length,
and pKa values of alcohols influence PET
depolymerization efficiency and pathways. Our findings indicate that
alkoxide ions (RO–) exhibit notably higher reactivity
than hydroxide ions (HO–), favoring an alcoholysis
pathway in the base/alcohol hybrid system. Experimental results across
a series of C1 to C5 alcohols show that longer-chain alcohols, particularly
1-butanol, achieve higher PET conversion, although this does not align
solely with simple nucleophilicity trends of alkoxides. While DFT
calculations reveal comparable activation energies for various alkoxides
in PET depolymerization, MD simulations underscore the significant
role of alcohol chain length, with longer-chain alcohols forming more
stable or frequent interactions with PET. Additionally, the alkoxide
concentration, influenced by the alcohol’s pKa, directly impacts PET conversion. These suggest that
PET depolymerization is governed by a balance between alkoxide concentration
and alkoxide-PET interactions, rather than activation energies or
nucleophilicity alone. From a practical perspective, incorporating
long-chain alcohols as cosolvents may enhance process efficiency but
increases raw material costs by approximately 30%. However, long-chain
alcohols present a safer and more sustainable alternative to hazardous
cosolvents such as dichloromethane. This work offers a molecular-level
understanding of PET depolymerization in base/alcohol systems and
provides insights into optimizing these systems for more efficient
and sustainable PET recycling processes.