TY - JOUR
T1 - Closed-Loop Recycling of Mixed Polyesters via Catalytic Methanolysis and Monomer Separations
AU - Curley, Julia
AU - Liang, Yuanzhe
AU - DesVeaux, Jason
AU - Choi, Hoon
AU - Clarke, Ryan
AU - Maurya, Anjani
AU - Michener, William
AU - Stanley, Lisa
AU - Wu, Yue
AU - Hesse, Sarah
AU - Baer, Andrea
AU - Neyer, Hudson
AU - Tassone, Christopher
AU - Jacobsen, Alan
AU - Mante, Ofei
AU - Beckham, Gregg
AU - Knauer, Katrina
PY - 2025
Y1 - 2025
N2 - A sustainable plastics future will require high recycling rates and the use of biogenic feedstocks, which together are catalyzing interest in replacing fossil fuel-derived, noncircular polyolefin packaging materials with bio-based, chemically recyclable polyesters. Here we present a catalytic methanolysis process capable of depolymerizing both fossil fuel- and bio-based polyesters, including polyethylene terephthalate (PET), polylactic acid, polybutylene adipate terephthalate and polybutylene succinate in one reactor under mild conditions with high monomer yields. We scaled this process to 1 kg and integrated separations engineering using activated carbon, crystallization, extraction and distillation to remove contaminants and recover individual monomers from depolymerized mixed polyesters with high yield and purity. PET synthesized from monomers isolated from postconsumer materials showed comparable mechanical and thermal properties to PET from commercial monomers. Techno-economic analysis and life cycle assessment show that this process is economically viable and exhibits lower environmental impacts than primary production of respective polymers.
AB - A sustainable plastics future will require high recycling rates and the use of biogenic feedstocks, which together are catalyzing interest in replacing fossil fuel-derived, noncircular polyolefin packaging materials with bio-based, chemically recyclable polyesters. Here we present a catalytic methanolysis process capable of depolymerizing both fossil fuel- and bio-based polyesters, including polyethylene terephthalate (PET), polylactic acid, polybutylene adipate terephthalate and polybutylene succinate in one reactor under mild conditions with high monomer yields. We scaled this process to 1 kg and integrated separations engineering using activated carbon, crystallization, extraction and distillation to remove contaminants and recover individual monomers from depolymerized mixed polyesters with high yield and purity. PET synthesized from monomers isolated from postconsumer materials showed comparable mechanical and thermal properties to PET from commercial monomers. Techno-economic analysis and life cycle assessment show that this process is economically viable and exhibits lower environmental impacts than primary production of respective polymers.
KW - catalytic methanolysis
KW - polybutylene adipate terephthalate (PBAT)
KW - polybutylene succinate (PBS)
KW - polyethylene terephthalate (PET)
KW - polylactic acid (PLA)
KW - recycling mixed polyesters
U2 - 10.1038/s44286-025-00275-x
DO - 10.1038/s44286-025-00275-x
M3 - Article
SN - 2948-1198
VL - 2
SP - 568
EP - 580
JO - Nature Chemical Engineering
JF - Nature Chemical Engineering
ER -