Upcycling waste polystyrene to adipic acid through a hybrid chemical and biological process

Oxidative catalytic depolymerization of polystyrene (PS) can produce benzoic acid, but the annual consumption of benzoic acid is ~40 times lower than PS. For this catalytic oxidation method to be a viable means to manage PS waste, benzoic acid should be converted to higher-volume chemicals. We demonstrate a hybrid chemical and biological process that uses PS as feedstock for production of adipic acid, a high-volume co-monomer for nylon 6,6 via benzoic acid. Mn/Br co-catalyzed autoxidation of PS to benzoic acid proceeds with a yield of up to 94% in a solvent mixture of benzoic acid and water. The PS-derived benzoic acid undergoes bioconversion at near-quantitative yield to muconic acid, which is readily converted to adipic acid through catalytic hydrogenation. Process modeling, techno-economic analysis, and life cycle assessment estimate an adipic acid minimum selling price of $3.18/kg, with a 61% decrease in greenhouse gas emissions relative to production from fossil fuels.

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Publication Details

Journal
Nature Communications
Published
2025-10-29
DOI
https://doi.org/10.1038/s41467-025-64561-1
Citations
2
Primary Topic
Polymer crystallization and properties
Type
article
Field-Weighted Citation Impact
1.21

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article

Upcycling waste polystyrene to adipic acid through a hybrid chemical and biological process

N. Meyer, Clarissa Lincoln, Joel Miscall, Gregg T. Beckham et al.
2 citations
Nature Communications
Polymer crystallization and properties
1.21
article

Upcycling waste polystyrene to adipic acid through a hybrid chemical and biological process

N. Meyer, Clarissa Lincoln, Joel Miscall, Gregg T. Beckham, Bruno Colling Klein, Davinia Salvachúa, Hyeongeon Lee, Stefan J. Haugen, Kwangjin An, Hannah Alt, Taylor Uekert, Christine A. Singer, Jason S. DesVeaux, Allison Z. Werner, Kelsey J. Ramirez, Shannon S. Stahl, Mikhail O. Konev, Christopher W. Johnson, Hyunjin Moon, Young-Saeng C. Avina, Elisabeth C. Van Roijen
article en
2 citations

Abstract

Oxidative catalytic depolymerization of polystyrene (PS) can produce benzoic acid, but the annual consumption of benzoic acid is ~40 times lower than PS. For this catalytic oxidation method to be a viable means to manage PS waste, benzoic acid should be converted to higher-volume chemicals. We demonstrate a hybrid chemical and biological process that uses PS as feedstock for production of adipic acid, a high-volume co-monomer for nylon 6,6 via benzoic acid. Mn/Br co-catalyzed autoxidation of PS to benzoic acid proceeds with a yield of up to 94% in a solvent mixture of benzoic acid and water. The PS-derived benzoic acid undergoes bioconversion at near-quantitative yield to muconic acid, which is readily converted to adipic acid through catalytic hydrogenation. Process modeling, techno-economic analysis, and life cycle assessment estimate an adipic acid minimum selling price of $3.18/kg, with a 61% decrease in greenhouse gas emissions relative to production from fossil fuels.

Nature CommunicationsVol. 16(1)
National Laboratory of the Rockies (US), University of Wisconsin–Madison (US), Stahl-Zentrum (Germany) (DE), Beckham Company (United States) (US), Ulsan National Institute of Science and Technology (KR)
U.S. Department of Energy, Office of Energy Efficiency and Renewable Energy, Bioenergy Technologies Office, Office of Energy Efficiency, National Renewable Energy Laboratory
Openalex Percentile: Top 19%
Polymer crystallization and properties
1.21
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