Selective Recycling of Mixed Polyesters via Heterogeneous Photothermal Catalysis

Y Yu Liu P Penglei Yan X Xiaodong Li (Hefei National Research Center for Physical Sciences at the Microscale, State Key Laboratory of Precision and Intelligent Chemistry) Q Qingye Li (State Key Laboratory of Bioinspired Interfacial Materials Science Institute of Functional Nano & Soft Materials (FUNSOM) Soochow University Suzhou 215123 P.R. China) S Shengming Li (School of Control Science and Engineering) H Hao Han M Mingyu Chu (Institute of Functional Nano and Soft Materials (FUNSOM), Jiangsu Key Laboratory of Advanced Negative Carbon Technologies, Soochow University, 199 Ren’ai Road, Suzhou, Jiangsu 215123, China) J Jie Fu (Institute of Functional Nano and Soft Materials (FUNSOM), Jiangsu Key Laboratory of Advanced Negative Carbon Technologies, Soochow University, 199 Ren’ai Road, Suzhou, Jiangsu 215123, China) M Muhan Cao (Institute of Functional Nano and Soft Materials (FUNSOM), Jiangsu Key Laboratory of Advanced Negative Carbon Technologies, Soochow University, 199 Ren’ai Road, Suzhou, Jiangsu 215123, China) P Panpan Xu Q Qiao Zhang L Le He (Institute of Functional Nano & Soft Materials (FUNSOM), Jiangsu Key Laboratory of Advanced Negative Carbon Technologies) J Jinxing Chen (Department of Chemistry)

Abstract

AbstractThe selective recycling of mixed plastic wastes with similar structural units is challenging. While heterogeneous catalysis shows potential for selective recycling, challenges such as complex mass transfer at multiphase interfaces and unclear catalytic mechanisms have slowed progress. In this study, a breakthrough in recycling mixed polyester wastes is introduced using heterogeneous photothermal catalysis. By adding co‐solvents, the difficulties associated with multiphase interfacial mass transfer are overcome. Grain boundary (GB)‐rich CeO2 photothermal catalysts are used to selectively glycolyze mixed poly(ethylene terephthalate) (PET) and poly(bisphenol A carbonate) (PC) plastics into bisphenol A (BPA) and bis(2‐hydroxyethyl) terephthalate (BHET), achieving yields of 97.8% and 93.4%, respectively. The high concentration of oxygen vacancies in GB‐rich CeO2 catalysts adjusts the adsorption energy of intermediates, leading to more selective and efficient depolymerization compared to GB‐poor CeO2 catalysts. The economic and environmental analysis demonstrates that this process, which utilizes heterogeneous photothermal catalysis, provides significant energy savings and carbon reduction, representing a major advancement in mixed plastic waste recycling.

Article Details

Volume / Issue Vol. 37, Issue 7
Published February 01, 2025
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (13)

Y

Yu Liu

P

Penglei Yan

X

Xiaodong Li

Hefei National Research Center for Physical Sciences at the Microscale, State Key Laboratory of Precision and Intelligent Chemistry

Q

Qingye Li

State Key Laboratory of Bioinspired Interfacial Materials Science Institute of Functional Nano & Soft Materials (FUNSOM) Soochow University Suzhou 215123 P.R. China

S

Shengming Li

School of Control Science and Engineering

H

Hao Han

M

Mingyu Chu

Institute of Functional Nano and Soft Materials (FUNSOM), Jiangsu Key Laboratory of Advanced Negative Carbon Technologies, Soochow University, 199 Ren’ai Road, Suzhou, Jiangsu 215123, China

J

Jie Fu

Institute of Functional Nano and Soft Materials (FUNSOM), Jiangsu Key Laboratory of Advanced Negative Carbon Technologies, Soochow University, 199 Ren’ai Road, Suzhou, Jiangsu 215123, China

M

Muhan Cao

Institute of Functional Nano and Soft Materials (FUNSOM), Jiangsu Key Laboratory of Advanced Negative Carbon Technologies, Soochow University, 199 Ren’ai Road, Suzhou, Jiangsu 215123, China

P

Panpan Xu

Q

Qiao Zhang

L

Le He

Institute of Functional Nano & Soft Materials (FUNSOM), Jiangsu Key Laboratory of Advanced Negative Carbon Technologies

J

Jinxing Chen

Department of Chemistry