Upcycling Poly(ethylene terephthalate) Into High‐Efficient Epoxy Toughener: Hyperbranched Oligomer Induced Nano‐Structural Heterogeneities

X Xin Wang Z Ziyu Liu (Department of Physics) J Jian Wang J Jingkai Liu (State Key Laboratory of Advanced Marine Materials Ningbo Institute of Materials Technology and Engineering Chinese Academy of Sciences Ningbo Zhejiang China) J Jinyue Dai (State Key Laboratory of Advanced Marine Materials Ningbo Institute of Materials Technology and Engineering Chinese Academy of Sciences Ningbo Zhejiang China) P Penglei Guo (State Key Laboratory of Advanced Marine Materials Ningbo Institute of Materials Technology and Engineering Chinese Academy of Sciences Ningbo Zhejiang China) X Xiaoling Liu (State Key Laboratory of Materials-Oriented Chemical Engineering, College of Chemical Engineering) X Xiaoqing Liu (School of Chemical Engineering and Light Industry)

Abstract

ABSTRACT The post‐consumer recycling efficacy of poly(ethylene terephthalate) (PET) has attracted considerable attention. Current chemical recycling of PET predominantly targets monomers, specialty chemicals, and functional materials, yet faces hurdles of costly purification/decolorization and limited market capacity. Here, we report an upcycling paradigm to directly transfer waste PET into highly efficient epoxy tougheners. Through a one‐pot process, PET is converted into hyperbranched oligomers (HBO) bearing a compact architecture and abundant terminal hydroxyl groups. This unique structure enables uniform dispersion and covalent integration into the epoxy network during curing, resulting in the formation of chemically seamless and homogeneous rigid nano‐structural heterogeneities. And these nano‐structural heterogeneities act as stress concentrators that activate localized plastic deformation, promote crack deflection and bridging, and induce microcracking, collectively establishing a multi‐scale energy dissipation network, rather than the cavity‐induced shear deformation process characteristic of conventional hyperbranched polymers. Remarkably, merely 0.3 wt.% incorporation enhances impact strength by 98.9% without compromising intrinsic processability, mechanical and thermal stability. Moreover, this method demonstrates strong feedstock versatility and has been validated at the kilogram scale, offering a viable and integrated pathway for high‐value plastic circularity.

Article Details

Volume / Issue Vol. 1, Issue 1
Published August 11, 2026
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (8)

X

Xin Wang

Z

Ziyu Liu

Department of Physics

J

Jian Wang

J

Jingkai Liu

State Key Laboratory of Advanced Marine Materials Ningbo Institute of Materials Technology and Engineering Chinese Academy of Sciences Ningbo Zhejiang China

J

Jinyue Dai

State Key Laboratory of Advanced Marine Materials Ningbo Institute of Materials Technology and Engineering Chinese Academy of Sciences Ningbo Zhejiang China

P

Penglei Guo

State Key Laboratory of Advanced Marine Materials Ningbo Institute of Materials Technology and Engineering Chinese Academy of Sciences Ningbo Zhejiang China

X

Xiaoling Liu

State Key Laboratory of Materials-Oriented Chemical Engineering, College of Chemical Engineering

X

Xiaoqing Liu

School of Chemical Engineering and Light Industry