Low‐temperature transesterification strategy for universal upcycling of waste polyesters into high‐value esters

Abstract Waste polyesters pose a severe environmental challenge and require transformative upcycling strategies to achieve a circular plastic economy. Distinct from conventional methanolysis relying on stoichiometric external alcohols or water‐triggered esterolysis, this study proposes a novel universal low‐temperature transesterification strategy for the upcycling of diverse polyesters into high‐value esters, using an internally driven self‐sustained transesterification cycle where, triggered by trace alcohols, dimethyl carbonate (DMC) dynamically exchanges its alkoxy groups with diols released from the polyester backbone. Typically, polyethylene terephthalate (PET) can be efficiently transesterified into dimethyl terephthalate (DMT) and ethylene carbonate (EC), reaching peak yields of 96% and 86%, respectively, under mild conditions. The self‐sustained transesterification strategy shows broad applicability to various types of polyesters, mixed textiles, post‐consumer plastics, and can also be extended to polyester upcycling using other alcohols and alkylating agents, which significantly reduces energy consumption and carbon emissions compared to traditional alcoholysis‐based systems, providing a scalable route for plastic circularity.

Authors

Institutions

Publication Details

Journal
AIChE Journal
Published
2026-07-22
DOI
https://doi.org/10.1002/aic.70514
Primary Topic
Carbon dioxide utilization in catalysis
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Low‐temperature transesterification strategy for universal upcycling of waste polyesters into high‐value esters

Ling Zhao, Weizhen Sun, Zhenhao Xi, Zhendong Pan et al.
AIChE Journal
Carbon dioxide utilization in catalysis
article

Low‐temperature transesterification strategy for universal upcycling of waste polyesters into high‐value esters

Ling Zhao, Weizhen Sun, Zhenhao Xi, Zhendong Pan, Weizhong Zheng, Shimei Xu, Zhihong Ma, Z Huang, Jingwen Qiu, Xin Wei
article en

Abstract

Abstract Waste polyesters pose a severe environmental challenge and require transformative upcycling strategies to achieve a circular plastic economy. Distinct from conventional methanolysis relying on stoichiometric external alcohols or water‐triggered esterolysis, this study proposes a novel universal low‐temperature transesterification strategy for the upcycling of diverse polyesters into high‐value esters, using an internally driven self‐sustained transesterification cycle where, triggered by trace alcohols, dimethyl carbonate (DMC) dynamically exchanges its alkoxy groups with diols released from the polyester backbone. Typically, polyethylene terephthalate (PET) can be efficiently transesterified into dimethyl terephthalate (DMT) and ethylene carbonate (EC), reaching peak yields of 96% and 86%, respectively, under mild conditions. The self‐sustained transesterification strategy shows broad applicability to various types of polyesters, mixed textiles, post‐consumer plastics, and can also be extended to polyester upcycling using other alcohols and alkylating agents, which significantly reduces energy consumption and carbon emissions compared to traditional alcoholysis‐based systems, providing a scalable route for plastic circularity.

AIChE Journal
East China University of Science and Technology (CN), Beibu Gulf University (CN), Ingenierie des Materiaux polymeres (FR), State Key Laboratory of Chemical Engineering (CN)
Affordable and clean energy
Openalex Percentile: Top 19%
Carbon dioxide utilization in catalysis
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.