TY - JOUR
T1 - Visible-light-driven photocatalytic depolymerization of post-consumer PET to terephthalic acid via cerium catalysis with batch-to-flow scalability
AU - Pang, Yujian
AU - Wu, Xiqun
AU - Li, Zhijie
AU - Sun, Jie
AU - Li, Zhenjiang
AU - Qiu, Jiang Kai
AU - Wang, Jian
AU - Ma, Canliang
AU - Guo, Kai
N1 - Publisher Copyright:
© 2025 The Royal Society of Chemistry.
PY - 2025
Y1 - 2025
N2 - Polyethylene terephthalate (PET), as one of the five major engineering plastics with an annual production exceeding 80 million metric tons, has created escalating environmental challenges. Currently, approximately 79% of discarded PET is treated through landfill or incineration, while conventional chemical recycling technologies (e.g., hydrolysis and alcoholysis) require harsh conditions such as high temperature, high pressure, and highly corrosive media, leading to issues including high energy consumption, severe equipment corrosion, and secondary pollution. This study pioneers a cerium-based photocatalytic system, achieving for the first time the efficient depolymerization of PET waste under visible-light-driven conditions. At ambient temperature and pressure, the cerium trichloride (CeCl3) photocatalyst activates visible light to depolymerize post-consumer PET (including plastic bottles and textile fibers) into high-purity terephthalic acid (PTA) without requiring strong alkali pretreatment, overcoming the equipment corrosion challenges inherent in conventional photocatalytic reforming technologies that rely on concentrated alkaline solutions. An innovatively designed microchannel reactor system leverages its high surface-to-volume ratio to enhance light utilization efficiency while resolving optical path decay issues, providing an engineered solution for large-scale processing. This breakthrough establishes a sustainable pathway for PET circular economy, addressing critical limitations of existing physical and chemical recycling methods.
AB - Polyethylene terephthalate (PET), as one of the five major engineering plastics with an annual production exceeding 80 million metric tons, has created escalating environmental challenges. Currently, approximately 79% of discarded PET is treated through landfill or incineration, while conventional chemical recycling technologies (e.g., hydrolysis and alcoholysis) require harsh conditions such as high temperature, high pressure, and highly corrosive media, leading to issues including high energy consumption, severe equipment corrosion, and secondary pollution. This study pioneers a cerium-based photocatalytic system, achieving for the first time the efficient depolymerization of PET waste under visible-light-driven conditions. At ambient temperature and pressure, the cerium trichloride (CeCl3) photocatalyst activates visible light to depolymerize post-consumer PET (including plastic bottles and textile fibers) into high-purity terephthalic acid (PTA) without requiring strong alkali pretreatment, overcoming the equipment corrosion challenges inherent in conventional photocatalytic reforming technologies that rely on concentrated alkaline solutions. An innovatively designed microchannel reactor system leverages its high surface-to-volume ratio to enhance light utilization efficiency while resolving optical path decay issues, providing an engineered solution for large-scale processing. This breakthrough establishes a sustainable pathway for PET circular economy, addressing critical limitations of existing physical and chemical recycling methods.
UR - http://www.scopus.com/inward/record.url?scp=105006762345&partnerID=8YFLogxK
U2 - 10.1039/d5gc01218j
DO - 10.1039/d5gc01218j
M3 - 文章
AN - SCOPUS:105006762345
SN - 1463-9262
JO - Green Chemistry
JF - Green Chemistry
ER -