Evidence map›Paper›PMID 42627287›Full record

ReviewChemSusChem2026

Photothermal Catalytic Depolymerization and Glycolytic Regeneration of Polyethylene Terephthalate.

Haishui Xu, Chao Chen, Zhang Cao, Jiabao Chen, Jiacheng Zhao, Guiyin Xu, Xijiang Chang

Abstract readReview
In one paragraph

Review in ChemSusChem, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Haishui XuCollege of Physics, Donghua University, Shanghai, China.
Chao ChenState Key Laboratory for Advanced Fiber Materials, College of Materials Science and Engineering, Donghua University, Shanghai, China.
Zhang CaoState Key Laboratory for Advanced Fiber Materials, College of Materials Science and Engineering, Donghua University, Shanghai, China.ORCID https://orcid.org/0000-0001-9726-2100
Jiabao ChenCollege of Physics, Donghua University, Shanghai, China.
Jiacheng ZhaoXin Feng Ming Group Huzhou Zhongshi Technology Co. Ltd., Hangzhou, China.
Guiyin XuState Key Laboratory for Advanced Fiber Materials, College of Materials Science and Engineering, Donghua University, Shanghai, China.ORCID https://orcid.org/0000-0002-5959-4814
Xijiang ChangCollege of Physics, Donghua University, Shanghai, China.ORCID https://orcid.org/0000-0002-3509-2713

Funding

Fundamental Research Funds for the Central Universities 2232025A-05International Cooperation Fund of the Science and Technology Commission of Shanghai Municipality 24520713300National Natural Science Foundation of China 12575269National Natural Science Foundation of China 22522807National Natural Science Foundation of China U25A20341Shanghai Rising-Star Program 24QA2700100
6 · The paper itself

Abstract

The efficient recycling of polyethylene terephthalate (PET) waste is essential for sustainable development, owing to the extensive utilization of this plastic in daily life. However, the high depolymerization energy barrier inherent to conventional single thermal catalytic technology constrains its reaction efficiency, necessitating substantial external heat input and energy consumption. Recently, photothermal synergistic catalysis has emerged as one of the most promising methods for PET glycolysis regeneration, with its core lying in the photothermal conversion and catalytic mechanism. In this review, the core mechanisms and recent advances in the photothermal catalytic depolymerization of PET to bis(2-hydroxyethyl) terephthalate (BHET) are systematically discussed. First, this review elucidates the critical role of photothermal conversion in PET recycling based on the structural characteristics of PET and the thermodynamic and kinetic principles governing its depolymerization. Particular emphasis is placed on how photothermal synergistic catalysis significantly lowers the depolymerization energy barrier and enhances reaction efficiency. Subsequently, the depolymerization mechanism of PET is analyzed in detail, with a focus on the synergistic promotion by catalyst active sites of electrophilicity of carbonyl groups in PET ester bonds and the nucleophilicity of the hydroxyl oxygen in ethylene glycol (EG), thereby achieving efficient transesterification.

Indexed as

bis(2‐hydroxyethyl) terephthalate (BHET)glycolysisphotothermal catalysispolyethylene terephthalate (PET)

Identifiers

PMID42627287
PMCPMC13496070

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.