Depolymerization of waste poly(ethylene terephthalate) into bis (2-hydroxyethyl) terephthalate: Catalytic glycolysis mechanism and kinetics

被引:0
作者
Li, Maoxin [1 ]
Chen, Wenxing
Chen, Shichang [1 ,2 ]
机构
[1] Zhejiang Sci Tech Univ, Sch Mat Sci & Engn, Hangzhou 310018, Peoples R China
[2] Zhejiang Sci Tech Univ, Natl & Local United Engn Lab Text Fiber Mat & Proc, Hangzhou 310018, Peoples R China
关键词
Polyethylene terephthalate; Glycolysis; Depolymerization mechanisms; Homogeneous; Pseudohomogeneous; Heterogeneous; Reaction kinetics; POLYETHYLENE TEREPHTHALATE; IONIC LIQUID; SUSTAINABLE CATALYST; PET WASTE; DEGRADATION; EFFICIENT; ACID; HYDROLYSIS; BIOMASS; NANOPARTICLES;
D O I
10.1016/j.cej.2024.157778
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Polyethylene terephthalate (PET) does not readily degrade in nature, leading to the accumulation of large quantities of PET waste in the ecosystem, posing a threat to both terrestrial and aquatic life. Consequently, proper recycling of post-consumer PET has become imperative for our society. This review focuses on PET glycolysis, emphasizing its associated mechanisms and kinetics. The degradation mechanisms are systematically summarized from the perspectives of homogeneous, pseudohomogeneous, and heterogeneous catalytic systems. Homogeneous catalysts demonstrate effective degradation but lack environmental friendliness, and are challenging to separate from the product for subsequent reuse. Conversely, pseudohomogeneous and heterogeneous catalysts offer greater stability and recyclability, rendering them advantageous for sustainable industrial-scale production. Moreover, this review surveys kinetic studies of PET glycolysis, categorizing them into homogeneous and heterogeneous systems. A comprehensive understanding of the kinetic modeling of various degradation processes is deemed essential for the design of efficient glycolytic reaction systems in the future.
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页数:25
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