Chemical Recycling Processes of Waste Polyethylene Terephthalate Using Solid Catalysts

被引:60
|
作者
Bohre, Ashish [1 ,2 ,3 ]
Jadhao, Prashant Ram [1 ]
Tripathi, Komal [1 ]
Pant, Kamal Kishore [1 ]
Likozar, Blaz [3 ]
Saha, Basudeb [4 ]
机构
[1] Indian Inst Technol Delhi, Dept Chem Engn, Delhi 110016, India
[2] Sardar Swaran Singh Natl Inst Bioenergy, Biomass & Energy Management Div, Kapurthala 1440603, Punjab, India
[3] Natl Inst Chem, Dept Catalysis & Chem React Engn, Hajdrihova 19, Ljubljana 1001, Slovenia
[4] RiKarbon Inc, 550 S Coll Ave, Delaware, DE 19716 USA
关键词
polymers; heterogeneous catalysts; chemical recycling; polyethylene terephthalate; plastic waste; PRODUCE DIOCTYL TEREPHTHALATE; DEEP EUTECTIC SOLVENTS; BENZENE-RICH OIL; POLY(ETHYLENE-TEREPHTHALATE) WASTE; PLASTIC WASTE; BENZOIC-ACID; PET-BOTTLES; DENSITY POLYETHYLENE; SUSTAINABLE CATALYST; SELECTIVE PRODUCTION;
D O I
10.1002/cssc.202300142
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Polyethylene terephthalate (PET) is a non-degradable single-use plastic and a major component of plastic waste in landfills. Chemical recycling is one of the most widely adopted methods to transform post-consumer PET into PET's building block chemicals. Non-catalytic depolymerization of PET is very slow and requires high temperatures and/or pressures. Recent advancements in the field of material science and catalysis have delivered several innovative strategies to promote PET depolymerization under mild reaction conditions. Particularly, heterogeneous catalysts assisted depolymerization of post-consumer PET to monomers and other value-added chemicals is the most industrially compatible method. This review includes current progresses on the heterogeneously catalyzed chemical recycling of PET. It describes four key pathways for PET depolymerization including, glycolysis, pyrolysis, alcoholysis, and reductive depolymerization. The catalyst function, active sites and structure-activity correlations are briefly outlined in each section. An outlook for future development is also presented.
引用
收藏
页数:24
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