解聚
聚对苯二甲酸乙二醇酯
粘胶
聚酯纤维
材料科学
对苯二甲酸
溶剂
化学工程
对苯二甲酸二甲酯
乙二醇
原材料
化学
制浆造纸工业
废物管理
有机化学
催化作用
高分子化学
复合材料
工程类
作者
Suthawan Muangmeesri,Kiran Reddy Baddigam,Kranti Navaré,Varvara Apostolopoulou‐Kalkavoura,Kuntawit Witthayolankowit,Helena Håkansson,Aji P. Mathew,Karel Van Acker,Joseph S. M. Samec
出处
期刊:ACS Sustainable Chemistry & Engineering
[American Chemical Society]
日期:2024-02-29
卷期号:12 (10): 4114-4120
标识
DOI:10.1021/acssuschemeng.3c07435
摘要
Polyethylene terephthalate (PET) is one of the most common plastics and can be cascaded mechanically during its life cycle. However, recycling affects the mechanical properties of the material, and the virgin material is constantly in demand. If a worn material could be depolymerized to its chemical building blocks, then a virgin polymer could be generated from old fibers. In this work, we have developed a benign organo-catalytic depolymerization of PET to yield dimethyl terephthalate (DMT) and ethylene glycol (EG) without the need for purification of generated monomers. By recirculating the solvent and organo-catalyst, a solvent/substrate ratio of 3:1 was achieved. The depolymerization was successfully applied to other polyesters, polycarbonates, and polycotton. The cotton isolated from the polycotton depolymerization was successfully processed into viscose fibers with a tenacity in the range of nonwaste cotton-derived viscose filaments. The global warming potential (GWP) of PET depolymerization was evaluated by using life cycle assessment (LCA). The GWP of 1 kg PET recycling is 2.206 kg CO2 equivalent, but the process produces DMT, EG, and heat, thereby avoiding the emissions equivalent to 4.075 kg CO2 equivalent from the DMT, EG, and steam-energy production through conventional pathways. Thus, the net result potentially avoids the emission of 1.88 kg of CO2 equivalent. The impact of this process is lower than that of waste PET incineration and conventional PET recycling technologies.
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