Simplified, fast, and efficient microwave assisted chemical recycling of poly (ethylene terephthalate) waste

被引:11
|
作者
Zangana, Karzan H. [1 ,2 ]
Fernandez, Antonio [3 ]
Holmes, Justin D. [1 ,2 ]
机构
[1] Univ Coll Cork, Sch Chem, Cork T12 YN60, Ireland
[2] Univ Coll Cork, Environm Res Inst ERI, AMBER Ctr, Lee Rd, Cork T23 XE10, Ireland
[3] Loughborough Univ, Sch Sci, Loughborough LE11 3TU, England
来源
基金
爱尔兰科学基金会;
关键词
PET waste; Microwave-assisted depolymerisation; Glycolysis; Transesterification; Heterogeneous catalysis; Calcium oxide; BIODIESEL PRODUCTION; POLYETHYLENE TEREPHTHALATE; HETEROGENEOUS CATALYSTS; ACTIVATED CARBON; CALCIUM-OXIDE; SUNFLOWER OIL; GLYCOLYSIS; POLY(ETHYLENE-TEREPHTHALATE); DEPOLYMERIZATION; OPTIMIZATION;
D O I
10.1016/j.mtcomm.2022.104588
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The widespread adoption of chemical recycling of poly (ethylene terephthalate) (PET) is hampered by long reaction times, high energy consumption and the use of metal catalysts that are either toxic or cost prohibitive for industrial use. Herein, we report a simple PET glycolytic process that combines an environmentally friendly and cheap heterogenous catalyst, calcium oxide (CaO) with microwave irradiation to obtain the monomer bis(2-hydroxyethyl) terephthalate (BHET), which can be easily separated by crystallisation. After the process opti-misation, depolymerisation of PET waste was achieved in 3.5 min under atmospheric pressure, to obtain highly crystalline BHET with a yield of 75%. To our knowledge, this is the fastest heterogeneous glycolytic process reported in the literature to-date, using a cheap and eco-friendly catalyst. Moreover, by using a heterogenous catalyst and avoiding the need for product precipitation by water addition, CaO and ethylene glycol materials were separated and reused, thus validating this protocol as a potential green and scalable route for PET recycling.
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页数:7
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