Waste-battery-derived multifunctional zinc catalysts for glycolysis and decolorization of polyethylene terephthalate

被引:20
|
作者
Chiao, Yu -Wen [1 ]
Liao, Weisheng [1 ]
Krisbiantoro, Philip Anggo [1 ,2 ,3 ]
Yu, Bor-Yih [1 ]
Wu, Kevin C. -W. [1 ,2 ]
机构
[1] Natl Taiwan Univ, Dept Chem Engn, Taipei 10617, Taiwan
[2] Acad Sinica, Mol Sci & Technol Program, Taiwan Int Grad Program, Taipei 11529, Taiwan
[3] Natl Taiwan Univ, Int Grad Program Mol Sci & Technol, Taipei 10617, Taiwan
关键词
Polyethylene terephthalate; Bis(2-hydroxyethyl) terephthalate; Glycolysis; Carbon -zinc batteries; Zero-valent zinc; Dye degradation; OXIDE NANOPARTICLES; ADVENTITIOUS CARBON; RAPID DEGRADATION; METHYL-ORANGE; POLY(ETHYLENE-TEREPHTHALATE); KINETICS; DEPOLYMERIZATION; GLYCOLATE; THERMODYNAMICS; LIQUID;
D O I
10.1016/j.apcatb.2022.122302
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In this study, novel and easily recyclable catalysts were prepared from waste batteries for efficient glycolysis and decolorization of polyethylene terephthalate (PET) to obtain bis(2-hydroxyethyl) terephthalate (BHET). At 190 degrees C and 5 h, the PET conversion and BHET yield reach 89.7 and 77.7%, respectively, which are comparable to the values obtained for the commonly used catalyst zinc acetate. Species generated from the reaction between ethylene glycol (EG) and zinc plates (e.g., Zn-glycolate, ZnO, and other metal species on zinc plates) demonstrate excellent catalytic performance. Furthermore, dye molecules released from several commercial-colored PET bottles during glycolysis can be degraded to colorless molecules using zinc plates, thereby facilitating BHET purification. The exposed zero-valent zinc from the zinc plates in EG is responsible for degrading the dye molecules. Finally, the scaled-up PET glycolysis process is conceptually designed using Aspen Plus software. The simulation results suggest that reducing the energy requirement in distillation is necessary for further improvement.
引用
收藏
页数:11
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