Microwave-carbon fiber cloth co-ignited catalytic degradation of waste plastic into high-yield hydrogen and carbon nanotubes

被引:6
|
作者
Zhang, Bowen [1 ]
Wang, Hui [1 ]
Yang, Yiyun [1 ]
Zhou, Yanping [1 ,2 ]
Zhang, Bing [1 ]
Huang, Kama [1 ,2 ]
机构
[1] Sichuan Univ, Coll Elect & Informat Engn, Chengdu 610065, Peoples R China
[2] Sichuan Univ, State Key Lab Polymer Mat Engn, Chengdu 610065, Peoples R China
来源
基金
中国国家自然科学基金;
关键词
Microwave-enhanced catalysis; Plastic cracking; Hydrogen production; Carbon nanotubes; Carbon fiber cloth; ABSORPTION PROPERTIES; PYROLYSIS; COPRODUCTION; PERFORMANCE; MECHANISM;
D O I
10.1016/j.jece.2023.109710
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Environmental pollution and waste of resources caused by the massive accumulation and landfill of plastic waste has been prompting the research considering its reclamation. In this work, a microwave-carbon fiber cloth (CFC) co-ignited cracking strategy is proposed for highly-efficient conversion of polyethylene to hydrogen and highquality carbon nanotubes conducted in a simple multimode microwave reactor. When FeAlOx@C is used as the catalyst, a hydrogen yield of 64.5 mmol g 1plastic is achieved while biochar powder as the ignitor only give yield to 30.6 mmol H2 g 1plastic, demonstrating the superiority of the CFC strategy where the carbon ignitor has little contact with the reactants. Further, FeAlOx@C treated by air plasma with rich oxygen vacancies is used as the catalyst. The yield is enhanced significantly, especially at low microwave power, resulting in a hydrogen yield of 67.3 mmol g  1 plastic at a microwave power of 900 W, which was the highest as far as we know in the literature under direct catalytic cracking processes. Notably, the integrity of the CFC piece is maintained well, and is highly recyclable. Numerical simulation suggests that the position of CFC plays a key role in initiating the enhanced catalytic cracking process enabled by direct microwave heating.
引用
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页数:10
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