中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Mechanistic understanding of metal-acid synergetic hydroconversion of polyethylene under mild conditions over a Ru/MOR catalyst

文献类型:期刊论文

作者Chen, Ruizhe1,2,3,4; Cheng, Leilei1,2,3,4; Gu, Jing1,2,3,4; Yuan, Haoran1,2,3,4; Chen, Yong1
刊名ENERGY CONVERSION AND MANAGEMENT
出版日期2024-01-15
卷号300页码:12
关键词Plastic waste Bifunctional catalysts Ru size Hydrogenolysis Hydrocracking
ISSN号0196-8904
DOI10.1016/j.enconman.2023.117983
通讯作者Yuan, Haoran(yuanhr@ms.giec.ac.cn)
英文摘要Hydroconversion has been demonstrated as a viable method to efficiently deconstruct polyolefins under relatively mild conditions. The hydrogenolysis of C-C bonds over Ru-based catalysts can convert polyolefins into liquid alkanes and methane. To suppress methane generation and obtain high-value isomer, further exploration of the mechanism for the cooperative deconstruction of polyolefins by bifunctional catalysts with metal-acid sites is necessary. In this study, we utilized ball milling to enhance the accessibility of acid sites within MOR zeolite, while the fragmented pore structure ensured that the loaded Ru metal was sufficiently accessible for longchain alkanes. The sequential accessibility of metal-acid sites boosted the hydroconversion efficiency of lowdensity polyethylene (LDPE). Through systematic investigations involving catalysts with various Ru loadings and Si/Al ratio of zeolites, it is discovered that the smaller-sized Ru particles not only facilitate the generation and desorption of olefinic intermediates in hydrocracking but also promote the hydrogenation and desorption of alkyls and suppress the cascade of terminal C-C bond cleavage in hydrogenolysis. Liquid fuel (C5-C21) yield was increased by 27% for the catalyst loaded with 0.7 wt% Ru on mMOR20 compared to 1.7 wt% loadings, while methane yield was only one-third of the latter. Concurrently, the distribution of acid sites on the zeolite surface affected the aggregation process of Ru atoms. This study deeply unveils the synergistic interaction of metal-acid sites, facilitating internal C-C bond cleavage to obtain liquid fuel and sheds light on catalyst design for waste polyolefins upcycling.
WOS关键词HYDROCRACKING
资助项目CAS Project for Young Scientists in Basic Research ; Guangdong Basic and Applied Basic Research Foundation ; [YSBR-044] ; [2021B1515020068]
WOS研究方向Thermodynamics ; Energy & Fuels ; Mechanics
语种英语
WOS记录号WOS:001138505100001
出版者PERGAMON-ELSEVIER SCIENCE LTD
资助机构CAS Project for Young Scientists in Basic Research ; Guangdong Basic and Applied Basic Research Foundation
源URL[http://ir.giec.ac.cn/handle/344007/40599]  
专题中国科学院广州能源研究所
通讯作者Yuan, Haoran
作者单位1.Univ Sci & Technol China, Sch Energy Sci & Engn, Hefei 230026, Peoples R China
2.Chinese Acad Sci, Guangzhou Inst Energy Convers, Guangzhou 510640, Peoples R China
3.CAS Key Lab Renewable Energy, Guangzhou 510640, Peoples R China
4.Guangdong Prov Key Lab New & Renewable Energy Res, Guangzhou 510640, Peoples R China
推荐引用方式
GB/T 7714
Chen, Ruizhe,Cheng, Leilei,Gu, Jing,et al. Mechanistic understanding of metal-acid synergetic hydroconversion of polyethylene under mild conditions over a Ru/MOR catalyst[J]. ENERGY CONVERSION AND MANAGEMENT,2024,300:12.
APA Chen, Ruizhe,Cheng, Leilei,Gu, Jing,Yuan, Haoran,&Chen, Yong.(2024).Mechanistic understanding of metal-acid synergetic hydroconversion of polyethylene under mild conditions over a Ru/MOR catalyst.ENERGY CONVERSION AND MANAGEMENT,300,12.
MLA Chen, Ruizhe,et al."Mechanistic understanding of metal-acid synergetic hydroconversion of polyethylene under mild conditions over a Ru/MOR catalyst".ENERGY CONVERSION AND MANAGEMENT 300(2024):12.

入库方式: OAI收割

来源:广州能源研究所

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