CO2 capture and in-situ conversion:recent progresses and perspectives

被引:0
|
作者
Bin Shao [1 ]
Yun Zhang [1 ]
Zheyi Sun [1 ]
Jianping Li [2 ,3 ]
Zihao Gao [1 ]
Zhicheng Xie [1 ]
Jun Hu [1 ,2 ]
Honglai Liu [1 ]
机构
[1] School of Chemistry and Molecular Engineering, East China University of Science and Technology
[2] ECUST School of Carbon Neutrality Future Technology, East China University of Science and Technology
[3] State Environmental Protection Key Laboratory of Environmental Risk Assessment and Control on Chemical Process, East China University of Science and Technology
基金
中国国家自然科学基金;
关键词
D O I
暂无
中图分类号
TQ426 [催化剂(触媒)]; X701 [废气的处理与利用];
学科分类号
080502 ; 081705 ; 083002 ;
摘要
Global warming caused by excess carbon dioxide(CO2) emission has been a focus of the world. The development of neutral carbon technologies becomes a strategic choice for the sustainable human society. Integrating CO2capture and conversion(iCCC) technology can simultaneously convert the captured CO2from flue gas into valueadded chemicals, which saves great energies and expenses incurred in CO2compression and transportation processes of conventional carbon capture, utilization, and storage(CCUS) technology. The present review critically discusses the dual-function materials(DFMs) and the iCCC technology at intermediate temperature for methane production and high temperature for syngas production. The design of reactor and optimization of operation conditions are emphasized from the perspective of industrial applications. The dual-fixed-bed reactors mode by switching the flue gas and reactant gases, and the dual-fluidized-bed reactors mode by the circulation of DFMs particles are comparatively reviewed. We hope this review can stimulate further studies including designing and fabricating feasible DFMs, exploring realistic catalytic process for CO2conversion to high value-added chemicals, developing workable reactor modes and optimizing operation conditions, and establishing industrial demonstration for real applications of iCCC technology in the future.
引用
收藏
页码:189 / 198
页数:10
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