中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Enhanced activity and sulfur resistance of Cu- and Fe-modified activated carbon for the reduction of NO by CO from regeneration gas

文献类型:期刊论文

作者Xu, Zhicheng2,3; Li, Yuran2; Lin, Yuting2; Wang, Bin2; Gao, Panting4; Zhu, Tingyu1,2
刊名CATALYSIS SCIENCE & TECHNOLOGY
出版日期2021-12-09
页码13
ISSN号2044-4753
DOI10.1039/d1cy01951a
英文摘要The reduction of NO by CO was proposed to be applied for regeneration gas to remove NOx from industrial flue gas with activated carbon purification technology. To improve the activity and sulfur resistance for the reduction of NO by CO in regeneration gas, Cu and Fe modifications on activated carbon were investigated. And various samples were characterized by XRD, XPS, TPD, H-2-TPR, in situ DRIFTS and DFT calculations to explain the reaction mechanism and poisoning mechanism. The synergistic effects of oxygen-containing functional groups and metal sites show that -COOH acts as an anchor site for metals and that C-O-C acts as a protective site for Fe3+ under a SO2 atmosphere. Cu2+ sites have a high activity at low temperatures due to the large amount of adsorbed NO and the intermediate NOx- participating in the reaction with the NOx- pathway. Fe3+ sites have a high activity at high temperatures due to the high N-O dissociation activity with the *N pathway and -NCO pathway. DFT calculations proved that the binding Cu2+ and Fe3+ sites have higher activity than free Cu2+ and Fe3+ sites. A high content of SO2 exhibits various poisoning effects, mainly including the sulfation of metal sites, deposition of S, and consumption of CO. AC-Fe-H exhibits excellent resistance and stability against SO2 and H2O due to less S deposition caused by consumption through the S-CO reaction, slight sulfation caused by the protective effect of Fe2+ and C-O-C on Fe3+ sites and better hydrophobicity.
WOS关键词SELECTIVE CATALYTIC-REDUCTION ; BINARY METAL-OXIDES ; PREFERENTIAL OXIDATION ; FUNCTIONAL-GROUPS ; SEMI-COKE ; FLUE-GAS ; REMOVAL ; SO2 ; ADSORPTION ; SURFACE
资助项目National Key R&D Program of China[2018YFC0213406] ; National Natural Science Foundation of China[U1810209]
WOS研究方向Chemistry
语种英语
WOS记录号WOS:000732838300001
出版者ROYAL SOC CHEMISTRY
资助机构National Key R&D Program of China ; National Natural Science Foundation of China
源URL[http://ir.ipe.ac.cn/handle/122111/51486]  
专题中国科学院过程工程研究所
通讯作者Li, Yuran; Zhu, Tingyu
作者单位1.Chinese Acad Sci, Ctr Excellence Reg Atmospher Environm, Inst Urban Environm, Xiamen 361021, Peoples R China
2.Chinese Acad Sci, Innovat Acad Green Manufacture, Inst Proc Engn, CAS Key Lab Green Proc & Engn, Beijing 100190, Peoples R China
3.Univ Chinese Acad Sci, Beijing 100049, Peoples R China
4.Taiyuan Univ Technol, State Key Lab Clean & Efficient Coal Utilizat, Taiyuan 030024, Peoples R China
推荐引用方式
GB/T 7714
Xu, Zhicheng,Li, Yuran,Lin, Yuting,et al. Enhanced activity and sulfur resistance of Cu- and Fe-modified activated carbon for the reduction of NO by CO from regeneration gas[J]. CATALYSIS SCIENCE & TECHNOLOGY,2021:13.
APA Xu, Zhicheng,Li, Yuran,Lin, Yuting,Wang, Bin,Gao, Panting,&Zhu, Tingyu.(2021).Enhanced activity and sulfur resistance of Cu- and Fe-modified activated carbon for the reduction of NO by CO from regeneration gas.CATALYSIS SCIENCE & TECHNOLOGY,13.
MLA Xu, Zhicheng,et al."Enhanced activity and sulfur resistance of Cu- and Fe-modified activated carbon for the reduction of NO by CO from regeneration gas".CATALYSIS SCIENCE & TECHNOLOGY (2021):13.

入库方式: OAI收割

来源:过程工程研究所

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