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 |
DOI | 10.1039/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
浏览0
下载0
收藏0
其他版本
除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。