中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Operando dual beam FTIR spectroscopy unravels the promotional effect of Zn on HZSM-5 in iso-butane aromatization

文献类型:期刊论文

作者Zhou, Wei1,2; Liu, Jiaxu1,2; He, Ning1,2; Shu, Miao3; Lin, Long1,2; Wang, Jilei1,2; Si, Rui3; Xiong, Guang1,2; Xin, Qin4; Guo, Hongchen1,2
刊名CATALYSIS SCIENCE & TECHNOLOGY
出版日期2019-04-07
卷号9期号:7页码:1609-1620
ISSN号2044-4753
DOI10.1039/c9cy00136k
通讯作者Guo, Hongchen(hongchenguo@dlut.edu.cn)
英文摘要Although zinc-promoted HZSM-5 catalysts have been widely used in the aromatization of short-chain hydrocarbons, the precise role of Zn in catalysis is still unclear due to the complex reaction mechanism and the lack of in situ or operando techniques. A home-built dual beam Fourier transform infrared (DB-FTIR) spectrometer, designed to eliminate the interference of gas-phase molecular vibration and heat irradiation through collecting reference and sample spectra simultaneously, can present an unimpeded view of the dynamic surface processes involved in gas/solid heterogeneous catalysis under real reaction conditions. With the aid of the DB-FTIR spectrometer, we directly observed the reaction process of iso-butane aromatization over HZSM-5 and Zn/HZSM-5. Unlike conventional studies, the aromatization was firstly performed under sub-atmospheric pressures using a home-built fixed-bed reactor. Comprehensive characterization results demonstrate that, besides their good dehydrogenation abilities, Zn species undergo strong interactions with olefin intermediates, even at sub-atmospheric pressures, but weaker interaction (or adsorption) with final aromatic products. Density functional theory studies certify that strong interactions could inhibit the desorption of olefin intermediates, which is beneficial for secondary chain-growth reactions relating to aromatics.
WOS关键词ZSM-5 ZEOLITES ; PROPANE AROMATIZATION ; LIGHT ALKANES ; TRANSFORMATION ; ACTIVATION ; CATALYSTS ; ETHANE ; ACID ; HYDROCARBONS ; ZN/HZSM-5
资助项目National Natural Science Foundation of China[21603023] ; Dalian high level talent innovation support program[2017RQ011]
WOS研究方向Chemistry
语种英语
WOS记录号WOS:000463950800005
出版者ROYAL SOC CHEMISTRY
资助机构National Natural Science Foundation of China ; National Natural Science Foundation of China ; Dalian high level talent innovation support program ; Dalian high level talent innovation support program ; National Natural Science Foundation of China ; National Natural Science Foundation of China ; Dalian high level talent innovation support program ; Dalian high level talent innovation support program ; National Natural Science Foundation of China ; National Natural Science Foundation of China ; Dalian high level talent innovation support program ; Dalian high level talent innovation support program ; National Natural Science Foundation of China ; National Natural Science Foundation of China ; Dalian high level talent innovation support program ; Dalian high level talent innovation support program
源URL[http://cas-ir.dicp.ac.cn/handle/321008/165648]  
专题大连化学物理研究所_中国科学院大连化学物理研究所
通讯作者Guo, Hongchen
作者单位1.Dalian Univ Technol, State Key Lab Fine Chem, Dalian 116023, Peoples R China
2.Dalian Univ Technol, Sch Chem Engn, Dalian 116023, Peoples R China
3.Chinese Acad Sci, Shanghai Inst Appl Phys, Shanghai Synchrotron Radiat Facil, Shanghai 201204, Peoples R China
4.Dalian Inst Chem Phys, State Key Lab Catalysis, Dalian 116023, Peoples R China
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Zhou, Wei,Liu, Jiaxu,He, Ning,et al. Operando dual beam FTIR spectroscopy unravels the promotional effect of Zn on HZSM-5 in iso-butane aromatization[J]. CATALYSIS SCIENCE & TECHNOLOGY,2019,9(7):1609-1620.
APA Zhou, Wei.,Liu, Jiaxu.,He, Ning.,Shu, Miao.,Lin, Long.,...&Guo, Hongchen.(2019).Operando dual beam FTIR spectroscopy unravels the promotional effect of Zn on HZSM-5 in iso-butane aromatization.CATALYSIS SCIENCE & TECHNOLOGY,9(7),1609-1620.
MLA Zhou, Wei,et al."Operando dual beam FTIR spectroscopy unravels the promotional effect of Zn on HZSM-5 in iso-butane aromatization".CATALYSIS SCIENCE & TECHNOLOGY 9.7(2019):1609-1620.

入库方式: OAI收割

来源:大连化学物理研究所

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