脱质子化
同步加速器
烯烃
化学
红外线的
解吸
碳氢化合物
沸石
甲醇
光化学
红外光谱学
催化作用
有机化学
吸附
核物理学
离子
物理
光学
作者
Ivalina B. Minova,Santhosh Kumar Matam,Alex G. Greenaway,C. Richard A. Catlow,Mark D. Frogley,Gianfelice Cinque,Paul A. Wright,Russell F. Howe
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2019-06-17
卷期号:9 (7): 6564-6570
被引量:80
标识
DOI:10.1021/acscatal.9b01820
摘要
Synchrotron infrared microspectroscopy has identified with high temporal resolution (down to 0.25 s) the initial events occurring when methanol vapor is in contact with a crystal of zeolite HZSM-5. The first alkenes are generated directly from methoxy groups formed at the acid sites via their deprotonation. These alkenes can either desorb directly or oligomerize and cyclize to form dimethylcyclopentenyl cations. The oligomeric and dimethylcyclopentenyl cations are the first major components of the hydrocarbon pool that precede aromatic hydrocarbons and lead to indirect alkene formation. The technique observes these events in real time.
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