Effects of the acidity and shape selectivity of dealuminated zeolite beta on butene transformations. (15th September 2021)
- Record Type:
- Journal Article
- Title:
- Effects of the acidity and shape selectivity of dealuminated zeolite beta on butene transformations. (15th September 2021)
- Main Title:
- Effects of the acidity and shape selectivity of dealuminated zeolite beta on butene transformations
- Authors:
- Yi, Fengjiao
Chen, Huimin
Huang, Lihua
Hu, Caixia
Wang, Jun
Li, Tao
Wang, Hongxing
Tao, Zhichao
Yang, Yong
Li, Yongwang - Abstract:
- Graphical abstract: Highlights: Mechanisms of Brønsted acids and weak Lewis acids from silanol nests are different. BAS catalysis follows carbenium ion mechanism contrast to allyl species on LAS. Butenes oligomerizations are affected by acidity and shape selectivity of zeolite. Abstract: The acidity and shape selectivity of zeolites are two important catalytic properties, and they have been extensively applied to the chemical and petrochemical industries. Here, we investigated the various effect mechanisms of Brønsted acid sites (BASs) from bridged hydroxyl groups in zeolite Beta and Lewis acid sites (LASs) from silanol nests in Si-Beta on butene transformation and their reaction pathways by diffuse-reflectance infrared Fourier-transform spectroscopy. BAS catalysis of butenes double bond activation and isomerization follows the classical carbenium ion mechanism, while catalysis by silanol nests as weak LASs due to hydrogen bond interaction is achieved by formation of allyl species and alkoxyl groups. Moreover, the oligomerization reactions of butene isomers are affected by the dynamic diameters and activation energies of the butene isomers and the synergy between acidity and shape selectivity of the zeolite. Oligomerization of n -butene and cis -2-butene is more likely to be affected by acids on the sample, while oligomerization of trans -2-butene and isobutene is influenced by the shape selectivity of the channel, in addition to the acidity on partly dealuminated zeoliteGraphical abstract: Highlights: Mechanisms of Brønsted acids and weak Lewis acids from silanol nests are different. BAS catalysis follows carbenium ion mechanism contrast to allyl species on LAS. Butenes oligomerizations are affected by acidity and shape selectivity of zeolite. Abstract: The acidity and shape selectivity of zeolites are two important catalytic properties, and they have been extensively applied to the chemical and petrochemical industries. Here, we investigated the various effect mechanisms of Brønsted acid sites (BASs) from bridged hydroxyl groups in zeolite Beta and Lewis acid sites (LASs) from silanol nests in Si-Beta on butene transformation and their reaction pathways by diffuse-reflectance infrared Fourier-transform spectroscopy. BAS catalysis of butenes double bond activation and isomerization follows the classical carbenium ion mechanism, while catalysis by silanol nests as weak LASs due to hydrogen bond interaction is achieved by formation of allyl species and alkoxyl groups. Moreover, the oligomerization reactions of butene isomers are affected by the dynamic diameters and activation energies of the butene isomers and the synergy between acidity and shape selectivity of the zeolite. Oligomerization of n -butene and cis -2-butene is more likely to be affected by acids on the sample, while oligomerization of trans -2-butene and isobutene is influenced by the shape selectivity of the channel, in addition to the acidity on partly dealuminated zeolite Beta. … (more)
- Is Part Of:
- Fuel. Volume 300(2021)
- Journal:
- Fuel
- Issue:
- Volume 300(2021)
- Issue Display:
- Volume 300, Issue 2021 (2021)
- Year:
- 2021
- Volume:
- 300
- Issue:
- 2021
- Issue Sort Value:
- 2021-0300-2021-0000
- Page Start:
- Page End:
- Publication Date:
- 2021-09-15
- Subjects:
- Acidity -- Shape selectivity -- Beta -- Butene -- Mechanism -- Oligomerization
Fuel -- Periodicals
Coal -- Periodicals
Coal
Fuel
Periodicals
662.6 - Journal URLs:
- http://www.sciencedirect.com/science/journal/latest/00162361 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.fuel.2021.120694 ↗
- Languages:
- English
- ISSNs:
- 0016-2361
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4048.000000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 16987.xml