Dehydration of ethanol over zeolites, silica alumina and alumina: Lewis acidity, Bronsted acidity and confinement effects

被引:172
|
作者
Thanh Khoa Phung [1 ]
Hernandez, Loriana Proietti [1 ]
Lagazzo, Alberto [1 ]
Busca, Guido [1 ]
机构
[1] Univ Genoa, Dept Civil Chem & Environm Engn, I-16129 Genoa, Italy
关键词
Ethanol dehydration; Zeolites; Silica alumina; Ethylene; Diethyl ether; Coking; METAL-OXIDE CATALYSTS; MODIFIED NANOCRYSTALLINE; RAMAN-SPECTROSCOPY; H-ZSM-5; CATALYSTS; CARBON NANOTUBES; PROBE MOLECULES; SURFACE-ACIDITY; RAW CHEMICALS; ACTIVE-SITES; RAPESEED OIL;
D O I
10.1016/j.apcata.2014.12.047
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Ethanol dehydration was investigated over commercial H-FER, H-MFI, H-MOR, H-BEA, H-Y and H-USY zeolite samples, and alumina and silica alumina for comparison. The catalysts were characterized using FT-IR spectroscopy of the surface OH groups and of adsorbed CO and pyridine. UV-vis, Raman and TG-DTA were applied to characterize coke, formed more on H-MOR and H-BEA. H-zeolites are definitely more active than silica alumina and alumina on catalyst weight base. The H-MOR sample is the most active but the H-MFI samples with Si/Al-2 ratios 280 and 50 show higher reaction rates per AI ion, H-PER and faujasites show highest ethylene yield (99.9% at 573 K). At lower temperature and higher space velocities, diethyl ether is formed with high yield (>70% at 453-473 K on H-BEA and H-MFI (50)). Overconversion of ethylene mainly to aromatics is observed on H-MFI (50). The different behaviour of protonic zeolites can predominantly be explained by confinement effects on the different zeolite cavities. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:77 / 89
页数:13
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