Effect of Ba impregnation on Al2O3 catalyst for 1-octene production by 1-octanol dehydration
- Authors
- Kim, Young-eun; Jung, Unho; Song, Dahye; Im, Hyo Been; Park, Ji Chan; Youn, Min Hye; Jeong, Heon-Do; Rhim, Geun Bae; Chun, Dong Hyun; Lee, Dong-Wook; Lee, Ki Bong; Koo, Kee Young
- Issue Date
- 1-12월-2020
- Publisher
- ELSEVIER SCI LTD
- Keywords
- Linear alpha-olefin; Alcohol dehydration; 1-Octene; 1-Octanol; Ba/Al2O3 catalyst
- Citation
- FUEL, v.281
- Indexed
- SCIE
SCOPUS
- Journal Title
- FUEL
- Volume
- 281
- URI
- https://scholar.korea.ac.kr/handle/2021.sw.korea/50868
- DOI
- 10.1016/j.fuel.2020.118791
- ISSN
- 0016-2361
- Abstract
- This study investigated the effect of impregnating Ba into an Al2O3 catalyst on the acid-base property and catalytic activity in the dehydration of 1-octanol to produce 1-octene. The Ba/Al2O3 catalysts were prepared by the incipient wetness method with different Ba contents of 0.0-3.0 wt%, and characterized by ICP-MS, BET-BJH, XRD, pyridine-FTIR, and CO2-TPD. The catalytic activity in 1-octanol dehydration was evaluated at 300, 350, and 400 degrees C with liquid hourly space velocity (LHSV) of 7-56 h(-1). As the amount of Ba increased, the density of the basic site on Ba/Al2O3 increased, and the strength distribution of the Lewis acid site (LAS) was changed. Under the reaction condition of 400 degrees C and LHSV = 7 h(-1), Ba/Al2O3 showed higher 1-octene selectivity and 1-octene purity compared with the pure Al2O3 even though the 1-octanol conversion was similar. This is because the added Ba eliminated the strong LAS, which, in turn, inhibited the side-reaction originating from the re adsorption of 1-octene. When LHSV > 21 h(-1), Ba/Al2O3 catalysts showed decreased 1-octanol conversion but maintained high 1-octene selectivity and 1-octene purity. As the Ba content reached 2.0 wt%, 1-octene selectivity was decreased as the formation of dioctyl ether became more active than olefin production. Therefore, 1.5 wt% Ba/Al2O3 is the optimal catalyst for producing 1-octene from 1-octanol in terms of 1-octanol conversion, 1-octene selectivity, and 1-octene yield.
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Collections - College of Engineering > Department of Chemical and Biological Engineering > 1. Journal Articles
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