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One-pot synthesis of ethylbenzene/1-phenylethanol and γ-butyrolactone from simultaneous acetophenone hydrogenation and 1,4-butanediol dehydrogenation over copper based catalysts: effects of the support

Authors
Kannapu, Hari Prasad ReddySuh, Young-WoongNarani, AnandVaddeboina, VeeralakshmiBurri, David RajuSeetha, Rama Rao Kamaraju
Issue Date
Dec-2016
Publisher
Royal Society of Chemistry
Citation
RSC Advances, v.7, no.56, pp 35346 - 35356
Pages
11
Indexed
SCIE
SCOPUS
Journal Title
RSC Advances
Volume
7
Number
56
Start Page
35346
End Page
35356
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/153256
DOI
10.1039/c7ra05558g
ISSN
2046-2069
2046-2069
Abstract
The effect of the support in the simultaneous hydrogenation of acetophenone and dehydrogenation of 1,4-butanediol was studied using supported (MgO, gamma-Al2O3, MgO-Al2O3 and SiO2) copper (10 wt%) catalysts, prepared via impregnation. In this process, acetophenone was transformed to 1-phenylethanol/ethylbenzene and 1,4-butanediol converted to gamma-butyrolactone/tetrahydrofuran under a hydrogen-free environment, indicating the major role of the supports. The Cu/MgO catalyst was active and highly selective towards the production of 1-phenylethanol and gamma-butyrolactone. However, an adverse behaviour was observed over Cu/MgO-Al2O3. An extraordinary catalytic performance was obtained over Cu/SiO2 with high selectivity for ethylbenzene (99%) and gamma-butyrolactone (99%). Contrarily, no hydrogenation of acetophenone was observed over Cu/g-Al2O3 due to the dehydration of 1,4-butanediol, yielding tetrahydrofuran. The main advantage of this process is that no external hydrogen is required for the hydrogenation of acetophenone. Copper dispersion, the reduction behaviour of copper, copper particle size and the acidity and basicity of the catalysts play important roles in the activity. All four catalysts were characterized using BET surface area, N2O pulse chemisorption, XRD, XRF, H-2-TPR, XPS, and TPD of NH3/CO2 to understand our results.
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