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In relation to this article, we declare that there is no conflict of interest.
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Received March 28, 2019
Accepted May 7, 2019
articles This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/bync/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
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Selective synthesis of acetonitrile by reaction of ethanol with ammonia over Ni/Al2O3 catalyst

Department of Chemical Engineering, Chungbuk National University, Cheongju, Chungbuk 28644, Korea
Chshin@chungbuk.ac.kr
Korean Journal of Chemical Engineering, July 2019, 36(7), 1051-1056(6), 10.1007/s11814-019-0294-y
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Abstract

A highly selective synthesis of acetonitrile was carried out by the reaction of ethanol with ammonia on a 10 wt% Ni/Al2O3 catalyst. The conversion of ethanol and selectivity to acetonitrile, ethylene, and monoethylamine were examined by varying experimental parameters such as ammonia partial pressure, reaction temperature, and space time. The increase in the ammonia partial pressure led to a considerable decrease in the conversion and small increase in the acetonitrile selectivity up to a molar ratio of NH3/ethanol of 3, followed by almost constant values. The partial reaction order of ethanol obtained by controlling the space time was one, while that of ammonia was negative, - 0.4. The deactivation behavior of the catalyst after 100 h on stream reaction at 230 °C was analyzed by X-ray photoelectron spectroscopy and temperature programmed oxidation of the catalyst used. The catalyst deactivation was attributed to the gradual formation of nickel carbonitride on the catalyst surface.

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