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Received October 20, 2009
Accepted December 21, 2009
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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
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Catalytic mechanism and reaction pathway of acetone ammoximation to acetone oxime over TS-1
1State Key Laboratory of Materials-Oriented Chemical Engineering, College of Chemistry and Chemical Engineering, Nanjing University of Technology, Nanjing 210009, China 2College of Chemistry and Biological Engineering, Changsha University of Science and Technology, Changsha 410076, China
xingwh@njut.edu.cn
Korean Journal of Chemical Engineering, September 2010, 27(5), 1423-1427(5)
https://doi.org/10.1007/s11814-010-0236-1
https://doi.org/10.1007/s11814-010-0236-1
Abstract
A series of two-step reactions and several special experiments were designed and carried out to discover the reaction pathway of acetone ammoximation to acetone oxime over titanium silicalites-1 (TS-1) employing 25 wt% ammonia and 30 wt% hydrogen peroxide as the ammoximation agents. The experimental results show that the acetone oxime can form even if there is no direct contact between acetone and TS-1 catalysts, indicating the hydroxylamine_x000D_
route may be the most important catalytic mechanism for the reaction. HPLC, GC/MS and ion chromatography characterization results show that hydrogen peroxide can oxidize acetone oxime to acetone, nitrite and nitrate in the presence of TS-1. In addition, nitrite and nitrate can form in the reaction of H2O2 and NH3 over TS-1. Based on these results, a possible overall reaction pathway of acetone ammoximation over TS-1 has been proposed.
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de Luis A, Lombrana JI, Varona F, Menendez A, Korean J. Chem. Eng., 26(1), 48 (2009)

