Abstract
Metal-modified molecular sieves (MNaY, M = Ni, Co, Cu) have been synthesized by the impregnation method, these catalysts were used for the study of liquid phase oxidation of p-tert-butyltoluene (PTBT) to synthesize p-tert-butylbenzaldehyde (PTBD) for the first time. The catalysts have been characterized by X-ray, XPS, SEM, BET, and TGA. The results show that the Ni/NaY exhibits suitable and stable catalytic activity. Recycle runs show that Ni/NaY was stable for at least five cycles. Under the optimized conditions of having a reaction time of 7 h, 6 mL of PTBT, 0.2 g of Ni/NaY, 0.1 g of N-hydroxyphthalimide (NHPI), 18 mL of acetonitrile, a reaction temperature of 70 °C, and a rotating speed 200 r/min, the conversion of PTBT reached 29.3–30.6% with a PTBD selectivity of 77.2%.
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10 March 2018
In the original version of this article, the corresponding author information was incorrect. This has been corrected with this erratum. The correct corresponding author is Dr. Jiang-Quan Ma.
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Acknowledgements
This work was financially supported by Industry Supporting Project of Zhenjiang of Jiangsu Province (GY2014037); and Industry Supporting Project of Changzhou of Jiangsu Province (CE20140077).
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(1)NaY molecular sieve: industrial products (Liaoning Haitai Technology Development Co., Ltd.); (2)cobalt acetate: AR (Shanghai Maike Lin Biochemical Technology Co., Ltd.); (3)nickel nitrate, copper nitrate: AR (MeiLan Industrial Shanghai Co., Ltd.); (4)P-tert-butyl toluene: industrial products (Jiangsu Lvyuan Fine Chemical Co., Ltd.); (5)N-hydroxy phthalimide (NHPI): 98% for research and development (Beijing Braunway Technology Co., Ltd.); (6)acetonitrile: AR (Shanghai Mai Ruier Chemical Technology Co., Ltd. Company).
A correction to this article is available online at https://doi.org/10.1007/s10562-018-2344-1.
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Yin, Q., Shen, TT., Ma, JQ. et al. Study on the Liquid Phase Oxidation of p-Tert-butyltoluene Over Ni/NaY. Catal Lett 147, 1214–1220 (2017). https://doi.org/10.1007/s10562-017-2018-4
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DOI: https://doi.org/10.1007/s10562-017-2018-4