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NiWS/Al2O3 Diesel Fraction Deep Hydrotreating Catalyst Synthesized Using Mesostructured Aluminum Hydroxide

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Abstract

On the basis of alumina synthesized via addition of mesostructured aluminum hydroxide gel, which is prepared by the hydrolysis of secondary aluminum butoxide in the presence of triblock copolymer Pluronic P123 to the AlOOH commercial powder, and the commercial reference sample, NiWS/Al2O3 catalysts are prepared using H3PW12O40 heteropolyacid and nickel citrate. The physicochemical properties of the supports and catalysts are studied by low-temperature nitrogen adsorption, temperature-programmed desorption of ammonia, and high-resolution transmission electron microscopy. The catalytic properties are investigated in the process of straight-run diesel fraction hydrotreating in a flow unit. It is shown that the use of the synthesized alumina as a catalyst support leads to an increase in the dispersity of nanosized particles of the NiWS active phase. The catalytic activity in targeted reactions also grows appreciably. The causes of these phenomena are discussed.

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ACKNOWLEDGMENTS

This work was supported by the Ministry of Education and Science of the Russian Federation within the scope of the Federal Target Program “Research and Development in Priority Directions of the Scientific and Technological Complex of Russia for 2014–2020,” agreement no. 14.576.21.0088 (unique project identifier RFMEFI57617X0088).

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Authors and Affiliations

  1. Samara State Technical University, 119991, Samara, Russia

    P. P. Minaev, M. S. Nikul’shina, A. V. Mozhaev & P. A. Nikul’shin

  2. All-Russia Research Institute of Oil Refining, 119991, Moscow, Russia

    P. P. Minaev & P. A. Nikul’shin

Authors
  1. P. P. Minaev
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  2. M. S. Nikul’shina
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  3. A. V. Mozhaev
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  4. P. A. Nikul’shin
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Correspondence to P. P. Minaev.

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Translated by T. Soboleva

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Minaev, P.P., Nikul’shina, M.S., Mozhaev, A.V. et al. NiWS/Al2O3 Diesel Fraction Deep Hydrotreating Catalyst Synthesized Using Mesostructured Aluminum Hydroxide. Pet. Chem. 58, 1186–1191 (2018). https://doi.org/10.1134/S0965544118140098

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