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Optimal choice of the preparation procedure and precursor composition for a bulk Ni–Mo–W catalyst K. A. Nadeina, S. V. Budukva, Y. V. Vatutina [et al.]

Contributor(s): Nadeina, Ksenia A | Budukva, Sergey V | Vatutina, Yuliya V | Mukhacheva, Polina P | Gerasimov, Evgeny Yu | Pakharukova, Vera P | Prosvirin, Igor P | Larina, Tatyana V | Klimov, Oleg V | Noskov, Aleksandr S | Atuchin, Victor VMaterial type: ArticleArticleContent type: Текст Media type: электронный Subject(s): прекурсоры | гидроочистка | гидрообессеривание | гидроденитрогенирование | катализаторыGenre/Form: статьи в журналах Online resources: Click here to access online In: Inorganics Vol. 11, № 2. P. 89 (1-23)Abstract: Among the known synthesis procedures and reagents for unsupported Ni–Mo–W catalysts, there is no consensus about optimal preparation conditions of their precursors. In the present work, Ni–Mo–W precursors were prepared via three preparation techniques—hydrothermal synthesis, precipitation method and spray drying—after the synthesis of complex compounds in solution. Ni–Mo–W precursors were studied by the XRD analysis, SEM methods, Raman and UV-vis spectroscopies and XPS measurements and used for the hydrotreatment of straight-run gasoil. Precursors prepared by hydrothermal synthesis contain particles with stacked plate shapes, while other methods provide spherical particles. The formation of different amounts of individual molybdates, tungstates or mixed phases such as W1−xMoxO3 possibly doped by Ni was detected. The precipitation technique results in the formation of spheres, with W located at the center and is unavailable for catalysis. The catalytic activity increased when all active metals are available for the feedstock, and a more mixed phase containing Ni, Mo and W is formed. This mixed phase is realized when the synthesis of the Ni–Mo–W precursors is carried out in solution followed by spray drying. The resulting catalyst has 1.2–4 times higher activity than catalysts prepared by other methods.
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Among the known synthesis procedures and reagents for unsupported Ni–Mo–W catalysts, there is no consensus about optimal preparation conditions of their precursors. In the present work, Ni–Mo–W precursors were prepared via three preparation techniques—hydrothermal synthesis, precipitation method and spray drying—after the synthesis of complex compounds in solution. Ni–Mo–W precursors were studied by the XRD analysis, SEM methods, Raman and UV-vis spectroscopies and XPS measurements and used for the hydrotreatment of straight-run gasoil. Precursors prepared by hydrothermal synthesis contain particles with stacked plate shapes, while other methods provide spherical particles. The formation of different amounts of individual molybdates, tungstates or mixed phases such as W1−xMoxO3 possibly doped by Ni was detected. The precipitation technique results in the formation of spheres, with W located at the center and is unavailable for catalysis. The catalytic activity increased when all active metals are available for the feedstock, and a more mixed phase containing Ni, Mo and W is formed. This mixed phase is realized when the synthesis of the Ni–Mo–W precursors is carried out in solution followed by spray drying. The resulting catalyst has 1.2–4 times higher activity than catalysts prepared by other methods.

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