4.7 Article

Tuning of activity and selectivity of Ni/(Al)SBA-15 catalysts in naphthalene hydrogenation

Journal

CATALYSIS TODAY
Volume 360, Issue -, Pages 27-37

Publisher

ELSEVIER
DOI: 10.1016/j.cattod.2019.09.018

Keywords

Nickel catalysts; (Al)SBA-15; Hydrogenation; Naphthalene; Activity; Selectivity

Funding

  1. Consejo Nacional de Ciencia y Tecnologia (CONACyT, Mexico) [CVU421070]
  2. DGAPA-UNAM, Mexico (PAPIIT) [IN-115218]

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The hydrogenation of naphthalene using nickel catalysts on SBA-15 and Al-SBA-15 supports was studied to evaluate the effect of support acidity. Catalysts prepared with Al-SBA-15 support and Ni:EDTA complex showed higher activity and selectivity towards decalins. This was attributed to better dispersion of metallic Ni species and higher total amount of acid sites.
The hydrogenation of naphthalene was performed with nickel catalysts (4 wt. % of Ni) supported on SBA-15 and Al-SBA-15 in order to evaluate the effect of the support's acidity on the activity and selectivity of the catalysts. The incorporation of aluminum into the SBA-15 support was performed during the hydrothermal synthesis of the material with the aim to reach the isomorphic substitution of Si4+ by Al3+ leading to the generation of Bronsted acid sites. Two different precursors (nickel nitrate and a Ni:EDTA complex) were used for the preparation of the catalysts on each support. Catalysts were characterized by nitrogen physisorption, powder X-ray diffraction, temperature programmed reduction, temperature programmed desorption of ammonia, scanning and high-resolution transmission electron microscopy. The Al-SBA-15 support was characterized by solid state Al-27 MAS-NMR. The results showed that the intrinsic activity of the catalysts (TOF) increased when the Al-SBA-15 support and the Ni:EDTA complex were used in the catalyst's preparation. The catalysts prepared using the Ni:EDTA complex showed high selectivity to decalins and higher proportion of trans-decalin in the products than the catalysts prepared with nickel nitrate, which was attributed to a higher dispersion of the metallic Ni species and the larger total amount of acid sites.

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