Effect of the nickel impregnation method on clay supports in the hydroconversion reaction of n-decane

Literature Information

Publication Date 2022-10-13
DOI 10.1039/D2RE00353H
Impact Factor 4.239
Authors

Jahaziel Amaya, Cesar Calderón, Rafael Molina, Sonia Moreno


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Abstract

Ni bifunctional catalysts supported on vermiculite, halloysite and bentonite previously modified by means of delamination or acid treatment were synthesized. The Ni was incorporated using three synthesis methods: auto-combustion (AC), microwave-assisted auto-combustion (AM) and the wet impregnation method (WI). The solids obtained were characterized under different conditions: i) as oxides prior to the reaction, using X-ray diffraction (XRD), N2 physisorption and temperature programmed reduction (H2-TPR), ii) under “in situ” reaction conditions using infrared spectroscopy with probe molecule (NH3-DRIFTS) accompanied by titration with HCl, iii) “ex situ” using high resolution transmission electron microscopy (HRTEM) and iv) post-reaction catalysts were characterized using thermogravimetric analysis (TGA-DSC), Raman and infrared spectroscopy. The catalytic performance of the materials was evaluated in the hydroconversion of decane (C10). In addition, the influence of the impregnation method on the mineral used was analyzed. In the case of the solids obtained from bentonite and halloysite, the methods that most favored the catalytic activity were those of auto-combustion, while in the case of the catalysts obtained with vermiculite as a support, the most favorable method was wet impregnation (WI), which was related to the number of reducible species, the dispersion and acid properties that each method favored depending on the clay mineral used. Finally, all the catalysts presented a high resistance to the formation of carbonaceous residues on their surface, indicating a high activity and low deactivation of the materials.

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Reaction Chemistry & Engineering

Reaction Chemistry & Engineering
CiteScore: 0
Self-citation Rate: 8.8%
Articles per Year: 284

Reaction Chemistry & Engineering is an interdisciplinary journal reporting cutting-edge research focused on enhancing the understanding and efficiency of reactions. Reaction engineering leverages the interface where fundamental molecular chemistry meets chemical engineering and technology. Challenges in chemistry can be overcome by the application of new technologies, while engineers may find improved solutions for process development from the latest developments in reaction chemistry. Reaction Chemistry & Engineering is a unique forum for researchers whose interests span the broad areas of chemical engineering and chemical sciences to come together in solving problems of importance to wider society. All papers should be written to be approachable by readers across the engineering and chemical sciences. Papers that consider multiple scales, from the laboratory up to and including plant scale, are particularly encouraged.

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