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Bifunctional MoS(2)/Al(2)O(3)-Zeolite Catalysts in the Hydroprocessing of Methyl Palmitate

A series of bifunctional catalysts, MoS(2)/Al(2)O(3) (70 wt.%), zeolite (30 wt.%) (zeolite—ZSM-5, ZSM-12, and ZSM-22), and silica aluminophosphate SAPO-11, were synthesized for hydroconversion of methyl palmitate (10 wt.% in dodecane) in a trickle-bed reactor. Mo loading was about 7 wt.%. Catalysts...

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Detalles Bibliográficos
Autores principales: Vlasova, Evgeniya, Zhao, Yiheng, Danilova, Irina, Aleksandrov, Pavel, Shamanaev, Ivan, Nuzhdin, Alexey, Suprun, Evgeniy, Pakharukova, Vera, Tsaplin, Dmitriy, Maksimov, Anton, Bukhtiyarova, Galina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10573751/
https://www.ncbi.nlm.nih.gov/pubmed/37834311
http://dx.doi.org/10.3390/ijms241914863
Descripción
Sumario:A series of bifunctional catalysts, MoS(2)/Al(2)O(3) (70 wt.%), zeolite (30 wt.%) (zeolite—ZSM-5, ZSM-12, and ZSM-22), and silica aluminophosphate SAPO-11, were synthesized for hydroconversion of methyl palmitate (10 wt.% in dodecane) in a trickle-bed reactor. Mo loading was about 7 wt.%. Catalysts and supports were characterized by different physical-chemical methods (HRTEM-EDX, SEM-EDX, XRD, N(2) physisorption, and FTIR spectroscopy). Hydroprocessing was performed at a temperature of 250–350 °C, hydrogen pressure of 3.0–5.0 MPa, liquid hourly space velocity (LHSV) of 36 h(−1), and an H(2)/feed ratio of 600 Nm(3)/m(3). Complete conversion of oxygen-containing compounds was achieved at 310 °C in the presence of MoS(2)/Al(2)O(3)-zeolite catalysts; the selectivity for the conversion of methyl palmitate via the ‘direct’ hydrodeoxygenation (HDO) route was over 85%. The yield of iso-alkanes gradually increases in order: MoS(2)/Al(2)O(3) < MoS(2)/Al(2)O(3)-ZSM-12 < MoS(2)/Al(2)O(3)-ZSM-5 < MoS(2)/Al(2)O(3)-SAPO-11 < MoS(2)/Al(2)O(3)-ZSM-22. The sample MoS(2)/Al(2)O(3)-ZSM-22 demonstrated the highest yield of iso-alkanes (40%). The hydroisomerization activity of the catalysts was in good correlation with the concentration of Brønsted acid sites in the synthesized supports.