Hydrogenation of aromatic hydrocarbons over nickel–tungsten sulfide catalysts containing mesoporous aluminosilicates of different nature
- Authors: Naranov E.R.1,2, Badeeva A.S.1, Sadovnikov A.A.3, Kardashev S.V.1, Maksimov A.L.1,2, Lysenko S.V.1, Vinokurov V.A.4, Karakhanov E.A.1
-
Affiliations:
- Faculty of Chemistry
- Topchiev Institute of Petrochemical Synthesis
- Kurnakov Institute of General and Inorganic Chemistry
- Gubkin State University of Oil and Gas
- Issue: Vol 56, No 7 (2016)
- Pages: 599-606
- Section: Article
- URL: https://journals.rcsi.science/0965-5441/article/view/178577
- DOI: https://doi.org/10.1134/S0965544116070124
- ID: 178577
Cite item
Abstract
The hydrogenation of naphthalene, toluene, and 2-methylnaphthalene used as model compounds; the hydrodearomatization of the methylnaphthalene fraction; and the hydrocracking of oil sludge over Ni–W sulfide catalysts supported on BEA/TUD, BEA/SBA-15, and ZSM-5/SBA-15 composites containing SBA-15 and TUD mesoporous silicates have been studied. Catalytic tests have been conducted in an autoclave at 300–400°C and an initial hydrogen pressure of 50–90 atm. It has been found that the highest activity is exhibited by the catalyst based on the ZSM-5/SBA-15 (1) composite prepared by the double-templating synthesis and characterized by a specific surface area of 400 m2/g and an acidity of 409 μmol/g. Thus, in the case of dearomatization of the methylnaphthalene fraction at 300°C and an H2 pressure of 50 atm, the content of diaromatic compounds has decreased from 99.0 to 53.4%, while the amount of sulfur compounds has decreased almost 15-fold. The hydrocracking of oil sludge over NiW/ZSM-5/SBA-15 (2) at 400°C and an H2 pressure of 90 atm has led to an increase in the content of light fractions to 52%.
About the authors
E. R. Naranov
Faculty of Chemistry; Topchiev Institute of Petrochemical Synthesis
Author for correspondence.
Email: naranov@petrol.chem.msu.ru
Russian Federation, Moscow; Moscow
A. S. Badeeva
Faculty of Chemistry
Email: naranov@petrol.chem.msu.ru
Russian Federation, Moscow
A. A. Sadovnikov
Kurnakov Institute of General and Inorganic Chemistry
Email: naranov@petrol.chem.msu.ru
Russian Federation, Moscow
S. V. Kardashev
Faculty of Chemistry
Email: naranov@petrol.chem.msu.ru
Russian Federation, Moscow
A. L. Maksimov
Faculty of Chemistry; Topchiev Institute of Petrochemical Synthesis
Email: naranov@petrol.chem.msu.ru
Russian Federation, Moscow; Moscow
S. V. Lysenko
Faculty of Chemistry
Email: naranov@petrol.chem.msu.ru
Russian Federation, Moscow
V. A. Vinokurov
Gubkin State University of Oil and Gas
Email: naranov@petrol.chem.msu.ru
Russian Federation, Moscow
E. A. Karakhanov
Faculty of Chemistry
Email: naranov@petrol.chem.msu.ru
Russian Federation, Moscow
Supplementary files
