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Transformations of n-undecane-indole model mixtures over the cracking catalysts resistant to nitrogen compounds Full article

Journal Fuel Processing Technology
ISSN: 0378-3820
Output data Year: 2018, Volume: 172, Pages: 172-178 Pages count : 7 DOI: 10.1016/j.fuproc.2017.12.020
Tags Catalytic cracking, Nitrogen poisoning, Indole, Acid activation of clays, Acid-base properties, Mg, Al – mixed oxides, Cu, Co, Zn, Ce on Mg, Al – Mixed oxides
Authors Bobkova T.V. 1 , Potapenko O.V. 1 , Doronin V.P. 1 , Sorokina T.P. 1
Affiliations
1 Institute of Hydrocarbons Processing, Siberian Branch of the Russian Academy of Sciences (IHP SB RAS)

Funding (1)

1 Ministry of Science and Higher Education of the Russian Federation 46.2.4

Abstract: Additives to a zeolite-containing cracking catalyst were synthesized and studied in order to enhance the resistance to the poisoning effect of nitrogen compounds (in particular indole) upon cracking of n-undecane as the model FCC hydrocarbon. The additives were represented by acid-activated clays and mixed oxides. The activation of clays in the catalyst by 5% sulfuric acid solutions was shown to enhance the resistance to nitrogen. The introduction of Mg, Al – mixed oxides in the catalytic system in the amount of 10 wt% increased its activity and resistance to indole. The highest resistance was observed for the systems containing magnesium ‑aluminum oxides with a Me2+ to Me3+ molar ratio equal to 0.5: 1. Cobalt modification of these mixed oxides enhanced the activity and nitrogen resistance of the cracking catalysts. Use of such nitrogen-resistant catalysts will allow cracking of heavy raw materials.
Cite: Bobkova T.V. , Potapenko O.V. , Doronin V.P. , Sorokina T.P.
Transformations of n-undecane-indole model mixtures over the cracking catalysts resistant to nitrogen compounds
Fuel Processing Technology. 2018. V.172. P.172-178. DOI: 10.1016/j.fuproc.2017.12.020 WOS Scopus РИНЦ OpenAlex
Dates:
Submitted: Sep 30, 2017
Accepted: Dec 25, 2017
Published online: Dec 29, 2017
Published print: Apr 1, 2018
Identifiers:
Web of science: WOS:000425205300019
Scopus: 2-s2.0-85040590676
Elibrary: 35532126
OpenAlex: W2779075131
Citing:
DB Citing
Web of science 9
Scopus 10
OpenAlex 10
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