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Optimal Pretreatment Conditions for Co–Mo Hydrotreatment Catalysts Prepared Using Ethylenediamine as a Chelating Agent Full article

Conference International Symposium on Advances in Hydroprocessing of Oil Fractions
09-14 Jun 2013 , Acapulco
Journal Catalysis Today
ISSN: 0920-5861 , E-ISSN: 1873-4308
Output data Year: 2014, Volume: 220-222, Pages: 327-336 Pages count : 10 DOI: 10.1016/j.cattod.2013.08.019
Tags Chelating agent, Ethylenediamine, Hydrotreating catalyst, Pretreatment temperature
Authors Leonova K.A. 1 , Klimov O.V. 1 , Kochubey D.I. 1 , Chesalov Yu.A. 1 , Gerasimov E.Yu. 1 , Prosvirin I.P. 1 , Noskov A.S. 1
Affiliations
1 Boreskov Institute of Catalysis, Siberian Branch, Russian Academy of Sciences, pr. ak. Lavrentiev 5, 630090 Novosibirsk, Russia

Abstract: Co–Mo/Al2O3 catalysts were prepared using bimetallic complexes consisting of ethylenediamine and polybasic carboxylic acid ligands coordinated to cobalt and molybdenum, respectively. The structures of the complex compounds remained unchanged upon initial adsorption to alumina. However, the chemical composition, morphology of the Co–Mo–S phase and thiophene hydrogenolysis activity of the catalysts were dependent on the pretreatment temperature before sulphidation. Nitrogen, a product of ligand decomposition, significantly inhibited catalytic activity. To attain the maximum thiophene hydrogenolysis activity, a 400 °C pretreatment was necessary. At this temperature, most of the nitrogen was removed, but the formation of Co and Mo compounds, which transform into low activity compounds during sulphidation, was not observed.
Cite: Leonova K.A. , Klimov O.V. , Kochubey D.I. , Chesalov Y.A. , Gerasimov E.Y. , Prosvirin I.P. , Noskov A.S.
Optimal Pretreatment Conditions for Co–Mo Hydrotreatment Catalysts Prepared Using Ethylenediamine as a Chelating Agent
Catalysis Today. 2014. V.220-222. P.327-336. DOI: 10.1016/j.cattod.2013.08.019 WOS Scopus РИНЦ ANCAN OpenAlex
Dates:
Submitted: Apr 1, 2013
Accepted: Aug 27, 2013
Published online: Sep 26, 2013
Published print: Mar 1, 2014
Identifiers:
Web of science: WOS:000328497600034
Scopus: 2-s2.0-84889648061
Elibrary: 21861610
Chemical Abstracts: 2013:1527033
Chemical Abstracts (print): 160:135833
OpenAlex: W1979507096
Citing:
DB Citing
Web of science 17
Scopus 20
Elibrary 26
OpenAlex 16
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