Reasons for the Rapid Deactivation of a Cobalt Catalyst
in the High-Efficiency Fischer–Tropsch Synthesis
of C19+ Hydrocarbons1
V. N. Soromotina, R. E. Yakovenkoa, A. V. Medvedeva, and S. A. Mitchenkoa, *
a Platov South-Russian State Polytechnic University (NPI), Novocherkassk, 346128 Russia
Correspondence to: *е-mail: samit_rpt@mail.ru
1Abbreviations and notation: FTS, Fischer–Tropsch synthesis; TEM, transmission electron microscopy; XRD, X-ray diffraction; GHSV, gas hourly space velocity; DSC, differential scanning calorimetry; DTA, differential thermal analysis.
Received 15 June, 2021
Abstract—The results of a study on the deactivation of an industrial Co–Al2O3/SiO2 catalyst under the conditions of highly productive Fischer–Tropsch synthesis of long-chained hydrocarbons at high pressure (6 MPa) are presented. It was found that an increase in the synthesis temperature led to a decrease in the rate of catalyst deactivation. The effect of the thermal agglomeration of cobalt particles and the carbonization of catalyst surface on the activity of the catalyst under the test conditions was insignificant. A correlation between the rate of catalyst deactivation and the selectivity for С19+ hydrocarbons was found; this correlation indicated the blocking of chain growth centers by synthesized waxes as the main reason for the rapid loss of catalyst activity.
Keywords: Fischer–Tropsch synthesis, cobalt catalyst, deactivation, С19+ hydrocarbons, process selectivity
DOI: 10.1134/S002315842106015X