Silica-Gel-Supported Cobalt Catalysts for the Selective Synthesis of Long-Chain Hydrocarbons (C19+)

This study investigates a silica-gel-supported cobalt catalyst for synthesizing long-chain hydrocarbons (C19+) from CO and H2. The process conditions were varied within the following ranges: pressure, 1.5–3.5 MPa; gas hourly space velocity (GHSV), 300–830 h–1; H2/CO ratio, 2.0–2.3; and temperature, 187–213°C. Catalytic testing revealed a correlation between the catalyst deactivation rate and the content of C19+ hydrocarbons in the products. When the C19+ content increased from approximately 40 to 55 wt %, the deactivation rate increased more than tenfold. Under optimized conditions (H2/CO = 2.3, P = 2.0 MPa, T = 193°C), the C19+ content reached ~46–50 wt %, and the deactivation rate was minimized. A long-term stability test over 500 h was used to project a catalyst cycle length, which was found to be at least 4000 h. The study results provide a foundation for optimizing Fischer–Tropsch process conditions to maximize catalyst lifetime and selectivity toward heavy hydrocarbons, supporting the recommendation of the proposed catalyst for industrial implementation.

Authors

Institutions

Publication Details

Journal
Petroleum Chemistry
Published
2025-12-01
DOI
https://doi.org/10.1134/s0965544125600195
Primary Topic
Catalysts for Methane Reforming
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Silica-Gel-Supported Cobalt Catalysts for the Selective Synthesis of Long-Chain Hydrocarbons (C19+)

R. E. Yakovenko, D. A. Ponomarev, I. N. Zubkov, M. A. Zubkova et al.
Petroleum Chemistry
Catalysts for Methane Reforming
article

Silica-Gel-Supported Cobalt Catalysts for the Selective Synthesis of Long-Chain Hydrocarbons (C19+)

R. E. Yakovenko, D. A. Ponomarev, I. N. Zubkov, M. A. Zubkova, A. A. Chemes, A. P. Savost’yanov, G. B. Narochnyi
article en

Abstract

This study investigates a silica-gel-supported cobalt catalyst for synthesizing long-chain hydrocarbons (C19+) from CO and H2. The process conditions were varied within the following ranges: pressure, 1.5–3.5 MPa; gas hourly space velocity (GHSV), 300–830 h–1; H2/CO ratio, 2.0–2.3; and temperature, 187–213°C. Catalytic testing revealed a correlation between the catalyst deactivation rate and the content of C19+ hydrocarbons in the products. When the C19+ content increased from approximately 40 to 55 wt %, the deactivation rate increased more than tenfold. Under optimized conditions (H2/CO = 2.3, P = 2.0 MPa, T = 193°C), the C19+ content reached ~46–50 wt %, and the deactivation rate was minimized. A long-term stability test over 500 h was used to project a catalyst cycle length, which was found to be at least 4000 h. The study results provide a foundation for optimizing Fischer–Tropsch process conditions to maximize catalyst lifetime and selectivity toward heavy hydrocarbons, supporting the recommendation of the proposed catalyst for industrial implementation.

Petroleum ChemistryVol. 65(11)
Platov South-Russian State Polytechnic University (RU)
Openalex Percentile: Top 50%
Catalysts for Methane Reforming
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.