CARBON ISOTOPE EFFECTS IN THE OPEN-SYSTEM FISCHER-TROPSCH SYNTHESIS
| dc.contributor.author | Taran Y.A. | |
| dc.contributor.author | Kliger G.A. | |
| dc.contributor.author | Sevastianov V.S. | |
| dc.date.accessioned | 2026-06-04T15:32:05Z | |
| dc.date.issued | 2007 | |
| dc.description.abstract | Carbon isotopic composition was measured for products of the Fischer-Tropsch synthesis: catalytic reaction between CO and H2 to produce CO, CO2, light hydrocarbons C1-C4 and "oil" fraction. Hydrogen isotopes were also measured in the oil fraction and the produced water. Experimental runs were conducted in the flow-through reactor at 260-310 °C and 30 bar using the synthesis gas composed of 5N2 + 3H2 + 2CO, on Fe-catalyst mixed with ZSM-5 synthetic zeolite. In the two of seven runs a Fe + Co-catalyst was used that gives a lower yield of unsaturated hydrocarbons in reaction products. The isotopic effects depended on the conversion of the carbon monoxide. Under steady-state conditions (CO conversion more than 90%) a strong kinetic fractionation was observed between CO and CO2 (~-10‰) and CO and hydrocarbons (~+38‰). At low conversion a clear "inverse" isotopic trend of the depletion in 13C of longer hydrocarbon chains was observed. On average, Δ12 = δ13C(CH4) - δ13C(C2H6) correlates well with the CO conversion: the C2H6 is ~6‰ isotopically lighter than CH4 at low conversion and ~2‰ heavier at steady-state regime. Under steady-state conditions there almost no difference was observed in the isotopic composition of methane and ethane and higher hydrocarbons. The chemical composition of light hydrocarbons in the products of flow-through, dynamic FTS is different from that found in the static FTS-type experiments with Fe-catalyst, but isotopic effects are similar. Our results suggest that the isotopic distribution of carbon found in so-called "abiogenic" hydrocarbons from some natural gases (δ13C1 > δ13C2 > δ13C3 >⋯) is somewhat similar to that at low conversion of CO, but do not resemble the distribution characteristic for the high conversion products, at least, on Fe-catalyst. Other processes (a simple mixing of two or more endmembers) or other P-T conditions of the carbon reduction could be responsible for the "inverse" isotopic trend found in meteorites and some natural gases. © 2007 Elsevier Ltd. All rights reserved. | |
| dc.identifier | https://elibrary.ru/item.asp?id=13535575 | |
| dc.identifier.citation | Geochimica et Cosmochimica Acta, 2007, 71, 18, 4474-4487 | |
| dc.identifier.doi | 10.1016/j.gca.2007.06.057 | |
| dc.identifier.issn | 0016-7037 | |
| dc.identifier.uri | https://repository.geologyscience.ru/handle/123456789/53183 | |
| dc.title | CARBON ISOTOPE EFFECTS IN THE OPEN-SYSTEM FISCHER-TROPSCH SYNTHESIS | |
| dc.type | Статья |
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