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Fischer-Tropsch synthesis. Effect of alkali, bicarbonate and chloride addition on activity and selectivity

  • Wenping Ma
  • , Gary Jacobs
  • , Jungshik Kang
  • , Dennis E. Sparks
  • , Muthu Kumaran Gnanamani
  • , Venkat Ramana Rao Pendyala
  • , Wilson D. Shafer
  • , Robert A. Keogh
  • , Uschi M. Graham
  • , Gerald A. Thomas
  • , Burtron H. Davis

Producción científica: Article › revisión exhaustiva

14 Citas (Scopus)

Resumen

The sensitivity of 100Fe/5.1Si/2Cu/3K Fischer-Tropsch synthesis (FTS) catalyst to the impurities of KCl, NaCl, KHCO3 and NaHCO3 in syngas (0.1-100 ppm) was studied in a slurry phase reactor at 533.2 or 543.2 K, H2/CO = 0.67-0.77, 1.31 MPa and 10 NL/g-cat/h. The impurities were co-fed with syngas, and the influence of each contaminant concentration on Fe catalyst behavior was examined for 72-144 h. The presence of up to 40 ppmw halide compounds (NaCl and KCl) or alkali bicarbonates (NaHCO3 and KHCO3) in syngas at 543.2 K or up to 100 ppm of NaCl and KCl at 533.2 K had little impact on the Fe catalyst activity and selectivities to CH 4, C5+ and C4 olefin and 1-olefin during 400 h (543.2 K) or 1400 h testing (533.2 K). CO2 selectivity slightly increased after feeding the impurity-containing solutions, which was due to enhanced water gas shift (WGS). ICP results for the Fe catalysts at the end of the FTS reaction test and of the FTS products (i.e., water, oil or wax phase) indicate that the impurity ions (K+, Na+ or Cl -) introduced were present in all phases of the FTS products, the greater part being retained in the wax. Therefore, the contaminant ions (i.e., Na, K or Cl) in the water solution injected appear to not strongly adsorb on the Fe catalyst surface at typical FTS conditions in the slurry phase reactor. This is assumed to be responsible for the lack of change in FTS behavior for the Fe catalyst using the contaminants studied.

Idioma originalEnglish
Páginas (desde-hasta)73-79
Número de páginas7
PublicaciónCatalysis Today
Volumen215
DOI
EstadoPublished - oct 15 2013

Nota bibliográfica

Funding Information:
This work was made possible by the financial support from DOE contract number DE-FC26-08NT0006368 and DOE contract number DE-NT0006289.

Financiación

This work was made possible by the financial support from DOE contract number DE-FC26-08NT0006368 and DOE contract number DE-NT0006289.

FinanciadoresNúmero del financiador
Michigan State University-U.S. Department of Energy (MSU-DOE) Plant Research LaboratoryDE-NT0006289, DE-FC26-08NT0006368

    ASJC Scopus subject areas

    • Catalysis
    • General Chemistry

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