Deutsch
 
Hilfe Datenschutzhinweis Impressum
  DetailsucheBrowse

Datensatz

DATENSATZ AKTIONENEXPORT

Freigegeben

Zeitschriftenartikel

Intermediate product regulation in tandem solid catalysts with multimodal porosity for high-yield synthetic fuel production

MPG-Autoren
/persons/resource/persons146595

Duyckaerts,  Nicolas
Research Department Schüth, Max-Planck-Institut für Kohlenforschung, Max Planck Society;

/persons/resource/persons132899

Trotus,  Ioan-Teodor
Research Department Schüth, Max-Planck-Institut für Kohlenforschung, Max Planck Society;

/persons/resource/persons58985

Schüth,  Ferdi
Research Department Schüth, Max-Planck-Institut für Kohlenforschung, Max Planck Society;

/persons/resource/persons141739

Prieto,  Gonzalo
Research Group Prieto, Max-Planck-Institut für Kohlenforschung, Max Planck Society;

Externe Ressourcen
Es sind keine externen Ressourcen hinterlegt
Volltexte (beschränkter Zugriff)
Für Ihren IP-Bereich sind aktuell keine Volltexte freigegeben.
Volltexte (frei zugänglich)
Es sind keine frei zugänglichen Volltexte in PuRe verfügbar
Ergänzendes Material (frei zugänglich)
Es sind keine frei zugänglichen Ergänzenden Materialien verfügbar
Zitation

Duyckaerts, N., Bartsch, M., Trotus, I.-T., Pfänder, N., Lorke, A., Schüth, F., et al. (2017). Intermediate product regulation in tandem solid catalysts with multimodal porosity for high-yield synthetic fuel production. Angewandte Chemie International Edition, 56(38), 11480-11484. doi:10.1002/anie.201705714.


Zitierlink: https://hdl.handle.net/11858/00-001M-0000-002D-C2EA-2
Zusammenfassung
Tandem catalysis is an attractive strategy to intensify chemical processes but simultaneous control over the individual and concerted catalyst performances poses a challenge. We show that enhanced pore transport within a Co/Al2O3 Fischer-Tropsch (FT) catalyst with a hierarchical porosity enables its tandem integration with a Pt/ZSM-5 zeolitic hydrotreating catalyst in a spatially distant fashion ‒ permitting a catalyst-specific temperature adjustment ‒ albeit resembling a close active site proximity ‒ by mitigating secondary reactions of primary FT α-olefin products. This approach enables the conciliation of in situ de-waxing with a minimum production of gases (18 wt%) and an up to two-fold higher (50 wt%) selectivity to middle-distillates compared to benchmark mesoporous FT catalysts. An overall 80% selectivity to liquid hydrocarbons from syngas is attained in one step, attesting for the potential of this strategy to increase the efficiency in intensified gas-to-liquid technologies.