Catalysts with iron high loading of 30 wt%, promoted with K (2.0 wt%) and Cu (3.75 wt%), have been synthesized according to three different methods: 1) the traditional impregnation method (TR); 2) Ultrasound (US) assisted TR method; 3) Microwave (MW) assisted TR method. All the samples have been fully characterized by BET, ICP/OES, XRPD, TG-DTA, FT-IR, TPR, SEM and TEM and tested in a laboratory pilot plant for Fischer -Tropsch synthesis working at 220°C and 20 bar. The results of the catalysts characterization indicated that the morphology of the samples strongly depends on the method of preparation. The best FTS results in term of C2+ yield (41%) has been obtained using MW with a good value of the selectivity towards heavy hydrocarbons, while in term of CO conversion (58%), using US. The samples prepared with non-traditional methods show FTS better results, probably due to a more wide and uniform distribution of Fe in the medium during the synthesis phase.

Biosyngas Fischer-Tropsch conversion by high Fe loaded supported catalysts prepared with ultrasound and microwave

Di Michele A.
2012

Abstract

Catalysts with iron high loading of 30 wt%, promoted with K (2.0 wt%) and Cu (3.75 wt%), have been synthesized according to three different methods: 1) the traditional impregnation method (TR); 2) Ultrasound (US) assisted TR method; 3) Microwave (MW) assisted TR method. All the samples have been fully characterized by BET, ICP/OES, XRPD, TG-DTA, FT-IR, TPR, SEM and TEM and tested in a laboratory pilot plant for Fischer -Tropsch synthesis working at 220°C and 20 bar. The results of the catalysts characterization indicated that the morphology of the samples strongly depends on the method of preparation. The best FTS results in term of C2+ yield (41%) has been obtained using MW with a good value of the selectivity towards heavy hydrocarbons, while in term of CO conversion (58%), using US. The samples prepared with non-traditional methods show FTS better results, probably due to a more wide and uniform distribution of Fe in the medium during the synthesis phase.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11391/1495251
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