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European Congress of Chemical Engineering - 6
Copenhagen 16-21 September 2007

Abstract 2178 - Catalyst Selection For The Coupled Methanol/paraffins Cracking Process

CATALYST SELECTION FOR THE COUPLED METHANOL/PARAFFINS CRACKING PROCESS

Sustainable process-product development & green chemistry

Sustainable & Clean Technologies - III: Combustion & Emission (T1-6P)

Mrs Diana Mier
University of Basque Country
Chemical Engineering
P.O.BOX-644, 48080 Bilbao
Tlf-94 601 5501/FAX-94 464 8500
Spain

Dr ANDRES T. AGUAYO
Universidad del País Vasco
Ingeniería Química
Apartado 644, 48080 Bilbao
Spain

Dr JAVIER EREÑA
Universidad del Pais Vasco
Ingeniería Química
Apartado 644, 48080 Bilbao
Spain

Mrs Ainhoa Alonso
University of the Basque Country
Chemical Engineering
P.O. Box-644, 48080 Bilbao
Spain

Dr JAVIER BILBAO
Universidad del País Vasco
Ingeniería Química
Apartado 644, 48080 Bilbao
Spain

Keywords: coupled methanol paraffins cracking, catalyst selection

The study of the basic steps of a catalytic process is proposed for the simultaneous cracking of n-butane and methanol, on acid catalysts with shape selectivity, with the aim of selectively obtaining C2-C4 olefins.
The transformation of both raw materials in an integrated process has advantages such us energy compensation because this process combines the exothermic methanol conversion with the highly endothermic hydrocarbon cracking, in a thermo-neutral reaction.

Because of the high temperature needed for the process and the presence of steam in the medium, catalysts with high hydrothermal stability are required. The performance of different catalysts, with different levels of shape selectivity has been studied: HZSM-5 (with Si/Al=30 and Si/Al=280), Ni-HZSM-5 (obtained by impregnation with 1 wt% Ni) and SAPO-18. The final catalysts consist of 25 wt% of active phase agglomerated by wet extrusion with bentonite as binder (30 wt%) and with inert alumina calcined at 1000 ºC as charge (45 wt%).

The kinetic behaviour of the catalysts has been tested in an automated reaction equipment provided with an isothermal fixed bed reactor connected on-line to a gas chromatograph.

Catalyst discrimination has been carried out based on their butane cracking capacity and olefin selectivity. HZSM-5 catalyst with Si/Al=30 has been proven to have the capacity required for cracking. However, the other catalysts produce a significant increase in the concentration of light olefins compared to that obtained with the HZSM-5 zeolite. Ni incorporation into the final catalyst does not contribute to butane cracking.
Finally, coke content deposited on the catalyst has been determinated subsequent to 5 h time-on-stream runs.

Presented Monday 17, 13:30 to 15:00, in session Sustainable & Clean Technologies - III: Combustion & Emission (T1-6P).

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