Scaling a bifunctional catalytic Fixed-Bed reactor for acetone-to-mesitylene Jet-Fuel additive production

• Mesitylene renewable jet-fuel additive by condensation of biomass-derived acetone. • Bench-scale demonstration using TiO 2 and Al-MCM-41 catalyst 1/8″ pellets. • Mass transfer in pellets limited the rate of reaction, so a model was fitted to data. • Mesitylene and isophorone yields were improved with catalyst pellets. • Increase in mesitylene yield by combination of both catalysts in consecutive beds. De-fossilization of the aviation sector will require the use of renewable synthetic jet fuels and additives that comply with strict regulations. One such additive, mesitylene, can be produced using a novel sustainable process based on the fermentation of biomass waste to acetone, followed by the self-condensation of acetone to mesitylene. This study addresses the viability of gas-phase self-condensation of acetone, catalyzed by TiO 2 and Al-MCM-41 acid catalysts, at a technological readiness level of TRL-4. The reactor used was a bench-scale fixed-bed reactor (28 mm diameter and 500 mm height) loaded with commercial-sized catalyst pellets (1/8″ diameter). It was equipped with a jacket for heat transfer using flowing thermal oil. The performance of commercial-scale reactors was approximated under conditions of 275 °C, 280 kPa, and a space velocity of 50–500 mol/kg·h. The catalyst pellets exhibited significant mass transfer resistances, which limited the reaction rate. This, in turn, reduced the deactivation rate caused by the adsorption of high-molecular-weight condensation products on the strongest acid sites. Additionally, the product distribution differed between pellet and powder forms of the catalysts, with higher yields of isophorone and mesitylene being observed on TiO 2 and Al-MCM-41 pellets, respectively. A reaction and mass transfer model was proposed and fitted to the bench-scale data. The study also considered the combination of both catalyst pellets in the same reactor for the bench-scale unit. It was demonstrated that mesitylene yield could be improved, with the best configuration being two separate beds placed consecutively in the reactor with a catalyst ratio of 1:2 (TiO 2 :MCM-41).

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Publication Details

Journal
Chemical Engineering Journal
Published
2024-08-12
DOI
https://doi.org/10.1016/j.cej.2024.154694
Citations
2
Primary Topic
Zeolite Catalysis and Synthesis
Type
article
Field-Weighted Citation Impact
0.32

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article

Scaling a bifunctional catalytic Fixed-Bed reactor for acetone-to-mesitylene Jet-Fuel additive production

A. Garcia, Pablo Marín, Salvador Ordóñez
2 citations
Chemical Engineering Journal
Zeolite Catalysis and Synthesis
0.32
article

Scaling a bifunctional catalytic Fixed-Bed reactor for acetone-to-mesitylene Jet-Fuel additive production

A. Garcia, Pablo Marín, Salvador Ordóñez
article en
2 citations

Abstract

• Mesitylene renewable jet-fuel additive by condensation of biomass-derived acetone. • Bench-scale demonstration using TiO 2 and Al-MCM-41 catalyst 1/8″ pellets. • Mass transfer in pellets limited the rate of reaction, so a model was fitted to data. • Mesitylene and isophorone yields were improved with catalyst pellets. • Increase in mesitylene yield by combination of both catalysts in consecutive beds. De-fossilization of the aviation sector will require the use of renewable synthetic jet fuels and additives that comply with strict regulations. One such additive, mesitylene, can be produced using a novel sustainable process based on the fermentation of biomass waste to acetone, followed by the self-condensation of acetone to mesitylene. This study addresses the viability of gas-phase self-condensation of acetone, catalyzed by TiO 2 and Al-MCM-41 acid catalysts, at a technological readiness level of TRL-4. The reactor used was a bench-scale fixed-bed reactor (28 mm diameter and 500 mm height) loaded with commercial-sized catalyst pellets (1/8″ diameter). It was equipped with a jacket for heat transfer using flowing thermal oil. The performance of commercial-scale reactors was approximated under conditions of 275 °C, 280 kPa, and a space velocity of 50–500 mol/kg·h. The catalyst pellets exhibited significant mass transfer resistances, which limited the reaction rate. This, in turn, reduced the deactivation rate caused by the adsorption of high-molecular-weight condensation products on the strongest acid sites. Additionally, the product distribution differed between pellet and powder forms of the catalysts, with higher yields of isophorone and mesitylene being observed on TiO 2 and Al-MCM-41 pellets, respectively. A reaction and mass transfer model was proposed and fitted to the bench-scale data. The study also considered the combination of both catalyst pellets in the same reactor for the bench-scale unit. It was demonstrated that mesitylene yield could be improved, with the best configuration being two separate beds placed consecutively in the reactor with a catalyst ratio of 1:2 (TiO 2 :MCM-41).

Chemical Engineering JournalVol. 497
Universidad de Oviedo (ES)
Ministerio de Ciencia, Innovación y Universidades, Spanish Clinical Research Network, Spanish National Plan for Scientific and Technical Research and Innovation
Affordable and clean energy
Openalex Percentile: Top 50%
Zeolite Catalysis and Synthesis
0.32
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