Jesper Ahrenfeldt
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Research Interests
Jesper Ahrenfeldt has a total of 144 co-authors. Here are the top co-authors by number of shared publications:
- Ulrik Birk Henriksen
Department of Chemical and Biochemical Engineering, Technical University of Denmark, 2800 Kgs. Lyngby, Denmark
64 shared publications - Tobias Pape Thomsen
Roskilde University
15 shared publications - Peter Arendt Jensen
Department of Chemical and Biochemical Engineering, Technical University of Denmark, So̷ltofts Plads, Building 229, DK-2800 Kongens Lyngby, Denmark
13 shared publications - Maria Puig-Arnavat
Department of Chemical and Biochemical Engineering, Technical University of Denmark, Kgs. Lyngby, Denmark
12 shared publications - Wolfgang Stelte
Technical University of Denmark
12 shared publications - Andreas Eschenbacher
Department of Chemical and Biochemical Engineering, Technical University of Denmark, 2800 Kgs. Lyngby, Denmark
11 shared publications
Latest Publications
- 9 June 2021
- Published by Springer Nature in Biomass Conversion and Biorefinery
- Vol. 13 (4) , 2985-3000
Influence of wood pellets properties on their grinding performance
- 9 June 2021
- Published by Springer Nature in Biomass Conversion and Biorefinery
- Vol. 13 (4) , 2985-3000
Influence of wood pellets properties on their grinding performance
- Open Access
- 1 September 2020
- Published by Elsevier in Journal of Analytical and Applied Pyrolysis
- Vol. 150, 104892
Performance-screening of metal-impregnated industrial HZSM-5/γ-Al2O3 extrudates for deoxygenation and hydrodeoxygenation of fast pyrolysis vapors
- 1 September 2020
- Published by Elsevier in Journal of Analytical and Applied Pyrolysis
- Vol. 150, 104892
Open AccessPerformance-screening of metal-impregnated industrial HZSM-5/γ-Al2O3 extrudates for deoxygenation and hydrodeoxygenation of fast pyrolysis vapors
- 1 September 2020
- Published by Elsevier in Journal of Analytical and Applied Pyrolysis
- Vol. 150
Micro-pyrolyzer screening of hydrodeoxygenation catalysts for efficient conversion of straw-derived pyrolysis vapors
- 1 September 2020
- Published by Elsevier in Journal of Analytical and Applied Pyrolysis
- Vol. 150
Micro-pyrolyzer screening of hydrodeoxygenation catalysts for efficient conversion of straw-derived pyrolysis vapors
- 1 August 2020
- Published by Elsevier in Chemical Engineering Journal
- Vol. 394
Deoxygenation of wheat straw fast pyrolysis vapors over Na-Al2O3 catalyst for production of bio-oil with low acidity
- 1 August 2020
- Published by Elsevier in Chemical Engineering Journal
- Vol. 394
Deoxygenation of wheat straw fast pyrolysis vapors over Na-Al2O3 catalyst for production of bio-oil with low acidity
- Open Access
Counteracting Rapid Catalyst Deactivation by Concomitant Temperature Increase during Catalytic Upgrading of Biomass Pyrolysis Vapors Using Solid Acid Catalysts
The treatment of biomass-derived fast pyrolysis vapors with solid acid catalysts (in particular HZSM-5 zeolite) improves the quality of liquid bio-oils. However, due to the highly reactive nature of the oxygenates, the catalysts deactivate rapidly due to coking. Within this study, the deactivation and product yields using steam-treated phosphorus-modified HZSM-5/γ-Al2O3 and bare γ-Al2O3 was studied with analytical Py-GC. While at a fixed catalyst temperature of 450 °C, a rapid breakthrough of oxygenates was observed with increased biomass feeding, this breakthrough was delayed and slower at higher catalyst temperatures (600 °C). Nevertheless, at all (constant) temperatures, there was a continuous decrease in the yield of oxygen-free hydrocarbons with increased biomass feeding. Raising the reaction temperature during the vapor treatment could successfully compensate for the loss in activity and allowed a more stable production of oxygen-free hydrocarbons. Since more biomass could be fed over the same amount of catalyst while maintaining good deoxygenation performance, this strategy reduces the frequency of regeneration in parallel fixed bed applications and provides a more stable product yield. The approach appears particularly interesting for catalysts that are robust under hydrothermal conditions and warrants further investigations at larger scales for the collection and analysis of liquid bio-oil.
Open AccessCounteracting Rapid Catalyst Deactivation by Concomitant Temperature Increase during Catalytic Upgrading of Biomass Pyrolysis Vapors Using Solid Acid Catalysts
The treatment of biomass-derived fast pyrolysis vapors with solid acid catalysts (in particular HZSM-5 zeolite) improves the quality of liquid bio-oils. However, due to the highly reactive nature of the oxygenates, the catalysts deactivate rapidly due to coking. Within this study, the deactivation and product yields using steam-treated phosphorus-modified HZSM-5/γ-Al2O3 and bare γ-Al2O3 was studied with analytical Py-GC. While at a fixed catalyst temperature of 450 °C, a rapid breakthrough of oxygenates was observed with increased biomass feeding, this breakthrough was delayed and slower at higher catalyst temperatures (600 °C). Nevertheless, at all (constant) temperatures, there was a continuous decrease in the yield of oxygen-free hydrocarbons with increased biomass feeding. Raising the reaction temperature during the vapor treatment could successfully compensate for the loss in activity and allowed a more stable production of oxygen-free hydrocarbons. Since more biomass could be fed over the same amount of catalyst while maintaining good deoxygenation performance, this strategy reduces the frequency of regeneration in parallel fixed bed applications and provides a more stable product yield. The approach appears particularly interesting for catalysts that are robust under hydrothermal conditions and warrants further investigations at larger scales for the collection and analysis of liquid bio-oil.