Reaction engineering of the hydrogenolysis of liquid n-Alkanes: Comparison of flow and batch reaction systems
Currently there is much interest in developing catalysts for the hydrogenolysis of long-chain alkanes for use in the recycling and upcycling of waste polyolefins. Understanding how reactor configurations affect reactivity and product distributions for this class of reactions is equally important. To...
Saved in:
Main Authors: | , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Elsevier
2025-03-01
|
Series: | Chemical Engineering Journal Advances |
Subjects: | |
Online Access: | http://www.sciencedirect.com/science/article/pii/S2666821124001182 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
_version_ | 1832557524461551616 |
---|---|
author | Zhuoming Feng Siwon Lee Raymond J. Gorte John M. Vohs |
author_facet | Zhuoming Feng Siwon Lee Raymond J. Gorte John M. Vohs |
author_sort | Zhuoming Feng |
collection | DOAJ |
description | Currently there is much interest in developing catalysts for the hydrogenolysis of long-chain alkanes for use in the recycling and upcycling of waste polyolefins. Understanding how reactor configurations affect reactivity and product distributions for this class of reactions is equally important. To aid in this effort, here we report a study of the hydrogenolysis of the alkane, n-hexatriacontane (C36H74), over a Ru/SiO2 catalyst in both batch and flow reactor configurations. For similar catalyst contact times and H2 pressures, the C36 hydrogenolysis rate was found to be significantly higher in the batch reactor compared to the flow reactor which can be attributed to H2 bubbles forming inactive dry zones on the catalyst surface in the flow reactor which are less prevalent in the batch reactor. In both reactor systems the hydrogenolysis rate was found to be negative order in H2 and that transport of the H2 through the liquid phase to the catalyst surface was not rate limiting. |
format | Article |
id | doaj-art-82e4713f0e2e4dbd885d49d3a12e1af3 |
institution | Kabale University |
issn | 2666-8211 |
language | English |
publishDate | 2025-03-01 |
publisher | Elsevier |
record_format | Article |
series | Chemical Engineering Journal Advances |
spelling | doaj-art-82e4713f0e2e4dbd885d49d3a12e1af32025-02-03T04:17:03ZengElsevierChemical Engineering Journal Advances2666-82112025-03-0121100701Reaction engineering of the hydrogenolysis of liquid n-Alkanes: Comparison of flow and batch reaction systemsZhuoming Feng0Siwon Lee1Raymond J. Gorte2John M. Vohs3Department of Chemical and Biomolecular Engineering, University of Pennsylvania, Philadelphia, PA 19104, USADepartment of Materials Science and Engineering, Hanbat National University, Daejeon 34158, Republic of KoreaDepartment of Chemical and Biomolecular Engineering, University of Pennsylvania, Philadelphia, PA 19104, USADepartment of Chemical and Biomolecular Engineering, University of Pennsylvania, Philadelphia, PA 19104, USA; Corresponding author.Currently there is much interest in developing catalysts for the hydrogenolysis of long-chain alkanes for use in the recycling and upcycling of waste polyolefins. Understanding how reactor configurations affect reactivity and product distributions for this class of reactions is equally important. To aid in this effort, here we report a study of the hydrogenolysis of the alkane, n-hexatriacontane (C36H74), over a Ru/SiO2 catalyst in both batch and flow reactor configurations. For similar catalyst contact times and H2 pressures, the C36 hydrogenolysis rate was found to be significantly higher in the batch reactor compared to the flow reactor which can be attributed to H2 bubbles forming inactive dry zones on the catalyst surface in the flow reactor which are less prevalent in the batch reactor. In both reactor systems the hydrogenolysis rate was found to be negative order in H2 and that transport of the H2 through the liquid phase to the catalyst surface was not rate limiting.http://www.sciencedirect.com/science/article/pii/S2666821124001182Polymer upcyclingHydrogenolysisN-hexatriacontanePolyethylene |
spellingShingle | Zhuoming Feng Siwon Lee Raymond J. Gorte John M. Vohs Reaction engineering of the hydrogenolysis of liquid n-Alkanes: Comparison of flow and batch reaction systems Chemical Engineering Journal Advances Polymer upcycling Hydrogenolysis N-hexatriacontane Polyethylene |
title | Reaction engineering of the hydrogenolysis of liquid n-Alkanes: Comparison of flow and batch reaction systems |
title_full | Reaction engineering of the hydrogenolysis of liquid n-Alkanes: Comparison of flow and batch reaction systems |
title_fullStr | Reaction engineering of the hydrogenolysis of liquid n-Alkanes: Comparison of flow and batch reaction systems |
title_full_unstemmed | Reaction engineering of the hydrogenolysis of liquid n-Alkanes: Comparison of flow and batch reaction systems |
title_short | Reaction engineering of the hydrogenolysis of liquid n-Alkanes: Comparison of flow and batch reaction systems |
title_sort | reaction engineering of the hydrogenolysis of liquid n alkanes comparison of flow and batch reaction systems |
topic | Polymer upcycling Hydrogenolysis N-hexatriacontane Polyethylene |
url | http://www.sciencedirect.com/science/article/pii/S2666821124001182 |
work_keys_str_mv | AT zhuomingfeng reactionengineeringofthehydrogenolysisofliquidnalkanescomparisonofflowandbatchreactionsystems AT siwonlee reactionengineeringofthehydrogenolysisofliquidnalkanescomparisonofflowandbatchreactionsystems AT raymondjgorte reactionengineeringofthehydrogenolysisofliquidnalkanescomparisonofflowandbatchreactionsystems AT johnmvohs reactionengineeringofthehydrogenolysisofliquidnalkanescomparisonofflowandbatchreactionsystems |