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Ruthenium nanoparticles supported on carbon: an active catalyst for the hydrogenation of lactic acid to 1,2-propanediol

Ruthenium nanoparticles supported on carbon: an active catalyst for the hydrogenation of lactic acid to 1,2-propanediol
Ruthenium nanoparticles supported on carbon: an active catalyst for the hydrogenation of lactic acid to 1,2-propanediol
The hydrogenation of lactic acid to form 1,2-propanediol has been investigated using Ru nanoparticles supported on carbon as a catalyst. Two series of catalysts which were prepared by wet impregnation and sol-immobilization were investigated. Their activity was contrasted with that of a standard commercial Ru/C catalyst (all catalysts comprise 5 wt % Ru). The catalyst prepared using sol-immobilization was found to be more active than the wet impregnation materials. In addition, the catalyst made by sol-immobilization was initially more active than the standard commercial catalyst. However, when reacted for an extended time or with successive reuse cycles, the sol-immobilized catalyst became less active, whereas the standard commercial catalyst became steadily more active. Furthermore, both catalysts exhibited an induction period during the first 1000 s of reaction. Detailed scanning transmission electron microscopy, X-ray photoelectron spectroscopy and X-ray absorption fine structure analysis data, when correlated with the catalytic performance results, showed that the high activity can be ascribed to highly dispersed Ru nanoparticles. Although the sol-immobilization method achieved these optimal discrete Ru nanoparticles immediately, as can be expected from this preparation methodology, the materials were unstable upon reuse. In addition, surface lactide species were detected on these particles using X-ray photoelectron spectroscopy, which could contribute to their deactivation. The commercial Ru/C catalysts, on the other hand, required treatment under reaction conditions to change from raft-like morphologies to the desired small nanoparticle morphology, during which time the catalytic performance progressively improved
2155-5435
5047-5059
Iqbal, Sarwat
1c0ca009-00c4-4103-97c8-1ba39d000e7d
Kondrat, Simon A.
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Jones, Daniel R.
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Schoenmakers, Daniël C.
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Edwards, Jennifer K.
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Lu, Li
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Yeo, Benjamin R.
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Wells, Peter
bc4fdc2d-a490-41bf-86cc-400edecf2266
Gibson, Emma K.
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Morgan, David J.
a54eaa5b-09bc-4185-8f18-dfc1eeeb310e
Kiely, Christopher J.
431afe51-dda4-44fb-a889-8f0e95a1b902
Hutchings, Graham J.
efab6909-c2f0-4992-a188-10b761075311
Iqbal, Sarwat
1c0ca009-00c4-4103-97c8-1ba39d000e7d
Kondrat, Simon A.
8f09c877-8bb6-4c82-8f81-564085479aff
Jones, Daniel R.
27173125-9036-41d7-8da2-4a19d5637654
Schoenmakers, Daniël C.
82986576-2c94-4180-99de-b0cdaf4afa4b
Edwards, Jennifer K.
c3b78bf8-181f-4878-bbff-a23e3ef9976c
Lu, Li
4f34edb1-6778-43e6-b0ad-ae556395f6c0
Yeo, Benjamin R.
fdf7f6f9-ac0c-4712-8878-289c5d7bb302
Wells, Peter
bc4fdc2d-a490-41bf-86cc-400edecf2266
Gibson, Emma K.
738c74e4-ab68-42fe-bda8-9d4a43669b31
Morgan, David J.
a54eaa5b-09bc-4185-8f18-dfc1eeeb310e
Kiely, Christopher J.
431afe51-dda4-44fb-a889-8f0e95a1b902
Hutchings, Graham J.
efab6909-c2f0-4992-a188-10b761075311

Iqbal, Sarwat, Kondrat, Simon A., Jones, Daniel R., Schoenmakers, Daniël C., Edwards, Jennifer K., Lu, Li, Yeo, Benjamin R., Wells, Peter, Gibson, Emma K., Morgan, David J., Kiely, Christopher J. and Hutchings, Graham J. (2015) Ruthenium nanoparticles supported on carbon: an active catalyst for the hydrogenation of lactic acid to 1,2-propanediol. ACS Catalysis, 5 (9), 5047-5059. (doi:10.1021/acscatal.5b00625).

Record type: Article

Abstract

The hydrogenation of lactic acid to form 1,2-propanediol has been investigated using Ru nanoparticles supported on carbon as a catalyst. Two series of catalysts which were prepared by wet impregnation and sol-immobilization were investigated. Their activity was contrasted with that of a standard commercial Ru/C catalyst (all catalysts comprise 5 wt % Ru). The catalyst prepared using sol-immobilization was found to be more active than the wet impregnation materials. In addition, the catalyst made by sol-immobilization was initially more active than the standard commercial catalyst. However, when reacted for an extended time or with successive reuse cycles, the sol-immobilized catalyst became less active, whereas the standard commercial catalyst became steadily more active. Furthermore, both catalysts exhibited an induction period during the first 1000 s of reaction. Detailed scanning transmission electron microscopy, X-ray photoelectron spectroscopy and X-ray absorption fine structure analysis data, when correlated with the catalytic performance results, showed that the high activity can be ascribed to highly dispersed Ru nanoparticles. Although the sol-immobilization method achieved these optimal discrete Ru nanoparticles immediately, as can be expected from this preparation methodology, the materials were unstable upon reuse. In addition, surface lactide species were detected on these particles using X-ray photoelectron spectroscopy, which could contribute to their deactivation. The commercial Ru/C catalysts, on the other hand, required treatment under reaction conditions to change from raft-like morphologies to the desired small nanoparticle morphology, during which time the catalytic performance progressively improved

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More information

Published date: 15 July 2015
Organisations: Organic Chemistry: SCF

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Local EPrints ID: 400586
URI: http://eprints.soton.ac.uk/id/eprint/400586
ISSN: 2155-5435
PURE UUID: 9c562afa-a331-4bed-a3c1-264c52e7c018
ORCID for Peter Wells: ORCID iD orcid.org/0000-0002-0859-9172

Catalogue record

Date deposited: 19 Sep 2016 13:22
Last modified: 15 Mar 2024 03:24

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Contributors

Author: Sarwat Iqbal
Author: Simon A. Kondrat
Author: Daniel R. Jones
Author: Daniël C. Schoenmakers
Author: Jennifer K. Edwards
Author: Li Lu
Author: Benjamin R. Yeo
Author: Peter Wells ORCID iD
Author: Emma K. Gibson
Author: David J. Morgan
Author: Christopher J. Kiely
Author: Graham J. Hutchings

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