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Copper-dolomite as effective catalyst for glycerol hydrogenolysis to 1,2-propanediol


Citation

Azri, Norsahida and Ramli, Irmawati and Nda-Umar, Usman Idris and Shamsuddin, Mohd Razali and Saiman, Mohd Izham and Yap, Taufiq Yun Hin (2020) Copper-dolomite as effective catalyst for glycerol hydrogenolysis to 1,2-propanediol. Journal of the Taiwan Institute of Chemical Engineers, 112. 34 - 51. ISSN 1876-1070

Abstract

A series of Cu/dolomite catalysts were synthesized using the impregnation technique, characterized using NH3–TPD, FTIR-Pyridine, XRD, H2-TPR, BET, BJH, FESEM-EDX, and XPS techniques and evaluated in glycerol hydrogenolysis into 1,2-propanediol (1,2-PDO). Remarkably, dolomite support exhibited high acidity, which is, to our knowledge the first acid characteristic revealed among the reported literatures. By doping copper on dolomite support, the acid amount and strength of the catalyst increased. N2O chemisorption analysis suggests that the metallic copper species were well dispersed on dolomite support while the copper surface area increased with copper loading. The formation of metallic copper on dolomite support agreed well with findings derived from XRD and XPS analysis. According to the results of XPS and H2-TPR, metallic copper species were enriched on the grain surfaces of dolomite and not in the bulk. The addition of copper to dolomite ameliorates the redox properties of the catalysts, owing to the reduction at a lower temperature than that of pure CuO and dolomite support. From the catalytic results, 20 wt% Cu/dolomite was the most active catalyst by giving 100% glycerol conversion and 92% selectivity toward 1,2-PDO at 180 ºC, 2 MPa H2 in 6 h reaction time.


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Additional Metadata

Item Type: Article
Divisions: Faculty of Science
DOI Number: https://doi.org/10.1016/j.jtice.2020.07.011
Publisher: Elsevier
Keywords: Glycerol hydrogenolysis; Copper; Dolomite; Acidity1-2-propanediol
Depositing User: Ms. Nuraida Ibrahim
Date Deposited: 10 Mar 2022 02:52
Last Modified: 24 Nov 2022 04:38
Altmetrics: http://www.altmetric.com/details.php?domain=psasir.upm.edu.my&doi=10.1016/j.jtice.2020.07.011
URI: http://psasir.upm.edu.my/id/eprint/88269
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