Simultaneous glycerol dehydration and in situhydrogenolysis over Cu-Al oxide under an inert atmosphere
Among various catalysts screened, the Cu-Al oxide catalyst, prepared by a co-precipitation method, exhibited excellent activity for simultaneous glycerol dehydration and its hydrogenolysis without external hydrogen. Detailed characterization by XRD, XPS, HR-TEM, TPR, etc., showed evidence of Cu supe...
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Veröffentlicht in: | Green chemistry : an international journal and green chemistry resource : GC 2012-10, Vol.14 (10), p.2780-2789 |
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Hauptverfasser: | , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Among various catalysts screened, the Cu-Al oxide catalyst, prepared by a co-precipitation method, exhibited excellent activity for simultaneous glycerol dehydration and its hydrogenolysis without external hydrogen. Detailed characterization by XRD, XPS, HR-TEM, TPR, etc., showed evidence of Cu super(2+) in the form of CuO and CuAl sub(2)O sub(4), along with Cu super(0) and Cu super(1+) species, which are responsible for their multifunctional roles in glycerol APR, dehydration and hydrogenolysis reactions under inert conditions. This catalyst also presented consistent activity for a duration of 400 h for autogeneous hydrogenolysis of refined glycerol with 36% selectivity to 1,2-propanediol (1,2-PDO). Manipulating the temperature and feed flow rate conditions, meant that the selectivity to acetol and 1,2-PDO could be tailored as desired. Substantial enhancement in 1,2-PDO selectivity (75%) was achieved for an aqueous bio-glycerol feed over the same catalyst for 50 h of testing. |
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ISSN: | 1463-9262 1463-9270 |
DOI: | 10.1039/c2gc35661a |