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Aqueous Phase Hydrogenolysis of Bio-Derivable Furfuryl Alcohol to Pentanediols Using Copper Catalysts

Götz, Dominik ; Lucas, Martin ; Claus, Peter (2017)
Aqueous Phase Hydrogenolysis of Bio-Derivable Furfuryl Alcohol to Pentanediols Using Copper Catalysts.
In: Catalysts, 7 (2)
doi: 10.3390/catal7020050
Artikel, Bibliographie

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Kurzbeschreibung (Abstract)

In the context of sustainable production processes based on bio-derivable feedstocks, the hydrogenolysis of furfuryl alcohol gives access to two important diols. This work evaluates the performance of commercial copper catalysts in the aqueous phase hydrogenolysis reaching a selectivity towards 1,2-pentanediol of up to 34%. In contrast to noble metal catalysts such as supported ruthenium, the selectivity of the hydrogenation product, tetrahydrofurfuryl alcohol, is significantly lower, so the desired diols are now the main products of this reaction. Catalysis experiments show that the performance is correlated to the catalyst composition rather than the free copper surface, indicating a strong influence of the supporting material. Although the formation of oligomeric and polymeric side products is still perturbing, copper catalysts represent promising candidates for this reaction due to their low cost and wide availability.

Typ des Eintrags: Artikel
Erschienen: 2017
Autor(en): Götz, Dominik ; Lucas, Martin ; Claus, Peter
Art des Eintrags: Bibliographie
Titel: Aqueous Phase Hydrogenolysis of Bio-Derivable Furfuryl Alcohol to Pentanediols Using Copper Catalysts
Sprache: Englisch
Publikationsjahr: 2017
Ort: Darmstadt
Verlag: MDPI
Titel der Zeitschrift, Zeitung oder Schriftenreihe: Catalysts
Jahrgang/Volume einer Zeitschrift: 7
(Heft-)Nummer: 2
DOI: 10.3390/catal7020050
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Kurzbeschreibung (Abstract):

In the context of sustainable production processes based on bio-derivable feedstocks, the hydrogenolysis of furfuryl alcohol gives access to two important diols. This work evaluates the performance of commercial copper catalysts in the aqueous phase hydrogenolysis reaching a selectivity towards 1,2-pentanediol of up to 34%. In contrast to noble metal catalysts such as supported ruthenium, the selectivity of the hydrogenation product, tetrahydrofurfuryl alcohol, is significantly lower, so the desired diols are now the main products of this reaction. Catalysis experiments show that the performance is correlated to the catalyst composition rather than the free copper surface, indicating a strong influence of the supporting material. Although the formation of oligomeric and polymeric side products is still perturbing, copper catalysts represent promising candidates for this reaction due to their low cost and wide availability.

Sachgruppe der Dewey Dezimalklassifikatin (DDC): 500 Naturwissenschaften und Mathematik > 540 Chemie
Fachbereich(e)/-gebiet(e): 07 Fachbereich Chemie
07 Fachbereich Chemie > Ernst-Berl-Institut
07 Fachbereich Chemie > Ernst-Berl-Institut > Fachgebiet Technische Chemie
07 Fachbereich Chemie > Ernst-Berl-Institut > Fachgebiet Technische Chemie > Technische Chemie II
Hinterlegungsdatum: 05 Jan 2024 09:18
Letzte Änderung: 01 Mär 2024 10:48
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