2017•CatalystsOpen access

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

Dominik Götz, Martin Lucas, Peter K. Claus

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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.

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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.

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Available 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.

Key concepts: Hydrogenolysis, Furfuryl alcohol, Catalysis, Copper, Chemistry, Selectivity, Alcohol, Aqueous solution

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Aqueous Phase Hydrogenolysis of Bio-Derivable Furfuryl Alcohol to Pentanediols Using Copper Catalysts — Research Paper | ScholarLens