Oxidative Hydrolysis of Cellobiose to Glucose |
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Authors: | Weiling Deng Rodrigo Lobo Worajit Setthapun Steven T Christensen Jeffrey W Elam Christopher L Marshall |
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Affiliation: | (1) Chemical Sciences and Engineering Division, Argonne National Laboratory, 9700 South Cass Avenue, Argonne, IL 60439, USA;(2) Energy Systems Division, Argonne National Laboratory, 9700 South Cass Avenue, Argonne, IL 60439, USA;(3) Present address: Chiang Mai Rajabhat University, Chiang Mai, 50300, Thailand; |
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Abstract: | Abstract Cellobiose hydrolysis into glucose was chosen as a model system for cellulose breakdown to investigate glycosidic bond cleavage.
The hydrolysis was enhanced by increased acidity in an inert gas medium, while air-assisted hydrolysis with a neutral solution
achieved over 70% glucose yield. Hydrogen peroxide, as a stronger oxidant than air, converted cellobiose to carboxyl compounds,
which lowered the glucose selectivity. At 150 °C, the selectivity from cellobiose to glucose was very low on porous γ-Al2O3 supported catalysts, even lower than without a catalyst. When the active metals were prepared on non-porous supports such
as spherical alumina (α phase), the overall yield of glucose was dramatically improved at 120 °C. Similar improvements were
obtained for another disaccharide model, sucrose, which achieved greater than 90% sucrose conversion with selectivity in excess
of 90% at 80 °C. |
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