Study of glucose isomerisation to fructose over three heterogeneous carbon-based aluminium-impregnated catalysts

Driven by the worldwide demand for sustainable resources and renewable energy, the synthesis of bio-based platform chemicals has attracted broad interest. The isomerisation of glucose to fructose acts as a critical intermediate step among many chemical synthesis routes. In this study, biochar (BC), graphitic oxide (GIO), and graphene oxide (GO) were used as carbon supports to synthesize Al-impregnated heterogeneous catalysts, which were then used for glucose isomerisation under microwave heating in the water at 140 °C. The kinetics model with parameters was used to reveal the interplay of the active sites and compare the activity of the three carbon-based catalysis systems. Catalyst characterisation results showed effective aluminium (Al) impregnation onto the three types of catalysts, and it was found that GIO-Al200 and GO-Al200 showed comparable catalytic activity (fructose yield of 34.3–35.0%) for glucose isomerisation. At the same time, BC-Al200 exhibited slightly lower catalytic activity (fructose yield of 29.4%). The conversion kinetics suggested similar catalytic mechanisms on the three catalysts while BC-Al200 manifested slower kinetics, possibly implying higher activation energy. The fructose selectivity decreased with increasing time due to the formation of side products, yet BC-Al200 resulted in less carbon loss than GIO-Al200 and GO-Al200, probably attributed to its lower catalytic activity and higher pH buffering capacity. A green synthesis route of this study promotes biomass valorisation and makes engineered biochar a promising carbon-based catalyst for sustainable biorefinery. [Display omitted] •Engineered catalysts are produced from biochar and graphite/graphene oxide.•Al-impregnated carbons catalyse glucose isomerisation with 29–35% fructose yields.•Kinetics analysis on the three heterogeneous catalysts are compared.•Al-impregnated biochar shows comparable activity as graphite-derived catalysts.•Green synthesis routes are explored for sustainable biorefinery.