The conversion of furfural into cyclopentanone over Ni–Cu bimetallic catalysts was studied under hydrogen atmosphere. Furfuryl alcohol, 4-hydroxy-2-cyclopentenone and 2-cyclopentenone were verified as three key intermediates. Rearrangement of the furan ring was independent of hydrogenation, starting from furfuryl alcohol rather than furfural. The opening and closure of the furan ring were closely related to the attack of a H₂O molecule on the 5-position of furfuryl alcohol. Prior hydrogenation of the aldehyde group accounted for the different reactivity of furfural and furfuryl alcohol. The high selectivity of cyclopentanone was ascribed to the presence of 2-cyclopentenone.

Furfural was converted to tetrahydrofurfuryl alcohol with high yield in water on alkaline earth metal modified Ni/Al₂O₃.

An isolated yield of MCP of 58% was obtained from HMF on Pd/Nb ₂ O ₅ , which was prepared using cyclohexene as a reductant, and Ca–Al.

Lithium-ion capacitors (LICs) are now drawing increasing attention because of their potential to overcome the current energy limitations of supercapacitors and power limitations of lithium-ion batteries. In this work, we designed LICs by combining an electric double-layer capacitor cathode and a lithium-ion battery anode. Both the cathode and anode are derived from graphene-modified phenolic resin with tunable porosity and microstructure. They exhibit high specific capacity, superior rate capability and good cycling stability. Benefiting from the graphene-enhanced electrode materials, the all graphene-based LICs demonstrate a high working voltage (4.2 V), high energy density of 142.9 Wh kg ⁻¹ , maximum power density of 12.1 kW kg ⁻¹ with energy density of 50 Wh kg ⁻¹ , and long stable cycling performance (with ∼88% capacity retention after 5000 cycles). Considering the high performance of the device, the cost-effective and facile preparation process of the active materials, this all graphene-based lithium-ion capacitor could have many promising applications in energy storage systems.