Understanding the role of pore structure and acidity of zeolite catalyst in the self-etherification of 5-hydroxymethylfurfural to 5,5′(oxy-bis(methylene))bis-2-furfural.

No abstract

The highly‐efficient conversion of 5‐hydroxymethylfurfural (HMF) to 2,5‐bis(ethoxymethyl)furan (BEMF) was achieved over the copper‐loaded hierarchically structured ZSM‐5 (Cu/HSZ) catalysts in the continuous fixed‐bed reactor. The main reaction path for BEMF synthesis on the Cu/HSZ catalysts was confirmed as following: HMF was firstly hydrogenated to BHMF intermediates over metal sites and then the formed BHMF was etherified by acid sites. Benefiting from the ammonia evaporation (AE) method promoted the dispersion of copper and reduced the acidity, the Cu/HSZ‐AE catalyst exhibited more excellent BEMF yield and stability than the catalyst prepared by conventional incipient‐wetness impregnation (Cu/HSZ‐IW). Indeed, the inactivation of Cu/HSZ‐IW catalyst was mainly attributed to the deactivation of copper by carbon species deposition.