糠醛
纳米材料基催化剂
层状双氢氧化物
催化作用
化学
羟醛缩合
共沉淀
介孔材料
选择性
纳米颗粒
化学工程
多相催化
冷凝
生物燃料
绿色化学
协同催化
有机化学
比表面积
材料科学
介孔二氧化硅
作者
Nilesh G. Gode,Atul S. Nagpure,Suresh B. Rewatkar,Shailesh K. Bhagat,Gajanan J. Deshmukh,Ajay Saini
标识
DOI:10.1002/cplu.202500416
摘要
Valorization of biomass‐derived chemicals into high‐quality compounds and biofuels is enormously fundamental to diminish dependence on fossil‐based resources. Furfural is a bio‐based valuable compound which can be proficiently upgraded to 4‐(2‐furyl)‐3‐buten‐2‐one ( FAc ) and 1,4‐pentadiene‐3‐one, 1,5‐di‐2‐furanyl ( F 2 Ac ) via aldol condensation of furfural with acetone. In the present work, efficient Cu‐doped MgAl layered double hydroxides ( LDH ) nanocatalysts are fabricated by coprecipitation and are exploited for furfural conversion to obtained FAc and F 2 Ac . The structure–activity relationship is scrutinized by characterizing fresh and spent nanocatalysts via numerous techniques. The good correlation between the amount of weak acidic‐weak basic catalytic sites and nanocatalysts performance is established. The superior performance of Cu‐0.1 nanocatalyst (Cu‐content = 1.85 wt%) in aldol condensation is attributed to the presence of optimum weak acidic sites (0.21 mmol g −1 ) and weak basic sites (0.36 mmol g −1 ), synergistic acidic‐basic effect, nano‐sized Cu(OH) 2 nanoparticles (1.6 nm), high BET surface area (181 m 2 g −1 ), and mesoporous architecture of material. Cu‐0.1 nanocatalyst delivered 98% FAc selectivity with 100% furfural conversion at 85 °C. Furthermore, at 100 °C, the nanocatalyst gives 55% F 2 Ac selectivity with 73% furfural conversion. The catalyst displays good recyclability (7 recycles) and stability. Plausible mechanistic pathway for transformation of furfural to FAc and F 2 Ac is proposed.
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