硅醇
催化作用
沸石
选择性
无定形固体
吸附
羟醛缩合
化学工程
材料科学
乙醇
化学
碳纤维
无定形碳
冷凝
多相催化
无机化学
化学稳定性
光化学
有机化学
原位
缩合反应
反应机理
葡萄酒
作者
Xinyu Qi,Zhenbo Li,Yaxin Jing,Yurong Yin,Lu Xiaoge,Liping He,Chengyi Dai,Chunshan Song,Xiaoxun Ma
标识
DOI:10.1021/acssuschemeng.6c00067
摘要
A novel amorphous zeolite catalyst (Zr–AZ) with abundant Zr–OH active sites and a hierarchical pore structure (micro-, meso-, and macropores) was developed for the ethanol-to-butadiene (ETB) reaction. Mechanically mixed with ZnO, the catalyst achieved 73% butadiene selectivity at 92% ethanol conversion and maintained stability over 100 h. Zr anchoring on silanol nests formed Zr–OH sites, while the hierarchical pores mitigated carbon deposition. FT-IR and 1H NMR identified surface hydroxyl types, and CO adsorption IR confirmed Zr–OH as the active sites. Reaction mechanism studies via EtOH-TPD, EtOH-TPSR, and in situ FT-IR revealed that ethanol dehydrogenates on ZnO to acetaldehyde, which then undergoes aldol condensation on Zr–OH sites to form butadiene. This design enhances both selectivity and stability for efficient ETB conversion.
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