催化作用
选择性
路易斯酸
无机化学
纤锌矿晶体结构
化学
四方晶系
锌
核化学
晶体结构
结晶学
有机化学
作者
Charles Beasley,Muthu Kumaran Gnanamani,Michela Martinelli,Kinga Góra‐Marek,Kaichiro Hamano,Wilson D. Shafer,Namal Wanninayake,Doo Young Kim
标识
DOI:10.1002/slct.201900400
摘要
Abstract Zn addition was found to affect both activity and selectivity of ZrO 2 for dehydration of 1,5‐pentanediol. ZrO 2 tends to produce more or less equimolar mixture of tetrahydropyran (THP) derivatives and 4‐penten‐1‐ol from 1,5‐pentanediol. The conversion of 1,5‐pentanediol on ZrO 2 increases with increasing Zn content up to 30–50 mole percent; however, catalyst containing Zn beyond 50 mole percent had an adverse effect on both conversion of diol and the selectivity for unsaturated alcohol (i. e., 4‐penten‐1‐ol). XRD and Raman analysis infer that the presence of tetragonal ZrO 2, the amorphous phase (ZrO 2 , ZrZnO x , ZnO), and hexagonal wurtzite structure of ZnO in the catalysts. The interplanar spacing of ZrO 2 (111) and ZnO (100) planes for catalysts indicate that Zn incorporates into ZrO 2 lattice and vice‐versa. Basicity assessed from CO 2 ‐TPD and acidity from FTIR‐pyridine adsorption techniques indicate that both basicity and Lewis acid sites density increases with increasing Zn proportion on ZrO 2 up to 50:50 molar ratios of Zn to Zr. An optimum Zn:Zr mole ratio is required to achieve higher density of oxygen vacant metal sites (i. e., Lewis acidity) and balanced acid‐base strength which improves the diol conversion.
科研通智能强力驱动
Strongly Powered by AbleSci AI