材料科学
苯酚
甲醛
八面体
选择性
产量(工程)
双酚A
化学工程
催化作用
金属
化学
形态学(生物学)
配体(生物化学)
无机化学
结晶学
有机化学
冶金
晶体结构
环氧树脂
工程类
受体
生物
生物化学
遗传学
作者
Xinnian Xia,Yingzhuang Xu,Chen You,Yutang Liu,Yanbing Lu,Luhua Shao
标识
DOI:10.1016/j.apcata.2018.04.020
摘要
The morphology and structure of metal organic frameworks (MOFs) are closely related to their properties. Herein, a flower-like morphology MOF (named as MIL-101(Cr/Al)A-f) was rationally designed in a acid-free environment and the Al3+ was transformed into the framework by the substitution process of cation exchange. During the preparation process of MIL-101(Cr/Al)A-f, we found that the acidity of the reaction mixture could regulate the morphology of MIL-101(Cr/Al)A-f by adjusting the coordination of the metal clusters and the ligand chains. The catalytic performance of MIL-101(Cr/Al)A-f was evaluated by the hydroxyalkylation of phenol with formaldehyde. Due to the larger surface area and high-density sites, MIL-101(Cr/Al)A-f showed a higher catalytic activity than the octahedron morphology MIL-101(Cr/Al)A-0.5 which was prepared with traditional method in acidic environment. In approximately equal Al3+ content, the MIL-101(Cr/Al)A-f showed a remarkably high yield (97.1%) and a excellent selectivity (98.3%) to bisphenol F at 60 °C for 30 min. Finally, a possible mechanism for the synthesis of bisphenol F was proposed and the hydroxyalkylation of phenol with formaldehyde to bisphenol F was fitted by the Langmuir-Hinshelwood kinetic model.
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