环己酮
苯酚
催化作用
选择性
多孔性
溶剂
化学
化学工程
金属有机骨架
纳米颗粒
材料科学
有机化学
纳米技术
吸附
工程类
作者
Mao Chao,Ziming Chen,Jiuxuan Zhang,Zhenchen Tang,Hong Jiang,Rizhi Chen
标识
DOI:10.1021/acs.iecr.3c01711
摘要
Cyclohexanone is a pivotal feedstock for the nylon industry that can be produced via one-step hydrogenation of phenol. Metal organic frameworks (MOFs) have wide applications in heterogeneous catalysis owing to their tuneable porous structures, compositions, and surface properties. Metal nanoparticles (NPs) supported on MOFs (M@MOFs) can effectively catalyze the phenol hydrogenation to cyclohexanone; however, the recyclability of M@MOFs is still not satisfactory, and the influences of the textural properties of M@MOFs are barely investigated. Herein, the surface properties and pore structures of UiO-66 were controllably modified through simply modulating the organic linkers and adjusting the composition of the synthesis solvent, and the synergistic effects of hierarchically porous structures and amino groups in Pd@UiO-66 for the selective hydrogenation of phenol were investigated in detail. Using 2-aminoterephthalic acid as the organic linker and introducing water in the synthesis solvent, Pd@HPUiO-NH2 with well-developed hierarchically porous structures and amino groups can be fabricated, and then, stable Pd NPs with good dispersion are achieved, resulting in superior catalytic performance in the phenol hydrogenation (97.9% phenol conversion with 93.7% cyclohexanone selectivity after six reaction cycles). Furthermore, the recycled Pd@HPUiO-NH2 exhibits a high turnover frequency, surpassing most of the reported MOF-based catalysts. These findings can aid the development of high-performance MOF-based catalysts and green cyclohexanone production.
科研通智能强力驱动
Strongly Powered by AbleSci AI