Identification of Vicinal Silanols and Promotion of Their Formation on MCM-41 via Ultrasonic Assisted One-Step Room-Temperature Synthesis for Beckmann Rearrangement

被引:19
作者
Wang, Zichun [1 ]
Jiang, Yijiao [2 ]
Zhang, Yunyao [1 ]
Shi, Jeffrey [1 ]
Stampfl, Catherine [3 ]
Hunger, Michael [4 ]
Huang, Jun [1 ]
机构
[1] Univ Sydney, Sch Chem & Biomol Engn, Lab Catalysis Engn, Sydney, NSW 2006, Australia
[2] Macquarie Univ, Dept Engn, Sydney, NSW 2109, Australia
[3] Univ Sydney, Sch Phys, Sydney, NSW 2006, Australia
[4] Univ Stuttgart, Inst Chem Technol, D-70550 Stuttgart, Germany
基金
澳大利亚研究理事会;
关键词
AL-MCM-41; MOLECULAR-SIEVES; SILICA-WATER INTERFACE; CYCLOHEXANONE OXIME; EPSILON-CAPROLACTAM; ACID SITES; SOLID-STATE; INFRARED-SPECTROSCOPY; MESOPOROUS SILICA; AMORPHOUS SILICA; ACTIVE-SITES;
D O I
10.1021/acs.iecr.8b00274
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Siliceous mesoporous MCM-41 materials were synthesized under ultrasonic treatment from 0.5 to 3 h. The obtained U-[Si]MCM-41 catalysts were applied in the Beckmann rearrangement of cyclohexanone oxime (CHO) to epsilon-caprolactam (CPL). The ultrasonic treatment can increase the pore wall thickness, while the density of surface SiOH groups increased slightly. Quantitative MAS NMR studies of the U-[Si]MCM-41 catalysts hint at the presence of isolated and vicinal silanols. After dehydration at 393 K, H-1 MAS NMR signals of poly-hydrogen-bonded vicinal silanols occurred, which are strongly reduced after dehydration at 473 K. Correspondingly, a much higher conversion of CHO to CPL was observed for U-[Si]MCM-41 dehydrated at 393 K in comparison with those dehydrated at 473 K. This finding indicates poly-hydrogen bonded SiOH groups can promote the reaction and improve the catalytic performance of siliceous catalytic materials in the Beckmann rearrangement of CHO in an energy economic way at a suitable activation temperature.
引用
收藏
页码:5550 / 5557
页数:8
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