甲醇
动力学
纳米笼
沸石
再结晶(地质)
ZSM-5型
催化作用
杂原子
化学工程
材料科学
硅酸铝
纳米晶
热液循环
纳米技术
化学
有机化学
古生物学
工程类
物理
生物
量子力学
戒指(化学)
作者
Guangrui Chen,Junyan Li,Sen Wang,Ji Won Han,Xingxing Wang,Peihong She,Weibin Fan,Bu Yuan Guan,Jihong Yu,Peng Tian
标识
DOI:10.1002/anie.202200677
摘要
We report an anisotropic-kinetics transformation strategy to prepare single-crystalline aluminosilicate MFI zeolites (ZSM-5) with highly open nanoarchitectures and hierarchical porosities. The methodology relies on the cooperative effect of in situ etching and recrystallization on the evolution of pure-silica MFI zeolite (silicalite-1) nanotemplates under hydrothermal conditions. The strategy enables a controllable preparation of ZSM-5 nanostructures with diverse open geometries by tuning the relative rate difference between etching and recrystallization processes. Meanwhile, it can also be extended to synthesize other heteroatom-substituted MFI zeolite nanocages. Compared with conventional ZSM-5 microcrystals, nanocrystals, and nanoboxes, the ZSM-5 nanocages with single-crystalline nature, highly open nanoarchitectures, and hierarchical porosities exhibit remarkably enhanced catalytic lifetime and low coking rate in the methanol-to-hydrocarbons (MTH) reaction.
科研通智能强力驱动
Strongly Powered by AbleSci AI