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 Han,Xingxing Wang,Peihong She,Weibin Fan,Buyuan Guan,Peng Tian,Jihong Yu
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.
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