沸石
微型多孔材料
结晶
硅酸盐
吸附
化学工程
多孔性
材料科学
方解石
四面体
冷凝
分子
催化作用
化学
纳米技术
拓扑(电路)
结晶学
有机化学
物理
工程类
热力学
数学
组合数学
作者
Jian Li,Zihao Gao,Qun Ying Lin,Chenxu Liu,Fangxin Gao,Cong Lin,Siyao Zhang,Hua Deng,Álvaro Mayoral,Wei Fan,Song Luo,Xiaobo Chen,Miguel Á. Camblor,Fei‐Jian Chen,Jihong Yu
标识
DOI:10.26434/chemrxiv-2022-3jtxh
摘要
Zeolites are microporous silicates that find an ample variety of applications as catalysts, adsorbents, and cation exchangers. Natural and synthetic zeolites possess a fully connected three-dimensional network of corner-sharing SiO4 tetrahedra (i.e. they are tectosilicates or framework silicates, with Si occasionally substituted by other atoms). Stable silica-based zeolites with increased porosity are of interest to allow processing of large molecules, but challenge our synthetic ability. Here we report a novel zeolite, ZEO-3, with a multidimensional, interconnected system of extra-large pores open through windows made by 16 and 14 SiO4 tetrahedra, which, with a specific surface area of over 1000 m2/g and an extraordinary performance for Volatile Organic Compounds abatement, is the less dense polymorph of silica known so far. This zeolite, however, is not directly synthesized as a tectosilicate but is the first three-dimensional zeolite that is obtained by topotactic condensation from a one-dimensional chain silicate (inosilicate, ZEO-2), a process that bears a 17% contraction of the structure but that does not alter the topology of the chain silicate (hence the term “topotactic”). This discovery challenges concepts deeply-rooted into zeolite science, and opens up the possibility of chain silicates as precursors for the crystallization of zeolites.
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