张维萍

个人信息Personal Information

教授

博士生导师

硕士生导师

性别:男

毕业院校:中科院大连化学物理研究所

学位:博士

所在单位:化工学院

学科:工业催化. 能源化工

办公地点:西部校区化工实验楼B-323

联系方式:0411-84986326

电子邮箱:wpzhang@dlut.edu.cn

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Interlayer expansion using metal-linker units: Crystalline microporous silicate zeolites with metal centers on specific framework sites

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论文类型:期刊论文

发表时间:2016-03-01

发表刊物:MICROPOROUS AND MESOPOROUS MATERIALS

收录刊物:EI、SCIE、Scopus

卷号:222

页面范围:235-240

ISSN号:1387-1811

关键字:Interlayer expanded zeolite; IEZ; Metal linker; Microporous metallo-silicate; Rietveld analysis

摘要:Interlayer expansion using silylating agents to connect layer silicates to 3D framework structures has shown to be a versatile synthesis route to new crystalline, microporous frameworks. We demonstrate here that also Me cations can be introduced on the linker sites applying the same synthesis procedure. An acidic aqueous Fe-chloride solution was used in a hydrothermal reaction to convert the layered hydrous silicate precursor RUB-36 into an interlayer expanded zeolite, containing Fe at the linker sites, Fe-IEZ-RUB-36, Si19.14Fe0.86O38(OH)(4). Structure analysis from powder X-ray data using the Rietveld technique confirmed that the porous framework is stable upon calcination and contains Fe on T-sites at the linker position. SEM-EDX analysis is in agreement with the analysis of the electron density maps showing that almost every other linker T-position is occupied by Fe-ions. The material crystallizes in the monoclinic space group Pm with a = 12.200(9) angstrom, b = 13.981(8) angstrom, c = 7.369(2) angstrom, and beta = 106.9(1)degrees. Applying a similar synthesis procedure, the Sn-analog, Sn-IEZ-RUB-36, Si38.6Sn1.4O76(OH)(8), has been obtained and structurally characterized. Despite its limited crystallinity, Rietveld analysis of the PXRD data set confirmed the materials framework topology and chemical composition (a = 23.856(14) angstrom, b = 14.103(7) angstrom, c = 7.412(7) angstrom, in SG Pnm2(1)). We conclude, that the synthesis procedure is flexible and, meanwhile, has been extended to other metal cations such as Ti, Zn, Eu and Al leading to microporous materials with potentially active metal cations on well defined sites of the silicate framework. (C) 2015 Elsevier Inc. All rights reserved.