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MFI型硅铁沸石水热合成、介孔改性与结构表征

韩静宇 王洪涛 张莉 张舒冬 封瑞江 金英杰

硅酸盐学报2017,Vol.45Issue(7):976-983,8.
硅酸盐学报2017,Vol.45Issue(7):976-983,8.DOI:10.14062/j.issn.0454-5648.2017.07.13

MFI型硅铁沸石水热合成、介孔改性与结构表征

Hydrothermal Synthesis, Mesoporous Modification and Structural Characterization of Ferrisilicate Zeolites with MFI Structure

韩静宇 1王洪涛 1张莉 1张舒冬 2封瑞江 1金英杰1

作者信息

  • 1. 辽宁石油化工大学化学化工与环境学部,辽宁抚顺 113001
  • 2. 中国石化抚顺石油化工研究院,辽宁抚顺 113001
  • 折叠

摘要

Abstract

MFI-type ferrisilicates with various Si/Fe molar ratios were hydrothermally synthesized using inorganic ferric and silica sources. The mesoporous modification of the MFI-type ferrisilicates in proton form was performed via a combined alkali-acid treatment. The crystal structure and porous distribution of precursor and modified zeolites were investigated by X-ray diffraction, Fourier transform infrared spectroscopy, ultraviolet-visible light absorption spectroscopy, N2-adsorption, scanning electron microscopy, and energy dispersive X-ray spectroscopy, respectively. The results show that the intra-grain mesoporostity and removal behavior of T-atoms (T= Si + Fe) are correlated to Si/Fe ratio in framework. The ferrisilicates as-prepared are MFI zeolites with a complete crystallinity, in which most Fe3+ atoms are incorporated into MFI framework. After being subjected to the alkali-acid treatment, the ferrisilicates preserve an adequate crystallinity, a high desilication selectivity and a mesoporosity, and present a two-level mesopore distribution. Moreover, the initial Si/Fe ratio in framework has a crucial effect on the controlled desilication for mesopore formation. The modified zeolites with initial Si/Fe ratios in the range of 60~120 have both greater mesoporostity and removal efficiency of T-atoms.

关键词

硅铁沸石/碱酸处理/硅铁比/多级介孔/脱硅选择性

Key words

ferrisilicate zeolite/alkali-acid treatment/Si/Fe ratio/hierarchical mesopore/desilication selectivity

分类

化学化工

引用本文复制引用

韩静宇,王洪涛,张莉,张舒冬,封瑞江,金英杰..MFI型硅铁沸石水热合成、介孔改性与结构表征[J].硅酸盐学报,2017,45(7):976-983,8.

基金项目

国家自然科学基金项目(21171083). (21171083)

硅酸盐学报

OA北大核心CSCDCSTPCD

0454-5648

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