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CXN天然沸石的研究VII. 骨架高硅超稳化改性
引用本文:程晓维,汪靖,张枚,钟鹰,黄强,龙英才.CXN天然沸石的研究VII. 骨架高硅超稳化改性[J].化学学报,2006,64(1):1-8.
作者姓名:程晓维  汪靖  张枚  钟鹰  黄强  龙英才
作者单位:[1]复旦大学化学系上海市分子催化与新材料重点实验室,上海200433 [2]昭通师范学院,昭通657000 [3]中非地质工程勘查研究院,北京100010
摘    要:以高硅超稳化辉沸石(STI)为基底沸石, 分别经盐酸脱铝或氟硅酸铵脱铝补硅处理后制备的改性H-STI沸石, 其非骨架铝含量明显减少, 而后者骨架硅铝比进一步提高. X射线荧光散射光谱(XRF), 27Al高分辨率魔角旋转固体核磁共振(MAS NMR), 红外(FT-IR)光谱等表征证明改性后的沸石骨架硅铝原子比分别为6.8和11.4. 低温氮吸附表明, 经盐酸处理的高硅STI沸石孔道开放完美, 但经氟硅酸铵处理的样品孔道被部分堵塞. 分段程序升温焙烧表明前者骨架热稳定性略差, 1000 ℃焙烧后结构基本被破坏, 而后者热稳定性较好, 经相同温度段焙烧后仍保持较高的结晶度和热稳定性, 其结构基本实现超稳化.

关 键 词:高硅STI沸石  超稳化  分段程序升温焙烧  固体核磁共振  氮吸附  红外光谱  脱铝改性
收稿时间:2005-07-15
修稿时间:2005-10-24

Studies on CXN Natural ZeoliteVII. High-silica and Ultra-stable Modification of Framework
CHENG Xiao-Wei,WANG Jing,ZHANG Mei,ZHONG Ying,HUANG Qiang,LONG Ying-Cai.Studies on CXN Natural ZeoliteVII. High-silica and Ultra-stable Modification of Framework[J].Acta Chimica Sinica,2006,64(1):1-8.
Authors:CHENG Xiao-Wei  WANG Jing  ZHANG Mei  ZHONG Ying  HUANG Qiang  LONG Ying-Cai
Institution:a Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Department of Chemistry, ;b Zhaotong Teacher College, Zhaotong 657000;c Zhongfei Geological Prospecting Researching Academy, Belting 100010
Abstract:Characterized with X-ray fluorescence scattering spectroscopy (XRF), 27Al MAS NMR and FT-IR techniques, the non-framework aluminum in the raw material of the ultra-stable high-silica stilbite (STI) zeolite has been proved to become decreased, and the zeolite framework Si/Al ratio to reach 6.8 and 11.4 after treatment by HCl or by ammonium hexafluorosilicate solution, respectively. N2 adsorptions indicate that the modified high-silica STI zeolites treated with HCl solution possessed open and perfect channels, and the pores of the zeolite samples treated with ammonium hexafluorosilicate soulution were partially blocked. Investigations on the samples obtained in the process of stage-temperature-programmed calcination with XRD proved that the structural stability of the former sample was weaker than that of the latter, which was collapsed under calcination at 1000 ℃. In comparison, the latter sample with better structural stability remained stable when calcined at the same temperatures, to possess high crystallinity, showing the ultra-stabilization of its framework.
Keywords:high-silica stilbite zeolite  nitra-stabilization  stage-temperature-programmed calcination  solid NMR  N2 adsorption  FT-IR spectrum  modification with dealumination
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