吡咯烷
铁白云石
沸石
四甲基铵
化学
分子
胺气处理
催化作用
有机化学
立体化学
离子
作者
Ana B. Pinar,Luis Gómez‐Hortigüela,Lynne B. McCusker,Joaquı́n Pérez-Pariente
摘要
Analysis of the structure of the zeolite ferrierite (framework type FER) synthesized using a combination of tetramethylammonium (TMA) and pyrrolidine as organic structure-directing agents (|((CH3)4N)0.4((CH2)4NH)3.6H1.7|[Si33.9Al2.1O72]) has revealed that TMA ions reside exclusively in the [586682] cavities of the FER framework, whereas pyrrolidine species are found in both the [586682] cavities and the main 10-ring channel. A similar, but not identical, arrangement of pyrrolidine molecules was found for a sample synthesized with pyrrolidine as the only SDA (|((CH2)4NH)4.2H2.2|[Si33.8Al2.2O72])). A comparison of the two structures shows the influence of TMA on the location of pyrrolidine and the framework Al. Pyrrolidine species establish stronger interactions with the zeolitic framework than does TMA, suggesting a different ability of the amine to exert an influence on the aluminum distribution of the zeolite. These findings have implications in the catalytic performance of the samples.
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