首页> 外文期刊>Microporous and mesoporous materials: The offical journal of the International Zeolite Association >Direct crystallization of CHA-type zeolite from amorphous aluminosilicate gel by seed-assisted method in the absence of organic-structure-directing agents
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Direct crystallization of CHA-type zeolite from amorphous aluminosilicate gel by seed-assisted method in the absence of organic-structure-directing agents

机译:在没有有机结构导向剂的情况下,通过晶种辅助方法从无定形硅铝酸盐凝胶中直接结晶CHA型沸石

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摘要

Highly crystalline CHA-type aluminosilicate zeolites with the Si/Al ratio of around 4-5 were successfully synthesized by a seed-assisted method in the absence of organic-structure-directing agents (OSDAs); a method for so-called "OSDA-free synthesis" of the CHA zeolite has been newly developed. In this OSDA-free system, in addition to the seeds with the CHA topology, a judicious use of potassium or cesium cations together with sodium cations is a crucial key to the crystallization of the amorphous aluminosilicate gel into the CHA structure. The Si/Al ratio of the CHA zeolite was increased by decreasing the total amount of alkali cations added and/or the use of cesium cations in place of potassium ones. Furthermore, the employment of the amorphous aluminosilicate gel containing boron species led to the formation of the CHA zeolite with a high Si/Al ratio of 6.1 compared with the synthetic chabazite crystallized through the interzeolite conversion of the FAU zeolite (Si/Al: 2.0). The catalytic performance of the prepared CHA zeolites was also evaluated. In the methanol-to-olefins reaction, the catalyst life was improved by increasing the Si/Al ratio of the CHA zeolite. (C) 2014 Elsevier Inc. All rights reserved.
机译:在没有有机结构导向剂(OSDA)的情况下,通过种子辅助方法成功合成了Si / Al比为4-5左右的高结晶度CHA型硅铝酸盐沸石。最近开发出一种用于CHA沸石的所谓“无OSDA合成”的方法。在此无OSDA的系统中,除了具有CHA拓扑的种子外,明智地使用钾或铯阳离子以及钠阳离子是非晶硅铝酸盐凝胶结晶成CHA结构的关键。通过减少添加的碱金属阳离子的总量和/或使用铯阳离子替代钾的阳离子,可提高CHA沸石的Si / Al比例。此外,与通过FAU沸石的中间沸石转化而结晶的合成菱沸石相比,使用含有硼物种的无定形硅铝酸盐凝胶导致形成了高Si / Al比6.1的CHA沸石。 。还评估了所制备的CHA沸石的催化性能。在甲醇与烯烃的反应中,通过增加CHA沸石的Si / Al比,可以提高催化剂寿命。 (C)2014 Elsevier Inc.保留所有权利。

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