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Development of a post-synthetic method for tuning the Al content of OSDA-free Beta as a catalyst for conversion of methanol to olefins

机译:开发用于调节无OSDA的Beta中Al含量的后合成方法,以作为甲醇转化为烯烃的催化剂

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摘要

Zeolites synthesized without any organic structure-directing agent (OSDA) have several advantages over conventional zeolites synthesized with OSDAs. Their Al-rich compositions, however, are sometimes not suitable for applications as catalysts. In the present study, post-synthetic modification was performed using an Al-rich Beta zeolite synthesized without any OSDAs (designated as “Beta(OF)”) to obtain high-silica Beta zeolites. We have successfully developed a facile post-synthetic method for tuning the Al content of Beta(OF) with the *BEA-type structure retained by calcination at >750 °C followed by acid treatment. Solid-state 29Si and 27Al MAS NMR analyses revealed that during calcination, framework Al atoms were isomorphously substituted with Si atoms to form high-silica frameworks and concomitant extra-framework Al species. The stability of the obtained frameworks against acid treatment was evaluated in terms of the framework Al content, finding that the framework with the Si/Al ratio higher than 12 is well stabilized enough for acid treatment. Thus, dealuminated Beta(OF) zeolites with high-silica compositions were found to be effective catalysts for the methanol-to-olefin (MTO) reaction; particularly, the Beta zeolite with the Si/Al ratio of 112 maintained the conversion of methanol over 90% with selectivity to C2–C4 olefins over 70% even at 40 hours on stream at WHSV = 3.2 h−1.
机译:不使用任何有机结构导向剂(OSDA)合成的沸石比使用OSDAs合成的常规沸石具有多个优势。但是,它们的富铝组合物有时不适合用作催化剂。在本研究中,合成后的修饰是使用不含任何OSDA(称为“ Beta(OF)”)合成的富含Al的Beta沸石进行的,以获得高二氧化硅Beta沸石。我们已经成功地开发了一种简便的合成后方法,用于通过在大于750°C的温度下煅烧并随后进行酸处理来保留带有* BEA型结构的Beta(OF)的Al含量。固态29Si和27Al MAS NMR分析表明,在煅烧过程中,骨架Al原子同构地被Si原子取代,形成高硅骨架和相应的骨架外Al物种。根据骨架Al的含量评价了所得骨架对酸处理的稳定性,发现Si / Al比高于12的骨架对于酸处理而言足够稳定。因此,发现具有高二氧化硅组成的脱铝的Beta(OF)沸石是甲醇制烯烃(MTO)反应的有效催化剂。尤其是,Si / Al比为112的Beta沸石即使在WHSV = 3.2 h-1的条件下运行40小时也能保持90%以上的甲醇转化率和70%以上的C2-C4烯烃选择性。

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