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Cracking of naphtha range alkanes and naphthenes over zeolites

机译:石脑油范围烷烃和环烷烃在沸石上的裂解

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摘要

Naphtha range alkanes and naphthenes can be activated over H-form of zeolites, which provide low temperature cracking pathways that are otherwise unavailable during conventional steam cracking. A range of zeolitic catalysts were tested for cracking naphtha. Due to their relatively larger kinetic diameter, isoalkanes and naphthenes exhibited lower reactivity than linear alkanes over 8-MR zeolites. 12-MR zeolites favored bimolecular hydride transfer pathways, which eventually increased the selectivity to light alkanes and to coke at the expense of ethylene and propylene. Hydride transfer and aromatization were suppressed by keeping the number of acid sites low. Primary reaction products n-butenes-butane showed low reactivity for secondary conversion over 12-MR zeolites, but showed relatively high reactivity over 10-MR zeolites. The highest ethylene and propylene yields were obtained over 10-MR zeolites such as Ferrierite.
机译:石脑油范围的烷烃和环烷烃可以在H型沸石上活化,这提供了低温裂解途径,而传统蒸汽裂解方法则无法提供这种途径。测试了一系列沸石催化剂的裂化石脑油。由于它们的相对较大的动力学直径,与8-MR沸石相比,异链烷烃和环烷烃的反应性比直链烷烃低。 12-MR沸石偏爱双分子氢化物转移途径,最终增加了对轻质烷烃和焦炭的选择性,但以乙烯和丙烯为代价。保持酸位低,可抑制氢化物的转移和芳香化。初级反应产物正丁烯/正丁烷对二次转化的反应性比12-MR沸石低,但对10-MR沸石的反应性相对较高。在10-MR沸石(诸如镁碱沸石)上获得了最高的乙烯和丙烯收率。

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