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Visualizing Dealumination of a Single Zeolite Domain in a Real‐Life Catalytic Cracking Particle

机译:可视化真实催化裂化颗粒中单个沸石结构域的脱铝

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摘要

Fluid catalytic cracking (FCC) catalysts play a central role in the chemical conversion of crude oil fractions. Using scanning transmission X‐ray microscopy (STXM) we investigate the chemistry of one fresh and two industrially deactivated (ECAT) FCC catalysts at the single zeolite domain level. Spectro‐microscopic data at the Fe L3, La M5, and Al K X‐ray absorption edges reveal differing levels of deposited Fe on the ECAT catalysts corresponding with an overall loss in tetrahedral Al within the zeolite domains. Using La as a localization marker, we have developed a novel methodology to map the changing Al distribution of single zeolite domains within real‐life FCC catalysts. It was found that significant changes in the zeolite domain size distributions as well as the loss of Al from the zeolite framework occur. Furthermore, inter‐ and intraparticle heterogeneities in the dealumination process were observed, revealing the complex interplay between metal‐mediated pore accessibility loss and zeolite dealumination.
机译:流化催化裂化(FCC)催化剂在原油馏分的化学转化中起着核心作用。使用扫描透射X射线显微镜(STXM),我们研究了一种新鲜和两种工业失活(ECAT)FCC催化剂在单个沸石域水平上的化学性质。 Fe L3,La M5和Al K X射线吸收边缘的光谱显微镜数据显示,ECAT催化剂上沉积的Fe含量不同,这与沸石域内四面体Al的总体损失相对应。使用La作为定位标记,我们开发了一种新颖的方法来绘制真实的FCC催化剂中单个沸石域的Al分布变化图。发现在沸石畴尺寸分布中发生了显着变化,以及从沸石骨架中损失了Al。此外,在脱铝过程中观察到颗粒间和颗粒内的异质性,揭示了金属介导的孔可及性损失与沸石脱铝之间的复杂相互作用。

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