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Quantification of active sites in yttrium containing dealuminated Beta zeolites during conversion of ethanol and acetaldehyde to butadiene

巴豆醛 乙醛 乙醇 滴定法 化学 吡啶 路易斯酸 化学吸附 铝酸盐 红外光谱学 傅里叶变换红外光谱 无机化学 有机化学 催化作用 化学工程 氧化物 考古 水泥 工程类 历史
作者
Shivangi N. Borate,Nohor “River” Samad,Stephen C. Purdy,Junyan Zhang,Carlos Bornes,Michael J. Cordon,Meijun Li,Luís Mafra,Andrew D. Sutton,Zhenglong Li,James W. Harris
出处
期刊:Journal of Catalysis [Elsevier BV]
卷期号:433: 115468-115468 被引量:1
标识
DOI:10.1016/j.jcat.2024.115468
摘要

In this work, yttrium containing dealuminated Beta zeolites (Y/deAlBeta) were synthesized and characterized by various spectroscopic techniques to improve understanding of ethanol upgrading over these materials. Characterization results indicate yttrium atoms partially condense with framework silanol nests formed during dealumination of parent Al-Beta supports. Active sites for conversion of ethanol and acetaldehyde to butadiene were quantified on a series of Y/deAlBeta catalysts (0.1–10 vawt% yttrium) via ex situ chemisorption and transmission Fourier transformed infrared (FTIR) spectroscopy measurements by first measuring the integrated molar extinction coefficient (IMEC) for pyridine bound to Lewis acidic yttrium sites. In situ titrations with pyridine demonstrate that the number of sites quantified by ex situ chemisorption IR is quantitatively similar to the number of sites that catalyze butadiene formation, which varies (from 0.05 to 0.35) across the series of catalysts. In situ pyridine titrations impact butadiene site time yields (STY), but not crotonaldehyde STY, indicating that a distribution of yttrium sites is present, and that discrete yttrium site types participate in distinct steps in the pathway from ethanol to butadiene. Apparent kinetic parameters including activation energies and reaction orders were measured, these suggest differences in reactant (or reactant-derived intermediate) surface coverages result in higher STYs (per mol Y or per Lewis acidic Y site) for samples with low Y loadings relative to those with higher Y loadings. Isotopic labeling experiments evince the existence of other kinetically relevant steps in addition to the crotonaldehyde transformation to crotyl alcohol. Together, these findings provide further guidance into the heterogeneities in site structures in yttrium-containing zeolites and their relevance for the various steps in the pathway from ethanol to C4 products useful for production of sustainable aviation fuel and renewable butadiene.
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