An efficient method for the synthesis of mixed phosphine–phosphine oxide ligands via Rh(I)-catalyzed C─H bond alkylation of biarylphosphines was developed. The resulting hemilabile ligands demonstrate high reactivity in Pd-catalyzed Buchwald–Hart...
Artikel
Correlating Structural Variation with Catalytic Performance of Hierarchical Zeolites Using Ultra‐High‐Field Solid‐State NMR
Von Wiley-VCH zur Verfügung gestellt
Ultra-high-field solid-state NMR spectroscopy unveils the effects of the microwave-assisted post-synthetic treatments of FAU Y on the structural integrity of the resulting zeolites with mesoporosity, as well as the role of various framework and extra framework species in the performance in catalytic cracking reactions.
Abstract
Ultra-high-field solid-state NMR spectroscopy (1.0 GHz, 23.5 T) was employed to reveal the structural evolution of aluminum species and thus their correlations to catalytic cracking performance of Y zeolites after post-synthetic treatments. Microwave-assisted treatments, including chelating dealumination and NH4OH treatment, induced significant changes in both framework and extra-framework aluminum species. NMR analysis identified that the interaction between extra-framework Al(V/VI) and Brønsted acid sites (BAS) play a crucial role in enhancing catalytic efficiency. The hierarchical zeolite Y-MWNH3-0.1–30 exhibited superior catalytic cracking performance, achieving high yields of light hydrocarbons (C1–C4), and excellent selectivity toward BTX during the cracking of bulky molecules. These findings provide new insights into how post-synthetic modifications can be used to tune aluminum species distribution and acid site interaction, optimizing zeolite catalysts for hydrocarbon conversion performance.
Zum VolltextÜberprüfung Ihres Anmeldestatus ...
Wenn Sie ein registrierter Benutzer sind, zeigen wir in Kürze den vollständigen Artikel.