Answers are grounded in this paper and cite their sources.
Vibrational spectroscopy reveals aniline adsorption orientation in palladium-alumina catalysts, suggesting implications for selectivity.
Vibrational spectroscopy (predominantly infrared (IR) spectroscopy) is applied to examine the adsorption of aniline over a 5 wt% Pd/Al2O3 catalyst. Diffuse-reflectance Fourier transform (FT-IR) spectroscopic measurements at 30°C, undertaken within a low-coverage regime, indicate aniline adsorption to occur in a parallel orientation with respect to the metal at the support/Pd interface. At higher coverages, aniline adsorption shifts to the alumina support. Temperature-programmed (TP-IR) spectroscopic measurements indicate that the adsorption strength of aniline partitioned between four adsorption sites to follow the trend: support/Pd interface < type III tri-bridged hydroxyls < type IIa bridged hydroxyls ≈ type IIb bridged hydroxyls. Computational (density functional theory (DFT)) studies concentrating on the geometry of the Pd-aniline adsorption complex in the low-coverage regime discern the parallel orientation to be the preferred structure, in agreement with the IR spectroscopic studies. The aniline adsorption in a parallel orientation with respect to the metal surface at the support/Pd interface positions the aromatic ring parallel with the active Pd surface, thereby enabling hydrogenation to cyclohexylamine, the first over-hydrogenation product associated with aniline. The predominant re-adsorption of aniline to the γ-Al2O3 support is proposed to limit product over-hydrogenation in nitrobenzene hydrogenation and, thus, contributes to the reported elevated aniline selectivity over Pd/Al2O3 catalysts. This article is part of the theme issue 'Surfaces, interfaces and heterogeneous catalysis'.
No takes yet. Share an insight, caveat, or question.
McCullagh et al. (2026) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: