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Transient Technique for Identification of True Reaction Intermediates: Hydroperoxide Species in Propylene Epoxidation on Gold/Titanosilicate Catalysts by X-ray Absorption Fine Structure Spectroscopy

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TLDR
In this paper, in situ ultraviolet-visible (UV−vis) diffuse reflectance spectroscopy was used in combination with in situ Ti K-edge X-ray absorption near-edge structure (XANES) to study the formation of Ti-hydroperoxo species during the gas-phase epoxidation of propylene with H2 and O2 at reaction conditions over a Au−Ba/Ti−SiO2 (Ti−TUD) catalyst.
Abstract
In situ ultraviolet−visible (UV−vis) diffuse reflectance spectroscopy was used in combination with in situ Ti K-edge X-ray absorption near-edge structure (XANES) to study the formation of Ti-hydroperoxo species during the gas-phase epoxidation of propylene with H2 and O2 at reaction conditions over a Au−Ba/Ti−SiO2 (Ti−TUD) catalyst. The in situ UV−vis measurements showed growth of a signal due to Ti-hydroperoxo species when the catalyst was put in contact with H2/O2/Ar (1/1/8) and C3H6/H2/O2/Ar (1/1/1/7) gas mixtures at 423 K and 0.1 MPa. Changes in the area of the pre-edge peak centered at 4968.9 eV present in the Ti K-edge XANES spectra of the catalyst were used to estimate the Ti-hydroperoxo species coverages (θ) under operating conditions. Transient Ti K-edge XANES experiments with H2/O2/Ar (1/1/8) and C3H6/H2/O2/Ar (1/1/1/7) gas mixtures allowed the estimation of the net epoxidation rate by a novel method involving the determination of dθ/dt. It is shown that the Ti-hydroperoxo species are true inter...

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Citations
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Gold-catalyzed carbon-heteroatom bond-forming reactions.

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Importance of Size and Contact Structure of Gold Nanoparticles for the Genesis of Unique Catalytic Processes.

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New trends in tailoring active sites in zeolite-based catalysts.

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Structure and surface chemistry of gold-based model catalysts.

TL;DR: Other Reactions Rettner and Auerbach studied the reaction dynamics of H atoms with Cl chemisorbed (via Cl2 decomposition at 400 K) on Au(111) employing molecular beam time-of-flight methods with quantum-state-specific detection and revealed the concurrence of two dynamically distinct mechanisms (Eley Rideal and Langmuir Hinshelwood) during the reaction.
References
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Journal ArticleDOI

Selective Vapor-Phase Epoxidation of Propylene over Au/TiO2Catalysts in the Presence of Oxygen and Hydrogen

TL;DR: In this article, it was shown that propylene adsorbed on a gold surface may react with oxygen species formed at the perimeter interface between the gold particles and the TiO2support through the reaction of oxygen with hydrogen.
Journal ArticleDOI

Synthesis of propylene oxide from propylene and hydrogen peroxide catalyzed by titanium silicalite

TL;DR: In this article, the epoxidation of propylene with hydrogen peroxide in the liquid phase, in the presence of titanium silicalite catalyst (TS-1), is described.
Journal ArticleDOI

Epoxidation of Lower Olefins with Hydrogen Peroxide and Titanium Silicalite

TL;DR: In this article, the epoxidation of lower olefins, catalysed by titanium silicalite (TS-1) under mild conditions, is reported. But the reaction may be performed at near room temperature, in dilute alcoholic or aqueous solutions of hydrogen peroxide.
Journal ArticleDOI

Lewis acids as catalysts in oxidation reactions: from homogeneous to heterogeneous systems.

TL;DR: This review is focused on the use of solid Lewis acids to promote catalytic oxidations, and the core of the review is organized to show the evolution from the simplest strategy for heterogeneizing homogeneous catalysts, to the more elaborate ones in which the active sites are part of the solid structure.
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