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Key properties promoting high activity and stability of supported PdSb/TiO2 catalysts in the acetoxylation of toluene to benzyl acetate

Paper ID Volume ID Publish Year Pages File Format Full-Text
41600 45894 2011 9 PDF Available
Title
Key properties promoting high activity and stability of supported PdSb/TiO2 catalysts in the acetoxylation of toluene to benzyl acetate
Abstract

The influence of thermal pretreatment in air, helium and 10% H2/He on the catalytic performance of a supported 9% Pd, 12% Sb/TiO2 catalyst in the gas phase acetoxylation of toluene has been studied by integrated evaluation of catalytic tests and catalyst characterization using mainly XRD, TEM and XPS. A pretreatment temperature of 600 °C is beneficial for shortening the activation period, while the atmosphere during thermal pretreatment influences the long-term stability. Highest catalytic performance with a good long-term stability was reached with pretreatment in He, which creates Sb-containing Pd particles, on which a mixed Pd0/PdO surface is formed during time on stream. Sb stabilizes oxidized Pd species and leads to more stable catalysts in contrast to air-calcined samples. The catalyst pretreated in H2/He was completely inactive, due to the formation of a stable Pd8Sb3 alloy.

Graphical abstractFigure optionsDownload full-size imageDownload high-quality image (102 K)Download as PowerPoint slideHighlights► Performance of PdSb/TiO2 catalysts is governed by thermal pretreatment. ► The pretreatment gives best catalyst, Pd with PdO surface and highly dispersed Sb. ► Crystalline PdSb alloys formed in 10%H2/He flow are totally inactive. ► New preparation method makes use of deactivating additives dispensable.

Keywords
Toluene; Benzyl acetate; Acetoxylation; TiO2 supported palladium; Deactivation; Thermal pretreatment
First Page Preview
Key properties promoting high activity and stability of supported PdSb/TiO2 catalysts in the acetoxylation of toluene to benzyl acetate
Publisher
Database: Elsevier - ScienceDirect
Journal: Applied Catalysis A: General - Volume 398, Issues 1–2, 15 May 2011, Pages 104–112
Authors
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Subjects
Physical Sciences and Engineering Chemical Engineering Catalysis