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Hydrogenation of aniline to cyclohexylamine in supercritical carbon dioxide: Significance of phase behaviour

Paper ID Volume ID Publish Year Pages File Format Full-Text
41695 45896 2011 8 PDF Available
Title
Hydrogenation of aniline to cyclohexylamine in supercritical carbon dioxide: Significance of phase behaviour
Abstract

Hydrogenation of aniline to cyclohexylamine was carried out in supercritical carbon dioxide using a variety of noble metal (Pt, Pd and Rh) catalysts. At 80 °C and 8 MPa of CO2 pressure, >95% of aniline conversion with 93% selectivity to cyclohexylamine was achieved on 5% Rh/Al2O3. A strong influence of phase behaviour related to the CO2 pressure was found on the conversion and selectivity. Optimization of reaction parameters resulted in a higher overall activity in the biphase (liquid substrate + gaseous H2 and CO2) than in the single phase (liquid substrate–CO2–H2) condition. It has been found that the interaction of CO2 with amine leads to the formation of solid carbamic acid, which enhanced the selectivity of cyclohexylamine, but reduced the conversion significantly. Furthermore, reaction temperature played a crucial role in preventing the formation of carbamic acid and also maintained a reasonably high reaction performance in terms of conversion and selectivity.

Graphical abstractFigure optionsDownload full-size imageDownload high-quality image (125 K)Download as PowerPoint slideResearch highlights► An example of tunability, the most claimed advantage of scCO2. ► High conversion and exceptionally high selectivity of cyclohexylamine. ► Phase behaviour has strong impact on the activity and selectivity. ► Temperature played a complex role to achieve high selectivity of the product.

Keywords
Supercritical carbon dioxide; Phase behaviour; Heterogeneous catalysis; Hydrogenation; Aniline; Cyclohexylamine
First Page Preview
Hydrogenation of aniline to cyclohexylamine in supercritical carbon dioxide: Significance of phase behaviour
Publisher
Database: Elsevier - ScienceDirect
Journal: Applied Catalysis A: General - Volume 396, Issues 1–2, 15 April 2011, Pages 186–193
Authors
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Subjects
Physical Sciences and Engineering Chemical Engineering Catalysis