468545 Highly Selective Synthesis of Primary Amines from Alcohols and Ammonia By Heterogeneous Nickel Catalysis

Tuesday, November 15, 2016: 3:59 PM
Franciscan A (Hilton San Francisco Union Square)
Andrew Leung, Chemical Engineering, Imperial College London, London, United Kingdom, Mimi Hii, Department of Chemistry, Imperial College London, London, United Kingdom and Klaus Hellgardt, Department of Chemical Engineering, Imperial College London, London, United Kingdom

Submit to: Reaction Chemistry and Engineering

Highly Selective Synthesis of Primary Amines from Alcohols and Ammonia by Heterogeneous Nickel Catalysis

N-alkylations of ammonia (NH3) with alcohols are important industrial processes. This study reports a heterogeneous catalyst system of Ni supported on Al2O3/SiO2. This catalyst achieves high conversions and selectivities when producing primary amines by reacting alcohols and gaseous NH3. This is a rare example of heterogeneous non-noble-metal catalytic system for this reaction, using the hydrogen borrowing mechanism, in which water is the only by-product and no external hydrogen is required. This catalyst is characterised and studied, and a new catalyst system is prepared with a comparable activity as the commercial one.

The reaction using benzyl alcohol is also compared with that of a gold catalyst on titania and their reaction kinetics are modelled and rates are determined. Kindly see attached figures below.

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