Support effects in the selective gas phase hydrogenation ofp-chloronitrobenzene over gold

The catalytic continuous gas phase hydrogenation of p-chloronitrobenzene ( P =1 atm; T =423 K) has been investigated over a series of oxide (Al 2 O 3 , TiO 2 , Fe 2 O 3 and CeO 2 ) supported Au (1 mol %) catalysts. The application of two catalyst synthesis routes, i.e. impregnation (IMP) and deposition-precipitation (DP), has been considered where the DP route generated smaller mean Au particle sizes (1.5-2.8 nm) compared with the IMP preparation (3.5-9.0 nm). The catalysts have been characterised in terms H2 chemisorption and BET area measurements where the formation of metallic Au post-activation has been verified by diffuse reflectance UV-Vis, XRD and HRTEM analyses. p -Chloroaniline was generated as the sole reaction product over all the Au catalysts with no evidence of C-Cl and/or C-NO 2 bond scission and/or aromatic ring reduction. The specific hydrogenation rate increased with decreasing Au particle size (from 9 to 3 nm), regardless of the nature of the support. This response extends to a reference Au/TiO 2 catalyst provided by the World Gold Council. A decrease in specific rate is in evidence for smaller particles (< 2 nm) and can be attributed to a quantum size effect. The results presented establish the basis for the design and development of a versatile catalytic system for the clean continuous production of high value amino compounds under mild reaction conditions.