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We report, for the first time, 100% selectivity in the continuous gas phase hydrogenation of m-dinitrobenzene to m-nitroaniline (m-NAN) over Au/Al 2 O 3 . The synthesis and application of an alumina supported Au-Ni alloy is also described where alloy formation is demonstrated by XRD, diffuse reflectance UV-Vis and HRTEM analyses. Under the same reaction conditions, Au/Al 2 O 3 delivered a higher (by close to an order of magnitude) hydrogenation rate compared with the alloy. Au-Ni/Al 2 O 3 promoted the formation of both m-NAN and m-phenylenediamine, i.e. partial and complete hydrogenation: the results are consistent with a stepwise reduction mechanism.

The effect of metal particle size on the aqueous-phase (T = 303 K) catalytic hydrodechlorination (HDC) of 2,4-dichlorophenol (2,4-DCP) over Pd/Al2O3 has been investigated. A range of palladium dispersions (8%−67%) was achieved using a H2 thermal treatment over the temperature range of 423 K ≤ T ≤ 1273 K. The catalyst samples have been characterized in terms of transmission electron microscopy (TEM), X-ray diffraction (XRD), surface area/porosity, H2 chemisorption, and point-of-zero-charge measurements. The HDC of 2,4-DCP is predominately a stepwise process, yielding 2-chlorophenol (2-CP) as the partially dechlorinated product, which is further converted to phenol and, ultimately, to cyclohexanone. The temporal dependence of product distribution is recorded and correlated to metal particle size/bulk solution pH changes. Structure sensitivity has been established where smaller palladium particles (≤5 nm) exhibit intrinsically higher specific activities. The HDC of 2,4-DCP has also been investigated under conditions of controlled pH (pHacid = 3 and pHbasic = 13). At pHacid, a greater palladium dispersion delivers greater 2-CP selectivities, as a result of repulsion between chlorophenolic species in solution and a supported Pd−H+ adduct; HDC selectivity at pHbasic is insensitive to palladium particle size. Bulk palladium was inactive under the same reaction conditions, necessitating lower Cl/Pd ratios, but it promoted the removal of both chlorines to a greater extent than that which was observed for Pd/Al2O3. We express, for the first time, HDC performance in terms of solution ecotoxicity and record an 81% decrease in toxicity for reaction at a higher palladium dispersion and pHbasic value. The results establish that catalytic HDC is an effective means of detoxifying chlorophenol-contaminated water.

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