Highly selective immobilized bimetallic Ni-Au nanoparticle catalyst for the partial hydrogenation of m-dinitrobenzene

Transition metal nanoparticles (NPs) are extensively used as catalysts for a wide and diverse range of organic transformations when immobilized on appropriate solid supports. We describe the development of a highly active and highly selective heterogeneous catalyst based on Ni-Au NPs supported on activated carbon fibers (ACFs) for the partial reduction of m-dinitrobenzene (m-DNB) to m-nitroaniline (m-NAN), an important platform chemical used in the synthesis of dyes and polymers. Initially, Ni NPs with narrow size distribution and ranging from 2 to 14 nm were prepared with poly-N-vinyl-2-pyrrolidone (PVP) as a stabilizer. Evaluation of the NPs as catalysts in the liquid-phase hydrogenation of m-dinitrobenzene led to the establishment of an antipathetic structure sensitivity, i.e. the larger NPs displayed a 6-fold higher turnover frequency than the smaller NPs. The selectivity to the target m-NAN product is independent of the size of the Ni NPs, possibly due to preferential PVP absorption of the NP edges and vertices. Consequently, Ni NPs of 2 nm were supported on ACFs and residual PVP was removed by a ultra-violet ozone (UVO) treatment, rendering a highly selective structured catalyst that affords m-NAN in almost 96% yield. A two-site (plane vs. edge Ni-atoms) Langmuir-Hinshelwood kinetic model is consistent with the experimental kinetic data confirming that low-coordination atoms (edges and vertices) are responsible for selective reaction. Consequently, we prepared bimetallic Ni-Au NPs (Ni:Au = 1:1) aiming to generate Ni surface sites mimicking the properties of edge and vertex atoms. The resulting UVO-treated Ni-Au NPs of 3 nm immobilized on ACFs afford m-NAN with a yield exceeding 98%. Such a high yield appears to be unprecedented and shows how careful nanocatalyst design, guided by detailed structural characterization and mechanistic studied, can lead to highly selective catalysts of industrial relevance.


Published in:
Applied Catalysis A-General, 542, 182-190
Year:
2017
Publisher:
Amsterdam, Elsevier Science Bv
ISSN:
0926-860X
Keywords:
Laboratories:




 Record created 2017-09-05, last modified 2018-12-03


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