Article ID Journal Published Year Pages File Type
6455814 Journal of Catalysis 2016 12 Pages PDF
Abstract

•Thermally reduced gold nanoparticles were prepared by carbonization of the matrix.•Particle morphology changed with neutral gold atoms in a low-coordination state.•Leaching- and aggregation-free gold was intercalated into spherical carbon.

In this study, we propose gold-intercalated ordered mesoporous carbon nanosphere catalysts in which gold nanoparticles are reduced by high-temperature carbonization of the carbonaceous matrix to catalyze the selective hydrogenation of aromatic nitro compounds. A spherical morphology of particles with size approximately 90 nm and ordered mesoporous arrays was clearly observed on the surface in the high-resolution scanning electron microscopy images. The X-ray photoelectron spectra and transmission electron microscopy images showed that the dispersed metallic gold nanoparticles (2.8 nm in diameter) were intercalated into a carbon framework. The IR spectra for CO chemisorption suggested the involvement of neutral gold atoms in a low-coordination state in clusters or a stepped surface. The gold nanocatalysts intercalated into the nanospherical mesoporous carbons exhibited high activity and selectivity for the hydrogenation of nitroarenes to the corresponding amines, using H2 as a reduction agent. The initial reaction rate reached 12.7 and 6.5 min−1 in the hydrogenation of p-chloronitrobenzene and 4-nitrophenol, respectively. This catalytic performance was retained for more than five catalytic runs with no obvious activity loss or gold leaching, indicative of high stability. The trapping test using a mercapto-functionalized SBA-15 solid revealed undetected soluble gold species in the reaction solution. The high activity and stability of the ordered mesoporous carbon nanosphere-supported gold catalysts was strongly correlated to the particle morphology change by thermal reduction, which can generate new low-coordinated gold atoms for intercalated gold NPs in the matrix.

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Related Topics
Physical Sciences and Engineering Chemical Engineering Catalysis
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