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Data · dataset · 2026

Catalytic performance of ZIF-derived metal catalysts for dimethyl carbonate synthesis from methanol

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A series of M-ZIF-8 precursors were synthesized by doping different metal species (M = Fe, Ni, Mn, Ce, In) and then converted into M-NC catalysts via high-temperature carbonization.

Description

The catalytic performance of the M-NC catalysts for dimethyl carbonate (DMC) synthesis through oxidative carbonylation of methanol was investigated. All as-synthesized precursors maintained the characteristic structure of ZIF-8.

After carbonization at 950 ℃, the Fe-NC and the supported Fe/NC*-950 catalyst displayed diffraction peaks corresponding to metallic Fe0, Fe2O3 and Fe3O4. Differently, Fe-NC shows Fe-N coordination sites, while the other M-NC samples exhibited amorphous structure. For Fe/NC catalyst and Fe/NC* catalysts with varied Fe loadings prepared by the impregnation method, only the diffraction signals of Fe3O4 were detected.

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Both Fe-NC and Fe/NC*-950 show that the methanol conversion reached 4.5%, while the Fe-NC exhibited higher DMC selectivity (98.3%) than the Fe/NC*-950 (96.2%). By contrast, the methanol conversion over Fe/NC, Fe/NC* and other M-NC catalysts was all lower than 1%. Increasing the total reaction pressure or temperature could effectively promote the methanol conversion, and the DMC selectivity was hardly affected by reaction pressure; however, increasing reaction temperature accelerated side reactions and decreased DMC selectivity.

The apparent activation energy of Fe-NC was found to be 30.1 kJ·mol–1, much lower than that of conventional copper-based catalysts for this reaction. This study presents a novel approach to design and application of iron-based catalysts in oxidative carbonylation and hydroformylation of methanol.

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ScienceDB10.57760/sciencedb.j00124.005528 d agoJSON v1
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