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    <responseDate>2026-10-10T22:00:51Z</responseDate>
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    <identifier>10.57760/sciencedb.j00124.00552</identifier>
    <datestamp>2026-07-06T22:11:53Z</datestamp>
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<oai_dc:dc xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:date>2026-07-06</dc:date>
  <dc:title>Catalytic performance of ZIF-derived metal catalysts for dimethyl carbonate synthesis from methanol</dc:title>
  <dc:identifier>doi:10.57760/sciencedb.j00124.00552</dc:identifier>
  <dc:language>en</dc:language>
  <dc:description>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. 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. 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&amp;middot;mol&amp;ndash;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.</dc:description>
  <dc:subject>methanol; dimethyl carbonate; ZIF-derived metal catalyst; iron-based catalyst; Fe-N coordination</dc:subject>
  <dc:creator>ZHANG Meng</dc:creator>
  <dc:creator>MENG Fanhui</dc:creator>
  <dc:creator>LIU Yufan</dc:creator>
  <dc:creator>ZHENG Huiling</dc:creator>
  <dc:creator>LI Haojie</dc:creator>
  <dc:creator>LI Zhong</dc:creator>
  <dc:rights>EMBARGO</dc:rights>
  <dc:rights>https://creativecommons.org/licenses/by-nc-nd/4.0/</dc:rights>
  <dc:type>dataset</dc:type>
  <dc:publisher>Science Data Bank</dc:publisher>
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