Abstract
TPR/TPD and FTIR are used to characterize “excessively ion-exchanged” Cu/Na-ZSM-5. After calcination in O2 at 773 K at least two copper-oxygen species are present in addition to Cu2+ ions; these have been identified as CuO and [Cu-O-Cu]2+. Reduction in H2 transforms all these into Cu0 below 773 K. [Cu-O-Cu]2+ is autoreduced to Cu+ during outgassing. Reoxidation of Cu0 by zeolite protons to Cu+ is observed above 723 K in He or Ar; in the presence of CO this process is considerably enhanced and observed at much lower temperature, because CO is strongly adsorbed on Cu+. At 293 K CO adsorption causes reversible changes in the FTIR spectra.
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On leave from: Center for Catalysis, Surface and Material Science, Department of Organic Chemistry, József Attila University, Dóm tér 8, Szeged, H-6720 Hungary.
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Sárkány, J., d'Itri, J.L. & Sachtler, W.M.H. Redox chemistry in excessively ion-exchanged Cu/Na-ZSM-5. Catal Lett 16, 241–249 (1992). https://doi.org/10.1007/BF00764336
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DOI: https://doi.org/10.1007/BF00764336