Journal
PHYSICAL CHEMISTRY CHEMICAL PHYSICS
Volume 12, Issue 24, Pages 6520-6531Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c000750a
Keywords
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Funding
- Deutsche Forschungsgemeinschaft
- Land Baden-Wurttemberg [SFB 706]
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The present study focuses on the characterization of the active sites for oxygen adsorption in both copper-free and copper-containing HZSM5 zeolites. FTIR, EPR, EXAFS and UV-Vis measurements offer insight into the initial state of the catalyst before oxygen adsorption. Both liquid and solid state ion exchanged samples contain a certain amount of Cu(II) and Cu(I) ions in the alpha 3, alpha 4 and gamma 6 position, their population ratio depending on the ion exchange temperature. They are accessible for interaction with the adsorbate, as the copper-oxygen spin exchange demonstrates. Both the sample magnetization and the EXAFS analysis indicate that 10-30% of the Cu(II) exists in the form of oxygen bridged Cu-Cu pairs. UV-Vis measurements prove that two different antiferromagnetically coupled copper peroxide complexes are formed during the sample preparation process, the bis(mu-oxo)- and (mu-eta(2) : eta(2)-peroxo) dimers. One of the complexes is susceptible to oxygen adsorption, which cleaves it irreversibly into two individual Cu(II)-O-2(-) units, while Cu(I) ions are oxidised to the same species. The Bronsted acid sites are also able to adsorb oxygen both at room and low temperatures. The presence of the different active sites may be an explanation for the high catalytic activity of the Cu/HZSM5 zeolite. The Bronsted sites near copper centers could protonate the peroxide complexes, leading to the in situ formation of hydrogen peroxide, a common oxidant. This peroxide would be a highly active species for catalytic reactions.
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