Effect of Copper State in Cu/H-ZSM-5 on Methane Activation by Bronsted Acid Sites, Studied by 1H MAS NMR In Situ Monitoring the H/D Hydrogen Exchange of the Alkane with Bronsted Acid Sites

With regard to possible involvement of zeolite Bronsted acid sites (BAS) in the activation of methane molecules for methane transformation to methanol, the effect of different Cu(II) species loaded in the zeolite on the kinetic parameters of the reaction of H/D hydrogen exchange of the alkane with BAS of Cu-modified ZSM-5 zeolites has been investigated with H-1 MAS NMR in situ at 533-563 K. It is found that the acceleration of the H/D exchange by 1 order of magnitude occurs for zeolite containing Cu2+ cations (Z(2)Cu(II) sites) or [Cu-3(mu-O)(3)](2+) oxo-clusters (Z(2) [Cu-3(mu-O)(3)] sites) compared to pure H-form zeolite. It is thus inferred that both Z(2)Cu(II) and Z(2)[Cu-3(mu-O)(3)] sites exhibit the promoting effect of copper on the activation of methane C-H bonds by BAS. Acceleration of the H/D exchange is rationalized by the change of the mechanism of the exchange accepted for the H-form zeolites for the mechanism that involves the formation of a transient molecular complex of methane with Cu(II) species, preceding the H/D exchange reaction. The formation of the complex of methane with both Z(2)Cu(II) and Z(2)[Cu-3(mu-O)(3)] sites is confirmed by DRIFTS. BASs with a higher strength than in H-ZSM-5, generated in the zeolite at copper loading, are concluded to not be responsible for the H/D exchange reaction acceleration.

Automated summary

The study investigated the impact of different Cu(II) species loaded in zeolite on the activation of methane molecules for methane transformation to methanol. It was found that Cu2+ cations or [Cu-3(μ-O)3]2+ oxo-clusters could accelerate the H/D exchange reaction, indicating their promoting effect on the activation of methane C-H bonds by BAS. The formation of a transient molecular complex of methane with Cu(II) species prior to the H/D exchange reaction was also observed.