TPR investigations on the reducibility of Cu supported on Al2O3, zeolite Y and SAPO-5

Reducibility of Cu supported on Al2O3, zeolite Y and silicoaluminophosphate SAPO-5 has been investigated in dependence on the Cu content using a method combining conventional temperature programmed reduction (TPR) by hydrogen with reoxidation in N2O followed by a second the so-called surface-TPR (s-TPR). The method enables discrimination and a quantitative estimation of the Cu oxidation states +2, +1 and 0. The quantitative results show that the initial oxidation state of Cu after calcination in air at 400 °C, independent on the nature of the support, is predominantly +2. Cu2+ supported on Al2O3 is quantitatively reduced by hydrogen to metallic Cu0. Comparing the TPR of the samples calcined in air and that of samples additionally pre-treated in argon reveals that in zeolite Y and SAPO-5 Cu2+ cations are stabilized as weakly and strongly forms. In both systems, strongly stabilized Cu2+ ions are not auto-reduced by pre-treatment in argon at 650 °C, but are reduced in hydrogen to form Cu+. The weakly stabilized Cu2+ ions, in contrast, may be auto-reduced by pre-treatment in argon at 650 °C forming Cu+ but are reduced in hydrogen to metallic Cu0.

Graphical AbstractTPR, TPR-(act), s-TPR and s-TPR-(act) profiles of (1.36)Cu/SAPO-5 (A), (4.55)Cu/SAPO-5 (B) and (9.19)Cu/SAPO-5 (C) samples. The intensities of TCD signals in (A) and (B) are multiplied by 4.5 and 2, respectively.Figure optionsDownload as PowerPoint slideHighlights
► Cu supported on SAPO-5, alumina and zeolite Y was investigated by TPR and s-TPR.
► Cu oxidation states can be discriminated and quantitatively determined.
► In zeolite Y and SAPO-5 Cu2+ cations are stabilized at weak and strong forms.
► Strongly stabilized Cu2+ cannot be auto-reduced in argon at 650 °C.