Identification and Quantification of Copper Sites in Zeolites by Electron Paramagnetic Resonance Spectroscopy

Topics in Catalysis - Tập 60 - Trang 13-29 - 2016
Anita Godiksen1, Peter N. R. Vennestrøm2, Søren B. Rasmussen2, Susanne Mossin1
1Department of Chemistry, Technical University of Denmark, Kgs. Lyngby, Denmark
2Haldor Topsøe A/S, Kgs. Lyngby, Denmark

Tóm tắt

Recent quantitative electron paramagnetic resonance spectroscopy (EPR) data on different copper species present in copper exchanged CHA zeolites are presented and put into context with the literature on other copper zeolites. Results presented herein were obtained using ex situ and in situ EPR on copper ion exchanged into a CHA zeolite with Si/Al = 14 ± 1 to obtain Cu/Al = 0.46 ± 0.02. The results shed light on the identity of different copper species present after activation in air. Since the EPR signal is quantifiable, the content of the different EPR active species has been elucidated and Cu2+ in 2Al positions in the 6-membered rings (6mr) of the CHA structure has been characterized. Some copper species are found not to give an EPR signal at ambient or high temperatures. Fortunately, treatments with different gasses under in situ conditions are able to trigger an EPR signal and thus reveal information about the reactivity and the quantity of some of the otherwise EPR silent species. In this way the [Cu–OH]+ species in copper substituted low-Al zeolites has been indirectly observed and quantified. EPR active Cu2+ species have been followed under reduction and oxidation with gas mixtures relevant for the selective catalytic reduction of NO with NH3 (NH3-SCR) revealing that all Cu2+ in 6mr are easily reduced and oxidized at 200 °C. Furthermore, a stable [Cu–NO3]+ species is identified in Cu-CHA after exposure to NO and O2, but is not stable in 2Al 6mr sites of the CHA structure under the applied conditions.

Tài liệu tham khảo

Deka U, Lezcano-Gonzalez I, Weckhuysen BM, Beale AM (2013) Local environment and nature of Cu active sites in zeolite-based catalysts for the selective catalytic reduction of NOx. ACS Catal 3:413–427

EU Commission (2011) Commission Regulation (EU) No 582/2011 of 25 May 2011. Off J Eur Union L 167: 1

Carl PJ, Larsen SC (2000) EPR study of copper-exchanged zeolites: effects of correlated g- and A-strain, Si/Al ratio, and parent zeolite. J Phys Chem B 104:6568–6575

Öpik U, Pryce MHL (1957) Jahn–Teller effect. I. A survey of the static problem. Proc R Soc Lond A 238:425–447

Bendix J (2004) Ligfield. Compr Coord Chem 2:673–676

Dědeček J, Kaucký D, Wichterlová B (2000) Co2+ ion siting in pentasil-containing zeolites, part 3. Co2+ ion sites and their occupation in ZSM-5: a VIS diffuse reflectance spectroscopy study. Micropor Mesopor Mater 35–36:483–494

Conesa JC, Soria J (1979) Electron spin resonance of copper-exchanged Y zeolites. J Chem Soc Faraday Trans 1(75):291–293

Deka U, Eilertsen EA, Emerich H et al (2012) Confirmation of isolated Cu2+ ions in SSZ-13 zeolite as active sites in NH3-selective catalytic reduction. J Phys Chem C 116:4809–4818

Schoonheydt RA (1993) Transition metal ions in zeolites: siting and energetics of Cu2+. Catal Rev 35:129–168

Kwak JH, Lee JH, Burton SD et al (2013) A common intermediate for N2 formation in enzymes and zeolites: side-on Cu-nitrosyl complexes. Angew Chem Int Ed Engl 52:9985–9989