Abstract

Iron zeolites with SiO 2 Al 2O 3 ratios in the range 5.8–10.7 were prepared for impregnating LZY-82 zeolite in an aqueous solution of iron(III) nitrate or iron(II) sulfate, and calcined at 500°C. Some of the samples were treated in an atmosphere of hydrogen at 400 or 450°C. Chemical forms and reduction behaviour of iron species in these modified iron(III) zeolites were examined by 57Fe Mössbauer and e.s.r. spectroscopies and by electron microscopy. Iron(III)-oxide clusters bonding with the zeolite framework and fine iron oxide with diameters less than 1.2 nm produced in the zeolite cavities were detected except for iron(III) located in the cationic sites of zeolites. The strength of bonding between the fine iron oxide and/or iron-oxide cluster and the zeolite lattice was influenced by the preparative conditions of the iron(III) impregnation. It was possible to make distinctions between irons(III) of the cationic sites for the iron zeolites reflexed in toluene by a Mössbauer spectroscopy.

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call