Abstract

Iron-incorporated zeolites were successfully synthesized at a low temperature such as 80°C by choosing appropriate starting materials and characterized by inductively coupled plasma atomic emission spectrometry (ICP-AES), wide-angle X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FT-IR), and magnetic susceptibility. ICP-AES showed␣that Fe component can be readily incorporated␣up to a maximum extent of Fe substitution, Fe/(Fe + Al) × 100 = 22.7%. XRD measurements suggested that the zeolites obtained have a crystal structure of gismondine type. The characterizations identified that the Fe component present in the products is all incorporated into the zeolite framework. The ammonia and water desorption profiles were compared for Fe-free and 22.7% Fe-zeolites ion-exchanged for NH4+ by means of TG-MS and DSC. The ammonia desorption peak temperatures considerably shifted toward lower temperatures by the introduction of Fe, suggesting decreased solid acidity. DSC thermograms of the as-synthesized gismondines revealed that they do not contain free water (i.e., water not coordinated to cations) in the pores irrespective of the Fe content. The enhanced catalytic reactivity of the Fe-incorporated gismondines was also confirmed from the decomposition of hydrogen peroxide. An apparent activation energy of 43 kJ mol−1 was obtained independent of the Fe contents in zeolites. This value was much lower than 70 kJ mol−1 for the same reaction in the homogeneous solution containing iron alum as a reference sample.

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