NIPPON KAGAKU KAISHI
Online ISSN : 2185-0925
Print ISSN : 0369-4577
Isomorphous Substitution of Iron in the Framework of Linde B Type Zeolites under Mild Conditions
Kazuko KATSUKIMiki OKAMOTOEmi ICHIKAWAAtsushi IWASHINAShingo KOIKEYasuhiro YAMAMOTOToshio TAKEUCHIYukichi YOSHINO
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1995 Volume 1995 Issue 9 Pages 689-696

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Abstract

At mild conditions such as 80°C and atmospheric pressure, zeolites containing iron (III) ions in the framework were prepared from a homogeneous solution or somewhat heterogeneous mixture as a starting material. Si nce iron (III) ions can be incorporated into excess silicate ions forming a soluble complex, [FeSiO(OH)3]2+, the iron (III) nitrate solution was first added to an excess of sodium metasilicate solution (Si/Fea≥50). Then various aluminium sources were added until Si/(Al+ Fe) and Fe/ (Al + Fe)become 20 and 0.00-0.40, respectively. When sodium aluminate was used as aluminium source, the solution became homogeneous (system 1), whereas aluminium nitrate lead to a partly heterogeneous mixture (system 2). The solid prod ucts obtained from both the systems were characterized by XRD, IR, SEM, ICP-AES and magnetic susceptibility methods. These analyses confirmed the formation of Linde B1 and B4 from the two systems and the presence of iron (III) in their zeolite lattice framwork. The extent of iron (III)substitution goes up to 40% in the products from system 1 and ca.25% in those from system 2. These values are fairly large as compared with those reported in the literatures. In conclusion, system 1 is a better starting material than system 2, because the former gives higher crystallinity and larger extent of iron substitution.

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