Clays and Clay Minerals, Vol. 58, No. 5, 589–595, 2010.

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Authors

Gutierrez, Marlen
Escudey, Mauricio
Escrig, Juan
Denardin, Juliano C.
Altbir, Dora
Fabris, Jose D.
Cavalcante, Luis C. D.
Garcia-gonzalez, Maria Teresa

Issue Date

2010

Type

Article

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Keywords

Periodicals , Geology , Coercivity , Fe Oxide , Isoelectric Point , Magnetite , Magnetic Zeolite , Mossbauer Spectroscopy

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Alternative Title

Preparation And Characterization Of Magnetic Composites Based On A Natural Zeolite

Abstract

A magnetic composite was prepared by wet-impregnating a powder of a natural zeolite with a magnetic Fe oxide-containing synthetic material. Both starting materials were first characterized with X-ray diffraction, scanning electron microscopy, Mo¨ssbauer spectroscopy, and by isoelectric-point using vibrating-sample magnetometry. The synthetic Fe oxide-containing material was characterized as a mixture of magnetite (Fe3O4) and goethite (a-FeOOH). From the 57Fe Mo¨ssbauer analysis, the relative subspectral area for magnetite corresponds to 93(2)%; the remaining spectrum is assignable to goethite. After the impregnation process, magnetite was still identified in the composite material as a magnetic layer surrounding the zeolite particles; no magnetically ordered goethite could be detected. The Mo¨ssbauer pattern for this sample indicates a much more complex structure than for the precursor material, based on Fe oxides, with some more altered magnetite and an intense central doublet of (super)paramagnetic Fe3+, probably due to small Fe (hydr)oxides and/or to a residual contribution of Fe-bearing species from the starting zeolite material. The composite preparation procedure also promoted the change of the characteristic A-type zeolite to mordenite. The resulting magnetic composite presented a magnetic coercivity of as much as 0.140 A m-1, at 77 K. The final composite is now being evaluated as an adsorbent: results to date confirm that this novel magnetic material may have applications in the remediation of contaminated water bodies.

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Citation

Clays and Clay Minerals, Vol. 58, No. 5, 589–595, 2010.

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The Clay Minerals Society

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Copyright © 2006-2018

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