Acs. Da Costa et al., Quantification and characterization of maghemite in soils derived from volcanic rocks in southern Brazil, CLAY CLAY M, 47(4), 1999, pp. 466-473
Many soils developed from volcanic rocks in southern Brazil exhibit spontan
eous magnetization caused by the presence of fine-grained maghemite (gamma-
Fe2O3), but few attempts were made to quantify or characterize this importa
nt soil component. To that end, clays were separated from freely drained so
ils derived from acid (greater than or equal to 63% SiO2), intermediate (54
-62% SiO2), and basic (less than or equal to 53% SiO2) igneous rocks produc
ed by the Parana flood volcanism. The sample set included soils with a wide
range of pedogenic development on different landscape positions. The Fe ox
ide mineralogy of these samples was examined by using a combination of sele
ctive dissolution, magnetic susceptibility, and X-ray diffraction (XRD) tec
hniques. Hematite and maghemite were the primary Fe oxides in mature soils
(Oxisols, Ultisols, and Alfisols) developed from basic rocks; whereas goeth
ite was dominant in all other soils, especially those formed from acid-inte
rmediate rocks. The association of maghemite with basic rock materials sugg
ests that it was primarily formed by oxidation of lithogenic magnetite. A s
trong, positive correlation (R-2 = 0.89) was obtained between mass specific
magnetic susceptibility (chi) of the clay fractions and maghemite contents
estimated by XRD. Either method could be used for quantitative analyses, b
ut chi was more sensitive than XRD at low maghemite concentrations (<2 wt.
LTC). The clay-sized maghemites were superparamagnetic with an estimated va
lue for the mass specific magnetic susceptibility (chi(If)) value of 91,000
x 10(-8) m(3) kg(-1) and frequency dependent Variations of 10-15%. The mag
hemites also had low unit cell constants, which, if attributed entirely to
replacement of Fe by Al, would correlate with Al substitutions in the range
of 5-16 mole %. Selective dissolution of the soil maghemites was achieved
by treatment of Fe oxide concentrates with 1.8 M H2SO4 at 75 degrees C for
7 h.