U. Schwertmann et al., IRON-OXIDES AND SMECTITES IN SEDIMENTS FROM THE ATLANTIS-II-DEEP, RED-SEA, European journal of mineralogy, 10(5), 1998, pp. 953-967
Solid-phase analysis was carried out on a 11 m sediment core of the At
lantis II Deep using chemical analysis, X-ray diffraction (XRD), elect
ron microscopy (TEM, EDX), Mossbauer (MS) and infrared (FTIR) spectros
copy. Iron oxides and smectites are the dominant minerals. Among the F
e oxides an extremely poorly crystalline nanometer-sized (nano-) hemat
ite with strong anisotropic XRD peak broadening comprised most of the
upper part of the column whereas well crystalline hematite prevailed i
n its lower part. Akaganeite dominated in an intermediate layer. The n
ano-hematite consisted of irregular particles ca. 5 nm in diameter and
of 2.4-2.8 nm thick curled fibers as revealed by TEM. Mainly due to i
ts small size the nano-hematite exhibits complex MS spectra. Both, the
nano- and the well crystalline hematite, could be subdivided on the b
asis of their magnetic hyperfine field and quadrupole shift. Further c
haracterization and semiquantification was based on MS spectra recorde
d at various temperatures. Di- and trioctahedral Fe-rich smectites com
prised the clay silicate fraction of the samples. The trioctahedral on
es dissolved in acid oxalate and were magnetically ordered at 4.2 K. I
t is speculated that the variety in Fe-oxide mineralogy reflects the t
ime dependent variations of the formation environment. Although we wer
e not successful in reproducing nano-hematite in the laboratory by var
ying parameters such as temperature (50-125 degrees C) and chemical co
mposition of the aqueous system we believe that variation of soluble S
i concentration is responsible for the large range in crystal perfecti
on of hematite. Akaganeite is most likely the result of Fe-III hydroly
sis at higher chloride concentration.