The rare Pb silicate jagoite, known only from the Långban and Pajsberg Mn–Fe oxide deposits in Värmland, Sweden, is associated with a more diverse mineral assemblage than originally described: alamosite, barysilite, hyttsjöite, margarosanite, melanotekite, nasonite and yangite and other, not fully characterised Pb silicates. Primary melanotekite and barysilite, formed as skarn (together with hematite, quartz, clinopyroxene and andradite) during regional metamorphism, are prone to alteration, with Cl⁻, SiO₂, Ca2⁺ and H₂O acting as modifying agents. In the process, newly formed Pb silicates exhibit increasing Si content, reflecting a higher degree of SiO₄ polymerisation at high pH and decreasing temperatures.

A refinement of the crystal structure of jagoite from X-ray diffraction data, to R1 = 1.2% [space group P$\bar 6$2c, a = 8.53926(5) Å and c = 33.3399(2) Å], confirms previous work, and provides significantly improved structural parameters. New data were also obtained with Mössbauer spectroscopy, laser-Raman micro-spectroscopy, electron-microprobe and laser-ablation inductively coupled plasma mass spectrometry analyses. The results indicate that jagoite accommodates minor elements, notably Al at an octahedrally coordinated Fe-dominated site and Mn3⁺, Zn and Mg at four-coordinated mixed Fe–Si sites, and small amounts of Ca+Na replacing Pb. Jagoite is also enriched in Be, Sb, Bi and Br, but those elements have a limited role in its crystal chemistry. Mössbauer measurements show that Fe3⁺ is distributed over three different crystallographic sites, two 4-coordinated and one 6-coordinated, and that jagoite remains paramagnetic down to 77 K. The ideal chemical formula for jagoite should be written Pb11Fe5Si12O41Cl3 for Z = 2.

Mössbauer spectroscopy of dioctahedral phyllosilicates showed that on dehydroxylation iron which originally occupied M(2) and M(l) sites became, respectively, 5- and 6-coordinated. The 6-coordinated sites are very distorted. No migration of cations occurs in the course of heating the specimens for 1–3 hr at 600°–700°C.

By using a combination of several physicochemical methods, different successive stages of the dehydroxylation process could be distinguished: (1) migration of protons; (2) localized dehydroxylation of individual associations without significant change in the overall configuration of the octahedral sheets; and (3) loss of most of the hydroxyl groups with concomitant changes in the cell dimensions. Penetration of Li into the octahedral sheets does not affect the course of the reaction, but reduces the dehydroxylation temperature and the stability of the products.

Dehydroxylation was preceded by or associated with the oxidation of any divalent iron present. Fe3+ derived from Fe2+ was indistinguishable by Mössbauer spectroscopy from iron initially present in the trivalent form. High concentrations of Fe lower the dehydroxylation temperature and reduce the stability of the dehydroxylate to the extent that partial disintegration may precede complete dehydroxylation.

Samples of nacrite, dickite, kaolinite, and halloysite were investigated using X-band electron paramagnetic resonance (EPR) and Mössbauer spectroscopy. Fe3+ gave rise to EPR signals at g ≃ 4 which differed with the individual polytype. Only nacrite had no resonance in this region of the spectrum, but it had one at g ≃ 2. Dickite had a quadruple line, kaolinite a triple line, and halloysite a single line in this region. The EPR spectra of these minerals are apparently dependent also on the orientation of adjacent layers in the structures. Other resonances were attributed to (1) clusters of ferric ions giving rise to broad resonance near g ≃ 2, (2) trapped holes, and (3) free radicals linked with organic matter. The Mössbauer spectroscopic results suggest that iron occurs in the ferric state (except in nacrite where Fe2+ is present also) as an ionic substitution (IS) in octahedral layers. This suggestion follows from the difference is the IS values between octahedral and tetrahedral symmetry sites occupied by Fe3+ equal to ∼0.4 mm/sec. Linewidths depend mainly on the way the layers stack; for monoclinic modifications represented by nacrite and dickite, the linewidths are narrow (Γ = 0.45 mm/sec and 0.56 mm/sec, respectively); pseudomonoclinic halloysites also gave narrow linewidths (Γ = 0.39 mm/sec and 0.48 mm/sec). The widest line was observed for triclinic kaolinite (Γ = 0.62 mm/sec and 0.71 mm/sec).

Fe3+ ions in palygorskite occupy sites at the edges and in the interior of the alumino-silicate chains. The Mössbauer parameters of the doublets associated with Fe3+ ions in edge sites indicate that the sites have a regular 6 coordination. Fe3+ ions in the interior of the chains occupy M(1) sites in three of the samples examined and M(2) sites in the fourth. Fe3+ ions in edge positions of palygorskite become 5-coordinated when water is lost on heating. They maintain this coordination on dehydroxylation, probably by cross-linking of the chains. The temperatures at which changes occur in the X-ray powder diffraction patterns and the Mössbauer and infrared (IR) spectra differ from sample to sample. The intermediate stages observed also vary, either due to different reaction paths or to different stabilities of the intermediate phases. The deduced distribution of cations in the octahedral sheets is in good qualitative agreement with the observed IR hydroxyl absorptions.

Feroxyhite (δ′-FeOOH) in association with goethite and lepidocrocite was found as a dominant mineral in some rusty precipitates from Finland. These precipitates formed in the interstices of sand grains from rapidly flowing, Fe(II)-containing water which was very quickly oxidized as it flowed through the sediment. The mineral is distinguished from other FeOOH forms and from ferrihydrite mainly by its X-ray powder diffractogram. Further characteristics are an acicular morphology (possibly thin, rolled plates), an internal magnetic field at 4°K of ∼510 kOe, Fe-OH stretching bands at ∼2900 cm−1 and Fe-OH bending bands at 1110, 920, 790, and 670 cm−1, and an oxalate solubility between ferrihydrite and goethite or lepidocrocite. Feroxyhites with very similar properties were synthesized by oxidation of an Fe(II) solution with H2O2 at a pH between 5 and 8.

Fe57 Mössbauer spectroscopy has been used to determine the nature of iron-containing minerals in Lower Greensand samples from an experimental lysimeter at Uffington, Oxfordshire, both before and after a three-year irrigation with a synthetic heavy metal leachate. Analysis of the spectra measured at 300°, 77°, and 4.2°K and at 4.2°K in an applied field of 45 kOe shows that iron is present in the uncontaminated sandstone in fine-grained goethite (α-FeOOH) and glauconite. In the irrigated samples iron is precipitated as a fine-grained ferric hydroxide gel having values for the hyperfine field at 4.2°K of 435 and 470 kOe. The stability of the gel over the three-year period of irrigation may be explained by surface energy considerations.

Mössbauer spectra of 9 glauconite samples from Upper Cretaceous and Lower Tertiary strata in the South Island of New Zealand contain a broad shoulder due to low intensity absorption continuous between 1.0 and 2.5 mm/sec when the absorber is at room temperature; the shoulder is absent, and sharp peaks are apparent in spectra taken with the absorber at 80°K. The data suggest that electron transfer occurs between adjacent Fe3+ and Fe2+ ions at room temperature. The low temperature spectra indicate that all Fe in the glauconites is in octahedral coordination. Fe3+ and Fe2+ ions occur in both eis and trans sites; Fe3+ shows a strong preference for eis sites whereas Fe2+ shows an even stronger preference for trans sites.

The partially variable oxidation state of Fe in glauconite is interpreted in terms of a geochemical model for glauconitization of a degraded or incomplete progenitor phyllosilicate. The model involves exchange of Fe2+ for other cations which temporarily stabilize the progenitor, followed by Fe2+-Fe3+ charge transfer reactions. Each reaction results from the system's tendency towards equilibrium. The model is supported by the observation that artificially leached glauconite increases both its Fe3+ and its Fe2+ content when placed in a solution containing Fe2+ as the only Fe ion present.

A rounded fragment of a multicoloured tourmaline crystal (2.5 cm diameter), collected from the secondary gem deposit of Mavuco, Alto Ligoña pegmatite district, Mozambique, has been investigated using a multi-analytical approach, with the objective of reconstructing its growth history. The sample represents a core-to-rim section, perpendicular to the c axis, of a crystal characterised by a variety of colours. These change from a black core to an intermediate zone with a series of colours, yellow, blue–green and purple, to a final dark-green prismatic overgrowth. These changes are the result of a wide variation in Fe, Mn, Ti and Cu concentrations and their redox state. The black core is characterised by enrichment in Fe and Mn, with iron present in its divalent state. The yellow zone shows a progressive depletion in Fe and its colouration is caused by Mn2+ and Mn2+-Ti4+ IVCT interactions. The progressive decrease in Mn coupled with the absence of Ti, and the lack of Fe, implies that Cu2+ acts as the only chromophore in the pale blue–green zone. The dominant colour-causing agent of the purplish zone is Mn3+, denoting a change in redox environment; however, even though the amount of Cu remains significant, its chromophore effect is obscured by Mn3+. The dark-green prismatic overgrowth, characterised by a sharp increase in Fe, Mn and also Ca, is interpreted as a late-stage partial re-opening of the geochemical system. This occurrence could potentially be related to mechanical instability of the cavity in which the crystal grew.

Adsorption isotherms and UV-visible and Mössbauer spectroscopic data point to specific interactions between flavomononucleotide (FMN) and Fe3+-smectite. The maximum amount of FMN adsorption was 0.3 mmole/g of Fe3+-smectite giving a 1:1 molar proportion of Fe3+ and FMN. The results suggest a Fe3+-FMN complex residing at the smectite surface. Other homoionic smectites (Cu2+, Zn2+, and Ca2+) exhibited lower levels of adsorption and less apparent specific interaction.

Glauconite from the oxidized and reduced zones of soil-geologic columns at two Coastal Plain sites, one in Maryland and one in New Jersey, was examined by Mössbauer spectroscopy. The data indicate that glauconite in the reduced zones had a higher proportion of its structural iron in the ferrous, as opposed to the ferric state. The Fe2+/Fe3+ ratio ranged from 0 to 0.2 for the glauconite from the oxidized zone and was about 0.35 for the glauconite in the reduced zones. Despite the presence of pyrite in the reduced zone, which might be expected to make ferric iron unstable because of the presence of sulfide S, about 75% of the Fe in the glauconite in the reduced zone was in the ferric state. Thin section analysis showed some glauconite in the reduced zones to be intimately associated with pyrite and some aggregates of fine pyrite crystals were locally present in cracks in glauconite pellets. In the oxidized zones, pyrite was absent and the glauconite was more yellow under plane-polarized light, as opposed to more green for the glauconite in the reduced zones. These data indicate that reports of studies of glauconite should stipulate whether samples are from the oxidized or reduced zone of soil-geologic columns.

Mössbauer spectra of 15 hematites with Al substitutions between 0 and 10 mole % were taken at room temperature. X-ray powder diffraction indicated dimensions of these hematites in the c-direction to range upwards from 27 nm to crystals large enough to show no line broadening. The Mössbauer spectra showed that magnetic hyperfine fields decreased both with increasing Al-for-Fe substitution and with decreasing crystal size. These relationships indicate that hyperfine field variations cannot, as has been done in the past, be unequivocally related to Al substitution alone. Hyperfine field reductions were paralleled by Mössbauer line broadening due to hyperfine field distributions. Only the hematites heated to 1000°C showed a significant variation of quadrupole splittings with Al substitution. No dependence of quadrupole splitting on crystal size was observed, indicating no detectable distortion of coordination polyhedra in the particle size range studied.

The mineralogy of the clay fraction was studied for soils and saprolite on two Blue Ridge Front mountain slopes. The clay fraction contained the weathering products of primary minerals in the mica gneiss and schist parent rocks. Gibbsite is most abundant in the saprolite and residual soil horizons, where only chemical weathering has been operable. In colluvial soil horizons, where both physical and chemical weathering have occurred, the clay fraction consists largely of comminuted primary phyllosilicates —muscovite, chlorite, and possibly biotite—and their weathering products: vermiculite, interstratified biotite/vermiculite (B/V), and kaolinite. The clay-size chlorite contains Fe2+ as indicated by Mössbauer spectroscopy, and is more resistant to weathering than biotite. The vermiculite and B/V, both weathering products of biotite, contain Fe3+. Vermiculite in colluvial soils and, especially, surface horizons is weakly hydroxy-interlayered. The kaolinite in the clay fraction resulted at least partly from the comminution of kaolinized biotite in coarser fractions.

The hematite content ranged from 0 to 8% of the clay fraction and strongly correlates (r =.95) with dry clay redness, as measured by the redness rating: RR = (10 - YR hue) × (chroma) ÷ (value). The hematite is largely a product of the weathering of almandine; thus, the soil redness is dependent on the amount of almandine in the parent materials and its degree of weathering in the soils. Goethite (13–22% of the clay fraction) imparts a yellow-brown hue to soils derived from almandine-free parent rocks. The release of Fe in relatively low concentrations during the weathering of Fe-bearing primary minerals, particularly biotite, appears to have promoted the formation of goethite.

The migration of interlayer Fe3+ cations into the structure of heated montmorillonite and Laponite has been studied by electron spin resonance (ESR), Mössbauer spectroscopy, and magnetic susceptibility measurements. The intensity of the ESR signal corresponding to interlayer Fe3+ in air-dried montmorillonite and Laponite increased linearly as the amount of interlayer Fe3+ increased. Changes in the spectra after thermal treatment indicate that Fe3+ cations migrated into the pseudohexagonal cavities of dehydrated montmorillonite and Laponite. The electrostatic interaction between the Fe3+ and the oxygen atoms defining the entrance to these cavities and the proton of the structural OH groups at the bottom of the cavities differ for the two smectites. Ferric cations were apparently bound more strongly within the pseudohexagonal cavities of the dehydrated montmorillonite than within the cavities of Laponite, because the montmorillonite did not rehydrate after heating. The differences in the binding of Fe3+ cations within the pseudohexagonal cavities of montmorillonite and Laponite were probably due to variations in the ability of the protons of the structural OH groups to reorient. An additional electronic interaction occurred in the heated Laponite, in which small cations were able to promote the formation of structural defects, which gave rise to a sharp ESR signal at g = 2.00. No evidence for the penetration of Fe3+ cations into the vacant octahedral sites of montmorillonite was found.

A series of synthetic goethites containing varying amounts of Si and P dopants were characterized by X-ray powder diffraction, electron diffraction, microbeam electron diffraction, and Mössbauer spectroscopy. Very low level incorporation produced materials having structural and spectral properties similar to those of poorly crystalline synthetic or natural goethite. At higher incorporation levels, mixtures of noncrystalline materials were obtained which exhibited Mössbauer spectra typical of noncrystalline materials mixed with a superparamagnetic component. Microbeam electron diffraction indicated that these mixtures contained poorly crystalline goethite, poorly crystalline ferrihydrite, and a noncrystalline component. If the material was prepared with no aging of the alkaline Fe3+ solution before the addition of Na2HPO4 or Na2SiO3, materials were obtained containing little if any superparamagnetic component. If the alkaline Fe3+ solution was aged for 48 hr before the addition, goethite nuclei formed and apparently promoted the precipitation of a superparamagnetic phase. The Mössbauer-effect hyperfme parameters and the saturation internal-hyperfine field obtained at 4.2 K were typical of those of goethite; however, the Mössbauer spectra indicated that the ordering temperature, as reflected in the relaxation rate and/or the blocking temperature, decreased with increasing incorporation of Si and P. The complete loss of crystallinity indicates that Si and P did not substitute for Fe, but rather adsorbed on crystal-growth sites, thereby preventing uniform crystal growth.

The 57Fe Mössbauer spectra of a series of untreated and Ca-saturated nontronites showed a predominant Fe3+ resonance which was computer-fitted with two Fe3+ doublets defining iron in non-equivalent cis-FeO4(OH)2 octahedral sites. In most spectra a doublet indicating tetrahedral Fe3+ was fitted and in one untreated sample a doublet indicating interlayer Fe3+ was identified. In a further untreated sample the interlayer iron was present as Fe2+. Upon Ca-saturation the interlayer iron was displaced. It also appears that the interlayer iron was present in at least two different interlayer sites. From the computer-fitted data it was clear that the interlayer cations have a significant effect on the Mössbauer resonances of iron in the two non-equivalent cis-octahedral and the tetrahedral sites of nontronite.

As part of the characterization of a Tunisian red soil profile, six samples, taken at different depths, were investigated by Mössbauer spectroscopy at room temperature and at 80 K to obtain information about the various types of Fe oxides present. By considering magnetic hyperfine field distributions, the spectra of goethite and hematite were well resolved. Chemical analyses of the samples revealed a partial substitution of Fe by Al and Mn. The spectral behavior of the goethite was predominantly influenced by crystallinity and amount of Al substitution which resulted in a reduction of the magnetic hyperfine field. The effect of Mn substitution was much more pronounced in the hematite spectrum as a consequence of a stronger suppression of the Morin transition by Mn than by Al.