Microbial reduction of clay mineral structural Fe(III) decreases the swelling of nontronite gels, most importantly at intermediate oxidation states (40 to 80 cmol Fe(II) kg−1 clay). The purpose of this study was to establish whether microbial reduction of structural Fe(III) decreased the swelling of other Fe-bearing smectites and to discern the influence that organic compounds of microbial origin (bacterial cells, cell fragments and/or exudates) may have on clay swelling and texture. Structural Fe(III) was reduced by incubating smectite suspensions with either a combination of Pseudomonas bacteria or a mixture of anaerobic bacteria. The influence of organics on clay swelling was estimated on smectites suspended in either organic or inorganic media in the absence of bacteria. The gravimetric water content of the reduced clay gels equilibrated at various applied pressures was recorded as a function of Fe oxidation state. Transmission electron microscopy (TEM) was employed to determine the influence of bacteria and type of media on the texture of reduced smectite gels. Reduction of structural Fe(III) by bacteria decreased the swelling pressure of all Fe-bearing smectites. Increased clay swelling, due to the presence of organics (organic medium, exudates or cell fragments), was correlated to the total Fe content, the extent of structural Fe reduction, as well as the initial swelling characteristics of the Fe-bearing smectites. High structural Fe(II) contents (>50 cmol Fe(II) kg−1) resulted in increased attractive forces between clay platelets that decreased clay swelling, even in organic medium suspensions. Microbial reduction resulted in increased face-face association of individual clay layers, forming larger and more distinct crystallite subunits than in nonreduced clay gels. But, perhaps more importantly, microbial reduction of structural Fe(III) resulted in an increased association between crystallite subunits and, thus, an overall larger particle size and pore size distribution, due to the interaction of bacteria ceils, cell fragments and organic exudates.

Kaolin is found in deposits of economic concentration in the Jabal Al-Harad/ Batn El-Ghoul area in southern Jordan. Ten representative kaolin samples were collected from the area and investigated for their mineralogical and chemical composition. Mineral characterization was carried using X-ray powder diffraction (XRD), thermogravimetrical analysis (TGA), differential thermal analysis (DTA), Fourier transform infrared spectroscopy (FTIR) and scanning electron microscopy (SEM). X-ray fluorescence (XRF) studies were conducted to determine the chemical composition of the kaolin deposits. Kaolinite was the predominant mineral, followed by quartz, with traces of illite-muscovite, Fe-bearing minerals (hematite), anatase and feldspar. The average chemical composition of the kaolin samples was 58.02 wt.% SiO2, 28.00% Al2O3, 1.48% Fe2O3, 1.26% TiO2 and 0.41% K2O (ignited basis). Dehydroxylation and mullitization temperatures (from DTA) were close to the theoretical values. Hexagonal booklets and stacks of kaolinite, as well as individual platelets, were present in the Jabal Al-Harad kaolin. Based on granulometric and descriptive mineralogical analyses, the mineral assemblages and kaolinite morphology, the Jabal Al-Harad kaolin deposit is thought to have originated from greatly weathered surfaces related to the Precambrian basement rocks. The kaolin was found to be suitable for manufacturing of common bricks, medium-fired bricks and sanitary ware, although a beneficiation process would be required; it could also be used in the refractory, white cement, paper and advanced ceramic industries.

Structural iron in smectites correlates with the cell edge length b and increases the refractive index. The cell edge length b is usually obtained from the position of the (060) reflection, but in this work we show that such b values differ from the values obtained from Rietveld fits because contributions from (hkl) reflections shift the position of the (060) reflection. The correlation between Fe and cell edge length b was significant (r2 > 0.99); the relationship is b [Å] = 8.9977(0.0035) + 0.1117(0.0032) × Fetot. Furthermore, we present for the first time measurements of the refractive index n of Fe-bearing smectites, applying a recently published turbidity method (Weidler & Friedrich, 2007). The refractive index correlates both with structural iron (r2 = 0.64) and with b (r2 = 0.94).

The clay-mineral fraction of samples from a bentonite deposit in the Zvolenská kotlina Basin (Slovakia), formed by the alteration of andesitic pyroclastics, was dominated by Fe-bearing montmorillonite of relatively low charge. The total Fe content of the samples ranged from 3.58 to 5.81 wt.% Fe. Variable-temperature Mössbauer spectroscopy revealed that structural Fe(III) in smectite accounts for 70–90% of the total Fe in the unfractionated samples. No structural Fe(II) was observed by Mössbauer spectroscopy, but a small amount was detected by wet chemical analysis. The remainder of the Fe is present in oxide and/or oxyhydroxide phases dominated by poorly ordered goethite and hematite. The hyperfine parameters of the Mössbauer spectra for the raw bentonite are consistent with structural Fe(III) in an aluminosilicate phase mixed with varying quantities of hematite, goethite and possibly maghemite. Except in the fine fraction of sample L28, the hematite failed to undergo the Morin transition, as shown by the negative values for quadrupole splitting at 298 K and 6 K.