High-quality kaolins are produced from two sites in the Capim River area in Pará State, northern Brazil. One mine is operated by Rio Capim Caulim (RCC) owned by Imerys and the other by Pará Pigmentos S.A. (PPSA) owned by Caemi (CVRD Group). The kaolin deposits are located on low-relief plateaux with a lateritic cap. The kaolin strata are in the Ipixuna Formation of Upper Cretaceous Age. There are two distinct kaolin layers, a 4–5 m thick soft kaolin which is overlain in the southern portion of the basin by a 4–5 m thick hard kaolin. The soft and hard designations refer to particle size, with the soft kaolin being relatively coarse and the hard kaolin very fine. The kaolin is mined, partially beneficiated, and pumped through pipelines to the port at Barcarena on the Guama River, a large tributary of the Amazon River. The PPSA kaolin is fully processed at the plant near the mine site and pumped to Barcarena where it is spray dried. The RCC kaolin is only partially processed at the mine site. This partially processed kaolin is pumped to Barcarena where it is beneficiated. The finished kaolin is high quality and is shipped to North and South American, European, and Asian paper-coating markets. More than 1.6M tons were shipped from Barcarena in 2005.

Fe-rich dioctahedral smectites are the main constituent of clays in Çamlıca Region of Turkey. The structural, chemical and morphological characteristics of these smectites after washing are examined by X-ray diffraction, electron microscopy, inductively coupled plasma mass spectrometry and Fourier transform infrared spectroscopy. Smectite particles occur as individual flakes 0.2–2.0 μm in size. These flakes are often aggregated into clusters up to 6.0 μm in size.

Given that reservoirs contain most of the leached materials from soils, we have studied the sediments accumulated in the bottom of two groups of reservoirs developed under different climatic conditions and thus with contrasting rates of weathering/erosion regimes. Through detailed comparative study of clay minerals of the parent rocks and soils with the clay fractions of the dam sediments, we have concluded that, during cycles of erosion-transport-deposition, the leached materials have complex transformation mechanisms, making them much more active in the environment. All clay-mineral groups are well represented in the reservoir sediments, including abundant mixed-layer and partly disordered minerals. Moreover, the sediments are nutrient-rich and potentially useful as agricultural fertilizers and hence in reversing the declining soil productivity in some regions.

Kaolinite-smectite mixed-layers have been found to have a complex structure with smectite and kaolinite domains within layers. Here we further investigate this structure in samples with 0–80% kaolinite layers, as determined by X-ray diffraction, by means of magic angle spinning nuclear magnetic resonance (MAS NMR) of 29Si and 6Li. The 29Si NMR experiments were carried out on two samples (55 and 80% kaolinite layers), before and after their exchange with Mn2+, a paramagnetic ion that causes NMR signal loss from neighbouring nuclei, in order to investigate the distance between Mn ions and Si atoms in kaolinite sites. The 29Si NMR intensity from such sites (at ~–91 ppm) was reduced upon Mn exchange, indicating that some Mn ions are located near kaolinite Si sites. The position of the 6Li peak changes slightly (–1.3 to –1.8 ppm) but progressively with increasing kaolinite content (0–80% kaolinite layers) of four K-S specimens, suggesting two slightly different chemical environments for interlayer Li, one related to smectite and the other to kaolinite. The two sets of experiments are consistent with a complex structure of kaolinite-smectite, including smectite and kaolinite domains within layers and/or interlayers of varying smectitic and kaolinitic character.

A mineralogical and microtextural study of Somosaguas Miocene deposits, located in the Madrid Basin (western Madrid, Spain), was carried out using X-ray diffraction, scanning electron microscopy, transmission electron microscopy and optical microscopy, whereas crystal chemistry data were obtained by analytical electron microscopy-transmission electron microscopy and electron icroprobe analysis. Four stratigraphic sections were studied, compising detrital rocks representing intermediate and distal facies from alluvial fan deposits. The predominant source area of these sediments was the granitic rocks of the Spanish Central System with a lesser contribution of metamorphic rocks. Clayey arkoses are the most abundant rocks of these sections, typical of granite alteration under warm, semi-arid climates. The mineralogy is characterized by phyllosilicates, followed by feldspars and quartz. The data obtained reveal mineral mixtures of detrital (quartz, feldspars, kaolinite, micas and chlorite), transformed (illite and beidellite) and neoformed (montmorillonite) origin. Clay minerals resulted from interactions between detrital minerals and meteoric waters. Two trends of degradation of micas are detected. The first shows a transition from muscovites and dioctahedral illites, to beidellites. The other trend is defined by the biotite degradation to beidellites with different layer charge and octahedral Fe content. Montmorillonites were neoformed from the hydrolysis and weathering of primary minerals (feldspars and muscovite). Magnesian clay minerals such as sepiolite, palygorskite and trioctahedral smectites, extremely abundant in the centre of the basin, were not detected in Somosaguas sediments.

Zeolite ZSM-5 was synthesized successfully, in situ, on pyrokaolin microspheres (PKM) under hydrothermal conditions, without the use of an organic amine template. The utility of alkali-modified pyrokaolin microspheres (AMKM) was also evaluated. The resulting products were characterized using X-ray diffraction, scanning electron microscopy (SEM) and N2-adsorption isotherm data. The material containing ZSM-5 synthesized from the system PKM-additional silica-water had a large surface area and pore volume with significant enhancements in the micropore surface area and micropore volume. The SEM images show that the synthesis of zeolite ZSM-5 from pyrokaolin microspheres (PKM) led to the formation of polycrystalline aggregates <2 μm in size. The purity of the zeolite ZSM-5 produced was affected by both the pH value of the reactant system and the reaction temperature. In the system containing AMKM-additional silica-water, very little of the synthesized zeolite resided on the kaolin microspheres.

A mixed-layer illite-smectite, illite-rich calcareous mudstone intruded by a basaltic dyke at the Perthus Pass (southern Massif Central, France) allows us to study the transformation of clays subjected to a brief thermal gradient. X-ray diffraction, scanning electron microscopy, electron microprobe and atomic absorption spectroscopy analyses were performed on samples at variable distances from the mudstone-dyke contacts.

A roughly similar evolution is seen on both sides of the dyke: quartz, calcite, kaolinite and illite disappear; Ca-silicates, albite and saponite-beidellite form, late meteoric halloysite crystallizes in open fractures.

Chemical and mineralogical transformations are related to heat diffusion from the dyke. Theoretical calculations highlight the influence of the dyke orientation. The mineralogical reactions observed in rocks are similar to those observed in experimental conditions. The formation of new swelling phases with a high retention capacity linked to a short duration, large-temperature increase, should constitute a positive process for Repository Performance Assessment.

Turkey has a long tradition (starting with prehistoric civilizations) and experience in exploring for raw clay materials and processing them into ceramic products. Many of these products, such as tiles and sanitary ware, are manufactured for domestic and export markets. Kaolin is one of the raw materials of major importance for the ceramic and paper industry, as well as for a number of auxiliary applications. There is ongoing interest in applying kaolin in the construction industry as a raw material in the production of white cement clinker and as an artificial pozzolanic additive for concrete (in the form of metakaolin). This report presents results related to search, assessment and evaluation of available resources for advanced cement and concrete additives.

A series of thin clayey beds topping shallow marine cyclothems was sampled from a Turonian succession in Israel and was analysed by XRD for the mineralogical composition of its clay fraction. The main goal was to search for potential relations between short-term shallowing and possible emergence events and clay mineralogy. The bulk (<2 μm), coarse (0.2–2 μm) and fine (–0.2 μm) clay fractions of a unique clay bed, dominated by R⩾1-type I-S were analysed for their chemical composition and dated by the K-Ar method. The fine clay fraction was dated at ~5 m.y. younger and the bulk clay to be slightly older than the known stratigraphic age, which means that the clay is mostly authigenic and formed at low-temperature, near-surface conditions. This is supported by the geological history of the region and by the variability of the clay assemblages and I-S composition within ~30 m vertical distance, neither of which indicates evidence for high temperatures. The sedimentological analysis suggests that the clay bed was deposited at marginal marine marshes where evaporated sea water turned into an alkaline solution of high K concentration. This is apparently the first study to provide convincing evidence for low-temperature, early diagenetic formation and preservation of I-S with R1-type, or similar ordering.

The colloidal state of aqueous Ca2+-montmorillonite dispersions was modified with three types of cationic end-capped poly(ethylene oxides). The macromolecules were not only adsorbed at the external surfaces but were also intercalated into the dispersed montmorillonite particles. The amounts adsorbed and the basal spacings (~1.7 nm) were comparable to the corresponding Na+-montmorillonite dispersions. The poly(ethylene oxides) protruding out of the interlayer spaces or adsorbed at the external surface determined the colloidal behaviour of the dispersions. The phase diagrams (sol-gel diagrams) of the Ca2+-montmorillonite dispersions differed from those of the corresponding Na+-montmorillonite because of the different colloidal states of both dispersions (Ca2+-montmorillonite particles vs. delaminated Na+-montmorillonite). The phase diagrams of the poly(ethylene oxide) containing Ca2+-montmorillonite dispersions showed fields of sol and flocs. Attractive gels were formed in a few cases only (TMA+-PEO 1500 and 4000, THA2+-PEO 1500, 4000 and 20,000) and with distinctly lower gel strength than in the presence of Na+ ions. On the basis of the sol-gel diagrams, conditions (type and concentration of poly(ethylene oxides), montmorillonite content) can be selected which lead to peptization of the Ca2+-montmorillonite particles into stable colloidal dispersions (sols). Addition of cationic poly(ethylene oxides) can enhance the salt tolerance up to 1000 mmol/l NaCl.