Five areally distinct mineral assemblages are recognized in the Inferior Oolite of S. England. In each area, vertical (stratigraphic) variations are insignificant. The five assemblages comprise varying proportions of illite, illite-smectite, kaolinite, chlorite and kaolinite-smectite, the mixed-layer clays being largely poorly crystalline and randomly interstratified. A predominantly detrital rather than authigenic origin is suggested for most of the clays. Shallow-water platform carbonates contain kaolinite with illite and illite-smectite. Kaolinite decreases in abundance away from former mid-Jurassic land areas, the deeper shelf and more basinal facies being dominated by illite and/or illite-smectite. Possible volcanic contributions to clay suites are suggested but cannot yet be fully evaluated. The palaeogeographic usefulness of clay mineral suites is confirmed, even in carbonate-dominated systems.

The adsorption of sulphur dioxide (SO2) on two bentonites from Unye, Turkey (Kavaktepe and Yemişlitepe deposits – denoted below as BK and BY) and on forms treated with 1 and 2 M HCl solutions was investigated. The bentonite samples were characterized using X-ray diffraction (XRD), X-ray fluorescence (XRF), thermogravimetry (TG-DTG), differential thermal analysis (DTA) and nitrogen adsorption methods. Adsorption capacities of SO2 were obtained using a standard volumetric apparatus at 293 K and 106 kPa. The SO2 adsorption capacity of the BY-2 (1.263 mmol g–1) sample was much greater than the BK-2 (1.126 mmol g–1) sample. As the concentration of acid increased, the specific surface areas and the uptakes of SO2 gas increased.

Studies of the thermal stability of organic compounds adsorbed on clay minerals are of interest from several points of view, e.g. the type and strength of bonding forces between the organics and the clay surfaces (Chou & McAtee, 1969; Yariv et al., 1971; Lacher et al., 1981), and the effect of the clay surface on stability or degradation mechanism of the organic compounds adsorbed on clays (Bodenheimer et al., 1966; Yariv et al., 1971; Durand et al., 1972).

A Quaternary or Recent tuff or pumice has weathered to an allophanic soil reminiscent of some described by Sudo. The soil has interesting engineering properties. Electronmicrographs show the apparent coalescence of alophane ribbons into a thin platy mineral, probably an early form of hydrated halloysite. The formation of crystals by the coalescence of mosaic crystallites is discussed.

A K+-saturated and an NH4+ -saturated smectite from Jelgov 37 Potok (Slovakia) was analysed by X-ray diffraction (XRD) after a series of I to 150 wetting and drying (WD) cycles, and the corresponding distribution functions were calculated using the Dyakonov method. From these data the thicknesses and proportions of different layers were determined. Three kinds of layers (A- 1-00 nm, B-1.26 nm and C-1-52 nm) were detected in the original samples. After 15 WD cycles only A and B type layers were identified in the K-smectite, whereas all three varieties were present during the whole WD treatment in the NH4-smectite. After initial changes the mutual proportion of layers seems to be stable. The 1.00 nm layer is the major layer type in the K-smectite and the 1.26 nm layer is the major layer type in the NH4-smectite. The layer thicknesses evolved during the WD experiments. The systematic changes observed for the NH4-smectite were greater than those for the K-smectite.

Textural, mineralogical and chemical characterization of archaeological ceramics (zellige) from El Badi Palace (Marrakech, Morocco), the main Islamic monument from the Saadian period (sixteenth century), has been performed to enhance restoration and to determine the technology of manufacturing. A multi-analytical approach based on optical and scanning electron microscopy, cathodoluminescence, X-ray fluorescence and X-ray diffraction was used. Re-firing tests on ceramic supports were also performed to determine the firing temperatures used by the Saadian artisans. A calcareous clay raw material was used to manufacture these decorative ceramics. The sherds were fired at a maximum temperature of 800°C in oxidizing atmosphere. The low firing temperature for ‘zellige’ facilitates cutting of the pieces, but also causes fragility in these materials due to the absence of vitreous phases.

The modification of halloysite nanotubes (HNTs) as fillers is very effective at improving the performance of polymers. A novel modification of HNTs through grafting dodecylamine onto their surfaces was conducted here. Owing to the improvement in dispersibility of HNTs in polytetrafluoroethylene (PTFE), the mechanical properties and wear resistance (in particular) of the dodecylamine-modified HNT-filled PTFE composite were enhanced significantly.

We have carried out optical microscopy, X-ray diffraction (XRD) and scanning and transmission electron microscopy (SEM and TEM) studies of phyllosilicates from black slates of very low to low-grade metamorphism. Such slates belong to a Middle/Late Devonian basin and an Early Carboniferous basin associated with the Porto–Tomar–Ferreira do Alentejo strike-slip shear zone (Ossa-Morena Zone, Portuguese Iberian Variscan Massif). These black slates are imbricated in an Upper Proterozoic substratum of higher metamorphic grade. Kübler Index values of white micas and mineral assemblages deduced from the XRD, SEM and TEM data (muscovite, chlorite and pyrophyllite) indicate high anchizonal and epizonal metamorphic conditions for slates from these basins. The b parameter and the phengitic contents of mica suggest the occurrence of low pressures (1–2 kbar) related to an extensional geotectonic setting. The dense fracture network shown by SEM images and the high density of crystal defects revealed by the TEM study in the eastern basin, adjacent to faults produced by shearing, suggest that their epizonal phyllosilicates were more affected during deformation than those belonging to the western basin, favouring the development of a retrograde association (siderite, kaolin group minerals and Al-smectite) on the epizonal paragenesis. Microcavities formed along phyllosilicate cleavage acted as channels for fluid transport favouring alteration under low-temperature conditions.

The design of nanostructured materials based on natural components, such as clay minerals, offers new solutions to biomedical challenges such as more efficient and storage-stable vaccines. Clay-lipid hybrid materials have proved useful as adjuvants in influenza vaccines and with a possible projection to leishmaniasis vaccines and other pathogens. Self-assembly of phospholipid molecules on the surface of microfibrous sepiolite and lamellar Mg/Al layered double hydroxide renders a biocompatible lipid bilayer membrane that ensures non-degrading immobilization of proteins and other biological species including viral particles and DNA (deoxyribonucleic acid). Immunization tests in mice showed the superior immunogenicity of a clay-lipid-supported virus compared to a commercial aluminium hydroxide adjuvant.

Two 20-cm long columns of MX-80 bentonite compacted at a nominal dry density of 1.7 g/cm3 with a water content of 17% were tested in thermo-hydraulic (TH) cells with the aim of simulating the conditions of a sealing material in a nuclear waste repository. On top of the columns a hydration surface simulated the host rock supplying groundwater and at the bottom a heater simulated the waste canister. The tests comprised two phases: a heating phase and a ‘heating + hydration’ phase. The temperatures at the ends of the columns were set during the last phase to 30°C at the top and 140°C at the bottom, respectively. The thermo-hydraulic treatment resulted in major changes along the bentonite columns. These changes led to significant gradients along the column with respect to the physical state (water content, dry density) and geochemistry of the bentonite. Smectite dissolution processes occurred. As a result, colloids were probably produced, particularly in the more hydrated areas. In the warmest part of the columns precipitation of carbonates took place, caused by their solubility decrease with temperature and the evaporation. The increase in water content reduced the ionic strength of the pore water in the more hydrated areas where species such as gypsum were dissolved. The solubilized ions were transported towards the bottom of the columns; Na+, Ca+, Mg2+ and SO42− moved at a similar rate and K+ and Cl− moved farther. These solubilized ions precipitated in the form of salts farther away along the columns as the test was longer. The TH treatment implied the loss of exchangeable positions in the smectite, particularly towards the heater. The cation exchange complex was also modified.

The expert system described in the first part of this paper has been applied to the identification of mixed-layer phyllosilicates (mica-smectite, mica-vermiculite, chlorite-smectite, chlorite-vermiculite, chlorite-swelling chlorite, chlorite-mica, chlorite-talc, kaolinite-smectite, talc-smectite), and to the determination of their structural parameters (Reichweite, R, and proportions of constituting layers, Wi). The expert system has been run utilizing the data extracted from (1) experimental XRD patterns for which structural parameters had been evaluated by comparison with calculated patterns, or (2) patterns calculated using pre-selected values of the structural parameters. In all cases examined, the expert system provided correct conclusions concerning the identification of a mixed-layer phyllosilicate and the value of the Reichweite, while the abundances of the component layers were evaluated with a margin of error usually <5%.

A systematic study has been made of the effects of aluminium fluoride on the thermal behaviour of kaolin, using differential thermal, thermogravimetric, X-ray and electron microscope techniques. It is shown that mullite can be formed at a temperature as low as 600°C; that in the presence of aluminium fluoride the exothermic reaction occurs at a lower temperature and is reduced in size; that the size of the mullite crystals is increased as a result of pretreatment with aluminium fluoride.

Transmission electron microscopy of ultramicrotomed thin-sections of Pleistocene and Eocene glass shards revealed the neoformation of (i) illite and (ii) halloysite at the glass periphery. According to previous experimental studies, halloysite neoformation in marine environments can occur on glass shards deposited in Si-rich sediments; an excess of Ca tends to inhibit the reaction.

Kaolins have been separated from sandstones from the Pugu Hills deposit, Tanzania, using a 15 mm glass hydrocyclone and a laboratory-scale multiple unit consisting of six 10 mm cyclones. Two types of sandstone were treated—containing a disordered kaolin (Pugu D) and a well-ordered variety (Pugu K)—to see whether products could be obtained that met particle-size specifications for paper manufacture. Pugu D gave a product that would meet specifications for both paper-filling and -coating applications with minimal processing, although the extremely fine-grained nature of this kaolin could lead to high viscosities in suspension. Processing of Pugu K gave products containing up to 97% kaolin and particle-size distributions that would meet specifications for filler and, possibly, coating clay. However, it was impossible to eliminate 3% or so of fine-grained quartz from these products and this could militate against use in paper manufacture.

A description is given of the widespread development in the U.S.S.R. of deposits of clay, largely kaolinitic in mineralogical content. These deposits also may be traced outside the U.S.S.R. Their origin is believed related to a period of intense weathering in Mesozoic times. It is pointed out that this thesis of an ancient crust of weathering would well repay application in other countries, where deposits normally regarded as of pneumatolytic origin might possibly be due to intense weathering.

A lamellar macroscopic Mg-vermiculite from Santa Olalla, Spain, which is accompanied by some talc and mica, shows a reversible expansion on glycolation due to the presence of layers with two different charges. The most probable origin of the vermiculite is by low-temperature hydrothermal transformation of phlogopite.