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.

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.

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.

Palygorskite and sepiolite occurrences and deposits are frequent in the Iberian Peninsula, mainly in the Tagus basin, in central Spain and Portugal (Galán & Castillo, 1984).

In Portugal, the first palygorskite occurrence was reported by Carvalho (1964) in the region of Ponte do Sor, Tagus basin, in Paleogene sediments. Later, Carvalho (1968) reported palygorskite occurrences in coarse detrital sediments that were occasionally carbonatic or hardened by silicification, and built up the Cenozoic base for the Tagus and Sado basins. Carvalho referred to such formations as the 'Attapulgite complex'. Overlying this attapulgite complex is the 'Montmorillonite complex', probably of Miocene age.

Stable isotope and chemical compositions of vesicle- and fissure-filling smectites (i.e. montmorillonite and saponite) in Penghu subaerial basalts were analysed to establish their possible formation conditions. The results show that montmorillonites have higher Fe contents (as FeOtotal), as well as higher O-isotope and H-isotope compositions than saponites. These differences may largely reflect dissimilar formation conditions and/or fluid compositions. It is suggested that saponites probably precipitated from fluids dominated by meteoric groundwaters at 40–50°C, whereas montmorillonites were probably formed at 20–40°C from mixtures of groundwaters and seawater. Considering all the possible uncertainties, the above estimated temperature conditions are suggested as reasonable lower limits.

It is established that the associated calcite is not in O-isotope equilibrium with the montmorillonite. The calcite might have been formed in environments with ambient fluid dominated by meteoric groundwaters at temperatures lower than those for montmorillonite.

The pore-size distribution of kaolinite has been studied by nitrogen desorption isotherms. A new method is proposed which takes account of the fact that the intraparticle or ‘internal’ area is small in comparison with the total surface area. The crystals form dihedral angles with one another, and the irregularities of the crystal edges form a slit-shaped internal pore system. When the nitrogen pressure increases, the condensed volume in the pores grows by an amount greater than predicted by de Boer's law. This excess is shown to result from capillary condensation in bevelled pores and this accounts for the main part of the intercrystalline or ‘external’ porosity. A model of condensation in bevelled capillaries has been developed and its range of validity determined.

The function of acid-activated sepiolite clay was evaluated for use in the clarification of apple juice. Optimizing the clarification process was done using response surface methodology (RSM) considering juice turbidity as a response. The efficiency of sepiolite in terms of clarification was compared to that of bentonite and a combination of these fining agents with gelatin and silica gel at optimal conditions. The conditions of 0.05% clay concentration at a temperature of 50°C for 7 h were deemed optimal in terms of juice clarification. The present results showed that treatment of sepiolitegelatin-silica gel was the most active fining agent with 99.7% reduction in apple-juice turbidity. The rate of turbidity, the viscosity, the total phenolic contents and the colour changes were fitted to first-, zero-, first- and zero-order kinetic models, respectively.

The clay mineralogy and chemical composition of the white veins, red matrix and both Fe- and Mn-bearing nodules occurring in a laterite profile in Hubei, south China were investigated using X-ray diffraction, scanning electron microscopy equipped with an energy-dispersive spectrometer, and high-resolution transmission electron microscopy. The results show that the mineral components of the red matrix are mainly quartz, kaolinite, halloysite, goethite and minor illite, whereas the white net-like veins contain mostly quartz, kaolinite, halloysite, and illite. In the net-like horizon, the chemical index of alteration (CIA, the ratio of Al2O3/(Al2O3+CaO+K2O+Na2O)) and the TiO2/Al2O3 ratio are 89.8% and 0.021 for the white vein and 90.7% and 0.025 for the red matrix, respectively. Both white-vein and red-matrix components have similar TiO2/Al2O3 ratios, and are similar to the ratio 0.027 of the unaltered bedrock. The similarity in TiO2/Al2O3 values indicates that all three portions of the laterite soil share the same origin. Also, although the white-vein and red-matrix components differ in Fe2O3 abundance, the similar CIA values do imply similar degrees of alteration. The Fe-bearing and Mn-bearing nodules were produced by the local accumulation of Fe2O3 and MnO, respectively. Halloysite in the weathering profile occurs in two different morphologies, tubular and platy crystals. Tubular halloysite occurs both in the red matrix and the Fe-bearing nodule whereas platy halloysite occurs only in the white vein and Mn-bearing nodule assemblages. Crystallization of small tubular halloysite from Si and Al concretions in the red matrix is observed, indicating that the morphology of these crystals in the weathering environment is mainly controlled by Fe3+ cations, whereas platy halloysite may be derived from the hydration of kaolinite.

This paper reports a statistical study of clay rocks both according to their geological character and their petrographic characteristics. The study was concerned almost entirely with rocks and not with present-day sediments. Further, typical sedimentary environments have been chosen: marine lagunar (saline and supersaline) and lacustrine. Deposits from river estuaries and moraines have not been considered, their conditions of genesis being more difficult to determine.

The origin of the regional and stratigraphical variation in the Triassic authigenic clay assemblages of England is discussed in relation to new estimates of the palaeotemperatures experienced by their host sediments and a preliminary study by transmission electron microscopy of their microtextural features. Spore colour index measurements, based on the spore type Deltoidospora s.l. occurring in the sediments (Penarth Group) at the very top of the Triassic sequence, give estimated palaeotemperatures ranging from 60–74°C (south Devon) to 89–97°C (northeast Yorkshire). Calculated palaeotemperatures, based on a gradient of 25°C/km, for the main zone of authigenic clay minerals range from 63–77°C to 89–97°C for the top to 71–85°C to 94–104°C for the base. Irregular mixed-layer smectite-chlorite, corrensite and Mg-rich chlorite are associated with calculated palaeotemperatures of 66–86°C, 66–104°C and 75–104°C respectively. The suggestion that elsewhere in the UK corrensite and Mg-rich chlorite were formed at temperatures in excess of 100°C finds no support. Geothermal gradients would have to have been of the order of at least 100–300°C/km to obtain these temperatures within the Triassic sediments; such values are associated typically with high-level magmatic intrusions or geothermal systems of which there is no geological evidence. The balance of evidence suggests that the Triassic authigenic clay assemblages formed by neoformation during the early stages of sediment diagenesis under the influence of variation in the alkalinity of the depositional environments.

Layered double hydroxides (LDHs) are known as ‘anionic clays’. They comprise a class of material with positively charged octahedral double hydroxyl layers and exchangeable anions. The Li/Al LDH term includes a group of LDHs with Li/Al octahedral double hydroxyl layers. We have demonstrated a modifed method, using Li/Al LDH-OH (OH− as interlayer anions) as the starting material, for preparing Li/Al LDH-X (X represents interlayer anions, including dioctyl sulphosuccinate (DOSS), dodecyl sulphate (DDS), mercaptoacetate (MA), EDTA, Tiron and dichromate) under mild acid conditions (pH in the range 4 to 5). However, in the case of acidsensitive anions, Fe(CN)64−, Li/Al LDH-Fe(CN)64− can be prepared by a two-step procedure using Li/Al LDH-DOSS or similar compounds as intermediates to react with acid-sensitive anions under mild alkaline conditions (pH ≈ 9).

L'arrangement des cations décylammonium échangés entre les feuillets de la vermiculite et de l'hectorite a été précisé à l'aide des spectrométries infrarouge (IR) et Raman. Les expériences de deutération et de dichroïsme faites par spectrométrie IR montrent que l'axe C3 du groupe NH3+ est confondu avec l'axe de la cavité hexagonale sous-jacente, dans le cas de la vermiculite comme dans celui de l'hectorite, et que dans la vermiculite, les groupes NH sont engagés dans des liaisons hydrogène avec les atomes d'oxygène des tétraèdres substitués. La spectrométrie Raman permet de comparer l'arrangement des chaînes alkyles dans les deux phyllosilicates. En effet, cette technique donne accès à des modes de vibration très sensibles à la conformation des chaînes carbonées, en particulier grâce à la décomposition des bandes de vibration de valence des groupements CH2 et CH3. Ainsi, dans la vermiculite, on montre que les chaînes sont linéaires, et que leur arrangement interdigité est proche de celui du chlorure de décylammonium cristallisé. Les spectres Raman obtenus pour l'hectorite mettent en évidence l'existence de conformations gauches dans les chaînes alkyles, qui caractérisent une rotation de la chaîne autour de la liaison C-C voisine du groupe NH3+ terminal. Les résultats obtenus en Raman montrent par ailleurs que les interactions entre les chaînes alkyles sont beaucoup plus faibles que dans le cas de la vermiculite et confortent le modèle proposé ici pour le complexe hectorite-décylammonium, pour lequel les chaînes sont parallèle aux surfaces des feuillets.

X-ray diffraction methods are effective and practical for the quantitative analysis of the often forgotten amorphous material phase in sediments. The method reported is simple, employing normal oriented samples, and quartz or fluorite as a diluent. However, special care must be taken to prepare the samples properly, to ensure optimum conditions for diffraction, and to measure accurately the scattering bands.