The alteration and transformation behaviour of the Tertiary Hammerschmiede Smectite and the Jurassic Opalinus Shale in an alkaline solution was studied in column experiments. The Hammerschmiede Smectite is proposed as potential backfill material and the Opalinus Shale as host rock for the Swiss low-level nuclear waste storage site. Over a period of 18 months, the evolution of permeability, pH and solution concentrations were measured. After the experiment, the columns were cut into pieces to study the mineralogical and the chemical evolution of the clays. X-ray diffraction (XRD) revealed no significant appearance or disappearance of diffraction peaks at the end of the experiments. The scanning electron micrographs of the clays revealed that both clays exhibited a precipitation zone, which extends from 0 to 2 cm below the infiltration surface. Both clays showed significant differences in the evolution of pH and hydraulic conductivity. The solution front crossed the Opalinus Shale column entirely after only 11 weeks and the initial values for K+ and Na+ were conserved in the solution. For both clays, the salt concentrations in the percolating fluids mirror the evolution of pH.

Diverse applications of chlorite thermometry have been considered for better understanding the formation process in nature. Here, an approach which combined a semi-empirical thermometer (Inoue et al., 2009) with the method of Walshe (1986) was tested to estimate the redox conditions (log fO2) and the formation temperature, using the literature data from Niger, Rouez and St Martin and new data for chlorite which coexists with pink-coloured epidote in the Noboribetsu geothermal field. The log fO2 predicted for the former data sets were compatible with those estimated by Vidal et al. (2016), suggesting that the present approach is valid for quantifying the variations in log fO2. The Noboribetsu chlorites have lower Fe/(Fe + Mn + Mg) and greater Fe3+/ΣFe ratios than those observed in adjacent propylite rocks. The peculiar mineral assemblage and chemical composition are attributed to the formation under higher fO2 conditions and possibly low Fe concentration in the alteration fluids.

L'étude expérimentale de l'adsorption d'ions La3+ sur une smectite, successivement saturée en ions K+, Na+ puis Ca2+, montre que la stoechiomérie de l'échange s'effectue dans le rapport des charges des cations participant à la réaction. Dans un domaine de force ionique suffisamment restreint, l'échange a lieu dans les rapports suivants: 1 La3+ pour 3 Na+ ou 3 K+, et 1 La3+ pour 1·4 Ca2+. L'adsorption de toutes les terres rares sur la smectite et une illite s'effectue sans ségrégation notable dans cette famille d'éléments, les terres rares les plus lourdes étant un peu plus adsorbées que les terres rares légères. La désorption des terres rares est plus difficile, leur charge trivalente devant les stabiliser en position interfoliaire dans les minéraux argileux.

A new method of measuring the layer charge of smectites by IR spectroscopy is proposed based on the integrated intensity measurement of the band assigned to the ammonium fundamental ν4 mode of NH+4-exchanged clays. Measurements are made before and after Li fixation (Hofman & Klemen effect). These allow the quantitative determination of the total charge, equivalent to CEC, and tetrahedral and octahedral charge distribution in both dioctahedral and trioctahedral smectites.

La sépiolite chauffée à 300°C et 480°C sous vide a été étudiée avec un microscope électronique en haute-résolution. Les clichés donnent une photographie réelle des structures de la sépiolite naturelle et de la sépiolite anhydre, telles qu'elles ont été calculées par la cristallographie. Les résultats obtenus sont en accord avec ceux de la diffraction des rayons X et de la spectroscopie infrarouge.

Ochre sediments from acid mine drainage in Cornwall have been investigated using X-ray diffraction, thermal methods, infrared spectroscopy, X-ray photoelectron spectroscopy, transmission electron microscopy and chemical methods in order to determine their mineralogical and chemical composition. Fresh sediments consist of ferrihydrite and goethite. Large fractions of these minerals are dissolved by the ammonium oxalate treatment reflecting their poorly crystalline structure. Fresh sediments contain large amounts of surface-adsorbed SO4 (up to 9.3%) which is readily desorbed by the PO4 treatment. Goethite is the only mineral present in relatively older sediments and the mineral is well crystallized with rod-shaped morphology. Environmental conditions, such as pH and SO4 content, are not favourable for the presence of schwertmannite at the site. Iron minerals appear to be precipitating around filamentous algae and the shape of algae is preserved in the Fe oxide matrix. The ubiquitous presence of algae in close association with Fe minerals indicate their possible role in the crystallization of Fe oxides.

The structure of an illite-smectite (I-S) sample (HSI) from the Tertiary–Cretaceous boundary layer at Stevns, Denmark, i.e. the so-called Fish Clay, is investigated in order to discuss the origin of this clay and its similarity to clays from Maastrichtian-Danian chalk of Denmark and the North Sea. The phase compositions and layer sequences have been determined by X-ray diffraction. The structural formulae are determined from chemical analysis and solid-state 27Al magic-angle spinning (MAS) nuclear magnetic resonance (NMR) spectroscopy. The octahedral vacancy pattern has been determined by thermal analysis and the particle shape by atomic force microscopy. The HSI sample I-S consists of two phases, a high-smectitic (HS) phase (70%) having 95% smectite and 5% illite (leucophyllite) layers, and a low-smectitic (LS) phase (30%) having 50% smectite and 50% illite (leucophyllite) layers. Both phases have trans-vacant dioctahedral sheets and contain only traces of IVAl, the charge of the illite (leucophyllite) layers being provided predominantly by octahedral Mg for Al substitution. The structure of the tetrahedral and octahedral sheets for the HSI are compared to the structure of an I-S sample (GRI) from the Maastrichtian chalk at Stevns below the Tertiary-Cretaceous boundary and to the standard smectite SAz-1 from Arizona. For all three samples the 27Al MAS NMR spectra show the presence of two resolved IVAl resonances, which indicate the presence of two different IVAl sites. The NMR, infrared spectroscopy and chemical data show that both HSI and GRI have highly ordered Mg for Al substitution in the octahedral sheet, each Al having one Mg and two Al neighbours, whereas substitution of Mg for Al in SAz-1 is random. For the HSI sample, both the HS and LS phases are probably formed from volcanic ash. The structural similarity of the phases in HSI and GRI shows that GRI formed from a material similar to HSI by illitization of the HS phase and chloritization of the LS phase.

New chemical and structural data on sepiolite-falcondoite in garnierite veins from the Falcondo Ni-laterite deposits, central Dominican Republic, are reported. Samples of Ni-sepiolite-falcondoite vary in colour from whitish green to green depending on the NiO content (wt.%) and the amount of silica present. The texture is normally schistose and friable but samples with considerable quartz and/or amorphous silica are compact and hard. Back-scattered electron images indicate that the samples are composed of at least three generations of Ni-sepiolite-falcondoite. The extreme refined cell parameters for Ni-sepiolite-falcondoite vary from 13.400(2), 27.006(4), 5.273(1) Å to 13.340(3), 27.001(6), 5.267(1) Å (space group Pncn). As the Ni content increases there is a small reduction in the a parameter. Chemical compositions determined by electron probe microanalysis cover a large interval of the Ni-sepiolite-falcondoite solid solution (Fal3 and Fal77). Individual samples show a considerable range in composition with the widest range determined in one sample from 4.63 to 22.40 wt.% NiO.

Una sepiolita procedente de Toledo (España) se ha activado por tratamiento con disoluciones 0·25, 0·50 y 0·75 n de NO3H, seguido de calentamiento durante 10 h a 110, 200, 300, 400 y 500°C. Para cualquier concentración ácida, un calentamiento de 110, 200 y, a veces, 300°C, produce un aumento del número de poros mientras que las temperaturas superiores significan un cierre de los mismos tanto mayor cuanto más elevada es la temperatura de tratamiento. El máximo desarrollo de la superficie accesible al N2 tiene lugar con una disolución 0·50 n de NO3Hy 200°C (449 m2/g, método de BET); la superficie específica de la sepiolita natural es de 321 m2/g.

The effect of temperature on the swelling of clay was studied by determining (1) the relation between the interlayer spacing, λ, and the swelling pressure,Π, at different values of the temperature, T, using the method of Viani et al. (1983) as modified by Wu et al. (1989); (2) the relation between λ and T at different values of Π; and (3) the relationship between Π and mw/mc, the mass ratio of water to clay, at different values of T using the method of Low (1980). The results showed that λ was essentially independent of T but that mw/mc decreased slightly with T at any value of Π. Such results are not consistent with electric double-layer theory. Therefore, it was concluded that the decrease in mw/mc with increasing T was due primarily to the thermal breakdown and consequent loss of water from the larger pores outside of the interlayer region.

In the Miller Field, diagenetic quartz abundance, isotopic compositions and salinities of quartz-cementing fluids display a distinct pattern which is related to the structural depth of the reservoir sandstones. Quartz cement volumes increase from the crest of the field (average 6.0±1.5%) towards the flanks of the field (average 13.2±2.1%) and directly reduce reservoir porosity. By integrating petrographic observations with results of fluid inclusion measurements and O isotope analyses of diagenetic quartz, the pattern of quartz cementation is seen to be related to the reservoir filling history. Oil filled the crest of the reservoir first and prevented extensive quartz cementation. At greater depth in the reservoir oil zone, quartz overgrowths continued to precipitate until inhibited by the developing oil column. Oxygen isotope compositions of diagenetic quartz imply that quartz cement continued to precipitate in the water zone of the reservoir up to the present day.

The low-charge dioctahedral 2:1 phyllosilicates are an important group of clay minerals that have a low degree of cation substitution and very weak interlayer interatomic interactions which are difficult to reproduce with quantum mechanical calculations. In order to study the crystallographic properties of these compounds with density functional theory (DFT) quantum-mechanical methods, an optimization of norm-conserving pseudopotentials of Al, Si, O, H and Na atoms has been carried out, and an optimization of the cutoff radii of the basis sets has been accomplished. Crystallographic properties and vibrational stretching frequencies of the OH groups, ν(OH), have been calculated, being consistent with previous computational and experimental results. All frequencies can be related to the different molecular environment of the OH groups. The effect of octahedral Fe3+ substitution on the ν(OH) frequency is reproduced. Several configurations of cation substitutions and interlayer cation (IC) positions are studied in low-charge dioctahedral 2:1 phyllosilicates, such as Al4(Si7–xAlx)O20(OH)4Nax, with x = 0.25, 0.50 and 0.75, indicating that the IVAl3+ is highly dispersed and the IC tends to be in the substituted ditrigonal hole. For the Al4(Si7Al)O20(OH)4Na composition, the trans-vacant form is more stable than the cis-vacant one.

Some minerals which have been referred to as corrensite are considered together with some related minerals. It is suggested that the name corrensite be retained for the original material so described—namely, a I:1 regular interstratification of chlorite and swelling chlorite. The possible constitution of swelling chlorite, its difference from vermiculite, and its relationship to labile chlorites produced synthetically are all discussed.

Halloysite with tubular morphology is formed in a wide range of geological environments from the alteration of various rock types. Intrusive acidic coarse-grained rocks, such as granites, pegmatites and anorthosite, with large potash and sodic feldspars contents, are subsequently altered to kaolinite, halloysite and other clay minerals by weathering or shallow hydrothermal fluid activity. Processing to separate the halloysite-kaolinite fraction from the altered host rock provides a product which can be used as a paper filler and in ceramics and fibreglass, among other uses, with various deposits in Brazil, China, Thailand and elsewhere. In the Kerikeri-Matauri Bay district of Northland, North Island, New Zealand, volcanic alkali rhyolite was extruded as domes and cooled rapidly with fine-grained feldspar subsequently altered to halloysite. The IMERYS plant in Matauri Bay separates the clay from the quartz-cristobalite matrix with an ∼20% yield of halloysite. The principal market is for high-quality porcelain and bone china that require low levels of Fe2O3 and TiO2. Deposits with high levels of halloysite occur in China, Turkey and the USA. The Dragon mine in Utah, USAwas recently reopened by Applied Minerals Inc. and now produces halloysite from zones of up to 100% white halloysite. Smaller occurrences of tubular halloysite are mined in China, Turkey and elsewhere from masses of comparatively pure clay that appear to have crystallized directly from solutions in which Al and Si were soluble.

Aniline, adsorbed from aqueous solution in 1% (w/v) clay suspensions, forms coloured complexes and polymerizes on Fe(III)- and Cu(II)-montmorillonite. As evidenced by the adsorption isotherms, and the coloration and spectroscopic (IR, ESR) characteristics of the organo-clay associations formed, the conditions under which these reactions take place and the mechanisms involved differ according to the exchange cation. Fe(III) interacts with the π electrons of the aromatic ring to give rise to radical cations or so-called type II complexes, provided the aniline concentration does not exceed 500 p.p.m. With Cu(II). an aniline concentration above 500 p.p.m. is required and the reaction occurs at the amine group, proceeding through coordination followed by free-radical formation.

This sub-committee consisting of Mr G. Brown (Chairman), Dr M. H. Hey, Dr D. M. C. MacEwan and Dr R. C. Mackenzie was asked to make proposals for the nomenclature of clay minerals and these proposals were presented in part at a C.I.P.E.A. meeting in Paris in July, 1954, where some useful discussion ensued. The outcome of that meeting was a suggestion that the proposals be published more fully. It is important to remember that these are proposals for consideration and not a set of rules. The Clay Minerals Group would welcome comments on these proposals (adverse or otherwise) or the comments may equally well be sent to C.I.P.E.A.

Chemical variations in individual chlorite crystals of diagenetic origin delineated by energy dispersive X-ray spectroscopy (EDS) in a transmission electron microscope (TEM) indicate a temperature dependent chemical zonation in each grain. Silicon decreases and Al increases with higher temperature resulting in a decreasing Si/Al ratio away from the crystal core reflecting the time and rate of the crystal growth. Chlorite particle-size distributions obtained by scanning electron microscopy (SEM) give steady state profiles which suggests that the chlorite growth is controlled by a grain coarsening process related to Ostwald ripening.

A bentonite sample from the Petreş ti deposit, Cluj County (Romania), was used to remove heavy-metal ions (Cd2+, Pb2+, Cr3+) from wastewaters. A representative sample of bentonite (P) was characterized using the Brunauer-Emmett-Teller (BET) method, wet chemical analyses, X-ray diffraction (XRD) and Fourier-transform infrared (FTIR) spectroscopy. The bentonite deposit from Petreş ti is present at the contact between Upper Jurassic limestones and basaltic andesites with subordinate basalt bodies. These rocks are composed of clay minerals (mainly smectite), with opal, quartz, feldspar and mica/illite as minor phases. The bentonite sample was used in powdered form (d < 0.2 mm) without any chemical treatment. The influence of the working regime, static and dynamic, on the process efficiency was studied using monocomponent synthetic wastewaters containing Cd, Pb and Cr ions. The bentonite sample proved to be efficient for the removal of these heavy-metal ions; removal efficiencies up to 100% (lead removal) were achieved.