Rock weathering has been investigated from atomic to global scales through the different but complementary approaches of mineralogy, petrography, geomorphology and geochemistry. The sequences of mineral reactions involved in the alteration process are now well known. They explain the global trend of weathering phenomena but do not account for the actual rock transformation dynamics. In particular, they ignore the intimate relation of the mineral reaction progress with the increase in connected porosity. At the hand specimen scale, heterogeneity is the rule: mineral reactions are controlled by local physicochemical conditions. Alteration processes depend largely on the rock microstructure properties. They proceed through nearly-closed, semi- and completely open microsystems which are interconnected by fractures or pores. Before being leached out by the solutions which flow in the large fractures (flux), the soluble elements migrate inside the connected porosity through chemical diffusion. The dissolution of the primary minerals is mediated through local gradients of chemical potential. With increasing alteration, the rock porosity increases, as does the length of the fluid passageways and their constrictivity and tortuosity. Consequently, the apparent diffusion coefficient for the most soluble elements decreases. The amplitude of the chemical potential gradients for the most soluble elements is reduced by the progressive coating of the reactive surfaces by clays and Fe oxyhydroxides. The residence time of these elements inside the weathered rock increases as alteration progresses; an effect enhanced by their temporary adsorption on the exchangeable sites of clays and Fe oxyhydroxides. Consequently, the weathering rate decreases with time. A possible new way to calculate weathering rates could be to measure the residence time of soluble elements inside the different microsystems during their migration towards the diluted solution which occurs in the large fractures.

Twenty nine Fe oxide concentrates of Thai soils formed on basalt, sandstone, shale/limestone and granite were investigated. Goethite and hematite are relatively more abundant in granitic and basaltic soils, respectively. Values of Feo/Fed range from 0.01 to 0.28 indicating that free Fe oxides are mostly crystalline.

There are no systematic differences in unit-cell dimensions for goethite and hematite in soils on different parent materials. Mean crystallite dimensions calculated from the 110 reflections are greater for hematite than for goethite. Aluminium substitution varies from 8 to 24 mole% for goethite and from 4 to 17 mole% for hematite. The dehydroxylation temperature for goethite ranges from 285ºC to 320ºC. The goethite in basaltic soils has a smaller crystal size and Al substitution, as well as a lower dehydroxylation temperature, compared to soils on other parent materials. The dehydroxylation temperature of goethite is positively related to Al substitution (R = +0.58), MCD110 (R = +0.49) and Ald (R = +0.53). The Mn, Ni, Cr, V and P in these soils occur in Fe oxides rather than as discrete minerals.

Iron cations in the octahedral sheet are a disadvantage to the industrial application of palygorskite clays. In this study, a palygorskite sample from eastern China (Mayaoshan deposit, Jiangsu Province) is shown to have an Fe content that is much greater than usual. The structural formula of the Fe-rich palygorskite sample was established as (Si7.48Al0.52) (Al1.24Fe0.94Mg1.77Ti0.03⁏1.02)O20(OH)2(OH2)4. The palygorskite is seen to be dioctahedral according to the structural formula, consistent with Fourier transform infrared data. Occurrences of AlFe3+ɏOH and Fe3+Fe3+ɏOH vibrations in the OH-stretching and -bending regions show that Fe atoms occupy inner sites of octahedral sheets. A Mössbauer spectrum confirmed that Fe ions occupy inner octahedral sites as trivalent Fe cations (Fe3+).

Rectorite (REC) was modified with dodecyl benzyl dimethyl ammonium chloride (1227) to form an organic-modified rectorite, termed OREC. The OREC was used as a filler additive to modify gel polymer electrolytes (GPEs) which consisted of polymethyl methacrylate (PMMA), propylene carbonate (PC) and LiClO4. Studies of ionic conductivity and viscosity of liquid electrolytes and pure PC, respectively, clearly showed that these properties are greatly influenced by temperature and the amount of OREC added; a consequence of the interactions between the components of CPEs. The Fourier transform infrared (FTIR) spectroscopy results indicated that there were two kinds of interaction: namely (1) a strong hydrogen bond between Si–OH and C=O of PC and (2) a weak interaction between Li+ and C=O. Inverse gas chromatography (IGC) research supported the FTIR interpretation, indicating that the two interactions exist and that the H bond is the stronger of the two. In CPEs, the polymer matrix of PMMA merely supports the active components and does not influence the interactions between them. The OREC greatly increased the crucial plasticizer maintenance property when the amount of clay added was optimum.

Ferric illite in the Neoproterozoic Penganga Group, southern India, occurs in a lenticular unit of reworked arkoses conformably enclosed in carbonate mudstones, deposited in a shelf-margin carbonate slope setting influenced by deep marine sediment gravity flows. The structures and textures of the arkoses suggest emplacement by fine-grained debris flows and deposition in channels incised into the carbonate slope.

Ferric illite is sparse in the arkoses and has small concentrations and grainsizes within the same size fraction of the associated detritus, uniform chemical composition and an association with reworked facies. It consists predominantly of granular grains that are mostly sorted spherical, ovoid, capsule-shaped and vermicular peloids; many broken and micaceous. These attributes provide a comprehensive framework for suggesting an allogenic origin for the ferric illite previously interpreted as authigenic. The methodology adopted here is a useful approach in the interpretation of in situ vs. reworked origins of glauconitic minerals.

Smectite formation in a vertisol developed from a granitic parent rock in the Kaélé region of Cameroon in a tropical, dry climate was studied by means of X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), transmission electron microscopy (TEM), chemical analyses, cation exchange capacity (CEC) and low temperature gas adsorption. The soil profile comprises three horizons (from base to top): (1) a saprolite, (2) an intermediate horizon, and (3) an upper dark grey horizon. In the saprolite, the progressive alteration of feldspars gave rise to the exclusive neoformation of beidellite exhibiting a typical honeycomb fabric. This process resulted in Al, Fe, Ca, Mg, Ti and Mn enrichment, a depletion of Si and Na and a significant negative Eu anomaly. In the upper horizons, beidellite evolves and is transformed into montmorillonite and kaolinite, probably through a series of smectite-kaolinite mixed layers. This transformation, from the saprolite to the upper horizons, causes the observed decrease in the CEC and the increase in specific surface area and mesoporosity of the clay. The REE patterns of the bulk soil and clay fraction display similar behaviour, indicating that the three horizons, and hence the clay minerals, have a common source in the underlying granite. Mass-balance calculations show that the intense weathering of the granite leads to a mass reduction of ~80–90%.

Metamorphic grade, palaeothermal history and the influence of tectonic strain on clay minerals and organic matter transformation were studied in the eastern part of the Teplá-Barrandian unit in the Czech Republic. The metamorphic grade of pelitic sediments ranges from the lower anchizone (IC ~0.30–0.36Δº2θ) to the lowermost epizone (IC ~0.24–0.26Δº2θ). Increase in metamorphic grade is paralleled by the development of anastomosing cleavage and lenticular quartz grains in the anchizone which give way to slaty cleavage and dynamically recrystallized ribbon quartz grains in the lower epizone. White mica in highly strained rocks generally has greater IC values whereas chlorite displays reduced values in deformed and cleaved samples. The organic matter dispersed in the sediments represents a complex assemblage of highly matured particles of uncertain origin, pyrobitumen and ‘transitional matter’. The reflectance of organic fragments generally varies from 3.1% to 7.7% of Rmax which suggests anthracite to meta-anthracite rank progrades to semigraphite in higher-grade samples, although the overall link between Rmax and IC values is weak, if present at all. Newly formed shear-induced graphite appears abruptly near the anchizone-epizone boundary and correlates with the onset of plastic deformation and dynamic recrystallization of quartz grains in the host sediments.

Maximum metamorphic temperatures within the Neoproterozoic sequence in the range of 250–350ºC were attained during the Cadomian (Pan-African) orogeny at 540–550 Ma. Apatite fission-track analysis reveals a subsequent decrease in rock temperature over the period 340–350 Ma that persisted throughout the late Palaeozoic. The most recent episode of accelerated cooling occurred between 20 and 40 Ma, corresponding with the regional uplift of the Bohemian Massif due to the Alpine orogeny.

This study focused on the structure and physical properties of acid-treated bentonite L45 from the Lieskovec deposit (Slovakia). New applications of near infrared and visible spectroscopies were used to follow Fe-montmorillonite dissolution and layer-charge reduction. Progressive dissolution of L45 results in the formation of a protonated amorphous silica phase. The OH overtone at 7312 cm–1 revealed the creation of Si–OH groups in the mildly treated samples. The area of the Si–O–Moct band, as obtained by a peak-fitting procedure, is a sensitive indicator of the changes in the octahedral sheets. Ultraviolet-visible (UV-VIS) spectroscopy of the smectite dispersions with methylene blue (MB) is an efficient method for controlling the acid activation process of bentonites. The results reveal that acid treatment causes a substantial layer-charge reduction, probably due to prevailing dissolution of MgO4(OH)2 polyhedra in the octahedral sheets. The layer-charge reduction is proportional to the structural changes and to the extent of mineral decomposition upon acid treatment.

The saponite examined occurs as two 0.1 m thick layers in a Pliocene sequence consisting of dolomite and dolomitic marl. To characterize this material, mineralogical and structural analyses (XRD, SEM and FTIR), thermal analyses (DTA, TG) and chemical analyses (ICP-ES) were performed. From XRD patterns of randomly-oriented powder samples, the first basal reflection appears as an asymmetric and broad peak with d001 values varying between 16.55 and 17.32 Å. In oriented and air-dried samples, this reflection occurs between 14.45 and 16.42 Å and is fairly symmetrical with FWHM of 2.7º2θ. Oriented and ethylene glycol-solvated samples produce a rational series of basal reflections, where 001 occurs at ~17.8 Å as an intense, narrow (1.1º2θ) and fairly symmetrical reflection. Upon solvation with glycerol, the 001 reflection shifts to ~18.7 Å.

The chemical composition of this saponite is similar to stevensite. However, the structural formula of Na0.114Ca0.013K0.003(Mg2.957Al0.004Fe0.028Ti0.004)(Si3.826Al0.174)O10(OH)2 indicates that vacancies in the octahedral sheet do not exist. The negative layer charge arises nearly entirely from the substitutions in the tetrahedral sheet, with the net layer charge of –0.148, smaller than for common smectites.

Due to the XRD characteristics and particularly the layer-charge distribution, it was concluded that this mineral is a Mg-rich saponite with low layer charge. The saponite was formed by direct precipitation in an alkaline lake environment from Mg- and Si-rich solutions at high pH.

Scanning electron microscopy/energy dispersive spectroscopy (SEM/EDS) analysis of smear slides of oriented <2 mm clay fractions is shown to be a reliable and rapid analytical technique for providing chemical data on clay mineral mixtures. Such smear slides are routinely prepared for clay mineral analysis by X-ray diffraction and the only additional treatment required for chemical analysis by EDS is carbon-coating to form an electronically conductive surface. Using standard clays, mixtures of standard clays, and sediment samples, it is shown that sample thickness, sample heterogeneity and surface roughness do not introduce significant analytical errors, although the presence of non-clay mineral phases such as calcite, dolomite, quartz and pyrite may introduce minor discrepancies. Chemical data complement the XRD analyses and increase their accuracy and reliability.

Poly(ethylene oxides) (PEOs) with sulphonate groups attached at both chain ends (S-PEOs) were strongly adsorbed by dispersed Na- and Ca-montmorillonite particles. The amounts adsorbed were very similar to those of cationic end-capped poly(ethylene oxides). In both cases bilayers of PEO chains were intercalated so that the basal spacing of the particles reached the same plateau values of ~1.73 nm. In contrast, the influence of anionic PEOs on the colloidal behaviour of the Na- and Ca-montmorillonite dispersions was very different from the effect of the cationic PEOs. The shorter chain S-PEOs (S-PEO 1500, 4000) destabilized the Na-montmorillonite dispersions by coagulation due to the Na+ ions introduced as counterions to the S-PEOs. The longer chain S-PEO 20000 and S-PEO 35000 did not coagulate the Na-montmorillonite sols because the corresponding Na+ concentration did not reach the critical coagulation value. The slightly enhanced salt tolerance indicated that the long-chain PEOs exerted a weak steric stabilization. In contrast, bridging of the particles by S-PEO molecules and Ca2+ ions played an important role in destabilizing the Ca-montmorillonite dispersions in the form of flocs and formation of gels.