The island-arc volcanics situated in the eastern part of the Căpîlnaş-Techereu nappe (South Apuseni Mountains, Romania) were studied to evaluate the temperature, fluid properties, and mineral chemistry during low-temperature metamorphism. Detailed observations of metamorphic mineral assemblages were conducted using powder X-ray diffraction and electron microprobe. The metamorphism involved albitization of plagioclase feldspar and the formation of mafic phyllosilicates, zeolites, and other hydrous Ca-Al-silicate minerals. Mafic phyllosilicates consisted of transitional dioctahedral-trioctahedral smectites, mixed-layer chlorite-smectite (C/S, 6–96% chlorite), and discrete chlorite. The zeolites were analcime, stilbite ± stellerite, heulandite, laumontite, epistilbite, and mordenite. Also present, as secondary minerals filling amygdales and veins, are prehnite, pumpellyite, and secondary amphibole. Two mineral assemblages were identified which provide important information about metamorphic conditions (temperature, reaction progress, and fluid properties): (1) heulandite + analcime + quartz; and (2) laumontite + albite + quartz + prehnite + pumpellyite ± amphibole. The types of and relations between minerals in the first assemblage suggest the occurrence of low-temperature hydrothermal metamorphism in the zeolite facies at ~125°C, whereas the second assemblage was metamorphosed at 200°C. The composition and variability of the mineral assemblages in the study area suggest that, due to slow reaction rates, the low-temperature transformations and mineral assemblages were influenced not only by temperature but also by local rock composition, fluid-rock ratio, and fluid chemistry.

A diapiric intrusion of clays in the Carlentini Formation (Tortonian) was discovered in a quarry at S. Demetrio High (Hyblean Plateau, Sicily, Italy). Seven clay samples were analyzed by different analytical methods, including X-ray powder diffraction (XRD) and Fourier-transform infrared (FTIR) spectroscopy, to determine the composition and mechanism of formation (sedimentary vs. hydrothermal) of these clays. Ferric saponite, carbonates (calcite and traces of ankerite), quartz, pyrite, and zeolites (phillipsite and harmotome) were detected using XRD and FTIR. This mineral assemblage, dominated by Fe-rich saponite, and the abundance of light rare-earth elements (LREE), Eu, fluid-mobile elements (FME > 10 × primordial mantle: Li, Be, B, As, Sb, Pb, U, Ba, Sr, Cs), and other incompatible elements (Zr = 169 ppm, Nb = 46 ppm, Th = 11 ppm, on average) imply that S. Demetrio clays precipitated from a mixture of hot Si-rich hydrothermal fluids (350–400°C) and cold seawater. The evidence is in accord with the affinity of clays for hydrothermally modified mafic and ultramafic rocks, forming the Hyblean lower crust, based on multi-element comparisons, and on the occurrence of trace amounts of chrysotile 2Mc1 and sepiolite. The association of long-chain aliphatic-aromatic hydrocarbons (intensity ratios I2927/I2957 > 0.5) with hydrothermal clays, the lack of fossils, and the similarity of the IR absorption bands with those of organic compounds detected previously in some metasomatized Hyblean gabbroic xenoliths suggest a possible abiogenic origin of hydrocarbons via a Fischer-Tropsch-type reaction. The S. Demetrio clay diapir was emplaced at shallow crustal levels in the Late Miocene as a consequence of the interaction, at a greater depth, of an uprising basalt magma and the products of an early, serpentinite-hosted hydrothermal system.

Microwave irradiation as a means for heating bentonites during acid activation has been investigated in the past but it has never been optimized for industrial applications. The purpose of this study was to apply a factorial 23 experimental design to a Serbian bentonite in order to determine the influence of microwave heating on the acid-activation process. The effect of acid activation under microwave irradiation on the textural and structural properties of bentonite was studied as a model reaction. A mathematical, second-order response surface model (RSM) was developed with a central composite design that incorporated the relationships among various process parameters (time, acid concentration, and microwave heating power) and the selected process response of specific surface area of the bentonite. The ranges of values for the process parameters chosen were: time, 5–21 min; acid concentration, 2–7 M; and microwave heating power, 63–172 W. The effect of individual variables and their interaction effects on the textural and structural properties of the bentonite were determined. Statistical analysis showed that the duration of microwave irradiation was less significant than the other two factors. The model showed that increasing the time and acid concentration improved the textural properties of bentonites, resulting in increased specific surface area. This model is useful for setting an optimum value of the activation parameters for achieving the maximum specific surface area. An optimum specific surface area of 142 m2g−1 was achieved with an acid concentration of 5.2 M, activation time of 7.4 min, and microwave power of 117 W.

Bentonite cake is usually formed on the excavated trench surface that is supported by the bentonite slurry during construction of slurry cutoff walls. The lower hydraulic conductivity of bentonite cakes formed during construction of slurry cutoff walls in comparison to backfill materials provides an additional benefit. In the present study, the hydraulic conductivities of bentonite cakes made using three different bentonites were estimated using the modified fluid-loss test under various pressures. Both the hydraulic conductivities of bentonite cakes and cutoff-wall backfill are important in evaluating the in situ hydraulic performance of slurry cutoff-wall construction. Three bentonite slurry concentrations of 4, 6, and 8% were used to fabricate bentonite cakes that represent common field conditions. X-ray diffraction, cation exchange capacity, and swell-index data were collected to characterize the bentonites. Two modified methods for analyzing fluid-loss test results were used to estimate bentonite cake hydraulic conductivities. In addition, the viscosity as a function of time was measured to explain the sealing capacities of the bentonite slurries. The bentonite-cake hydraulic conductivities ranged from 2.15×10−11 m/s to 2.88×10−10 m/s, which were 10 to 500 times lower than the cutoff wall backfill design. Experimental results for 4 and 6% bentonite slurries were relatively similar, but the 8% slurries were noticeably different. Calculated bentonite-cake thickness and stress distribution indicated that the local void ratio and hydraulic conductivity may vary across the cake thickness. The considerably lower bentonite-cake hydraulic conductivities compared to the cutoff wall backfill design show its significance in slurry cutoff-wall construction practices.

The collector for separating diasporic bauxite serves as a type of flotation reagent by adsorbing selectively on diaspore to make it hydrophobic enough to separate it from the aluminosilicates. Although the flotation process is considered economical in the desilication of Chinese diasporic bauxite, the existing collectors fail to separate these ores because of their poor adsorption selectivity over other minerals. The present study was an attempt to seek a collector for selective flotation of diaspore over aluminosilicates. A novel carboxyl hydroxamic acid compound, 2,2-bis(hydroxycarbamoyl) decanoic acid (BHDA), was designed and synthesized, and the flotation behavior of diaspore, kaolinite, and illite was investigated by flotation tests with BHDA. The interactions between the BHDA and the minerals were also explored by Fourier-transform infrared spectroscopy (FTIR), zeta-potential measurement, and density functional theory (DFT) calculation. Using BHDA as the collector, the pulp pH value affected the floatability of diaspore significantly while the floatability of kaolinite or illite was unaffected or only slightly affected. The dosage of BHDA had little effect on the floatability of the three minerals. The greatest difference in floatability between diaspore and aluminosilicates occurred at mid-range pulp pH (7). Large shifts in characteristic absorption peaks and new absorption peaks were observed for BHDA-treated diaspore but were absent from BHDA-treated aluminosilicates. The change in the negative zeta potential of diaspore was also greater than those of aluminosilicates in the presence of BHDA. The O atoms in the carboxyl and hydroxycarbamoyl of BHDA have highly negative charges, and favorable stereo conditions existed to form five- or six-membered rings, resulting in their coordination with the Al atoms of diaspore, leading to chemisorption in chelate rings; the adsorption of BHDA on kaolinite or illite, on the other hand, was mainly physical in nature. The BHDA was, therefore, highly selective in the flotation between diaspore and aluminosilicates and possibly suitable for the separation of diasporic bauxite.

This study uses the data from Miocene rocks of the Carpathian Foredeep to test the performance of the computer programs QUANTA and BESTMIN in aiding the interpretation of geophysical log data. These programs were designed to help trace trends in the mineral composition of rocks, the chemical composition of minerals, and the effects of these data on petrophysical and geophysical logging parameters. Chemical and X-ray diffraction data for 65 samples of shales, sandstones, and carbonates taken from cored wells in the molasse basin of the Carpathian Foredeep were processed. Compositional differences were detected between rocks sourced from the platform and rocks sourced from the Carpathians. Quartz, K-feldspar, and zircon were more abundant in the coarse-grained rocks (sandstones), while calcite, ankerite, siderite, pyrite, barite, halite, celestite, apatite, anatase, chlorite, 2:1 minerals, and organic matter were more abundant in the fine-grained rocks (shales). Plagioclase reached its maximum in coarse shales. Ankerite, chlorite, and dioctahedral 2:1 minerals had more Fe in the coarse-grained rocks. The dioctahedral 2:1 minerals in fine-grained rocks had a greater concentration of smectitic layers. This information permitted the precise calculation of grain density, porosity, adsorbed water, and some geophysical logging parameters. It also permitted the calibration of well-log response, in particular, the macroscopic neutron absorption cross-section (Σa) combined with the photoelectric absorption factor (P{e}) or with Pe + Ca (calcium content, measurable in wells by spectroscopic techniques) with porosity and cation exchange capacity (CEC). The NaCl concentration in the pore waters was found to range from the values typical for seawater in shales to the freshwater level in clean sandstones.

Recognizing weathering effects is significant for any work carried out on glauconites at the surface. The mineralogy and chemistry of glauconite grains exposed to weathering in a hot arid climate for a maximum of 42 y were studied here. The objective of the study was to find the mineralogical and chemical differences between weathered glauconite from the surface and fresh glauconite from the subsurface.

One specific glauconite-bearing layer at the surface (Layer 16) of the Abu Tartur phosphate mine, located in the Western Desert of Egypt, was studied in detail and compared to a fresh, subsurface glauconitic sandstone from the underground mine.

Even within this single surface layer, the brownish-green glauconite grains vary in color and chemical composition. From top to bottom, the grains show an increase in Fe and K and a decrease in Al and S. In addition, the grains show an internal color zonation caused by variation of Fe and K contents between the center and rim of the grains. The differences in color and chemical composition are even more pronounced between the weathered-glauconite grains from the surface and the fresh glauconite grains from the subsurface which are dark green and enriched in Fe and K.

The clay fractions consisted of mixed-layer glauconite (illite)-smectite, with the surface samples containing more expandable smectite (50%) than the subsurface samples (20%). In the charge-distribution diagram for muscovite-pyrophyllite-celadonite, the weathered glauconites at the surface showed a clear trend from smectitic glauconite at the top to illitic glauconite at the bottom of the layer, whereas the fresh subsurface sample plotted exactly in the glauconite field.

The color, mineralogy, and chemistry indicate that the surface samples were strongly altered by weathering processes and that glauconite transformed progressively into Fe-rich mixed-layer illite-smectite and then into smectites.Weathering can thus completely reverse the glauconitization process. For any chemical and mineralogical characterization of glauconites at the surface, these weathering effects must be taken into consideration.

Particle concentration, charge, solution chemistry (i.e. ionic strength), and the nature of organic matter (OM) are the major factors controlling particle flocculation in aqueous environments. In the present study, the nature of clay fabric associated with clay—OM interaction at a range of ionic strengths was the focus. In the flocculation experiments, the aqueous suspension of montmorillonite and chitin was mixed with NaCl/MgSO4 electrolyte solution. Advanced sample-preparation techniques and visualization methods using transmission electron microscopy were used to observe directly the micro- and nano-scale clay—OM fabric of the resulting flocs. Such direct observation elucidated the role of OM in clay flocculation; few attempts have been made in the past due to the technical difficulties in preserving the original structure. A comparison of clay fabric at two different ionic strengths of 0 and 0.14 M revealed that the individual hexagonal clay particles settled slowly with little intra-aggregate void space (void ratio: 0.07) at 0 M while rapid flocculation and settling of clay particles at 0.14 M, with or without OM, resulted in a more open fabric with greater void space (void ratio: 0.33). The silver-staining technique demonstrated effectively the location of electron-transparent chitin in montmorillonite aggregates. Chitin appeared to link the face-to-face (FF) contacts of clay domains by bridging between negatively charged face surfaces. However, the resultant void ratio and the average hydrodynamic diameter (dH) values were lower than in the OM-free system after flocculation. The results indicated that the interplay between ionic strength and OM content affected the floc architecture and void ratio.