Although fluorescence detection is a sensitive method in the field of pollutant analysis, its application is restricted due to the fluorescence shown by organic material being quenched after aggregation and to low photo-thermal stability. To address these issues, a novel mineral/dye composite material was prepared by intercalating a fluorescence molecule, Rhodamine (R6G), into the interlayer space of montmorillonite (Mnt). This composite material greatly enhanced the light stability and efficiency of R6G. After enhancement, the fluorescence lifetime of R6G-Mnt was eight times longer than originally and the luminous intensity was 20 times greater. Chromium at the mmol/L (mM) level can be detected by the naked eye when its enhanced fluorescent property is fabricated into a solid test paper, even though a fluorescence spectrophotometer should be used for detection at the 0.01 μmol/L level in the sensing range 0.01 μmol/L to 100 mmol/L. These results can provide new avenues as well as a theoretical and experimental foundation for the development of novel supramolecular luminescent material.

The cation exchange capacity (CEC) is a characteristic property of expandable clay minerals, such as smectites and vermiculites. The aim of this work was to examine the cation exchange behavior of vermiculite using the Cu-triethylenetetramine (Cu-trien) CEC method and the influence of mechanical and chemical pretreatment, with the ammonium acetate method serving as a reference. The Cu-trien method makes rapid and direct CEC measurements possible. Three different kinds of mill were used to grind a vermiculite sample from Russia, in order to reduce the particle size to <10 µm. The Netzsch CGS 10 dry mill reduced the particle size more effectively than the other grinding methods. Chemical pretreatments were used to remove carbonates, organic matter, Fe oxides, and divalent exchangeable cations from vermiculite samples prior to CEC measurements. Subsamples of ground and chemically pretreated vermiculite samples were saturated with Na, Li, Mg, Ca, and Cu cations to determine the effect of exchangeable cations on measured CEC values. Chemical pretreatment, monovalent cation pretreatment, and 48 h of shaking time were needed to measure vermiculite CEC values effectively using the Cu-trien method.

During the Gilded Age and Progressive Era, thousands of middle-class youths published their own amateur newspapers. These periodicals were printed using the so-called toy (or “novelty”) press, a portable tabletop device that helped democratize word processing. Children often used their presses to compose miniature novels and short stories. They then shared their prose with a national community of fellow juvenile writers collectively known as “Amateurdom.” Adolescent fiction explored an array of subjects, but the frontier, territorial expansion, and empire in the West became some of its particular fixations. All that imperial storytelling, however, possessed a rich subtext. Boys and girls, reacting to late-nineteenth-century changes in the lived experience of childhood, used their printing presses to challenge various constraints imposed upon them. But in so doing, they both perpetuated and reinforced a pernicious culture of settler colonialism that celebrated the subjugation of American Indians. Ultimately, the amateur publications of children remind us that fiction is not exclusively an adult enterprise. The creative output of young people provides important insight into an underexplored realm of the Gilded Age and Progressive Era’s literary world.

Microstructural changes induced by the microbial reduction of Fe(III) in nontronite by Shewanella oneidensis were studied using environmental cell (EC)-transmission electron microscopy (TEM), conventional TEM, and X-ray powder diffraction (XRD). Direct observations of clays by EC-TEM in their hydrated state allowed for the first time an accurate and unambiguous TEM measurement of basal layer spacings and the contraction of layer spacing caused by microbial effects, most likely those of Fe(III) reduction. Non-reduced and Fe(III)-reduced nontronite, observed by EC-TEM, exhibited fringes with mean d001 spacings of 1.50 nm (standard deviation, σ = 0.08 nm) and 1.26 nm (σ = 0.10 nm), respectively. In comparison, the same samples embedded with Nanoplast resin, sectioned by microtome, and observed using conventional TEM, displayed layer spacings of 1.0–1.1 nm (non-reduced) and 1.0 nm (reduced). The results from Nanoplast-embedded samples are typical of conventional TEM studies, which have measured nearly identical layer spacings regardless of Fe oxidation state. Following Fe(III) reduction, both EC- and conventional TEM showed an increase in the order of nontronite selected area electron diffraction patterns while the images exhibited fewer wavy fringes and fewer layer terminations. An increase in stacking order in reduced nontronite was also suggested by XRD measurements. In particular, the ratio of the valley to peak intensity (v/p) of the 1.7 nm basal 001 peak of ethylene glycolated nontronite was measured at 0.65 (non-reduced) and 0.85 (microbially reduced).

What are the distributional consequences of migration, and how do they affect attitudes toward migration? In this paper we leverage a natural experiment generated by the ousting of former Libyan dictator Muammar Gaddafi, which created an unprecedented influx of economic migrants from African countries to Europe. This surge of low-skilled labor benefited low-productivity firms by lowering their production costs and expanding their labor supply. Employing a triple difference-in-differences design, we document that attitudes toward migration became more positive in Western European regions with large shares of migrants and low-productivity firms. Evidence from Sweden, which provides finely grained geographical data, confirms these findings. We then test the economic microfoundations of this attitudinal shift. We show that the surge in the supply of low-skilled labor increased the profitability of low-productivity firms more in areas that experienced larger migration flows. We find no evidence that migration worsened natives’ labor market conditions.

We used high-resolution X-ray texture goniometry to quantify changes in the mm-scale orientation of phyllosilicate minerals in a suite of Paleogene mudstones from the Podhale Basin in southern Poland. The sample set covers an estimated range of burial depths between 2.4 and 7.0 km, corresponding to a temperature range of 60–160°C. Although mechanical compaction has reduced porosities to ∼10% in the shallowest samples, the phyllosilicate fabric is only modestly aligned. Coarser-grained (>10 µm) detrital chlorite and mica appear to be more strongly aligned with (001) parallel to bedding, suggesting their deposition as single grains rather than as isotropic flocs or aggregates. From 2.4 to 4.6 km, R0 illite-smectite with 40–50% illite layers changes to R1 illite-smectite with 70–80%) illite layers. At the same time kaolinite is lost and diagenetic chlorite is formed. The mineralogical changes are accompanied by a strong increase in the alignment of illite-smectite, chlorite, and detrital illite, parallel to bedding and normal to the presumed principal effective stress. We propose that the development of a more aligned I-S fabric results from the dissolution of smectite and the growth of illite with (001) normal to the maximum effective stress. Water released by illitization may act as a lubricant for the rotation of all platy minerals into nanoporosity transiently formed by the illitization reaction. At greater depths and temperatures, further illitization is inhibited through the exhaustion of K-feldspar. After the cessation of illitization, a further 2.4 km of burial only results in a small increase in phyllosilicate alignment. At such small values for porosity and pore size, increasing stress does not substantially reorient phyllosilicates in the absence of mineralogical change.

Particle-size analysis (obtained by Galai CIS 1) was used to determine the following statistical parameters of aqueous suspensions of Na-, Ca- and Mn-montmorillonite: the size distributions, the diameters of the largest and of the median and mean particles, and the percentage of particles with diameters <1.5 µm. Dilution or shaking had almost no effect on the particle-size distribution curves and statistical parameters of Ca- and Mn-montmorillonites but the curves and the statistical parameters of Na-montmorillonite were very much affected by these treatments. The median and mean diameters of Na-montmorillonite range from 0.8 to 10.5 µm and 0.8 to 11.6 µm, respectively, the median and mean diameters of Ca-montmorillonite range from 1.5 to 3.6 µm and 2.12 to 4.2 µm, respectively, and those for Mn-montmorillonite from 1.2 to 2.3 µm and 1.5 to 2.5 µm, respectively. The presence of large particles of Na-montmorillonite was attributed to the extensive swelling of this clay in aqueous suspensions by osmotic water adsorption. The median and mean diameters of aged Na-montmorillonite suspensions indicate that swelling increases with dilution. The swelling of Ca- and Mn-montmorillonite, on the other hand, is limited and their particle size does not increase with dilution.

Clays are used widely as facial masks to remove excess sebum, an oily substance released onto the skin. Smectite, illite, kaolinite, and in some cases, chlorite, are the dominant phyllosilicates in most commonly used clay facial masks. To date, the adsorption of human sebum has been proved only on smectite clays; in the present study the adsorption of two organic compounds found in human sebum by illitic, kaolinitic, and chloritic phyllosilicates was investigated. Illitic clays are often used in cosmetic clay masks, but usually contain some fine-grained non-clay minerals. The presence of carbonate, for example, can cause skin irritation because of its alkaline nature, and iron oxides and hydroxides reduce the adsorption properties of clays. The influence of the removal of these compounds on the adsorption properties of illitic clays was also investigated. The amounts of both compounds adsorbed were established by UV-VIS spectrophotometry. All samples were characterized by mineralogical composition, particlesize distribution, specific surface area, and cation exchange capacity (CEC). Oleic acid and squalene were adsorbed on all clay samples, but illitic and chloritic phyllosilicates showed the greatest adsorption capacity. After purification, the sizes of the particles decreased and the CEC values increased. Nevertheless, the dissolution of carbonates essentially had no influence on the adsorption properties, whereas the removal of iron oxides and hydroxides increased significantly the amounts adsorbed of both oleic acid and squalene.

Nanostructural analysis of pillared clay samples using high-resolution transmission electron microscopy has been developed. Montmorillonite samples were pillared using partially hydrolyzed Al and Fe solutions. Two samples, M01 and M05, corresponding to Fe/(Fe+Al) ratios of 0.1 and 0.5, respectively, were analyzed. The different steps of image filtration, resulting from filtration by ring-shaped masks, are illustrated and discussed from lattice imaging of sample M01. This procedure is used to show the heterogeneous distribution of the basal spacings in the different ordered domains. Domains of mesoporosity and distribution of the different Fe species are studied specifically in the sample M05. The quantitative HRTEM results are discussed and compared with X-ray diffraction patterns obtained from the same sample.

The use of waste materials from mineral ore processing has much potential for immobilizing pollutants such as arsenic (As) in natural soils and waters. The purpose of the present study was to investigate red mud (RM, a finely textured bauxite-ore residue) as a sequestering agent for arsenate and phosphate, including characterization of the types of surface complexes formed. The mineralogical and structural changes occurring in RM were investigated after exchange with arsenate [As(V)-RM] and phosphate [P(V)-RM] anions at pH 4.0, 7.0, and 10.0. Eight different phases were present in the untreated red mud (RMnt), though 80 wt.% of the crystalline phase consisted of sodalite, hematite, gibbsite, and boehmite. The X-ray diffraction (XRD) data for As(V)-RM revealed an anion-promoted dissolution of the gibbsite, suggesting that this phase was the most active for As(V) sequestration. In addition, the lattice parameters of cancrinite were different in As(V)-RM at pH 7.0 and 10.0 from those in RMnt. The changes may be related to the incorporation of arsenate in the cancrinite cages. X-ray diffraction patterns of P(V)-RM at pH 4.0 and 7.0 revealed the dissolution of sodalite, hematite, and gibbsite, and the formation of a novel phase, berlinite [(α,β)AlPO4]. The new phases detected through XRD and thermal (TG/DTG) analysis in P(V)-RM probably originated through an initial phosphate-promoted dissolution of some RM phases, followed by a precipitation reaction between the phosphate and Al/Fe ions. The results obtained suggest that phosphate and arsenate, though with different reactivities, were strongly bound to some RM phases, such as gibbsite, cancrinite, sodalite, and hematite through mechanisms such as chemical sorption and coprecipitation reactions. The knowledge acquired will be helpful in selecting alternative materials such as red muds, which currently pose critical economic and environmental challenges related to their disposal, for the decontamination of soils and waters polluted with As.

The Upper Silurian–Lower Devonian section of the Dniester gorge in Podolia and samples from boreholes located S and N of this area were studied in order to reconstruct the thermal history of Lower Paleozoic sedimentary rocks in the Dniester segment of the Peri-Tornquist margin of the East European Craton which is the most eastern part of a major shale-gas target in Europe. X-ray diffraction data for illite-smectite from shales and carbonates indicate very advanced diagenesis and maximum paleotemperatures of ~200ºC, higher than interpreted from the ‘conodont alteration index’ (CAI) data. Diagenesis of the Devonian section is slightly less advanced than that of the underlying Silurian section, indicating that it is a regional feature and the result of burial. The regional distribution of the diagenetic grade based on illite matches well with the pattern established from the CAI data. K-Ar dating of illite-smectite from Silurian bentonites and shales gave a consistent set of dates ranging from 390 to 312 Ma. To explain such advanced levels of diagenesis and such K-Ar dates, the extension of the Carboniferous foreland basin (which today is only preserved to the NW of L’viv) toward the SE on the craton margin has to be assumed. The diagenetic zonation pattern of the Carboniferous coals supports this hypothesis. The Carboniferous cover may have been either sedimentary or partially tectonic (Variscan intracratonic duplexes) in origin and the thickness, necessary for the observed level of diagenesis, may have been reduced by an elevated heat flow along the major tectonic zone at the edge of the craton (TESZ). The presence of such cover is confirmed by completely reset Cretaceous apatite fission track (AFT) ages of the Silurian bentonites. The AFT dates also imply a Tertiary heating event in the area.

The 10 Å clay mineral present in the dolomitic part of the profile (Silurian), both in bentonites and in other rocks, is aluminoceladonite or intermediate between illite and aluminoceladonite, while in the Devonian shale section only illite was documented. Chlorite is also common in the studied rocks and is at least partially authigenic. It is non-expandable in the samples from boreholes, while often expandable to variable extents in the samples from outcrops, which also contain goethite. Such variation in chlorite is attributed to contemporary weathering.

This review is concerned with the synthesis and physical-chemical characteristics of a specific type of modified clay material: Ti-PILCs. The two general synthetic procedures and the main problems associated with the scale-up synthesis of these pillared materials are discussed in detail. The general characteristics of Ti-PILCs in terms of basal spacing, pillar homogeneity, surface area, microporosity, mesoporosity, pore size and distribution, thermal resistance and acidity are discussed in depth. Likewise, the most important synthesis parameters that have a clear and marked influence on the final characteristics of the materials are summarized.

Aiming to identify the complexing mechanisms of heavy metal cations on edge surfaces of 2:1-type clay minerals, systemic first-principles molecular dynamics (FPMD) simulations were conducted and the microscopic structures and complex free energies were obtained. Taking Cd(II) as a model cation, the structures on both (010) and (110) edges of the complexes were derived for the three possible binding sites (≡SiO, ≡Al(OH)2/≡AlOH≡AlSiO, and vacant sites). The stable complexes adsorbed on the three binding sites on both terminations had similar structures. The free energies of the complexes on (010) edges were calculated by using the constrained FPMD method. The free energies of complexes on the ≡SiO and ≡Al(OH)2 sites were similar and they were both significantly lower than the free energy of the complex on the octahedral vacant site. In association with the concept of high energy site (HES) and low energy site (LES) in the 2 Site Protolysis Non Electrostatic Surface Complexation and Cation Exchange (2SPNE SC/CE) sorption model, the vacant site was assigned to HES and the other two sites to LES, respectively.

K-Ar measurements were used in this study of upland Savannah River Site soils to distinguish between sorbed K and the K remaining in remnants of primary minerals. Study of sorbed K contributes to understanding further the interaction of alkali metals (Cs in particular) with the soils. Primary mineral K and the associated radiogenic Ar were studied to characterize soil mica with respect to its provenance and its relationship to hydroxy-interlayered vermiculite. K-Ar age values of Na-saturated clay fractions from five samples of these soils range in age from 270 to 370 Ma. After a moderate acid treatment (6% HNO3 v/v, ~1 mol dm-3, 3 h, 80°C) of the clay fractions, K-Ar age values (270-325 Ma) were little changed on the whole, but they were more closely grouped near 300 Ma. Earlier work had shown that most of the K in these soils is found in material resistant to moderate acid extraction. The K-Ar age values show that this acid-resistant material is much older than any pedogenic minerals could be, even much older than the sedimentary parent rocks from which the soils were derived. These observations support earlier inferences by others that the K in these well leached soils is largely in remnants of primary muscovite from the parent sediments. Age values near 300 Ma suggest that the muscovite is largely from proximal Piedmont terranes of the Appalachian orogen, where the K-Ar relationship in most micas was set by Alleghanian tectonic processes late in the Paleozoic Era. The structural location of the K within mica, shown by the retention of the associated radiogenic Ar, is in contrast to the sorption-dominated behavior of the Cs and most of the Rb in these soils during pedogenesis. Stronger acid treatment (~6 mol dm-3 HNO3, 3 h, 100°C) extracted substantial fractions of both the K and the radiogenic Ar from bulk-soil portions, indicating destruction of some of the primary mica. K-Ar age values for the sand-rich bulk soils were not useful for this study because the sand contains excess radiogenic Ar, probably in sand-sized vein quartz.

Numerous experiments have verified that smectites can adsorb aflatoxin B1 (AfB1) effectively and the efficiency of this process depends heavily on the chemical, physical, and mineralogical characteristics of the smectite. Several relationships between these characteristics and AfB1 sorption have been determined experimentally, but the molecular mechanisms underlying these were not investigated. In the current study the effects of charge density, type of exchange cation, and charge origin (octahedral vs. tetrahedral) on AfB1 sorption on smectites were analyzed by a series of molecular simulations. The calculations confirmed the formation of water bridges between carbonyl groups of AfB1 molecules and interlayer cations. Flat orientation of AfB1 molecules on smectite surfaces was also confirmed. For larger amounts of AfB1 molecules in the intercalates, self-association of two AfB1 molecules bound by π–π interaction was shown. The thermodynamics of AfB1 sorption depends heavily on the water content in the structure, being optimal for basal distances corresponding to two layers of water. A clear preference for sorption of AfB1 on smectites with bivalent cations (Ba2+, Ca2+) and an octahedral origin of its layer charge was confirmed and this was explained as steric hindrance between hydrated ions and AfB1 molecules, which tend to lie flat on smectite surfaces devoid of ions. Ba-montmorillonite with a charge of 0.4 per half unit cell was shown to have the smallest and thus the best potential energy of adsorption compared to the other layer charges.

We investigated the sorption of Ni to gibbsite of two different surface areas at pH 7.5, in the presence and absence of citrate, over a time period of 180 days. Extended X-ray absorption fine-structure spectroscopy was employed to elucidate the sorption mechanisms at the molecular level. In agreement with former results, Ni-Al layered double hydroxide (LDH) formed in the presence of gibbsite of low surface area. However, gibbsite of high surface area suppressed the formation of the surface precipitate. Instead, two Al atoms neighboring Ni at distances of 2.95–2.98 Å indicated formation of an inner-sphere sorption complex, where each NiO6-octahedron shares edges with two AlO6-octahedra. Focused multiple scattering arising from Al atoms at a distance of 6 Å suggest that sorbed Ni(OH)2(OH2)4 monomers epitaxially extend the hexagonal arrangement of Al atoms in gibbsite. Only after 30 days or more was a small amount of LDH formed. The presence of citrate prevented the formation of LDH, while maintaining the formation of inner-sphere sorption complexes.

Theoretical models of the mechanical properties of hydrated smectites, saturated with a variety of cations, are of much value in determining the potential for their use in various applications, including clay-polymer nanocomposites, but the development of such models is still in its infancy. The purpose of this study was to calculate the effects of divalent cations on the structural and mechanical elasticity of montmorillonite under different degrees of hydration. A theoretical study of the swelling and hydration behavior of montmorillonite was, therefore, undertaken using density functional theory (DFT) to investigate the basal spacing behavior of the homoionic montmorillonite with varying amounts of water in the interlayer space. The effect of the degree of the hydration of divalent interlayer cations (Mg2+/Ca2+/ Sr2+/Ba2+) on the structure expansion of the interlayer space was analyzed. In addition, the results obtained were compared to calculations performed on the montmorillonite model with a monovalent cation (Na+). The basal spacing (d001) is governed by the size and the degree of hydration of the countercations. The structures containing divalent cations are more compact than structures with monovalent cations. Ba-exchanged montmorillonite was found to have the largest d001 value for any degree of hydration (‘dry,’ one water layer, or two layers). The basal spacings of ‘dry’ montmorillonite exchanged with small cations, Mg2+ and Ca2+, are very similar. In hydrated models, the d001 expansion correlates with the ionic radius of the interlayer cation. The dependence of the total electronic energy on the volume expansion was calculated. From the energetic curves, bulk modulus (B0) was obtained by fitting in order to show how the compliance of the material depends on the type of interlayer cation and on the degree of hydration. With increasing water content in the interlayer space, the bulk modulus decreased, suggesting that the c-axial compression becomes easier with increasing hydration of the clay mineral. The values of the bulk modulus in hydrated systems are less sensitive to the type of the interlayer cation.

Lubricants are an essential component in high-performance mechanical equipment, but traditional lubricants are becoming inadequate for meeting the increasing demands for anti-friction and anti-wear properties and they discharge harmful chemicals to the environment. The purpose of the present study was to explore the use of sepiolite as a novel oil additive to extend the performance of lubricants. Sepiolite nanofibers were first treated by acid followed by a dry air flow, aimed at increasing the pore volume and decreasing the particle size. Then the nanofibers were further modified by an organosilane coupling agent to reduce the surface free energy and to improve the dispersion stability in lubricant. A significant improvement in the performance of the lubricant was achieved by using the modified sepiolite nanofibers as an additive. When the amount of modified sepiolite nanofibers added was 1.5 wt.%, the best performance was demonstrated by the lubricant, showing a viscosity increase at 40°C and 100°C, and an increase in resistance to oxidation. Moreover, the acid value and pour point decreased, and the copper sheet corrosion level dropped to its lowest value.

The aim of the present study was to synthesize a photocatalyst on the basis of TiO2 with kaolin as the support material. Properties such as layered structure and a suitable particle size of kaolin could be beneficial in the production of a high-quality and relatively cheap photocatalyst on an industrial scale. Homogeneous hydrolysis with urea as a precipitation agent and kaolin as support material was used to obtain a kaolin surface covered with TiO2. Samples were characterized by means of X-ray powder diffraction, infrared and Raman spectroscopy, high-resolution transmission electron microscopy, Brunauer-Emmett-Teller surface area, and Barrett-Joyner-Halenda porosity determination. Photocatalytic activity was assessed by a Reactive Black 5 azo dye discoloration in a water suspension and by acetone decomposition on a thin layer of sample in a gas phase. The characterization confirmed that the well crystallized TiO2 was distributed effectively over the whole surface of a kaolin substrate, and photocatalytic tests revealed that the active surface layer of titania particles on kaolin performed well, suggesting that kaolin acts as a suitable support.