Differences were found in the differential thermal analysis curves and in the temperatures of new-phase development between allophanes of high (1.91–1.99) and low (1.47–1.53) SiO2/Al2O3 ratios. The endothermic peak due to continuous dehydration and dehydroxylation was at higher temperatures (153°-185°C) for allophanes with high SiO2/Al2O3 ratios and at lower temperatures (148°–165°C) for those with low SiO2/Al2O3 ratios. The temperature of the exothermic peak was lower and the height affected more by the exchangeable cation content for allophanes with high ratios than for those with low ratios. New phases did not develop in allophanes having high Si02/Al2O3 ratios even after they were heated to 1000°C, above the temperature of the exothermic peak. In contrast, a symptomatic development of new phases was noted in allophanes with low SiO2/Al2O3 ratios at 900°C, below the temperature of the exothermic peak. The effect of SiO2/Al2O3 ratio in the thermal behavior of allophane strongly suggests that differences in the structure are closely associated with the chemical composition of this material.

The hot spring water discharging from a flank of an active volcano is precipitating unique monomineralic manganese deposits over volcanic terrain. The major and trace element chemistry, XRD mineralogy, DTA, and SEM observations indicate that the deposits consist of 10 Å phyllomanganate (buserite) accommodating inter-layer Ca and Mg with negligible amounts of detrital minerals. Other metallic elements can be accommodated by buserite, but concentrations are negligible ranging less than 10 ppm to 500 ppm. Abundance and pattern of REE (less than 100 ppm in total) are similar to those from hydrothermal manganese deposits. The buserite is enriched in Ca and Mg but depleted in Na in comparison with those in the spring water. The distribution coefficients for Ca, Mg and Na between the buserite and the host water were calculated assuming an ion-exchange equilibrium in the Yuno-Taki Fails, which proved applicable to other manganese deposits from surficial environments on land and oceans.

OH-Cr smectites were prepared with different mmol Cr/g smectite: 0.5, 1.5, 3.5, 5, 10 and 20 by treatment with hydroxy-chromium solution prepared at 60°C and one day of hydrolysis with OH/Cr = 2. The samples were characterized by X-ray diffraction (XRD), differential thermal analyses (DTA) and N2 adsorption-desorption isotherms.

The d(001) spacings of OH-Cr-smectite were different according to Cr added/g smectite. Larger d(001) spacings: 1.95, 2.05 and 2.07 nm were obtained with 5, 10 and 20 mmol Cr per gram of sample. DTA diagrams of smectite treated with OH-Cr solution showed exothermic peak at 420°C corresponding to Cr203 (confirmed by XRD). N2 adsorption-desorption isotherms of smectite treated with different amounts of Cr preserved the same slit-shaped pores than original sample, but with different micropore volume. This behavior was maintained until treatment temperature of 380°C. The specific area of smectite was increased from 36 to 175 m2/g after treatment with OH-Cr solution. The textural characteristics of OH- Cr smectite heated up to 420°C were changed. The specific area decreased and mesopore volume was produced. The different Cr added modified the structural and textural behavior.

The residual kaolin deposits near Lastarria, South-Central Chile, were formed by weathering of subvolcanic quartz porphyry stocks, which intruded the metamorphic basement of the Coastal Cordillera. The clay fractions (<2 µm) consist mainly of poorly-ordered, very fine-grained kaolinite and lath-shaped illite (17–38 wt. %) with minor amounts of quartz, sanidine, and goethite. A sample from the top of the deposit contains major quantities of gibbsite morphologically indistinguishable from kaolinite flakes. The gibbsite-free clays contain 35.5–36.6 wt. % Al2O3, 0.4–2.6 wt. % Fe2O3, 1.3–3.9 wt. % K2O, and have low TiO2 concentrations (<0.02 wt. %). The absence of quartz veining, the abundance of melt inclusions, and the scarcity of secondary fluid inclusions in quartz phenocrysts from altered rocks imply a lack of significant hydrothermal activity in the quartz porphyries. The δ 18O and δD values of the kaolins indicate formation in a weathering environment at significantly higher annual mean air temperatures (∼12°C) than present mean temperatures of ∼9.4°C. Uplift of the region alone probably cannot account for the change in climate. The stable isotope composition of gibbsite is consistent with an origin of desilication of kaolinite at superficial temperatures. Various criteria proposed to distinguish supergene from hypogene kaolins are discussed.

The Şile Region contains discontinuous, cyclic, thin coal beds and industrial clay deposits that were accumulated in lacustrine basins which received extensive volcanoclastic sediments due to transport of highly weathered calc-alkaline volcanic rocks. The Sülüklü area has the largest kaolin deposit in this region. Cyclic kaolinization depended on the degree of leaching of Si and alkalis in cyclic swamp environments and, therefore, kaolinite contents vary in each discontinuous lens-shaped clay bed and underclay within the basin. The kaolins comprise disordered kaolinite, illite, smectite, gibbsite, quartz, pyrite, anatase, K-feldspar and goethite. Depth-related changes in the distribution of clay minerals, associated with coal beds, are indicative of organic acid-mineral reactions. Kaolinite crystallization initiated at the edges of sericitic mica sheets in the form of composite kaolinite stacks. The small size (<1 µm), morphology and poor crystallinity of kaolinite crystals suggest that kaolinization post dated transportation. Primary or secondary origins of particles can be determined from the stacking sequences of kaolinite particles using high-resolution transmission electron microscopy images. Kaolinite stacks always contain a small amount of illite, but smectite is only present in the middle and upper levels. Gibbsite is a main constituent of refractory bauxitic clays locally found as discontinuous lenses and exploited from the lower level of the basin.

Genesis of kaolin deposits took place in two stages: first, there was in situ weathering of the oldest andesitic agglomerates, tuffs and ashes at the base of the lacustrine basin coupled with discharge of shallow thermal waters which were initiated by local hydrothermal alteration; second, surface weathering enhanced transportation of altered rocks from the surrounding hills into the lacustrine basin. Kaolinization took place in cyclic swamp environments, as indicated by the presence of cyclic thin- to thick-bedded coals that provided necessary humic and fulvic acids for the post-depositional alteration of altered volcanic rocks to kaolin in dysaerobic, relatively low-pH conditions in saturated groundwater zones.

The thermal stability of surfactant-modified clays plays a key role in the synthesis and processing of organoclay-based nanocomposites. Differential thermal analysis (DTA), thermogravimetric measurement and differential scanning calorimetry (DSC) were used in this study to characterize the thermal stability of hexadecyltrimethylammonium bromide-modified montmorillonites prepared at different surfactant concentrations. Analysis by DSC shows that the molecular environment of the surfactant within the montmorillonite galleries is different from that in the bulk state. The endothermic peak at 70–100°C in the DTA curves of the modified montmorillonites is attributed to both the surfactant phase transformation and the loss of free and interlayer water. With an increase of surfactant-packing density, the amount of water residing in the modified montmorillonite decreases gradually, reflecting the improvement of the hydrophobic property for the organoclay. However, the increase in the surfactant packing density within the galleries leads to a decrease in the thermal stability of the organoclays.

With an increase of initial surfactant concentration for the preparation of organoclays, the surfactant- packing density increases gradually to a ‘saturated’ state. It was found that the cationic surfactant was introduced into the montmorillonite interlayer not only by cation exchange but also by physical adsorption.

Emanation thermal analysis (ETA), based on radon release measurements from previously labeled samples, was used for the first time in the characterization of the thermal behavior of natural Mg2+-vermiculite (Santa Olalla, Huelva, Spain) and of Na+- and ${\text{NH}}_4^{+}$-exchanged vermiculite samples. In addition, vermiculite samples subjected to a chemical treatment with an aqueous solution of (NH4)2SiF6 and partially or totally re-saturated with Na+ ions were also investigated by ETA. The ETA results of natural Mg2+-vermiculite, Na+-vermiculite and ${\text{NH}}_4^{+}$-vermiculite gave supplementary information about microstructure changes of the samples observed under dynamic heating conditions. The method has proved to be very useful for characterization of microstructure changes due to modification in the interlayer space of samples during the heat treatment. The crystallization of vermiculite into new phases, such as enstatite (for ${\text{NH}}_4^{+}$-vermiculite and Mg2+-vermiculite) and forsterite (for Na+-vermiculite) was also observed by ETA.

What, if anything, is the import of Hayek to epistemic democracy? Although Hayek is revered by epistemic democrats for his insights into the epistemic aspects of the market sphere, it is generally believed that his theory is moot with respect to democratic reason. This paper aims to challenge this verdict. I argue that a Hayekian analysis of inclusive public deliberation contributes at least three valuable lessons: (1) Hayek makes the case that under certain conditions even unbiased deliberators are permanently unable to converge on the best available policy option. Call this the problem of ‘persistent hidden policy champions’. (2) He demonstrates that to unlock hidden policy champions, reasonable minority factions need the opportunity to act on their own evidential standards. (3) He challenges epistemic democrats to think more carefully about how to design the “epistemic basic structure” (Kurtulmus and Irzik 2017) of society in order to account for persistent hidden policy champions.

The thermal decomposition of hydrotalcite (HT), with chemical composition Mg1-xAlx(OH)2(CO3)x/2.(1-3x/2)H2O, (0.20 < x ≤ 0.33), is a complex sequence of dehydration, dehydroxylation and decarbonization and leads to the formation of a series of metaphases: HT-D (dehydrated HT), HT-B (partially dehydroxylated HT) and MO (mixed oxides with periclase-like structure). The evolution of water and CO2 in natural and synthetic hydrotalcites (a Mg/Al ratio between 2:1and 3.7:1), heated to 800°C, was investigated by differential thermal analysis, thermogravimetry and evolved gas analysis. At least six endothermic and two exothermic effects were established by computer-aided resolving of the curves. The formation of each HT metaphase was related to the release of a discrete number of water molecules depending on the Al content in the samples and each appeared as a corresponding endothermic peak in the DTA curves. The exothermic processes associated with the crystallization of HT-B and MO metaphases were specified by decomposition of DTA curves. The evolution of CO2 during the thermal decomposition of the carbonate groups was found to be different for the samples studied. The preservation of CO3 even at high temperatures was established for synthetic samples with a high Al content. The release of volatile H2O and CO2 (which comprise ~40% of the sample mass) provokes fine cracking both along and across the layers.

Li8(Al6Si6O24)Cl2, a synthetic member of the sodalite family (Henderson and Taylor, 1977), was prepared by heating natural sodalite, Na8(Al- 6Si6O24)Cl2 (from Låven, Norway), in molten LiC1 at 800 °C for 2h, washing uncombined LiC1 from the product and drying at 110 °C Chemical analyses of the natural sodalite and the Li-sodalite are given in Table 1. The cell edge of the Lisodalite was 8.4476(9) Å (Si as internal standard: a = 5.43065/Å at 25 °C in good agreement with literature values (Henderson and Taylor, 1977).

Most electrolytic zinc plants have to deal with dissolved magnesium in their process liquors, as zinc sulphide concentrates contain small amounts of magnesium. Applied magnesium bleed methods are generally expensive and environmentally unfriendly. Recently, a new approach was suggested and discussed, which involves selective magnesium fluoride precipitation from purified zinc sulphate solutions. X-ray fluorescence measurements of these precipitates indicated that the ratio Mg:F is not 1:2 as would be expected if the precipitate was MgF2, which should be formed on a theoretical basis. It was inferred that fluoride was partly substituted by hydroxyl groups. Analytical techniques such as infrared absorption spectrometry, X-ray diffraction, and thermogravimetry were combined in order to verify this hypothesis. The precipitate indeed appeared to be a magnesium fluoro- hydroxide compound containing physically bound water. The results contribute to the understanding of the required operating conditions of the proposed process.