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The interlayer space of the highly charged synthetic Na-Mica-4 can be modified by ion-exchange reactions involving the exchange of inorganic Na + cations by surfactant molecules, which results in the formation of an organophilic interlayer space. The swelling and structural properties of this highly charged mica upon intercalation with n-alkylammonium (RNH 3 ) + cations with varying alkyl chain lengths (R = C12, C14, C16, and C18) have been reported. The stability, fine structure, and evolution of gaseous species from alkylammonium Mica-4 are investigated in detail by conventional thermogravimetric analysis (TGA), Fourier transform infrared spectroscopy (FTIR), in situ X-ray diffraction (XRD), and solid-state nuclear magnetic resonance (MAS NMR) techniques. The results clearly show the total adsorption of n-alkylammonium cations in the interlayer space which expands as needed to accommodate intercalated surfactants. The surfactant packing is quite ordered at room temperature, mainly involving a paraffin-type bilayer with an all-trans conformation, in agreement with the high density of the organic compounds in the interlayer space. At temperatures above 160 °C, the surfactant molecules undergo a transformation that leads to a liquid-like conformation, which results in a more disordered phase and expansion of the interlayer space.

A family of organomicas was synthesized using synthetic swelling micas with high layer charge (Na n Si 8-n Al n Mg 6 F 4 O 20 •XH 2 O, where n = 2, 3, and 4) exchanged with dodecylammonium and octadecylammonium cations. The molecular arrangement of the surfactant was elucidated on the basis on XRD patterns and DTA. The ordering conformation of the surfactant molecules into the interlayer space of micas was investigated by 13 C, 27 Al, and 29 Si MAS NMR. The arrangement of alkylammonium ions in these high-charge synthetic micas depends on the combined effects of the layer charge of the mica and the chain length of the cation. In the organomicas with dodecylammonium, a transition from a parallel layer to a bilayer-paraffin arrangement is observed when the layer charge of the mica increases. However, when octadecylammonium is the interlayer cation, the molecular arrangement of the surfactant was found to follow the bilayer-paraffin model for all values of layer charge. The amount of ordered conformation all-trans is directly proportional of layer charge.

In this research, the adsorption capacity of diatomaceous earth in the removal of the crystal violet dye (CV) in aqueous solution was evaluated. The experimental methodology began with the determination of the texture properties by adsorption-desorption isotherms with N2 a 77 K, the identification of functional groups by Fourier transform infrared spectrophotometry (FTIR), morphology by scanning electron microscopy (SEM) and, the pH of the isoelectric point by the point of zero charge (PZC). A categorical multifactorial design was developed with factors such as the initial concentration of the dye (300-1000 mg/dm3), the temperature (30, 35 and 40ºC) and the initial pH of the solution (5, 6, 7 and 8). The maximum adsorption capacity was of 96.1 mg/g up 30ºC and pH 8, satisfactorily fitting the experimental data to the Langmuir isotherm model with R2 = 0.99, suggesting a monolayer adsorption mechanism on a homogeneous surface. In conclusion, diatomaceous earth can be considered as an efficient adsorbent in the removal of CV in aqueous solution.

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