The fluoride content in groundwater varies depending on geological configuration. Fluoride problems tend to occur in places where these minerals are most abundant in rocks. The objective of the present work was to synthesize four biopolymers based on chitosan-polyvinyl alcohol (Ch-PVA) cross-linked with sodium tripolyphosphate pentabasic (TPP) and ethylene glycol diglycidyl ether (EGDE) and determine their ability to remove fluoride from water. The characterization of the Ch-PVA beads was performed by way of Scanning Electron Microscopy (SEM) and Fourier-transform infrared spectroscopy (FTIR). The percentage of humidity and the point of zero charge were determined. The Ch-PVA beads showed a surface area of 63.87 m² g⁻¹, a pore size of 7.6 nm, a point of zero charge of 7.4, and 98.6% humidity. The kinetic adsorption study was adjusted to the pseudo-second-order model and the adsorption equilibrium data were adjusted to the Freundlich adsorption isotherm, showing a maximum fluoride adsorption capacity of 12.64 mg g⁻¹ at pH 7 and 30 °C, for the beads of Ch-PVA-NaOH-TPP. According to the thermodynamic parameters: −∆G°, +∆H° and −∆S°, fluoride adsorption is spontaneous, endothermic in nature and there is no random energy change in the solid/liquid interface during the adsorption process.

Dental and emaciated fluorosis is derived from the chronic intake of fluoride ions (F⁻) by consumption of food, tooth products and drinking water from groundwater. Recent reports indicate that in some regions of Mexico, the incidence of fluorosis in temporary and permanent dentitions have increased in recent years. The purpose of the present investigation was to determine the presence and distribution of F⁻ ions in semi-confined aquifers, located in the basins of Lerma-Chapala and Valley of México. Temperature (T), pH, electrical conductivity (EC) and alkalinity were determined in situ, in 27 groundwater wells. The hardness, chloride ions (Cl⁻), free chlorine (Cl₂), total dissolved solids (TDS) and bicarbonates (HCO₃⁻), were determined in the laboratory. The high content of bicarbonate ions (HCO₃⁻) is associated with the alteration of silicates and the presence of chloride ions (Cl⁻) due to the anthropogenic activity. The highest value of fluoride ions (F⁻) (1.31 mg/L) was identified in a well of the Lerma-Chapala basin and in 25% of the samples (1.056 mg/L) of the Valley of México basin. The groundwater in the Lerma-Chapala basin is of the Ca-HCO₃ type and the water in the Valley of Mexico basin is Na-HCO₃ and Ca-HCO₃. According to the Gibbs diagram, the water of the Toluca Valley aquifer is recharged by local meteoric precipitation and consequent the water-rock interaction occurs. The correlation analysis shows the significant relationship between F⁻ and CE (R = 0.5933), F⁻ and alkalinity (R = 0.6924), F⁻ and HCO₃⁻ (R = 0.6924) and F⁻ and TDS (R = 0.5933). The correlations confirm that the content of fluoride ions present in groundwater is associated with high concentrations of bicarbonate ions and the presence of sodium, due to a process of alteration of the silicates.

Layered double hydroxides (LDH) M²⁺M³⁺CO₃²⁻ were synthesized following the sol-gel methodology using Mg-Al, Mg-Fe, and Zn-Al as cation pairs for subsequent use in the preparation of TiO₂/LDH materials. The samples were characterized by infrared spectroscopy (IR), scanning electron microscopy (SEM), and the Brunauer–Emmett–Teller (BET) technique to determine the surface area (SA); the results of which were used to determine the roughness of the samples in terms of surface fractal dimension (D). The prepared materials exhibited both adsorption and photocatalytic properties in the removal of phenol in aqueous solution under ultraviolet irradiation. This work studies the relationship between the textural parameters of the materials obtained in relation to their photocatalytic efficiency and adsorption capacity, finding that the surface of the solids, their structural heterogeneity, and roughness condition the photodegradation and adsorption processes, using phenol as reference organic pollutant. The results show that different cation in LDH influences in photocatalytic capacity; the TiO₂/ZnAl was the best material in one test, but after 10 times of test, the TiO₂/MgFe gave the better photodegradation material. In adsorption capacity, TiO₂/ZnAl and TiO₂/MgFe have a close rate for phenol adsorption and both were better than TiO₂/MgAl. The differences in textural characteristics (surface area, surface roughness, and pore-size distribution) affected phenol adsorption and photodegradation efficiency.

Synthetic dyes are increasingly relevant pollutants due to their widespread use and discharge into water bodies. This study examines how the solution pH affects the morphology of chitosan–cellulose cryogel (Ch-C-EGDE) and its impact on dye transport to adsorption sites. Adsorption tests with dyes Y5, R2, and B1 over a pH range of 2–12 revealed optimal performance at pH 2.5. High hydronium ion concentrations significantly improved adsorption capacities (945–1605 mg/g), with a hierarchy B1 > R2 > Y5 at 250 mg/L initial concentration. The dependence of the dye adsorption on the acidic pH of the solution suggests that there is a mechanism of adsorption by electrostatic forces due mainly to the protonation of the amino group (NH₃⁺). During the dye adsorption studies, a decrease in the diameter of the cryogel beads was observed, as well as a possible “zipper effect” in the pores of the Ch-C-EGDE cryogel beads, which depends on the pH at which the anionic molecules of the dyes attract the positively charged chitosan-based adsorbent walls, which physically closes the pores and results in a decrease in pore size as well as a geometric and/or load-bearing impediment. The experimental data fitted well with the pseudo-second-order kinetic models and the Sips isotherm model, indicating multilayer and heterogeneous adsorption behavior. In the Sips model, a value of n > 1 was obtained, which confirms favorable adsorption conditions and suggests strong dye-adsorbent material interactions, especially at higher dye concentrations.