Biochar is a carbonaceous and porous material with limited adsorption capacity, which increases by modifying its surface. Many of the biochars modified with magnetic nanoparticles reported previously were obtained in two steps: first, the biomass was pyrolyzed, and then the modification was performed. In this research, a biochar with Fe₃O₄ particles was obtained during the pyrolysis process. Corn cob residues were used to obtain the biochar (i.e., BCM) and the magnetic one (i.e., BCM_Fe). The BCM_Fe biochar was synthesized by a chemical coprecipitation technique prior to the pyrolysis process. The biochars obtained were characterized to determine their physicochemical, surface, and structural properties. The characterization revealed a porous surface with a 1013.52 m²/g area for BCM and 903.67 m²/g for BCM_Fe. The pores were uniformly distributed, as observed in SEM images. BCM_Fe showed Fe₃O₄ particles on the surface with a spherical shape and a uniform distribution. According to FTIR analysis, the functional groups formed on the surface were aliphatic and carbonyl functional groups. Ash content in the biochar was 4.0% in BCM and 8.0% in BCM_Fe; the difference corresponded to the presence of inorganic elements. The TGA showed that BCM lost 93.8 wt% while BCM_Fe was more thermally stable due to the inorganic species on the biochar surface, with a weight loss of 78.6%. Both biochars were tested as adsorbent materials for methylene blue. BCM and BCM_Fe obtained a maximum adsorption capacity (q_m) of 23.17 mg/g and 39.66 mg/g, respectively. The obtained biochars are promising materials for the efficient removal of organic pollutants.

In this study new compounds consisting of activated carbon cloths (ACC) modified with calcium silicate (CaSiO₃) were prepared for hydroxyapatite (HAP) generation. ACC samples were oxidized with 8 M HNO₃ at different times (15 min and 2 h), to increase oxygenated functional groups. The CaSiO₃ fine powders were prepared by chemical coprecipitation using Ca(NO₃)₂∙4H₂O and Si(OC₂H₅)₄, and 5 M NaOH was used as precipitant. The resulting powders were mixed with ethanol by ultrasound stirring and the previously oxidized activated carbon fibers were placed leaving under stirring for 30 min to allow particle dispersion. Once the formed compounds were dried, the samples were immersed in a simulated body fluid (SBF) solution for 21 days in conical tubes at 36.5 °C to allow the HAP formation on the ACC/CaSiO₃ composite surface. The results indicated that the increase in oxidation time improves HAP formation on the surface from ACC/CaSiO₃ compounds and this bioactive composite may be a potential material for bone regeneration.

Many adsorbent materials are now commercially available; however, studies have focused on modifying them to enhance their properties. In this study, an activated carbon (AC) and hydroxyapatite (HAp) composite was synthesized by the immersion of ACs in a simulated body fluid solution, varying the AC oxidation degree along with the addition of CaSiO₃. The resulting composites were characterized by ash %, X-ray fluorescence (XRF), Fourier-transformed infrared spectroscopy (FTIR), scanning electron microscopy (SEM), and point of zero charge (PZC). The characterization results indicated that the addition of CaSiO₃ and the oxygenated functional groups in the AC surface are key factors for HAp growth. The composites were tested on methylene blue (MB) adsorption as a potential application for the synthesized materials. Adsorption isotherms were modeled with Langmuir and Freundlich isotherms, and the composites were fitted to a Langmuir model with the highest q_max value of 9.82. The kinetic results indicated that for the pseudo-second-order model, the composites fitted, with a contact time of 180 min to remove a 95.61% average of the MB. The results indicate that composite materials can be an efficient adsorbent for the removal of MB from aqueous solutions at low concentrations since the material with the highest amount of HAp growth removed 99.8% of the MB in 180 min.

The presence of calcium sulfate in the process water during the coal flotation greatly influences the recovery and selectivity of the separation. The concentrations of calcium and sulfate ions modify mineral hydrophobicity by altering surface properties resulting in depression or activation of the mineral species. An investigation to evaluate the statistical significance of the effect of the pH and concentration of calcium and sulfate ions on coal flotation was carried out; for this purpose, a 2³ factorial design was implemented. A p-value < 0.05 was determined for the effect of calcium and sulfate ion concentrations, indicating that it is statistically significant. The interactions between factors (pH × calcium, pH × sulfate, calcium × sulfate and pH × calcium × sulfate) are also statistically significant, but the interaction between the concentration of calcium and sulfate ions has a notable influence according to the F statistic value. Employing 800 and 1920 mg/L of calcium and sulfate ions as experimental conditions yields a recovery of 90.4% with a concentrate containing 13% ash.