The main purpose of this research was to explain the differences in the adsorption mechanisms and adsorption capacities of natural and Fe(III)-modified zeolite for Pb2+, Zn2+ and Cd2+ ions. The adsorbents were characterized with respect to their phase composition, morphology, specific surface area, cation exchange capacity and point of zero charge. Batch adsorption experiments were performed as a function of the initial ion concentration and temperature, at constant initial pH value of 5.5 ? 0.1. The adsorption isotherms at 25, 40, 55 and 70?C suggest that the sequence of adsorption efficiency of both zeolites is Pb2+ > Zn2+ > Cd2+. The adsorption capacities of both zeolites increased with increasing temperature. The equilibrium adsorption data were best described by the Langmuir adsorption isotherm. This study revealed that the adsorption capacity of the Fe(III)-modified zeolite is much higher than that of natural zeolite for all investigated ions owing to the higher: specific adsorption caused by the new functional groups formed on the zeolite surface; ion exchange due to the presence of easily exchangeable ions; and hydroxide precipitation caused by higher point of zero charge of the Fe(III)-modified zeolite compared to natural zeolite.

Composites for efficient removal of hexavalent chromium Cr(VI) from industrial wastewater were obtained by deposition of nano-zero-valent iron (nZVI), synthesized by environmentally friendly synthesis using oak leaf extract, on inexpensive, natural, readily available and cheap natural raw materials, sepiolite (SEP) or kaolinite/illite (KUb) clay, as support. nZVI particles were deposited from the FeCl₃ solution of different concentrations, with the same volume ratio extract/FeCl₃ solution (3:1), and with different masses of SEP or KUb. Physico–chemical characterization (SEM/EDS, FTIR, BET, determination of point of zero charge) of the composites and nZVI was performed. The results of SEM and BET analyses suggested more homogeneous deposition of nZVI onto SEP than onto KUb, which ensures greater availability of the nZVI surface for Cr(VI) anions. Therefore, the higher Cr(VI) removal at all investigated initial pH values (pH_i) of the solution (3, 4 and 5) was achieved with the SEP composites. The adsorption results indicated that the elimination of Cr(VI) was achieved via the combined effect of reduction and adsorption. The removal of total chromium at pH_i = 3 was approximately the same as that of Cr(VI) removal for the KUb composites, but lower for the SEP composites, indicating lower removal of Cr(III) compared to the reduced Cr(VI). The SEP/nZVI composite with the highest removal efficiency was applied for Cr(VI) removal from real wastewater at pH_i = 3 and pH_i = 5. The results demonstrated the high Cr(VI) removal capacity, validated the assumption that a good dispersion of nZVI particles is beneficial for Cr(VI) removal and showed that the produced green composites can be efficient materials for the removal of Cr(VI) from wastewater.

The restoration of large bone defects caused by trauma, tumor resection, or infection is a major clinical problem in orthopedics and dentistry because postoperative infections, corrosion, and limited osteointegration of metal implants can lead to loosening of the implant. The aim of this study was to improve the surface properties of a 3D-printed (electron beam melting) Ti6Al4V-based macroporous scaffold by multilayer coating with bioactive silicate glasses (BAGs) and hydroxyapatite doped with a silver (AgHAP) or AgHAP additionally sonochemically modified with ZnO (ZnO-AgHAP). The coated scaffolds AgHAP_BAGs_Ti and ZnO-AgHAP_BAGs_Ti enhanced cytocompatibility in L929 and MRC5 cell lines and expressed bioactivity in simulated body fluid. A lower release of vanadium ions in coated samples compared to bare Ti scaffold indicates decreased dissolution of Ti alloy in coated samples. The coated samples reduced growth of Escherichia coli and Staphylococcus aureus for 4–6 orders of magnitude. Therefore, the 3D-printed Ti-based scaffolds coated with BAGs and (ZnO-)AgHAP have great potential for application as a multifunctional implant with antibacterial properties for the restoration of defects in load-bearing bones.

The sepiolite/ZrO₂ composites were prepared by sepiolite (Sep) modification with zirconium propoxide in toluene at room temperature for 24 h (Sep–ZrI) or 95 °C for 4 h (sample Sep–ZrII). The efficiency of the obtained composites for the removal of phosphate from aqueous solutions at initial pH = 4 and pH = 8 was investigated. Characterization of the samples shows that synthesis at a higher temperature for a shorter time provides a slightly higher content of amorphous Zr phase, which is deposited on the sepiolite fibers as a thin layer and agglomerated nanoparticles. Compared to Sep, the composites have a lower point of zero charge and higher specific surface area and pore volume. The adsorption kinetics follow the pseudo second-order model. The adsorption capacities of the composites are approximately the same at both initial pH and higher at initial pH = 4 than at pH = 8. The XPS and ATR-FTIR of Sep–ZrI before and after adsorption identifies the formation of inner-sphere complexes as the mechanism of phosphate adsorption. The slow release during desorption with NaOH solution confirms the strong bonds of the phosphates with the surface of the composites.